Hansen's Disease
Comment: A few commenters thought 
that there are still sufficient cases of Hansen's disease to warrant its 
retention in the listings.
Response: We did not adopt the 
comment. The incidence (new cases per year) of Hansen's disease (leprosy) 
in the United States is very low, less than 135 in the past few years. 
Moreover, we do not need a separate listing because the dermatological and 
neurological manifestations of this disorder are addressed in the sections 
pertaining to those body systems.
9.00 and 9.09 Obesity
Comment: One comment we received 
said that we should not move the obesity listing to the endocrine system 
section, but that it should stay with the impairments in the multiple body 
system section.
Response: We did not adopt the 
comment. With the exception of obesity and Hansen's disease (which we have 
deleted), we have moved all the impairments from the adult multiple body 
systems section to the newly established "Immune System." Rather 
than keep obesity as the sole impairment in a body system, we believe that 
the most appropriate location for it would be the endocrine system, which 
is now titled: "Endocrine System and Obesity."
Comment: A comment asked whether the 
reference to the "spine" in proposed Listing 9.09A was meant to 
include the cervical and thoracic regions of the spine. Another comment 
said that the listing for obesity should state that the history of pain, 
limitation of motion, and arthritis caused by obesity in any 
weight-bearing joint or spine need only be minimal to satisfy the 
listing's requirements.
Response: We agreed with the first 
comment that the references to the "spine" in former Listing 
10.10A and proposed Listing 9.09A could be made clearer. The listing has 
always applied only to the weight-bearing parts of the spine (i.e., the 
lumbosacral regions). Therefore we have clarified the language in final 
Listing 9.09. This is not a substantive change from the prior rules or the 
NPRM, but a clarification of our intent that the phrase 
"weight-bearing" modify both "joint" and 
"spine" in the listing.
We did not adopt the second comment because it is implicit in the language 
of the rule. The fact that the degrees of pain,limitation of motion, and 
arthritis in the weight-bearing structures are not quantified indicates 
the intentional absence of threshold criteria.
Comment: A comment stated that the 
adult obesity listing is inadequate for assessing obesity in children. The 
comment also suggested that we consult with pediatricians to develop a 
childhood obesity listing by which to assess whether a child is 
functioning independently, appropriately, and effectively in an 
age-appropriate manner.
Response: We did not adopt the 
comment because the creation of a childhood obesity listing is beyond the 
scope of these rules. When we consider revising the childhood endocrine 
section, we will consider whether we need to add a listing for 
obesity.
14.00 and 114.00 
Immune System—Non-HIV Listings
Connective Tissue Disorders—General Comments
Comment: One comment stated that the 
term "rheumatic diseases" better describes conditions such as 
juvenile arthritis, systemic lupus erythematosus, dermatomyositis, and 
scleroderma than does the term "connective tissue 
disorders."
Response: We did not adopt the 
comment. Inflammatory arthritides (which are types of connective tissue 
disorders), including rheumatoid arthritis, psoriatic arthritis, Reiter's 
syndrome, and ankylosing spondylitis, are included in the musculoskeletal 
body system listings in 1.00 and 101.00. Therefore, we prefer the term 
"connective tissue disorders" because it better describes the 
disorders in 14.00 and 114.00.
Comment: Another comment said that 
systemic lupus erythematosus, systemic sclerosis, and polymyositis are 
rheumatic disorders that should be retained under the multiple body system 
section, or grouped into a new section titled, "Rheumatic 
Disorders." The comment added that any listing of the immune system 
should include multiple sclerosis and myasthenia gravis.
Response: We did not adopt the 
comment. We agree that all immune system disorders are not included in 
this listing. There are many disorders of immune regulation that are 
covered in other body systems, depending on the primary target organs. For 
example, multiple sclerosis (Listing 11.09) and myasthenia gravis (Listing 
11.12) are evaluated under the neurological body system because 
neurological dysfunction is the primary outcome of these impairments. 
However, in the immune system listings we have grouped a number of 
connective tissue disorders that are characterized by autoimmune 
abnormality.
Comment: A few commenters called for 
rheumatoid arthritis to be grouped with systemic lupus erythematosus 
(Listings 14.02 and 114.02), systemic vasculitis (Listings 14.03 and 
114.03), systemic sclerosis (Listings 14.04 and 114.04), and polymyositis 
(Listings 14.05 and 114.05). One of their comments said that the inclusion 
of rheumatoid arthritis would be consistent with our emphasis on 
functional aspects rather than labeling or diagnosis, inasmuch as the 
effects of all of these disorders on joints and internal organs are very 
similar.
Response: We did not adopt the 
comment in these final rules. However, we will consider the comment when 
we consider any revisions to the musculoskeletal body system 
listings.
Comment: A few commenters called for 
separate listing subsections for Sjögren's syndrome, sarcoidosis, 
psoriatic arthritis, Ehlers-Danlos syndrome, Marfan's syndrome, and, in 
the adult section, congenital immune deficiencies, such as genetic 
dwarfism. They also stated that consideration of Raynaud's phenomena 
should not be limited to systemic sclerosis and scleroderma. One of their 
comments suggested the addition of listings subsections for 
spondyloarthropathies, reactive arthritides, Bechet's syndrome, familial 
Mediterranean fever, and inflammatory myopathies other than polymyositis, 
such as body myositis. The comment also stated that the listings should 
consider the effects of therapy, which can cause bone thinning, pathologic 
fractures, and growth failure.
Response: We did not adopt the 
comments, but we did add guidance to 114.00B of the childhood rules in 
response to the last comment. The listings are only examples of 
impairments, not an all-inclusive list, and serve as a screening device by 
which we can quickly identify individuals who are disabled as a result of 
commonly occurring impairments. Even though they include many impairments, 
they have never been intended to include all impairments. It would not be 
feasible to attempt to provide a listing for every known disease. 
Generally, when a specific disease is not listed, we use the listing that 
provides the findings most closely analogous to the findings associated 
with the unlisted impairment.
Sjögren's syndrome is evaluated under the applicable body system depending 
on the presenting manifestation (e.g., kerato-conjunctivitis under 2.00 or 
102.00, xerostomia under 5.00 or 105.00, arthritis under 1.02 or 101.02, 
and other connective tissue involvement under 14.00 or 114.00). The most 
common rheumatic manifestation of sarcoidosis is acute arthritis, which 
may be evaluated under the musculoskeletal system (Listings 1.02 and 
101.02). When chronic arthritis occurs, the predominant impairment is due 
to involvement of the lungs, spleen, bone marrow, and bone. Hence, 
sarcoidosis, the cause of which is unknown, should also be evaluated under 
the applicable body system, depending on the disease manifestations. 
Psoriatic arthritis and spondylitis may be evaluated under 1.00, 101.00, 
or 8.00. Raynaud's phenomena are seen in several connective tissue 
disorders, but are particularly common in systemic sclerosis (Listings 
14.04 and 114.04) and undifferentiated connective tissue disorders 
(Listings 14.06 and 114.06). When they occur in these or other connective 
tissue disorders and are characterized by digital ulceration, ischemia, or 
gangrene, equivalence to Listing 14.04 or 114.04 could be found.
Although Ehlers-Danlos syndrome and Marfan's syndrome are connective 
tissue disorders, they are not immune disorders, but genetic disorders, 
and, therefore, should not be included in the immune system listings. 
These syndromes are evaluated under the listings for the affected body 
system, (e.g., cardiovascular, visual, musculoskeletal, 
gastrointestinal).
Listings 14.07 and 114.07 provide criteria for immunoglobulin deficiency 
states and non-HIV cell-mediated immune deficiency. Myositis and myopathy 
may occur in a wide spectrum of diseases, and should be evaluated under 
the body system applicable to the primary disorder associated with the 
myopathy (e.g., 6.00 or 106.00 for hyperthyroidism, 11.00 or 111.00 for 
myasthenia gravis, or 14.00 or 114.00 for connective tissue disorders). 
Equivalence to 14.05 or 114.05, polymyositis, may be found when the 
criteria are applicable but the cause of the myopathy is other than 
polymyositis. Muscle weakness associated with myopathies may also manifest 
equivalent severity under the neurological listings. Spondyloarthropathies 
and "reactive" arthritides may be evaluated under 1.00 or 
101.00. Bechet's syndrome is rare, its manifestations diverse, and 
etiology unknown. The major findings are genital and oral ulcers, skin 
lesions, and ocular lesions. Evaluation should be under the applicable 
body system for the manifestation(s). Mediterranean fever is an inherited 
disorder and not due to immune dysregulation. It is characterized by 
acute, self-limited attacks of fever, abdominal pain, pleuritic pain and, 
occasionally, arthritis. Evaluation for equivalence under rules applicable 
to other episodic illnesses is appropriate.
We do consider the effects of treatment in all cases. The fifth paragraph 
of 14.00B (both in the NPRM and the final rule) indicates that in addition 
to the limitations caused by the connective tissue disorder itself, the 
chronic adverse effects of treatment may result in functional loss. 
However, even though this principle is fundamental to all disability 
adjudications, the last comment made us realize that we had stated it 
explicitly in the preface to the adult rules but not in the preface to the 
childhood rules. Therefore, in response to the comment, we have added a 
new fourth paragraph to final 114.00B which is identical to the 
corresponding paragraph in the adult rules and underscores the need to 
consider the adverse effects of treatment (such as corticosteroid therapy) 
when evaluating connective tissue disorders in children.
Comment: We received a comment 
stating that because of the vast number of rare "orphan 
diseases," the primary factor that we should use to determine 
disability should be functional limitations caused by symptoms of any 
etiology.
Response: As noted previously, the 
listings are only examples of commonly occurring impairments and are not 
intended to include all impairments, especially rare ones. Many listings, 
including final Listings 14.02-14.06 and 114.02-114.06 do include 
functioning among their criteria; when we use these listings for 
comparison to evaluate unlisted impairments, we also consider functioning 
within the context of the listings. Moreover, for children who apply for 
SSI benefits based on disability, we also provide a "functional 
equivalence" determination.
Even if the individual's severe impairment(s) does not meet or equal in 
severity any listing, we still always assess the functional limitations 
caused by the impairment(s) and use that assessment to determine whether 
the individual is disabled at the later steps of the sequential evaluation 
processes for adults and children. As with all claims where the individual 
has a severe impairment(s) that does not meet or equal the severity of a 
listed impairment, the individual's claim is evaluated further and 
residual functional capacity is assessed to determine if he or she has the 
ability to do past relevant work. If the individual cannot perform his or 
her past work, we will determine if there are other jobs the individual 
can perform. In the case of a child under 18 who is applying for SSI, we 
perform an individualized functional assessment to determine if he or she 
is able to function independently, appropriately, and effectively in an 
age-appropriate manner.
Comment: One comment said that, 
beyond the information needed to make a medical diagnosis, there should be 
more specific guidelines in the listings on assessing function because of 
the imperfect relationship between a person's capacity and his or her 
function.
Response: We did not adopt the 
comment. We already have very detailed standards on assessing function for 
all impairments. The instructions address the need to consider the 
specific effects of each person's impairment(s) on his or her ability to 
function and recognize that one individual's limitations may differ from 
another's even though they may have the same impairment(s).
Comment: Another comment suggested 
adding listing criteria for chronic fatigue syndrome which, the comment 
said, is an immunological disorder that affects millions of 
individuals.
Response: We did not adopt the 
comment. Due to the divergence of medical opinion on chronic fatigue 
syndrome, we do not believe that it is either possible or appropriate to 
establish listing criteria. Further, such a listing would be beyond the 
scope of these rules.
Comment: One comment questioned 
whether adults who have impairments that would meet the childhood criteria 
may be found disabled using the part B criteria. The comment also asked if 
children who have impairments that meet the childhood criteria will remain 
eligible upon attainment of age 18, or whether they will then have to 
demonstrate that they have impairments that meet the part A 
criteria.
Response: As set forth in 
§§ 404.1525(b)(2) and 416.925(b)(2) of our regulations, the 
criteria in part B apply only to the evaluation of impairments in persons 
under age 18. Therefore, the listings in part B may not be used to find an 
adult disabled.
We do not require children to reestablish disability based on adult 
criteria when they attain age 18. However, we do periodically review the 
claims of disabled people to determine whether they are still disabled. 
When we determine whether disability continues, we apply a medical 
improvement review standard required by the statute. Under this standard, 
if a beneficiary who is now an adult was most recently found disabled (or 
still disabled) because his or her impairment(s) met the childhood 
criteria, we use those childhood criteria, even after the individual has 
attained age 18, as a basis of comparison to determine whether there has 
been any medical improvement in the individual's impairment(s) that is 
related to the ability to work.
14.00A and B, and 114.00A and B 
Preface
Comment: One comment said that the 
discussion on polymyositis and dermatomyositis in 14.00B4 omitted any 
other inflammatory myopathies and implies that if there is weakness, pain 
or tenderness in any muscles other than the proximal limb-girdle, 
cervical, cricopharyngeal, or intercostal muscles or the diaphragm, then 
one does not meet this criterion.
Response: We accommodated the 
comment by indicating in final 14.00B4 that the descriptions are only 
meant to describe the criteria in Listing 14.05. The muscles described in 
Listing 14.05 and in final 14.00B4 are the ones usually involved in 
polymyositis or dermatomyositis. If other muscles are involved, the 
underlying disorder—which may not be polymyositis—should be 
identified if possible and considered under the appropriate body system 
listings. If the impairment is found to be severe at the second step of 
the sequential evaluation processes but does not meet or equal in severity 
any listing at the third step of the processes, we will do an 
individualized assessment of its impact on the person's functioning and 
decide disability at the last steps of the sequential evaluation 
processes.
Comment: Another comment stated that 
weight loss as a constitutional symptom, which is recognized in 14.00B of 
the adult listings, should also be recognized in the childhood 
listings.
Response: We did not adopt the 
comment because the proposed childhood listings already included weight 
loss in the fourth paragraph of proposed 114.00B. That same language 
appears in the last sentence of final 114.00B.
14.02-14.06 and 114.02-114.06 
Connective Tissue Disorder Listings
Comment: One comment noted that the 
phrase "with the expectation that the disease will remain active for 
12 months" appeared repeatedly in the proposed connective tissue 
disorder listings (in proposed Listings 14.02-14.06 and 114.02) and asked 
how we make such a prediction. The comment said that unless we describe 
how physicians are to make the prediction, claimants who have had active 
disease for 10 or 11 months will be denied benefits.
Response: Even though we disagree 
with the conclusion that we would deny claims filed by individuals who 
have had active, listing-level disease for almost a year, we partially 
adopted the aacomment. We frequently make findings of disability based on 
an expectation that a disabling impairment(s) is expected to last for at 
least 12 months. In most cases in which the evidence substantiates a 
finding of disability, it is readily apparent from the same evidence 
whether or not the impairment is expected to last 12 months from the onset 
of disability. When the application is being adjudicated before the 
impairment has lasted 12 months, the nature of the impairment, the 
therapeutic history, and the prescribed treatment serve as the basis for 
concluding whether the impairment is expected to continue to prevent the 
individual from working for the required 12 months' duration.
However, we are not describing this in the listings because it is 
longstanding practice that applies to all types of impairments, not just 
connective tissue disorders.
This comment and others made us realize that the discussions on duration 
in proposed Listings 14.02-14.06 and 114.02 made the proposed listings 
unnecessarily complex. More importantly, they only repeated the general 
listings requirements in §§ 404.1525(a) and 416.925(a). There 
is, therefore, no reason to repeat the provision in each of these 
listings. Therefore, in response to this and other comments, we removed 
the repetitive language from each of the proposed listings and added a 
single discussion on duration in 14.00B and 114.00B as a reminder of the 
basic rules. For consistency, we also removed the statements in each of 
the listings requiring a 3-month longitudinal clinical record, inasmuch as 
we already make the statement in 14.00B and 114.00B. We also moved the 
requirement that the disorder remain active, "despite prescribed 
therapy" into the same sections of the preface. (We also changed the 
word "therapy" to "treatment" for reasons explained 
elsewhere in this preamble.) The result is that final Listings 14.02-14.06 
and 114.02 are much simpler to read, even though there is no substantive 
change in the rules as a result of these editorial changes.
Finally, we will not generally find an individual who has had active, 
listing-level disease for 10 or 11 months to be not disabled. Unless the 
impairment has significantly improved to the point at which it is no 
longer disabling at the second, fourth, or fifth steps of the sequential 
evaluation process for adults (or the second or fourth steps of the 
sequential evaluation process for children claiming SSI benefits) before 
the end of 12 months after onset, an allowance would be appropriate. We 
are confident that our adjudicators understand this principle.
Comment: A comment suggested 
editorial changes to the statements regarding duration in Listings 14.02 
and 14.03, apparently to remove redundancies.
Response: We adopted the comment in 
part by moving references pertaining to durational requirements from all 
of the listings that used this language to one location in 14.00B and 
114.00B.
Comment: One comment we received 
said that there were problems with including in Listing 114.02A 
cross-references to other listings criteria as a means of describing the 
multiple organ dysfunction of systemic lupus erythematosus. The comment 
said that the type and pattern of organ involvement in systemic lupus 
erythematosus is not always the same as in other disorders and that muscle 
involvement in scleroderma and systemic sclerosis is not necessarily 
similar or identical to the muscle involvement of polymyositis or 
dermatomyositis. The comment also questioned the propriety of referencing 
some of the childhood connective tissue disorders to adult criteria 
because the disorders are not always identical in children and 
adults.
Response: We did not adopt the 
comment. Connective tissue disorders may involve many different organs and 
body systems. Establishing specific criteria for every organ in each body 
system would make the listing unnecessarily complicated. Consequently, we 
believe that cross-references to existing listings are the best solution. 
We cross-referenced the childhood systemic lupus erythematosus listing 
(final Listing 114.02) to other body systems, the scleroderma and systemic 
sclerosis childhood listing (final Listing 114.04) and polymyositis and 
dermatomyositis childhood listing (final Listing 114.05) to the 
corresponding adult rules in final Listings 14.04 and 14.05, and the 
childhood undifferentiated connective tissue disorders listing (final 
Listing 114.06) to the childhood listings for systemic lupus erythematosus 
and systemic sclerosis and scleroderma (final Listings 114.02 and 114.04), 
because their manifestations can be identical, even though the causes of 
the problems are not the same. Cross-referencing provides a means to find 
the existence of a disabling impairment when a single manifestation of 
disease is at the same level of severity described in the cross-referenced 
listing.
Comment: A comment asked whether 
severe fatigue, fever, malaise, and weight loss must all be present to 
satisfy the criteria in Listings 14.02B, 14.03B, and 14.04B (and, 
presumably, 114.02B).
Response: We adopted the comment. 
The parenthetical "e.g." in the proposed rules was an error. We 
have corrected final Listings 14.02B, 14.03B, 14.04B and 114.02B to show 
that all four symptoms and signs must be present. However, instead of 
replacing the proposed "e.g." with "i.e.," as we 
originally intended, we have revised the sentence to make our intent 
clearer. The final provisions state that the disorders must be "* * * 
associated with significant constitutional symptoms and signs of severe 
fatigue, fever, malaise, and weight loss." We chose the particular 
symptoms and signs shown in the listings because they are the most common 
and are most likely to be present.
Comment: Another comment asked that 
we define the terms "severe" and "moderate" used 
throughout the listings for connective tissue disorders.
Response: We did not adopt the 
comment. Even though, as we explain later, we changed the term 
"severe" in places where it could have been confused with other 
terms ("incapacitating" and "major"), we retained the 
terms "severe" and "moderate" where we believe they 
are appropriate and unambiguous. The terms are widely used to describe 
relative values on a rating scale, and their meanings are commonly 
understood. But because their meanings are somewhat nonspecific, use of 
these terms in Listings 14.02, 14.03, 14.04, and 114.02 unquestionably 
requires a degree of judgment, as do many other aspects of our disability 
evaluation process. Our adjudicators are accustomed to making these 
judgments on a case-by-care bases, and we believe that attempting to 
devise specific definitions for terms that are, by their nature, 
non-specific, would only make the listings confusing. However, in response 
to this comment, we have also provided clarification in 14.00B and 114.00B 
that we use the word "severe" in these listings in its medical 
sense, not in the functional sense associated with the second step of our 
sequential evaluation processes. We explain this provision in a later 
response, below.
14.02 and 114.02 
Systemic Lupus Erythematosus
Comment: One comment noted our 
statement in proposed 14.00B1 that, "[g]enerally" the medical 
evidence will show that patients with systemic lupus erythematosus will 
fulfill the 1982 "Revised Criteria for the Classification of Systemic 
Lupus Erythematosus" of the American College of Rheumatology 
(formerly, the American Rheumatism Association). The comment also noted 
that this implies that an individual can have systemic lupus erythematosus 
and not fulfill these criteria, and asked why similar latitude is not 
provided for other conditions.
Response: We did not adopt the 
comment. We used the word "generally" because the diagnosis is 
not invariably made strictly according to the criteria. To meet the 
American College of Rheumatology diagnostic criteria for systemic lupus 
erythematosus an individual must have four manifestations out of a list of 
11 criteria, and the vast majority of people with this disorder will meet 
these criteria. However, a doctor will occasionally make a diagnosis of 
systemic lupus erythematosus when an individual has only three out of 11 
manifestations, or other findings, when it appears likely that the 
diagnosis is appropriate.
Latitude is built into all the connective tissue disorder criteria. The 
guidance in final 14.00B3 for evaluations under Listing 14.04, Systemic 
sclerosis and scleroderma does not require that any specific pattern of 
disease manifestations be present to establish the diagnosis. The criteria 
in Listing 14.04 are similar to those for the other connective tissue 
disorders, providing references to other listings. As in thoseother 
listings, it also provides alternative criteria for multisystem 
manifestations associated with constitutional symptoms and signs. This is 
also true of polymyositis, 14.00B4 and final Listing 14.05, and 
undifferentiated connective tissue disorder, 14.00B5 and final Listing 
14.06.
Systemic vasculitis, 14.00B2 and final Listing 14.03, comprises several 
diverse clinical syndromes and is characterized diagnostically by a tissue 
biopsy showing necrotizing vascular inflammation. Hence, a tissue biopsy 
or an angiogram showing the characteristic vascular abnormalities is 
necessary to confirm the clinically suspected diagnosis. However, when the 
findings of a referenced listing are present or multisystem involvement is 
evident with constitutional symptoms and signs, listing-level severity may 
be found even if there has not been a definitive diagnosis. Hence, this 
listing also provides latitude.
Comment: A few commenters said that 
they were not sure that the medical community at large is familiar with 
the 1982 "Revised Criteria for the Classification of Systemic Lupus 
Erythematosus" of the American College of Rheumatology. They 
suggested that, instead of referencing it, the material should be included 
in the listing itself or in a readily available supplement. One of their 
comments asked why we proposed to use the American College of Rheumatology 
criteria for systemic lupus erythematosus, but not for the other 
connective tissue disorders. The comment also said that most of the 
rheumatic diseases are syndromes and the diagnoses are made by meeting 
specific criteria.
Response: We did not adopt the first 
comment because we do not think that it is necessary to publish the 
diagnostic criteria in the regulations. The American College of 
Rheumatology diagnostic criteria are widely available and widely 
known.
Systemic lupus erythematosus is a relatively common disease, the diagnosis 
of which is based upon the presence of several non-specific clinical and 
laboratory abnormalities. Because of the lack of a single set of 
diagnostic findings, individuals may be erroneously diagnosed because of a 
non-specific laboratory result. It is, therefore, appropriate to refer to 
the published American College of Rheumatology diagnostic criteria. The 
vasculitides, on the other hand, are rare and difficult to diagnose 
clinically. The hallmark for and the diagnosis of vasculitis is almost 
invariably based upon characteristic clinical findings and tissue biopsy 
showing necrotizing vascular inflammation. Moreover, there are no 
published specific diagnostic criteria based upon clinical observations 
and laboratory tests. Therefore, referral to published diagnostic criteria 
is not possible.
Comment: A few commenters said that, 
because the type and pattern of joint involvement in rheumatoid arthritis 
and juvenile rheumatoid arthritis differs from that seen in systemic lupus 
erythematosus, the rheumatoid arthritis and juvenile rheumatoid arthritis 
criteria in Listings 1.02 and 101.02 should not be applied as reference 
listings to the evaluation of systemic lupus erythematosus under Listings 
14.02A1 and 114.02A2. One of their comments noted further that, if there 
is joint involvement consistent with rheumatoid arthritis or juvenile 
rheumatoid arthritis in the presence of other findings consistent with 
systemic lupus erythematosus, then, by our definition, this would be an 
undifferentiated connective tissue disorder, which should be evaluated 
under Listings 14.06 and 114.06.
Response: We did not adopt the 
comment. In referencing proposed Listing 14.02A1 to Listing 1.02, and 
proposed Listing 114.02A2 to Listing 101.02, we were providing a means to 
determine the presence of a disabling impairment when a single 
manifestation of disease is at the same level of severity as that 
described in the reference listing. We did not mean to imply that systemic 
lupus erythematosus and rheumatoid arthritis have identical 
characteristics. To make this point even clearer, we have revised the 
cross-references in the final rules to the generic body system headings, 
1.00 and 101.00, in order to include any musculoskeletal effects of 
systemic lupus erythematosus that are at the listing level of 
severity.
A diagnosis of undifferentiated connective tissue disorder is appropriate 
where the impairment has features suggestive of a connective tissue 
disorder but not diagnostic of any one disorder. We did not intend to 
suggest otherwise in Listings 14.02A1 and 114.02A2, which describe 
properly diagnosed systemic lupus erythematosus.
Comment: One comment noted that the 
adult listing for systemic lupus erythematosus included a criterion for 
muscle involvement (Listing 14.02A2), but proposed childhood Listing 
114.02 did not.
Response: In response to the 
comment, we added muscle involvement to final Listing 114.02A3. Because of 
this addition, we renumbered the subsequent criteria accordingly.
Comment: Another comment suggested 
that Listing 114.02 include cross-references to criteria in the hemic 
system and to the listings for depression and Raynaud's phenomena.
Response: We adopted the comment. 
Although proposed childhood Listings 114.02A8 and 114.02A12 did include 
cross-references to specific hemic listings (Listings 7.02 and 107.06) and 
mental disorders listings (Listings 112.02, 112.03, and 112.04), we 
revised final Listings 114.02A9 and 114.02A13 so that they refer to the 
hemic and lymphatic and mental "body systems" in general (107.00 
and 112.00), instead of to specific listings. In this way, no hemic or 
mental manifestations will be overlooked and the listing will remain 
up-to-date should we revise the hemic and mental listings in the future. 
Even though Raynaud's phenomena are not a primary feature of childhood 
systemic lupus erythematosus, we added a cross-reference to Listing 14.04D 
in final Listing 114.02A6 for those situations in which children do have 
such manifestations at the listing level. For consistency, we also added a 
cross-reference to Listing 14.04D in the corresponding adult rule, final 
Listing 14.02A5.
Comment: One comment suggested that 
in proposed Listing 14.02B the requirement that the individual demonstrate 
"severe" and "incapacitating" signs and symptoms was 
extreme, especially when a full 12 months of this level of severity must 
be anticipated.
Response: We adopted the comment in 
part. We agree that "incapacitating" is a higher level of 
severity than is needed to show listing-level severity. Furthermore, the 
comment made us realize that we had proposed slightly different language 
(using the terms "severe," "incapacitating," and 
"major") for corresponding paragraphs in proposed Listings 
14.02B, 14.03B, 14.04B, and 114.02B, when we intended to say the same 
thing in each section. Furthermore, the word "major," which we 
had proposed in Listing 14.04B, could have caused confusion because it has 
a particular meaning in the medical community, referring to kinds of 
infections. Therefore, we replaced all these terms with the word 
"significant," which conveys the intended meaning consistently 
throughout these final listings.
We also realized that referring to "severe" symptoms and signs 
in these listings could have caused confusion because "severe" 
has a specific meaning when we use the word in the phrase "severe 
impairment" to describe the functional impact of an impairment(s) 
(see §§ 404.1520, 404.1521, 416.920, 416.921, and 416.924). For 
this reason, we have added a sentence at the end of the sixth paragraph of 
final 14.00B and 114.00B to explain that we use the term 
"severe" in these listings to describe medical severity and that 
it does not have the same meaning as it does when we use it in connection 
with a finding at the second step of the sequential evaluation processes 
for adults and children.
14.03 and 114.03 
Systemic Vasculitis
Comment: One comment said that 
proposed Listing 14.03 on vasculitis was stricter and more detailed than 
then-current Listing 10.03, which required only signs of generalized 
arterial involvement.
Response: Listing 14.03 is more 
detailed than prior Listing 10.03, but the criteria are not stricter. 
Rather, they are more medically accurate and reflect state-of-the-art 
practice. They also now include all forms of systemic vasculitis, and 
ensure more consistent and valid determinations.
14.04 and 114.04 
Systemic Sclerosis and Scleroderma
Comment: A comment suggested that we 
delete the word "generalized" before "scleroderma" in 
Listing 14.04C. Another comment questioned why we provided a listing for 
linear scleroderma for children (Listing 114.04B) but no similar listing 
for adults, and noted that 14.00B3 omits mention of the differences 
between limited and diffuse scleroderma.
Response: We have retained the term 
"generalized" in final Listing 14.04C because adults rarely 
manifest localized scleroderma; if they do, equivalence to a listing in 
1.00 or a residual functional capacity assessment may lead to a finding of 
disability because of destructive or mutilating lesions of the extremities 
or the head. We provided criteria for localized scleroderma for children 
because destructive and mutilating lesions involving the extremities, 
head, and scalp not only interfere with walking and using the upper 
extremities, but also with growth and development; scalp and facial 
lesions in children may also be accompanied by seizures.
"Limited" cutaneous scleroderma is not the same thing as 
"localized" or "linear" scleroderma, but a systemic 
form of the disorder. We did not mention the differences between limited 
and diffuse cutaneous scleroderma in the preface because the differences 
are not needed for application of the criteria in final Listings 14.04 and 
114.04.
Comment: A comment said that, 
although severe Raynaud's phenomena were included in the proposed Listing 
14.04D criteria, they were not defined.
Response: We have clarified the 
listing in response to the comment. In fact, proposed Listing 14.04D did 
describe severe Raynaud's phenomena, which are characterized by digital 
ulcerations, ischemia, or gangrene. However, we realized that the language 
of the proposed rule, "Raynaud's phenomena with" these findings, 
was not clear. We have, therefore, changed the word "with" to 
"characterized by" in the final listing to make clear that the 
findings of digital ulcerations, ischemia, or gangrene define severe 
Raynaud's phenomena.
14.05 and 114.05 
Polymyositis and Dermatomyositis
Comment: One comment stated that 
proposed Listing 14.05, for polymyositis and dermatomyositis, was too 
strict. The comment said that an individual who satisfied the criteria in 
the opening paragraph of the listing (which required 3 months of active 
disease, severe proximal muscle weakness despite prescribed treatment, and 
an expected duration of 12 months) should be found to meet the listing 
without also having to satisfy the criteria in proposed Listing 14.05A or 
14.05B.
Response: We partially adopted the 
comment. The commenters misunderstood our intent in proposed Listing 
14.05. The criteria in proposed Listings 14.05A and 14.05B were not 
additional criteria, but were meant to define the "severe proximal 
muscle weakness" in the opening paragraph. However, the comment made 
us realize that the listing could be made clearer. Therefore, we 
have clarified the requirements in final Listing 14.05 by removing 
the opening paragraph, which was redundant of the criteria for 
documentation, duration, and severity, discussed in other parts of the 
listings, and which is now in final 14.00B.
Comment: Another comment suggested 
that we provide more detail about the required severity of proximal muscle 
weakness. The comment said that proposed Listing 14.05 required shoulder 
or pelvic muscle weakness as described in Listing 11.12, which pertains 
only to muscle weakness of the extremities. The comment also questioned 
how swallowing and impairment of respiration are to be evaluated under 
Listings 14.05B1 and 14.05B2.
Response: In response to the 
comment, we deleted the cross-reference to Listing 11.12B in final Listing 
14.05A and instead provided a discussion of the intent of the provision in 
final 14.00B4. We also provided a more detailed description of the 
criteria in final Listing 14.05B1 for cricopharyngeal weakness. However, 
we think that proposed Listing 14.05B2 was clear and have made no changes 
in that final listing.
Comment: Another comment questioned 
why there was no adult listing corresponding to Listing 114.05B for 
polymyositis or dermatomyositis with severe multiple joint contracture or 
diffuse cutaneous calcification, and why swallowing or respiratory 
difficulties are limited to adult Listing 14.05B1.
Response: Both multiple joint 
contractures and diffuse cutaneous calcification are extremely uncommon 
findings in adults with these disorders; however, if an adult has these 
findings their specific impact on the individual must be assessed. 
Multiple joint contractures in an adult that are of listing-level severity 
should be evaluated under the criteria in 1.00ff, the musculoskeletal body 
system. Listing-level cutaneous calcification may be evaluated under 
Listing 14.04, Systemic sclerosis and scleroderma.
Swallowing and respiratory difficulties are not limited to Listing 14.05B. 
Childhood Listing 114.05A indicates that impairment should be evaluated 
according to Listing 14.05. Therefore, all of the criteria in Listing 
14.05 apply to children.
14.06 and 114.06 
Undifferentiated Connective Tissue Disorder
Comment: One comment questioned 
whether the term "undifferentiated connective tissue disorder" 
used in Listings 14.06 and 114.06 is synonymous with "mixed 
connective tissue disorder." The comment also questioned why chronic 
undifferentiated tissue disorder is evaluated by reference to the criteria 
in Listing 14.02, Systemic lupus erythematosus, and stated that the 
disorder is either systemic lupus erythematosus or it is not.
Response: We partially adopted the 
comment. We added a discussion of overlap syndromes to final 14.00B5 
(which is also referred to in 114.00B) and noted that these syndromes 
should be evaluated under Listings 14.06 and 114.06. Although most 
individuals with undifferentiated connective tissue disorders have 
features of systemic lupus erythematosus, we recognize that some may have 
features of systemic sclerosis and scleroderma. Therefore, we added to 
Listings 14.06 and 114.06 cross-references to Listings 14.04 and 114.04. 
However, we prefer to confine Listings 14.06 and 114.06 to 
undifferentiated connective tissue disorders to indicate the lack of a 
specific diagnosis, with its attendant specific prognosis. We also have 
retained the title.
Comment: Another comment stated that 
there is a distinction between the undifferentiated connective tissue 
disorders (i.e., where a connective tissue disorder is present but 
unknown) and the overlap syndromes (i.e., where there are elements of more 
than one connective tissue disorder present). This comment also said that 
both types should be recognized under the listing and that, because some 
of these disorders are not undifferentiated, Listings 14.06 and 114.06 
should be titled: "Other Connective Tissue Disorders."
Response: We did not adopt the 
comment, except to the extent that we added the aforementioned discussion 
about overlap syndromes to final 14.00B5. "Undifferentiated 
connective tissue disorder" is similar to, but not synonymous with, 
"overlap syndrome" and "mixed connective tissue 
disorder," but the latter two classifications depend upon 
constellations of non-specific features. Undifferentiated connective 
tissue disorders have the clinical and immunologic features of several 
connective tissue disorders, none of which satisfies the criteria for any 
of the disorders described. Overlap syndromes have clinical features of 
more than one established connective tissue disorder, and mixed connective 
tissue disorders usually have features of systemic lupus erythematosus, 
systemic sclerosis, and myositis. Most individuals with mixed connective 
tissue disorders eventually will be shown to have either systemic lupus 
erythematosus, systemic sclerosis, or Sjögren's syndrome, but a few remain 
undiagnosed and should be labeled "undifferentiated."
Comment: A comment stated that the 
criteria for evaluation of childhood undifferentiated connective tissue 
disorders in Listing 114.06 were a confusing series of cross-references, 
noting that Listing 114.06 referred to evaluation under corresponding 
adult Listing 14.06 which, in turn, referred to Listing 14.02.
Response: We adopted the comment. 
Final Listing 114.06 now indicates that undifferentiated connective tissue 
disorders should be evaluated by reference to Listings 114.02 or 
114.04.
14.07 and 114.07 
Immunoglobulin Deficiency Syndromes or Congenital Immune Deficiency Disease
Comment: One comment said that the 
criteria for the evaluation of immune deficiency disease in Listings 14.07 
and 114.07 are too restrictive because they consider only immunoglobulin 
deficiency syndromes or deficiencies of cell-mediated immunity, and 
exclude other immune deficiencies or immune dysregulatory states. The 
comment also noted our statement in proposed 14.00A that the " * * * 
disorders include impairments involving deficiency of one or more 
components of the immune system * * *." The comment said that, 
although a number of examples are listed in this section, many of the 
potential immune system impairments are absent from Listings 14.07 and 
114.07.
Response: We did not adopt the 
comment. As we have stated, the listings are only examples of commonly 
occurring impairments, and are not meant to be all-inclusive. 
Immunoglobulin deficiency syndromes or deficiencies of cell-mediated 
immunity are the most common immune deficiencies. Immune deficiency 
disorders not specified in Listing 14.07 or 114.07, but that are of 
listing-level severity, may be found equivalent in severity to the listed 
14.00 and 114.00 Immune System: General Comments On The HIV Listings
Populations Covered By the Rules
Comment: Various commenters asserted 
that the proposed rules did not include manifestations of HIV infection 
that affect women, persons of color, gay and lesbian people, and the 
poor.
Response: On the basis of 
information we received from individual medical and other experts who 
study, treat, and work with people who have HIV infection, as well as our 
review of the medical literature, we do not agree that the proposed rules 
excluded these groups of people. Based on our experience since December 
17, 1991, using our revised operating procedures, we know that the 
proposed listings would have included the vast majority of people who were 
disabled by HIV infection. Nevertheless, as we have already explained 
above in the summary of the final provisions, we have further revised the 
final listings to make them even more inclusive. Among the new criteria 
are several new criteria in both the adult and childhood listings that 
include more of the manifestations of HIV infection unique to women and 
girls. We are confident that these final rules provide criteria for 
evaluating all of the manifestations of HIV infection suffered by various 
populations.
Comment: One of the comments said 
that the proposed listing did not recognize the medical conditions that 
affect drug abusers, and that some chronic conditions were not 
listed.
Response: This comment did not 
identify any additional conditions that were not listed. The 
manifestations in proposed Listing 14.08M2 (with the exception of Kaposi's 
sarcoma), as well as many others throughout the proposed listing, are 
conditions that affect drug abusers. The conditions in proposed Listing 
14.08M2 are now in the final rules as stand-alone medical listings, 
without functional requirements.
Comment: Many commenters thought 
that, despite our assertion to the contrary in the NPRM (56 FR at 65703), 
the proposed rules had not broken the link to the CDC surveillance 
definition of AIDS. They said the listings were unfair and discriminatory 
to women, poor people, those who do not have CDC-defined AIDS, and those 
with no continuity of health care. They indicated that, although we had 
proposed to include manifestations that the CDC uses to define AIDS 
without functional criteria, other illnesses (the kind not associated with 
CDC-defined AIDS, but frequently found in women, intravenous drug users 
and others who tend to be poor and have limited access to health care) 
required that functional criteria be met.
Response: We disagree with the 
comments, but we have revised the rules in response to these and other 
comments to explicitly include even more manifestations without a 
functional requirement. Therefore, even though we have included many of 
the criteria of the CDC's surveillance definition of AIDS, we have also 
provided many other criteria for people who have symptomatic HIV infection 
but who do not meet the CDC surveillance definition.
For example, we added as stand-alone conditions as many HIV-related 
conditions from proposed Listings 14.08M and 114.08L and 114.08M as 
possible, including endocarditis, syphilis and neurosyphilis, meningitis, 
pulmonary tuberculosis, and pneumonia. These manifestations are not 
stand-alone criteria in the CDC surveillance definition of AIDS but, we 
believe, can be sufficiently severe to be disabling in an individual with 
HIV infection. In addition, we created a stand-alone listing that includes 
pelvic inflammatory disease (final Listings 14.08A5 and 114.08A6) and 
another that includes vulvovaginal candidiasis (final Listings 14.08F and 
114.08F).
Standard of Disability
Comment: Many commenters believed 
the proposed listings did not take into account the progressive nature of 
HIV infection in adults or children. They suggested that claimants with 
HIV infection should be found disabled at commensurately lower levels of 
severity than claimants with other diseases. A few commenters suggested 
that we adopt the broadest permissible definition of disability so as to 
get medical care to as many HIV-infected individuals as early as possible. 
They said this was important because the degenerative nature of 
HIV-related conditions guarantees that if someone is nearly disabled 
today, he or she will become disabled in the near future. One of their 
comments said that, although our stringent disability standards make sense 
with impairments that are relatively stable and capable of improvement, 
such eligibility requirements are less necessary when dealing with rapidly 
degenerative illnesses such as those associated with HIV. This is because 
there is little need to consider whether applicants will remain ill long 
enough to be classified as disabled—those impaired by such illnesses 
simply do not get better. Another comment noted that, only through a 
combination of Federal, State and local funding could early treatment and 
care, including drug trials, be provided, and that tightening the listing 
criteria would result in the City and State governments bearing the entire 
responsibility for this continuum of care.
Some commenters cited the rapid deterioration experienced by children with 
HIV infection, and the fact that few of these children live to adulthood, 
especially those who acquire the virus from their mothers. The commenters 
said that our childhood neoplastic listings (i.e., the listings in 113.00) 
permit a finding of disability before marked functional loss has occurred 
and thus set a precedent for doing something similar in the case of 
children with HIV infection.
Response: We believe that these 
rules provide the broadest permissible definition of listing-level 
severity, consistent with the definition of disability contained in the 
Act. Moreover, we do not have the authority to apply a different 
definition of disability for some people than the standard of disability 
in the Act. The Act requires that an individual be currently disabled, and 
does not permit us to find an individual disabled based on a prediction of 
future disability.
However, these rules are not stricter than our previous criteria. To the 
contrary, both the proposed rules and these final rules provide more ways 
in which people with HIV infection may establish that they have 
listing-level impairments.
Our criteria take into account the unique course and history of HIV 
disease in both adults and children, including its progressive nature. In 
cases in which a claimant is experiencing a manifestation(s) of HIV 
disease that is indicative of a rapid decline in an adult's ability to 
engage in any gainful activity, or an SSI child claimant's ability to 
function independently, appropriately, and effectively in an 
age-appropriate manner, we have defined criteria that do not necessarily 
require continuous HIV are rapidly degenerative, or that individuals with 
HIV functional loss following the onset of the initial manifestation. 
Rather, the manifestation of HIV infection can be found disabling even 
though it includes periods of improvement. However, even though HIV 
infection is progressive and ultimately fatal, it is not true that all 
illnesses or other manifestations associated with infection cannot recover 
from HIV-related manifestations. Many manifestations are treatable, and 
many individuals can return to a good level of functioning following a 
period of severe illness. The impact of HIV and its manifestations is 
highly individual, and our disability adjudication system, which affords 
an individualized determination to every claimant, recognizes this.
We believe that this approach is consistent with the approach we take in 
the neoplastic listings. Neither the HIV listings nor the neoplastic 
listings describe impairments of lower severity than other listings. 
Rather, they recognize the medical realities of the conditions in terms of 
prognosis, overall functioning on a longitudinal basis, and the impact of 
treatment on functioning.
It is also very important to remember that no individual will be denied 
benefits simply because his or her impairment(s) does not meet or equal 
the severity of a listing. If an individual's impairment(s) does not meet 
or equal the severity of a listing, he or she can be found disabled at 
later steps of the sequential evaluation processes for adults and 
children.
Finally, we want to assure the commenters that we share their concerns, 
and are aware of the poor prognosis for individuals with HIV infection. We 
believe the promulgation of these listings addresses those concerns.
Comment: Some commenters thought 
that we should find any individual with symptomatic HIV infection to be 
disabled.
Response: We do not agree that any 
individual with symptomatic HIV infection of any type should be found 
disabled. There are, in fact, many such conditions that are amenable to 
treatment without significant after-effects, and others that are simply 
not so severe as to render an individual unable to work or unable to 
engage in age-appropriate activities. In both instances individuals may 
continue to function well for long periods, and we believe that it is 
reasonable to provide regulatory criteria that allow for the 
individualized assessment of the effects of a person's impairment(s) on 
him or her, as we have done in final Listings 14.08N and 114.08O.
Comment: A few commenters said that 
the criteria for HIV infection should recognize that persons who have 
asymptomatic HIV infection should have the right to treat their condition 
and prolong their lives through rest and stress reduction, and not be 
exposed to further compromise of their medical condition in a 
workplace.
Response: We did not adopt the 
comment. The standard of disability for adults under the statute is the 
inability to engage in substantial gainful activity by reason of a 
medically determinable physical or mental impairment(s), or for children 
under age 18 who apply for SSI based on disability an impairment(s) of 
comparable severity to one that would disable an adult. Even though we 
agree that people who have asymptomatic HIV infection will ultimately 
become ill, they are not functionally limited until the infection begins 
to become symptomatic; i.e., until they begin to experience manifestations 
of the HIV infection. Once individuals do become symptomatic, however, 
these rules do not require that they be continuously symptomatic. The 
rules require that their impairments be evaluated on a longitudinal basis 
in order to form a picture of how the individual is able to function over 
time. Indeed, we have provided a separate listing, final Listing 14.08N, 
that includes individuals who suffer periodic manifestations of HIV 
infection but who may not be continuously limited between the 
episodes.
We would also like to clarify that we do not require people to work. The 
Act uses the ability to work as a way of describing the level of severity 
of impairment that constitutes a "disability." The Act does not 
say that a person who does not meet the definition of disability must 
work; it simply says that such a person is not disabled within the meaning 
of the Act. Indeed, to underscore this point, the statute explicitly 
excludes from consideration the factors of whether a job exists in the 
area in which the person lives, whether there are job openings, or whether 
the person would be hired to do a job. Thus, the listings are not intended 
for use in determining whether or not an individual should work, but to 
provide examples of impairments that satisfy the definition of disability 
in the Act because they are considered severe enough to prevent an adult 
from engaging in any gainful activity, or an SSI claimant under the age of 
18 from functioning independently, appropriately, and effectively in an 
age-appropriate manner.
Comment: One comment said that any 
claimant whose physician reports positive HIV infection and a resulting 
inability to work should be considered disabled, regardless of whether or 
not the individual presents opportunistic infections.
Response: We did not adopt the 
comment. As we have said, an individual with asymptomatic HIV infection 
will not be functionally limited by the impairment. Under our rules for 
evaluating medical opinion evidence in §§ 404.1527(e) and 
416.927(e), the Secretary is responsible for determining whether an 
individual is "disabled" under the Act; a statement by a medical 
source that the individual is "unable to work" is not sufficient 
in itself to establish that an individual is disabled within the meaning 
of the Act. However, in making our determination, we review all of the 
medical findings and other evidence in the individual's case record that 
support a medical source's statement that the individual is disabled and 
will recontact the source, if necessary, to obtain additional information 
in support of the opinion.
Comment: A number of commenters 
suggested that we give special consideration to the 
"socioeconomic" factors that can affect HIV-infected claimants, 
such as poor nutrition, limited or no access to ongoing health care, 
inadequate housing, and adverse family factors.
Response: We did not adopt the 
comments, but we have revised several provisions in response to these and 
other comments to make clear that we do consider some of the factors the 
commenters suggested, though not as "socioeconomic" 
factors.
The Act requires that disability must be established on the basis of a 
medically determinable physical or mental impairment(s) that results from 
anatomical, physiological, or psychological abnormalities which are 
demonstrable by medically acceptable clinical and laboratory diagnostic 
techniques. It does not permit direct consideration of 
"socioeconomic" factors as determinants of disability. For 
example, under the Act we cannot consider whether a claimant lives in 
inadequate housing or receives substandard medical care in making a 
disability determination.
However, we do consider some of the factors the commenters believed to be 
"socioeconomic" factors because they are medical factors under 
our program. For example, under our program poor nutrition (i.e., 
malnutrition) is a medical condition and can be a disabling impairment in 
and of itself if it is of sufficient severity and duration. Even if it is 
not of listing-level severity, it can limit an individual's ability to 
function and cause disability, or combine with other impairments to cause 
disability. Individuals who receive substandard medical 
care—especially individuals who have HIV infection—will often 
be more severely impaired than other individuals because of more frequent 
illness or failure to adequately recover from infections and other 
manifestations that might be treatable with proper care, resulting in a 
generally more severe medical and functional picture.
Thus, it is not necessary for us to consider "socioeconomic" 
factors, which are ancillary to the determination of how the person is 
actually affected by his or her impairment(s). For the purpose of deciding 
disability, we need only know the nature and severity of the individual's 
impairment(s) and its effects on his or her functioning. We do not use 
factors like the quality of medical care or housing to determine whether a 
person is medically disabled, just as we would not use such factors to 
find a claimant not disabled.
However, in part because we agree with the commenters that many claimants 
have limited access to ongoing health care, we have clarified the 
documentation requirements in final 14.00D3 and 14.00D4, and 114.00D3 and 
114.00D4 to make it clear that HIV infection or its manifestations may be 
documented without definitive laboratory evidence if the documentation is 
consistent with the prevailing state of medical knowledge and current 
medical practice and is consistent with the other evidence. We do not 
require specific diagnostic tests in all cases.
Comment: A few commenters proposed 
that we should also assess the effect of an HIV-infected individual's home 
situation on the ability to work when the individual is a parent caring 
for a child or children who also show symptoms of HIV and are, therefore, 
in need of more intensive care. These commenters observed that, because 
such children require frequent administration of medication and regular 
clinic visits and are not allowed to receive day care, they would be a 
burden on a healthy parent; parents with HIV infection are already 
required to miss work frequently because of their own conditions, and the 
situation is exacerbated when the parent must also take time off from work 
to care for sick children.
Response: We did not adopt the 
comment. Under the Act, disability must result from the individual's 
medically determinable impairment(s). We are, therefore, unable to provide 
for a finding of disability when an adult is unable to attend work because 
of the need to care for an ailing child and not because of a medically 
determinable impairment(s). However, when we consider the extent to which 
an individual's HIV-related manifestations affect his or her ability to 
function, we consider the individual's ability to care for her or his 
children.
Organization of the Listings
Comment: Many commenters requested 
that we simplify the HIV listings. Some commenters thought that it was 
unnecessary to publish all of the CDC's criteria for diagnosing AIDS in 
our listings because some of the CDC criteria are redundant. They pointed 
out, for example, that every manifestation in proposed Listings 14.08A and 
114.08A was repeated somewhere in proposed Listings 14.08B-I and 
114.08B-H; the only difference was that a person's manifestations would 
meet Listings 14.08A or 114.08A if the person did not have laboratory 
evidence confirming the presence of HIV infection, but would meet one of 
the other listings if he or she did have such evidence. The commenters 
noted that, whereas the CDC might have good reasons for distinguishing 
between the two situations, the fact was that we would find an individual 
who had one of these manifestations to be disabled under the listings 
whether or not there was laboratory evidence of HIV infection. Therefore, 
there was no reason for us to list the same manifestation more than 
once.
Some commenters said that this complexity had led to inconsistencies in 
the proposed rules. They pointed to various sections of the proposed 
listings where the same conditions and the same evidence needed to 
document those conditions were described in slightly different terms, 
suggesting that the criteria were different even though they clearly were 
not meant to be. They stated that these discrepancies and other 
inconsistencies in the language would be confusing to both adjudicators 
and the general public.
Some commenters pointed out repetitious language that we could delete (for 
instance, the statement "Documentation of HIV infection as described 
in 14.00D" at the beginning of every listing under proposed 14.08 and 
114.08); others suggested ways to reorganize the listings. One of their 
comments said that dividing the proposed listing by pathogenic process did 
not increase the ease of reference and thought the repetition of section 
headings added clutter. The comment recommended that we combine the 
proposed listings into a single listing with all of the manifestations 
arranged alphabetically.
Many commenters objected to the many different proposed criteria for 
documenting the existence of the various manifestations in the listings. 
We address the substantive comments in a separate section below, but as 
pertinent here, the commenters pointed out that the numerous specific 
criteria for documenting each of the different manifestations made the 
listings very complex and difficult to use.
Response: We adopted the comments. 
As we have already explained in the summary of the final provisions, we 
have simplified the language and organization of the final rules and have 
eliminated the redundancies of the proposed listings. In response to 
comments we describe later in this section, we removed all of the various 
specific requirements for documenting the presence of the manifestations 
in lieu of the guidance we now provide in final 14.00D4 and 114.00D4. We 
also revised the language throughout part A and part B to make them both 
internally consistent and consistent with each other where 
appropriate.
We chose to retain an organization that lists some of the manifestations 
under general headings for the type of organism, and others according to 
the affected body system or type of manifestation. We did not adopt the 
suggestion that we list all the manifestations alphabetically, although we 
did try it to see if it would work. We found that an alphabetical list was 
more cumbersome than the system in these final rules. To begin with, the 
list was very long; there are over 50 separate named manifestations in 
final Listing 14.08. In addition, it was sometimes difficult to decide how 
a given impairment should be of alphabetized (i.e., by specific organism, 
affected organ, or kind of manifestation), and in some cases, impairments 
that naturally seemed to group together (for example, cryptosporidiosis, 
isosporiasis, and microsporidiosis, which are all protozoans that cause 
diarrhea) were widely separated only because of the alphabetical artifice. 
Moreover, we believe that the system we decided to use in the final rules 
carries an advantage that simple alphabetization would not. By grouping 
impairments according to etiology where possible and, elsewhere, into 
other logical categories (such as body system or organ affected) we have 
provided implicit guidance that will be more useful for finding medical 
equivalence for unlisted manifestations than an alphabetized system 
would.
Comment: One comment suggested 
editorial revisions in 14.00D. The comment suggested that we consolidate 
the definition and description of HIV infection into one location, giving 
more emphasis to the progressive nature of the disease, that we 
consolidate all information about evaluation of HIV infection cases under 
the sequential evaluation process into one location, and that we eliminate 
superfluous language. The commenter provided alternative language for 
parts of proposed 14.00D.
Response: Although we have not 
adopted the specific language suggested in the comment, we have rewritten 
and reorganized all of the paragraphs in 14.00D of the final rule, and 
removed repetitious language. In the final rule, we have revised the 
definition of HIV infection in 14.00D1, consolidated the explanation of 
how to evaluate individuals with HIV infection under the sequential 
evaluation process in 14.00D6, and made other changes throughout 14.00D. 
We discuss these changes in greater detail in the explanation of the final 
rules and in response to public comments about specific issues addressed 
in final 14.00D.
Comment: One comment suggested that 
it was not necessary to list Hodgkin's and non-Hodgkin's lymphomas 
separately, as we had proposed in Listings 14.08I and 14.08J. The comment 
noted that, under the proposed rules, any individual with any type of 
lymphoma would be found to have an impairment that met a listing; 
therefore, it would be simpler to have one listing that included all 
lymphomas. Another comment said that we should provide separate criteria 
for immunoblastic sarcoma, which we had included with the lymphomas in 
proposed Listing 14.08I2, because there is a controversy over whether it 
is a true lymphoma.
Response: We adopted the first 
comment. Final Listing 14.08E3 now includes all lymphomas. In a 
parenthetical statement, the final listing names some of the various 
lymphomas we had proposed in the NPRM, but characterizes them as examples 
to emphasize that all lymphomas are included. This is because all 
lymphomas in HIV-infected individuals carry a poor prognosis. We made the 
same revisions in the childhood rules, at final Listing 114.08E3.
Even though we acknowledge that there is a dispute about whether 
immunoblastic sarcoma is a lymphoma, we did not adopt the second comment. 
Inasmuch as the prognosis is poor in all such cases with HIV infection and 
the mere existence of the manifestation establishes listing-level 
severity, there is no practical reason for establishing a separate listing 
under our rules.
Documentation
Comment: A number of commenters said 
that the proposed requirements for documentation of HIV infection were too 
difficult and burdensome to meet, especially for indigent persons who do 
not have a primary care physician and have inadequate access to health 
care. The commenters also said that the tests we required in the proposed 
rules to document a diagnosis of HIV infection are too expensive for 
indigent persons to afford, and that proposed 14.00D required individuals 
to undergo specific laboratory tests or invasive medical procedures to 
establish a diagnosis or meet the listing. Several commenters also 
expressed concern that requiring specific laboratory tests, such as an HIV 
antibody test or a CD4 count, might inappropriately cause denials or the 
early obsolescence of the criteria for establishing disability related to 
HIV infection. Several commenters suggested that we consider clinical 
judgment or generally acceptable means of diagnosis consistent with the 
current state of medical knowledge. One commenter suggested specific 
language about the standards for documenting HIV infection without 
laboratory evidence, and included suggested language for the fourth 
paragraph of proposed 14.00D to explain why a positive screening test for 
HIV infection, such as ELISA, needs confirmation by a more definitive 
test.
Response: We adopted the comments, 
even though we did not require as much testing as the commenters believed. 
For instance, in the fifth and sixth paragraphs of proposed 14.00D we 
explained that a diagnosis of HIV infection could be accepted without 
laboratory documentation based on the existence of a disease predictive of 
a defect in cell-mediated immunity with no known cause of diminished 
resistance to that disease. We also said that, in such cases, the 
documentation of HIV infection will rely on the clinical history, physical 
examination, exclusion of other causes for clinical abnormalities, and 
treating source opinion. We also added language to final 14.00D3a and 
114.00D3a to explain why a positive ELISA test must be confirmed by a more 
definitive test.
However, recognizing the reality of limited access to health care for many 
individuals, we have revised and expanded the language in final 14.00D3b 
and 114.00D3b, Other acceptable documentation of HIV infection, to provide 
that the existence of HIV infection may be documented without definitive 
laboratory evidence when definitive laboratory evidence is not available. 
We did not adopt the specific language suggested by one commenter. If no 
definitive laboratory evidence is available, documentation may be by 
medical history, clinical and laboratory findings, and diagnoses indicated 
in the medical evidence, provided that it is consistent with the 
prevailing state of medical knowledge and clinical practice and is 
consistent with the other evidence. This would be true, for example, when 
an individual has an opportunistic disease predictive of a defect in 
cell-mediated immunity, and there is no other known cause of diminished 
resistance to the disease (as we provided in the NPRM). We use the clause, 
"If no definitive laboratory evidence is available," in the 
final rules to make clear that we include individuals who may have 
undergone HIV testing anonymously or when there are privacy 
considerations. Of course, if laboratory tests have been performed and the 
results are available, we will make every reasonable effort to obtain 
them.
We have also made other changes in the rules. We made similar revisions to 
our rules regarding the documentation of manifestations of HIV disease in 
final 14.00D4b and 114.00D4b. We also no longer include separate listings 
in final Listings 14.08 and 114.08 for manifestations of HIV with and 
without documentation.
Comment: Some commenters believed 
that diagnosis without definitive laboratory evidence should be accepted 
for every manifestation in the proposed listings. Other commenters 
requested clarification of which manifestations of HIV infection could be 
diagnosed without definitive laboratory evidence and which required 
definitive documentation.
Response: We did not adopt the 
comments. We cannot make a blanket rule that permits diagnosis of every 
listed manifestation in Listings 14.08 and 114.08 without definitive 
laboratory evidence because some of the manifestations, such as Salmonella 
bacteremia (Listing 14.08A3), lymphoma (Listing 14.08E3), nephropathy 
(Listing 14.08L), and radiographically documented sinusitis (Listing 
14.08M6), will by their very nature require laboratory testing. However, 
we also do not want to specify exactly which of the manifestations may be 
diagnosed without definitive laboratory evidence because we want to leave 
the listings flexible to accommodate future medical practices. For this 
reason, we provide in final 14.00D3b and 14.00D4b (as well as the 
corresponding childhood sections) that the diagnosis of HIV and its 
manifestations may be established by methods of documentation that are 
"consistent with the prevailing state of medical knowledge and 
clinical practice and consistent with the other evidence."
Comment: Another comment said that 
the proposed rule's heavy reliance on documented HIV test results 
disadvantaged persons who test positive for HIV infection at an anonymous 
test site before developing HIV-related symptoms. Giving the example of an 
individual applying for disability benefits under title II after she 
tested positive for HIV infection at an anonymous test site and 
subsequently developed an HIV-related condition, the comment recommended 
that we apply later evidence of HIV infection retroactively to the date 
when HIV-related symptoms first developed.
Response: We partially adopted the 
comment. As we explained above, we introduced the clause, "If no 
definitive laboratory evidence is available," in final 14.00D3 and 
14.00D4, and 114.00D3 and 114.00D4, to underscore the fact that we include 
the situation in which an individual may have undergone HIV testing 
anonymously.
We did not add explicit rules on determining retroactivity. Our general 
disability rules already permit us to establish an onset date in the past 
based on an inference drawn from the medical and other evidence in the 
case record. This does not mean, however, that we will find all 
individuals with HIV infection to be disabled from the moment that they 
tested positive for the HIV. As we have said, individuals with HIV 
infection who are otherwise asymptomatic and do not yet have any 
limitations are not disabled under the definition of disability in the 
Act. On the other hand, it is possible for us to find disabled as of the 
date the manifestation(s) first occurred, an individual who began 
experiencing manifestations of HIV infection before she knew that she had 
HIV infection. As we always do, we will determine an individual's onset 
date based on the facts of the specific case.
Treatment
Comment: A few commenters said that 
we did not address the adverse side effects caused by treatment or explain 
how to evaluate improvement caused by AZT therapy.
Response: Although we did include a 
general discussion of the need to consider the effects of treatment in the 
fourteenth paragraph of proposed 14.00D, we have expanded the discussion 
in antiretroviral agents as an example of a type of treatment that may 
ameliorate the condition or cause side effects. AZT is a kind of 
antiretroviral agent; we did not mention it specifically because final 
14.00D7, Effect of treatment, in response to the comments. The final 
section contains three paragraphs. The first paragraph stresses the 
importance of considering both the positive and negative effects of 
treatment. In the paragraph, we mention we would like the rules to remain 
current if new treatments are devised in the future that supplant the use 
of AZT.
In the second and third paragraphs of the final rule, we provide guidance 
about how to evaluate the effects of treatment. We stress the need to take 
into consideration on a case-by-case basis both the positive and negative 
effects of treatment on the individual's ability to function. In these 
same paragraphs, we also point out that some individuals may respond to 
treatment more successfully than others and that the effects of treatment 
may be temporary or long-term. As in the NPRM, the final section provides 
that it is essential to obtain a specific description of the drugs or 
treatment given, and a description of the complications or any other 
response to treatment.
Equivalence
Comment: A few commenters suggested 
that we include in the listing preface more instructions to be used in 
determining when unlisted conditions equal the severity of listed 
conditions. They said that an applicant would have no way of knowing what 
he or she would have to prove, because program physicians determine 
whether an unlisted illness has a level of severity equivalent to a listed 
impairment. One of their comments suggested that, even though such things 
are not amenable to exact quantitative measurement, the approximate levels 
of pain, fatigue, and physical impairment associated with each listed 
illness, along with any other relevant factors, such as frequency and 
duration of episodes, could be specified, so any illness that meets the 
least restrictive of these descriptions could qualify as a 
disability.
Response: We did not add guidance to 
the listings about how to determine equivalence, but we have provided more 
of the kind of detail the commenters requested in the final rules. We do 
not provide substantive instructions for determining equivalence in any of 
the listings sections in part A or part B. We have separate rules in 
§§ 404.1526, 416.926, and 416.926a of our regulations which set 
forth criteria for determining equivalence. The rules on equivalence 
include rules in § 416.926a for assessing a child's functional 
limitations to determine whether they are the same as the disabling 
functional consequences of any impairment in the listings.
The majority of our listings describe conditions for which medical 
criteria can be specified that are of such severity that it is unnecessary 
to consider the kinds of factors mentioned by the commenters. Final 
Listings 14.08 and 114.08 are no exception; the criteria for all of the 
manifestations in Listings 14.08A-M and 114.08A-N are met without the need 
to consider or specify whether there are symptoms or limitations; the 
levels of fatigue, pain, or "physical impairment" these 
impairments may cause are implicit in the listings. Only final Listings 
14.08N and 114.08O, which employ functional criteria as a measure of 
severity, require such considerations. As we have already explained, we 
have extensively revised the functional rules in response to these and 
other comments, and we believe that we have provided more detail about the 
kinds of symptoms and the extent of limitations necessary to meet these 
listings within the listings themselves and in 14.00D and 114.00D.
In addition to symptoms (such as fatigue and pain) and limitations, the 
commenters also suggested that we better define other factors, such as the 
frequency and duration of episodes mentioned in various listings. We 
believe we have responded to this comment as well in the extensive 
revisions in final 14.00D and 114.00D. In these sections, we have, among 
other changes, provided definitions of the terms "resistant to 
treatment" and "recurrent," included language about the 
need to consider an individual's medical and functional status on a 
longitudinal basis, and provided explicit guidance (in final 14.00D8) 
about the meaning of the term "repeated" in final Listing 
14.08N. In the listings themselves, we added specific criteria for the 
frequency, duration, and severity of episodes of manifestations wherever 
it was relevant. For example, final Listings 14.08A5 and 114.08A6 specify 
that the multiple or recurrent bacterial infections must require 
hospitalization or intravenous antibiotic treatment at least 3 times in 1 
year.
Finally, an individual does not have to know what he or she has to prove 
to us in order for us to make a finding of equivalence or any other 
finding regarding disability. We assist the individual by requesting the 
evidence we need for our determination. Moreover, an individual does not 
have to "prove" equivalence to us to be found disabled. If we 
determine that the individual's impairment(s) is equivalent in severity to 
a listed impairment, we will find that the individual is disabled. 
However, if we determine that an individual's impairment or impairments 
are "severe," but that they are not listed and are not 
equivalent in severity to a listed impairment, our evaluation will proceed 
through the final steps of the sequential evaluation process before we 
make any determination about whether the individual is disabled.
Proposed 14.08M, 114.08L, and 114.08M: 
The Functional Listings
Proposed 14.08M1-M3, 114.08L1-L2, and 114.08M1-M3: 
The Medical Criteria
Comment: A number of commenters said 
that the manifestations of HIV infection in proposed Listings 14.08M2 and 
14.08M3, 114.08L1 and 114.08L2, and 114.08M2 and 114.08M3 were severe 
enough to be disabling without meeting a functional test, or had their own 
functional ramifications. Some commenters indicated that the manner in 
which the diseases were ranked did not accurately reflect the true 
disabling effects of some of the conditions. A number of commenters 
specifically questioned the need for functional requirements for people 
with Kaposi's sarcoma in proposed Listing 14.08M2h. Some commenters noted 
that there was a range of severity for Kaposi's sarcoma. (CD4 lymphocyte 
count, the other criterion associated with the functional criteria in 
proposed Listings 14.08M1 and 114.08M1, is addressed in a separate comment 
and response, below.)
Some commenters thought that our use of the terms "persistent" 
and "resistant" to describe the severity of the manifestations 
was confusing. They said we should define the terms.
Response: We adopted many of the 
comments. As we have already explained in the summary of the final 
provisions above, we devised stand-alone medical listings for most of the 
manifestations we had proposed in the functional listings. We also removed 
all of the specific manifestations we had proposed to list in lieu of more 
general descriptive rules that include any kind of manifestation of HIV 
infection, not only those that were in the proposed functional listings. 
Our changes were based on the public comments, additional medical 
information received from doctors—including pediatricians and 
physicians specializing in the treatment of HIV infection in 
women—and from other professionals with expertise in treating and 
studying individuals with HIV infection.
We converted all eight HIV manifestations included in proposed Listings 
14.08M2, 114.08L1, and 114.08M2 into stand-alone listing criteria. We 
agreed for the most part with commenters who stated that the first six of 
the eight listed manifestations would be listing-level impairments if they 
were "persistent and/or resistant to therapy," as described in 
the proposed rules, without the need to consider functional deficits. In 
the final listings, pulmonary tuberculosis is in Listings 14.08A1 and 
114.08A1; pneumonia, sepsis, meningitis, septic arthritis, and 
endocarditis are in final Listings 14.08M and 114.08N.
The final rules require that these conditions be "resistant to 
treatment" instead of "persistent and/or resistant to 
therapy." We made this change for a number of reasons. We used the 
word "treatment" instead of "therapy" only to make the 
language of the final rules consistent with other sections in the 
listings; this is merely an editorial change. The phrase "persistent 
and/or resistant to therapy," however, was redundant and could have 
been confusing. The phrase "and/or" was unnecessary in that, 
because of the disjunctive, "or," a person would have had an 
impairment that met the listings with either persistence or resistance to 
treatment; therefore, the conjunctive, "and," was superfluous. 
Also, in most situations, "persistent" would have been redundant 
of "resistant to therapy" because, if a person was receiving 
treatment and the manifestation persisted, the manifestation was 
implicitly resistant to treatment.
Moreover, the word "persistent" was also ambiguous and difficult 
to define. Some manifestations can respond to treatment without being 
cured. They can technically "persist" because the organisms that 
cause them are still present, but not necessarily be disabling. If we said 
the manifestations had to persist at a disabling level, the individual 
would have to be in treatment and the manifestation resistant to 
treatment: Individuals with persistent disabling pneumonia, pulmonary 
tuberculosis, sepsis, and meningitis require treatment or they will die; 
septic arthritis is usually a sign of a more pervasive infection and is so 
debilitating that the individual would also require treatment.
Therefore, we deleted the word, "persistent," from the final 
rules. However, we also provided alternative criteria for the 
manifestations in final Listings 14.08M and 114.08N by which individuals 
whose manifestations respond to treatment only to recur may establish 
listing-level severity.
We did not agree with the commenters who thought that we could list the 
remaining two manifestations proposed in Listings 14.08M2, 114.08L1 and 
114.08M2, peripheral neuropathy and Kaposi's sarcoma, without some other 
indication of medical severity. Both Kaposi's sarcoma and peripheral 
neuropathy vary widely in severity. These disorders, even when not 
amenable to treatment, may not seriously impair functioning, even in 
individuals with HIV infection. Therefore, the medical criteria we 
developed require more than resistance to treatment and are more 
descriptive of listing-level severity. The final criteria for evaluating 
Kaposi's sarcoma (final Listings 14.08E2 and 114.08E2) require more than 
limited superficial lesions; they require extensive oral lesions, or 
visceral involvement, or skin or mucous membrane lesions of sufficient 
severity to satisfy the criteria in final Listings 14.08F and 114.08F, 
Conditions of the skin or mucous membranes. Of course, the condition may 
also be evaluated under the final functional listings in 14.08N and 
114.08O. In the case of peripheral neuropathy (final Listings 14.08H2 and 
114.08H), the disorder must be assessed either under the appropriate 
neurological listings in 11.00 and 111.00 or on the basis of functional 
limitations under final Listings 14.08N and 114.08O. In order to make 
clear that HIV-related peripheral neuropathy may be evaluated under the 
neurological listings, we added cross-references to those listings 
sections in final Listings 14.08H2 and 114.08H.
In addition, we developed criteria for evaluating most of the other HIV 
manifestations in proposed Listings 14.08M3, 114.08L2 and 114.08M3. As we 
did for peripheral neuropathy, we required the three blood disorders now 
in final Listings 14.08G and 114.08G—anemia (proposed Listings 
14.08M3a and 114.08M3a), granulocytopenia (proposed Listings 14.08M3b and 
114.08M3b), and thrombocytopenia (proposed Listings 14.08M3c and 
114.08M3c)—to meet the criteria of other listings (in 7.00 and 
107.00, the listings for the hemic and lymphatic system). Even in the case 
of an individual with HIV infection, the blood count figures alone do not 
show how an individual is able to function.
We also developed stand-alone medical listings for mucosal candidiasis, 
including vulvovaginal candidiasis (proposed Listings 14.08M3f and 
114.08M3f, final Listings 14.08F and 114.08F), Herpes zoster (proposed 
Listings 14.08M3h and 114.08M3h, final Listings 14.08D and 114.08D), 
dermatological conditions such as eczema and psoriasis (proposed Listings 
14.08M3i, 114.08L2g, and 114.08M3i, final Listings 14.08F and 114.08F), 
diarrhea (proposed Listings 14.08M3j, 114.08L2f, and 114.08M3j, final 
Listings 14.08J and 114.08J), and radiographically documented sinusitis 
(proposed Listings 14.08M3k, 114.08L2i, and 114.08M3k, final Listings 
14.08M6 and 114.08N6).
Although we agree with the comment that the remaining manifestations in 
proposed Listings 14.08M3, 114.08L2 and 114.08M3 (fever, weight loss, 
hepatomegaly, splenomegaly, parotitis, oral hairy leukoplakia, and 
lymphadenopathy) can have functional ramifications, their effects on an 
adult's ability to work or a child's ability to function in an 
age-appropriate manner vary from individual to individual and, thus, 
listing-level severity cannot be defined in solely medical terms. 
Therefore, these manifestations, along with other manifestations of HIV 
infection that do not meet the criteria in final Listings 14.08A-M or 
114.08A-114.08N, will continue to be evaluated with functional criteria 
under final Listings 14.08N and 114.08O.
Comment: Another comment questioned 
the addition of functional requirements to the criteria for HIV wasting 
syndrome.
Response: We did not list HIV 
wasting syndrome in proposed Listing 14.08M3 (or proposed childhood 
Listing 114.08M3); we proposed a separate Listing 14.08H (final Listing 
14.08I) which provided that any person with HIV wasting syndrome had an 
impairment that met the listing. In the childhood listings, we provided a 
cross-reference to the proposed adult rule, in the ninth paragraph of 
proposed 114.00C.
We believe that the commenters misunderstood our intent in proposed 
Listings 14.08M3 and 114.08M3. HIV wasting syndrome is defined as an 
involuntary weight loss of more than 10 percent of baseline body weight 
and either chronic diarrhea or chronic weakness and documented fever 
greater than 100.4o F (38o C) for the majority of 1 month or longer. 
Although it is true that in proposed Listings 14.08M3 and 114.08M3 we 
listed all three of the criteria that may define HIV wasting syndrome 
(fever, weight loss, and diarrhea), we did not intend to list true HIV 
wasting syndrome in the functional listing but a lesser manifestation of 
HIV infection. An individual with true HIV wasting syndrome would have 
already been found to have an impairment that met the criteria of proposed 
Listing 14.08H. The individuals who could have met the criteria of 
proposed Listing 14.08M3 were those who did not have all of the findings 
needed to define HIV wasting syndrome, but who were nevertheless 
significantly limited in their functioning because of their 
manifestations.
For reasons we have already explained in the summary of provisions, we 
have established separate listings, final Listings 14.08J and 114.08J, to 
make diarrhea a stand-alone medical condition, but we have not listed 
fever and weight loss separately, except insofar as they define HIV 
wasting syndrome. However, these two medical findings, as well as diarrhea 
of lesser severity than in the stand-alone medical listings, may still be 
found to be of listing-level severity under final Listings 14.08N and 
114.08O.
Comment: Some commenters suggested 
that we consider additional manifestations of HIV infection in conjunction 
with the functional standards in proposed Listing 14.08M3. The commenters 
suggested many specific manifestations, including joint aches, arthritis, 
or arthralgias, recurrent cystitis, fatigue, chronic headaches, chronic 
sleep disturbance, chronic shortness of breath or exertional dyspnea, and 
HIV-related mental disorders. Various comments on the childhood listings 
also suggested that we add chronic and recurrent otitis media associated 
with functional limitations.
Response: As we have said, instead 
of making the lists longer, but still finite, we decided to revise the 
functional listings so that they would include any possible manifestation 
of HIV infection. Therefore, we no longer list any manifestations 
explicitly, only a few examples. The revisions in final Listing 114.08O 
are sufficient to allow adjudicators to evaluate chronic and recurrent 
otitis media when it is a manifestation of HIV infection. Additionally, 
sequelae from otitis media, such as hearing loss or brain abscess, or any 
other manifestations of HIV infection in children or adults, can be 
evaluated under the appropriate listing or at the last steps of the 
sequential evaluation processes.
Comment: A number of commenters 
believed that the CD4 lymphocyte count required in proposed Listings 
14.08M1 and 114.08M1 should be considered enough to establish 
listing-level severity without the additional requirement to meet the 
functional criteria. Some commenters stated that the proposed CD4 count 
less than or equal to 200 cells/mm3 (or 14 percent or less lymphocytes) 
was too low, especially if we linked it to functioning; others stated that 
it was too high.
Many suggested various alternatives. At least one comment asked us not to 
use any particular CD4 count as a measure of disability at all because 
each individual situation is different; the comment said that it would be 
unfair to label as disabled all individuals with low CD4 counts, when many 
such individuals are still functioning well. One commenter suggested a 
specific description of the standard for using CD4 lymphocyte counts, and 
suggested specific language to clarify the discussion of CD4 lymphocyte 
counts in the third paragraph of proposed 14.00D.
Response: We have deleted the CD4 
criterion from the final rules. We realize that, although a decreased CD4 
count is a gauge of an individual's potential for developing a serious 
opportunistic infection or other manifestation of HIV, with improved 
treatment and prophylaxis for certain opportunistic diseases one cannot 
reliably predict when an individual will develop a disabling 
manifestation. Further, the laboratory finding does not show whether the 
individual is functionally limited. There are many cases of individuals 
with very low CD4 counts (often far below 200) who exhibited few or no 
functional restrictions, and other individuals with much higher CD4 counts 
who were seriously impaired. Indeed, we received comments from such an 
individual, who related his own story of living with HIV infection and 
working even though his CD4 count was below 100.
We agreed completely with the many commenters who stated that such 
individuals are at risk of becoming disabled. However, our disability 
programs require an assessment of whether an individual is disabled 
currently, without regard to whether the individual may become disabled at 
some point in the future. Because there is so much variability in the 
state of health and functioning of individuals with any given CD4 count we 
could not adopt the suggestions to use a specific CD4 count alone (at any 
level) as a listing criterion.
Proposed 14.08M4, 114.08L3, and 114.08M4: 
The Functional Criteria
Comment: Many commenters said that 
the functional criteria were overly burdensome and restrictive and should 
be eliminated entirely. Some of these commenters believed that linking 
manifestations of HIV disease to a functional test ignored the progressive 
nature of the disease and created a higher level of severity than 
established by other listings. One commenter suggested extensive revisions 
in the paragraphs explaining the functional criteria in proposed 14.00D, 
and provided specific language for such revisions.
Response: For reasons we have given 
in the explanation of the final rules, we did not eliminate the functional 
criteria. Our intent in proposing the functional criteria in Listings 
14.08M, 114.08L, and 114.08M was to include in the listings many 
individuals for whom we thought we could not provide solely medical 
criteria. For instance, the functional listings include a group of 
individuals who would be very difficult to describe in strictly medical 
terms—individuals who become ill then improve, only to repeatedly 
become ill again, either with the same manifestation of HIV infection or 
with something different. The functional listings also provide a listing 
for those individuals whose impairments might not be at listing-level 
severity for all individuals, but that are actually of listing-level 
severity for the particular individuals given their effects, such as pain, 
other symptoms, and the consequences of medication, that vary greatly with 
the individual. They help to ensure a finding of disability for any person 
whose impairment(s) actually prevents him or her from engaging in any 
gainful activity, or of any SSI claimant child whose impairment(s) 
actually prevents him or her from independently, appropriately, and 
effectively engaging in age-appropriate activities, even though that 
impairment(s) might not impose similar limitations on other 
individuals.
Moreover, we believe that, in view of the fact that we have made most of 
the proposed manifestations into stand-alone medical listings, we have 
accommodated the comments that asked us to delete the functional listings. 
The functional criteria now only provide another way to find disabled 
individuals who have most of the manifestations we proposed in Listings 
14.08M, 114.08L, and 114.08M.
Based on other comments, however, we have significantly modified the 
proposed functional criteria to make them more applicable to cases 
involving HIV infection and to better express our original intent. We have 
also revised the paragraphs in the final rules that explain the functional 
criteria (final 14.00D8). The functional criteria for both adults and 
children are no longer tied to a finite list of specific medical 
conditions; any manifestation or combination of manifestations may now be 
evaluated under this listing. Additionally, the final rules require an 
adult to demonstrate limitations of functioning in only one of three areas 
of functioning, rather than the proposed two of four. We describe these 
rules and our reasons for the changes in subsequent comments.
Comment: Many commenters pointed out 
that under the functional equivalence policy in § 416.926a(b)(3), any 
child who has listing-level deficits in the functional domains of the 
listings in 112.00 is considered disabled regardless of the nature of the 
impairment. They said it was, therefore, not necessary to include the 
functional criteria in proposed Listings 114.08L and 114.08M, because 
these criteria did no more than recodify existing policy.
Response: We disagree. The part B 
listings are used to evaluate claims filed under both title II and title 
XVI of the Act if the claimant is under age 18. The functional equivalence 
policy in § 416.926a(b)(3), however, applies only to claims for SSI 
filed under title XVI. Even though SSI claims constitute the great 
majority of childhood disability applications, it is possible for 
individuals under age 18 to apply for disability benefits (both as 
disabled minor children and as workers) under title II. Functional 
equivalence does not apply in these cases, and such children could be 
disadvantaged by removal of the rule.
Comment: Many commenters said that 
the proposed HIV listing was the first and only adult physical impairment 
listing to require a functional test in order to qualify for benefits, and 
to do so violated various antidiscrimination laws. One comment indicated 
that the listing should exist solely to provide SSA with medical criteria 
for the purpose of making disability determinations.
Response: The commenters were not 
correct. Even though the listing for evaluation of HIV infection is the 
first to contain functional criteria similar to those in the mental body 
system, other physical body system listings, such as (but not limited to) 
several in the neurological and musculoskeletal body systems, include 
functional criteria among their requirements. We also believe that we have 
the statutory authority to include functional criteria in the listings 
because the listings are not intended to include all possible impairments 
(see, e.g., Sullivan v. Zebley, 493 U.S 521 (1990)) and because our rules 
ensure that all disabled individuals have an opportunity to establish that 
they are disabled under the Act. In any case, we have provided stand-alone 
criteria for most of the manifestations we had proposed to link to 
functioning, as well as some others that affect women, girls, and other 
groups of people with HIV infection. Therefore, the final rules do not 
discriminate against any group of people, but broaden the listings to 
include more people.
We also do not agree that the listings may include only medical criteria. 
Functional criteria not only provide an important avenue to allow 
individuals whose HIV-related conditions impose functional limitations, 
but, perhaps most importantly, they reflect a true outcome of the illness. 
Even the strictly medical criteria in the listings have implied functional 
consequences. By definition, claimants with impairments meeting or 
equaling listed medical criteria cannot work, and this inability to 
work—a functional assessment—is the underlying statutory 
criterion on which the entire disability program is based.
Comment: Several commenters said 
that requiring functional criteria in the adult listing would prevent 
adults with HIV infection from establishing their disabilities at the 
earliest possible point in time. They said that the functional criteria 
could cause the same delays for gathering and weighing evidence as the 
commenters believe occur when we assess residual functional capacity when 
a claimant's severe impairment(s) does not meet or equal in severity any 
listing. Some commenters said that the requirement for 2 months' 
persistence of the manifestations in proposed Listings 14.08M3 and 
114.08M3 would create a 2-month processing delay.
Response: The effect of the 
functional criteria may actually be to expedite case processing. The 
functional criteria do not come into play unless the individual does not 
have an impairment that meets the requirements of one of the preceding 
listings. We also follow a general policy in all cases of curtailing 
development when there is sufficient evidence to properly allow a claim; 
if the evidence shows medical equivalence to one of the listings, we would 
not further develop the claim simply to establish whether the individual 
has an impairment that meets final Listing 14.08N. Therefore, the 
provision applies only to individuals for whom we would have to assess 
functioning at later steps of the sequential evaluation process: 
Individuals who have severe impairments that do not meet the medical 
listings and for whom we would have to perform a residual functional 
capacity assessment if we did not have this listing.
The assessment of residual functional capacity is a much more refined 
evaluation than is required under final Listing 14.08N. Whereas final 
Listing 14.08N only requires a judgment about whether an individual is 
markedly impaired in a broad area of functioning, a residual functional 
capacity assessment is a detailed evaluation of the claimant's ability to 
do particular physical and mental work-related activities. Both 
evaluations rely on the same kinds of evidence, so the new listing will 
not require additional time spent to develop evidence. If anything, 
individuals who meet this listing may not have to present as much evidence 
of their ability to function as to function as they would have to for the 
more detailed residual functional capacity assessment. Furthermore, the 
actual assessment of functioning under the listing is quicker than the 
residual functional capacity assessment and does not require evaluation 
under the medical-vocational rules.
In fact, there has been no evidence that using functional criteria since 
December 17, 1991, has delayed decisions made on cases involving HIV 
infection. We updated our procedures for evaluating HIV infection under an 
interpretive ruling we have been following since December 17, 1991 
(Social Security Ruling (SSR) 91-8p, 
"Titles II and XVI: Evaluation of Human Immunodeficiency Virus 
Infection," 56 FR 65498, December 17, 1991). The experience we have 
using SSR 91-8p 
indicates that claims involving HIV infection are being processed 
expeditiously. We believe, therefore, that—far from delaying case 
adjudication—the new listing will speed the processing of many 
claims and permit more cases to be adjudicated at the listing level than 
would otherwise be possible.
With regard to the comment about the delays that might have been caused by 
the criteria requiring 2 months' persistence of the manifestations in 
proposed Listings 14.08M3 and 114.08M3, we have deleted those rules, as 
already explained.
Comment: Many commenters said that 
if we retained functional criteria in the final adult and childhood 
listings, the requirement should be to demonstrate marked limitations in 
only one area of functioning (for adults) or one functional domain (for 
children). They thought that for adults this was equivalent to the 
threshold we previously used in our operating instructions in effect prior 
to December 17, 1991. Some commenters were particularly concerned that the 
proposed rules for adults would be stricter than the rules they would 
replace by requiring a higher level of functional impairment.
Response: Even though we have 
changed the standard for adults to require marked limitations in one of 
the three functional areas, we do not agree that the proposed rules set a 
higher level of severity than was in our previous operating instructions, 
nor was that our intent. Indeed, under our prior instructions, an 
individual needed help with most activity, including climbing stairs, 
shopping, cooking, and housework, in order to establish a 
"marked" restriction of activities of daily living. In the 
nineteenth paragraph of 14.00D of the NPRM, an individual who was unable 
to perform activities independently most of the time had a 
"marked" limitation of activities of daily living. We further 
defined a "marked" limitation in the seventeenth paragraph of 
the section as arising "when several activities or function are 
impaired or even when only one is impaired, so long as the degree of 
limitation is such as to seriously interfere with the ability to function 
independently, appropriately, and effectively."
More fundamentally, and as we have already explained in the summary of 
provisions above, the proposed functional criteria for adults effectively 
permitted a finding of disability based on marked limitations in only one 
functional area if the individual also suffered episodic bouts of illness. 
Whereas activities of daily living, social functioning, and concentration, 
persistence or pace clearly describe functioning, the fourth area, 
repeated episodes of deterioration or decompensation in work or work-like 
settings, referred to episodes of illness. (This is not true for people 
with mental disorders, where the episodes of deterioration or 
decompensation may result from the stress of the work or work-like 
setting, but it is true in the context of HIV infection.) Thus, an 
individual who experienced the required episodes of illness in proposed 
Listing 14.08M4d and met only one of the three functional criteria in 
proposed Listing 14.08M4a-c would have had an impairment that met the 
listing.
This is not to say that all individuals could have met the listing in this 
way. Some would not have suffered episodic manifestations and, therefore, 
would have had to meet two of the three functional criteria in proposed 
Listing 14.08M4a-c. However, it has been our experience, contrary to the 
beliefs of many commenters, that individuals who are markedly limited in 
one of the areas of functioning also demonstrate marked limitations in one 
of the other areas; the requirement for limitations in two areas merely 
validated the finding of disability. Indeed, we have been using the same 
procedures under 
SSR 91-8p and have 
allowed many cases under this interpretive ruling.
As we have already explained in the summary, and in response to the 
comments, we revised final Listing 14.08M inasmuch as the fourth proposed 
functional criterion described the universe of individuals we were trying 
to capture in the listing. In the final rule, the fourth criterion from 
the proposed listing is now the threshold criterion for the listing and 
the individual must meet one of three functional criteria.
A similar change in the number of functional domains that must be limited 
in a childhood case is not appropriate. The criteria a child has to meet 
to be considered under the listing (i.e., the child must have a 
manifestation of HIV infection that does not satisfy any of the criteria 
in final Listings 114.08A-N) are not repeated in the functional domains, 
are not analogous to the areas of functioning used in evaluating adult 
cases, and differ with the age of the child.
Comment: Many commenters thought 
that the "marked" level of restriction required in the proposed 
adult functional criteria was too severe. They were particularly critical 
of the definition of "marked" as occurring "most of the 
time" in the paragraphs that defined the first three functional 
criteria. Some commenters suggested that "marked" connoted a 
level of functional restriction commensurate with almost total 
incapacitation, i.e., bed confinement or requiring nursing home care, and 
said that this reflected a higher level of restriction than is required to 
establish disability under the Act. Some also suggested that individuals 
would be disabled even if they were not limited "most of the 
time" but were limited to some lesser extent.
Response: We never intended 
"marked" to be interpreted as requiring total incapacitation 
(as, indeed, it does not in the mental body system listings). We proposed 
language to underscore this intent in the seventeenth paragraph of 14.00D 
in the NPRM, which, with minor language changes, is now the fifth 
paragraph of 14.00D8 in the final rules. In that paragraph, we first 
defined "marked" as being on a continuum between 
"moderate" and "extreme" to make the point that there 
is a more severe limitation than a "marked" limitation; that is, 
an "extreme" limitation. If "marked" meant total 
debility, it clearly would have left no room on the scale of severity for 
"extreme" limitation. We then stated that a marked limitation 
could arise "when several activities or functions are impaired or 
even when only one is impaired, so long as the degree of limitation is 
such as to seriously interfere with the ability to function independently, 
appropriately, and effectively." By indicating that a marked 
limitation might result from limitations of only several activities, or 
even only one activity, and by using the phrase "seriously 
interfere," we again meant to say that the individual need not have 
been totally debilitated.
We did, however, intend to establish a level of limitation that is higher 
than is required to establish disability under the Act. This is because 
all listed impairments in part A and part B define a more severe level of 
disability than is defined in the Act. The standard of disability in the 
statute is based on an inability to engage in "any substantial 
gainful activity" (see sections 216(i), 223(d), and 1614(a) of the 
Act). Under §§ 404.1525(a) and 416.925(a) of our regulations, 
however, we explain that the listings describe impairments that are 
considered severe enough to prevent a person from doing "any gainful 
activity." Similarly, the regulations defining disability in children 
provide that "comparable severity" to a disability in an adult 
means a substantial reduction in the ability to function independently, 
appropriately, and effectively in an age-appropriate manner (see § 
416.924(a)). The listings, however, describe impairments that 
"prevent" a child from functioning independently,appropriately, 
and effectively in an age-appropriate manner (see §§ 416.924(e) 
and 416.926a(a)).
The point is that the listings are meant to be a screening device by which 
we can decide relatively quickly that an individual is disabled, without 
the need to proceed to the final steps of the sequential evaluation 
processes. It is at the final steps of the sequential evaluation processes 
for adults and children that we determine whether individuals have 
impairments that meet the statutory definition of disability. Disability 
under the listings is so severe that we know that there is no need to 
proceed further because a finding of disability would result even if we 
proceeded through all the steps of the sequential evaluation 
processes.
Nevertheless, the comments made us realize two things: First, that we 
could have more clearly stated that "marked" does not mean total 
incapacity, and second, that the standard of "most of the time" 
was unnecessarily inflexible. Consequently, we revised the description of 
"marked" to explain our intent more clearly. We now state 
plainly in the fifth paragraph of final 14.00D8 that "an individual 
need not be totally precluded from performing an activity to have a marked 
limitation * * *." We also added language in the fifth paragraph that 
describes "marked" in qualitative terms and makes clear that a 
"marked" restriction in function is not defined by any frequency 
of occurrences but by the degree of interference with function. We also 
state plainly that "marked" is not intended to imply that a 
person is confined to bed, hospitalized, or in a nursing home. This allows 
us the flexibility to determine whether a limitation is "marked" 
on a case-by-case basis. In each of the sixth, seventh, and eighth 
paragraphs of final 14.00D8 (which define the three functional areas, and 
correspond to the nineteenth, twentieth, and twenty-first paragraphs of 
proposed 14.00D) we eliminated the sentences that included the phrase 
"most of the time" and revised the remaining discussions to be 
more descriptive of our intent.
We did not simply revise "most of the time" to a shorter period, 
as some commenters suggested, because we believe the attempt was fraught 
with the same pitfalls that the commenters pointed out for the phrase we 
proposed. Furthermore, because we say that "marked" may involve 
only one activity or several activities, a criterion for less frequent 
interference could result in unintended variations in severity levels 
depending on which activities or other functions were limited.
Comment: Many commenters thought 
that it was inappropriate to use, nearly verbatim, the functional criteria 
language from the mental listings to describe the functional limitations 
in proposed Listings 14.08M, 114.08L and 114.08M. Although some commenters 
said they could appreciate the need to link functional limitations to 
physical disorders, they thought it was inappropriate to apply mental 
listing criteria to physical impairments.
Response: We do not agree that it is 
inappropriate to apply these functional criteria to physical disorders 
because the criteria are generic; they do not describe mental functions, 
but broad areas of functioning that are relevant to any adult's ability to 
work or any child's ability to independently, appropriately and 
effectively engage in age-appropriate activity. As we have explained in 
the summary of the final rules, these activities describe what people do 
and how well they do it on a day-to-day basis. For our purposes, it is 
immaterial whether an individual has difficulty doing chores or 
maintaining concentration because of a mental disorder or because of 
fatigue, weakness, pain, headaches, frequent diarrhea, or any other 
physical problem; the person still has the limitation that results from a 
medically determinable impairment(s).
However, as we have also said, we have modified the proposed language in 
final 14.00D8 to make it even more specific to individuals with HIV 
infection. As we have previously explained, we also removed the fourth 
"functional" criterion in proposed Listing 14.08M4d.
We also repeat that, by revising proposed Listings 14.08M, 114.08L and 
114.08M to make most of the proposed manifestations into stand-alone 
medical listings and to broaden the applicability of the final functional 
listings to include any manifestation or combinations of manifestations, 
final Listings 14.08N and 114.08O are only advantageous to claimants. They 
merely provide another means for people to show that they are disabled 
under the listings.
Comment: A number of commenters 
specifically commented that the area of social functioning is meant to 
measure an individual's psychiatric condition and is not appropriate for 
the evaluation of HIV. They were especially concerned that an individual 
could be denied disability benefits because he or she 
"socialized" with family and friends.
Response: The commenters 
misunderstood our intent; we have, therefore, clarified the rules. We have 
always recognized that there is a difference between visiting with family 
and close friends, who may make special allowances for an impaired 
individual, and independent social functioning. Furthermore, the ability 
to interact with other people can be affected by a physical impairment. 
For instance, an individual who is fatigued my have difficulty going out 
or sustaining conversation. In addition, many individuals with 
manifestations of HIV infection do have mental findings (such as anxiety, 
depression, and apathy) that can interfere with their social functioning. 
Even if the mental findings are not manifestations of HIV infection, or 
are the only manifestations of the HIV infection, we still consider their 
effect on the individual's functioning together with any other 
manifestations.
To make our intent clearer, we have revised the language of the seventh 
paragraph of final 14.00D8 in response to the comments. Final 14.00D8 
states that marked difficulty of social functioning means that an 
individual "cannot engage in social interaction on a sustained basis 
(even though he or she is able to communicate with close friends or 
relatives) * * *." It is also important to note that, under the final 
listing, social functioning is only one area of functioning among three, 
each one of which can establish disability at the listing level.
Comment: Several commenters thought 
that the fourth functional test requirement in the adult listing, i.e., 
"repeated episodes of decompensation," was too severe and went 
beyond what is necessary to prevent an adult from working. The commenters 
suggested that this criterion be revised to more accurately reflect the 
reality of the exacerbations and remissions in HIV-related illnesses and 
the need to be absent from work for treatment.
Response: We have already explained 
how we revised proposed Listing 14.08M in the summary of provisions and 
the foregoing responses. In the third paragraph of final 14.08D8, we 
retained the provision for manifestations occurring on an average of 3 
times a year, or once every 4 months, and each lasting at least 2 weeks, 
but changed it to one provision among several alternatives instead of an 
absolute requirement. We now also provide that the manifestations may last 
for less than 2 weeks and occur substantially more frequently than 3 times 
a year or every 4 months, or that they may occur less frequently than 3 
times a year or once every 4 months but last substantially longer than 2 
weeks each time. We believe this better reflects the variety of patterns 
of episodic illness experienced by persons with HIV infection.
We do not agree, however, that the proposed criterion was incompatible 
with the ability to work in and of itself. It described an individual who 
missed 6 weeks of work during the course of a whole year because of 
illness. Although we do not mean to suggest that missing work for 2 weeks 
at a time 3 times in a year is not serious, we do not believe that it is 
so serious in itself that we could conclude that the individual was 
disabled for 12 months, as required by the statute. This is why we also 
require an accompanying indication of marked functional limitations in the 
final rule.
Comment: Several commenters stated 
that in setting the adult functional standards, we should evaluate 
individuals based on both current functional ability and likely future 
loss of capacity.
Response: The Act requires that an 
individual be disabled during the period covered by the individual's 
application. This usually means that the individual must be currently 
disabled, although we may find disability in the past under title II 
within the time limits covered by the application. However, we are never 
permitted to find an individual disabled based on a prediction that the 
individual will become disabled in the future. There is no provision in 
the statute that would permit us to overlook a claimant's current 
favorable level of function because it is expected his or her condition 
will worsen at some future time. Our policy is to advise individuals to 
reapply for disability benefits at such time as the condition precludes 
substantial work activity.
Comment: Numerous commenters 
suggested that we use functional tests like the Karnofsky Performance 
Status instead of the proposed functional criteria.
Response: We did not adopt the 
comments. The Karnofsky Performance Status is not a "functional 
test," but a physician's estimate of functional status. We do not 
think, however, that the Karnofsky or other available tests are 
sufficiently broad or objective to use in place of our functional 
criteria, as the standard for measuring functional capacity in HIV-related 
disability claims.
Comment: Several commenters said 
that we should develop a special form to capture information regarding a 
claimant's functional limitations and train our Field Office and State 
agency personnel to properly elicit this information. Some were interested 
in working with us to develop the form, as well as to develop a national 
800-number and telefax service for the dictation of physician narratives 
and medical documentation.
Response: Developing evidence of 
functional limitations is not new to Field Office or State agency 
employees. The disability application forms include basic questions 
regarding evidence of functional limitations and are sufficient to make a 
determination in many cases. The State agencies develop additional 
evidence regarding function from a variety of medical and non-medical 
sources when that is necessary. Although we appreciate the commenters' 
offers, at this time we do not believe a special form is needed for either 
the Field Offices or the State agencies. Also, because medical 
determinations are made locally, a national telephone/telefax service for 
physician narratives and medical documentation would not be practical. We 
believe these kinds of services are best when designed and implemented 
locally in order to meet the particular needs of the area.
HIV Manifestations Suggested as Additions to the Listings
Comment: A number of commenters 
suggested adding other manifestations of HIV infection to the listings, 
such as: anemia, arthritis, oral candidiasis (oral thrush), chronic 
shortness of breath or exertional dyspnea, chronic sleep disorders, 
hepatitis (including hepatitis caused by cytomegalovirus), extrapulmonary 
pneumocystis, fatigue, HIV myositis, leukemia, lymphocytic interstitial 
pneumonitis, microsporidiosis, mucormycosis, neoplasia, pancytopenia, 
pulmonary aspergillosis, recurrent giardiasis, renal failure, squamous 
carcinoma of the genitals, side effects of antiretroviral therapy, 
syphilis and neurosyphilis. (We discuss other suggested additions to the 
listings—including several that are specific to women—in 
subsequent comments and responses).
Some of these commenters suggested specific criteria to be included (e.g., 
chronic anemia with persistent hemoglobin of less than 10 percent or 
hematocrit of less than 30 percent, or requiring transfusions more often 
than twice yearly). Other commenters simply identified the symptoms (e.g., 
dyspnea) or conditions they thought should be included, without describing 
any particular level of severity. When a commenter suggested adding a 
medical condition to the listing but did not include criteria describing 
impairment severity, we were often unable to discern whether the commenter 
was asking that we develop listing criteria for that manifestation, or 
asking that we consider the mere existence of the manifestation in an 
individual with HIV infection to be listing-level severity. In order to 
ensure that we considered every comment, we considered both possible 
interpretations of the comment.
Response: We adopted some of these 
comments, partially adopted others, and did not adopt others.
In response to the comments, we added the following manifestations of HIV 
infection to the listing without any qualifying criteria: extrapulmonary 
pneumocystis carinii infection (final Listings 14.08C2 and 114.08C2); 
mucormycosis (final Listings 14.08B6 and 114.08B6); and aspergillosis 
(final Listings 14.08B1 and 114.08B1). An individual with HIV infection 
and any one of these manifestations has an impairment that meets the 
listing.
To the extent that the commenters were suggesting that we include any 
other manifestations in the HIV listings without any qualifying criteria, 
we did not adopt the suggestions. The information we obtained and the 
medical literature indicated that, although the other manifestations 
suggested by the commenters can be disabling, they need not be. 
Consequently, the assessment of severity must be made based on criteria 
beyond the mere presence of the manifestation. In order to be responsive 
to the comments, we attempted to develop a listing-level standard for each 
suggested addition to the listings, using qualifying criteria to indicate 
impairment severity.
The listings now include microsporidiosis (final Listings 14.08C1 and 
114.08C1), if it results in diarrhea lasting for 1 month or longer; and 
septic arthritis (final Listings 14.08M4 and 114.08N4) if it is resistant 
to treatment or requires hospitalization or intravenous treatment 3 or 
more times in 1 year. These criteria were developed based on the 
information we obtained.
Some of the HIV manifestations that commenters suggested as additions to 
the listings may be evaluated under existing listings; consequently, we 
did not add new criteria for them. These include: oral candidiasis (which 
is evaluated under final Listings 14.08F and 114.08F, Conditions of the 
skin or mucous membranes, or 14.08M and 114.08N, for other multiple 
infection, or under the appropriate body system listing); leukemia (which 
is evaluated under the criteria in Listing 7.11, 7.12, 13.27, or 107.11); 
giardiasis (which is evaluated under final Listings 14.08J and 114.08J); 
and pancytopenia (which is evaluated under final Listings 14.08G and 
114.08G or under the criteria in 7.00ff and 107.00ff).
Syphilis and neurosyphilis are also manifestations that may be evaluated 
under existing listings. However, because of their frequency in 
individuals with HIV infection, we added Listings 14.08A4 and 114.08A4 to 
remind adjudicators that HIV infection can make this illness more 
difficult to treat and to ensure that they look for sequelae of the 
disease. For the same reason, we added Listings 14.08D5 and 114.08D5 for 
evaluating viral hepatitis. We did not distinguish in the final listings 
between CMV hepatitis and other forms; therefore, CMV hepatitis is 
included under these final listings.
The NPRM included criteria for evaluating various malignant neoplasms. 
Final Listings 14.08E and 114.08E are expressly for the evaluation of 
malignant neoplasms. The NPRM also included criteria for renal failure, in 
proposed Listing 14.08L. The general term "nephropathy" means 
disease of the kidneys and would, therefore, encompass renal (i.e., 
kidney) failure. Nephropathy is now included in both the adult and 
childhood listings at final Listings 14.08L and 114.08M, which are 
cross-references to the criteria in 6.00ff and 106.00ff.
We did not adopt the suggestions to add listing criteria for the following 
manifestations of HIV infection because the manifestations are either 
symptoms, signs, or medical findings that must be evaluated based on the 
underlying medical condition: dyspnea, sleep disorder, or fatigue.
We did not adopt the suggestion to include criteria for squamous cell 
carcinoma of the genitals because the condition is not necessarily 
disabling, even in an individual with HIV infection, and may be evaluated 
under the listings for malignant neoplasms in 13.00 and 113.00 or as other 
skin conditions under the criteria in final Listings 14.08F and 
114.08F.
Likewise, HIV myositis and arthritis are not necessarily disabling in 
individuals with HIV infection, and these disorders may be evaluated under 
existing criteria in 1.00ff. HIV myositis may also be evaluated under the 
criteria in final Listings 14.05 and 114.05, and septic arthritis under 
the criteria in final Listings 14.08M and 114.08N.
The NPRM included criteria for lymphocytic interstitial pneumonia (LIP) in 
children. We did not adopt the suggestion to add criteria for adults 
because the condition is uncommon in adults, is usually accompanied by 
other manifestations of HIV infection, and would likely cause respiratory 
symptoms that could be evaluated appropriately under 3.00ff., or under 
final Listing 14.08N.
The term "recurrent cystitis" describes many different types of 
bladder inflammation that occur commonly in individuals who have HIV 
infection and individuals who do not. Evaluation under the listings will 
depend on the type of inflammation (e.g., bacterial cystitis may be 
evaluated under final Listings 14.08A5 and 114.08A6). Separate criteria 
for cystitis are not warranted because the condition is often not 
functionally limiting. If it is, and if it does not meet the criteria of 
any of the stand-alone medical listings, it may still meet the criteria of 
the functional listings, 14.08N and 114.08O.
In response to the comment about the side-effects of antiretroviral 
therapy, we supplemented the discussion of the effects of treatment in 
final 14.00D7 and 114.00D7, to make it clearer that we always consider the 
effects of treatment when evaluating disability. We have included 
"antiretroviral agents" as an example of treatment in these 
sections.
It is important to remember that any severe HIV manifestations not 
specifically included in the listings (including any of the manifestations 
discussed above that we declined to add) may still be evaluated based on 
their functional consequences under final Listings 14.08N and 114.08O, or 
at later steps of the sequential evaluation processes for adults and 
children.
Comment: A few commenters questioned 
whether the HIV infection listing adequately considered the effects of 
mental disorders such as depression or anxiety, which are common among 
HIV-infected individuals. They expressed concern that an individual who 
had HIV infection would nevertheless have to meet a specific mental 
disorder listing without consideration of the factors of HIV infection and 
its symptoms. Some commenters suggested that we add depression and anxiety 
as manifestations of HIV infection.
Response: We agree that many 
individuals with HIV infection display signs and symptoms of mental 
disorders, such as anxiety and depression. In some cases, this is a 
reaction to the condition, similar to that of many individuals afflicted 
with other serious disorders, such as cancer or heart disease, and may be 
a mental disorder in itself. In some cases, the mental findings may be 
manifestations of the underlying HIV infection. For example, mental signs 
associated with HIV encephalopathy are, of course, manifestations of the 
illness. Some people who have HIV infection may have mental disorders that 
are unrelated to the HIV infection but nevertheless contribute to their 
limitations; for example, individuals who abuse drugs may have a mental 
disorder related to their use of drugs.
However, regardless of whether the mental findings are signs or symptoms 
of an underlying disorder, mental impairments in and of themselves, or 
symptoms of mental impairments, can vary in their severity and impact on 
each individual's functioning. We, therefore, believe that it is 
appropriate to evaluate these kinds of mental findings either under our 
mental listings or under final Listings 14.08N and 114.08O, in both of 
which we are required to consider their impact on the person's 
functioning. The mental listings contain criteria not only for the 
evaluation of depression and anxiety disorders (Listings 12.04, 12.06, 
112.04 and 112.06) but other disorders that include these findings among 
their signs and symptoms. Moreover, Listings 12.02 and 112.02, Organic 
mental disorders, are listings specifically for people who experience 
psychological or behavioral abnormalities associated with organic brain 
dysfunction. Therefore, these listings would include mental manifestations 
caused by HIV.
We also repeat that the test of disability involves much more than a 
requirement that an impairment meet (or equal in severity) any listing, 
and that disability may also be established at the last steps of the 
sequential evaluation processes.
Comment: Many commenters suggested 
including listing criteria for genital ulcers or genital herpes. Some 
suggested specific listing criteria, such as chronic genital ulcers; 
chronic genital ulcers persisting for more than 1 month; chronic gential 
ulcers that fail to respond to treatment and persist for more than 4 
weeks; chronic genital ulcers caused by a sexually transmitted disease 
that fail to respond to treatment and persist for more than 4 weeks; 
recurrent herpes simplex; recurrent herpes with lesions that have not been 
documented to last 4 weeks, but that recur more often than every 8 weeks 
or that are incompletely suppressed despite continuous maintenance 
therapy.
Other commenters simply identified the conditions they thought should be 
included (e.g., genital herpes), without describing any particular level 
of severity.
Response: As we noted above, we 
considered both possible interpretations of these comments; i.e., that the 
commenters thought the mere existence of the condition was sufficient to 
establish disability or that the commenters thought we could devise 
severity criteria. To the extent that the commenters were suggesting that 
we include these conditions without additional criteria describing 
impairment severity (such that any individual with HIV infection and 
genital ulcers would have an impairment that meets the listings), we did 
not adopt the suggestions. Although genital ulcerative disease can be of 
disabling severity, it is not necessarily disabling. Consequently, the 
assessment of severity must be based on criteria beyond the mere presence 
of the disease.
Some of the comments demonstrated that our proposed criteria for Herpes 
simplex (proposed Listings 14.08A5, 14.08E2, 114.08A5, and 114.08E2) were 
not clear. (Many commenters recommended criteria that were essentially the 
same as the criteria we proposed.) Therefore, we reorganized the proposed 
listings (which became final Listings 14.08D2 and 114.08D2) to make it 
clearer that genital ulcers caused by Herpes simplex that persist for 1 
month or longer meet the criteria of the listing. We did not adopt the 
suggestion to include Herpes simplex infection that does not last for 1 
month, but recurs, because recurrence alone is not a reliable indicator of 
impairment severity; an individual with recurrent minor lesions of short 
duration may be completely unimpaired. Recurrent manifestations of HIV 
infection may be evaluated based on the functional consequences of the 
disorder in final Listings 14.08N and 114.08O.
In further response to these and other comments, we also developed general 
criteria in final Listings 14.08F and 114.08F for conditions affecting the 
skin and mucous membranes, which include genital ulcerative disease. For 
reasons we have already given in the explanation of the final rules, the 
criteria are based on the severity of the resulting lesions ("with 
extensive fungating or ulcerating lesions") and the response to 
treatment ("not responding to treatment").
We did not adopt the suggestion to include criteria limiting the 
evaluation to ulcers caused by a sexually transmitted disease, or the 
suggestion to require that the conditions be both resistant to treatment 
and of a specific duration. Adopting these suggestions would have resulted 
in an unnecessarily restrictive listing.
HIV Manifestations Specific to Women
Comment: Many commenters suggested 
adding criteria for evaluating pelvic inflammatory disease, often called 
PID. They suggested various medical criteria for describing listing-level 
pelvic inflammatory disease, including: pelvic inflammatory disease 
resulting in severe pain; recurrent or refractory pelvic inflammatory 
disease; pelvic inflammatory disease that is persistent or resistant to 
treatment; pelvic inflammatory disease of more than 1 month's duration 
that does not respond to treatment; pelvic inflammatory disease with a 
specific number of episodes (e.g., three or more episodes); pelvic 
inflammatory disease with one episode requiring hospitalization; pelvic 
inflammatory disease with one episode requiring pelvic surgery; pelvic 
inflammatory disease with one episode resulting in documented chronic pain 
syndrome; or some combination of the above.
Response: We responded to these 
comments by developing stand-alone medical criteria that may be used to 
evaluate pelvic inflammatory disease in final Listings 14.08A5 and 
114.08A6. We included pelvic inflammatory disease in the childhood 
listings because there are many adolescent girls who have the disease. 
Although we did not fully adopt any one of the suggestions for specific 
criteria to describe listing-level severity, we derived our criteria from 
many of the suggestions.
We did not adopt some of the specific suggestions because they did not 
represent listing-level severity. For example, we did not include a 
blanket rule for pelvic inflammatory disease requiring surgery because 
pelvic inflammatory disease (whether in the general population or in 
individuals with HIV infection) usually responds to surgical treatment 
and, therefore, will not always meet the statutory duration requirement. 
Moreover, a single episode of pelvic inflammatory disease requiring 
hospitalization is not an accurate predictor of continuing impairment 
severity because individuals often recover satisfactorily from such an 
isolated episode.
The criteria in these final rules (i.e., pelvic inflammatory disease 
requiring hospitalization or intravenous antibiotic treatment 3 or more 
times in 1 year) are similar to a number of the commenters' suggestions 
(e.g., recurrent or refractory pelvic inflammatory disease; pelvic 
inflammatory disease that is persistent or resistant to treatment; pelvic 
inflammatory disease of more than a month's duration that does not respond 
to treatment; pelvic inflammatory disease with a specific number of 
episodes). The criteria are also based on the same premise as those 
suggestions—that disability from pelvic inflammatory disease can be 
measured most accurately by the persistence and severity of the infection. 
We believe that the final rules are less stringent than some of the 
commenters' suggestions, especially those that require more-or-less 
continuous disease. The final rules may be used to evaluate claims filed 
by women and girls who may recover from bouts of infection, but who suffer 
from repeated infections, or who may have their infections controlled for 
a time only to suffer exacerbations.
The criteria in final Listings 14.08A5 and 114.08A6 do not apply only to 
pelvic inflammatory disease, but to any other multiple or recurrent 
bacterial infections requiring hospitalization or intravenous antibiotic 
treatment 3 or more times in 1 year. Bacterial infections, including 
pelvic inflammatory disease, that do not meet these criteria but that may 
be disabling because of pain, chronic illness, or other symptoms and signs 
may also be evaluated under the functional criteria in final Listings 
14.08N and 114.08O.
Comment: Many commenters recommended 
that we revise the proposed listing-level criteria for invasive cervical 
cancer, FIGO stage II, in proposed Listing 14.08J2. Some suggested that we 
use stage IB because cancer at that stage usually requires the same 
treatment as cancer at stage II (i.e., surgery and radiation therapy). 
Other commenters suggested stage I (without indicating IA or IB), or made 
no specific recommendation.
In addition, some commenters recommended that we allow evaluation of 
cervical cancer not yet at FIGO stage II under the functional test in 
proposed Listing 14.08M3.
Response: We did not adopt the 
recommendations to list cervical cancer less than FIGO stage II as a 
stand-alone listing. Impairment severity in the case of malignant tumors 
is assessed by considering the site of the lesion and extent of 
involvement, histogenesis of the tumor, adequacy of and response to 
treatment, and any post-therapeutic residuals. We chose FIGO stage II as 
the listing-level criterion for cervical cancer as a manifestation of HIV 
infection because that is the minimal point at which the cancer has 
advanced beyond the cervix. In FIGO stage I, the cancer is confined to the 
cervix—stage IA indicates cancer that can only be seen 
microscopically, and stage IB indicates a larger amount, deeper in the 
tissues of the cervix, but still confined to the cervix. In stage II, 
however, the cancer has spread beyond the cervix into the uterus or upper 
vagina. Stage I (including IB) cervical lesions are usuallyamenable to 
treatment, even in individuals with HIV infection.
The fact that the recommended treatment is the same for stages IB and II 
may have clinical significance, but it says little about the potential for 
ongoing functional restrictions.
Our revisions in final Listings 14.08N and 114.08O address the suggestion 
to evaluate cervical cancer of a severity less than FIGO stage II at the 
listing level in conjunction with functional restrictions. As we have 
already explained, final Listing 14.08N allows for a finding that 
manifestation of HIV infection (including cervical cancer not meeting the 
criteria in Listing 14.08J) may be found to meet the listing based on the 
functional consequences of the impairment.
Comment: Many commenters identified 
other manifestations of HIV infection that they considered disabling to 
women, and suggested that we include those manifestations in Listing 
14.08. They cited many of the same manifestations that commenters 
suggested as general additions to the adult listings (which we have 
already discussed above), or as conditions that should not have been tied 
to the functional criteria in proposed Listings 14.08M, 114.08L, and 
114.08M (also discussed above). They also suggested that we add abscess of 
an internal organ or body cavity, cervical dysplasia, chronic headaches, 
vulvovaginal candidiasis, human papillomavirus, and vaginal condyloma. (As 
noted previously, when a comment suggested adding one of these 
manifestations to the listing but did not include criteria describing 
impairment severity, we analyzed both possible interpretations of the 
comment.) One commenter suggested extensive revisions in the tenth, 
eleventh, and twelfth paragraphs of proposed 14.00D, the proposed 
paragraphs discussing the evaluation of HIV infection in women. The 
commenter provided specific language for such revisions.
Response: We have added to the final 
listings most of the conditions suggested by the commenters by drafting 
specific criteria describing listing-level severity for a wide range of 
HIV-related conditions common in women. We could not, however, adopt the 
suggestions to include these conditions without additional criteria 
describing impairment severity. None of the conditions suggested are 
necessarily disabling solely by virtue of being present with HIV 
infection.
We considered all the criteria the commenters suggested for describing 
impairment severity, but decided to draft original criteria based on the 
suggestions and on other information about the severity and consequences 
of the conditions. In many cases, the criteria we decided to use are 
similar to the suggested criteria. For example, a comment suggested adding 
vulvovaginal candidiasis of more than 1 month's duration that does not 
respond to therapy; we decided to include all skin and mucosal conditions 
with extensive ulcerating lesions not responding to treatment in final 
Listings 14.08F and 114.08F. Whenever we decided to use criteria 
significantly different from that suggested by the commenters, we did so 
based on what is known about the severity and consequences of the 
conditions.
Final Listings 14.08F and 114.08F include criteria for vulvovaginal 
candidiasis and condyloma caused by human papillomavirus. Because these 
conditions can affect both adults and children, especially adolescent 
children, we incorporated the criteria into both part A and part B of the 
listings.
Although abscesses of an internal organ or body cavity are not 
specifically referred to in the final rules, they may be evaluated under 
final Listings 14.08A5 and 114.08A6, which apply to multiple or recurrent 
bacterial infections.
We did not adopt the suggestions to include criteria for cervical 
dysplasia or headaches. Cervical dysplasia is a clinical finding, a 
deviation from normal in the cells in the lining of the cervix, which may 
or may not cause symptoms or progress to a more serious condition. We did 
not list it as a separate condition because, although clinically 
meaningful, dysplasia alone does not necessarily result in functional 
limitation, and evaluation of such a condition will depend on its impact 
on the individual on a case-by-case basis. Headaches are symptoms that may 
be associated with a wide range of medical conditions, and should be 
evaluated according to the underlying condition and our rules for the 
evaluation of symptoms, including pain, in §§ 404.1529 and 
416.929, which we have recently updated and made more detailed.
In the final rules, we deleted the paragraphs the last commenter asked us 
to edit because vulvovaginal candidiasis, genital herpes, and pelvic 
inflammatory disease are now specifically included in the final listings 
as stand-alone medical conditions. Based on these revisions, the 
additional language suggested by the commenter was not needed. The 
guidance in final 14.00D5, Manifestations specific to women, is more 
general and addresses issues of evaluation instead of specific 
manifestations.
Comment: A comment suggested that we 
add a discussion of HIV infection in pregnant women to the preface and 
that we use different listing criteria for pregnant women. The comment 
said that immunological alterations associated with pregnancy and the fact 
that the CD4 count typically decreases during pregnancy raise the 
possibility that HIV infection could be accelerated. For example, pregnant 
women may develop opportunistic infections when their CD4 counts fall 
below 300.
Response: We did not adopt the 
comment. We agree that medical literature reports that the rate of CD4 
cell loss in HIV-infected pregnant women is faster than in HIV-negative 
pregnant women or HIV-infected men. However, as we state in final 14.00D4a 
and 114.00D4a, a CD4 count in itself is not an indicator of the severity 
of the HIV infection or its functional effects, or a reliable predictor of 
when manifestations will occur. If pregnant women develop manifestations 
of HIV, we will evaluate them in the same way that we do in other women, 
examining the particular effects of their conditions on a case-by-case 
basis.
Comment: Another comment noted that 
we had included gynecological conditions associated with HIV infection and 
functional limitations in the proposed listings. The comment said that, 
since the conditions are also prevalent in HIV-negative women, we should 
add listings for gynecological conditions associated with conditions other 
than HIV infection, and resulting in functional limitations.
Response: We did not adopt the 
comment, which was beyond the scope of these rules. However, in evaluating 
the claim of a woman with or without a compromised immune system under the 
listings, we will consider whether the medical findings for any 
gynecological impairment, in combination with other impairments or 
standing alone, are listed or are medically equivalent in severity to the 
findings for the most closely analogous listed impairment.
The Childhood Listings: Other Comments
General
Comment: A number of commenters 
expressed concern that the proposed childhood HIV listings did not 
adequately reflect the course of the disease in children, but were merely 
an extension, with minor changes, of the adult HIV listings. One comment 
recommended that we limit the childhood HIV listings to those aspects 
peculiar to children that are not covered by the adult HIV listings.
Response: We partially adopted the 
comments, even though it is not true that the proposed childhood listings 
were only an extension of the adult listings. It is simply a fact that 
many of the manifestations of HIV infection in children are the same as 
those in adults. Although the course of these manifestations may differ 
somewhat in a child, in most instances the mere existence of a 
manifestation is sufficient to establish listing-level severity. For that 
reason, there was no need to provide criteria distinguishing the childhood 
manifestations from criteria in the adult rules. Where the differences did 
matter—for instance, in proposed Listing 114.08F (final Listing 
114.08A5) (for two pyogenic bacterial infections in 2 years) and proposed 
Listing 114.08J (final Listing 114.08H) (for HIV encephalopathy)—we 
proposed criteria that recognized these differences.
However, we agree with the general suggestion to make the childhood 
listings better reflect the course and manifestations of the disease in 
children, and have revised the final listings accordingly. We revised the 
discussion about the course and manifestations of HIV infection in 
children in final 114.00D5, deleted most cross-references to the adult 
rules, and provided more listing criteria that describe the unique 
presentation of some manifestations in children. We describe the listings 
changes in other comments and responses, below.
The final childhood listings still contain many of the same criteria as 
the adult listings because they are appropriate to the evaluation of both 
adults and children. We included these criteria in both listings, as we do 
in many other body systems, to ensure the public understands the rules and 
to increase ease and accuracy of adjudication by decisionmakers. Indeed, 
we have added several new listings to the childhood listings that are the 
same as adult listings—such as listings describing manifestations 
that affect women—because we believe that it is not self-evident 
that many children (especially adolescents) are unfortunately in the same 
risk groups for HIV infection as many adults and, therefore, suffer from 
the same manifestations.
Documentation
Comment: One comment stated that the 
HIV evaluation criteria for children in the proposed rules were too vague 
to be properly applied.
Response: We have responded to the 
comment by clarifying 114.00D3 and 114.00D4 of the final rules, the 
documentation standards for evaluating children with HIV infection, final 
114.00D6, Evaluation of HIV infection in children, and final 114.00D7, 
Effect of treatment.
Evidence of HIV Infection
Comment: We received many comments 
about our proposal in the fifth paragraph of proposed 114.00C to use CD4 
(T4) lymphocyte counts to establish the existence of HIV infection. Some 
commenters agreed with the proposal that CD4 counts of 1500/mm3 or less or 
20 percent or less are evidence of HIV infection for children from birth 
to age 1. A few commenters believed that a CD4 count of 1000/mm3 or less 
should by itself be evidence of HIV infection for children 12 to 15 months 
of age. Other commenters said that CD4 counts of 750/mm3 or less should be 
evidence of HIV infection for children 12 to 24 months of age.
One comment suggested that we provide language discussing the change in 
CD4 counts with age.
Some commenters believed that CD4 counts of 750/mm3 or less should be the 
standard for children 1 to 15 years of age. One comment said that the CD4 
counts used in the childhood listings were not consistent with CDC 
guidelines.
Response: We partially adopted the 
comments. As we make clear in 114.00D3, antibody testing for HIV infection 
is not definitive in young children because the mother's antibodies can 
persist in a child up to 24 months of age, even if the child is not 
infected. Therefore, we need to include criteria that would help identify 
when infants who test positive for HIV antibodies are actually infected. 
CD4 counts alone are generally not used to definitively diagnose HIV 
infection in children, in part because there is still some debate in the 
medical community about what the norms for CD4 counts in children should 
be. However, the CD4 counts in these rules are used by the medical 
community to begin prophylaxis for Pneumocystis carinii pneumonia, and are 
sufficiently suggestive in an infant who has tested positive for HIV 
antibodies to presume the existence of HIV infection.
Because of the continuing debate about the norms in children, we cannot 
adopt the recommendation to use a higher CD4 count for children age 12 
months to 15 months of age. However, even though we have not increased the 
CD4 count threshold in the final rules, we have extended the age range for 
CD4 counts of 750/mm3 or less to cover children up to 24 months of age to 
make them consistent with the CDC guidelines for prophylaxis, in response 
to some of the comments, and based on other information we received. We 
also added two additional ways of establishing the presence of HIV 
infection in response to a comment we summarize below.
We did not extend the use of CD4 counts to aid in the diagnosis of HIV 
infection in children age 2 years or older because antibody testing is 
definitive in these children.
Comment: One comment suggested that 
we find infants who have HIV antibodies automatically eligible until such 
time as their infection status can be definitively established. Another 
comment suggested that we establish a listing that would allow for a 
finding of disability for a child between birth and age 15 months who has 
HIV antibodies and exhibits failure to thrive, diffuse lymphadenopathy, or 
any form of candidiasis. The commenters stated that the presence of HIV 
infection in young children can be difficult to confirm through laboratory 
testing, which can be expensive and may be inconclusive.
Response: We did not adopt these 
suggestions because the Act requires that disability be established in 
order for the claimant to receive benefits. As one medical organization 
that submitted comments noted, only about one in three infants born with 
HIV antibodies actually has HIV infection.
However, in response to these and other comments, we revised final 
114.00D3 to allow HIV infection to be documented based on medical history, 
clinical and laboratory evidence (other than the laboratory evidence that 
definitively diagnoses the impairment), and diagnoses. The documentation 
must be consistent with the prevailing state of medical knowledge and 
clinical practice and consistent with the other evidence. Thus, a 
diagnosis of HIV infection could be established under the final rules for 
a child who has HIV antibodies and exhibits failure to thrive, diffuse 
lymphadenopathy, or any form of candidiasis. However, we cannot make a 
blanket statement that this would, or should, always be the case, because 
diagnoses of HIV infection in such cases rely on clinical judgment and the 
documented facts of the individual case. For example, oral candidiasis 
(oral thrush) is a very common condition in babies. If this were the only 
finding in an infant with HIV serum antibodies, a doctor would have to 
make a judgment, based on such factors as the severity, frequency, 
duration, and response to treatment of the infection, and whether there 
are other accompanying clinical findings, to decide whether the infection 
is a routine infection of infancy or a sign of HIV infection.
In addition, even if the suggested signs result in a presumed diagnosis of 
HIV infection, this alone would not speak to the severity of the 
manifestations or their effects on the child's ability to function. HIV 
infection alone, without any serious manifestations, will seldom interfere 
with a child's ability to function.
Once HIV infection is documented, the child, like any person with HIV 
infection, can be found disabled if his or her manifestations satisfy, or 
are equivalent in severity to, the criteria in any of the HIV listings or 
other listings appropriate for the evaluation of the manifestations. If 
the impairment(s) of a child claimant for SSI does not meet or equal in 
severity any listing, the effects of the impairment(s) on the child's 
ability to function will be evaluated at the last step in the sequential 
evaluation process for children.
In addition, it is important to remember that we consider all the 
impairments the child has, whether related to HIV or not. Thus, if the 
child could be found disabled on some other basis, e.g., a child less than 
1 year of age who weighed under 1200 grams at birth, consideration of HIV 
infection would not be necessary.
Comment: One comment suggested that 
we include abnormal CD4/CD8 ratios and immunoglobulin G (IgG) levels 
greater than or less than the normal range for age as laboratory evidence 
of HIV infection in children.
Response: We adopted the comment in 
final 114.00D3b(iii) and (iv). These laboratory findings are acceptable 
documentation of the existence of HIV infection in children up to age 24 
months who have serum antibodies for the HIV.
Comment: One comment suggested 
language to revise the fifth paragraph of proposed 114.00C to expand the 
discussion about the transmission of HIV antibodies and HIV infection from 
mother to child and the significance of CD4 counts. The comment suggested 
adding information about the low prenatal and natal HIV transmission rate 
to infants, and the duration of HIV antibody persistence, and put the list 
of laboratory findings in a separate paragraph.
Response: We modified and adopted 
the suggested language in final 114.00D3a and b.
Comment: Another comment noted that, 
although proposed 114.00C stated that the mean age of diagnosis of 
children infected before or shortly after birth is 17 months, various mean 
ages of diagnosis of HIV infection have been determined and diagnosis is 
often made earlier.
Response: We have adopted this 
comment by removing the language concerning the mean age of diagnosis of 
children infected before or shortly after birth. Final 114.00D3b permits 
HIV infection to be documented in children from birth to the attainment of 
24 months of age based on any of four specific laboratory findings, or 
based on documentation consistent with the prevailing state of medical 
knowledge and clinical practice.
Comment: Several commenters said we 
should delete the language in the ninth paragraph of proposed 114.00C 
describing how pediatric populations may contract HIV because it was 
inappropriate and irrelevant to the purpose of disability 
determination.
Response: We adopted the 
comment.
Symptoms and Response to Treatment
Comment: One comment said that the 
criteria incorrectly assumed that children will adequately express and 
document pain, fatigue, complications and/or reactions to therapy.
Response: We recognize that some 
children may have a limited ability to report history, symptoms, and other 
information, but we do not believe that this will have an adverse effect 
on their claims. Most of the listings in final 114.08 do not include 
symptoms among their criteria; rather, the criteria consist of clinical 
signs and laboratory findings that will be documented in the child's 
medical records. Furthermore, our experience in processing childhood 
disability claims has shown that a child's symptoms will generally be 
observed by a parent or other caregiver who will provide this information 
to the physician and to us.
Although some children may not be able to verbally describe their 
symptoms, these symptoms may be expressed in other ways, such as otherwise 
unexplained changes in demeanor, behavior, eating habits, and sleeping 
habits. These changes would be readily discernible to the child's parents 
or other caregivers, a physician or other professionals experienced in 
evaluating and treating children, as well as to other people who see the 
children, such as relatives, teachers, social workers, and ministers. 
Older children should be more able to express their symptoms and any 
adverse effects of treatment, if this information is needed for 
adjudication.
Adolescents
Comment: Many commenters requested 
that we eliminate the proposed criteria that distinguished between 
children under age 13 and over age 13. Many of the commenters questioned 
our statements in the ninth paragraph of proposed 114.00C that the course 
and spectrum of disease in children age 13 and older is generally similar 
to that of adults, and that older children with HIV encephalopathy and HIV 
wasting syndrome should be evaluated under the appropriate adult listings. 
One comment asserted that scientific and medical literature point to 
distinctive differences between the course and spectrum of HIV infection 
in adolescents and adults, and referred us to the "Journal of 
Pediatrics," Volume 119, July 1991, Number 1, Part 2, titled 
"Guidelines for the Care of Children and Adolescents with HIV 
Infection. Report of the New York State Department of Health AIDS 
Institute Criteria Committee for the Care of HIV-Infected 
Children."
Response: We partially adopted the 
comments. Our statement in the ninth paragraph of proposed 114.00C that 
the course and spectrum of the disease in children age 13 and older is the 
same as in adults was correct and was confirmed by various pediatric 
authorities, including some who specialize in the study and treatment of 
adolescents. We disagree with the comment suggesting that the scientific 
and medical literature supports a contrary view. Indeed, the article cited 
in the comment does not say that there are significant differences between 
adolescents and adults in the manifestations of HIV infection; it says 
that there are differences in epidemiology—i.e., the modes of 
disease transmission. Our disability determination, however, is based on 
the effects of the disease on a child's ability to function in an 
age-appropriate manner, not on how the child acquired HIV disease.
Nevertheless, in response to the comments we deleted the statement about 
the course and spectrum of the disease in adolescents, and revised the 
statement (now in final 114.00D5) about the manifestations and course of 
disease in younger children. The proposed statement about the disease in 
adolescents did not provide guidance that was especially relevant to the 
determination of disability and, therefore, was superfluous.
Comment: A number of commenters 
thought that it was more difficult for some children with HIV infection to 
qualify for disability than it was for children with other impairments. 
The commenters gave as an example a child over age 13 with HIV 
encephalopathy. The ninth paragraph of 114.00C of the proposed rules had 
indicated that such a child should be evaluated under proposed adult 
Listing 14.08G (which, in turn, cross-referred to criteria in the eighth 
paragraph of 14.00D), and would have required the child to show 
progressive motor dysfunction and the absence of a concurrent illness. The 
commenters suggested that this proposed listing was more severe than the 
children's neurologic Listing 111.06, which the commenters thought 
requires only interference with age-appropriate major daily 
activities.
Response: We do not agree that any 
of the proposed listings made it more difficult for children with HIV 
infection to qualify for disability than children with other impairments, 
for reasons we have already given in an earlier comment and 
response.
The proposed criteria for HIV encephalopathy for children were not more 
stringent than Listing 111.06. The criteria in the eighth paragraph of 
proposed 14.00D, which would have been applied to children, required only 
that there be HIV encephalopathy "characterized by" cognitive or 
motor dysfunction that limited function and progressed, and that there not 
be a concurrent illness that could otherwise explain the neurological 
findings. Thus, the criteria only defined the syndrome of HIV 
encephalopathy; that is, how one can tell that a person has HIV 
encephalopathy without invasive testing. Childhood Listing 111.06, on the 
other hand, requires more than mere interference with age-appropriate 
activities; it requires persistent disorganization or deficit of motor 
function involving two extremities that, despite prescribed therapy, 
interferes with age-appropriate major daily activities and results in 
disruption of fine and gross movements or gait and station.
However, as we have already said, we believe that the proposed criteria 
for evaluating HIV encephalopathy in children could be simplified because 
they appeared only in proposed 114.00C, not in the listing, and required a 
cross-reference to an adult listing that itself cross-referred to 14.00D 
of the adult rules. Therefore, we revised final Listing 114.08H (which 
replaces proposed Listing 114.08J) to include HIV encephalopathy and 
criteria specifically for children. We also provided guidance in final 
114.00D5 specifically for the evaluation of neurological abnormalities, 
such as HIV encephalopathy, in children. We also deleted the requirement 
for ruling out other causes, as we did in the corresponding adult 
rule.
Comment: Some comments questioned 
our proposals in Listings 114.08F and 114.08G to limit the criteria for 
multiple bacterial infections and lymphoid interstitial 
pneumonia/pulmonary lymphoid hyperplasia to children under age 13. 
Similarly, some comments questioned the proposal to pair different 
manifestations with functional requirements, for the two age groups in 
proposed Listings 114.08L and 114.08M.
Response: We adopted most of the 
comments. We eliminated the age reference in final Listing 114.08L, 
Lymphoid interstitial pneumonia/pulmonary lymphoid hyperplasia, so that it 
now applies to children of all ages. We had proposed the distinction only 
because the manifestation is quite rare in older children, as it is in 
adults. However, it is possible that an older child could have the 
disorder, especially as more and more children who contracted HIV 
perinatally or early in life are surviving into adolescence. For reasons 
we have already given, however, we have also revised final Listing 114.08L 
to better describe listing-level severity.
The functional listing, final Listing 114.08O, which replaces proposed 
Listings 114.08L and 114.08M, no longer lists specific medical 
manifestations. Therefore, there is no longer a need to distinguish 
between adolescents and younger children.
We have retained the age limit in final Listing 114.08A5, Multiple or 
recurrent pyogenic bacterial infections, because these types of infections 
are more serious and more indicative of a rapid decline in younger 
children, and age 13 is medically an appropriate dividing line. Although 
we could have confined the rule to younger children, we decided to retain 
the rule because age 13 is fair and consistent with prevailing medical 
practice, and we want these listings to be as inclusive as possible. 
Furthermore, unlike the proposed rules, the final rules include a new 
Listing 114.08A6 under which all children, including adolescents, may 
establish that they have impairments of listing-level severity as the 
result of multiple bacterial infections of any type.
Comment: Another comment recommended 
that we address the special needs of adolescents with HIV infection, 
including feelings and fears regarding HIV testing, effective ways of 
counseling adolescents, coping strategies of adolescents with HIV 
infection, and the role of social support in the lives of adolescents with 
HIV infection. The comment also recommended that we establish a group of 
experts within SSA to focus on the specific needs of adolescents with HIV 
infection.
Response: We share these concerns 
about the impact of HIV infection on adolescents. However, the 
recommendations involve areas of social services policy that are beyond 
our authority under the Act and, thus, cannot be addressed within the 
context of these rules.
Final 114.08H Neurological Manifestations
Comment: One comment recommended 
that we add "the sudden acquisition of new learning 
disabilities" as a fourth criterion in proposed Listing 114.08J 
(final Listing 114.08H).
Response: We adopted the comment. We 
added language to the second paragraph of final 114.00D5 and a 
parenthetical statement in final Listing 114.08H1 (which replaces proposed 
Listing 114.08J1) to state clearly that the loss of previously acquired, 
or marked delay in achieving, developmental milestones or intellectual 
ability, includes "the sudden acquisition of a new learning 
disability." This addition is only a clarification of our original 
intent in the proposed rules.
Final 114.08I Growth Disturbance
Comment: Many commenters suggested 
we clarify our criteria for assessing failure to thrive. Some commenters 
thought we were using the height criteria specified in Listing 100.02 to 
assess failure to thrive under proposed Listing 114.08K. The commenters 
indicated that, because the term "failure to thrive" generally 
refers to infants and children who fail to gain weight at an appropriate 
rate or who lose weight, the listing should contain criteria based on 
weight.
Other commenters stated that the 10 percent weight loss required by 
proposed Listings 114.08L and 114.08M, which was the same standard used in 
the adult HIV listings, was too strict. They pointed out that a standard 
of weight loss can make sense for adults because adults are fully grown 
and are expected to maintain a static weight. However, because children 
are growing, it is possible for a child to be gaining weight but falling 
behind what is normal, so that the resulting impairment would be as severe 
as a serious weight loss. The majority of these commenters suggested using 
a 5 percent weight loss as a standard for children. Another suggestion was 
to base our criteria on a failure to follow age-appropriate growth curves 
on standard growth charts.
Response: We adopted several of the 
comments. We revised final Listing 114.08I, which is now headed 
"Growth disturbance" to include weight criteria for failure to 
thrive in addition to the height criteria. The first two criteria of final 
Listing 114.08I describe children who have either lost weight or who have 
failed to gain weight at an appropriate rate, so that there is persistence 
of a fall of 15 percentiles on a standard growth chart or persistence of 
weight below the third percentile on a standard growth chart. We have 
determined that this approach provides a more accurate method of 
assessment than basing our criteria solely on a percentage of weight loss 
because, as the commenters stated, children can, in fact, be gaining 
weight and still be failing to thrive.
We have, however, also retained the criterion of a 10 percent weight loss 
in final Listing 114.08I3 (formerly in proposed Listings 114.08L and 
114.08M) because in some cases 10 percent weight loss will still be less 
than 15 percentiles on a standard growth chart or result in a weight above 
the third percentile. We believe that a 5 percent weight loss would be too 
small to be a reliable standard in the listings, and that children with 
this amount of weight loss will have to be evaluated on an individualized 
basis under the rules for equivalence and the last step of the sequential 
evaluation process.
We have also retained the rules providing for loss of height or length, as 
described in the growth impairment listings in 100.00. Both the 10 percent 
weight loss provision and the cross-reference to the growth impairment 
listings merely provide alternative criteria by which children may be 
found disabled under the listings.
Comment: A number of commenters were 
also concerned about assessing HIV-related growth impairments in children 
by reference to the criteria of Listing 100.02. The commenters said that 
Listing 100.02 defines when a growth impairment is disabling in itself and 
not because HIV infection has interfered with growth. The commenters also 
questioned whether the longitudinal approach required by Listing 100.02 is 
appropriate for children with a progressive disease such as HIV 
infection.
Response: Listing 100.02 is 
appropriate to use because it is a listing for evaluating growth 
impairment caused by a known medically determinable impairment, such as 
HIV infection. It is, thus, a very appropriate listing for evaluating 
growth impairment caused by HIV infection. (However, we revised the 
reference to 100.00ff for consistency with our other revisions.) In any 
event, by expanding final Listing 114.08I, we have made the reference to 
the growth impairment listing only one alternative among four by which a 
child's impairment may meet the listing, not the sole criterion as in the 
NPRM.
We believe the longitudinal approach required by the growth impairment 
listings is reasonable. Multiple measurements are needed to properly 
assess the decline in the child's growth and its persistence.
Final 114.08O1: 
The Functional Criteria for Infants
Comment: One comment objected to the 
criteria in Listing 112.12, the description of functional deficit we used 
to describe listing-level severity for infants from birth to age 1 in 
proposed Listing 114.08L3. The comment stated that our standard of 
one-half chronological age for these children appeared to be more 
restrictive than the standard for older children and adults, especially 
considering how quickly infants change over time. Also, the comment 
suggested that impairment at the level specified need only be documented 
at one assessment.
Response: The functional standard 
for children from birth to the attainment of age 1 (and for many children 
age 1 to the attainment of age 3), now in final Listing 114.08O, is not 
more restrictive than the standard used for older children and adults. In 
the Mental Disorders listings, older children and adults are found 
disabled at the listing level if their impairments result in marked 
limitations in two areas of functioning. In Listings 112.12A and B (and in 
Listings 112.02B1 for children age 1 to 3), however, a young child has an 
impairment that meets the functional requirements of the listings if he or 
she has either one "extreme" limitation or two 
"marked" limitations. An extreme limitation may result when the 
function or developmental milestone is limited to no more than one-half 
the child's chronological age, while marked limitations result with less 
severe limitations—more than one-half but no more than two-thirds of 
the child's chronological age.
For this reason, we provide two ways for children from birth to the 
attainment of age 3 to establish listing-level severity. Under the 
functional criteria in Listings 112.02B1a, b, and c, and in Listings 
112.12A and B, children can establish that their impairments are of 
listing-level severity by showing functioning or delays at no more than 
one-half of their chronological age. Alternatively, under Listings 
112.02B1d and 112.12E, they can establish listing-level severity in the 
same way that older children and adults do: by showing marked 
impairment—i.e., functioning at more than one-half but less than 
two-thirds of chronological age—in two functional areas.
We recognize the problems involved in assessing infants, who do change 
rapidly over time. Because of this, we cannot state that determinations of 
disability can always be based on a single evaluation. The amount of 
evidence needed for each claim has to be determined based on the facts of 
that specific claim, which include the nature and progression of the 
impairment, the interventions and treatments available, the response to 
those interventions and treatments, and—perhaps most 
importantly—the individual infant's own response to the 
illness.
Other Comments
Error in Proposed Listing 
14.08D
Comment: Several commenters pointed 
out that the 2-month timeframe set out in the ninth paragraph of proposed 
14.00D for chronic diarrhea or documented fever caused by HIV wasting 
syndrome was longer than the 1 month required by the CDC's surveillance 
definition.
Response: The criterion in the NPRM 
was an editorial error. In fact, we have been using a 1-month standard in 
our operating instructions, consistent with the CDC surveillance 
definition of HIV wasting syndrome. We have corrected the final rule, 
which is in final Listing 14.08I.
Administrative Procedure Act
Comment: A few commenters expressed 
a concern that we had released guidelines on the evaluation of HIV 
infection in the form of a Social Security Ruling (SSR), in effect 
implementing the proposed rules in the NPRM in advance of public comments. 
Some commenters saw this as a breach of faith or a violation of the 
Administrative Procedure Act (APA).
Response: We have issued SSRs 
(SSRs 
84-19 and 86-20) 
and manualized instructions concerning HIV infection on various occasions 
since 1983, as medical and scientific knowledge about this disease became 
available, to provide guidance to our decisionmakers concerning how claims 
involving HIV infection could be evaluated within the context of the law 
and regulations. On December 17, 1991, we published the latest of these 
instructions, an interpretative ruling, 
SSR 
91-8p, in the FEDERAL REGISTER (56 FR 65498), to announce and to 
state our criteria for evaluating HIV infection. We have been applying 
this interpretive ruling in our adjudication of claims filed by of people 
with HIV infection. Since January 11, 1990, we have published SSRs in the 
FEDERAL REGISTER pursuant to the provisions of § 422.406(b) of part 
422, of title 20 of the Code of Federal Regulations. Statements of policy 
in SSRs continue to be binding on all components of SSA, just as they have 
been since before the regulatory change in 1990 that provided for their 
publication in the FEDERAL REGISTER.
The purpose of these criteria has been to permit our decisionmakers to 
make findings of disability when a particular AIDS- or HIV-related 
condition could "meet" or "equal" a listing under the 
existing regulatory framework. If we had not published them but had waited 
for these final rules, we would have followed our prior instructions 
which, as we have stated, were not as inclusive as the criteria we 
published in SSR 91-8p. 
The effect would have been only to delay needlessly claims that we have 
now been able to allow.
Advisory Council
Comment: A number of commenters 
recommended that we convene a group of experts, an advisory council, or 
other knowledgeable specialists to evaluate and revise the proposed 
listings on HIV infection, and to regularly review the listings to keep 
the criteria for HIV-related diseases current. Some commenters also 
thought that the proposed rules for evaluating HIV infection in children 
did not reflect the expertise of childhood medical specialists. They 
pointed out that no childhood specialty groups, such as the American 
Academy of Pediatrics (AAP), or public interest advocacy groups were among 
the list of medical specialty groups listed in the NPRM as providing 
information in developing the HIV criteria in proposed Part B. They 
questioned whether any of the experts listed were pediatricians and 
whether they were independent of SSA. A few commenters also said the 
implementation of the proposed rules should be delayed until we consult 
with childhood HIV experts.
Response: We did not adopt the 
recommendation to establish an advisory council to assist us in preparing 
these rules. We solicited information from individual medical experts, 
including pediatricians, in developing the proposed rules. Establishing a 
separate group of experts following the publication of the NPRM would 
likely have duplicated many of the steps we had already undertaken and, 
most importantly, such duplication would have caused unnecessary delay in 
the publication of these final rules, to the disadvantage of claimants 
with HIV infection. Moreover, the public comments in response to the NPRM 
came from a broad spectrum of the medical, legal, and advocacy 
communities, and, hence, included some of the kind of input recommended by 
the commenters.
Nevertheless, and partly in response to the comments, we have sought 
additional information from a wide range of individual medical 
specialists. Other experts assisted us on an individual basis as we 
finalized these rules and responded to the comments.
With regard to the proposed rules for evaluating HIV infection in 
children, although we did not obtain information from the AAP during the 
development of the proposed rules, we did obtain information from 
pediatricians at Johns Hopkins Hospital, the Centers for Disease Control, 
and other Federal agencies, all of which were independent of SSA. 
Furthermore, during the process of developing the final rules, we obtained 
information from additional pediatricians and other individuals with 
knowledge and treatment experience in pediatric HIV infection in all 
childhood populations, including adolescents. Among these individuals were 
some recommended by members of the AAP and a physician to whom we were 
specifically referred by the AAP. Finally, the AAP, as well as other 
pediatric specialty groups and other children's advocacy groups, have 
submitted comments on the NPRM expressing their interest or concern about 
its content and publication. By submitting these comments, these groups 
have participated in the formulation of the final rules.
Timely Updates
Comment: A number of commenters 
responded to our request for suggestions on alternatives to our regulatory 
process consistent with the APA and that would enable us to issue timely 
updates to the listings for HIV infection (56 FR at 65704). One comment 
suggested that we develop a decisionmaking protocol, which would be 
subject to the normal regulatory process, that would establish a procedure 
for evaluating when changes would be appropriate in the listings. Other 
comments proposed that we create an ongoing advisory panel composed of a 
range of experts committed to assisting us in updating and refining these 
procedures in a timely fashion as medical knowledge on HIV improves.
Response: We appreciate these 
suggestions, and will give them further study. We will study whether any 
of the suggestions we received can be used given the constraints of the 
Act and our regulations. We have always attempted to update the medical 
listings to reflect advancements in medical technology, disability 
evaluation and treatment, and changes in knowledge and new disease 
processes. We monitor the listings on an ongoing basis to ensure that they 
continue to meet program purposes and, when changes are found to be 
warranted, the listings for that body system are updated through the 
normal regulatory process.
We recognize that the HIV listings may need to be changed as we learn more 
about the course of HIV infection in different populations, and as new 
tests and treatments are developed. We will update the listings as it 
becomes necessary, and will issue new instructions to our adjudicators as 
this becomes necessary.
Excessive Paperwork
Comment: A number of commenters were 
concerned that the proposed rules were complicated and would require too 
much paperwork on the part of health care providers and claimants to 
document a claimant's eligibility. They were also concerned that the 
proposed rules would not produce timely disability determinations, which 
would be harmful to individuals affected by HIV infection.
Response: We agree that paperwork 
and the effort required to establish a disabling impairment should be kept 
to a minimum. We have made changes in the final listings that will 
facilitate the documentation and adjudication of HIV claims. These changes 
include revising the criteria for documenting the existence of HIV 
infection and its manifestations to permit documentation of HIV infection 
or its manifestations in the absence of a definitive diagnosis and to 
permit a finding of "meets" for most of the impairments formerly 
tied to functional criteria in proposed Listing 14.08M when the medical 
evidence indicates listing-level severity. In addition, we give these 
claims priority handling.
Training
Comment: Several commenters 
expressed the need for extensive training for health care officials, 
physicians, advocates, Social Security personnel, and the general 
public.
Response: We agree, and have already 
begun a public awareness campaign and training initiative with respect to 
HIV including the design, printing, and distribution of brochures, 
television and radio public service announcements (in both English and 
Spanish), and video news releases. We are also working with the medical 
community, service providers, and advocacy groups to ensure that the 
important message about the potential for Social Security Disability 
Insurance (SSDI) and SSI benefits reaches those with HIV infection. We 
have also provided training to our adjudicators and will continue to 
provide training as necessary.
Trust Fund
Comment: A few commenters expressed 
concern about the cost of adding manifestations of HIV infection to the 
Listing of Impairments on the Social Security and health care financing 
systems.
Response: These final rules 
establish a listing for HIV infection to replace the adjudicative criteria 
we have been using to evaluate manifestations of this disease. These final 
rules represent only the latest refinement of the criteria we have been 
using since we began receiving these cases shortly after AIDS was first 
identified. Consequently, we do not expect their publication to have a 
significant additional effect on the Federal Disability Insurance Trust 
Fund or the Federal Hospital Insurance and Federal Supplementary Medical 
Insurance Trust Funds. It should also be noted that SSI benefits are not 
paid from the Social Security trust funds, but from the general 
revenues.
Waiting Period for Cash and Medicare Benefits
Comment: A comment suggested that we 
waive the 24-month waiting period to qualify for Medicare for individuals 
with HIV infection, which, the comment indicated, we do for other 
conditions, such as end-stage renal disease. The comment also noted that 
the 5-month waiting period requirement for SSDI benefits is inappropriate 
in HIV-infection cases, in view of the short life expectancy that follows 
a diagnosis of AIDS.
Response: We certainly empathize 
with the need for medical care for people who are HIV-infected. The 
comments are, however, outside the scope of these regulations. More 
importantly, the waiting periods for Medicare (including the exception for 
end-stage renal disease) and for SSDI benefits are specified in the Act, 
and cannot be "waived" without a legislative change.
Critical Payments
Comment: One comment recommended 
that the regulations require Social Security disability adjudicators to 
notify claimants of the availability of immediate critical payments at the 
time they are found eligible for disability benefits.
Response: We did not adopt this 
comment because it is outside the scope of these regulations and has been 
dealt with in our operating instructions. One of our goals is to pay all 
benefits due on time, and in the vast majority of cases we meet this goal 
through routine processing. However, our operating instructions provide 
for expedited payment by various means if a claimant has a financial 
emergency. These methods include the one-time emergency advance payment 
(EAP) procedure, which can be made in SSI cases in accordance with § 
416.520 of our regulations when the individual is presumptively eligible 
for SSI payments and has a financial emergency. Our Field Offices and 
processing centers also have the capability to make expedited payments in 
other critical Social Security and SSI case situations.
Determinations at Steps 4 and 5; Younger Individuals
Comment: A number of commenters 
supported the philosophy of awarding as many claimants as possible at the 
listing level. They pointed out that most adult claimants with HIV 
infection are "younger" individuals (i.e., people under 50 years 
old) under our rules in §§ 404.1563(b) and 416.963(b). The 
commenters said that, if these individuals are not found to have an 
impairment(s) that meets a listing, they would probably be denied at the 
last step of the sequential evaluation processes. One comment said that we 
almost never do an equivalence analysis. Other comments said that it was 
insufficient to rely on the rest of the sequential evaluation process to 
adjust for the "inadequacies" of the medical standard.
Response: As we have explained, the 
listings do not represent the standard of disability in the Act, but a 
higher level of disability, because they are intended only to be a method 
by which we can quickly pay claims that clearly would be allowed at later 
steps in the sequential evaluation processes. Indeed, the Act does not 
require us to have a set of listings at all; the listings are simply a 
means by which we can process some claims more timely and 
efficiently.
Therefore, the question is not about any "inadequacies" in the 
listings, but about whether we will find disabled all individuals who have 
disabling impairments. We are committed to ensuring that all individuals 
who are disabled because of HIV infection receive timely and correct 
determinations under our rules, whether at the listing-level or beyond. 
This means that we will provide assessments of equivalence and of residual 
functional capacity (or of a child's functioning) to people who do not 
have impairments that meet the requirements of any of these listings, and 
allow those individuals who are disabled within the meaning of the 
Act.
But the fact that the great majority of people disabled with HIV infection 
are found to have listing-level impairments also attests to two things: 
that HIV infection is a terrible disease and that we have made our listing 
criteria broad enough to include most people who are disabled by HIV 
infection. We believe that some of the changes in the final 
rules—the listings for manifestations that affect women and girls, 
the new stand-alone medical criteria and other new medical criteria we 
have added, and the improvements to the functional criteria—will 
include even more disabled people at the listing level.
Beyond that, we can only say that we are as concerned about people with 
HIV infection as the commenters are. It is never acceptable to deny an 
individual who is disabled, even more so when the individual has an 
illness like HIV infection. Nevertheless, we are bound to follow the 
statute, there are many individuals who have HIV infection and are not yet 
disabled under the statute, and we have a responsibility to ensure that 
only individuals who are disabled receive benefits.