Program Operations Manual System (POMS)
TN 31 (08-20)
COMPASSIONATE ALLOWANCES INFORMATION
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ENDOMYOCARDIAL FIBROSIS
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ALTERNATE NAMES
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EMF; Davies Disease; Fibroelastic Endocarditis, Loeffler Endomyocardial Fibrosis with
Eosinophilia; Loeffler Fibroplastic Parietal Endocarditis; Loeffler’s Disease
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DESCRIPTION |
Endomyocardial Fibrosis (EMF) is a rare progressive type of heart disease of unknown origin (idiopathic). It is
illustrated by progressive fibrosis (the development of excess fibrous connective
tissue) of the lining of one or both lower heart chambers. This results in constriction
of the heart cavity and can involve the heart valves and other structures. The overall
prognosis is poor and depends on the extent and distribution of disease within the
various heart chambers and valves of the heart. EMF is an idiopathic disorder of the
tropical and subtropical regions of the world characterized by the development of
restrictive cardiomyopathy. Women and children are more commonly affected than men.
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DIAGNOSTIC TESTING, PHYSICAL FINDINGS, AND
ICD-9-CM/ICD-10-CM
CODING
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Diagnostic testing:
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Clinical examination describing physical findings;
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Complete blood count showing anemia and eosinophilia;
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Chest x-ray showing cardiomegaly;
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Imaging studies showing enlargement of the atria;
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Angiography showing distortion of the heart chambers;
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Electron beam computed tomography; and
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Cardiovascular magnetic resonance imaging (MRI) showing obliterative changes in the
ventricles, atrial dilation, and regurgitant antrioventricular valves.
Physical findings: Signs of this disease include:
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Restricted ventricle; and
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ICD-9:
288.3
ICD-10:
142.3
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TREATMENT
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There is no definitive cure for this condition. Palliative treatment aimed at controlling
symptoms, utilizing diuretics, digoxin, beta-blockers, endocardiectomy, cardiopulmonary
bypass, and immunosuppressive therapy.
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PROGRESSION
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Most people have extensive disease at the time of diagnosis. The disease is usually
fatal within one to three years after onset of symptoms. Prognosis for this condition
is poor with high incidences of sudden cardiac death from fatal arrhythmias or from
progressive cardiac failure.
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SUGGESTED PROGRAMMATIC
ASSESSMENT* |
Suggested MER for Evaluation:
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Clinical history and examination that describes the diagnostic features of the impairment;
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Complete blood count (CBC);
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Cardiac catheterization; and cardiovascular magnetic resonance imaging (MRI).
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Suggested Listings for Evaluation:
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DETERMINATION |
LISTING
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REMARKS |
Meets |
4.02 |
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4.05 |
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Equals |
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* Adjudicators may, at their discretion, use the Medical Evidence of Record or the
listings suggested to evaluate the claim. However, the decision to allow or deny the
claim rests with the adjudicator.
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