Circulation, Vol 75, 1012-1017, Copyright © 1987 by American Heart Association
MH Schoenfeld, EW Supple, GW Dec Jr, JT Fallon and IF Palacios
Despite careful clinical, noninvasive, and hemodynamic assessment of
patients with constrictive/restrictive physiology, the differentiation of
restrictive cardiomyopathy from constrictive pericarditis remains
difficult. We examined the role of right ventricular endomyocardial biopsy
in defining the underlying process in 54 patients with evidence of
constrictive/restrictive physiology, including 38 patients with profound
symptoms of heart failure in whom diagnostic/therapeutic thoracotomy was
contemplated (group I) and 16 patients with milder symptoms (group II). All
patients in group I had NYHA class III or IV heart failure with depressed
cardiac index (mean 2.5 liters/min/m2), right atrial hypertension (mean 15
mm Hg), and normal left ventricular ejection fraction (mean 59%).
Endomyocardial biopsy identified a specific source of restrictive
cardiomyopathy in 15 of 38 patients (39%) (11 amyloid, four myocarditis).
Of the 23 remaining patients with either normal biopsy findings or
nonspecific abnormalities on biopsy, 18 had intraoperative or autopsy
evaluation of their pericardium, and constriction was found in 14 (77%). A
specific form of restrictive cardiomyopathy was also identified in four of
the 16 patients with milder symptoms (group II). We conclude that
endomyocardial biopsy is useful in patients with severe
constrictive/restrictive physiology. It identifies a large subset of
patients with specific forms of restrictive cardiomyopathy in whom
thoracotomy should be avoided. It supports the need for thoracotomy and the
likelihood of finding pericardial constriction in patients without specific
pathologic findings.
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Restrictive cardiomyopathy versus constrictive pericarditis: role of endomyocardial biopsy in avoiding unnecessary thoracotomy
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