Literature DB >> 857628

Systolic and diastolic ventricular function in cardiac amyloidosis. Studies in six cases diagnosed with endomyocardial biopsy.

R H Swanton, I A Brooksby, M J Davies, D J Coltart, B S Jenkins, M M Webb-Peploe.   

Abstract

Five cases of cardiac amyloidosis diagnosed after endomyocardial biopsy are described. Systolic function was normal in three cases as assessed by cardiac index, ejection fraction and maximal velocity of contractile element shortening at zero developed pressure. The diastolic dip and plateau wave form was a characteristic but not an invariable finding. Increased ventricular end-diastolic pressure but normal end-diastolic volume indexes in all cases implied a disorder of diastolic compliance. The diastolic pressure-volume plots suggested a sudden decrease in distensibility after normal early filling of the ventricle. The functional defect did not necessarily differ from that of other diseases of heart muscle. Therefore, hemodynamic data should not be relied upon for diagnostic purposes. Electron microscopy was the most reliable aid in making the diagnosis from the endomyocardial biopsy specimens especially in the presence of fibrosis. It may not be valid to assume a diagnosis of cardiac amyloidosis from the finding of amyloid in other organs.

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Year:  1977        PMID: 857628     DOI: 10.1016/s0002-9149(77)80125-2

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN: 0002-9149            Impact factor:   2.778


  19 in total

1.  Pattern of myocardial 99mTc-HMDP uptake and impact on myocardial function in patients with transthyretin cardiac amyloidosis.

Authors:  Sarah Pradel; Stéphanie Brun; Gérard Victor; Pierre Pascal; Pauline Fournier; David Ribes; Yoan Lavie-Badie; Michel Galinier; Didier Carrié; Isabelle Berry; Olivier Lairez
Journal:  J Nucl Cardiol       Date:  2018-06-07       Impact factor: 5.952

Review 2.  Restrictive cardiomyopathy.

Authors:  P T Wilmshurst; D Katritsis
Journal:  Br Heart J       Date:  1990-06

3.  Familial restrictive cardiomyopathy with atrioventricular block and skeletal myopathy.

Authors:  A P Fitzpatrick; L M Shapiro; A F Rickards; P A Poole-Wilson
Journal:  Br Heart J       Date:  1990-02

Review 4.  Sudden death in nondilated cardiomyopathies: pathophysiology and prevention.

Authors:  Anand Soni; Paul LeLorier
Journal:  Curr Heart Fail Rep       Date:  2005-09

5.  Systemic lambda light-chain deposition presenting with predominant cardiac involvement.

Authors:  M J Garton; S Walton; S W Ewen
Journal:  Postgrad Med J       Date:  1993-07       Impact factor: 2.401

6.  Current therapeutic strategies in cardiac amyloidosis.

Authors:  Shailja Parikh; James A de Lemos
Journal:  Curr Treat Options Cardiovasc Med       Date:  2005-12

7.  Is technetium-99 m-pyrophosphate scintigraphy valuable in the diagnosis of cardiac amyloidosis?

Authors:  A Hartmann; J Frenkel; R Hopf; R P Baum; G Hör; M Schneider; M Kaltenbach
Journal:  Int J Card Imaging       Date:  1990

8.  Impaired left ventricular diastolic filling in patients with familial amyloid polyneuropathy: a pulsed Doppler echocardiographic study.

Authors:  O Kinoshita; M Hongo; H Yamada; T Misawa; J Kono; S Okubo; S Ikeda
Journal:  Br Heart J       Date:  1989-02

9.  Radionuclide angiography and magnetic resonance imaging: complementary non-invasive methods in the diagnosis of constrictive pericarditis.

Authors:  A Furber; P Pézard; J J Jeune; P Geslin; A Tadei; P Jallet
Journal:  Eur J Nucl Med       Date:  1995-11

10.  Primary cardiac amyloidosis in a young man presenting with angina pectoris.

Authors:  S Saltissi; P J Kertes; D G Julian
Journal:  Br Heart J       Date:  1984-08
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