Document Detail

The spectrum of left ventricular size in dilated cardiomyopathy: clinical correlates and prognostic implications. SPIC (Italian Multicenter Cardiomyopathy Study) Group.
MedLine Citation:
PMID:  8427135     Owner:  NLM     Status:  MEDLINE    
To address the issues of variability and prognostic role of left ventricular dimensions in dilated cardiomyopathy (DCM), 144 patients with DCM were studied. They were arbitrarily assigned to two groups according to an echocardiographic left ventricular end-diastolic diameter index < or = 15% (45 patients with mildly dilated cardiomyopathy) and above 15% (99 patients with typically dilated cardiomyopathy) of the upper normality range. Among the patients with mildly dilated cardiomyopathy, there were more men (89% vs 66%; p < 0.01). This group of patients also had a greater prevalence of atrial fibrillation (22% vs 3%; p < 0.001) higher left ventricular fractional shortening (15 +/- 6% vs 13 +/- 5%; p < 0.05), higher ejection fraction (28 +/- 8% vs 24 +/- 8%; p < 0.01), and a lower exercise tolerance (5 +/- 2 MET vs 6 +/- 2 MET; p < 0.05). At the time of follow-up examination (30 +/- 15 months), event-free survival was not significantly different between patients with mildly dilated cardiomyopathy and those with typically dilated cardiomyopathy. Pulmonary capillary wedge pressure (p < 0.001) and left atrial dimension index (p < 0.01) were significant predictors of prognosis as determined by Cox multivariate analysis. Minimal or mild ventricular dilatation is not uncommon in DCM, and it identifies a heterogenous group of patients--some who are in the early stages of disease and others with severe pump dysfunction and persistently small hearts. Ventricular dilatation is not an independent predictor of prognosis.
A Gavazzi; R De Maria; G Renosto; A Moro; M Borgia; A Caroli; G Castelli; M Ciaccheri; D Pavan; C De Vita
Related Documents :
20592665 - Isolated dynamic left ventricular outflow tract obstruction can cause hypotension that ...
20453225 - Sudden death associated with hypertrophic cardiomyopathy in an alpaca (llama pacos).
6685465 - The cardiomyopathies. a pathophysiologic approach to therapeutic management.
17502765 - Hypertrophic cardiomyopathy in a patient with down's syndrome.
317205 - Cardiac involvement in progressive systemic sclerosis.
23673175 - Bidirectional ventricular tachycardia of unknown etiology.
Publication Detail:
Type:  Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  American heart journal     Volume:  125     ISSN:  0002-8703     ISO Abbreviation:  Am. Heart J.     Publication Date:  1993 Feb 
Date Detail:
Created Date:  1993-03-04     Completed Date:  1993-03-04     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  0370465     Medline TA:  Am Heart J     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  410-22     Citation Subset:  AIM; IM    
Divisione di Cardiologia, IRCCS Policlinico San Matteo, Pavia, Italy.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Cardiomyopathy, Dilated / mortality,  pathology*,  physiopathology
Follow-Up Studies
Heart Ventricles / pathology*
Middle Aged
Multivariate Analysis
Prospective Studies
Survival Analysis

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Biphasic versus sequential pulse defibrillation: a direct comparison in humans.
Next Document:  Long-term outcome of enoximone therapy in patients with refractory heart failure.