Literature DB >> 25140066

Prognostic implications of the systolic to diastolic duration ratio in children with idiopathic or familial dilated cardiomyopathy.

Tapas Mondal1, Cameron Slorach1, Cedric Manlhiot1, Wei Hui1, Paul F Kantor1, Brian W McCrindle1, Luc Mertens1, Mark K Friedberg2.   

Abstract

BACKGROUND: Childhood dilated cardiomyopathy (DCM) carries high morbidity and mortality. The echocardiographic systolic to diastolic (S:D) duration ratio, an indicator of global cardiac performance, is elevated in DCM; however, its prognostic implications have not been investigated in this population. METHODS AND
RESULTS: We investigated systolic and diastolic durations and the resultant S:D ratio using pulsed tissue Doppler imaging in children with idiopathic or familial DCM. We studied serial echocardiograms from presentation until the last follow-up echo. Results were compared with heart rate-matched controls and between DCM subgroups based on an acute or insidious presentation. The association between S:D ratio and death or need for transplant was analyzed. All analyses were adjusted for repeated measures per patient. We studied 200 serial echocardiograms of 48 children with DCM (7.0±6.0 years) and 25 controls. Adjusted for repeated measures through a compound symmetry covariance structure, the S:D ratio was higher in DCM patients (-0.425 [0.072]; P<0.001) because of shortened diastole. A S:D ratio >1.2 at presentation and on serial evaluation was associated with a hazard ratio of 10.5 (95% confidence interval, 3.9-27.8; P<0.001) for death or transplant. In combined multivariable analysis, a S:D ratio >1.2 remained significantly associated with hazard of death/transplant (hazard ratio, 9.1; P=0.04) after adjustment for ejection fraction (hazard ratio: 2.2 per -10%; P<0.001).
CONCLUSIONS: A high S:D ratio is associated with increased risk for death or need for transplant in children with DCM across the spectrum of heart rates and may be a useful prognostic index for serial evaluation of children with DCM.
© 2014 American Heart Association, Inc.

Entities:  

Keywords:  cardiomyopathy, dilated; echocardiography; pediatrics; prognosis

Mesh:

Year:  2014        PMID: 25140066     DOI: 10.1161/CIRCIMAGING.114.002120

Source DB:  PubMed          Journal:  Circ Cardiovasc Imaging        ISSN: 1941-9651            Impact factor:   7.792


  3 in total

1.  Sarcomere-based genetic enhancement of systolic cardiac function in a murine model of dilated cardiomyopathy.

Authors:  Jiayang Li; Kenneth S Gresham; Ranganath Mamidi; Chang Yoon Doh; Xiaoping Wan; Isabelle Deschenes; Julian E Stelzer
Journal:  Int J Cardiol       Date:  2018-09-21       Impact factor: 4.164

2.  Right ventricular function as assessed by cardiac magnetic resonance imaging-derived strain parameters compared to high-fidelity micromanometer catheter measurements.

Authors:  Takahiro Sato; Bharath Ambale-Venkatesh; Stefan L Zimmerman; Ryan J Tedford; Steven Hsu; Ela Chamera; Tomoki Fujii; Christopher J Mullin; Valentina Mercurio; Rubina Khair; Celia P Corona-Villalobos; Catherine E Simpson; Rachel L Damico; Todd M Kolb; Stephen C Mathai; Joao A C Lima; David A Kass; Ichizo Tsujino; Paul M Hassoun
Journal:  Pulm Circ       Date:  2021-09-24       Impact factor: 2.886

3.  Study of the Correlation Between the Ratio of Diastolic to Systolic Durations and Echocardiography Measurements and Its Application to the Classification of Heart Failure Phenotypes.

Authors:  Lifang Cheng; Kangla Liao; Yingying Wang; Fajin Lv; Xingming Guo; Yineng Zheng; Jian Qin
Journal:  Int J Gen Med       Date:  2021-09-10
  3 in total

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