An association between right ventricular dysfunction and sudden cardiac death.


Journal

Heart rhythm
ISSN: 1556-3871
Titre abrégé: Heart Rhythm
Pays: United States
ID NLM: 101200317

Informations de publication

Date de publication:
02 2020
Historique:
received: 31 07 2019
pubmed: 22 10 2019
medline: 28 4 2021
entrez: 22 10 2019
Statut: ppublish

Résumé

The effectiveness of severely reduced left ventricular ejection fraction (LVEF <35%) as a predictor of sudden cardiac death (SCD) has diminished, and improvements in risk stratification await discovery of novel markers. Right ventricular (RV) abnormalities can be observed in conditions such as chronic obstructive pulmonary disease and sleep apnea, which have been linked to SCD. The purpose of this study was to evaluate whether RV abnormalities were associated with SCD after accounting for LVEF and other patient characteristics. In a large, prospective ongoing community-based study of SCD in the Portland, Oregon, metropolitan area, SCD cases (age ≥18 years; 2002-2014) were compared to controls with coronary artery disease but no SCD. Using a novel archive of digital echocardiograms, a standardized approach was used to evaluate RV basal diameter, RV end-diastolic area, and right ventricular fractional area change (RVFAC). A total of 350 subjects were studied, including 81 SCD cases (age 68.7 ± 13.6 years; 73% male) and 269 controls (age 66.5 ± 10.2 years; 69% male). In multivariate analysis, RVFAC was significantly associated with SCD (odds ratio 1.14 for each 5% decrease; 95% confidence interval 1.03-1.25; P = .01). When modeled with LVEF ≤35%, RVFAC ≤35% was significantly associated with increased risk of SCD. Individuals with both left ventricular and RV dysfunction had a 3× higher odds of SCD than those with neither (odds ratio 3.19; 95% confidence interval 1.33-7.68; P = .01). RV dysfunction was associated with a significantly increased risk of SCD independent of LVEF and, when combined with LVEF, had additive effects on SCD risk.

Sections du résumé

BACKGROUND
The effectiveness of severely reduced left ventricular ejection fraction (LVEF <35%) as a predictor of sudden cardiac death (SCD) has diminished, and improvements in risk stratification await discovery of novel markers. Right ventricular (RV) abnormalities can be observed in conditions such as chronic obstructive pulmonary disease and sleep apnea, which have been linked to SCD.
OBJECTIVE
The purpose of this study was to evaluate whether RV abnormalities were associated with SCD after accounting for LVEF and other patient characteristics.
METHODS
In a large, prospective ongoing community-based study of SCD in the Portland, Oregon, metropolitan area, SCD cases (age ≥18 years; 2002-2014) were compared to controls with coronary artery disease but no SCD. Using a novel archive of digital echocardiograms, a standardized approach was used to evaluate RV basal diameter, RV end-diastolic area, and right ventricular fractional area change (RVFAC).
RESULTS
A total of 350 subjects were studied, including 81 SCD cases (age 68.7 ± 13.6 years; 73% male) and 269 controls (age 66.5 ± 10.2 years; 69% male). In multivariate analysis, RVFAC was significantly associated with SCD (odds ratio 1.14 for each 5% decrease; 95% confidence interval 1.03-1.25; P = .01). When modeled with LVEF ≤35%, RVFAC ≤35% was significantly associated with increased risk of SCD. Individuals with both left ventricular and RV dysfunction had a 3× higher odds of SCD than those with neither (odds ratio 3.19; 95% confidence interval 1.33-7.68; P = .01).
CONCLUSION
RV dysfunction was associated with a significantly increased risk of SCD independent of LVEF and, when combined with LVEF, had additive effects on SCD risk.

Identifiants

pubmed: 31634617
pii: S1547-5271(19)30943-9
doi: 10.1016/j.hrthm.2019.10.021
pmc: PMC8078030
mid: NIHMS1544613
pii:
doi:

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

169-174

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL122492
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL126938
Pays : United States

Informations de copyright

Copyright © 2019 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.

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Auteurs

Summit Pandat (S)

Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California.

Takafumi Nagaura (T)

Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California.

Sandeep G Nair (SG)

Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California.

Audrey Uy-Evanado (A)

Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California.

Eric C Stecker (EC)

Knight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon.

Gregory A Nichols (GA)

Kaiser Permanente Center for Health Research, Portland, Oregon.

Jonathan Jui (J)

Department of Emergency Medicine, Oregon Health & Science University, Portland, Oregon.

Takahiro Shiota (T)

Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California.

Sumeet S Chugh (SS)

Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California.

Kyndaron Reinier (K)

Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California. Electronic address: kyndaron.reinier@cshs.org.

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Classifications MeSH