Atrial arrhythmias are associated with increased mortality in pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is a deadly vascular disease, characterized by increased pulmonary arterial pressures and right heart failure. Considering prior non-US studies of atrial arrhythmias in PAH, this retrospective, regional multi-center US study sought to define more completely the...

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Main Authors: Benjamin Smith, Michael V. Genuardi, Agnes Koczo, Richard H. Zou, Floyd W. Thoma, Adam Handen, Ethan Craig, Caroline M. Hogan, Timothy Girard, Andrew D. Althouse, Stephen Y. Chan
Format: Article
Language:English
Published: SAGE Publishing 2018-07-01
Series:Pulmonary Circulation
Online Access:https://doi.org/10.1177/2045894018790316
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spelling doaj-897a785c626846f089d9978e074f7dcf2020-11-25T03:17:37ZengSAGE PublishingPulmonary Circulation2045-89402018-07-01810.1177/2045894018790316Atrial arrhythmias are associated with increased mortality in pulmonary arterial hypertensionBenjamin Smith0Michael V. Genuardi1Agnes Koczo2Richard H. Zou3Floyd W. Thoma4Adam Handen5Ethan Craig6Caroline M. Hogan7Timothy Girard8Andrew D. Althouse9Stephen Y. Chan10Department of Medicine, University of Pittsburgh, USACenter for Pulmonary Vascular Biology and Medicine, Pittsburgh Heart, Lung, and Blood Vascular Medicine Institute, Division of Cardiology, Department of Medicine, University of Pittsburgh Medical Center, USADepartment of Medicine, University of Pittsburgh, USADepartment of Medicine, University of Pittsburgh, USADepartment of Medicine, University of Pittsburgh, USACenter for Pulmonary Vascular Biology and Medicine, Pittsburgh Heart, Lung, and Blood Vascular Medicine Institute, Division of Cardiology, Department of Medicine, University of Pittsburgh Medical Center, USADepartment of Medicine, University of Pittsburgh, USADepartment of Medicine, University of Pittsburgh, USAClinical Research, Investigation, and Systems Modeling of Acute illness (CRISMA) Center; Department of Critical Care Medicine, University of Pittsburgh School of Medicine, USADepartment of Medicine, University of Pittsburgh, USACenter for Pulmonary Vascular Biology and Medicine, Pittsburgh Heart, Lung, and Blood Vascular Medicine Institute, Division of Cardiology, Department of Medicine, University of Pittsburgh Medical Center, USAPulmonary arterial hypertension (PAH) is a deadly vascular disease, characterized by increased pulmonary arterial pressures and right heart failure. Considering prior non-US studies of atrial arrhythmias in PAH, this retrospective, regional multi-center US study sought to define more completely the risk factors and impact of paroxysmal and non-paroxysmal forms of atrial fibrillation and flutter (AF/AFL) on mortality in this disease. We identified patients seen between 2010 and 2014 at UPMC (Pittsburgh) hospitals with hemodynamic and clinical criteria for PAH or chronic thromboembolic pulmonary hypertension (CTEPH) and determined those meeting electrocardiographic criteria for AF/AFL. We used Cox proportional hazards regression with time-varying covariates to analyze the association between AF/AFL occurrence and survival with adjustments for potential cofounders and hemodynamic severity. Of 297 patients with PAH/CTEPH, 79 (26.5%) suffered from AF/AFL at some point. AF/AFL was first identified after PAH diagnosis in 42 (53.2%), identified prior to PAH diagnosis in 27 (34.2%), and had unclear timing in the remainder. AF/AFL patients were older, more often male, had lower left ventricular ejection fractions, and greater left atrial volume indices and right atrial areas than patients without AF/AFL. AF/AFL (whether diagnosed before or after PAH) was associated with a 3.81-fold increase in the hazard of death (95% CI 2.64–5.52, p  < 0.001). This finding was consistent with multivariable adjustment of hemodynamic, cardiac structural, and heart rate indices as well as in sensitivity analyses of patients with paroxysmal versus non-paroxysmal arrhythmias. In these PAH/CTEPH patients, presence of AF/AFL significantly increased mortality risk. Mortality remained elevated in the absence of a high burden of uncontrolled or persistent arrhythmias, thus suggesting additional etiologies beyond rapid heart rate as an explanation. Future studies are warranted to confirm this observation and interrogate whether other therapies beyond rate and rhythm control are necessary to mitigate this risk.https://doi.org/10.1177/2045894018790316
collection DOAJ
language English
format Article
sources DOAJ
author Benjamin Smith
Michael V. Genuardi
Agnes Koczo
Richard H. Zou
Floyd W. Thoma
Adam Handen
Ethan Craig
Caroline M. Hogan
Timothy Girard
Andrew D. Althouse
Stephen Y. Chan
spellingShingle Benjamin Smith
Michael V. Genuardi
Agnes Koczo
Richard H. Zou
Floyd W. Thoma
Adam Handen
Ethan Craig
Caroline M. Hogan
Timothy Girard
Andrew D. Althouse
Stephen Y. Chan
Atrial arrhythmias are associated with increased mortality in pulmonary arterial hypertension
Pulmonary Circulation
author_facet Benjamin Smith
Michael V. Genuardi
Agnes Koczo
Richard H. Zou
Floyd W. Thoma
Adam Handen
Ethan Craig
Caroline M. Hogan
Timothy Girard
Andrew D. Althouse
Stephen Y. Chan
author_sort Benjamin Smith
title Atrial arrhythmias are associated with increased mortality in pulmonary arterial hypertension
title_short Atrial arrhythmias are associated with increased mortality in pulmonary arterial hypertension
title_full Atrial arrhythmias are associated with increased mortality in pulmonary arterial hypertension
title_fullStr Atrial arrhythmias are associated with increased mortality in pulmonary arterial hypertension
title_full_unstemmed Atrial arrhythmias are associated with increased mortality in pulmonary arterial hypertension
title_sort atrial arrhythmias are associated with increased mortality in pulmonary arterial hypertension
publisher SAGE Publishing
series Pulmonary Circulation
issn 2045-8940
publishDate 2018-07-01
description Pulmonary arterial hypertension (PAH) is a deadly vascular disease, characterized by increased pulmonary arterial pressures and right heart failure. Considering prior non-US studies of atrial arrhythmias in PAH, this retrospective, regional multi-center US study sought to define more completely the risk factors and impact of paroxysmal and non-paroxysmal forms of atrial fibrillation and flutter (AF/AFL) on mortality in this disease. We identified patients seen between 2010 and 2014 at UPMC (Pittsburgh) hospitals with hemodynamic and clinical criteria for PAH or chronic thromboembolic pulmonary hypertension (CTEPH) and determined those meeting electrocardiographic criteria for AF/AFL. We used Cox proportional hazards regression with time-varying covariates to analyze the association between AF/AFL occurrence and survival with adjustments for potential cofounders and hemodynamic severity. Of 297 patients with PAH/CTEPH, 79 (26.5%) suffered from AF/AFL at some point. AF/AFL was first identified after PAH diagnosis in 42 (53.2%), identified prior to PAH diagnosis in 27 (34.2%), and had unclear timing in the remainder. AF/AFL patients were older, more often male, had lower left ventricular ejection fractions, and greater left atrial volume indices and right atrial areas than patients without AF/AFL. AF/AFL (whether diagnosed before or after PAH) was associated with a 3.81-fold increase in the hazard of death (95% CI 2.64–5.52, p  < 0.001). This finding was consistent with multivariable adjustment of hemodynamic, cardiac structural, and heart rate indices as well as in sensitivity analyses of patients with paroxysmal versus non-paroxysmal arrhythmias. In these PAH/CTEPH patients, presence of AF/AFL significantly increased mortality risk. Mortality remained elevated in the absence of a high burden of uncontrolled or persistent arrhythmias, thus suggesting additional etiologies beyond rapid heart rate as an explanation. Future studies are warranted to confirm this observation and interrogate whether other therapies beyond rate and rhythm control are necessary to mitigate this risk.
url https://doi.org/10.1177/2045894018790316
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