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Atrioventricular Conduction Delay Predicts Impaired Exercise Capacity in Patients with Heart Failure with Reduced Ejection Fraction
BACKGROUND: Atrioventricular conduction delay (AVCD) impairs left ventricular (LV) filling and consequently leads to a reduction of cardiac output. We hypothesized that in patients with severely depressed LV function and coexisting intraventricular conduction disturbances (IVCD), AVCD can affect exe...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5572778/ https://www.ncbi.nlm.nih.gov/pubmed/28819094 http://dx.doi.org/10.12659/MSM.902908 |
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author | Stępniewski, Jakub Kopeć, Grzegorz Magoń, Wojciech Podolec, Piotr |
author_facet | Stępniewski, Jakub Kopeć, Grzegorz Magoń, Wojciech Podolec, Piotr |
author_sort | Stępniewski, Jakub |
collection | PubMed |
description | BACKGROUND: Atrioventricular conduction delay (AVCD) impairs left ventricular (LV) filling and consequently leads to a reduction of cardiac output. We hypothesized that in patients with severely depressed LV function and coexisting intraventricular conduction disturbances (IVCD), AVCD can affect exercise performance. Therefore, we evaluated the association of AVCD and exercise capacity in patients with heart failure (HFREF) and coexisting IVCD. MATERIAL/METHODS: We included patients with stable, chronic HFREF, LVEF <35%, sinus rhythm, and QRS ≥120 ms. PR interval and peak oxygen consumption (VO(2 peak)) were specifically investigated. Multiple regression analysis was used to adjust the association between PR interval and VO(2 peak) for possible confounders. RESULTS: Most (57.5%) of the 40 included patients [20% female, aged 63±12, 47.5% of ischemic etiology (IHD)] were in NYHA class III. Mean PR interval was 196±38.1 ms. There were 26 (65%) patients with PR interval ≤200 ms and 14 (35%) with >200 ms. Groups were similar in clinical, laboratory, echocardiographic parameters, QRS morphology, and treatment regimens. VO(2 peak) was lower in patients with longer PR interval group as compared to shorter PR interval group (12.3±4.1 vs. 17.06±4.4, p=0.002). In the regression model, PR interval, female sex, and IHD remained important predictors of VO(2 peak) ((partial)=−0.50, p=0.003; r(partial)=−0.48, p=0.005; r(partial)=−0.44, p=0.01; R(2)=0.61). CONCLUSIONS: Delayed AV conduction contributes to decreased exercise capacity in patients with HFREF and coexisting IVCD. |
format | Online Article Text |
id | pubmed-5572778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55727782017-09-01 Atrioventricular Conduction Delay Predicts Impaired Exercise Capacity in Patients with Heart Failure with Reduced Ejection Fraction Stępniewski, Jakub Kopeć, Grzegorz Magoń, Wojciech Podolec, Piotr Med Sci Monit Clinical Research BACKGROUND: Atrioventricular conduction delay (AVCD) impairs left ventricular (LV) filling and consequently leads to a reduction of cardiac output. We hypothesized that in patients with severely depressed LV function and coexisting intraventricular conduction disturbances (IVCD), AVCD can affect exercise performance. Therefore, we evaluated the association of AVCD and exercise capacity in patients with heart failure (HFREF) and coexisting IVCD. MATERIAL/METHODS: We included patients with stable, chronic HFREF, LVEF <35%, sinus rhythm, and QRS ≥120 ms. PR interval and peak oxygen consumption (VO(2 peak)) were specifically investigated. Multiple regression analysis was used to adjust the association between PR interval and VO(2 peak) for possible confounders. RESULTS: Most (57.5%) of the 40 included patients [20% female, aged 63±12, 47.5% of ischemic etiology (IHD)] were in NYHA class III. Mean PR interval was 196±38.1 ms. There were 26 (65%) patients with PR interval ≤200 ms and 14 (35%) with >200 ms. Groups were similar in clinical, laboratory, echocardiographic parameters, QRS morphology, and treatment regimens. VO(2 peak) was lower in patients with longer PR interval group as compared to shorter PR interval group (12.3±4.1 vs. 17.06±4.4, p=0.002). In the regression model, PR interval, female sex, and IHD remained important predictors of VO(2 peak) ((partial)=−0.50, p=0.003; r(partial)=−0.48, p=0.005; r(partial)=−0.44, p=0.01; R(2)=0.61). CONCLUSIONS: Delayed AV conduction contributes to decreased exercise capacity in patients with HFREF and coexisting IVCD. International Scientific Literature, Inc. 2017-08-18 /pmc/articles/PMC5572778/ /pubmed/28819094 http://dx.doi.org/10.12659/MSM.902908 Text en © Med Sci Monit, 2017 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Clinical Research Stępniewski, Jakub Kopeć, Grzegorz Magoń, Wojciech Podolec, Piotr Atrioventricular Conduction Delay Predicts Impaired Exercise Capacity in Patients with Heart Failure with Reduced Ejection Fraction |
title | Atrioventricular Conduction Delay Predicts Impaired Exercise Capacity in Patients with Heart Failure with Reduced Ejection Fraction |
title_full | Atrioventricular Conduction Delay Predicts Impaired Exercise Capacity in Patients with Heart Failure with Reduced Ejection Fraction |
title_fullStr | Atrioventricular Conduction Delay Predicts Impaired Exercise Capacity in Patients with Heart Failure with Reduced Ejection Fraction |
title_full_unstemmed | Atrioventricular Conduction Delay Predicts Impaired Exercise Capacity in Patients with Heart Failure with Reduced Ejection Fraction |
title_short | Atrioventricular Conduction Delay Predicts Impaired Exercise Capacity in Patients with Heart Failure with Reduced Ejection Fraction |
title_sort | atrioventricular conduction delay predicts impaired exercise capacity in patients with heart failure with reduced ejection fraction |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5572778/ https://www.ncbi.nlm.nih.gov/pubmed/28819094 http://dx.doi.org/10.12659/MSM.902908 |
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