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Atrial Fibrillation Is Associated With Mortality in Intermediate Surgical Risk Patients With Severe Aortic Stenosis: Analyses From the PARTNER 2A and PARTNER S3i Trials
BACKGROUND: The impact of atrial fibrillation (AF) in intermediate surgical risk patients with severe aortic stenosis who undergo either transcatheter or surgical aortic valve replacement (AVR) is not well established. METHODS AND RESULTS: Data were assessed in 2663 patients from the PARTNER (Placem...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8174321/ https://www.ncbi.nlm.nih.gov/pubmed/33754803 http://dx.doi.org/10.1161/JAHA.120.019584 |
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author | Brener, Michael I. George, Isaac Kosmidou, Ioanna Nazif, Tamim Zhang, Zixuan Dizon, Jose M. Garan, Hasan Malaisrie, S. Chris Makkar, Raj Mack, Michael Szeto, Wilson Y. Fearon, William F. Thourani, Vinod H. Leon, Martin B. Kodali, Susheel Biviano, Angelo B. |
author_facet | Brener, Michael I. George, Isaac Kosmidou, Ioanna Nazif, Tamim Zhang, Zixuan Dizon, Jose M. Garan, Hasan Malaisrie, S. Chris Makkar, Raj Mack, Michael Szeto, Wilson Y. Fearon, William F. Thourani, Vinod H. Leon, Martin B. Kodali, Susheel Biviano, Angelo B. |
author_sort | Brener, Michael I. |
collection | PubMed |
description | BACKGROUND: The impact of atrial fibrillation (AF) in intermediate surgical risk patients with severe aortic stenosis who undergo either transcatheter or surgical aortic valve replacement (AVR) is not well established. METHODS AND RESULTS: Data were assessed in 2663 patients from the PARTNER (Placement of Aortic Transcatheter Valve) 2A or S3i trials. Analyses grouped patients into 3 categories according to their baseline and discharge rhythms (ie, sinus rhythm [SR]/SR, SR/AF, or AF/AF). Among patients with transcatheter AVR (n=1867), 79.2% had SR/SR, 17.6% had AF/AF, and 3.2% had SR/AF. Among patients with surgical AVR (n=796), 71.7% had SR/SR, 14.1% had AF/AF, and 14.2% had SR/AF. Patients with transcatheter AVR in AF at discharge had increased 2‐year mortality (SR/AF versus SR/SR; hazard ratio [HR], 2.73; 95% CI, 1.68–4.44; P<0.0001; AF/AF versus SR/SR; HR, 1.56; 95% CI, 1.16–2.09; P=0.003); patients with SR/AF also experienced increased 2‐year mortality relative to patients with AF/AF (HR, 1.77; 95% CI, 1.04–3.00; P=0.03). For patients with surgicalAVR, the presence of AF at discharge was also associated with increased 2‐year mortality (SR/AF versus SR/SR; HR, 1.93; 95% CI, 1.25–2.96; P=0.002; and AF/AF versus SR/SR; HR, 1.67; 95% CI, 1.06–2.63; P=0.027). Rehospitalization and persistent advanced heart failure symptoms were also more common among patients with transcatheter AVR and surgical AVR discharged in AF, and major bleeding was more common in the transcatheter AVR cohort. CONCLUSIONS: The presence of AF at discharge in patients with intermediate surgical risk aortic stenosis was associated with worse outcomes—especially in patients with baseline SR—including increased all‐cause mortality at 2‐year follow‐up. REGISTRATION: URL: https://www.clinicaltrials.gov; Unique identifiers: NCT01314313 and NCT03222128. |
format | Online Article Text |
id | pubmed-8174321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81743212021-06-11 Atrial Fibrillation Is Associated With Mortality in Intermediate Surgical Risk Patients With Severe Aortic Stenosis: Analyses From the PARTNER 2A and PARTNER S3i Trials Brener, Michael I. George, Isaac Kosmidou, Ioanna Nazif, Tamim Zhang, Zixuan Dizon, Jose M. Garan, Hasan Malaisrie, S. Chris Makkar, Raj Mack, Michael Szeto, Wilson Y. Fearon, William F. Thourani, Vinod H. Leon, Martin B. Kodali, Susheel Biviano, Angelo B. J Am Heart Assoc Original Research BACKGROUND: The impact of atrial fibrillation (AF) in intermediate surgical risk patients with severe aortic stenosis who undergo either transcatheter or surgical aortic valve replacement (AVR) is not well established. METHODS AND RESULTS: Data were assessed in 2663 patients from the PARTNER (Placement of Aortic Transcatheter Valve) 2A or S3i trials. Analyses grouped patients into 3 categories according to their baseline and discharge rhythms (ie, sinus rhythm [SR]/SR, SR/AF, or AF/AF). Among patients with transcatheter AVR (n=1867), 79.2% had SR/SR, 17.6% had AF/AF, and 3.2% had SR/AF. Among patients with surgical AVR (n=796), 71.7% had SR/SR, 14.1% had AF/AF, and 14.2% had SR/AF. Patients with transcatheter AVR in AF at discharge had increased 2‐year mortality (SR/AF versus SR/SR; hazard ratio [HR], 2.73; 95% CI, 1.68–4.44; P<0.0001; AF/AF versus SR/SR; HR, 1.56; 95% CI, 1.16–2.09; P=0.003); patients with SR/AF also experienced increased 2‐year mortality relative to patients with AF/AF (HR, 1.77; 95% CI, 1.04–3.00; P=0.03). For patients with surgicalAVR, the presence of AF at discharge was also associated with increased 2‐year mortality (SR/AF versus SR/SR; HR, 1.93; 95% CI, 1.25–2.96; P=0.002; and AF/AF versus SR/SR; HR, 1.67; 95% CI, 1.06–2.63; P=0.027). Rehospitalization and persistent advanced heart failure symptoms were also more common among patients with transcatheter AVR and surgical AVR discharged in AF, and major bleeding was more common in the transcatheter AVR cohort. CONCLUSIONS: The presence of AF at discharge in patients with intermediate surgical risk aortic stenosis was associated with worse outcomes—especially in patients with baseline SR—including increased all‐cause mortality at 2‐year follow‐up. REGISTRATION: URL: https://www.clinicaltrials.gov; Unique identifiers: NCT01314313 and NCT03222128. John Wiley and Sons Inc. 2021-03-23 /pmc/articles/PMC8174321/ /pubmed/33754803 http://dx.doi.org/10.1161/JAHA.120.019584 Text en © 2021 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Research Brener, Michael I. George, Isaac Kosmidou, Ioanna Nazif, Tamim Zhang, Zixuan Dizon, Jose M. Garan, Hasan Malaisrie, S. Chris Makkar, Raj Mack, Michael Szeto, Wilson Y. Fearon, William F. Thourani, Vinod H. Leon, Martin B. Kodali, Susheel Biviano, Angelo B. Atrial Fibrillation Is Associated With Mortality in Intermediate Surgical Risk Patients With Severe Aortic Stenosis: Analyses From the PARTNER 2A and PARTNER S3i Trials |
title | Atrial Fibrillation Is Associated With Mortality in Intermediate Surgical Risk Patients With Severe Aortic Stenosis: Analyses From the PARTNER 2A and PARTNER S3i Trials |
title_full | Atrial Fibrillation Is Associated With Mortality in Intermediate Surgical Risk Patients With Severe Aortic Stenosis: Analyses From the PARTNER 2A and PARTNER S3i Trials |
title_fullStr | Atrial Fibrillation Is Associated With Mortality in Intermediate Surgical Risk Patients With Severe Aortic Stenosis: Analyses From the PARTNER 2A and PARTNER S3i Trials |
title_full_unstemmed | Atrial Fibrillation Is Associated With Mortality in Intermediate Surgical Risk Patients With Severe Aortic Stenosis: Analyses From the PARTNER 2A and PARTNER S3i Trials |
title_short | Atrial Fibrillation Is Associated With Mortality in Intermediate Surgical Risk Patients With Severe Aortic Stenosis: Analyses From the PARTNER 2A and PARTNER S3i Trials |
title_sort | atrial fibrillation is associated with mortality in intermediate surgical risk patients with severe aortic stenosis: analyses from the partner 2a and partner s3i trials |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8174321/ https://www.ncbi.nlm.nih.gov/pubmed/33754803 http://dx.doi.org/10.1161/JAHA.120.019584 |
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