Impact of Transcatheter Aortic Valve Replacement on Severity of Chronic Kidney Disease.


Journal

Journal of the American College of Cardiology
ISSN: 1558-3597
Titre abrégé: J Am Coll Cardiol
Pays: United States
ID NLM: 8301365

Informations de publication

Date de publication:
22 09 2020
Historique:
received: 03 06 2020
revised: 15 07 2020
accepted: 20 07 2020
entrez: 18 9 2020
pubmed: 19 9 2020
medline: 2 2 2021
Statut: ppublish

Résumé

The effect of transcatheter aortic valve replacement (TAVR) on kidney function stage in patients with aortic stenosis remains poorly understood. We hypothesized that in some patients, TAVR results in improved kidney function by alleviating cardiorenal syndrome. The purpose of this study was to assess change in chronic kidney disease (CKD) stage following TAVR, identify variables associated with pre- and post-TAVR estimated glomerular filtration rate (eGFR), and assess association of post-TAVR eGFR with mortality. Patients (n = 5,190) receiving TAVR in the PARTNER (Placement of Aortic Transcatheter Valves) 1, 2, and PARTNER 2 S3 trials between April 2007 and October 2014 were included. Pre-TAVR and procedural variables associated with post-TAVR eGFR, change in CKD stage at ≤7 days post-TAVR, and association of post-TAVR eGFR on intermediate-term mortality were assessed. At baseline, CKD stage ≥2 was present in 91% of patients. CKD stage either improved or was unchanged following TAVR in the majority of patients (77% stage 1, 90% stage 2, 89% stage 3A, 94% stage 3B, and 99% stage 4). Progression to CKD stage 5 occurred in 1 (0.035%) of 2,892 patients within 7 days post-TAVR. Of 3,546 patients in whom data were available, 70 (2.0%) underwent post-TAVR dialysis. Higher pre-TAVR eGFR and transfemoral approach were strongly associated with higher post-TAVR eGFR. Lower baseline and longitudinal post-TAVR eGFR were associated with lower intermediate-term survival. In patients with severe aortic stenosis undergoing TAVR, even with baseline impaired eGFR, CKD stage is more likely to stay the same or improve than worsen. Aortic stenosis may contribute to cardiorenal syndrome that improves with TAVR.

Sections du résumé

BACKGROUND
The effect of transcatheter aortic valve replacement (TAVR) on kidney function stage in patients with aortic stenosis remains poorly understood. We hypothesized that in some patients, TAVR results in improved kidney function by alleviating cardiorenal syndrome.
OBJECTIVES
The purpose of this study was to assess change in chronic kidney disease (CKD) stage following TAVR, identify variables associated with pre- and post-TAVR estimated glomerular filtration rate (eGFR), and assess association of post-TAVR eGFR with mortality.
METHODS
Patients (n = 5,190) receiving TAVR in the PARTNER (Placement of Aortic Transcatheter Valves) 1, 2, and PARTNER 2 S3 trials between April 2007 and October 2014 were included. Pre-TAVR and procedural variables associated with post-TAVR eGFR, change in CKD stage at ≤7 days post-TAVR, and association of post-TAVR eGFR on intermediate-term mortality were assessed.
RESULTS
At baseline, CKD stage ≥2 was present in 91% of patients. CKD stage either improved or was unchanged following TAVR in the majority of patients (77% stage 1, 90% stage 2, 89% stage 3A, 94% stage 3B, and 99% stage 4). Progression to CKD stage 5 occurred in 1 (0.035%) of 2,892 patients within 7 days post-TAVR. Of 3,546 patients in whom data were available, 70 (2.0%) underwent post-TAVR dialysis. Higher pre-TAVR eGFR and transfemoral approach were strongly associated with higher post-TAVR eGFR. Lower baseline and longitudinal post-TAVR eGFR were associated with lower intermediate-term survival.
CONCLUSIONS
In patients with severe aortic stenosis undergoing TAVR, even with baseline impaired eGFR, CKD stage is more likely to stay the same or improve than worsen. Aortic stenosis may contribute to cardiorenal syndrome that improves with TAVR.

Identifiants

pubmed: 32943158
pii: S0735-1097(20)36112-X
doi: 10.1016/j.jacc.2020.07.048
pii:
doi:

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1410-1421

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Auteurs

Robert J Cubeddu (RJ)

Cardiovascular Medicine, Heart and Vascular Institute, Cleveland Clinic Weston, Weston, Florida. Electronic address: CUBEDDR@ccf.org.

Craig R Asher (CR)

Cardiovascular Medicine, Heart and Vascular Institute, Cleveland Clinic Weston, Weston, Florida.

Ashley M Lowry (AM)

Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.

Eugene H Blackstone (EH)

Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio; Thoracic and Cardiovascular Surgery, Heart, Vascular, and Thoracic Institute, Cleveland Clinic, Cleveland, Ohio.

Samir R Kapadia (SR)

Cardiovascular Medicine, Heart, Vascular, and Thoracic Institute, Cleveland Clinic, Cleveland, Ohio.

Maria C Alu (MC)

Center for Interventional Vascular Therapy, Columbia University Medical Center/New York Presbyterian Hospital, New York, New York.

Vinod H Thourani (VH)

Cardiovascular Surgery, Marcus Heart and Vascular Center, Piedmont Heart and Vascular Institute, Atlanta, Georgia.

Michael J Mack (MJ)

Cardiothoracic Surery, Baylor Scott & White Health, Plano, Texas.

Susheel K Kodali (SK)

Structural Heart and Valve Center, Columbia University Medical Center/New York Presbyterian Hospital, New York, New York.

Howard C Herrmann (HC)

Cardiology, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania.

Jessica Forcillo (J)

Cardiac Surgery, University of Montreal Hospital Centre, Montreal, Quebec, Canada.

Vasilis C Babaliaros (VC)

Structural Heart and Valve Center, Emory University School of Medicine, Atlanta, Georgia.

Chandan M Devireddy (CM)

Cardiology, Emory University School of Medicine, Atlanta, Georgia.

S Chris Malaisrie (SC)

Cardiac Surgery, Northwestern University Feinberg School of Medicine and Northwestern Memorial Hospital, Chicago, Illinois.

Charles J Davidson (CJ)

Cardiovascular Medicine, Northwestern University Feinberg School of Medicine and Northwestern Memorial Hospital, Chicago, Illinois.

Wael A Jaber (WA)

Cardiovascular Medicine, Heart, Vascular, and Thoracic Institute, Cleveland Clinic, Cleveland, Ohio.

Martin B Leon (MB)

Center for Interventional Vascular Therapy, Columbia University Medical Center/New York Presbyterian Hospital, New York, New York.

Lars G Svensson (LG)

Thoracic and Cardiovascular Surgery, Heart, Vascular, and Thoracic Institute, Cleveland Clinic, Cleveland, Ohio.

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Classifications MeSH