Baseline NT-proBNP predicts acute kidney injury following transcatheter aortic valve implantation.

AKI NT-proBNP TAVI

Journal

Cardiovascular revascularization medicine : including molecular interventions
ISSN: 1878-0938
Titre abrégé: Cardiovasc Revasc Med
Pays: United States
ID NLM: 101238551

Informations de publication

Date de publication:
30 Mar 2024
Historique:
received: 01 12 2023
revised: 22 02 2024
accepted: 26 03 2024
medline: 11 4 2024
pubmed: 11 4 2024
entrez: 10 4 2024
Statut: aheadofprint

Résumé

Acute kidney injury (AKI) after transcatheter aortic valve implantation (TAVI) increases morbidity and mortality. Our study aimed to investigate the role of baseline N-terminal pro B-type natriuretic peptide (NT-proBNP) as a predictor of AKI following TAVI. All consecutive TAVI patients were included in the analysis, except patients with dialysis and those with a GFR < 15 ml/min/1.73 m We included 1973 patients treated with TAVI between January 2006 and December 2016. Median [IQR] age was 81.0 [77.0;84.0] years, the STS score was 6.2 [3.9;9.0], and the logEuroScore was 14.5 [9.0;23.0]. 30-day and one-year mortality was 5.1 % and 16.1 % for all patients, respectively. Multivariate analysis revealed that patients with NT-proBNP levels higher than two times above the upper level of normal (ULN) had an increased risk for AKI after TAVI compared to patients with NT-proBNP levels < 2× ULN (OR 1.40 [1.03-1.91]). Routine assessment of baseline NT-proBNP levels might be an additional tool to identify patients at increased risk for AKI after TAVI.

Sections du résumé

BACKGROUND/PURPOSE OBJECTIVE
Acute kidney injury (AKI) after transcatheter aortic valve implantation (TAVI) increases morbidity and mortality. Our study aimed to investigate the role of baseline N-terminal pro B-type natriuretic peptide (NT-proBNP) as a predictor of AKI following TAVI.
METHODS METHODS
All consecutive TAVI patients were included in the analysis, except patients with dialysis and those with a GFR < 15 ml/min/1.73 m
RESULTS RESULTS
We included 1973 patients treated with TAVI between January 2006 and December 2016. Median [IQR] age was 81.0 [77.0;84.0] years, the STS score was 6.2 [3.9;9.0], and the logEuroScore was 14.5 [9.0;23.0]. 30-day and one-year mortality was 5.1 % and 16.1 % for all patients, respectively. Multivariate analysis revealed that patients with NT-proBNP levels higher than two times above the upper level of normal (ULN) had an increased risk for AKI after TAVI compared to patients with NT-proBNP levels < 2× ULN (OR 1.40 [1.03-1.91]).
CONCLUSIONS CONCLUSIONS
Routine assessment of baseline NT-proBNP levels might be an additional tool to identify patients at increased risk for AKI after TAVI.

Identifiants

pubmed: 38599917
pii: S1553-8389(24)00115-5
doi: 10.1016/j.carrev.2024.03.027
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of competing interest Christina Eckrich has no conflict of interest. Sandra Erbs has no conflict of interest. Norman Mangner reports speaker's honoraria from Edwards, Medtronic, Novartis, Sanofi Genzyme, and Astra Zeneca, consultant honoraria from Biotronik, outside the submitted work. Felix Woitek has no conflict of interest. Philipp Kiefer has no conflict of interest. Florian Schlotter has no conflict of interest. Georg Stachel has no conflict of interest. Sergey Leontyev reports personal fees from St. Jude Medical and Medtronic, outside the submitted work. David Holzhey reports personal fees from Symetis and Medtronic, outside the submitted work. Michael A. Borger reports speakers' honoraria and consulting fees from Edwards Lifesciences, Medtronic, and CryoLife, outside the submitted work. Axel Linke reports grants and personal fees from Medtronic, personal fees from St. Jude Medical, grants from Claret Medical, personal fees and other from Claret Medical, personal fees from Boston Scientific, personal fees from Bard, personal fees from Edwards, outside the submitted work. Stephan Haussig reports speakers' honoraria and consulting fees from Edwards Lifesciences, Abbott, Cardiac Dimensions, and Boston Scientific, outside the submitted work

Auteurs

Kristina Eckrich (K)

Helios Park-Klinikum Leipzig, Department of Internal Medicine and Cardiology, Leipzig, Germany.

Norman Mangner (N)

Herzzentrum Dresden, University Clinic, Technische Universitaet Dresden, Department of Internal Medicine and Cardiology, Dresden, Germany.

Sandra Erbs (S)

University of Leipzig - Heart Center, Department of Internal Medicine and Cardiology, Leipzig, Germany.

Felix Woitek (F)

Herzzentrum Dresden, University Clinic, Technische Universitaet Dresden, Department of Internal Medicine and Cardiology, Dresden, Germany.

Philipp Kiefer (P)

University of Leipzig - Heart Center, Department of Cardiac Surgery, Leipzig, Germany.

Florian Schlotter (F)

University of Leipzig - Heart Center, Department of Internal Medicine and Cardiology, Leipzig, Germany.

Georg Stachel (G)

Klinik und Poliklinik für Kardiologie, Leipzig University Clinic, Leipzig, Germany.

Sergey Leontyev (S)

University of Leipzig - Heart Center, Department of Cardiac Surgery, Leipzig, Germany.

David Holzhey (D)

Helios Heart Center Wuppertal, Department of Cardiac Surgery, Witten/Herdecke University, Wuppertal, Germany.

Michael A Borger (MA)

University of Leipzig - Heart Center, Department of Cardiac Surgery, Leipzig, Germany.

Axel Linke (A)

Herzzentrum Dresden, University Clinic, Technische Universitaet Dresden, Department of Internal Medicine and Cardiology, Dresden, Germany.

Stephan Haussig (S)

Herzzentrum Dresden, University Clinic, Technische Universitaet Dresden, Department of Internal Medicine and Cardiology, Dresden, Germany. Electronic address: stephan.haussig@tu-dresden.de.

Classifications MeSH