Development and Validation of a Practical Model to Identify Patients at Risk of Bleeding After TAVR.


Journal

JACC. Cardiovascular interventions
ISSN: 1876-7605
Titre abrégé: JACC Cardiovasc Interv
Pays: United States
ID NLM: 101467004

Informations de publication

Date de publication:
14 06 2021
Historique:
received: 04 12 2020
revised: 05 03 2021
accepted: 09 03 2021
entrez: 11 6 2021
pubmed: 12 6 2021
medline: 28 10 2021
Statut: ppublish

Résumé

No standardized algorithm exists to identify patients at risk of bleeding after transcatheter aortic valve replacement (TAVR). The aim of this study was to generate and validate a useful predictive model. Bleeding events after TAVR influence prognosis and quality of life and may be preventable. Using machine learning and multivariate regression, more than 100 clinical variables from 5,185 consecutive patients undergoing TAVR in the prospective multicenter RISPEVA (Registro Italiano GISE sull'Impianto di Valvola Aortica Percutanea; NCT02713932) registry were analyzed in relation to Valve Academic Research Consortium-2 bleeding episodes at 1 month. The model's performance was externally validated in 5,043 TAVR patients from the prospective multicenter POL-TAVI (Polish Registry of Transcatheter Aortic Valve Implantation) database. Derivation analyses generated a 6-item score (PREDICT-TAVR) comprising blood hemoglobin and serum iron concentrations, oral anticoagulation and dual antiplatelet therapy, common femoral artery diameter, and creatinine clearance. The 30-day area under the receiver-operating characteristic curve (AUC) was 0.80 (95% confidence interval [CI]: 0.75-0.83). Internal validation by optimism bootstrap-corrected AUC was 0.79 (95% CI: 0.75-0.83). Score quartiles were in graded relation to 30-day events (0.8%, 1.1%, 2.5%, and 8.5%; overall p <0.001). External validation produced a 30-day AUC of 0.78 (95% CI: 0.72-0.82). A simple nomogram and a web-based calculator were developed to predict individual patient probabilities. Landmark cumulative event analysis showed greatest bleeding risk differences for top versus lower score quartiles in the first 30 days, when most events occurred. Predictivity was maintained when omitting serum iron values. PREDICT-TAVR is a practical, validated, 6-item tool to identify patients at risk of bleeding post-TAVR that can assist in decision making and event prevention.

Sections du résumé

OBJECTIVES
No standardized algorithm exists to identify patients at risk of bleeding after transcatheter aortic valve replacement (TAVR). The aim of this study was to generate and validate a useful predictive model.
BACKGROUND
Bleeding events after TAVR influence prognosis and quality of life and may be preventable.
METHODS
Using machine learning and multivariate regression, more than 100 clinical variables from 5,185 consecutive patients undergoing TAVR in the prospective multicenter RISPEVA (Registro Italiano GISE sull'Impianto di Valvola Aortica Percutanea; NCT02713932) registry were analyzed in relation to Valve Academic Research Consortium-2 bleeding episodes at 1 month. The model's performance was externally validated in 5,043 TAVR patients from the prospective multicenter POL-TAVI (Polish Registry of Transcatheter Aortic Valve Implantation) database.
RESULTS
Derivation analyses generated a 6-item score (PREDICT-TAVR) comprising blood hemoglobin and serum iron concentrations, oral anticoagulation and dual antiplatelet therapy, common femoral artery diameter, and creatinine clearance. The 30-day area under the receiver-operating characteristic curve (AUC) was 0.80 (95% confidence interval [CI]: 0.75-0.83). Internal validation by optimism bootstrap-corrected AUC was 0.79 (95% CI: 0.75-0.83). Score quartiles were in graded relation to 30-day events (0.8%, 1.1%, 2.5%, and 8.5%; overall p <0.001). External validation produced a 30-day AUC of 0.78 (95% CI: 0.72-0.82). A simple nomogram and a web-based calculator were developed to predict individual patient probabilities. Landmark cumulative event analysis showed greatest bleeding risk differences for top versus lower score quartiles in the first 30 days, when most events occurred. Predictivity was maintained when omitting serum iron values.
CONCLUSIONS
PREDICT-TAVR is a practical, validated, 6-item tool to identify patients at risk of bleeding post-TAVR that can assist in decision making and event prevention.

Identifiants

pubmed: 34112454
pii: S1936-8798(21)00481-7
doi: 10.1016/j.jcin.2021.03.024
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT02713932']

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1196-1206

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures Dr. Navarese has received research grants from Abbott, Amgen, and Medtronic; and has received lecture fees and honoraria from Amgen, AstraZeneca, Bayer, Pfizer, and Sanofi-Regeneron, outside the submitted work. Dr. Kubica has received personal fees from AstraZeneca, outside the submitted work. Dr. Berti has been a proctor for Abbott. Dr. Andreotti has received speaker and consulting fees from Amgen, Bayer, Bristol Myers Squibb/Pfizer, and Daiichi-Sankyo, outside the submitted work. Dr. Wojakowski has received speaker or consulting fees from Abbott, Boston Scientific, and Medtronic, outside the submitted work. Dr. Witkowski is a proctor for Edwards Lifesciences and Medtronic. Dr. Dudek has received personal fees from Abbott, Boston Scientific, Edwards Lifesciences, and Medtronic, outside the submitted work. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Eliano Pio Navarese (EP)

Interventional Cardiology and Cardiovascular Medicine Research, Department of Cardiology and Internal Medicine, Nicolaus Copernicus University, Bydgoszcz, Poland; Faculty of Medicine, University of Alberta, Edmonton, Alberta, Canada; SIRIO MEDICINE Research Network, Bydgoszcz, Poland. Electronic address: elianonavarese@gmail.com.

Zhongheng Zhang (Z)

Department of Emergency Medicine, Sir Run-Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.

Jacek Kubica (J)

Interventional Cardiology and Cardiovascular Medicine Research, Department of Cardiology and Internal Medicine, Nicolaus Copernicus University, Bydgoszcz, Poland; SIRIO MEDICINE Research Network, Bydgoszcz, Poland.

Felicita Andreotti (F)

Department of Cardiovascular and Thoracic Sciences, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Antonella Farinaccio (A)

Department of Biotechnology and Biosciences, University of Milano-Bicocca, Italy.

Antonio L Bartorelli (AL)

Centro Monzino, IRCCS and Department of Biomedical and Clinical Sciences "Luigi Sacco," University of Milan, Milan, Italy.

Francesco Bedogni (F)

Department of Clinical and Interventional Cardiology, IRCCS Policlinico San Donato, Milan, Italy.

Manali Rupji (M)

Winship Cancer Institute of Emory University, Atlanta, Georgia, USA.

Fabrizio Tomai (F)

Division of Cardiology, European Hospital, Rome, Italy.

Arturo Giordano (A)

Unità Operativa di Interventistica Cardiovascolare, Pineta Grande Hospital, Castel Volturno, Italy.

Bernard Reimers (B)

Division of Cardiology, CCU and Interventional, Cardiology, Cardio Center, Humanitas Research Hospital IRCCS, Rozzano-Milan, Italy.

Carmen Spaccarotella (C)

Cardiovascular Research Center, University Magna Graecia, Catanzaro, Italy.

Krzysztof Wilczek (K)

Cardiac and Lung Transplantation Mechanical Circulatory Support, Silesian Center for Heart Diseases, Pomeranian Medical University, Szczecin, Poland.

Janina Stepinska (J)

National Institute of Cardiology, Warsaw, Poland.

Adam Witkowski (A)

National Institute of Cardiology, Warsaw, Poland.

Marek Grygier (M)

Medical University of Poznań, Poznań, Poland.

Tomasz Kukulski (T)

Cardiac and Lung Transplantation Mechanical Circulatory Support, Silesian Center for Heart Diseases, Pomeranian Medical University, Szczecin, Poland.

Wojciech Wanha (W)

Department of Cardiology and Structural Heart Diseases, Medical University of Silesia, Katowice, Poland.

Wojciech Wojakowski (W)

Department of Cardiology and Structural Heart Diseases, Medical University of Silesia, Katowice, Poland.

Maciej Lesiak (M)

Department of Cardiology, Poznań University of Medical Sciences, Poznań, Poland.

Dariusz Dudek (D)

Institute of Cardiology, Jagiellonian University Medical College, Krakow, Poland.

Michal O Zembala (MO)

Cardiac and Lung Transplantation Mechanical Circulatory Support, Silesian Center for Heart Diseases, Pomeranian Medical University, Szczecin, Poland.

Sergio Berti (S)

Department of Diagnostic and Interventional Cardiology, Gabriele Monasterio Tuscany Foundation, G. Pasquinucci Heart Hospital, Massa, Italy.

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Classifications MeSH