Development and validation of a decision support tool for the diagnosis of acute heart failure: systematic review, meta-analysis, and modelling study.
Author
Lee, Kuan KenDoudesis, Dimitrios
Anwar, Mohamed
Astengo, Federica
Chenevier-Gobeaux, Camille
Claessens, Yann-Erick
Wussler, Desiree
Kozhuharov, Nikola
Strebel, Ivo
Sabti, Zaid
deFilippi, Christopher
Seliger, Stephen
Moe, Gordon
Fernando, Carlos
Bayes-Genis, Antoni
van Kimmenade, Roland R J
Pinto, Yigal
Gaggin, Hanna K
Wiemer, Jan C
Möckel, Martin
Rutten, Joost H W
van den Meiracker, Anton H
Gargani, Luna
Pugliese, Nicola R
Pemberton, Christopher
Ibrahim, Irwani
Gegenhuber, Alfons
Mueller, Thomas
Neumaier, Michael
Behnes, Michael
Akin, Ibrahim
Bombelli, Michele
Grassi, Guido
Nazerian, Peiman
Albano, Giovanni
Bahrmann, Philipp
Newby, David E
Japp, Alan G
Tsanas, Athanasios
Shah, Anoop S V
Richards, A Mark
McMurray, John J V
Mueller, Christian
Januzzi, James L
Mills, Nicholas L
Date
2022-06-13Journal
BMJ (Clinical Research Ed.)Publisher
BMJ Publishing GroupType
Article
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Objectives: To evaluate the diagnostic performance of N-terminal pro-B-type natriuretic peptide (NT-proBNP) thresholds for acute heart failure and to develop and validate a decision support tool that combines NT-proBNP concentrations with clinical characteristics. Design: Individual patient level data meta-analysis and modelling study. Setting: Fourteen studies from 13 countries, including randomised controlled trials and prospective observational studies. Participants: Individual patient level data for 10 369 patients with suspected acute heart failure were pooled for the meta-analysis to evaluate NT-proBNP thresholds. A decision support tool (Collaboration for the Diagnosis and Evaluation of Heart Failure (CoDE-HF)) that combines NT-proBNP with clinical variables to report the probability of acute heart failure for an individual patient was developed and validated. Main outcome measure: Adjudicated diagnosis of acute heart failure. Results: Overall, 43.9% (4549/10 369) of patients had an adjudicated diagnosis of acute heart failure (73.3% (2286/3119) and 29.0% (1802/6208) in those with and without previous heart failure, respectively). The negative predictive value of the guideline recommended rule-out threshold of 300 pg/mL was 94.6% (95% confidence interval 91.9% to 96.4%); despite use of age specific rule-in thresholds, the positive predictive value varied at 61.0% (55.3% to 66.4%), 73.5% (62.3% to 82.3%), and 80.2% (70.9% to 87.1%), in patients aged <50 years, 50-75 years, and >75 years, respectively. Performance varied in most subgroups, particularly patients with obesity, renal impairment, or previous heart failure. CoDE-HF was well calibrated, with excellent discrimination in patients with and without previous heart failure (area under the receiver operator curve 0.846 (0.830 to 0.862) and 0.925 (0.919 to 0.932) and Brier scores of 0.130 and 0.099, respectively). In patients without previous heart failure, the diagnostic performance was consistent across all subgroups, with 40.3% (2502/6208) identified at low probability (negative predictive value of 98.6%, 97.8% to 99.1%) and 28.0% (1737/6208) at high probability (positive predictive value of 75.0%, 65.7% to 82.5%) of having acute heart failure. Conclusions: In an international, collaborative evaluation of the diagnostic performance of NT-proBNP, guideline recommended thresholds to diagnose acute heart failure varied substantially in important patient subgroups. The CoDE-HF decision support tool incorporating NT-proBNP as a continuous measure and other clinical variables provides a more consistent, accurate, and individualised approach. Study registration: PROSPERO CRD42019159407.Rights/Terms
© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. No commercial re-use. See rights and permissions. Published by BMJ.Identifier to cite or link to this item
http://hdl.handle.net/10713/19188ae974a485f413a2113503eed53cd6c53
10.1136/bmj-2021-068424
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