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Development and validation of a decision support tool for the diagnosis of acute heart failure: systematic review, meta-analysis, and modelling study.
Lee, Kuan Ken; Doudesis, 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.
Afiliação
  • Lee KK; British Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
  • Doudesis D; Contributed equally.
  • Anwar M; British Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
  • Astengo F; Usher Institute, University of Edinburgh, Edinburgh, UK.
  • Chenevier-Gobeaux C; Contributed equally.
  • Claessens YE; British Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
  • Wussler D; Contributed equally.
  • Kozhuharov N; British Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
  • Strebel I; Department of Biochemistry, Cochin Hospital, Assistance Publique-Hopitaux de Paris, Paris, France.
  • Sabti Z; Department of Emergency Medicine, Princess Grace Hospital Center, Monaco, Principality of Monaco.
  • deFilippi C; Cardiovascular Research Institute of Basel, Department of Cardiology, University Hospital Basel, Basel, Switzerland.
  • Seliger S; Department of Internal Medicine, University Hospital Basel, University of Basel, Switzerland.
  • Moe G; Cardiovascular Research Institute of Basel, Department of Cardiology, University Hospital Basel, Basel, Switzerland.
  • Fernando C; Liverpool Heart and Chest Hospital, Liverpool, UK.
  • Bayes-Genis A; Cardiovascular Research Institute of Basel, Department of Cardiology, University Hospital Basel, Basel, Switzerland.
  • van Kimmenade RRJ; Cardiovascular Research Institute of Basel, Department of Cardiology, University Hospital Basel, Basel, Switzerland.
  • Pinto Y; Inova Heart and Vascular Institute, Falls Church, VA, USA.
  • Gaggin HK; Division of Nephrology, University of Maryland School of Medicine, Baltimore, MD, USA.
  • Wiemer JC; University of Toronto, St Michael's Hospital, Toronto, ON, Canada.
  • Möckel M; University of Toronto, St Michael's Hospital, Toronto, ON, Canada.
  • Rutten JHW; Heart Institute, Hospital Universitari Germans Trias i Pujol, Badalona, CIBERCV, Spain.
  • van den Meiracker AH; Department of Cardiology, Radboud University Medical Center, Nijmegen, Netherlands.
  • Gargani L; University of Amsterdam, Amsterdam, Netherlands.
  • Pugliese NR; Harvard Medical School, Boston, MA, USA.
  • Pemberton C; Division of Cardiology, Massachusetts General Hospital, Boston, MA, USA.
  • Ibrahim I; BRAHMS, Thermo Fisher Scientific, Hennigsdorf, Germany.
  • Gegenhuber A; Department of Emergency and Acute Medicine with Chest Pain Units, Charité - Universitätsmedizin Berlin, Campus Mitte and Virchow, Berlin, Germany.
  • Mueller T; Department of Internal Medicine, Radboud University Medical Center, Nijmegen, Netherlands.
  • Neumaier M; Department of Internal Medicine, Division of Pharmacology and Vascular Medicine, Erasmus Medical Center, Rotterdam, Netherlands.
  • Behnes M; Department of Surgical, Medical and Molecular Pathology and Critical Care Medicine, University of Pisa, Pisa, Italy.
  • Akin I; Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
  • Bombelli M; Christchurch Heart Institute, University of Otago, Christchurch, New Zealand.
  • Grassi G; Emergency Medicine Department, National University Hospital, Singapore.
  • Nazerian P; Department of Internal Medicine, Krankenhaus Bad Ischl, Bad Ischl, Austria.
  • Albano G; Department of Laboratory Medicine, Hospital Voecklabruck, Voecklabruck, Austria.
  • Bahrmann P; Institute for Clinical Chemistry, University Medical Centre Mannheim, Faculty of Medicine Mannheim, University of Heidelberg, Mannheim, Germany.
  • Newby DE; First Department of Medicine, University Medical Centre Mannheim, Faculty of Medicine Mannheim, University of Heidelberg, Mannheim, Germany.
  • Japp AG; First Department of Medicine, University Medical Centre Mannheim, Faculty of Medicine Mannheim, University of Heidelberg, Mannheim, Germany.
  • Tsanas A; University of Milan Bicocca, ASST-Brianza, Pio XI Hospital of Desio, Internal Medicine, Desio, Italy.
  • Shah ASV; Clinica Medica, University Milan Bicocca, Milan, Italy.
  • Richards AM; Department of Emergency Medicine, Azienda Ospedaliero-Universitaria Careggi, Florence, Italy.
  • McMurray JJV; Department of Emergency Medicine, Azienda Ospedaliero-Universitaria Careggi, Florence, Italy.
  • Mueller C; Department of Internal Medicine III, Division of Cardiology, University Hospital of Heidelberg, Ruprecht-Karls University Heidelberg, Heidelberg, Germany.
  • Januzzi JL; British Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
  • Mills NL; British Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
BMJ ; 377: e068424, 2022 06 13.
Article em En | MEDLINE | ID: mdl-35697365
ABSTRACT

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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeo Natriurético Encefálico / Insuficiência Cardíaca Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Revista: BMJ Assunto da revista: MEDICINA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeo Natriurético Encefálico / Insuficiência Cardíaca Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Revista: BMJ Assunto da revista: MEDICINA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido