Development and Validation of an Abridged Version of the REVEAL 2.0 Risk Score Calculator, REVEAL Lite 2, for Use in Patients With Pulmonary Arterial Hypertension.


Journal

Chest
ISSN: 1931-3543
Titre abrégé: Chest
Pays: United States
ID NLM: 0231335

Informations de publication

Date de publication:
01 2021
Historique:
received: 14 04 2020
revised: 12 08 2020
accepted: 16 08 2020
pubmed: 4 9 2020
medline: 12 6 2021
entrez: 4 9 2020
Statut: ppublish

Résumé

Achievement of low-risk status is a treatment goal in pulmonary arterial hypertension (PAH). Risk assessment often is performed using multiparameter tools, such as the Registry to Evaluate Early and Long-Term PAH Disease Management (REVEAL) risk calculator. Risk calculators that assess fewer variables without compromising validity may expedite risk assessment in the routine clinic setting. We describe the development and validation of REVEAL Lite 2, an abridged version of REVEAL 2.0. Can a simplified version of the REVEAL 2.0 risk assessment calculator for patients with PAH be developed and validated? REVEAL Lite 2 includes six noninvasive variables-functional class (FC), vital signs (systolic BP [SBP] and heart rate), 6-min walk distance (6MWD), brain natriuretic peptide (BNP)/N-terminal prohormone of brain natriuretic peptide (NT-proBNP), and renal insufficiency (by estimated glomerular filtration rate [eGFR])-and was validated in a series of analyses (Kaplan-Meier, concordance index, Cox proportional hazard model, and multivariate analysis). REVEAL Lite 2 approximates REVEAL 2.0 at discriminating low, intermediate, and high risk for 1-year mortality in patients in the REVEAL registry. The model indicated that the most highly predictive REVEAL Lite 2 parameter was BNP/NT-proBNP, followed by 6MWD and FC. Even if multiple, less predictive variables (heart rate, SBP, eGFR) were missing, REVEAL Lite 2 still discriminated among risk groups. REVEAL Lite 2, an abridged version of REVEAL 2.0, provides a simplified method of risk assessment that can be implemented routinely in daily clinical practice. REVEAL Lite 2 is a robust tool that provides discrimination among patients at low, intermediate, and high risk of 1-year mortality. ClinicalTrials.gov; No.: NCT00370214; URL: www.clinicaltrials.gov.

Sections du résumé

BACKGROUND
Achievement of low-risk status is a treatment goal in pulmonary arterial hypertension (PAH). Risk assessment often is performed using multiparameter tools, such as the Registry to Evaluate Early and Long-Term PAH Disease Management (REVEAL) risk calculator. Risk calculators that assess fewer variables without compromising validity may expedite risk assessment in the routine clinic setting. We describe the development and validation of REVEAL Lite 2, an abridged version of REVEAL 2.0.
RESEARCH QUESTION
Can a simplified version of the REVEAL 2.0 risk assessment calculator for patients with PAH be developed and validated?
STUDY DESIGN AND METHODS
REVEAL Lite 2 includes six noninvasive variables-functional class (FC), vital signs (systolic BP [SBP] and heart rate), 6-min walk distance (6MWD), brain natriuretic peptide (BNP)/N-terminal prohormone of brain natriuretic peptide (NT-proBNP), and renal insufficiency (by estimated glomerular filtration rate [eGFR])-and was validated in a series of analyses (Kaplan-Meier, concordance index, Cox proportional hazard model, and multivariate analysis).
RESULTS
REVEAL Lite 2 approximates REVEAL 2.0 at discriminating low, intermediate, and high risk for 1-year mortality in patients in the REVEAL registry. The model indicated that the most highly predictive REVEAL Lite 2 parameter was BNP/NT-proBNP, followed by 6MWD and FC. Even if multiple, less predictive variables (heart rate, SBP, eGFR) were missing, REVEAL Lite 2 still discriminated among risk groups.
INTERPRETATION
REVEAL Lite 2, an abridged version of REVEAL 2.0, provides a simplified method of risk assessment that can be implemented routinely in daily clinical practice. REVEAL Lite 2 is a robust tool that provides discrimination among patients at low, intermediate, and high risk of 1-year mortality.
TRIAL REGISTRY
ClinicalTrials.gov; No.: NCT00370214; URL: www.clinicaltrials.gov.

Identifiants

pubmed: 32882243
pii: S0012-3692(20)34296-3
doi: 10.1016/j.chest.2020.08.2069
pmc: PMC7462639
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT00370214']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

337-346

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.

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Auteurs

Raymond L Benza (RL)

Ohio State University, Columbus, OH. Electronic address: Raymond.Benza@osumc.edu.

Manreet K Kanwar (MK)

Allegheny General Hospital, Pittsburgh, PA.

Amresh Raina (A)

Allegheny General Hospital, Pittsburgh, PA.

Jacqueline V Scott (JV)

Carnegie Mellon University, Pittsburgh, PA.

Carol L Zhao (CL)

Janssen Pharmaceuticals, Inc, South San Francisco, CA.

Mona Selej (M)

Janssen Pharmaceuticals, Inc, South San Francisco, CA.

C Greg Elliott (CG)

Intermountain Medical Center and the University of Utah, Salt Lake City, UT.

Harrison W Farber (HW)

Tufts Medical Center, Boston, MA.

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Classifications MeSH