Associations Between New York Heart Association Classification, Objective Measures, and Long-term Prognosis in Mild Heart Failure

Author:

Rohde Luis E.12,Zimerman André12,Vaduganathan Muthiah3,Claggett Brian L.3,Packer Milton4,Desai Akshay S.3,Zile Michael5,Rouleau Jean6,Swedberg Karl7,Lefkowitz Martin8,Shi Victor8,McMurray John J. V.9,Solomon Scott D.3

Affiliation:

1. Postgraduate Program in Cardiology and Cardiovascular Sciences, Medical School, Universidade Federal do Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil

2. Cardiovascular Division, Hospital de Clínicas de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil

3. Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston, Massachusetts

4. Baylor Heart and Vascular Institute, Baylor University Medical Center, Dallas, Texas

5. Medical University of South Carolina and Ralph H. Johnson Veterans Administration Medical Center, Charleston

6. Institut de Cardiologie de Montréal, Université de Montréal, Montreal, Quebec, Canada

7. Department of Molecular and Clinical Medicine, University of Gothenburg, Gothenburg, Sweden

8. Novartis, East Hanover, New Jersey

9. BHF Cardiovascular Research Centre, University of Glasgow, Glasgow, United Kingdom

Abstract

ImportanceHeart failure (HF) treatment recommendations are centered on New York Heart Association (NYHA) classification, such that most apparently asymptomatic patients are not eligible for disease-modifying therapies.ObjectivesTo assess within-patient variation in NYHA classification over time, the association between NYHA class and an objective measure of HF severity (N-terminal pro–B-type natriuretic peptide [NT-proBNP] level), and their association with long-term prognosis in the PARADIGM-HF trial.Design, Setting, and ParticipantsAll patients in PARADIGM-HF were in NYHA class II or higher at baseline and were treated with sacubitril-valsartan during a 6- to 10-week run-in period before randomization. Patients classified as NYHA class I, II, and III in PARADIGM-HF were compared at randomization.ExposuresNYHA class at randomization after 6 to 10 weeks of the run-in period.Main Outcomes and MeasuresPrimary outcome was cardiovascular death or first HF hospitalization. Logistic regression models, areas under the receiver operating characteristic curve (AUC), kernel density estimation overlaps, and Cox proportional hazards models were used.ResultsThe analysis included 8326 patients with known NYHA classification at randomization. Of 389 patients in NYHA class I, 228 (58%) changed functional class during the first year after randomization. Level of NT-proBNP was a poor discriminator of NYHA classification: for NYHA class I vs II, the AUC was 0.51 (95% CI, 0.48-0.54). For NT-proBNP level, estimated kernel density overlap was 93% between NYHA class I vs II, 79% between NYHA I vs III, and 83% between NYHA II vs III. Patients classified as NYHA III displayed a distinctively higher rate of cardiovascular events (NYHA III vs I, hazard ratio [HR], 1.84; 95% CI, 1.44-2.37; NYHA III vs II, HR, 1.49; 95% CI, 1.35-1.64). Patients in NYHA class I and II revealed lower event rates (NYHA II vs I, HR, 1.24; 95% CI, 0.97-1.58). Stratification by NT-proBNP level (<1600 pg/mL or ≥1600 pg/mL) identified subgroups with distinctive risk, such that NYHA class I patients with high NT-proBNP levels (n = 175) had a numerically higher event rate than patients with low NT-proBNP levels from any NYHA class (vs I, HR, 3.43; 95% CI, 2.03-5.87; vs II, HR, 2.12; 95% CI, 1.58-2.86; vs III, HR, 1.37; 95% CI, 1.00-1.88).Conclusions and RelevanceIn this study, patients in NYHA class I and II overlapped substantially in objective measures and long-term prognosis. Physician-defined “asymptomatic” functional class concealed patients who were at substantial risk for adverse outcomes. NYHA classification might be limited to differentiate mild forms of HF.Trial RegistrationClinicalTrials.gov Identifier: NCT01035255

Publisher

American Medical Association (AMA)

Subject

Cardiology and Cardiovascular Medicine

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