Clinical Implications of the New York Heart Association Classification

Author:

Caraballo César1,Desai Nihar R.1,Mulder Hillary2,Alhanti Brooke2,Wilson F. Perry3,Fiuzat Mona2,Felker G. Michael2,Piña Ileana L.4,O'Connor Christopher M.5,Lindenfeld Joanne6,Januzzi James L.7,Cohen Lawrence S.3,Ahmad Tariq1

Affiliation:

1. Section of Cardiovascular Medicine Center for Outcomes Research Evaluation (CORE) Yale University School of Medicine New Haven CT

2. Duke Clinical Research Institute Durham NC

3. Program of Applied Translational Research Yale University School of Medicine New Haven CT

4. Detroit Medical Center Detroit MI

5. Inova Heart and Vascular Institute Fairfax VA

6. Vanderbilt University Medical Center Nashville TN

7. Massachusetts General Hospital and Baim Institute for Clinical Research Boston MA

Abstract

Background The New York Heart Association ( NYHA ) classification has served as a fundamental tool for risk stratification of heart failure ( HF ) and determines clinical trial eligibility and candidacy for drugs and devices. However, its ability to adequately stratify risk is unclear. Methods and Results To compare NYHA class with objective assessments and survival in patients with HF , we performed secondary analyses of 4 multicenter National Institutes of Health–funded HF clinical trials that included patients classified as NYHA class II or III: TOPCAT (Treatment of Preserved Cardiac Function Heart Failure with an Aldosterone Antagonist), DIG (The Effect of Digoxin on Mortality and Morbidity in Patients With Heart Failure), HF‐ACTION (Efficacy and Safety of Exercise Training in Patients With Chronic Heart Failure), and GUIDE‐IT (Guiding Evidence‐Based Therapy Using Biomarker Intensified Treatment in Heart Failure). Twenty‐month cumulative survival was compared between classes using Kaplan–Meier curves and the log rank test. NT ‐proBNP (N‐terminal pro–B‐type natriuretic peptide), Kansas City Cardiomyopathy Questionnaire ( KCCQ ) scores, 6‐minute walk distances, left ventricular ejection fraction, and cardiopulmonary test parameters were compared using Wilcoxon rank sum tests and percentage overlap using kernel density estimations. Cumulative mortality varied significantly across NYHA classes and HF clinical trials (likelihood ratio, P <0.001). Mortality at 20 months for NYHA class II ranged from 7% for patients in HFACTION to 15% in GUIDEIT , whereas mortality for NYHA class III ranged from 12% in TOPCAT to 26% in GUIDEIT . There was substantial percentage overlap in values for NT ‐pro BNP levels (79% and 69%), KCCQ scores (63% and 54%), 6‐minute walk distances (63% and 54%), and left ventricular ejection fraction (88% and 83%). Similarly, there was substantial overall in values for minute ventilation–carbon dioxide production relationship (71%), maximal oxygen uptake (54%), and exercise duration (53%). Conclusions The NYHA system poorly discriminates HF patients across the spectrum of functional impairment. These findings raise important questions about the need for improved phenotyping of these patients to facilitate risk stratification and response to interventions.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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