Association Between Myocardial Infarction and Quality of Life in the ISCHEMIA Trial.
Pubmed ID: 40272347
Journal: JACC. Cardiovascular interventions
Publication Date: May 26, 2025
MeSH Terms: Humans, Male, Female, Aged, Risk Factors, Middle Aged, Treatment Outcome, Quality of Life, Myocardial Infarction, Time Factors, Health Status, Surveys and Questionnaires, Percutaneous Coronary Intervention, ST Elevation Myocardial Infarction, Non-ST Elevated Myocardial Infarction
Grants: R01 HL152021
Authors: Bhatt DL, Stone GW, Kim J, Gaudino M, Alexander JH, Devereaux PJ, Redfors B, Biondi-Zoccai G, Caldonazo T, Puskas J, Sandner S, Heise RS, Harik L, Masterson-Creber R, Spertus J
Cite As: Gaudino M, Stone GW, Heise RS, Caldonazo T, Kim J, Harik L, Sandner S, Biondi-Zoccai G, Masterson-Creber R, Alexander JH, Bhatt DL, Puskas J, Devereaux PJ, Spertus J, Redfors B. Association Between Myocardial Infarction and Quality of Life in the ISCHEMIA Trial. JACC Cardiovasc Interv 2025 May 26;18(10):1263-1272. Epub 2025 Apr 23.
Studies:
Abstract
BACKGROUND: The association between myocardial infarction (MI) subtypes (procedural MI [PMI] and spontaneous MI [SMI]) and subsequent quality of life (QoL) is incompletely understood. OBJECTIVES: The authors analyzed the association between PMI and SMI and generic and disease-specific QoL in the ISCHEMIA (International Study of Comparative Health Effectiveness with Medical and Invasive Approaches) trial. METHODS: QoL was assessed before randomization and at 1.5, 3, and 6 months, and every 6 months thereafter. European Quality of Life-5 dimensions visual analog scale (EQ-5D VAS) (generic) and Seattle Angina Questionnaire (SAQ-7) summary score (disease-specific) were used. The primary analysis was a linear, repeated-measures, multivariable-adjusted, mixed-effects model, with a random intercept for patient. QoL assessments occurring <3 months after MI were defined as early QoL and those occurring >3 months after MI were defined as late QoL. RESULTS: A total of 4,375 randomized patients were included in the primary analysis population. The median duration of follow-up was 36.2 months (Q1-Q3: 23.8-49.5 months). In the primary analysis population, a total of 84 PMIs and 352 SMIs occurred. SMI was associated with significant decreases in both early (adjusted difference -5.7; 95% CI: -7.3 to -4.1 points) and late EQ-5D VAS (-3.1 points; 95% CI: -4.3 to -1.9 points) and in early (-7.7 points; 95% CI: -9.4 to -6.1 points) and late SAQ-7 (-1.9 points; 95% CI: -3.2 to -0.7 points). PMI was not associated with early (adjusted difference -0.8 points; 95% CI: -3.3 to 1.8 points) or late (-0.7 points; 95% CI: -2.7 to 1.2 points) changes in EQ-5D VAS, and was associated with a reduction in early (-3.0 points; 95% CI: -5.7 to -0.4) but not late SAQ-7 (-0.2 points; 95% CI -2.2 to 1.8 points). CONCLUSIONS: In ISCHEMIA, SMI was associated with reductions in both early and late generic and disease-specific QoL, whereas PMI was only associated with a transient reduction in disease-specific QoL.