Why the study?
The optimal approach to classifying multimorbidity burden when evaluating treatment-associated outcomes using real-world data remains uncertain.
Does a simple count of chronic conditions perform similarly to a weighted multimorbidity score in assessing outcomes associated with beta-blocker use in adults with heart failure?
Does a simple count of chronic conditions perform similarly to a weighted multimorbidity score in assessing outcomes associated with beta-blocker use in adults with heart failure?
Simple counts of chronic conditions perform similarly to complex weighted multimorbidity scores for risk adjustment in observational studies of heart failure therapies.
Simple counts of chronic conditions yield similar HF outcome estimates as weighted multimorbidity scores; supports simpler adjustment in future observational therapy studies.
BACKGROUND: The optimal approach to classifying multimorbidity burden in assessing treatment-associated outcomes using real-world data remains uncertain. We assessed whether 2 measurement approaches to characterize multimorbidity influenced observed associations of β-blocker use with outcomes in adults with heart failure (HF). METHODS: We conducted a retrospective study on adults with HF from 4 integrated health care delivery systems. Multimorbidity burden was characterized by either (1) simple counts of chronic conditions or (2) a weighted multiple chronic conditions score using data from electronic health records. We assessed the impact of these 2 approaches to characterizing multimorbidity on associations between exposure to β-blockers and subsequent all-cause death, hospitalization for HF, and hospitalization for any cause. RESULTS: The study population characterized by a count of chronic conditions included 9988 adults with HF who had a mean (SD) age of 76.4 (12.5) years, with 48.7% women and 24.7% racial/ethnic minorities. The cohort characterized by weighted multiple chronic conditions included 10,082 adults with HF who had a mean (SD) age of 76.4 (12.4) years, 48.9% women, and 25.5% racial/ethnic minorities. The multivariable associations of risks of death or hospitalizations for HF or for any cause associated with incident β-blocker use were similar regardless of how multimorbidity burden was characterized. CONCLUSIONS: Simple counts of chronic conditions performed similarly to a weighted multimorbidity score in predicting outcomes using real-world data to examine clinical outcomes associated with β-blocker therapy in HF. Our findings challenge conventional wisdom that more complex measures of multimorbidity are always necessary to characterize patients in observational studies examining therapy-associated outcomes.
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Tisminetzky et al. (2023) studied this question.
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