Frailty as an instrument for evaluation of elderly patients with non-ST-segment elevation myocardial infarction: A follow-up after more than 5 years.

Published

Journal Article

BACKGROUND: There is a growing body of evidence on the relevance of using frailty measures also in a cardiovascular context. The estimated time to death is crucial in clinical decision-making in cardiology. However, data on the importance of frailty in long-term mortality are very scarce. The aim of the study was to assess the prognostic value of frailty on mortality at long-term follow-up of more than 5 years in patients 75 years or older hospitalised for non-ST-segment elevation myocardial infarction. We hypothesised that frailty is independently associated with long-term mortality. DESIGN: This was a prospective, observational study conducted at three centres. METHODS AND RESULTS: Frailty was assessed according to the Canadian Study of Health and Aging clinical frailty scale (CFS). Of 307 patients, 149 (48.5%) were considered frail according to the study instrument (degree 5-7 on the scale). The long-term all-cause mortality of more than 5 years (median 6.7 years) was significantly higher among frail patients (128, 85.9%) than non-frail patients (85, 53.8%), ( P < 0.001). In Cox regression analysis, frailty was independently associated with mortality from the index hospital admission to the end of follow-up (hazard ratio 2.06, 95% confidence interval 1.51-2.81; P < 0.001) together with age ( P < 0.001), ejection fraction ( P = 0.012) and Charlson comorbidity index ( P = 0.018). CONCLUSIONS: In elderly non-ST-segment elevation myocardial infarction patients, frailty was independently associated with all-cause mortality at long-term follow-up of more than 6 years. The combined use of frailty and comorbidity may be the ultimate risk prediction concept in the context of cardiovascular patients with complex needs.

Full Text

Duke Authors

Cited Authors

  • Ekerstad, N; Pettersson, S; Alexander, K; Andersson, D; Eriksson, S; Janzon, M; Lindenberger, M; Swahn, E; Alfredsson, J

Published Date

  • November 2018

Published In

Volume / Issue

  • 25 / 17

Start / End Page

  • 1813 - 1821

PubMed ID

  • 30247067

Pubmed Central ID

  • 30247067

Electronic International Standard Serial Number (EISSN)

  • 2047-4881

Digital Object Identifier (DOI)

  • 10.1177/2047487318799438

Language

  • eng

Conference Location

  • England