Can risk models accurately predict 1-year mortality, readmission for myocardial infarction, and progression to kidney failure in patients with chronic kidney disease and non-ST-segment-elevation ACS?
Adults with chronic kidney disease admitted for non-ST-segment-elevation acute coronary syndrome (NSTE-ACS). Derivation cohort n=11,980; temporal validation cohort n=4,204; geographic validation cohort n=1,787.
Risk prediction models (Cox proportional hazard and Fine and Gray competing risk models)
1-year mortality, readmission for myocardial infarction, and progression to kidney failure following ACShard clinical
Newly developed and validated risk models can accurately predict 1-year mortality, MI readmission, and kidney failure in patients with CKD and NSTE-ACS, facilitating shared decision-making.
Background: Patients with chronic kidney disease are at high risk of adverse outcomes after acute coronary syndrome (ACS) and need optimized treatment decisions. We derived and validated a series of risk models for predicting 1‐year mortality, readmission for myocardial infarction, and progression to kidney failure following ACS. Methods: The development cohort included adults with chronic kidney disease who had an admission for non‐ST‐segment–elevation ACS, in Alberta, Canada between April 1, 2004 and March 31, 2017. Cox proportional hazard and Fine and Gray competing risk models were externally validated and updated in a temporally distinct cohort of patients in Alberta and a geographically distinct cohort of patients with chronic kidney disease and ACS in British Columbia, Canada. Results: The derivation cohort included 11 980 patients, the temporal validation cohort 4204, and the geographic validation cohort 1787. All models showed comparable discrimination and calibration in the temporal validation cohort; comparable model performance was achieved in the geographic validation cohort after updating. In the temporal and geographic validation cohorts, respectively, discrimination was very good for kidney failure (C‐indexes, 0.93 95% CI, 0.89–0.97 and 0.80 95% CI, 0.78–0.82), and modest for mortality (0.77 95% CI, 0.75–0.78 and 0.71 95% CI, 0.69–0.73), and readmission for myocardial infarction (0.65 95% CI, 0.62–0.67 and 0.57 95% CI, 0.53–0.62). All models were well calibrated after updating. Conclusions: We have developed, validated, and updated risk models for cardiac and renal outcomes in patients with chronic kidney disease and ACS, which can help facilitate shared decision‐making surrounding diagnostic testing, treatment, and monitoring of these patients.
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Wilson et al. (Tue,) studied this question.
www.synapsesocial.com/papers/69d893a86c1944d70ce04a53 — DOI: https://doi.org/10.1161/jaha.125.045139
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:
Todd Wilson
Lee Er
Tolulope T. Sajobi
Journal of the American Heart Association
University of British Columbia
University of Alberta
University of Calgary
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