Why the study?
The long-term impact of renin-angiotensin system inhibitors for secondary prevention in patients with chronic kidney disease and coexisting coronary artery disease remains unclear.
Does RAS inhibitor use reduce 3P-MACE in patients with CKD who underwent their first PCI?
Does RAS inhibitor use reduce 3P-MACE in patients with CKD who underwent their first PCI?
Long-term RAS inhibitor use in patients with CKD after PCI may reduce major adverse cardiovascular events but is associated with an increased risk of heart failure admission.
Answers are grounded in this paper and cite their sources.
RAS inhibitors post-PCI in CKD were associated with lower 3P-MACE yet higher HF admissions; leaves open net benefit for randomized trials.
Introduction: The long-term impact of renin-angiotensin system (RAS) inhibitors for secondary prevention in patients with chronic kidney disease (CKD) and coexisting coronary artery disease remains unclear. Methods: Altogether, 1,160 consecutive patients with CKD (mean age, 70 ± 9 years; 78% men) who underwent their first percutaneous coronary intervention (PCI) between 2000 and 2018 were included and analyzed. Based on their RAS inhibitor use, 674 patients (58%) were allocated to the RAS inhibitor group, and 486 patients (42%) were allocated to the non-RAS inhibitor group. This study evaluated the incidence of 3-point major adverse cardiovascular events (3P-MACE), including cardiovascular death, nonfatal acute coronary syndrome and nonfatal stroke, admission for heart failure (HF), target vessel revascularization (TVR), and all-cause death. Results: During a median follow-up duration of 7.8 years, 280 patients (24.1%) developed 3P-MACE, 134 patients (11.6%) were hospitalized for HF, 171 patients (14.7%) underwent TVR, and 348 patients (30.0%) died of any causes. The cumulative incidence rate of 3P-MACE in the RAS inhibitor group was significantly lower than in the non-RAS inhibitor group (31.7% vs. 39.0%, log-rank test, p = 0.034); however, that of admission for HF in the RAS inhibitor group was significantly higher than in the non-RAS inhibitor group (28.1% vs. 13.3%, log-rank test, p < 0.001). The subgroup of preserved ejection fraction, non-acute myocardial infarction, and non-proteinuria tended to promote the onset of HF rather than cardiovascular prevention by RAS inhibitors. Conclusion: The long-term RAS inhibitor use for patients with CKD after PCI might prevent cardiovascular events but increase the risk of HF.
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Fukase et al. (2023) studied this question.
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