ECLIPSES: Early initiation of sodium glucose cotransporter-2 inhibitors for cardiovascular protection in patients with type 2 diabetes following acute coronary syndrome and subsequent coronary artery bypass graft surgery.

IF 2.9 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Pharmacotherapy Pub Date : 2024-10-25 DOI:10.1002/phar.4620
Lena Makortoff, Karen L Then, Melissa Dutchak, Meng Lin, Erik Youngson, Cheryl Harten
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引用次数: 0

Abstract

Introduction: There is a paucity of data evaluating early initiation of sodium-glucose cotransporter-2 inhibitors (SGLT2i) in patients with diabetes following acute coronary syndrome (ACS) and coronary artery bypass graft surgery (CABG).

Objectives: To describe the efficacy and safety of SGLT2i initiated early after CABG in patients with type 2 diabetes who experienced ACS.

Methods: This is a retrospective cohort study of patients with type 2 diabetes (T2DM) who experienced ACS and subsequent CABG with follow up at 3 and 12 months. Patients who filled a SGLT2i prescription within 14 days of discharge were allocated to the SGLT2i group and those who did not were included in the no SGLT2i group. The primary efficacy end point was first occurrence of a 4-point Major Adverse Cardiovascular Event (MACE), and the primary safety end point was a composite of hypoglycemia, hypotension, diabetic ketoacidosis, acute kidney injury, and urinary tract infection. Secondary end points included a comparative analysis of the primary outcome, 30-day readmission rates, and subgroup analyses of key populations.

Results: A total of 1629 patients were included: 226 received a SGLT2i within 14 days of discharge and 1403 did not. At 12 months, 8.9% and 15.3% of patients experienced MACE in the SGLT2i and no SGLT2i groups, respectively (adjusted Hazard Ratio [aHR] 0.65, 95% confidence interval [CI] 0.41-1.04). The primary safety outcome occurred in 12.0% of the SGLT2i group and 19.1% of the no SGLT2i group at 12 months (aHR 0.68, 95% CI 0.45-1.01).

Conclusion: Early initiation of SGLT2i use was not associated with a reduction in MACE in patients with T2DM who experienced ACS and underwent subsequent CABG surgery. However, no apparent safety concerns were identified. Adequately powered trials are required to confirm this finding.

ECLIPSES:急性冠状动脉综合征和随后的冠状动脉旁路移植手术后的 2 型糖尿病患者早期使用钠葡萄糖共转运体-2 抑制剂保护心血管。
简介:评估急性冠状动脉综合征(ACS)和冠状动脉旁路移植手术(CABG)后糖尿病患者早期使用钠-葡萄糖共转运体-2抑制剂(SGLT2i)的数据很少:描述急性冠状动脉综合征(ACS)和冠状动脉旁路移植手术(CABG)后的 2 型糖尿病患者在 CABG 术后早期使用 SGLT2i 的疗效和安全性:这是一项回顾性队列研究,研究对象为经历过 ACS 并随后接受过 CABG 的 2 型糖尿病患者,随访时间为 3 个月和 12 个月。出院后14天内开具SGLT2i处方的患者被分配到SGLT2i组,未开具SGLT2i处方的患者被纳入无SGLT2i组。主要疗效终点是首次出现 4 点主要心血管不良事件 (MACE),主要安全性终点是低血糖、低血压、糖尿病酮症酸中毒、急性肾损伤和尿路感染的复合终点。次要终点包括主要结果的比较分析、30 天再入院率以及关键人群的亚组分析:结果:共纳入了 1629 名患者:结果:共纳入1629名患者:226人在出院后14天内接受了SGLT2i治疗,1403人未接受治疗。12个月时,SGLT2i组和未使用SGLT2i组分别有8.9%和15.3%的患者发生MACE(调整危险比[aHR] 0.65,95%置信区间[CI] 0.41-1.04)。12个月时,12.0%的SGLT2i组和19.1%的无SGLT2i组出现了主要安全性结果(aHR 0.68,95% CI 0.45-1.01):结论:在发生 ACS 并随后接受 CABG 手术的 T2DM 患者中,早期开始使用 SGLT2i 与减少 MACE 无关。不过,并未发现明显的安全性问题。要证实这一发现,还需要进行充分的试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmacotherapy
Pharmacotherapy 医学-药学
CiteScore
7.80
自引率
2.40%
发文量
93
审稿时长
4-8 weeks
期刊介绍: Pharmacotherapy is devoted to publication of original research articles on all aspects of human pharmacology and review articles on drugs and drug therapy. The Editors and Editorial Board invite original research reports on pharmacokinetic, bioavailability, and drug interaction studies, clinical trials, investigations of specific pharmacological properties of drugs, and related topics.
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