Safety of concomitant use of oral anticoagulants and antidiabetic drugs: a systematic review of observational studies.

Paraskevi Tassopoulou, Wanqi Wang, Fabian Maximilian Meinert, Thomas G Riemer, Antonios Douros
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Abstract

Introduction: We systematically reviewed observational studies assessing the safety of concomitant use of oral anticoagulants (OACs) and antidiabetic drugs (ADs).

Methods: We systematically searched MEDLINE/PubMed and EMBASE up to 10/2024 for cohort, case-control, and case-only studies on concomitant use of OACs and ADs and the risk of adverse outcomes (hypoglycemia, bleeding). Risk of bias was assessed using the Risk Of Bias In Non-randomized Studies of Interventions (ROBINS-I) tool.

Results: We identified five cohort studies and two self-controlled case-series (n = 1,370,036). Concomitant use of sulfonylureas and warfarin was mostly associated with increased risks of hypoglycemia versus sulfonylurea use alone (five studies); results were heterogeneous when comparing concomitant use of sulfonylureas and warfarin versus concomitant use of sulfonylureas and DOACs (two studies) and concomitant use of non-sulfonylurea ADs and warfarin versus non-sulfonylurea AD use alone (two studies). Concomitant use of warfarin and sulfonylureas was not associated with the risk of bleeding versus warfarin use alone (one study). Via ROBINS-I, four studies were at moderate, one at serious, and two at critical risk of bias.

Conclusions: Given inconsistent findings and a non-negligible risk of bias, observational studies do not suggest major clinical hazards due to concomitant use of OACs and ADs. (PROSPERO registration: CRD42024505475).

同时使用口服抗凝血剂和降糖药的安全性:观察性研究的系统回顾。
我们系统地回顾了评估口服抗凝剂(OACs)和降糖药(ADs)合用安全性的观察性研究。方法:我们系统地检索MEDLINE/PubMed和EMBASE截至10/2024的队列、病例对照和仅病例研究,以了解OACs和ad的联合使用以及不良结局(低血糖、出血)的风险。使用非随机干预研究的偏倚风险(ROBINS-I)工具评估偏倚风险。结果:我们确定了5个队列研究和2个自我对照病例系列(n = 1,370,036)。与单独使用磺脲类药物相比,同时使用磺脲类药物和华法林主要与低血糖风险增加相关(5项研究);当比较磺脲类药物和华法林与磺脲类药物和doac的合用(两项研究)以及非磺脲类药物和华法林与非磺脲类药物的合用(两项研究)时,结果是不一致的。与单独使用华法林相比,同时使用华法林和磺脲类药物与出血风险无关(一项研究)。通过ROBINS-I,四项研究为中度偏倚风险,一项为严重偏倚风险,两项为严重偏倚风险。结论:鉴于不一致的研究结果和不可忽略的偏倚风险,观察性研究未提示OACs和ad同时使用的主要临床危害(PROSPERO注册号:CRD42024505475)。
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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