Emergency Department, Clermont-Ferrand University Hospital, 58 Rue Montalembert, 63003, Clermont-Ferrand, France.
EA 4679, Université Clermont Auvergne, 63000, Clermont-Ferrand, France.
Clin Drug Investig. 2017 Oct;37(10):929-936. doi: 10.1007/s40261-017-0545-9.
Several studies have suggested a link exists between L-thyroxine and the coagulation system, and, according to some drug interaction studies, L-thyroxine can potentiate the effect of warfarin. This study sought to assess whether thyroid hormone therapy could impact the risk of bleeding in patients receiving vitamin K antagonists (VKAs).
We conducted a monocentric, retrospective study on prospectively collected data from consecutive patients enrolled in the Registry of patient with AntiThrombotic agents admitted to an Emergency Department (RATED) database, and compared the hemorrhage rates (both major and nonmajor) of patients receiving treatment with and without L-thyroxine. Propensity score matching analysis was performed to reduce the differences between patients receiving L-thyroxine and those not receiving L-thyroxine in order to reassess bleeding outcomes in patients receiving VKAs.
From January 2014 to June 2015, 1454 patients receiving VKAs were recruited into the RATED database. Overall, 187 patients (12.8%) received L-thyroxine. Patients receiving L-thyroxine were more likely to be female than those not receiving L-thyroxine (78.1 vs. 55%) and more likely to exhibit hypertension (65.5 vs. 55.7%; p = 0.015), but less likely to have history of myocardial infarction (9.6 vs. 16.6%; p = 0.022) or higher creatinine levels (96.1 vs. 112.1 μmol/L; p = 0.04). After propensity score matching, bleeding outcomes were not significantly different between patients receiving L-thyroxine and those not receiving L-thyroxine.
Our study revealed no evidence that L-thyroxine could increase bleeding risk in patients receiving VKAs. However, physicians must be aware that patients with thyroid disease receiving VKA therapy could have other drug interactions, particularly with amiodarone therapy. CLINICALTRIALS.
NCT02706080.
几项研究表明 L-甲状腺素与凝血系统之间存在关联,并且根据一些药物相互作用研究,L-甲状腺素可以增强华法林的作用。本研究旨在评估甲状腺激素治疗是否会影响接受维生素 K 拮抗剂(VKA)治疗的患者出血的风险。
我们对连续入组于急诊部抗血栓药物患者登记处(RATED)数据库的前瞻性收集数据进行了单中心回顾性研究,并比较了接受 L-甲状腺素治疗和未接受 L-甲状腺素治疗的患者的出血率(包括主要出血和非主要出血)。采用倾向评分匹配分析来减少接受 L-甲状腺素和未接受 L-甲状腺素治疗的患者之间的差异,以便重新评估接受 VKA 治疗的患者的出血结局。
从 2014 年 1 月至 2015 年 6 月,共有 1454 例接受 VKA 的患者入组 RATED 数据库。总体而言,187 例(12.8%)患者接受 L-甲状腺素治疗。与未接受 L-甲状腺素治疗的患者相比,接受 L-甲状腺素治疗的患者更可能为女性(78.1%比 55%),更可能患有高血压(65.5%比 55.7%;p=0.015),但更不可能患有心肌梗死史(9.6%比 16.6%;p=0.022)或更高的肌酐水平(96.1%比 112.1 μmol/L;p=0.04)。经倾向评分匹配后,接受 L-甲状腺素治疗和未接受 L-甲状腺素治疗的患者的出血结局无显著差异。
本研究未发现 L-甲状腺素可增加接受 VKA 治疗的患者出血风险的证据。然而,医生必须意识到接受 VKA 治疗的甲状腺疾病患者可能存在其他药物相互作用,特别是与胺碘酮治疗有关。临床试验.gov 编号:NCT02706080。