School of Pharmacy and Pharmacology, University of Tasmania, Hobart, Australia.
Launceston Clinical School, Tasmanian School of Medicine, University of Tasmania, Launceston, Australia.
Expert Rev Clin Pharmacol. 2022 Aug;15(8):1003-1010. doi: 10.1080/17512433.2022.2103540. Epub 2022 Jul 21.
We aimed to compare the risk of developing osteoporosis in patients prescribed warfarin or direct-acting oral anticoagulants (DOACs) with those with no therapy.
We included 37,632 patients aged between 18 and 111 years with a recorded diagnosis of AF between 1 January 2013 and 31 December 2017. Patients were followed until the diagnosis of osteoporosis, switch or discontinuation of the OAC, last clinical visit, or end of the study period, whichever occurred first. The incidences of new-onset osteoporosis were calculated using the Cox proportional hazards model.
Of total, 16,995 (45.2%) had no recorded OAC prescription, and 20,637 had a recorded prescription of warfarin (6,609) or DOAC (14,028). Compared with those not prescribed an OAC, the risk of being diagnosed with new-onset osteoporosis increased in patients prescribed warfarin (HR 2.22, 95% CI 2.00-2.47, p < 0.001) and DOACs (HR 1.42, 95% CI 1.29-1.58, p < 0.001). However, the effect of DOACs was not statistically significant (HR 1.07, 95% CI 0.86-1.33, p < 0.535) after excluding patients with at least one recorded prescription of systemic corticosteroids, antiepileptics, or proton pump inhibitors.
Use of warfarin or DOACs was associated with a significantly increased risk of developing osteoporosis compared with no OAC treatment.
我们旨在比较华法林或直接口服抗凝剂(DOACs)与无治疗患者发生骨质疏松症的风险。
我们纳入了 2013 年 1 月 1 日至 2017 年 12 月 31 日期间记录有房颤诊断的 37632 名年龄在 18 至 111 岁之间的患者。患者随访至诊断为骨质疏松症、OAC 转换或停药、最后一次临床就诊或研究期结束,以先发生者为准。使用 Cox 比例风险模型计算新发骨质疏松症的发生率。
共有 16995 名(45.2%)患者未记录有 OAC 处方,20637 名患者记录有华法林(6609 名)或 DOAC(14028 名)处方。与未处方 OAC 的患者相比,处方华法林(HR 2.22,95%CI 2.00-2.47,p < 0.001)和 DOAC(HR 1.42,95%CI 1.29-1.58,p < 0.001)的患者诊断为新发骨质疏松症的风险增加。然而,在排除至少有一次记录处方全身皮质激素、抗癫痫药或质子泵抑制剂的患者后,DOAC 的作用无统计学意义(HR 1.07,95%CI 0.86-1.33,p < 0.535)。
与无 OAC 治疗相比,使用华法林或 DOAC 与发生骨质疏松症的风险显著增加相关。