Hargrove Jennifer L, Golightly Yvonne M, Pate Virginia, Casteel Carri H, Loehr Laura R, Marshall Stephen W, Stürmer Til
Gillings School of Global Public Health, The University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
College of Public Health, The University of Iowa, Iowa City, IA, USA.
Inj Epidemiol. 2017 Oct 18;4(1):27. doi: 10.1186/s40621-017-0125-8.
Research suggests antihypertensive medications are associated with fractures in older adults, however results are inconsistent and few have examined how the association varies over time. We sought to examine the association between antihypertensive class and incident non-vertebral fractures among older adults initiating monotherapy according to time since initiation.
We used a new-user cohort design to identify Medicare beneficiaries (≥ 65 years of age) initiating antihypertensive monotherapy during 2008-2011 using a 20% random sample of Fee-For-Service Medicare beneficiaries enrolled in parts A (inpatient services), B (outpatient services), and D (prescription medication) coverage. Starting the day after the initial antihypertensive prescription, we followed beneficiaries for incident non-vertebral fractures. We used multinomial logistic regression models to estimate propensity scores for initiating each antihypertensive drug class. Using these propensity scores, we weighted beneficiaries to achieve the same baseline covariate distribution as beneficiaries initiating with angiotensin-converting enzyme inhibitors. Lastly, we used weighted Cox proportional hazard models to estimate hazard ratios (HRs) of having an incident fractures according to antihypertensive class and time since initiation.
During 2008-2011, 122,629 Medicare beneficiaries initiated antihypertensive monotherapy (mean age 75, 61% women, 86% White). Fracture rates varied according to days since initiation and antihypertensive class. Beneficiaries initiating with thiazides had the highest fracture rate in the first 14 days following initiation (438 per 10,000 person-years, 95% confidence interval (CI): 294-628; HR: 1.40, 0.78-2.52). However, beneficiaries initiating with calcium channel blockers had the highest fracture rate during the 15-365 days after initiation (435 per 10,000 person-years, 95% CI: 404-468; HR: 1.11, 1.00-1.24). Beneficiaries initiating with angiotensin-receptor blockers had the lowest fracture rates during the initial 14 days (333 per 10,000 person-years, 190-546, HR: 0.92, 0.49-1.75) and during 15-365 days after initiation (321 per 10,000 person-years, 287-358, HR: 0.96, 0.84-1.09).
The association between antihypertensives and fractures varied according to class and time since initiation. Results suggest that when deciding upon antihypertensive therapy, clinicians may want to consider possible fracture risks when choosing between antihypertensive drug classes.
研究表明,抗高血压药物与老年人骨折有关,然而结果并不一致,很少有研究探讨这种关联如何随时间变化。我们试图根据开始治疗后的时间,研究抗高血压药物类别与开始单一疗法的老年人发生非椎体骨折之间的关联。
我们采用新用户队列设计,从参加A部分(住院服务)、B部分(门诊服务)和D部分(处方药)保险的按服务收费的医疗保险受益人的20%随机样本中,确定2008 - 2011年开始抗高血压单一疗法的医疗保险受益人(≥65岁)。从首次抗高血压处方后的第二天开始,我们对受益人进行随访,观察其非椎体骨折的发生情况。我们使用多项逻辑回归模型来估计开始使用每种抗高血压药物类别的倾向得分。利用这些倾向得分,我们对受益人进行加权,以使基线协变量分布与开始使用血管紧张素转换酶抑制剂的受益人相同。最后,我们使用加权Cox比例风险模型,根据抗高血压药物类别和开始治疗后的时间,估计发生骨折的风险比(HRs)。
在2008 - 2011年期间,122,629名医疗保险受益人开始抗高血压单一疗法(平均年龄75岁,61%为女性,86%为白人)。骨折发生率根据开始治疗后的天数和抗高血压药物类别而有所不同。开始使用噻嗪类药物的受益人在开始治疗后的前14天骨折发生率最高(每10,000人年438例,95%置信区间(CI):294 - 628;HR:1.40,0.78 - 2.52)。然而,开始使用钙通道阻滞剂的受益人在开始治疗后的15 - 365天骨折发生率最高(每10,000人年435例,95%CI:404 - 468;HR:1.11,1.00 - 1.24)。开始使用血管紧张素受体阻滞剂的受益人在最初14天(每10,000人年333例,190 - 546,HR:0.92,0.49 - 1.75)和开始治疗后的15 - 365天(每10,000人年321例,287 - 358,HR:0.96,0.84 - 1.09)骨折发生率最低。
抗高血压药物与骨折之间的关联因药物类别和开始治疗后的时间而异。结果表明,在决定抗高血压治疗方案时,临床医生在选择抗高血压药物类别时可能需要考虑可能的骨折风险。