Donnelly Karen, Bracchi Robert, Hewitt Jonathan, Routledge Philip A, Carter Ben
Pharmacology, Therapeutics and Toxicology, Cardiff University School of Medicine, Academic Centre, University Hospital Llandough, Cardiff, United Kingdom.
Institute of Primary Care and Public Health, Cardiff University, School of Medicine, Neuadd Meirionnydd, Cardiff, United Kingdom.
PLoS One. 2017 Apr 27;12(4):e0174730. doi: 10.1371/journal.pone.0174730. eCollection 2017.
Hip fractures in the older person lead to an increased risk of mortality, poorer quality of life and increased morbidity. Benzodiazepine (BNZ) use is associated with increased hip fracture rate, consequently Z-drugs are fast becoming the physician's hypnotic prescription of choice yet data on their use is limited. We compared the risk of hip fracture associated with Z-drugs and BNZ medications, respectively, and examined if this risk varied with longer-term use.
We carried out a systematic review of the literature and meta-analysis. MEDLINE and SCOPUS were searched to identify studies involving BNZ or Z-drugs and the risk of hip fracture up to May 2015. Each included study was quality-assessed. A pooled relative risk of hip fracture was calculated using the generic inverse variance method, with a random effects model, with the length of hypnotic usage as a subgroup. Both BNZ, and Z-drug use respectively, were significantly associated with an increased risk of hip fracture (RR = 1.52, 95% CI 1.37-1.68; and RR = 1.90, 95% CI 1.68-2.13). Short-term use of BNZ and Z-drugs respectively, was also associated with the greatest risk of hip fracture (RR = 2.40, 95% CI 1.88-3.05 and RR = 2.39, 95% CI 1.74-3.29).
There is strong evidence that both BNZ and Z-drugs are associated with an increased risk of hip fracture in the older person, and there is little difference between their respective risks. Patients newly prescribed these medicines are at the greatest risk of hip fracture. Clinicians and policy makers need to consider the increased risk of fallings and hip fracture particularly amongst new users of these medications.
老年人髋部骨折会导致死亡风险增加、生活质量下降和发病率上升。使用苯二氮䓬类药物(BNZ)会使髋部骨折率升高,因此Z类药物正迅速成为医生首选的催眠处方药物,但关于其使用的数据有限。我们分别比较了与Z类药物和BNZ药物相关的髋部骨折风险,并研究了这种风险是否会因长期使用而有所不同。
我们进行了一项文献系统综述和荟萃分析。检索了MEDLINE和SCOPUS数据库,以确定截至2015年5月涉及BNZ或Z类药物以及髋部骨折风险的研究。对每项纳入研究进行质量评估。使用通用逆方差法和随机效应模型计算髋部骨折的合并相对风险,并将催眠药物使用时长作为一个亚组。使用BNZ和使用Z类药物均分别与髋部骨折风险增加显著相关(相对风险[RR]=1.52,95%置信区间[CI]为1.37 - 1.68;RR = 1.90,95% CI为1.68 - 2.13)。分别短期使用BNZ和Z类药物也与最高的髋部骨折风险相关(RR = 2.40,95% CI为1.88 - 3.05;RR = 2.39,95% CI为1.74 - 3.29)。
有充分证据表明,BNZ和Z类药物均与老年人髋部骨折风险增加相关,且它们各自的风险差异不大。新开具这些药物的患者髋部骨折风险最高。临床医生和政策制定者需要考虑跌倒和髋部骨折风险增加的问题,尤其是在这些药物的新使用者中。