Department of Orthopaedic Surgery, Keelung Chang Gung Memorial Hospital, Keelung 204, Taiwan; Department of Medicine, College of Medicine, Chang Gung University, Kwei-Shan, Taoyuan 259, Taiwan; Osteoporosis Prevention and Treatment Center, Keelung Chang Gung Memorial Hospital, Keelung 204, Taiwan.
Osteoporosis Prevention and Treatment Center, Keelung Chang Gung Memorial Hospital, Keelung 204, Taiwan; Department of General Surgery, Keelung Chang Gung Memorial Hospital, Keelung 204, Taiwan; Department of Chinese Medicine, College of Medicine, Chang Gung University, Kwei-Shan, Taoyuan 259, Taiwan; Department of Ophthalmology, Keelung Chang Gung Memorial Hospital, Keelung 204, Taiwan.
Bone. 2022 Jan;154:116239. doi: 10.1016/j.bone.2021.116239. Epub 2021 Oct 22.
The aim of this study is to investigate the impact of bisphosphonate treatment on the prognosis of patients with initial hip fracture. Patients aged fifty years and older with initial hip fracture were identified from the Taiwan National Health Insurance Research Database between 2002 and 2011. A multi-state model was established to evaluate the transition between "first to second hip fracture", "first hip fracture to death", and "second hip fracture to death". Transition probability and cumulative hazards were used to compare the prognosis of initial hip fracture in a bisphosphonate treated cohort versus non-treated cohort. In addition, Deyo-Charlson comorbidities, both vertebral and non-vertebral fractures, and cataracts were also included for analysis. After 10-year follow-up, there is decreased cumulative transition probability for both second hip fracture and mortality after both first and second hip fracture in the bisphosphonate treated cohort. Multivariable, transition-specific time-dependent Cox model revealed that bisphosphonate treatment significantly reduced risk for second hip fracture in the first 5 years of the treatment (HR 0.88; 95% CI 0.79-0.99; P: 0.034), first hip fracture mortality (HR 0.88; 95% CI 0.83-0.93; P < 0.001), and second hip fracture mortality in the first 2 years of the treatment (HR 0.78; 95% CI 0.65-0.95; P = 0.011). Female sex, both vertebral and non-vertebral fractures, cataracts, dementia in the first 2 years, and DM with complication were all significantly associated with risk of a second hip fracture. Cerebrovascular disease and hemiplegia comorbidities had less risk of a second hip fracture. The risk of mortality after both first and second hip fracture was significantly associated with congestive heart failure, renal disease, myocardial infarction, and moderate to severe liver disease. Our study demonstrated that bisphosphonate treatment and strict management of comorbidities after the initial hip fracture significantly decrease the risk for a second hip fracture and mortality.
本研究旨在探讨双膦酸盐治疗对初发性髋部骨折患者预后的影响。我们从 2002 年至 2011 年的台湾全民健康保险研究数据库中确定了年龄在 50 岁及以上的初发性髋部骨折患者。我们建立了多状态模型来评估“初次髋部骨折至第二次髋部骨折”、“初次髋部骨折至死亡”和“第二次髋部骨折至死亡”之间的转移。我们使用转移概率和累积风险来比较双膦酸盐治疗组与未治疗组初发性髋部骨折的预后。此外,我们还纳入了 Deyo-Charlson 合并症、椎体和非椎体骨折以及白内障进行分析。10 年随访后,在双膦酸盐治疗组中,第二次髋部骨折和第一次及第二次髋部骨折后死亡率的累积转移概率均降低。多变量、转移特异性时间依赖性 Cox 模型显示,双膦酸盐治疗在治疗的前 5 年内显著降低了第二次髋部骨折的风险(HR 0.88;95%CI 0.79-0.99;P:0.034)、第一次髋部骨折死亡率(HR 0.88;95%CI 0.83-0.93;P<0.001)和治疗的前 2 年内第二次髋部骨折死亡率(HR 0.78;95%CI 0.65-0.95;P=0.011)。女性、椎体和非椎体骨折、白内障、治疗前 2 年内痴呆以及合并并发症的糖尿病与第二次髋部骨折风险显著相关。脑血管疾病和偏瘫合并症发生第二次髋部骨折的风险较低。初次及第二次髋部骨折后死亡率与充血性心力衰竭、肾脏疾病、心肌梗死和中重度肝脏疾病显著相关。我们的研究表明,初发性髋部骨折后双膦酸盐治疗和合并症的严格管理显著降低了第二次髋部骨折和死亡率的风险。