Elizabeth Rieger, Andrew Fuqua, Alyssa Woltemath, Jacob M Wilson, Christian Pean, Alejandro Gonzalez Della Valle, Ajay Premkumar
{"title":"错失良机?股骨颈骨折后骨质疏松治疗:降低继发性髋部骨折的风险。","authors":"Elizabeth Rieger, Andrew Fuqua, Alyssa Woltemath, Jacob M Wilson, Christian Pean, Alejandro Gonzalez Della Valle, Ajay Premkumar","doi":"10.1016/j.arth.2025.07.028","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Hip fractures represent devastating injuries with extensive morbidity and mortality. Despite guidelines recommending osteoporosis pharmacotherapy after hip fracture, treatment rates remain low. This study sought to determine the effect of osteoporosis pharmacotherapy on the secondary hip fracture rate in patients undergoing operative treatment for femoral neck fractures (FNFx).</p><p><strong>Methods: </strong>A large national database was queried for patients ≥ 50 years old who underwent operative fixation of FNFx between 2009 and 2022. Age, sex, comorbidities, and pharmaceutical records were collected from the database. Among the 17,128 study patients, the mean age was 79 years (range, 50 to 103), and 65% were women. Patients previously treated for osteoporosis were excluded. Kaplan-Meier and Cox proportional hazards analyses were used to compare secondary hip fracture rates in patients who were medically treated for osteoporosis within one year of index FNFx versus those who were never treated for osteoporosis. Cumulative rates of osteoporosis pharmacotherapy initiation and secondary hip fracture were determined.</p><p><strong>Results: </strong>Treatment initiation within one year was associated with a significantly reduced hip fracture hazard at three years (HR [hazard ratio] 0.56, 95% CI [confidence interval] 0.32 to 0.95, P = 0.03), five years (HR 0.63, 95% CI 0.40 to 0.98, P = 0.04), and 10 years (HR 0.57, 95% CI 0.37 to 0.87, P = 0.01) following FNFx. Only 6.3% of study patients were initiated on osteoporosis medication within one year following FNFx. The cumulative rate of secondary hip fracture over 10 years was 5.3%.</p><p><strong>Conclusions: </strong>Despite established guidelines, low rates of osteoporotic pharmacotherapy were seen in patients who had FNFx. Pharmacotherapy initiation within one year of FNFx was associated with a reduced rate of secondary hip fracture. In adherence to guidelines, physicians should educate patients and initiate osteoporosis treatment along with operative management of FNFx, given its association with reduced rates of subsequent hip fractures.</p>","PeriodicalId":51077,"journal":{"name":"Journal of Arthroplasty","volume":" ","pages":""},"PeriodicalIF":3.4000,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Missed Opportunity? Osteoporosis Treatment Following Femoral Neck Fractures: Reducing the Risk of Secondary Hip Fracture.\",\"authors\":\"Elizabeth Rieger, Andrew Fuqua, Alyssa Woltemath, Jacob M Wilson, Christian Pean, Alejandro Gonzalez Della Valle, Ajay Premkumar\",\"doi\":\"10.1016/j.arth.2025.07.028\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Hip fractures represent devastating injuries with extensive morbidity and mortality. Despite guidelines recommending osteoporosis pharmacotherapy after hip fracture, treatment rates remain low. This study sought to determine the effect of osteoporosis pharmacotherapy on the secondary hip fracture rate in patients undergoing operative treatment for femoral neck fractures (FNFx).</p><p><strong>Methods: </strong>A large national database was queried for patients ≥ 50 years old who underwent operative fixation of FNFx between 2009 and 2022. Age, sex, comorbidities, and pharmaceutical records were collected from the database. Among the 17,128 study patients, the mean age was 79 years (range, 50 to 103), and 65% were women. Patients previously treated for osteoporosis were excluded. Kaplan-Meier and Cox proportional hazards analyses were used to compare secondary hip fracture rates in patients who were medically treated for osteoporosis within one year of index FNFx versus those who were never treated for osteoporosis. Cumulative rates of osteoporosis pharmacotherapy initiation and secondary hip fracture were determined.</p><p><strong>Results: </strong>Treatment initiation within one year was associated with a significantly reduced hip fracture hazard at three years (HR [hazard ratio] 0.56, 95% CI [confidence interval] 0.32 to 0.95, P = 0.03), five years (HR 0.63, 95% CI 0.40 to 0.98, P = 0.04), and 10 years (HR 0.57, 95% CI 0.37 to 0.87, P = 0.01) following FNFx. Only 6.3% of study patients were initiated on osteoporosis medication within one year following FNFx. The cumulative rate of secondary hip fracture over 10 years was 5.3%.</p><p><strong>Conclusions: </strong>Despite established guidelines, low rates of osteoporotic pharmacotherapy were seen in patients who had FNFx. Pharmacotherapy initiation within one year of FNFx was associated with a reduced rate of secondary hip fracture. 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引用次数: 0
摘要
背景:髋部骨折是具有广泛发病率和死亡率的破坏性损伤。尽管指南建议髋部骨折后进行骨质疏松药物治疗,但治愈率仍然很低。本研究旨在确定骨质疏松药物治疗对股骨颈骨折(FNFx)手术治疗患者继发髋部骨折率的影响。方法:对2009年至2022年间接受FNFx手术固定的≥50岁患者的大型国家数据库进行查询。从数据库中收集年龄、性别、合并症和用药记录。在17128例研究患者中,平均年龄为79岁(50 - 103岁),65%为女性。先前接受过骨质疏松治疗的患者被排除在外。Kaplan-Meier和Cox比例风险分析用于比较在FNFx指数一年内接受骨质疏松医学治疗的患者与从未接受骨质疏松治疗的患者的继发性髋部骨折发生率。测定骨质疏松症药物治疗开始和继发性髋部骨折的累积率。结果:一年内开始治疗与FNFx术后3年(HR[风险比]0.56,95% CI[置信区间]0.32至0.95,P = 0.03)、5年(HR 0.63, 95% CI 0.40至0.98,P = 0.04)和10年(HR 0.57, 95% CI 0.37至0.87,P = 0.01)髋部骨折风险显著降低相关。只有6.3%的研究患者在FNFx后一年内开始接受骨质疏松药物治疗。10年内继发性髋部骨折的累计发生率为5.3%。结论:尽管有既定的指南,但在FNFx患者中骨质疏松药物治疗的比例很低。FNFx治疗一年内开始药物治疗与继发性髋部骨折发生率降低相关。在遵循指南的前提下,医生应该教育患者并开始骨质疏松治疗以及FNFx的手术管理,因为它与后续髋部骨折的发生率降低有关。
A Missed Opportunity? Osteoporosis Treatment Following Femoral Neck Fractures: Reducing the Risk of Secondary Hip Fracture.
Background: Hip fractures represent devastating injuries with extensive morbidity and mortality. Despite guidelines recommending osteoporosis pharmacotherapy after hip fracture, treatment rates remain low. This study sought to determine the effect of osteoporosis pharmacotherapy on the secondary hip fracture rate in patients undergoing operative treatment for femoral neck fractures (FNFx).
Methods: A large national database was queried for patients ≥ 50 years old who underwent operative fixation of FNFx between 2009 and 2022. Age, sex, comorbidities, and pharmaceutical records were collected from the database. Among the 17,128 study patients, the mean age was 79 years (range, 50 to 103), and 65% were women. Patients previously treated for osteoporosis were excluded. Kaplan-Meier and Cox proportional hazards analyses were used to compare secondary hip fracture rates in patients who were medically treated for osteoporosis within one year of index FNFx versus those who were never treated for osteoporosis. Cumulative rates of osteoporosis pharmacotherapy initiation and secondary hip fracture were determined.
Results: Treatment initiation within one year was associated with a significantly reduced hip fracture hazard at three years (HR [hazard ratio] 0.56, 95% CI [confidence interval] 0.32 to 0.95, P = 0.03), five years (HR 0.63, 95% CI 0.40 to 0.98, P = 0.04), and 10 years (HR 0.57, 95% CI 0.37 to 0.87, P = 0.01) following FNFx. Only 6.3% of study patients were initiated on osteoporosis medication within one year following FNFx. The cumulative rate of secondary hip fracture over 10 years was 5.3%.
Conclusions: Despite established guidelines, low rates of osteoporotic pharmacotherapy were seen in patients who had FNFx. Pharmacotherapy initiation within one year of FNFx was associated with a reduced rate of secondary hip fracture. In adherence to guidelines, physicians should educate patients and initiate osteoporosis treatment along with operative management of FNFx, given its association with reduced rates of subsequent hip fractures.
期刊介绍:
The Journal of Arthroplasty brings together the clinical and scientific foundations for joint replacement. This peer-reviewed journal publishes original research and manuscripts of the highest quality from all areas relating to joint replacement or the treatment of its complications, including those dealing with clinical series and experience, prosthetic design, biomechanics, biomaterials, metallurgy, biologic response to arthroplasty materials in vivo and in vitro.