Nakatoh Shinichi, Fujimori Kenji, Ishii Shigeyuki, Tamaki Junko, Okimoto Nobukazu, Ogawa Sumito, Iki Masayuki
Department of Orthopedic Surgery, Asahi General Hospital, 477 Tomari, Asahimachi, Shimo-Niikawa-gun, Toyama, 939-0798, Japan.
National Database Japan-Osteoporosis Management Study Group, Department of Public Health, Kindai University Faculty of Medicine, 377-2 Oono-higashi, Osaka-Sayama, Osaka, 589-8511, Japan.
J Bone Miner Metab. 2023 Mar;41(2):248-257. doi: 10.1007/s00774-023-01411-4. Epub 2023 Feb 28.
This study aimed to assess the association between pharmacotherapy and secondary hip fracture incidence.
The correlation between secondary hip fracture incidence and the presence, type, and medication possession ratio (MPR) of pharmacotherapy was investigated using medical insurance data acquired from the National Database of Health Insurance Claims and Specific Health Checkups of Japan.
Data collected from female patients (n = 1,435,347) were analyzed. The 2-year secondary hip fracture incidence was 3.48% (n = 49,921). Secondary hip fracture was significantly more common in patients without medications (3.80%) than in those with medications (3.00%). Patients receiving selective estrogen receptor modulators (SERMs) had the lowest average age. The crude incidence of secondary hip fracture was the lowest in patients receiving SERMs (n = 2088 [2.52%]), followed by those taking bisphosphonates (n = 11,355 [2.88%]), denosumab (n = 1118 [2.90%]), no medications (n = 32,747 [3.80%]), and parathyroid hormone (PTH: n = 2163 [4.55%]), whereas the age-adjusted incidence was the lowest in patients administered denosumab (2.27%), followed by those taking bisphosphonates (2.47%), SERMs (2.55%), PTH (3.67%), and no medications (3.80%). The mean MPR was the highest in patients taking denosumab (64.9%), followed by those receiving bisphosphonates (58.7%), SERMs (58.2%), and PTH (40.6%) in the no hip fracture group.
Secondary hip fractures were less likely to occur with medication versus no medication. Differences in the crude incidence of secondary hip fracture based on medications usage might be attributed to background characteristics.
本研究旨在评估药物治疗与继发性髋部骨折发生率之间的关联。
利用从日本国民健康保险索赔和特定健康检查国家数据库获取的医疗保险数据,研究继发性髋部骨折发生率与药物治疗的存在、类型及药物持有率(MPR)之间的相关性。
对收集的女性患者(n = 1,435,347)数据进行分析。2年继发性髋部骨折发生率为3.48%(n = 49,921)。未用药患者的继发性髋部骨折明显比用药患者更常见(3.80%对3.00%)。接受选择性雌激素受体调节剂(SERM)治疗的患者平均年龄最低。接受SERM治疗的患者继发性髋部骨折的粗发病率最低(n = 2088 [2.52%]),其次是服用双膦酸盐的患者(n = 11,355 [2.88%])、地诺单抗(n = 1118 [2.90%])、未用药患者(n = 32,747 [3.80%])和甲状旁腺激素(PTH:n = 2163 [4.55%]),而年龄调整发病率在接受地诺单抗治疗的患者中最低(2.27%),其次是服用双膦酸盐的患者(2.47%)、SERM(2.55%)、PTH(3.67%)和未用药患者(3.80%)。在无髋部骨折组中,服用地诺单抗的患者平均MPR最高(64.9%),其次是接受双膦酸盐治疗的患者(58.7%)、SERM(58.2%)和PTH(40.6%)。
与未用药相比,用药时继发性髋部骨折发生的可能性较小。基于药物使用情况的继发性髋部骨折粗发病率差异可能归因于背景特征。