Department of Orthopedic Surgery, Sasayama Hospital, Hyogo College of Medicine, Sasayama, Japan.
Curr Med Res Opin. 2012 Nov;28(11):1757-66. doi: 10.1185/03007995.2012.736860. Epub 2012 Oct 26.
To assess changes in quality of life (QOL) and pain in raloxifene-treated Japanese women with postmenopausal osteoporosis.
This prospective, postmarketing observational study was conducted at 60 Japanese hospitals from September 2007 to February 2009 and included Japanese women with postmenopausal osteoporosis who were new to standard treatment with raloxifene (60 mg/day). Primary outcome measures (QOL and pain) were assessed using the Short Form-8 (SF-8), European Quality of Life Instrument (EQ-5D), osteoporosis-specific Japanese Osteoporosis Quality of Life Questionnaire (JOQOL), a visual analogue scale (VAS-pain), and a pain frequency survey. Assessments were performed at baseline and 8 (except JOQOL) and 24 weeks after first administration of raloxifene. Adverse drug reactions were recorded. Japan Pharmaceutical Information Center registration number: JapicCTI-070465.
A total of 506 participants, mean (±standard deviation [SD]) age = 70.7 ± 8.7 years, completed ≥1 follow-up assessment and were included in the analyses. All QOL scores increased from baseline during follow-up. All SF-8 domain scores increased significantly from baseline after 8 and 24 weeks (P < 0.001). Mean (±SD) EQ-5D scores increased significantly from baseline (0.70 ± 0.17) by 0.05 ± 0.15 after 8 weeks and 0.07 ± 0.17 after 24 weeks (P < 0.001). The mean (±SD) total JOQOL score increased significantly from baseline (66.8 ± 16.5) by 3.8 ± 11.3 after 24 weeks (P < 0.001). The percentage of participants with a ≥20 mm reduction in VAS-pain was 32.6% (120/368) and 39.5% (115/291) after 8 and 24 weeks, respectively. The frequency of pain reported by participants decreased after 8 and 24 weeks. Forty adverse drug reactions were reported by 34 participants.
Limitations include the lack of a control group, the possibility of the changes being due to the natural disease course, and potential selection bias.
Our findings suggest that standard treatment with raloxifene improves QOL and relieves pain in Japanese women with postmenopausal osteoporosis in a real-world clinical setting.
评估雷洛昔芬治疗绝经后骨质疏松症日本女性的生活质量(QOL)和疼痛变化。
本项前瞻性、上市后观察性研究于 2007 年 9 月至 2009 年 2 月在 60 家日本医院进行,纳入了开始接受雷洛昔芬(60mg/天)标准治疗的新诊断为绝经后骨质疏松症的日本女性。主要结局评估指标(QOL 和疼痛)采用简易 8 项健康调查量表(SF-8)、欧洲生命质量量表(EQ-5D)、骨质疏松症特异性日本骨质疏松症生活质量问卷(JOQOL)、视觉模拟量表(VAS-pain)和疼痛频率调查进行评估。在雷洛昔芬首次给药后 8 周(除 JOQOL 外)和 24 周时进行基线和 8 次评估。记录药物不良反应。日本药品信息中心注册号:JapicCTI-070465。
共有 506 名参与者完成了至少 1 次随访评估并纳入分析,其平均(±标准差 [SD])年龄为 70.7±8.7 岁。在随访期间,所有 QOL 评分均自基线升高。所有 SF-8 领域评分在 8 周和 24 周后均较基线显著升高(P<0.001)。平均(±SD)EQ-5D 评分自基线(0.70±0.17)升高 0.05±0.15,8 周后升高 0.07±0.17,24 周后升高 0.07±0.17(P<0.001)。JOQOL 总分平均(±SD)自基线(66.8±16.5)升高 3.8±11.3,24 周后升高 3.8±11.3(P<0.001)。8 周和 24 周时,VAS-pain 疼痛缓解≥20mm 的参与者比例分别为 32.6%(120/368)和 39.5%(115/291)。8 周和 24 周后,参与者报告的疼痛频率均降低。34 名参与者报告了 40 起药物不良反应。
局限性包括缺乏对照组、变化可能是由自然病程引起的以及潜在的选择偏倚。
我们的研究结果表明,雷洛昔芬标准治疗可改善日本绝经后骨质疏松症女性的生活质量并缓解疼痛。