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雷洛昔芬可预防绝经后女性非骨水泥全髋关节置换术后早期假体周围骨丢失:一项随机安慰剂对照临床试验。

Raloxifene Prevents Early Periprosthetic Bone Loss for Postmenopausal Women after Uncemented Total Hip Arthroplasty: A Randomized Placebo-Controlled Clinical Trial.

机构信息

Department of Orthopaedic Surgery, China-Japan Friendship Hospital, Peking Union Medical College, Chinese Academy of Medical College, Beijing, China.

Department of Obstetrics and Gynecology, West China Second University Hospital of Sichuan University, Chengdu, China.

出版信息

Orthop Surg. 2020 Aug;12(4):1074-1083. doi: 10.1111/os.12696. Epub 2020 Jul 19.

Abstract

OBJECTIVE

To examine the results of raloxifene for prevention of periprosthetic bone loss around the femoral stem in patients undergoing total hip arthroplasty (THA).

METHODS

Between January 2015 and May 2017, 240 female patients between 55 and 80 years underwent primary THA and were randomly allocated to receive 60 mg raloxifene hydrochloride per day (treatment group, TG, n = 120) or placebo (control group, CG, n = 120) orally at bedtime using computer-generated randomization sequence generation. Baseline data, the Western Ontario McMaster Universities Osteoarthritis Index (WOMAC), women's quality of life (QoL) score, bone mineral density (BMD) around the prosthesis, and adverse events were compared between the two groups. The measuring range of BMD around the prosthesis was divided into seven regions of interest (ROI). The sample size was calculated to detect a mean difference in BMD of 0.15 g/cm with a standard deviation (SD) of 0.3. The error was set at 0.05 and the power level at 90% with additional compensation for a possible dropout rate of 20%.

RESULTS

A total of 240 participants in the study up to 24 months after THA. There were no significant differences in the mean BMD of all the zones between groups before surgery (all P > 0.05). However, there were significant differences in the BMD of Gruen zones 4 and 7 between groups at 6 months postoperatively (both P < 0.05); there were significant differences in Gruen zones 1, 4, 6, and 7 at 12 months postoperatively (all P < 0.01); there were significant differences in Gruen zones 1, 2, 4, 6, and 7 at 24 months postoperatively (all P < 0.001). Patients taking raloxifene reported higher QoL scores, with better improvement in BMD in all areas except in zones 3 and 5 compared with the control group. There were no significant differences in WOMAC pain (P = 0.4045), WOMAC function (P = 0.4456) and women's QoL scores (P = 0.5983) between groups before surgery. However, WOMAC pain, WOMAC function and women's QoL score in the treatment group were significantly better at all time points (all P < 0.05). Patients in the treatment group showed no increased adverse events, including cardiac events, stroke, venous thromboembolism, and gynecological cancer (all P > 0.05), but did show decreased odds of breast cancer in comparison with those using a placebo (P = 0.0437).

CONCLUSION

Raloxifene can help inhibit bone loss around the prosthesis and improve the QoL of postmenopausal women after THA with no increased adverse events, and can even decrease the odds of breast cancer.

摘要

目的

研究雷洛昔芬对预防全髋关节置换术(THA)患者股骨柄周围假体周围骨丢失的效果。

方法

2015 年 1 月至 2017 年 5 月,240 名 55 至 80 岁的女性患者接受了初次 THA,并随机分为接受盐酸雷洛昔芬 60mg/天(治疗组,TG,n=120)或安慰剂(对照组,CG,n=120)组。采用计算机生成的随机序列生成方法,在睡前口服。比较两组患者的基线数据、西部安大略省麦克马斯特大学骨关节炎指数(WOMAC)、女性生活质量(QoL)评分、假体周围骨密度(BMD)和不良事件。假体周围 BMD 的测量范围分为七个感兴趣区(ROI)。根据标准偏差(SD)为 0.3,预计平均 BMD 差值为 0.15g/cm,计算样本量。误差设定为 0.05,效能设定为 90%,并考虑到 20%的可能脱落率进行了额外补偿。

结果

共有 240 名患者在 THA 后 24 个月接受了研究。两组患者在手术前所有区域的平均 BMD 均无显著差异(均 P>0.05)。然而,术后 6 个月时,Gruen 区 4 和 7 的 BMD 有显著差异(均 P<0.05);术后 12 个月时,Gruen 区 1、4、6 和 7 的 BMD 有显著差异(均 P<0.01);术后 24 个月时,Gruen 区 1、2、4、6 和 7 的 BMD 有显著差异(均 P<0.001)。服用雷洛昔芬的患者报告了更高的 QoL 评分,除了区域 3 和 5 之外,所有区域的 BMD 都有更好的改善,与对照组相比。两组患者在手术前的 WOMAC 疼痛(P=0.4045)、WOMAC 功能(P=0.4456)和女性 QoL 评分(P=0.5983)均无显著差异。然而,治疗组在所有时间点的 WOMAC 疼痛、WOMAC 功能和女性 QoL 评分均显著改善(均 P<0.05)。治疗组患者无不良事件增加,包括心脏事件、中风、静脉血栓栓塞和妇科癌症(均 P>0.05),但与安慰剂组相比,乳腺癌的几率降低(P=0.0437)。

结论

雷洛昔芬可抑制假体周围骨丢失,提高绝经后妇女 THA 后的生活质量,且无不良事件增加,并可能降低乳腺癌的几率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aba/7454213/64358e8747bc/OS-12-1074-g001.jpg

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