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双磷酸盐类药物可维持全髋关节置换术后的假体周围骨密度,但在感兴趣区域 5 存在争议。

Bisphosphonates Can Maintain Periprosthetic Bone Mass Density after Total Hip Replacement, with Controversy in Region of Interest 5.

机构信息

Shanxi Bethune Hospital, Taiyuan, Shanxi Province, China.

Changzhi Medical College, Changzhi, Shanxi, China.

出版信息

Curr Pharm Des. 2020;26(38):4925-4933. doi: 10.2174/1381612826666200422093213.

Abstract

BACKGROUND

Total hip replacement (THR) is the standard surgical treatment of hip diseases. Periprosthetic bone mass density (BMD) loss may be a cause for revision surgery. Bisphosphonates (BPs) are now the principal class medications for osteoporosis.

OBJECTIVE

To demonstrate the effect of BPs on treating periprosthetic osteoporosis after THR via a meta-analysis of randomized controlled trials (RCTs).

METHODS

A comprehensive search of PubMed, EMBASE, the Web of Science and the Cochrane Central Register of Controlled Trials was performed for RCTs on the effect of BPs on treating periprosthetic osteoporosis after THR and clinical outcomes relative to controls. The primary outcome measures were the change in BMD in each region of interest (ROI), the change in serum bone turnover marker levels, the change in functional parameters and the risk of adverse effects (AEs). The final search was performed in March, 2020.

RESULTS

Nine RCTs were included. A total of 359 patients met the inclusion criteria. BPs can clearly maintain periprosthetic BMD in ROIs at 1, 2, 3, 4, 6 and 7 at 6, 12 and 24 months. In addition, BPs can clearly decrease serum procollagen type 1 N-terminal propeptide (P1NP) levels at 12 months. There was no significant difference in the risk of AEs between the BP and control groups; however, BPs can cause more patients to decline participation.

CONCLUSION

BPs can effectively maintain overall periprosthetic BMD, but BMD in ROI 5 remains controversial. In addition, the safety of BPs is relatively high, but the compliance may be relatively low.

摘要

背景

全髋关节置换术(THR)是治疗髋关节疾病的标准手术。假体周围骨量密度(BMD)丢失可能是翻修手术的原因。双膦酸盐(BPs)现在是治疗骨质疏松症的主要药物类别。

目的

通过对 THR 后 BPs 治疗假体周围骨质疏松症的随机对照试验(RCT)的荟萃分析,证明 BPs 的疗效。

方法

对 PubMed、EMBASE、Web of Science 和 Cochrane 对照试验中心注册库进行全面检索,以获取关于 BPs 治疗 THR 后假体周围骨质疏松症以及与对照组相关的临床结局的 RCT 研究。主要结局指标是每个感兴趣区域(ROI)的 BMD 变化、血清骨转换标志物水平的变化、功能参数的变化和不良事件(AEs)的风险。最后一次检索是在 2020 年 3 月进行的。

结果

纳入了 9 项 RCT。共有 359 名患者符合纳入标准。BPs 可以清楚地维持 ROI 中假体周围的 BMD 在 1、2、3、4、6 和 7 处,在 6、12 和 24 个月时。此外,BPs 可以清楚地降低血清 1 型前胶原 N 端前肽(P1NP)水平在 12 个月时。BPs 组与对照组之间的 AEs 风险无显著差异;然而,BPs 会导致更多的患者拒绝参与。

结论

BPs 可以有效地维持整体假体周围的 BMD,但 ROI 5 处的 BMD 仍存在争议。此外,BPs 的安全性相对较高,但顺应性可能相对较低。

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