Liu Yuan, Xu Jia-Wen, Li Ming-Yang, Wu Li-Min, Zeng Yi, Shen Bin
Department of Orthopedics, National Clinical Research Center for Geriatrics, Orthopedics Research Institute, West China Hospital, Sichuan University, Chengdu, China.
Front Med (Lausanne). 2021 Dec 23;8:801282. doi: 10.3389/fmed.2021.801282. eCollection 2021.
Periprosthetic bone mineral density (BMD) loss following total hip arthroplasty (THA) may threaten the survival of the implant, especially in patients with osteoporosis. Zoledronic acid (ZA) is the representative of the third generation of bisphosphonates, which were effective in reducing bone loss in conditions associated with accelerated bone turnover. The aim of this study was to evaluate the efficacy and safety of ZA in patients with osteoporosis after THA. Randomized controlled trials (RCTs) associated with ZA and THA were searched from the MEDLINE, PubMed, EMBASE, Wanfang database, and the Web of Science (August 2021). Other methods, such as hand search and email request were also tried. The methodological quality was assessed by the Risk of Bias (RoB) 2.0. Relevant data were abstracted from the included RCTs and authors were contacted when necessary. In this study, six RCTs involving a total of 307 patients were finally included and analyzed. The pooled data demonstrated that significantly less periprosthetic BMD loss in Gruen zone seven had occurred in the ZA-treated patients than in the control patients at 3 months (mean difference [MD] = 4.03%; 95% : 0.29-7.76%; = 0.03), 6 months (MD = 7.04%; 95% : 2.12-11.96%; = 0.005), and 12 months (MD = 7.12%; 95% : 0.33-13.92%; = 0.04). The Harris Hip Score (HHS) was also significantly increased in ZA group at 6 and 12 months after operation ( = 0.03 and = 0.02, respectively). Influenza-like symptom was found related to the usage of ZA [relative risk () = 7.03, < 0.0001]. A meta-analysis of six RCTs suggested that ZA was beneficial in maintaining the periprosthetic BMD in patients with osteoporosis at 6 and 12 months after THA. In addition, the HHS was significantly improved in patients treated with ZA. However, the short length of follow-up of the available studies resulted in the lack of analyses regarding the survival of implants including the rate of aseptic loosing, periprosthetic fracture, and revision. It still needs to be determined in research with longer follow-up period. Researchregistry.com, identifier: reviewregistry1087.
全髋关节置换术(THA)后假体周围骨密度(BMD)的丢失可能会威胁植入物的存活,尤其是在骨质疏松症患者中。唑来膦酸(ZA)是第三代双膦酸盐的代表药物,在减少与骨转换加速相关疾病中的骨质流失方面有效。本研究的目的是评估ZA在THA后骨质疏松症患者中的疗效和安全性。从MEDLINE、PubMed、EMBASE、万方数据库和Web of Science(2021年8月)中检索与ZA和THA相关的随机对照试验(RCT)。还尝试了其他方法,如手工检索和电子邮件询问。采用偏倚风险(RoB)2.0评估方法学质量。从纳入的RCT中提取相关数据,并在必要时联系作者。在本研究中,最终纳入并分析了6项RCT,共涉及307例患者。汇总数据表明,在3个月时,ZA治疗组患者Gruen 7区假体周围BMD的丢失明显少于对照组(平均差[MD]=4.03%;95%:0.29 - 7.76%;P = 0.03),6个月时(MD = 7.04%;95%:2.12 - 11.96%;P = 0.005),以及12个月时(MD = 7.12%;95%:0.33 - 13.92%;P = 0.04)。术后6个月和12个月时,ZA组的Harris髋关节评分(HHS)也显著提高(分别为P = 0.03和P = 0.02)。发现流感样症状与ZA的使用有关[相对风险(RR)= 7.03,P < 0.0001]。六项RCT的荟萃分析表明,ZA有利于在THA后6个月和12个月时维持骨质疏松症患者的假体周围BMD。此外,接受ZA治疗的患者HHS显著改善。然而,现有研究的随访时间较短,导致缺乏关于植入物存活情况的分析,包括无菌性松动率、假体周围骨折和翻修情况。在随访期更长的研究中仍需确定。Researchregistry.com,标识符:reviewregistry1087。