Pegios Vasileios F, Kenanidis Eustathios, Tsotsolis Stavros, Potoupnis Michael, Tsiridis Eleftherios
Academic Orthopaedic Department, Aristotle University Medical School, General Hospital Papageorgiou, Thessaloniki, Greece.
Centre of Orthopaedic and Regenerative Medicine (CORE), Center for Interdisciplinary Research and Innovation (CIRI)-Aristotle University of Thessaloniki (AUTH), Balkan Center, Thessaloniki, Greece.
EFORT Open Rev. 2023 Nov 1;8(11):798-808. doi: 10.1530/EOR-22-0121.
The main indication of bisphosphonates (BPs) is osteoporosis treatment. However, there is growing interest in the peri- and postoperative use of BPs to mitigate total hip arthroplasty (THA) aseptic loosening (AL) risk. This systematic review aimed to evaluate the implant survival and the AL rate in patients with elective THA receiving BPs compared to those that do not receive BPs. Secondary outcomes included the comparison of revision rate, postoperative complications, and patients' functional scores.
This systematic review was conducted under the PRISMA 2020 guidelines with a pre-registered PROSPERO protocol. Three engines and grey literature were searched up until May 2022. Randomized and nonrandomized controlled trials and comparative cohort studies assessing BP and control therapy impact on THA survival were included.
Twelve studies embraced the inclusion criteria. A total of 99 678 patients and 99 696 THAs were included; 10 025 patients received BPs (BP group), and 89 129 made up the control group. The overall revision and AL rates were lower in the BP group (2.17% and 1.85%) than in the control group (4.06% and 3.2%). Periprosthetic fracture (PPF) cases were higher in the BP group (0.24%) than in the control group (0.04%); however, the majority of PPF cases were derived from a single study. Further complication risk was similar between groups. Most studies reported comparable functional scores between groups.
BP treatment after elective THA seems to reduce the overall revision and AL risk. Other complications' risk and functional scores were similar between groups. Further high-quality studies are needed to validate the results due to the multifactorial AL pathogenesis.
双膦酸盐(BPs)的主要适应证是骨质疏松症治疗。然而,人们越来越关注在围手术期和术后使用双膦酸盐以降低全髋关节置换术(THA)无菌性松动(AL)的风险。本系统评价旨在评估接受双膦酸盐治疗的择期THA患者与未接受双膦酸盐治疗的患者相比,植入物的生存率和AL发生率。次要结局包括翻修率、术后并发症和患者功能评分的比较。
本系统评价按照PRISMA 2020指南进行,并采用预先注册的PROSPERO方案。检索了三个数据库和灰色文献,检索截止至2022年5月。纳入评估双膦酸盐和对照治疗对THA生存率影响的随机和非随机对照试验以及比较队列研究。
12项研究符合纳入标准。共纳入99678例患者和99696例THA;10025例患者接受双膦酸盐治疗(双膦酸盐组),89129例构成对照组。双膦酸盐组的总体翻修率和AL发生率(分别为2.17%和1.85%)低于对照组(分别为4.06%和3.2%)。双膦酸盐组的假体周围骨折(PPF)病例(0.24%)高于对照组(0.04%);然而,大多数PPF病例来自一项研究。两组之间的进一步并发症风险相似。大多数研究报告两组之间的功能评分相当。
择期THA术后使用双膦酸盐治疗似乎可降低总体翻修率和AL风险。两组之间其他并发症风险和功能评分相似。由于AL发病机制的多因素性,需要进一步的高质量研究来验证这些结果。