da Cruz Vinícius Furtado, Machinski Elcio, da Silva Oliveira Filho André Richard, Conde Rodrigo Arruda, Varone Bruno Butturi, Gobbi Riccardo Gomes, Helito Camilo Partezani, Leal Daniel Peixoto
Pontifícia Universidade Católica do Paraná, Londrina, Brazil.
Universidade Estadual de Ponta Grossa (UEPG), Ponta Grossa, Brazil.
J Orthop. 2025 Jan 4;66:25-33. doi: 10.1016/j.jor.2024.12.025. eCollection 2025 Aug.
This study aimed to evaluate the effectiveness and safety of intra-articular vancomycin powder in reducing prosthetic joint infections (PJIs) in primary hip and knee arthroplasty through a meta-analysis of randomized controlled trials (RCTs).
A research in Pubmed, Embase and Cochrane databases was performed to identify randomized clinical trials comparing intra-articular vancomycin use to conventional antibiotic prophylaxis in total hip or knee arthroplasty patients, assessing postoperative infection rates, adverse drug reactions, and venous thrombotic events. Statistical analysis was performed using R (RStudio 2024.04.2), and heterogeneity was assessed with the I test.
A total of 1485 patients from five randomized clinical trials were included, with 737 receiving intra-articular vancomycin. The infection rate was 0.54 % in the intervention group and 1.73 % in the control group (RR 0.37; 95 % CI 0.02-8.95; p = 0.369; I = 49 %), showing no statistically significant difference between the groups. Adverse reactions to the glycopeptide were reported in six cases (0.8 %) in the intervention group compared to four cases (0.5 %) in the control group (RR 1.50; 95 % CI 1.50-150; p = 0.001; I = 0 %). Regarding thrombotic events, there was one case in 647 patients in the intervention group and three cases in 660 patients in the control group (RR 0.45; 95 % CI 0.03-7.02; p = 0.169; I = 0 %).
Although no significant difference was found, the intervention group showed a trend toward lower infection rates. Additional RCTs with larger sample sizes are required to confirm these findings
The prospective registration of the meta-analysis was conducted on PROSPERO in July 2024 with the protocol number 565988.
本研究旨在通过对随机对照试验(RCT)的荟萃分析,评估关节腔内注射万古霉素粉末在降低初次髋膝关节置换术中假体关节感染(PJI)方面的有效性和安全性。
在PubMed、Embase和Cochrane数据库中进行检索,以确定比较关节腔内使用万古霉素与全髋或全膝关节置换术患者常规抗生素预防的随机临床试验,评估术后感染率、药物不良反应和静脉血栓形成事件。使用R(RStudio 2024.04.2)进行统计分析,并用I²检验评估异质性。
共纳入五项随机临床试验的1485例患者,其中737例接受关节腔内注射万古霉素。干预组感染率为0.54%,对照组为1.73%(风险比[RR] 0.37;95%置信区间[CI] 0.02 - 8.95;p = 0.369;I² = 49%),两组间无统计学显著差异。干预组有6例(0.8%)报告了对糖肽类药物的不良反应,对照组有4例(0.5%)(RR 1.50;95% CI 1.50 - 150;p = 0.001;I² = 0%)。关于血栓形成事件,干预组647例患者中有1例,对照组660例患者中有3例(RR 0.45;95% CI 0.03 - 7.02;p = 0.169;I² = 0%)。
尽管未发现显著差异,但干预组显示出感染率较低的趋势。需要更多样本量更大的随机对照试验来证实这些发现。
该荟萃分析于2024年7月在PROSPERO上进行前瞻性注册,方案编号为565988。