A pilot, masked, randomized controlled trial to evaluate local gentamicin versus saline in open tibial fractures (pGO-Tibia).

Billy T Haonga, Patrick Ngunyale, Ericka P von Kaeppler, Claire A Donnelley, Nae Y Won, Edmund N Eliezer, Kelsey Brown, Michael Flores, Jamieson M O'Marr, Patricia Rodarte, Mayur Urva, Abigail Cortez, Travis Porco, Saam Morshed, David W Shearer
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Abstract

Background: Open tibial fractures have a high risk of infection that can lead to severe morbidity. Antibiotics administered locally at the site of the open wound are a potentially effective preventive measure, but there are limited data evaluating aminoglycoside antibiotics. The objective of this study was to assess the feasibility of a clinical trial to test the efficacy of local gentamicin in reducing the risk of fracture-related infection after open tibial fracture.

Methods: This study is a single-center, pilot, masked, randomized controlled trial conducted at the Muhimbili Orthopaedic Institute. Participants were randomized intraoperatively after wound closure to receive gentamicin solution or normal saline solution injected at the fracture site. Follow-ups were completed at 2 weeks, 6 weeks, 3 months, 6 months, 9 months, and 1 year postoperatively. The primary feasibility outcomes were the rate of enrollment and retention. The primary clinical outcome was the occurrence of fracture-related infection.

Results: Of 199 patients screened, 100 eligible patients were successfully enrolled and randomized over 9 months (11.1 patients/month). Complete data were recorded at baseline and follow-up for >95% of cases. The rate of follow-up at 6 weeks, 3 months, 6 months, 9 months, and 1 year were 70%, 68%, 69%, 61%, and 80%, respectively. There was no difference in adverse events or any of the measured primary and secondary outcomes.

Conclusion: This pilot study is among the first to evaluate locally administered gentamicin in open tibial fractures. Results indicate a rigorous clinical trial with acceptable rates of enrollment and follow-up to address this topic is possible in this setting.

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一项蒙面随机对照试验,评估开放性胫骨骨折中局部庆大霉素与生理盐水的对比(pGO-胫骨)。
背景:胫骨开放性骨折的感染风险很高,可导致严重的发病率。在开放性伤口局部使用抗生素是一种潜在有效的预防措施,但评估氨基糖苷类抗生素的数据有限。本研究的目的是评估临床试验的可行性,以测试局部使用庆大霉素对降低开放性胫骨骨折后骨折相关感染风险的疗效:本研究是在穆汉比利骨科研究所进行的一项单中心、试验性、蒙面随机对照试验。参与者在术中伤口闭合后随机接受庆大霉素溶液或生理盐水溶液注射。随访时间分别为术后 2 周、6 周、3 个月、6 个月、9 个月和 1 年。主要的可行性结果是入选率和保留率。主要临床结果是骨折相关感染的发生率:结果:在筛选出的 199 名患者中,有 100 名符合条件的患者在 9 个月内成功入组并接受随机治疗(11.1 人/月)。95%以上的病例在基线和随访时记录了完整的数据。6周、3个月、6个月、9个月和1年的随访率分别为70%、68%、69%、61%和80%。不良事件或任何主要和次要测量结果均无差异:这项试点研究是首批对开放性胫骨骨折局部注射庆大霉素进行评估的研究之一。研究结果表明,在这种情况下,可以通过严格的临床试验,以可接受的入组率和随访率来解决这一问题。
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