抗菌机制和制备抗生素浸渍水泥涂层锁定板治疗感染性骨不连。

IF 1 Q3 ORTHOPEDICS
Robert Kaspar Wagner, Clara Guarch-Pérez, Alje P van Dam, Sebastian Aj Zaat, Peter Kloen
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引用次数: 0

摘要

背景:在感染性骨不连的两阶段治疗中,抗生素浸渍水泥涂层板(ACPs)已成功用于分期之间的临时内固定。我们描述了我们使用ACP分期治疗甲氧西林耐药金黄色葡萄球菌(MRSA)感染的全髋关节假体下股骨远端不愈合的方法。此外,我们还介绍了一项体外实验的结果,以深入了解ACP在(i)处理残留生物膜和(ii)防止细菌再定植方面的能力。材料和方法:在第一阶段,我们使用涂有手动混合PALACOS和万古霉素(PAL-V)的LISS钛板进行临时内固定,并结合商业制备的庆大霉素和万古霉素(COP-GV)的COPAL来填充节段缺损。在第二阶段,采用双钢板固定和骨移植治疗不愈合。进行Kirby-Bauer琼脂盘扩散测定以测定ACP的抗微生物活性,并进行药物释放测定以测量抗生素随时间的释放。还进行了生物膜杀死测定,以确定释放的抗生素是否能够减少或根除患者MRSA菌株的生物膜。结果:在一年的随访中,在之前的不愈合中出现了完全的骨桥接。病人没有疼痛,可以走动,无需进一步手术。具有COP-GV和PAL-V的ACP都对MRSA菌株产生了抗微生物作用,抗生素的峰值浓度在最初的24小时内释放。体外前24小时从COP-GV释放的浓度导致生物膜中的集落形成单位(CFU)减少7.7倍对数。在第50天,COP-GV和PAL-V仍释放出高于各自最低抑制浓度(MIC)的抗生素浓度,这可能有助于积极的临床结果。结论:在感染不愈合的临床情况下,ACP的使用提供了稳定性和感染控制。这在体外得到了证实,其中ACP释放抗生素的特征是早期爆发,然后在MIC以上持续释放延长至50天。COP-GV的突然释放降低了生物膜中的CFU,并通过释放的万古霉素和庆大霉素的协同活性防止了早期的再定植。临床意义:抗生素浸渍水泥涂层接骨板是外科医生器械的一个有用补充,可以在没有外固定缺点的情况下提供临时内固定,并有助于控制感染非大学的感染。如何引用这篇文章:Wagner RK,Guardh-Pérez C,van Dam AP等人。抗菌机制和制备抗生素浸渍水泥涂层锁定板治疗感染性骨不连。2023年创伤肢体康复策略;18(2):73-81。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Antimicrobial Mechanisms and Preparation of Antibiotic-impregnated Cement-coated Locking Plates in the Treatment of Infected Non-unions.

Antimicrobial Mechanisms and Preparation of Antibiotic-impregnated Cement-coated Locking Plates in the Treatment of Infected Non-unions.

Antimicrobial Mechanisms and Preparation of Antibiotic-impregnated Cement-coated Locking Plates in the Treatment of Infected Non-unions.

Antimicrobial Mechanisms and Preparation of Antibiotic-impregnated Cement-coated Locking Plates in the Treatment of Infected Non-unions.

Background: Antibiotic-impregnated cement-coated plates (ACPs) have been used successfully for temporary internal fixation between stages in the two-stage treatment of infected non-unions. We describe our approach of using an ACP in the staged treatment of a methicillin-resistant Staphylococcus aureus (MRSA)-infected distal femoral non-union below a total hip prosthesis. In addition, we present the results of an in vitro experiment to provide an in-depth insight into the capacity of ACPs in (i) treating residual biofilm and (ii) preventing bacterial recolonisation.

Materials and methods: In the first stage, we used a titanium LISS plate coated with hand-mixed PALACOS with vancomycin (PAL-V) for temporary internal fixation combined with commercially prepared COPAL with gentamicin and vancomycin (COP-GV) to fill the segmental defect. In the second stage, the non-union was treated with double-plate fixation and bone grafting.A Kirby-Bauer agar disc diffusion assay was performed to determine the antimicrobial activity of both ACPs and a drug-release assay to measure antibiotic release over time. A biofilm killing assay was also carried out to determine if the antibiotic released was able to reduce or eradicate biofilm of the patient's MRSA strain.

Results: At one-year follow-up, there was complete bone-bridging across the previous non-union. The patient was pain-free and ambulatory without need for further surgery. Both ACPs with COP-GV and PAL-V exerted an antimicrobial effect against the MRSA strain with peak concentrations of antibiotic released within the first 24 hours. Concentrations released from COP-GV in the first 24 hours in vitro caused a 7.7-fold log reduction of colony-forming units (CFU) in the biofilm. At day 50, both COP-GV and PAL-V still released concentrations of antibiotic above the respective minimal inhibitory concentrations (MIC), likely contributing to the positive clinical outcome.

Conclusion: The use of an ACP provides stability and infection control in the clinical scenario of an infected non-union. This is confirmed in vitro where the release of antibiotics from ACPs is characterised by an early burst followed by a prolonged sustained release above the MIC until 50 days. The burst release from COP-GV reduces CFU in the biofilm and prevents early recolonisation through synergistic activity of the released vancomycin and gentamicin.

Clinical significance: An antibiotic-impregnated cement-coated plate is a useful addition to the surgeon's armamentarium to provide temporary internal fixation without the disadvantages of external fixation and contribute to infection control in an infected non-union.

How to cite this article: Wagner RK, Guarch-Pérez C, van Dam AP, et al. Antimicrobial Mechanisms and Preparation of Antibiotic-impregnated Cement-coated Locking Plates in the Treatment of Infected Non-unions. Strategies Trauma Limb Reconstr 2023;18(2):73-81.

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来源期刊
Strategies in Trauma and Limb Reconstruction
Strategies in Trauma and Limb Reconstruction Medicine-Orthopedics and Sports Medicine
CiteScore
1.50
自引率
0.00%
发文量
31
期刊介绍: Strategies in Trauma and Limb Reconstruction is dedicated to surgeons, allied medical professionals and researchers in the field of orthopaedics and trauma. The scope of the journal is to discuss the fields of skeletal injury, and the complications thereof, congenital and acquired limb deformities and deficiencies, and orthopaedic-related infection, together with their surgical and non-surgical treatments. The journal publishes original articles, reviews, case reports, descriptions of new or recognised treatment techniques, forum discussions of clinical scenarios and relevant correspondence. It aims to provide a widely accessible source of useful information to practitioners in the field through the problem- or technique-based approach of published articles.
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