Do Antibiotic-Impregnated Envelopes Prevent Deep Brain Stimulation Implantable Pulse Generator Infections? A Prospective Cohort Study.

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Accounts of Chemical Research Pub Date : 2024-01-01 Epub Date: 2024-03-08 DOI:10.1159/000536478
Michael Colditz, Tomas Heard, Peter Silburn, Terry Coyne
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引用次数: 0

Abstract

Introduction: Infection after deep brain stimulation (DBS) implanted pulse generator (IPG) replacement is uncommon but when it occurs can cause significant clinical morbidity, often resulting in partial or complete DBS system removal. An antibiotic absorbable envelope developed for cardiac implantable electronic devices (IEDs), which releases minocycline and rifampicin for a minimum of 7 days, was shown in the WRAP-IT study to reduce cardiac IED infections for high-risk cardiac patients. We aimed to assess whether placing an IPG in the same antibiotic envelope at the time of IPG replacement reduced the IPG infection rate.

Methods: Following institutional ethics approval (UnitingCare HREC), patients scheduled for IPG change due to impending battery depletion were prospectively randomised to receive IPG replacement with or without an antibiotic envelope. Patients with a past history of DBS system infection were excluded. Patients underwent surgery with standard aseptic neurosurgical technique [J Neurol Sci. 2017;383:135-41]. Subsequent infection requiring antibiotic therapy and/or IPG removal or revision was recorded.

Results: A total of 427 consecutive patients were randomised from 2018 to 2021 and followed for a minimum of 12 months. No patients were lost to follow-up. At the time of IPG replacement, 200 patients received antibiotic envelope (54 female, 146 male, mean age 72 years), and 227 did not (43 female, 184 male, mean age 71 years). The two groups were homogenous for risk factors of infection. The IPG replacement infection rate was 2.1% (9/427). There were six infections, which required antibiotic therapy and/or IPG removal, in the antibiotic envelope group (6/200) and three in the non-envelope group (3/227) (p = 0.66).

Conclusion: This prospective randomised study did not find that an antibiotic envelope reduced the IPG infection rate in our 427 patients undergoing routine DBS IPG replacement. Further research to reduce IPG revisions and infections in a cost-effective manner is required.

抗生素浸渍包膜能预防脑深部刺激植入式脉冲发生器感染吗?一项前瞻性队列研究。
导言:更换脑深部刺激(DBS)植入式脉冲发生器(IPG)后发生感染的情况并不常见,但一旦发生感染,就会造成严重的临床并发症,通常会导致部分或全部拆除 DBS 系统。WRAP-IT 研究显示,为心脏植入式电子设备(IED)开发的抗生素可吸收包膜可释放米诺环素和利福平至少 7 天,可减少高危心脏病患者的心脏 IED 感染。我们的目的是评估在更换 IPG 时将 IPG 放在相同的抗生素包膜中是否会降低 IPG 感染率:在获得机构伦理批准后(UnitingCare HREC),因电池即将耗尽而计划更换 IPG 的患者被前瞻性地随机分配到带或不带抗生素包膜的 IPG 更换中。既往有 DBS 系统感染病史的患者被排除在外。患者采用标准无菌神经外科技术进行手术[J Neurol Sci.]结果:从2018年到2021年,共有427名连续患者接受了随机治疗,并随访了至少12个月。没有患者失去随访机会。在更换 IPG 时,200 名患者接受了抗生素治疗(54 名女性,146 名男性,平均年龄 72 岁),227 名患者没有接受抗生素治疗(43 名女性,184 名男性,平均年龄 71 岁)。两组患者的感染风险因素相同。IPG 置换感染率为 2.1%(9/427)。抗生素包膜组(6/200)和非包膜组(3/227)分别发生了六例需要抗生素治疗和/或取出 IPG 的感染(P = 0.66):这项前瞻性随机研究并未发现抗生素包膜能降低427例行DBS IPG置换术患者的IPG感染率。需要进一步研究如何以具有成本效益的方式减少 IPG 改造和感染。
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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