Joshua R Porto, Monish S Lavu, Christian J Hecht, Atul F Kamath
{"title":"你的手术头盔系统是否危及无菌领域?全关节置换术中污染风险及预防措施的系统综述。","authors":"Joshua R Porto, Monish S Lavu, Christian J Hecht, Atul F Kamath","doi":"10.1097/CORR.0000000000003383","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Surgical helmet systems remain widely used in total joint arthroplasty (TJA) despite evidence to suggest that they may increase infection risk via contamination of sterile equipment and operating room air. However, the challenging nature of conducting high-quality clinical trials to study outcomes with low incidence, such as prosthetic joint infection (PJI), has made drawing definitive conclusions from the available experimental studies difficult. Therefore, a comprehensive analysis of the best available evidence is needed to clarify the association between surgical helmet system use and contamination and infection risk and to provide clinical recommendations for use in TJA.</p><p><strong>Questions/purposes: </strong>This systematic review aimed to address the following questions: (1) What is the level of sterility of surgical helmet systems and concomitantly used personal protective equipment (PPE)? (2) Is there an association between surgical helmet systems and air contamination within the operating room? (3) Does the use of a surgical helmet system affect wound contamination and/or infection?</p><p><strong>Methods: </strong>PubMed, Medline, EBSCOhost, and Google Scholar were queried on July 31, 2024, to identify studies published from inception to July 2024 that have evaluated the impact of surgical helmet system use in TJA on sterile field contamination (operating room air, PPE, sterile equipment), wound contamination and infection, or practices that may impact related outcomes. Inclusion criteria were that the study evaluate the sterility, donning, or intraoperative use (including mock TJA) of a surgical helmet system in association with contamination or infection. The following articles were excluded: case reports, case series, reviews, commentaries, editorials, duplicate studies among databases, gray literature, studies specific to a procedure other than TJA, and studies unavailable as a full-text English manuscript. After screening 536 articles, 21 were included. The 13 studies that evaluated the sterility of surgical helmet systems and concomitantly used PPE comprised 126 gowning simulations, 445 mock TJA procedures, and 191 patients who had undergone TJA. The seven studies that evaluated contamination of operating room air comprised 38 gowning simulations, 82 mock TJA procedures, and 96 patients who had undergone TJA. Three studies directly evaluated wound contamination or infection, comprising 83,888 patients who had undergone TJA. Risk of bias was determined via the Methodological Index for Nonrandomized Studies (MINORS) tool, with a mean ± SD score of 20 ± 1.4 (of 24) for comparative studies and 14 ± 0.8 (of 16) for noncomparative studies, indicating good study quality. Notably, the quality of evidence was limited by the inclusion of experimental study designs that did not directly measure infection; however, the inclusion of such studies is necessitated by the infeasibly large study population required to directly evaluate the association between surgical helmet systems and infection prospectively. Heterogeneity among studies precluded meta-analysis, and a qualitative synthesis was instead conducted.</p><p><strong>Results: </strong>The best available evidence suggests that surgical helmet systems frequently harbor microbes known to be common causes of SSI and PJI, and that their improper donning and use (for example, activation of the exhaust fan before fully gowned) can lead to the contamination of gowns and sterile gloves worn by surgical personnel. Furthermore, several studies suggest that the exhaust from surgical helmet systems presents a potential source of operating room air contamination, although there were mixed findings based on the location of air sampling and whether or not a toga was used and the gown-glove interface was sealed (both of which were shown to mitigate airborne contaminants). However, whether there is a direct association between surgical helmet system use and wound infection remains understudied and unclear, with one retrospective comparative analysis demonstrating no difference in odds of infection when comparing surgical helmet systems used to a standard gown during TJA, and another reporting reduced odds of revision for deep infection with a 12-month follow-up time when a surgical helmet system was used (adjusted OR 0.55).</p><p><strong>Conclusion: </strong>Although the best available evidence suggests that the use of surgical helmet systems in TJA can increase the likelihood of sterile field contamination, including sterile surgical attire and equipment, as well as operating room air, that finding derives largely from experimental studies with effect sizes (based on endpoints like colony counts) that are difficult or impossible to convert to real-world infection risk. Robust investigations into the association between surgical helmet systems and infection are limited by the need for infeasibly large study populations to conduct sufficiently powered clinical trials, with no evidence found by this review to directly implicate surgical helmet systems in increased infection risk. Still, because the risk for contamination has been shown to be driven substantially by donning technique and the type of gown used, we recommend waiting to activate the surgical helmet system fan until fully gowned, taping the gown cuff at the inner glove, utilizing a toga system set up, and implementing sterilization protocols for reusable helmets.</p><p><strong>Clinical relevance: </strong>When used appropriately, there is insufficient high-quality evidence to suggest that surgical helmet systems pose meaningful harm to patient safety. However, the persistent lack of evidence to demonstrate their effectiveness in achieving the initial purpose of reducing infection warrants careful evaluation of their utility in TJA. Ample consideration must be given to their role as personal protection systems for surgical personnel, as studies have demonstrated superior protection from surgical debris and splatter compared with conventional surgical attire. While the added cost of surgical helmet systems may therefore be justified, surgeons wishing to continue utilizing surgical helmet systems in their practice should do so while taking proper precautionary measures to mitigate contamination risks.</p>","PeriodicalId":10404,"journal":{"name":"Clinical Orthopaedics and Related Research®","volume":" ","pages":"972-990"},"PeriodicalIF":4.2000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12106205/pdf/","citationCount":"0","resultStr":"{\"title\":\"Is Your Surgical Helmet System Compromising the Sterile Field? 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Therefore, a comprehensive analysis of the best available evidence is needed to clarify the association between surgical helmet system use and contamination and infection risk and to provide clinical recommendations for use in TJA.</p><p><strong>Questions/purposes: </strong>This systematic review aimed to address the following questions: (1) What is the level of sterility of surgical helmet systems and concomitantly used personal protective equipment (PPE)? (2) Is there an association between surgical helmet systems and air contamination within the operating room? (3) Does the use of a surgical helmet system affect wound contamination and/or infection?</p><p><strong>Methods: </strong>PubMed, Medline, EBSCOhost, and Google Scholar were queried on July 31, 2024, to identify studies published from inception to July 2024 that have evaluated the impact of surgical helmet system use in TJA on sterile field contamination (operating room air, PPE, sterile equipment), wound contamination and infection, or practices that may impact related outcomes. Inclusion criteria were that the study evaluate the sterility, donning, or intraoperative use (including mock TJA) of a surgical helmet system in association with contamination or infection. The following articles were excluded: case reports, case series, reviews, commentaries, editorials, duplicate studies among databases, gray literature, studies specific to a procedure other than TJA, and studies unavailable as a full-text English manuscript. After screening 536 articles, 21 were included. The 13 studies that evaluated the sterility of surgical helmet systems and concomitantly used PPE comprised 126 gowning simulations, 445 mock TJA procedures, and 191 patients who had undergone TJA. The seven studies that evaluated contamination of operating room air comprised 38 gowning simulations, 82 mock TJA procedures, and 96 patients who had undergone TJA. Three studies directly evaluated wound contamination or infection, comprising 83,888 patients who had undergone TJA. Risk of bias was determined via the Methodological Index for Nonrandomized Studies (MINORS) tool, with a mean ± SD score of 20 ± 1.4 (of 24) for comparative studies and 14 ± 0.8 (of 16) for noncomparative studies, indicating good study quality. Notably, the quality of evidence was limited by the inclusion of experimental study designs that did not directly measure infection; however, the inclusion of such studies is necessitated by the infeasibly large study population required to directly evaluate the association between surgical helmet systems and infection prospectively. Heterogeneity among studies precluded meta-analysis, and a qualitative synthesis was instead conducted.</p><p><strong>Results: </strong>The best available evidence suggests that surgical helmet systems frequently harbor microbes known to be common causes of SSI and PJI, and that their improper donning and use (for example, activation of the exhaust fan before fully gowned) can lead to the contamination of gowns and sterile gloves worn by surgical personnel. Furthermore, several studies suggest that the exhaust from surgical helmet systems presents a potential source of operating room air contamination, although there were mixed findings based on the location of air sampling and whether or not a toga was used and the gown-glove interface was sealed (both of which were shown to mitigate airborne contaminants). However, whether there is a direct association between surgical helmet system use and wound infection remains understudied and unclear, with one retrospective comparative analysis demonstrating no difference in odds of infection when comparing surgical helmet systems used to a standard gown during TJA, and another reporting reduced odds of revision for deep infection with a 12-month follow-up time when a surgical helmet system was used (adjusted OR 0.55).</p><p><strong>Conclusion: </strong>Although the best available evidence suggests that the use of surgical helmet systems in TJA can increase the likelihood of sterile field contamination, including sterile surgical attire and equipment, as well as operating room air, that finding derives largely from experimental studies with effect sizes (based on endpoints like colony counts) that are difficult or impossible to convert to real-world infection risk. Robust investigations into the association between surgical helmet systems and infection are limited by the need for infeasibly large study populations to conduct sufficiently powered clinical trials, with no evidence found by this review to directly implicate surgical helmet systems in increased infection risk. Still, because the risk for contamination has been shown to be driven substantially by donning technique and the type of gown used, we recommend waiting to activate the surgical helmet system fan until fully gowned, taping the gown cuff at the inner glove, utilizing a toga system set up, and implementing sterilization protocols for reusable helmets.</p><p><strong>Clinical relevance: </strong>When used appropriately, there is insufficient high-quality evidence to suggest that surgical helmet systems pose meaningful harm to patient safety. 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引用次数: 0
摘要
背景:手术头盔系统仍然广泛应用于全关节置换术(TJA),尽管有证据表明它们可能通过无菌设备和手术室空气的污染增加感染风险。然而,开展高质量的临床试验来研究低发病率的结果(如假体关节感染(PJI))具有挑战性,这使得从现有的实验研究中得出明确的结论变得困难。因此,需要对现有的最佳证据进行全面分析,以明确手术头盔系统的使用与污染和感染风险之间的关系,并为TJA的使用提供临床建议。问题/目的:本系统综述旨在解决以下问题:(1)手术头盔系统和伴随使用的个人防护装备(PPE)的无菌水平是什么?(2)手术头盔系统与手术室空气污染之间是否存在关联?(3)手术头盔系统的使用是否会影响伤口污染和/或感染?方法:于2024年7月31日查询PubMed、Medline、EBSCOhost和谷歌Scholar,以确定从成立到2024年7月发表的评估TJA手术头盔系统使用对无菌现场污染(手术室空气、PPE、无菌设备)、伤口污染和感染或可能影响相关结果的实践影响的研究。纳入标准是研究评估与污染或感染相关的手术头盔系统的无菌性、佩戴或术中使用(包括模拟TJA)。以下文章被排除:病例报告、病例系列、综述、评论、社论、数据库中的重复研究、灰色文献、TJA以外的特定研究以及无法作为全文英文手稿的研究。经536篇文献筛选,纳入21篇。13项研究评估了手术头盔系统和伴随使用的PPE的无菌性,其中包括126例长袍模拟,445例模拟TJA手术,以及191例接受过TJA的患者。评估手术室空气污染的七项研究包括38例长袍模拟,82例模拟TJA手术,以及96例接受过TJA的患者。三项研究直接评估了伤口污染或感染,包括83,888例接受TJA的患者。偏倚风险通过非随机研究方法学指数(Methodological Index for Nonrandomized Studies,未成年人)工具确定,比较研究的平均±SD评分为20±1.4(24项),非比较研究的平均±SD评分为14±0.8(16项),表明研究质量较好。值得注意的是,证据的质量受到没有直接测量感染的实验研究设计的限制;然而,纳入这些研究是必要的,因为需要大量的研究人群来直接评估手术头盔系统与感染之间的关系。研究间的异质性妨碍了meta分析,因此进行了定性综合。结果:现有的最佳证据表明,手术头盔系统经常含有已知的导致SSI和PJI的常见原因的微生物,并且其不当穿戴和使用(例如,在完全穿上工作服之前激活排气扇)可能导致手术人员所穿的工作服和无菌手套受到污染。此外,几项研究表明,手术头盔系统排出的废气是手术室空气污染的潜在来源,尽管基于空气采样的位置以及是否使用长袍和长袍-手套界面密封(两者都被证明可以减轻空气中的污染物),结果好坏参半。然而,手术头盔系统的使用与伤口感染之间是否存在直接关联仍未得到充分研究和明确,一项回顾性比较分析显示,在TJA期间,使用手术头盔系统与标准长袍相比,感染的几率没有差异,另一项报告显示,在12个月的随访时间内,使用手术头盔系统后,深度感染的翻修几率降低(调整OR 0.55)。结论:尽管现有的最佳证据表明,在TJA中使用手术头盔系统会增加无菌现场污染的可能性,包括无菌手术服装和设备,以及手术室空气,但这一发现主要来自实验研究,其效应大小(基于菌落计数等终点)难以或不可能转化为现实世界的感染风险。 手术头盔系统与感染之间的关联的有力调查受到限制,因为需要不可行的大规模研究人群来进行足够有力的临床试验,本综述没有发现任何证据直接表明手术头盔系统与感染风险增加有关。尽管如此,由于污染的风险已经被证明是由穿着技术和使用的长袍类型驱动的,我们建议等到完全穿好长袍后再启动手术头盔系统风扇,在内手套处绑好长袍袖口,利用长袍系统设置,并实施可重复使用的头盔消毒方案。临床相关性:如果使用得当,没有足够的高质量证据表明手术头盔系统对患者安全构成有意义的危害。然而,一直缺乏证据证明它们在实现减少感染的初始目的方面的有效性,因此需要仔细评估它们在TJA中的效用。必须充分考虑其作为手术人员个人保护系统的作用,因为研究表明,与传统的手术服装相比,它们具有更好的手术碎片和飞溅保护作用。虽然手术头盔系统的额外成本可能因此是合理的,但希望在实践中继续使用手术头盔系统的外科医生应该在采取适当的预防措施以减轻污染风险的同时这样做。
Is Your Surgical Helmet System Compromising the Sterile Field? A Systematic Review of Contamination Risks and Preventive Measures in Total Joint Arthroplasty.
Background: Surgical helmet systems remain widely used in total joint arthroplasty (TJA) despite evidence to suggest that they may increase infection risk via contamination of sterile equipment and operating room air. However, the challenging nature of conducting high-quality clinical trials to study outcomes with low incidence, such as prosthetic joint infection (PJI), has made drawing definitive conclusions from the available experimental studies difficult. Therefore, a comprehensive analysis of the best available evidence is needed to clarify the association between surgical helmet system use and contamination and infection risk and to provide clinical recommendations for use in TJA.
Questions/purposes: This systematic review aimed to address the following questions: (1) What is the level of sterility of surgical helmet systems and concomitantly used personal protective equipment (PPE)? (2) Is there an association between surgical helmet systems and air contamination within the operating room? (3) Does the use of a surgical helmet system affect wound contamination and/or infection?
Methods: PubMed, Medline, EBSCOhost, and Google Scholar were queried on July 31, 2024, to identify studies published from inception to July 2024 that have evaluated the impact of surgical helmet system use in TJA on sterile field contamination (operating room air, PPE, sterile equipment), wound contamination and infection, or practices that may impact related outcomes. Inclusion criteria were that the study evaluate the sterility, donning, or intraoperative use (including mock TJA) of a surgical helmet system in association with contamination or infection. The following articles were excluded: case reports, case series, reviews, commentaries, editorials, duplicate studies among databases, gray literature, studies specific to a procedure other than TJA, and studies unavailable as a full-text English manuscript. After screening 536 articles, 21 were included. The 13 studies that evaluated the sterility of surgical helmet systems and concomitantly used PPE comprised 126 gowning simulations, 445 mock TJA procedures, and 191 patients who had undergone TJA. The seven studies that evaluated contamination of operating room air comprised 38 gowning simulations, 82 mock TJA procedures, and 96 patients who had undergone TJA. Three studies directly evaluated wound contamination or infection, comprising 83,888 patients who had undergone TJA. Risk of bias was determined via the Methodological Index for Nonrandomized Studies (MINORS) tool, with a mean ± SD score of 20 ± 1.4 (of 24) for comparative studies and 14 ± 0.8 (of 16) for noncomparative studies, indicating good study quality. Notably, the quality of evidence was limited by the inclusion of experimental study designs that did not directly measure infection; however, the inclusion of such studies is necessitated by the infeasibly large study population required to directly evaluate the association between surgical helmet systems and infection prospectively. Heterogeneity among studies precluded meta-analysis, and a qualitative synthesis was instead conducted.
Results: The best available evidence suggests that surgical helmet systems frequently harbor microbes known to be common causes of SSI and PJI, and that their improper donning and use (for example, activation of the exhaust fan before fully gowned) can lead to the contamination of gowns and sterile gloves worn by surgical personnel. Furthermore, several studies suggest that the exhaust from surgical helmet systems presents a potential source of operating room air contamination, although there were mixed findings based on the location of air sampling and whether or not a toga was used and the gown-glove interface was sealed (both of which were shown to mitigate airborne contaminants). However, whether there is a direct association between surgical helmet system use and wound infection remains understudied and unclear, with one retrospective comparative analysis demonstrating no difference in odds of infection when comparing surgical helmet systems used to a standard gown during TJA, and another reporting reduced odds of revision for deep infection with a 12-month follow-up time when a surgical helmet system was used (adjusted OR 0.55).
Conclusion: Although the best available evidence suggests that the use of surgical helmet systems in TJA can increase the likelihood of sterile field contamination, including sterile surgical attire and equipment, as well as operating room air, that finding derives largely from experimental studies with effect sizes (based on endpoints like colony counts) that are difficult or impossible to convert to real-world infection risk. Robust investigations into the association between surgical helmet systems and infection are limited by the need for infeasibly large study populations to conduct sufficiently powered clinical trials, with no evidence found by this review to directly implicate surgical helmet systems in increased infection risk. Still, because the risk for contamination has been shown to be driven substantially by donning technique and the type of gown used, we recommend waiting to activate the surgical helmet system fan until fully gowned, taping the gown cuff at the inner glove, utilizing a toga system set up, and implementing sterilization protocols for reusable helmets.
Clinical relevance: When used appropriately, there is insufficient high-quality evidence to suggest that surgical helmet systems pose meaningful harm to patient safety. However, the persistent lack of evidence to demonstrate their effectiveness in achieving the initial purpose of reducing infection warrants careful evaluation of their utility in TJA. Ample consideration must be given to their role as personal protection systems for surgical personnel, as studies have demonstrated superior protection from surgical debris and splatter compared with conventional surgical attire. While the added cost of surgical helmet systems may therefore be justified, surgeons wishing to continue utilizing surgical helmet systems in their practice should do so while taking proper precautionary measures to mitigate contamination risks.
期刊介绍:
Clinical Orthopaedics and Related Research® is a leading peer-reviewed journal devoted to the dissemination of new and important orthopaedic knowledge.
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