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万古霉素粉末在脊柱手术中的使用选择压力:一项荟萃分析。

Selection pressures of vancomycin powder use in spine surgery: a meta-analysis.

机构信息

Department of Orthopedic Surgery, University of California, 101 S. City Drive, Irvine, Orange, CA, 92868, USA.

School of Medicine, University of California, 1001 Health Sciences Rd, Irvine, CA, 92697, USA.

出版信息

Spine J. 2019 Jun;19(6):1076-1084. doi: 10.1016/j.spinee.2019.01.002. Epub 2019 Jan 17.

Abstract

BACKGROUND CONTEXT

Surgical site infection (SSI) is a serious and costly complication of spine surgery. Many surgeons apply vancomycin powder to the surgical wound to prevent SSIs. While multiple studies have reported reduced rates of SSI, others have suggested that widespread use of intrawound vancomycin may increase the incidence of vancomycin-resistant, gram-negative, or polymicrobial spinal infections.

PURPOSE

To systematically review the current literature on vancomycin powder in spine surgery and its impact on SSI culture profiles.

STUDY DESIGN

Meta-analysis.

SAMPLE

We included observational studies, retrospective chart reviews, and randomized controlled trials of patients who underwent spine surgeries with and without vancomycin powder application to surgical wounds and reported SSI rates.

OUTCOME MEASURES

The primary outcome was postoperative SSIs. Subgroup analyses compared rates of postoperative SSIs.

METHODS

We performed a comprehensive search of numerous electronic databases and conference proceedings pertaining to this topic. Our meta-analysis was conducted according to Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines. Inclusion criteria consisted of spine surgeries with or without use of vancomycin powder, case-control design, sample sizes of at least 10 in each arm, SSIs identified with bacterial cultures, and follow-up of at least 1 month. Data extracted from eligible studies included, but was not limited to, SSI rates, cultured organisms, and vancomycin powder dose. Chi-square analyses were used to assess pooled risk-estimates of intrawound vancomycin powder on reducing SSIs and selecting for gram-negative and/or polymicrobial organisms compared to controls. Pooled odds ratios, relative risks, and relative risk increase for observed outcomes were calculated. A meta-analysis was then performed with a forest plot to determine risk estimates' heterogeneity with I index, Q-statistic, and p value under a fixed-effects model. Funnel plot was used to assess publication bias. None of the authors received funding or other support for this review.

RESULTS

After reviewing nearly 400 titles and abstracts, 28 articles met inclusion criteria. They included two randomized controlled trials, one observational study, and 25 retrospective analyses. There were 412 cases of SSI (3.8%) in the control group (N=10,846) compared to 197 SSIs (2.3%) in the vancomycin powder group (N=8,456). The pooled odds ratio was 0.60 (95% confidence intervalCI 0.51-0.71, p<.05). The rate of gram-positive SSI was significantly higher in the control group compared to the vancomycin group (70% vs. 45.1%, p<.05). The rate of gram-negative and polymicrobial SSI was significantly higher in the vancomycin group (35.8% vs. 18.5%, p<.05). The risk of developing a gram-negative or polymicrobial SSI was nearly twice (93.5% higher) in the vancomycin group. Study heterogeneity and synthesizing mostly retrospective data were primary limitations.

CONCLUSIONS

Widespread use of prophylactic intrawound vancomycin may increase the incidence of gram-negative and polymicrobial SSIs. Vancomycin powder should likely be restricted to procedures and patients most at risk for infection.

摘要

背景信息

手术部位感染(SSI)是脊柱手术的一种严重且代价高昂的并发症。许多外科医生会在手术伤口上涂抹万古霉素粉末以预防 SSI。虽然多项研究报告 SSI 发生率降低,但其他研究表明,广泛使用局部万古霉素可能会增加耐万古霉素的革兰氏阴性菌或混合微生物脊柱感染的发生率。

目的

系统回顾关于脊柱手术中万古霉素粉末的现有文献及其对 SSI 培养谱的影响。

研究设计

荟萃分析。

样本

我们纳入了观察性研究、回顾性图表审查和随机对照试验,这些研究的对象是接受了有或没有在手术伤口中应用万古霉素粉末的脊柱手术,并报告了 SSI 发生率。

主要结局指标

术后 SSI。亚组分析比较了术后 SSI 的发生率。

方法

我们对大量与该主题相关的电子数据库和会议记录进行了全面搜索。我们的荟萃分析根据系统评价和荟萃分析的首选报告项目进行。纳入标准包括有或没有使用万古霉素粉末的脊柱手术、病例对照设计、每组至少 10 例的样本量、通过细菌培养鉴定的 SSI,以及至少 1 个月的随访。从合格研究中提取的数据包括但不限于 SSI 发生率、培养的生物体和万古霉素粉末剂量。卡方分析用于评估与对照组相比,局部使用万古霉素粉末是否可以降低 SSI 发生率并选择革兰氏阴性菌和/或混合微生物。计算了观察结局的汇总优势比、相对风险和相对风险增加。然后进行了荟萃分析,并使用森林图确定 I 指数、Q 统计量和 p 值下固定效应模型的风险估计值的异质性。漏斗图用于评估发表偏倚。本综述的作者均未因这项研究而获得任何资金或其他支持。

结果

在回顾了近 400 篇标题和摘要后,有 28 篇文章符合纳入标准。其中包括两项随机对照试验、一项观察性研究和 25 项回顾性分析。在对照组(N=10846)中,有 412 例 SSI(3.8%),而在万古霉素粉末组(N=8456)中,有 197 例 SSI(2.3%)。汇总优势比为 0.60(95%置信区间 0.51-0.71,p<.05)。对照组的革兰氏阳性 SSI 发生率明显高于万古霉素组(70%比 45.1%,p<.05)。革兰氏阴性菌和混合微生物 SSI 的发生率在万古霉素组明显更高(35.8%比 18.5%,p<.05)。革兰氏阴性菌或混合微生物 SSI 的风险增加了近两倍(高 93.5%)。研究异质性和主要使用回顾性数据是主要的局限性。

结论

广泛使用预防性局部万古霉素可能会增加革兰氏阴性菌和混合微生物 SSI 的发生率。万古霉素粉末可能应仅限于感染风险最高的手术和患者。

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