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2 期翻修全关节置换术患者再植入前诊断试验的效用:系统评价和荟萃分析。

Utility of Diagnostic Tests Before Reimplantation in Patients Undergoing 2-Stage Revision Total Joint Arthroplasty: A Systematic Review and Meta-analysis.

机构信息

Rothman Orthopaedic Institute at Thomas Jefferson University, Philadelphia, Pennsylvania.

Department of Orthopaedic Surgery, University of Alabama at Birmingham, Birmingham, Alabama.

出版信息

JBJS Rev. 2023 Mar 22;11(3). doi: e22.00201. eCollection 2023 Mar 1.

Abstract

INTRODUCTION

Periprosthetic joint infection (PJI) is a devastating complication after total joint arthroplasty (TJA), with treatment failure occurring in 12% to 28% after 2-stage revision. It is vital to identify diagnostic tools indicative of persistent infection or treatment failure after 2-stage revision for PJI.

METHODS

The Cochrane Library, PubMed (MEDLINE), and EMBASE were searched for randomized controlled trials and comparative observational studies published before October 3, 2021, which evaluated the utility of serum/plasma biomarkers (erythrocyte sedimentation rate [ESR], C-reactive protein [CRP], interleukin-6 [IL-6], fibrinogen, D-dimer), synovial biomarkers (white blood cell [WBC] count, neutrophil percentage [PMN %], alpha-defensin [AD], leukocyte esterase [LE]), tissue frozen section, tissue culture, synovial fluid culture, or sonicated spacer fluid culture indicative of persistent infection before the second stage of 2-stage revision for PJI or treatment failure after 2-stage revision for PJI.

RESULTS

A total of 47 studies including 6,605 diagnostic tests among 3,781 2-stage revisions for PJI were analyzed. Among those cases, 723 (19.1%) experienced persistent infection or treatment failure. Synovial LE (sensitivity 0.25 [0.10-0.47], specificity 0.99 [0.93-1.00], positive likelihood ratio 14.0 [1.45-135.58]) and serum IL-6 (sensitivity 0.52 [0.33-0.70], specificity 0.92 [0.85-0.96], positive likelihood ratio 7.90 [0.86-72.61]) had the highest diagnostic accuracy. However, no biomarker was associated with a clinically useful negative likelihood ratio. In subgroup analysis, synovial PMN %, synovial fluid culture, serum ESR, and serum CRP had limited utility for detecting persistent infection before reimplantation (positive likelihood ratios ranging 2.33-3.74; negative likelihood ratios ranging 0.31-0.9) and no utility for predicting failure after the second stage of 2-stage revision.

CONCLUSIONS

Synovial WBC count, synovial PMN %, synovial fluid culture, serum ESR, and serum CRP have modest sensitivity and specificity for predicting persistent infection during the second stage of 2-stage revision, suggesting some combination of these diagnostic tests might be useful before reimplantation. No biomarker or culture accurately predicted treatment failure after reimplantation.

LEVEL OF EVIDENCE

Level III. See Instructions for Authors for a complete description of levels of evidence.

摘要

简介

假体周围关节感染(PJI)是全关节置换术后的一种毁灭性并发症,2 期翻修后治疗失败的发生率为 12%至 28%。对于 2 期翻修后 PJI 持续感染或治疗失败,识别有诊断价值的工具至关重要。

方法

检索 Cochrane 图书馆、PubMed(MEDLINE)和 EMBASE,以获取 2021 年 10 月 3 日之前发表的评估血清/血浆生物标志物(红细胞沉降率 [ESR]、C 反应蛋白 [CRP]、白细胞介素-6 [IL-6]、纤维蛋白原、D-二聚体)、滑膜生物标志物(白细胞计数 [WBC]、中性粒细胞百分比 [PMN%]、α-防御素 [AD]、白细胞酯酶 [LE])、组织冷冻切片、组织培养、滑膜液培养或超声空化间隔液培养对 2 期翻修后 PJI 第 2 阶段前持续感染或治疗失败的诊断价值的随机对照试验和比较观察性研究。

结果

共分析了 47 项研究,涉及 3781 例 PJI 2 期翻修术的 6605 项诊断试验。其中 723 例(19.1%)发生持续感染或治疗失败。滑膜白细胞酯酶(敏感度 0.25 [0.10-0.47],特异度 0.99 [0.93-1.00],阳性似然比 14.0 [1.45-135.58])和血清白细胞介素-6(敏感度 0.52 [0.33-0.70],特异度 0.92 [0.85-0.96],阳性似然比 7.90 [0.86-72.61])具有最高的诊断准确性。然而,没有一种生物标志物与有临床意义的阴性似然比相关。在亚组分析中,滑膜中性粒细胞百分比、滑膜液培养、血清 ESR 和血清 CRP 对检测再植入前持续感染的能力有限(阳性似然比范围 2.33-3.74;阴性似然比范围 0.31-0.9),对预测 2 期翻修后失败无作用。

结论

滑膜白细胞计数、滑膜中性粒细胞百分比、滑膜液培养、血清 ESR 和血清 CRP 对预测 2 期翻修期间持续感染有一定的敏感度和特异度,提示这些诊断试验的某种组合可能在再植入前有用。没有生物标志物或培养物能准确预测再植入后的治疗失败。

证据水平

III 级。详见作者指南,了解证据水平的完整描述。

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