Rothenberg Adam C, Wilson Alan E, Hayes John P, O'Malley Michael J, Klatt Brian A
Department of Orthopaedic Surgery, University of Pittsburgh, 3471 5th Avenue, Suite 1010, Pittsburgh, PA, 15213, USA.
Clin Orthop Relat Res. 2017 Jul;475(7):1827-1836. doi: 10.1007/s11999-017-5315-8.
There is evidence that sonication of explanted prosthetic hip and knee arthroplasty components with culture of the sonication fluid may enhance diagnostic sensitivity. Previous studies on the use of implant sonicate cultures have evaluated diagnostic thresholds but did not elaborate on the clinical importance of positive implant sonicate cultures in the setting of presumed aseptic revisions and did not utilize consensus statements on periprosthetic joint infection (PJI) diagnosis when defining their gold standard for infection.
QUESTIONS/PURPOSES: (1) How do implant sonicate cultures compare with preoperative synovial fluid cultures and intraoperative tissue cultures in the diagnosis of PJI in both THA and TKA when compared against Musculoskeletal Infection Society (MSIS) criteria for PJI? (2) Utilizing implant sonicate cultures, what is the relative prevalence of bacterial species identified in PJIs? (3) What is the incidence of positive implant sonicate cultures in the setting of presumed aseptic revision hip and knee arthroplasty procedures, and what treatments did they receive?
Between 2012 and 2016 we performed implant sonicate fluid cultures on surgically removed implants from 565 revision THAs and TKAs. Exclusion criteria including insufficient data to determine Musculoskeletal Infection Society (MSIS) classification, fungal-only cultures, and absence of reported colony-forming units decreased the number of procedures to 503. Procedures represented each instance of revision surgery (sometimes multiple in the same patient). Of those, a definitive diagnosis of infection was made using the MSIS criteria in 178 of 503 (35%), whereas the others (325 of 503 [65%]) were diagnosed as without infection. A total of 53 of 325 (16%) were considered without infection based on MSIS criteria but had a positive implant sonicate culture. Twenty-five of 53 (47%) of these patients were followed for at least 2 years. The diagnosis of PJI was determined using the MSIS criteria.
Sensitivity of implant sonicate culture was greater than synovial fluid culture and tissue culture (97% [89%-99%] versus 57% [44%-69%], p < 0.001; 97% [89%-99%] versus 70% [58%-80%], p < 0.001, respectively). The specificity of implant sonicate culture was not different from synovial fluid culture or tissue culture with the numbers available (90% [72%-97%] versus 100% [86%-100%], p = 0.833; 90% [72%-97%] versus 97% [81%-100%], p = 0.317, respectively). Coagulase-negative Staphylococcus was the most prevalent organism for both procedure types. In PJIs, the five most frequent bacteria identified by synovial fluid, tissue, and/or implant sonicate cultures were coagulase-negative Staphylococcus (26% [89 of 267]), methicillin-susceptible Staphylococcus aureus (19% [65 of 267]), methicillin-resistant S. aureus (12% [43 of 267]), α-hemolytic Streptococci (5% [19 of 267]), and Enterococcus faecalis (5% [19 of 267]). Fifty-three of 325 (16%) presumed aseptic revisions had a positive sonication culture. Thirty-four percent (18 of 53) of culture-positive aseptic revision patients received antibiotic treatment for infection and 8% (4 of 53) underwent a secondary revision.
The routine use of implant sonicate cultures in arthroplasty revisions improves the diagnostic sensitivity for detecting the presence of bacteria in both clinical and occult infections. Future studies will need to refine colony-forming unit thresholds for determining clinical infection and indications for treatment.
Level III, diagnostic study.
有证据表明,对外植的人工髋关节和膝关节置换部件进行超声处理并培养超声处理后的液体,可能会提高诊断敏感性。以往关于使用植入物超声培养物的研究评估了诊断阈值,但未详细阐述在假定为无菌翻修的情况下,植入物超声培养阳性在临床中的重要性,并且在确定其感染金标准时未采用关于假体周围关节感染(PJI)诊断的共识声明。
问题/目的:(1)与肌肉骨骼感染学会(MSIS)的PJI标准相比,在全髋关节置换术(THA)和全膝关节置换术(TKA)中,植入物超声培养物与术前滑液培养物和术中组织培养物在PJI诊断方面相比如何?(2)利用植入物超声培养物,PJI中鉴定出的细菌种类的相对患病率是多少?(3)在假定为无菌的髋关节和膝关节置换翻修手术中,植入物超声培养阳性的发生率是多少,以及他们接受了哪些治疗?
2012年至2016年期间,我们对565例翻修THA和TKA手术中手术取出的植入物进行了植入物超声液体培养。排除标准包括数据不足以确定肌肉骨骼感染学会(MSIS)分类、仅真菌培养以及未报告菌落形成单位,这使得手术数量减少至503例。手术代表了每次翻修手术实例(同一患者有时进行多次)。其中,根据MSIS标准,503例中有178例(35%)被明确诊断为感染,而其他患者(503例中的325例[65%])被诊断为无感染。325例中共有53例(16%)根据MSIS标准被认为无感染,但植入物超声培养呈阳性。这些患者中有25例(47%)至少随访了2年。PJI的诊断采用MSIS标准确定。
植入物超声培养的敏感性高于滑液培养和组织培养(分别为97%[89%-99%]对57%[44%-69%],p<0.001;97%[89%-99%]对70%[58%-80%],p<0.001)。根据现有数据,植入物超声培养的特异性与滑液培养或组织培养无差异(分别为90%[72%-97%]对100%[86%-100%],p = 0.833;90%[72%-97%]对97%[81%-100%],p = 0.317)。凝固酶阴性葡萄球菌是两种手术类型中最常见的病原体。在PJI中,通过滑液、组织和/或植入物超声培养鉴定出的五种最常见细菌为凝固酶阴性葡萄球菌(26%[267例中的89例])、甲氧西林敏感金黄色葡萄球菌(19%[267例中的65例])、甲氧西林耐药金黄色葡萄球菌(12%[267例中的43例])、α溶血性链球菌(5%[267例中的19例])和粪肠球菌(5%[267例中的19例])。325例假定为无菌翻修中有53例(16%)超声培养呈阳性。培养阳性的无菌翻修患者中有34%(53例中的18例)接受了抗感染抗生素治疗,8%(53例中的4例)接受了二次翻修。
在关节置换翻修术中常规使用植入物超声培养可提高检测临床和隐匿性感染中细菌存在的诊断敏感性。未来的研究需要完善用于确定临床感染和治疗指征的菌落形成单位阈值。
III级,诊断性研究。