Department of Orthopaedics, Joint Replacement & Reconstruction, University at Buffalo, SUNY, Buffalo, NY.
Department of Infectious Diseases, Hospital for Special Surgery, New York, NY.
J Arthroplasty. 2021 Jul;36(7S):S4-S10. doi: 10.1016/j.arth.2021.01.073. Epub 2021 Feb 2.
The concordance between preoperative synovial fluid culture and multiple intraoperative tissue cultures for identifying pathogenic microorganisms in periprosthetic joint infection (PJI) remains unknown. Our aim is to determine the diagnostic performance of synovial fluid culture for early organism identification.
A total of 363 patients who met Musculoskeletal Infection Society criteria for PJI following primary total joint arthroplasty were identified from a retrospective joint infection database. Inclusion criteria required a positive preoperative intra-articular synovial fluid sample within 90 days of intraoperative tissue culture(s) at revision surgery. Concordance was defined as matching organism(s) in aspirate and intraoperative specimens.
Concordance was identified in 279 (76.8%) patients with similar rates among total hip arthroplasties (77.2%) and total knee arthroplasties (76.4%, P = .86). Culture discordance occurred in 84 (23.1%) patients; 37 (10.2%) had no intraoperative culture growth and 33 (90.1%) were polymicrobial. Monomicrobial Staphylococcal PJI cases had high sensitivity (0.96, 95% confidence interval [CI] 0.92-0.98) and specificity (0.85, 95% CI 0.80-0.90). Polymicrobial infections had the lowest sensitivity (0.06, 95% CI 0.01-0.19).
Aspiration culture has favorable sensitivity and specificity when compared to tissue culture for identifying the majority of PJI organisms. Clinicians can guide surgical treatment and postoperative antibiotics based on monomicrobial aspiration results, but they should strongly consider collecting multiple tissue cultures to maximize the chance of identifying an underlying polymicrobial PJI.
Level III.
术前滑液培养与多次术中组织培养在识别假体周围关节感染(PJI)中的致病微生物的一致性尚不清楚。我们的目的是确定滑液培养在早期鉴定病原体方面的诊断性能。
从回顾性关节感染数据库中确定了 363 名符合 Musculoskeletal Infection Society 标准的原发性全关节置换术后 PJI 患者。纳入标准要求在翻修手术时的术中组织培养(s)之前 90 天内进行阳性术前关节内滑液样本。一致性定义为抽吸液和术中标本中匹配的生物体(s)。
在 279 名(76.8%)患者中发现了一致性,全髋关节置换术和全膝关节置换术的发生率相似(77.2%和 76.4%,P=0.86)。84 名(23.1%)患者存在培养不相符;37 名(10.2%)术中无培养生长,33 名(90.1%)为混合感染。单一微生物葡萄球菌 PJI 病例具有较高的敏感性(0.96,95%置信区间 [CI] 0.92-0.98)和特异性(0.85,95% CI 0.80-0.90)。混合感染的敏感性最低(0.06,95%CI 0.01-0.19)。
与组织培养相比,抽吸培养在识别大多数 PJI 病原体方面具有良好的敏感性和特异性。临床医生可以根据单一微生物抽吸结果指导手术治疗和术后抗生素治疗,但他们应强烈考虑收集多个组织培养物,以最大程度地识别潜在的混合性 PJI。
III 级。