Departamento de Medicina Tropical - Universidade Federal de Pernambuco - UFPE, Recife, Brazil.
Departamento de Microbiologia - Instituto Aggeu Magalhães - Fiocruz, Recife, Brazil.
Front Cell Infect Microbiol. 2024 May 13;14:1398461. doi: 10.3389/fcimb.2024.1398461. eCollection 2024.
Addressing the existing problem in the microbiological diagnosis of infections associated with implants and the current debate about the real power of precision of sonicated fluid culture (SFC), the objective of this review is to describe the methodology and analyze and compare the results obtained in current studies on the subject. Furthermore, the present study also discusses and suggests the best parameters for performing sonication. A search was carried out for recent studies in the literature (2019-2023) that addressed this research topic. As a result, different sonication protocols were adopted in the studies analyzed, as expected, and consequently, there was significant variability between the results obtained regarding the sensitivity and specificity of the technique in relation to the traditional culture method (periprosthetic tissue culture - PTC). Coagulase-negative (CoNS) and were identified as the main etiological agents by SFC and PTC, with SFC being important for the identification of pathogens of low virulence that are difficult to detect. Compared to chemical biofilm displacement methods, EDTA and DTT, SFC also produced variable results. In this context, this review provided an overview of the most current scenarios on the topic and theoretical support to improve sonication performance, especially with regard to sensitivity and specificity, by scoring the best parameters from various aspects, including sample collection, storage conditions, cultivation methods, microorganism identification techniques (both phenotypic and molecular) and the cutoff point for colony forming unit (CFU) counts. This study demonstrated the need for standardization of the technique and provided a theoretical basis for a sonication protocol that aims to achieve the highest levels of sensitivity and specificity for the reliable microbiological diagnosis of infections associated with implants and prosthetic devices, such as prosthetic joint infections (PJIs). However, practical application and additional complementary studies are still needed.
针对与植入物相关感染的微生物学诊断中存在的问题以及目前关于超声液培养(SFC)精准度实际能力的争议,本综述旨在描述该方法,并分析和比较当前研究中获得的结果。此外,本研究还讨论并提出了执行超声处理的最佳参数。在文献中对最近的研究进行了检索(2019-2023 年),以解决这一研究课题。结果显示,分析的研究中采用了不同的超声处理方案,这是意料之中的,因此,与传统培养方法(假体周围组织培养-PTC)相比,技术的敏感性和特异性的结果存在显著差异。凝固酶阴性葡萄球菌(CoNS)和革兰氏阳性球菌被 SFC 和 PTC 鉴定为主要的病原体,SFC 对于鉴定低毒力且难以检测的病原体非常重要。与化学生物膜置换方法 EDTA 和 DTT 相比,SFC 也产生了不同的结果。在这种情况下,本综述提供了该主题的最新情况概述,并从包括样本采集、储存条件、培养方法、微生物鉴定技术(表型和分子)以及菌落形成单位(CFU)计数的截止值等各个方面提供了理论支持,以改善超声处理的性能,特别是在敏感性和特异性方面。本研究证明了标准化技术的必要性,并为超声处理协议提供了理论基础,该协议旨在实现对与植入物和假体相关感染的可靠微生物学诊断的最高敏感性和特异性,例如人工关节感染(PJIs)。然而,仍需要实际应用和更多的补充研究。