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Prospective study on the diagnostics and susceptibility testing of infections associated with osseointegrated percutaneous implants

机译:对骨整向性经皮植入物相关的诊断和易感性试验的前瞻性研究

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Introduction: Biomaterial-associated infections (BAI) are among the main reasons for implant failure, often leading to long-term antimicrobial treatment and implant removal. BAI are mainly caused by biofilm producing bacteria with increased antimicrobial resistance. Proper and rapid diagnosis is important for successful treatment. Sonication is an alternative method for the diagnosis of prosthetic infections with higher sensitivity than standard tissue cultures. The aims of the study were to: ⅰ) identify and quantify bacteria causing osteomyelitis associated with osseointegrated percutaneous amputation prostheses by sonication of explanted implants; ⅱ) characterise the isolated strains by their biofilm production abilities and antimicrobial susceptibility. In parallel, the diagnostic laboratory at the hospital performed standard culturing techniques of bone tissue and blood marrow samples. Materials and Methods: A bone-anchored part (fixture) of a prosthesis was extracted due to suspicion of infection according to clinical evaluation. The retrieved fixture was placed in sterile saline, sonicated at 47 KHz for 5 min and vortexed for 1 min. The implant was removed, the remaining solution was centrifuged, pellet was re-suspended in saline and quantitative cultures were made on general purpose agar (blood agar for aerobic and brucella agar for anaerobic cultures) and selective agar plates (staphylococci agar, enterococci agar, streptococci agar, chromogenic orientation agar and pseudomonas agar). Crystal violet (CV) staining and Congo Red (CR) agar plate test was performed to evaluate the biofilm production. Identification of the staphylococcal strains was performed using API Staph. The Calgary Biofilm Device and a custom-made antimicrobial susceptibility plate were used to determine minimum biofilm eradication concentrations (MBEC) and minimum inhibitory concentrations (MIC) to 10 antimicrobial agents. Results and Discussion: We report the first results of an ongoing prospective study where the method has been tested real-time. In the first patient, Enterococcus faecalis (5×10~4 CFU/implant) and Escherichia coli (10~2 CFU/implant) were detected after sonication. These strains were both biofilm-producing strains according to CV and CR tests. Biofilms showed increased tolerance to the antimicrobials compared with the standard planktonic MIC values (Table 1). Escherichia coli was the only species detected by standard tissue cultures; in contrast, by the use of sonication, Enterococcus faecalis was further identified indicating the possibility of a polymicrobial infection with potential implications for the choice of the optimal treatment strategy for the patient. Conclusions: An increased detection of the potential causative agents by sonication of retrieved implants may improve the current diagnostics of BAI. In addition, determination of MBEC for clinically relevant antimicrobial agents has the potential to optimize the treatment choices for patients.
机译:介绍:生物材料相关的感染(BAI)是植入损伤的主要原因,通常导致长期抗微生物处理和植入物去除。 Bai主要由生物膜产生细菌,具有增加的抗微生物抗性。适当和快速的诊断对于成功治疗是重要的。超声处理是诊断比标准组织培养更高敏感性的假体感染的替代方法。该研究的目的是:Ⅰ)通过超声处理植入物鉴定和量化导致骨髓炎与骨细胞炎相关的骨髓炎的假体; Ⅱ)通过生物膜生产能力和抗微生物易感性表征分离菌株。同时,医院的诊断实验室表现了骨组织和血骨样品的标准培养技术。材料和方法:根据临床评价,由于感染感染而提取假体的骨锚定部分(夹具)。将所检索的夹具置于无菌盐水中,在47kHz处超声处理5分钟并涡旋1分钟。除去植入物,离心剩余的溶液,将沉淀重新悬浮在盐水中,在通用琼脂(用于有氧和Brucella琼脂的血糖和厌氧培养物中的血琼脂)和选择性琼脂平板(肠球菌琼脂,)中进行定量培养物(肠球菌琼脂,链球菌琼脂,发色取向琼脂和假单胞菌琼脂)。进行晶体紫(CV)染色和刚果红色(CR)琼脂板试验进行评估生物膜生产。使用API​​ Staph进行葡萄球菌菌株的鉴定。 Calgary Biofilm器件和定制的抗微生物敏感板用于确定最小生物膜根除浓度(MBEC)和最小抑制浓度(MIC)至10次抗菌剂。结果与讨论:我们报告了该方法实时测试的持续前瞻性研究的第一个结果。在第一个患者中,在超声处理后检测到肠球菌粪便(5×10〜4 CFU /植入物)和大肠杆菌(10〜2 CFU /植入物)。这些菌株根据CV和Cr试验是生物膜产生的菌株。与标准浮游麦克风值相比,生物膜显示对抗微生物的耐受性增加(表1)。大肠杆菌是标准组织培养物唯一检测到的物种;相反,通过使用超声处理,进一步鉴定了肠球菌粪便,表明具有对患者最佳治疗策略的潜在影响的多发性感染的可能性。结论:通过超声处理检索植入物的潜在致病剂的检测增加可以改善白皮书的当前诊断。此外,用于临床相关抗微生物剂的MBEC的测定有可能优化患者的治疗选择。

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