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Diagnosis of venous access port colonization requires cultures from multiple sites: Should guidelines be amended?

机译:静脉通路端口定植的诊断需要多个部位的培养:是否应修订指南?

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Data on microbiological management of withdrawn venous access ports (VAPs) are scarce. The aim of our study was to assess the validity of Gram stain and culture performed on VAPs to detect colonization and VAP-related bloodstream infection (VAP-RBSI). We prospectively performed cultures of the following: catheter tip (roll-plate and sonication), port content aspirate before and after sonication, port sonication fluid (PSF), and port internal surface biofilm (ISB). The gold standard of VAP colonization was positivity of at least 1 of the cultures mentioned above. We collected 223 VAPs in which no single culture had validity values reliable enough to predict colonization and VAP-RBSI. The best validity values were those obtained when cultures of catheter tip (roll-plate), PSF, and port ISB were combined. Cultures from several areas on the VAP are necessary to ensure suitable assessment of colonization and VAP-RBSI.
机译:撤回静脉通道(VAP)的微生物管理数据很少。我们研究的目的是评估革兰氏染色和在VAP上进行培养以检测定植和VAP相关血流感染(VAP-RBSI)的有效性。我们前瞻性地进行了以下培养:导管尖端(滚动板和超声处理),超声处理前后的端口内容物抽吸,端口超声处理液(PSF)和端口内部表面生物膜(ISB)。 VAP定殖的金标准是上述至少一种培养物的阳性。我们收集了223个VAP,其中没有单一培养物具有足够可靠的有效性值来预测定植和VAP-RBSI。最佳效度值是将导管尖端(滚动板),PSF和端口ISB的培养物合并使用时获得的值。 VAP多个区域的培养对于确保正确评估定植和VAP-RBSI是必要的。

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