Behera B, Mathur P, Gupta B
Department of Microbiology, Jai Prakash Narayan Apex Trauma Centre, All India Institute of Medical Sciences, New Delhi - 110 029, India.
Indian J Med Microbiol. 2010 Apr-Jun;28(2):138-42. doi: 10.4103/0255-0857.62491.
The purpose of this study was to ascertain if the simple practice of Gram stain, acridine orange stain and direct sensitivity determination of positive blood culture bottles could be used to guide early and appropriate treatment in trauma patients with clinical suspicion of sepsis. The study also aimed to evaluate the error in interpreting antimicrobial sensitivity by direct method when compared to standard method and find out if specific antibiotic-organism combination had more discrepancies. Findings from consecutive episodes of blood stream infection at an Apex Trauma centre over a 12-month period are summarized.
A total of 509 consecutive positive blood cultures were subjected to Gram staining. AO staining was done in BacT/ALERT-positive Gram-stain negative blood cultures. Direct sensitivity was performed from 369 blood culture broths, showing single type of growth in Gram and acridine orange staining. Results of direct sensitivity were compared to conventional sensitivity for errors.
No 'very major' discrepancy was found in this study. About 5.2 and 1.8% minor error rates were noted in gram-positive and gram-negative bacteria, respectively, while comparing the two methods. Most of the discrepancies in gram-negative bacteria were noted in beta lactam - beta lactamase inhibitor combinations. Direct sensitivity testing was not reliable for reporting of methicillin and vancomycin resistance in Staphylococci.
Gram stain result together with direct sensitivity testing is required for optimizing initial antimicrobial therapy in trauma patients with clinical suspicion of sepsis. Gram staining and AO staining proved particularly helpful in the early detection of candidaemia.
本研究的目的是确定革兰氏染色、吖啶橙染色以及对阳性血培养瓶进行直接药敏测定这种简单做法是否可用于指导对临床怀疑有败血症的创伤患者进行早期且恰当的治疗。该研究还旨在评估与标准方法相比,直接法在解读抗菌药敏时的误差,并查明特定抗生素 - 病原体组合是否存在更多差异。总结了一家顶级创伤中心在12个月期间连续发生的血流感染事件的研究结果。
对总共509份连续的阳性血培养标本进行革兰氏染色。对BacT/ALERT阳性且革兰氏染色阴性的血培养标本进行吖啶橙染色。从369份在革兰氏和吖啶橙染色中显示单一类型生长的血培养肉汤中进行直接药敏测定。将直接药敏结果与传统药敏结果进行误差比较。
本研究未发现“非常重大”的差异。在比较两种方法时,革兰氏阳性菌和革兰氏阴性菌的轻微误差率分别约为5.2%和1.8%。革兰氏阴性菌的大多数差异见于β - 内酰胺 - β - 内酰胺酶抑制剂组合。直接药敏试验在报告葡萄球菌对甲氧西林和万古霉素的耐药性方面不可靠。
对于临床怀疑有败血症的创伤患者,优化初始抗菌治疗需要革兰氏染色结果以及直接药敏试验。革兰氏染色和吖啶橙染色在念珠菌血症的早期检测中被证明特别有用。