{"title":"MALDI-TOF质谱法早期鉴定阳性血培养瓶细菌分离株及儿科肿瘤患者早期药敏试验","authors":"M. Elanany, T. Mansour, R. Hassan, Hany Maher","doi":"10.59566/ijbs.2018.14026","DOIUrl":null,"url":null,"abstract":"Background: Final identification and susceptibility results of positive blood cultures would take 24 to 48 h by conventional methods. Every hour of early treatment, could be life-saving for septic immunocompromised patients. We conducted a pilot study to determine the earliest timing for performing identification and antimicrobial susceptibility testing of microorganisms isolated, after positive blood culture bottles with the most accurate results. Materials and Methods: Positive blood culture samples were inoculated onto two blood agar plates at 37°C. The growth on one plate was used every one hour repeatedly identification by MALDI-TOF MS (bioMérieux Vitek MS IVD system) and antimicrobial susceptibility testing Vitek 2 system. A total of 600 ID and MIC testing were done (13 Gram positive and 12 Gram negative). Results: Identification of all isolates showed 100% agreement between testing initial 3-hour growth and testing over-night growth. MIC showed 100% agreement when testing at mean hours of 5.6 (SD+/- 2.5) and 9 (SD +/- 2.5) for Gram negative and positive organisms respectively. The total time needed for accurate MIC results from start of positive BC sub-culturing was 16.1 h & 22 h for Gram negative and positive organisms respectively. Conclusion: Identification of causative pathogens using MALDI-TOF MS could be achieved accurately after 3h of sub-culturing. MIC testing can be performed after 5.6 h, 9 h incubation. Applying this methodology provided final accurate rapid results and early treatment of septic patients.","PeriodicalId":13852,"journal":{"name":"International Journal of Biomedical Science : IJBS","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2018-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Early Identification of Bacterial Isolates from Positive Blood Culture Bottles using MALDI-TOF MS and Early Antimicrobial Susceptibility Testing on Pediatric Oncology Patients\",\"authors\":\"M. Elanany, T. Mansour, R. Hassan, Hany Maher\",\"doi\":\"10.59566/ijbs.2018.14026\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Final identification and susceptibility results of positive blood cultures would take 24 to 48 h by conventional methods. Every hour of early treatment, could be life-saving for septic immunocompromised patients. We conducted a pilot study to determine the earliest timing for performing identification and antimicrobial susceptibility testing of microorganisms isolated, after positive blood culture bottles with the most accurate results. Materials and Methods: Positive blood culture samples were inoculated onto two blood agar plates at 37°C. The growth on one plate was used every one hour repeatedly identification by MALDI-TOF MS (bioMérieux Vitek MS IVD system) and antimicrobial susceptibility testing Vitek 2 system. A total of 600 ID and MIC testing were done (13 Gram positive and 12 Gram negative). Results: Identification of all isolates showed 100% agreement between testing initial 3-hour growth and testing over-night growth. MIC showed 100% agreement when testing at mean hours of 5.6 (SD+/- 2.5) and 9 (SD +/- 2.5) for Gram negative and positive organisms respectively. The total time needed for accurate MIC results from start of positive BC sub-culturing was 16.1 h & 22 h for Gram negative and positive organisms respectively. Conclusion: Identification of causative pathogens using MALDI-TOF MS could be achieved accurately after 3h of sub-culturing. MIC testing can be performed after 5.6 h, 9 h incubation. Applying this methodology provided final accurate rapid results and early treatment of septic patients.\",\"PeriodicalId\":13852,\"journal\":{\"name\":\"International Journal of Biomedical Science : IJBS\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-09-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Biomedical Science : IJBS\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.59566/ijbs.2018.14026\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Biomedical Science : IJBS","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.59566/ijbs.2018.14026","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
摘要
背景:常规方法对阳性血培养的最终鉴定和药敏结果需要24 ~ 48 h。每一个小时的早期治疗,都可能挽救脓毒性免疫功能低下患者的生命。我们进行了一项初步研究,以确定在血培养瓶阳性后对分离的微生物进行鉴定和抗菌药敏试验的最早时机,结果最准确。材料与方法:将阳性血培养标本接种于2块血琼脂板上,温度为37℃。每隔1 h用MALDI-TOF MS (biomrieux Vitek MS IVD系统)和Vitek 2系统对1个平板上的生长进行重复鉴定。共进行了600例ID和MIC检测(革兰氏阳性13例,革兰氏阴性12例)。结果:所有分离株的鉴定结果表明,初始3小时生长试验和过夜生长试验100%一致。在革兰氏阴性菌和阳性菌的平均检测时间分别为5.6 (SD+/- 2.5)和9 (SD+/- 2.5)时,MIC显示了100%的一致性。从阳性BC继代培养开始获得准确MIC结果所需的总时间为革兰氏阴性和阳性菌分别为16.1 h和22 h。结论:传代培养3h后,MALDI-TOF质谱法可准确鉴定病原菌。孵育5.6 h、9 h后即可进行MIC检测。应用这种方法提供了最终准确快速的结果和早期治疗脓毒症患者。
Early Identification of Bacterial Isolates from Positive Blood Culture Bottles using MALDI-TOF MS and Early Antimicrobial Susceptibility Testing on Pediatric Oncology Patients
Background: Final identification and susceptibility results of positive blood cultures would take 24 to 48 h by conventional methods. Every hour of early treatment, could be life-saving for septic immunocompromised patients. We conducted a pilot study to determine the earliest timing for performing identification and antimicrobial susceptibility testing of microorganisms isolated, after positive blood culture bottles with the most accurate results. Materials and Methods: Positive blood culture samples were inoculated onto two blood agar plates at 37°C. The growth on one plate was used every one hour repeatedly identification by MALDI-TOF MS (bioMérieux Vitek MS IVD system) and antimicrobial susceptibility testing Vitek 2 system. A total of 600 ID and MIC testing were done (13 Gram positive and 12 Gram negative). Results: Identification of all isolates showed 100% agreement between testing initial 3-hour growth and testing over-night growth. MIC showed 100% agreement when testing at mean hours of 5.6 (SD+/- 2.5) and 9 (SD +/- 2.5) for Gram negative and positive organisms respectively. The total time needed for accurate MIC results from start of positive BC sub-culturing was 16.1 h & 22 h for Gram negative and positive organisms respectively. Conclusion: Identification of causative pathogens using MALDI-TOF MS could be achieved accurately after 3h of sub-culturing. MIC testing can be performed after 5.6 h, 9 h incubation. Applying this methodology provided final accurate rapid results and early treatment of septic patients.