Haytham Ahmed Mahrous, Tahia Ahmed Mohamed, Abeer Elhawary, Ahmed Mohammed, Elsayed S. Abd elbaser
{"title":"埃及患者中的嗜肺军团菌感染:最新诊断测试和评估","authors":"Haytham Ahmed Mahrous, Tahia Ahmed Mohamed, Abeer Elhawary, Ahmed Mohammed, Elsayed S. Abd elbaser","doi":"10.21608/aeji.2024.234274.1318","DOIUrl":null,"url":null,"abstract":"and q Real Time (RT) PCR for detection of L. pneumophila mip gene. Results: Prevalence of L. pneumophila in Zagazig university hospitals was 17% detected by L. pneumophila urinary antigen testing (LPUAT), 15% of samples were positive by q RT PCR based mip gene and 12 % positive by respiratory sample cultures. In comparison to respiratory sample culture, the gold standard, q RT PCR evaluation showed sensitivity 83.3%, specificity 94.3%, positive predictive value 66.7%, Negative predictive value 97.6% and accuracy of 93.0%. Conclusion: Molecular assays and UAT are promising methods that can be used in the rapid and early diagnosis of Legionella infections but they seem not to be sufficient to replace microbial cultures which must associate these techniques.","PeriodicalId":261891,"journal":{"name":"Afro-Egyptian Journal of Infectious and Endemic Diseases","volume":"8 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Legionella Pneumophila Infections among Egyptian Patients: Updated Diagnostic Tests and Evaluation\",\"authors\":\"Haytham Ahmed Mahrous, Tahia Ahmed Mohamed, Abeer Elhawary, Ahmed Mohammed, Elsayed S. Abd elbaser\",\"doi\":\"10.21608/aeji.2024.234274.1318\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"and q Real Time (RT) PCR for detection of L. pneumophila mip gene. Results: Prevalence of L. pneumophila in Zagazig university hospitals was 17% detected by L. pneumophila urinary antigen testing (LPUAT), 15% of samples were positive by q RT PCR based mip gene and 12 % positive by respiratory sample cultures. In comparison to respiratory sample culture, the gold standard, q RT PCR evaluation showed sensitivity 83.3%, specificity 94.3%, positive predictive value 66.7%, Negative predictive value 97.6% and accuracy of 93.0%. Conclusion: Molecular assays and UAT are promising methods that can be used in the rapid and early diagnosis of Legionella infections but they seem not to be sufficient to replace microbial cultures which must associate these techniques.\",\"PeriodicalId\":261891,\"journal\":{\"name\":\"Afro-Egyptian Journal of Infectious and Endemic Diseases\",\"volume\":\"8 3\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Afro-Egyptian Journal of Infectious and Endemic Diseases\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21608/aeji.2024.234274.1318\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Afro-Egyptian Journal of Infectious and Endemic Diseases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21608/aeji.2024.234274.1318","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Legionella Pneumophila Infections among Egyptian Patients: Updated Diagnostic Tests and Evaluation
and q Real Time (RT) PCR for detection of L. pneumophila mip gene. Results: Prevalence of L. pneumophila in Zagazig university hospitals was 17% detected by L. pneumophila urinary antigen testing (LPUAT), 15% of samples were positive by q RT PCR based mip gene and 12 % positive by respiratory sample cultures. In comparison to respiratory sample culture, the gold standard, q RT PCR evaluation showed sensitivity 83.3%, specificity 94.3%, positive predictive value 66.7%, Negative predictive value 97.6% and accuracy of 93.0%. Conclusion: Molecular assays and UAT are promising methods that can be used in the rapid and early diagnosis of Legionella infections but they seem not to be sufficient to replace microbial cultures which must associate these techniques.