Evaluation of the Luminex xTAG Respiratory Viral Panel FAST v2 assay for detection of multiple respiratory viral pathogens in nasal and throat swabs in Vietnam

التفاصيل البيبلوغرافية
العنوان: Evaluation of the Luminex xTAG Respiratory Viral Panel FAST v2 assay for detection of multiple respiratory viral pathogens in nasal and throat swabs in Vietnam
المؤلفون: Tran Tinh Hien, Tran My Phuc, Pham Nhu Hiep, Nguyen Van Hung, Pham Thi Thanh Tam, H. Rogier van Doorn, Nguyen Thi Han Ny, Nguyen Anh Vu, Ho Dang Trung Nghia, Guy E. Thwaites, Vu Thi Ty Hang, Stephen Baker, Nguyen Van Dong, Le Van Tan, Nguyen Van Xang, Dang Thao Huong, Maia A. Rabaa, Pham Thi Hong Phuong
المصدر: Wellcome Open Research
بيانات النشر: F1000 Research Ltd, 2017.
سنة النشر: 2017
مصطلحات موضوعية: RVP FAST v2, 0301 basic medicine, medicine.drug_class, Antibiotics, 030106 microbiology, Medicine (miscellaneous), Methods for Diagnostic & Therapeutic Studies, Rapid detection, Virus, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, 0302 clinical medicine, Virology, Throat, Luminex, medicine, Multiplex, 030212 general & internal medicine, Respiratory system, Nose, biology, business.industry, Human bocavirus, Articles, biology.organism_classification, respiratory tract diseases, 3. Good health, medicine.anatomical_structure, Vietnam, business, Research Article
الوصف: Background: Acute respiratory infections (ARI) are among the leading causes of hospitalization in children ≤5 years old. Rapid diagnostics of viral pathogens is essential to avoid unnecessary antibiotic treatment, thereby slowing down antibiotic-resistance. We evaluated the diagnostic performance of the Luminex xTAG Respiratory Viral Panel FAST v2 against viral specific PCR as reference assays for ARI in Vietnam.Methods: Four hundred and forty two nose and throat swabs were collected in viral transport medium, and were tested with Luminex xTAG Respiratory Viral Panel FAST v2. Multiplex RT-PCR and single RT-PCR were used as references. Results: Overall, sensitivity of the Luminex against reference assays was 91.8%, 95% CI 88.1-94.7 (270/294), whilst 112/6336 (1.8%, 95% CI, 1.4-2.1) of pathogens were detected by the Luminex, but not by reference assays. Frequency of pathogens detected by Luminex and reference assays was 379 and 292, respectively. The diagnostic yield was 66.7% (295/442, 95%CI 62.1-71.1%) for the Luminex assay and 54.1% (239/442, 95% CI, 49.3-58.8%) for reference assays. The Luminex kit had higher yields for all viruses except influenza B virus, respiratory syncytial virus, and human bocavirus. High agreements between both methods [mean (range): 0.91 (0.83-1.00)] were found for 10/15 viral agents.Conclusions: The Luminex assay is a high throughput multiplex platform for rapid detection of common viral pathogens causing ARI. Although the current high cost may prevent Luminex assays from being widely used, especially in limited resource settings where ARI are felt most, its introduction in clinical diagnostics may help reduce unnecessary use of antibiotic prescription.
وصف الملف: application/pdf
تدمد: 2398-502X
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07fdbb194b97493bdea9700c1db4690dTest
https://doi.org/10.12688/wellcomeopenres.12429.1Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....07fdbb194b97493bdea9700c1db4690d
قاعدة البيانات: OpenAIRE