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DC Field | Value | Language |
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dc.contributor.author | Sheikh Ariful Hoque | en_US |
dc.contributor.author | Itoe Iizuka | en_US |
dc.contributor.author | Masaaki Kobayashi | en_US |
dc.contributor.author | Sayaka Takanashi | en_US |
dc.contributor.author | Kazi Selim Anwar | en_US |
dc.contributor.author | Mohammad Tajul Islam | en_US |
dc.contributor.author | Sk Azimul Hoque | en_US |
dc.contributor.author | Pattara Khamrin | en_US |
dc.contributor.author | Shoko Okitsu | en_US |
dc.contributor.author | Satoshi Hayakawa | en_US |
dc.contributor.author | Hiroshi Ushijima | en_US |
dc.date.accessioned | 2019-09-16T12:47:16Z | - |
dc.date.available | 2019-09-16T12:47:16Z | - |
dc.date.issued | 2019-09-16 | en_US |
dc.identifier.issn | 18732518 | en_US |
dc.identifier.issn | 0264410X | en_US |
dc.identifier.other | 2-s2.0-85071077344 | en_US |
dc.identifier.other | 10.1016/j.vaccine.2019.07.091 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85071077344&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/66579 | - |
dc.description.abstract | © 2019 Elsevier Ltd Introduction: Because of the large animal reservoirs and reassortment capacity of rotaviruses (RVs) that pose the possibilities of waning the effectiveness of RV-vaccines, it remains essential to monitor vaccine effectiveness (VE) regularly. Although reverse transcription polymerase chain reaction (RT-PCR) remains sensitive for RV detection, physicians, especially in Japan, frequently use immunochromatography (IC)-based kits for RV diagnosis. Recently, IC is being used to calculate VE also. Herein, we investigated the validity of VEs determined by IC compared to that by RT-PCR during an outbreak in Shizuoka Prefecture, Japan. Methods: RVs in the stool or rectal swabs from children with acute gastroenteritis (AGE) were tested first by IC in the clinic and then by RT-PCR in the laboratory. A test-negative study design was used to examine VE. Results: Although the specificity of IC assay revealed 100%, its sensitivity remained weaker (67%) than that of RT-PCR that increased up to 88% depending on disease severity. VE assessed by IC remained stronger than that by RT-PCR: 79% (95% CI: 39–93%) by IC, and 58% (95% CI: −20% to 90%) by RT-PCR. However, VEs by IC and RT-PCR appeared almost similar in higher disease severity: 81.5% (95% CI: 40–94%) by IC and 72% (95% CI: 7–92%) by RT-PCR at severity ≥7, while 97.5% (95% CI: 77–99.7%) by IC and 92% (95% CI: 58–98%) by RT-PCR at severity ≥11. We showed that RV-vaccinated children had 80% [OR = 0.192 (95% CI: 0.052–0.709) less chance to be detected by IC. Conclusion: Although the sensitivity and specificity of IC differ by brand type, generally, IC is not as sensitive as RT-PCR. Despite the VEs remain higher by IC, it looks comparable with that of RT-PCR in severe cases implying that VEs evaluated by IC against severe illness remain useful for VE-monitoring. | en_US |
dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Immunology and Microbiology | en_US |
dc.subject | Medicine | en_US |
dc.subject | Veterinary | en_US |
dc.title | Determining effectiveness of rotavirus vaccine by immunochromatography and reverse transcriptase polymerase chain reaction: A comparison | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Vaccine | en_US |
article.volume | 37 | en_US |
article.stream.affiliations | International University of Health and Welfare | en_US |
article.stream.affiliations | Save the Children Fund | en_US |
article.stream.affiliations | University of Tokyo | en_US |
article.stream.affiliations | University of Dhaka | en_US |
article.stream.affiliations | Nihon University School of Medicine | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
article.stream.affiliations | National Institute of Neurosciences and Hospital | en_US |
article.stream.affiliations | Kobayashi Pediatric Clinic | en_US |
Appears in Collections: | CMUL: Journal Articles |
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