<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Sohn YJ</submitter><pubmed_abstract>OBJECTIVES:In Korea, the National Immunization Program provided trivalent inactivated influenza vaccines (IIV3) to all children aged 6 - 59 months during the 2017-2018 season. In this study, we aimed to evaluate the vaccine effectiveness (VE) of IIV3 in children during the 2017-2018 season. METHODS:Children aged 6 -59 months who were tested for influenza for their acute respiratory illness were included in four hospitals during the 2017-2018 influenza season. We estimated the VE of IIV3 by test-negative case-control design based on the rapid influenza diagnostic test (RIDT) or reverse transcription polymerase chain reaction (RT-PCR) test results. RESULTS:A total of 4,738 children were included in this study. The number of laboratory-confirmed influenza cases was 845 (17.8%), and there were 478 cases of influenza A, 362 cases of influenza B. The adjusted VE based on RT-PCR was 53.4% (95% CI, 25.3-70.5) against any influenza, 68.8% (95% CI, 38.7-84.1) against influenza A, and 29.7% (95% CI, -35.1-61.8) for influenza B. The adjusted VE based on RIDT was 14.8% (95% CI, -4.4-30.0) against any influenza, 24.2% (95% CI, 3.1-40.2) against influenza A, and -5.1% (95% CI, -42.6-21.4) against influenza B. Age-specific VE based on RT-PCR against any influenza was 44.1% (95% CI, -0.2-67.8) in children aged 6 months to 2 years and 59.3% (95% CI, 8.8-81.9) in children aged 3 to 5 years. CONCLUSION:Our results suggest moderate protection (53.4%) of IIV3 against RT-PCR laboratory-confirmed influenza in children in the 2017-2018 influenza season. However, the RIDT hampered the validity to assess VE during influenza season. Caution is needed when interpreting RIDT-based test negative design influenza VE study.</pubmed_abstract><journal>International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7381399</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Effectiveness of Trivalent Inactivated Influenza Vaccines in Children during 2017-2018 Season in Korea: Comparison of Test-Negative Analysis by Rapid and RT-PCR Influenza Tests.</pubmed_title><pmcid>PMC7381399</pmcid><pubmed_authors>Choi EH</pubmed_authors><pubmed_authors>Choe YJ</pubmed_authors><pubmed_authors>Sohn YJ</pubmed_authors><pubmed_authors>Choi YY</pubmed_authors><pubmed_authors>Park JY</pubmed_authors><pubmed_authors>Kim YK</pubmed_authors><pubmed_authors>Han MS</pubmed_authors><pubmed_authors>Kim K</pubmed_authors><pubmed_authors>Lee JK</pubmed_authors><pubmed_authors>Choi JH</pubmed_authors><pubmed_authors>Song SH</pubmed_authors><pubmed_authors>Ahn B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effectiveness of Trivalent Inactivated Influenza Vaccines in Children during 2017-2018 Season in Korea: Comparison of Test-Negative Analysis by Rapid and RT-PCR Influenza Tests.</name><description>OBJECTIVES:In Korea, the National Immunization Program provided trivalent inactivated influenza vaccines (IIV3) to all children aged 6 - 59 months during the 2017-2018 season. In this study, we aimed to evaluate the vaccine effectiveness (VE) of IIV3 in children during the 2017-2018 season. METHODS:Children aged 6 -59 months who were tested for influenza for their acute respiratory illness were included in four hospitals during the 2017-2018 influenza season. We estimated the VE of IIV3 by test-negative case-control design based on the rapid influenza diagnostic test (RIDT) or reverse transcription polymerase chain reaction (RT-PCR) test results. RESULTS:A total of 4,738 children were included in this study. The number of laboratory-confirmed influenza cases was 845 (17.8%), and there were 478 cases of influenza A, 362 cases of influenza B. The adjusted VE based on RT-PCR was 53.4% (95% CI, 25.3-70.5) against any influenza, 68.8% (95% CI, 38.7-84.1) against influenza A, and 29.7% (95% CI, -35.1-61.8) for influenza B. The adjusted VE based on RIDT was 14.8% (95% CI, -4.4-30.0) against any influenza, 24.2% (95% CI, 3.1-40.2) against influenza A, and -5.1% (95% CI, -42.6-21.4) against influenza B. Age-specific VE based on RT-PCR against any influenza was 44.1% (95% CI, -0.2-67.8) in children aged 6 months to 2 years and 59.3% (95% CI, 8.8-81.9) in children aged 3 to 5 years. CONCLUSION:Our results suggest moderate protection (53.4%) of IIV3 against RT-PCR laboratory-confirmed influenza in children in the 2017-2018 influenza season. However, the RIDT hampered the validity to assess VE during influenza season. Caution is needed when interpreting RIDT-based test negative design influenza VE study.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jul</publication><modification>2020-08-27T07:01:19Z</modification><creation>2020-08-27T07:01:19Z</creation></dates><accession>S-EPMC7381399</accession><cross_references><pubmed>32717398</pubmed><doi>10.1016/j.ijid.2020.07.032</doi></cross_references></HashMap>