K. Hughes, D. Middleton, M. Nowalk, G. Balasubramani, E. Martin, M. Gaglani, H. Talbot, M. Patel, J. Ferdinands, R. Zimmerman, F. Silveira, R. Zimmerman, D. Middleton, F. Silveira, K. Hughes, H. Eng, Theresa M. Sax, Sean G. Saul, Charles Rinaldo, Balasubramani Goundappa, M. Nowalk, Lori Steiffel, J. Williams, Monika Johnson, M. Gaglani, Kempapura Murthy, T. McNeal, Shekar Ghamande, V. Escobedo, Anne Robertson, Lydia Clipper, A. Rao, K-H Chang, Marcus Volz, K. Walker, A. Arroliga, A. Monto, Emily K. Martin, R. Malosh, J. Petrie, A. Lauring, Caroline K. Cheng, H. Segaloff, E. McSpadden, Emileigh Johnson, Rachel K Truscon, L. Lamerato, S. Davis, M. Zervos, H. Talbot, Dayna Wyatt, Yuwei Zhu, Zhouwen Liu, Rendie Mchenry, N. Halasa, Sandra Alvarez Calvillo, Stephanie Longmire, Laura S. Stewart, J. Ferdinands, A. Fry, E. Alyanak, Emily R Smith, Courtney Strickland, Sarah M. Spencer, B. Flannery, J. Chung, Xiyan Xu, Stephen L. Lindstrom, L. Berman, W. Sessions, Rebecca J. Kondor, M. Patel
{"title":"流感疫苗预防免疫功能低下成人经实验室证实的流感住院的有效性","authors":"K. Hughes, D. Middleton, M. Nowalk, G. Balasubramani, E. Martin, M. Gaglani, H. Talbot, M. Patel, J. Ferdinands, R. Zimmerman, F. Silveira, R. Zimmerman, D. Middleton, F. Silveira, K. Hughes, H. Eng, Theresa M. Sax, Sean G. Saul, Charles Rinaldo, Balasubramani Goundappa, M. Nowalk, Lori Steiffel, J. Williams, Monika Johnson, M. Gaglani, Kempapura Murthy, T. McNeal, Shekar Ghamande, V. Escobedo, Anne Robertson, Lydia Clipper, A. Rao, K-H Chang, Marcus Volz, K. Walker, A. Arroliga, A. Monto, Emily K. Martin, R. Malosh, J. Petrie, A. Lauring, Caroline K. Cheng, H. Segaloff, E. McSpadden, Emileigh Johnson, Rachel K Truscon, L. Lamerato, S. Davis, M. Zervos, H. Talbot, Dayna Wyatt, Yuwei Zhu, Zhouwen Liu, Rendie Mchenry, N. Halasa, Sandra Alvarez Calvillo, Stephanie Longmire, Laura S. Stewart, J. Ferdinands, A. Fry, E. Alyanak, Emily R Smith, Courtney Strickland, Sarah M. Spencer, B. Flannery, J. Chung, Xiyan Xu, Stephen L. Lindstrom, L. Berman, W. Sessions, Rebecca J. Kondor, M. Patel","doi":"10.1101/2020.10.08.20208579","DOIUrl":null,"url":null,"abstract":"Background: Yearly influenza immunization is recommended for immunocompromised (IC) individuals, although immune responses are lower than that for the non-immunocompromised and the data on vaccine effectiveness (VE) in the IC is scarce. We evaluated VE against influenza-associated hospitalization among IC adults. Methods: We analyzed data from adults [≥] 18 years hospitalized with acute respiratory illness (ARI) during the 2017-2018 influenza season at 10 hospitals in the United States. IC adults were identified using pre-specified case-definitions, utilizing electronic medical record data. VE was evaluated with a test-negative case-control design using multivariate logistic regression with PCR-confirmed influenza as the outcome and vaccination status as the exposure, adjusting for age, enrolling site, illness onset date, race, days from onset to specimen collection, self-reported health, and self-reported hospitalizations. Results: Of 3,524 adults hospitalized with ARI, 1,210 (34.3%) had an immunocompromising condition. IC adults were more likely to be vaccinated than non-IC (69.5% vs 65.2%), and less likely to have influenza (22% vs 27.8%). The mean age did not differ among IC and non-IC (61.4 vs 60.8 years old). The overall VE against influenza hospitalization, including immunocompetent adults, was 33% (95% CI, 21% to 44%). VE among IC vs non-IC adults was lower at 5% (-29% to 31%) vs. 41% (27% to 52%) (p<0.05 for interaction term). Conclusions: VE in one influenza season was very low among IC individuals. Future efforts should include evaluation of VE among the different immunocompromising conditions and whether enhanced vaccines improve the suboptimal effectiveness among the immunocompromised.","PeriodicalId":10421,"journal":{"name":"Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America","volume":"38 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"16","resultStr":"{\"title\":\"Effectiveness of Influenza Vaccine for Preventing Laboratory-Confirmed Influenza Hospitalizations in Immunocompromised Adults\",\"authors\":\"K. Hughes, D. Middleton, M. Nowalk, G. Balasubramani, E. Martin, M. Gaglani, H. Talbot, M. Patel, J. Ferdinands, R. Zimmerman, F. Silveira, R. Zimmerman, D. Middleton, F. Silveira, K. Hughes, H. Eng, Theresa M. Sax, Sean G. Saul, Charles Rinaldo, Balasubramani Goundappa, M. Nowalk, Lori Steiffel, J. Williams, Monika Johnson, M. Gaglani, Kempapura Murthy, T. McNeal, Shekar Ghamande, V. Escobedo, Anne Robertson, Lydia Clipper, A. Rao, K-H Chang, Marcus Volz, K. Walker, A. Arroliga, A. Monto, Emily K. Martin, R. Malosh, J. Petrie, A. Lauring, Caroline K. Cheng, H. Segaloff, E. McSpadden, Emileigh Johnson, Rachel K Truscon, L. Lamerato, S. Davis, M. Zervos, H. Talbot, Dayna Wyatt, Yuwei Zhu, Zhouwen Liu, Rendie Mchenry, N. Halasa, Sandra Alvarez Calvillo, Stephanie Longmire, Laura S. Stewart, J. Ferdinands, A. Fry, E. Alyanak, Emily R Smith, Courtney Strickland, Sarah M. Spencer, B. Flannery, J. Chung, Xiyan Xu, Stephen L. Lindstrom, L. Berman, W. Sessions, Rebecca J. Kondor, M. Patel\",\"doi\":\"10.1101/2020.10.08.20208579\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Yearly influenza immunization is recommended for immunocompromised (IC) individuals, although immune responses are lower than that for the non-immunocompromised and the data on vaccine effectiveness (VE) in the IC is scarce. We evaluated VE against influenza-associated hospitalization among IC adults. Methods: We analyzed data from adults [≥] 18 years hospitalized with acute respiratory illness (ARI) during the 2017-2018 influenza season at 10 hospitals in the United States. IC adults were identified using pre-specified case-definitions, utilizing electronic medical record data. VE was evaluated with a test-negative case-control design using multivariate logistic regression with PCR-confirmed influenza as the outcome and vaccination status as the exposure, adjusting for age, enrolling site, illness onset date, race, days from onset to specimen collection, self-reported health, and self-reported hospitalizations. Results: Of 3,524 adults hospitalized with ARI, 1,210 (34.3%) had an immunocompromising condition. IC adults were more likely to be vaccinated than non-IC (69.5% vs 65.2%), and less likely to have influenza (22% vs 27.8%). The mean age did not differ among IC and non-IC (61.4 vs 60.8 years old). The overall VE against influenza hospitalization, including immunocompetent adults, was 33% (95% CI, 21% to 44%). VE among IC vs non-IC adults was lower at 5% (-29% to 31%) vs. 41% (27% to 52%) (p<0.05 for interaction term). Conclusions: VE in one influenza season was very low among IC individuals. Future efforts should include evaluation of VE among the different immunocompromising conditions and whether enhanced vaccines improve the suboptimal effectiveness among the immunocompromised.\",\"PeriodicalId\":10421,\"journal\":{\"name\":\"Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America\",\"volume\":\"38 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-10-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"16\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1101/2020.10.08.20208579\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2020.10.08.20208579","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Effectiveness of Influenza Vaccine for Preventing Laboratory-Confirmed Influenza Hospitalizations in Immunocompromised Adults
Background: Yearly influenza immunization is recommended for immunocompromised (IC) individuals, although immune responses are lower than that for the non-immunocompromised and the data on vaccine effectiveness (VE) in the IC is scarce. We evaluated VE against influenza-associated hospitalization among IC adults. Methods: We analyzed data from adults [≥] 18 years hospitalized with acute respiratory illness (ARI) during the 2017-2018 influenza season at 10 hospitals in the United States. IC adults were identified using pre-specified case-definitions, utilizing electronic medical record data. VE was evaluated with a test-negative case-control design using multivariate logistic regression with PCR-confirmed influenza as the outcome and vaccination status as the exposure, adjusting for age, enrolling site, illness onset date, race, days from onset to specimen collection, self-reported health, and self-reported hospitalizations. Results: Of 3,524 adults hospitalized with ARI, 1,210 (34.3%) had an immunocompromising condition. IC adults were more likely to be vaccinated than non-IC (69.5% vs 65.2%), and less likely to have influenza (22% vs 27.8%). The mean age did not differ among IC and non-IC (61.4 vs 60.8 years old). The overall VE against influenza hospitalization, including immunocompetent adults, was 33% (95% CI, 21% to 44%). VE among IC vs non-IC adults was lower at 5% (-29% to 31%) vs. 41% (27% to 52%) (p<0.05 for interaction term). Conclusions: VE in one influenza season was very low among IC individuals. Future efforts should include evaluation of VE among the different immunocompromising conditions and whether enhanced vaccines improve the suboptimal effectiveness among the immunocompromised.