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2517. Seasonal Influenza 2017–2018: Epidemiological Review and Experience at a Veterans Affairs Medical Center in New York
BACKGROUND: The 2017–2018 influenza (INF) season started early with widespread activity throughout the country which was covered extensively in the media. The season peaked in February and subsided nationally in March and April. The CDC reported decreased effectiveness of this season’s vaccine. The...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254165/ http://dx.doi.org/10.1093/ofid/ofy210.2169 |
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author | Fisher, Matthew Bailey, Lisa Lemaitre, Beth Psevdos, George |
author_facet | Fisher, Matthew Bailey, Lisa Lemaitre, Beth Psevdos, George |
author_sort | Fisher, Matthew |
collection | PubMed |
description | BACKGROUND: The 2017–2018 influenza (INF) season started early with widespread activity throughout the country which was covered extensively in the media. The season peaked in February and subsided nationally in March and April. The CDC reported decreased effectiveness of this season’s vaccine. The latter had the B/Brisbane/60/2008-like (B/Victoria lineage) component for INF B. We report our hospital’s experience of seasonal INF activity. METHODS: Retrospective chart review of every Veteran who tested positive for INF A or B at Northport Veterans Medical Center, Long Island New York. RESULTS: 160 Veterans were diagnosed with INF from December 1, 2017 to April 26, 2018. 106 had INF A, 54 INF B. Of the 160 cases, 15 were in DEC, 61 in JAN, 69 in FEB, 13 in MAR, 2 in APRIL 10 INF A isolates subtyped as: 9 H3N2, 1 H1N1pdm09. 5 INF B isolates subtyped as Yamagata lineage. Demographics: Median age: 63 years (23–93); Race: 79% Caucasian, 16% Black, 1% Asian, 1% Pacific Island, 3% Hispanic. 95% men. Medical History: 11% had history of CHF, 12% CAD, 19% HTN, 24% DM, and 12% COPD. The median BMI was 29 (17–51.5). 101 tested in ER; 36 in clinics, 5 in our related adult and nursing homes, and 17 during their hospitalization. 56 (35%) had received the INF vaccine this season. The median duration from vaccination to diagnosis was 100.5 days (2–175 days). 25 required hospitalization with 5 of them in ICU; 40% of the hospitalized patients had received the INF vaccine. The median length of stay was 4.5 days. 139 received oseltamivir (OSE), 13 supportive treatment, 8 antibiotics alone, and 7 OSE+antibiotics. 5 patients expired (3 INF A, 2 INF B) 3 were not vaccinated; one patient developed NSTEMI and survived. Hospitalized patients were older 73 vs. 60, P:0.018, more likely to have COPD (P = 0.0009), CHF (P = 0.0066), and history of lung cancer. There was no difference in risk for hospitalization between vaccinated and unvaccinated Veterans, P = 0.649. CONCLUSION: The months of JAN and FEB had the highest flu activity, mirroring the INF activity in our nation as reported by the CDC. The majority of our patients were not vaccinated. 5 fatalities were noted. Not surprisingly, the vaccine was not as effective this season; also our INF B cases were Yamagata lineage (not part of this season’s vaccine). Our data show need for improvement of both the efficacy of INF vaccination (universal) and vaccination rate for our Veterans. DISCLOSURES: All authors: No reported disclosures. |
format | Online Article Text |
id | pubmed-6254165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62541652018-11-28 2517. Seasonal Influenza 2017–2018: Epidemiological Review and Experience at a Veterans Affairs Medical Center in New York Fisher, Matthew Bailey, Lisa Lemaitre, Beth Psevdos, George Open Forum Infect Dis Abstracts BACKGROUND: The 2017–2018 influenza (INF) season started early with widespread activity throughout the country which was covered extensively in the media. The season peaked in February and subsided nationally in March and April. The CDC reported decreased effectiveness of this season’s vaccine. The latter had the B/Brisbane/60/2008-like (B/Victoria lineage) component for INF B. We report our hospital’s experience of seasonal INF activity. METHODS: Retrospective chart review of every Veteran who tested positive for INF A or B at Northport Veterans Medical Center, Long Island New York. RESULTS: 160 Veterans were diagnosed with INF from December 1, 2017 to April 26, 2018. 106 had INF A, 54 INF B. Of the 160 cases, 15 were in DEC, 61 in JAN, 69 in FEB, 13 in MAR, 2 in APRIL 10 INF A isolates subtyped as: 9 H3N2, 1 H1N1pdm09. 5 INF B isolates subtyped as Yamagata lineage. Demographics: Median age: 63 years (23–93); Race: 79% Caucasian, 16% Black, 1% Asian, 1% Pacific Island, 3% Hispanic. 95% men. Medical History: 11% had history of CHF, 12% CAD, 19% HTN, 24% DM, and 12% COPD. The median BMI was 29 (17–51.5). 101 tested in ER; 36 in clinics, 5 in our related adult and nursing homes, and 17 during their hospitalization. 56 (35%) had received the INF vaccine this season. The median duration from vaccination to diagnosis was 100.5 days (2–175 days). 25 required hospitalization with 5 of them in ICU; 40% of the hospitalized patients had received the INF vaccine. The median length of stay was 4.5 days. 139 received oseltamivir (OSE), 13 supportive treatment, 8 antibiotics alone, and 7 OSE+antibiotics. 5 patients expired (3 INF A, 2 INF B) 3 were not vaccinated; one patient developed NSTEMI and survived. Hospitalized patients were older 73 vs. 60, P:0.018, more likely to have COPD (P = 0.0009), CHF (P = 0.0066), and history of lung cancer. There was no difference in risk for hospitalization between vaccinated and unvaccinated Veterans, P = 0.649. CONCLUSION: The months of JAN and FEB had the highest flu activity, mirroring the INF activity in our nation as reported by the CDC. The majority of our patients were not vaccinated. 5 fatalities were noted. Not surprisingly, the vaccine was not as effective this season; also our INF B cases were Yamagata lineage (not part of this season’s vaccine). Our data show need for improvement of both the efficacy of INF vaccination (universal) and vaccination rate for our Veterans. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6254165/ http://dx.doi.org/10.1093/ofid/ofy210.2169 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Fisher, Matthew Bailey, Lisa Lemaitre, Beth Psevdos, George 2517. Seasonal Influenza 2017–2018: Epidemiological Review and Experience at a Veterans Affairs Medical Center in New York |
title | 2517. Seasonal Influenza 2017–2018: Epidemiological Review and Experience at a Veterans Affairs Medical Center in New York |
title_full | 2517. Seasonal Influenza 2017–2018: Epidemiological Review and Experience at a Veterans Affairs Medical Center in New York |
title_fullStr | 2517. Seasonal Influenza 2017–2018: Epidemiological Review and Experience at a Veterans Affairs Medical Center in New York |
title_full_unstemmed | 2517. Seasonal Influenza 2017–2018: Epidemiological Review and Experience at a Veterans Affairs Medical Center in New York |
title_short | 2517. Seasonal Influenza 2017–2018: Epidemiological Review and Experience at a Veterans Affairs Medical Center in New York |
title_sort | 2517. seasonal influenza 2017–2018: epidemiological review and experience at a veterans affairs medical center in new york |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254165/ http://dx.doi.org/10.1093/ofid/ofy210.2169 |
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