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Hospital-acquired influenza in an Australian tertiary Centre 2017: a surveillance based study
BACKGROUND: In 2017, Australia experienced its highest levels of influenza virus activity since the 2009 pandemic. This allowed detailed comparison of the characteristics of patients with community and hospital-acquired influenza, and infection control factors that contributed to influenza spread. M...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469028/ https://www.ncbi.nlm.nih.gov/pubmed/30991976 http://dx.doi.org/10.1186/s12890-019-0842-6 |
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author | Parkash, Nikita Beckingham, Wendy Andersson, Patiyan Kelly, Paul Senanayake, Sanjaya Coatsworth, Nicholas |
author_facet | Parkash, Nikita Beckingham, Wendy Andersson, Patiyan Kelly, Paul Senanayake, Sanjaya Coatsworth, Nicholas |
author_sort | Parkash, Nikita |
collection | PubMed |
description | BACKGROUND: In 2017, Australia experienced its highest levels of influenza virus activity since the 2009 pandemic. This allowed detailed comparison of the characteristics of patients with community and hospital-acquired influenza, and infection control factors that contributed to influenza spread. METHODS: A surveillance based study was conducted on hospitalised patients with laboratory-confirmed influenza at the Canberra Hospital during April–October 2017. Differences between the hospital-acquired and community-acquired patient characteristics and outcomes were assessed by univariate analysis. Epidemiologic curves were developed and cluster distribution within the hospital was determined. RESULTS: Two hundred and ninety-two patients were included in the study. Twenty-eight (9.6%) acquired influenza in hospital, representing a higher proportion than any of the previous 5 years (range 0.9–5.8%). These patients were more likely to have influenza A (p = 0.021), had higher rates of diabetes (p = 0.015), malignancy (p = 0.046) and chronic liver disease (p = 0.043). Patients acquiring influenza in hospital met clinical criteria for influenza like illness in 25% of cases, compared with 64.4% for community-acquired cases (p < 0.001). Hospital-acquired influenza cases occurred in two distinct clusters. Patients were moved an average of 5 times after diagnosis. Mean length of stay following diagnosis was 13 days compared to 5 days for community-acquired cases (p < 0.001). Of the patients with hospital-acquired influenza, 22 were in shared rooms during their incubation period and 9 were not isolated in single rooms following diagnosis. Treatment was initiated within the recommended 48 h period following symptom onset for 62.5% of hospital-acquired cases compared with 39.8% of community-acquired cases (p = 0.033). CONCLUSIONS: Our results show that clinical presentation differed between patients with hospital-acquired influenza compared with those who acquired influenza in the community. Cases occurred in two clusters suggesting intra-hospital transmission rather than random importation from the community, highlighting the importance of infection control measures to limit influenza spread. Patients with hospital-acquired influenza may present without classical features of an influenza-like illness and this should promote earlier diagnostic testing and isolation to limit spread. Movement of patients after diagnosis is likely to facilitate spread within the hospital. |
format | Online Article Text |
id | pubmed-6469028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64690282019-04-23 Hospital-acquired influenza in an Australian tertiary Centre 2017: a surveillance based study Parkash, Nikita Beckingham, Wendy Andersson, Patiyan Kelly, Paul Senanayake, Sanjaya Coatsworth, Nicholas BMC Pulm Med Research Article BACKGROUND: In 2017, Australia experienced its highest levels of influenza virus activity since the 2009 pandemic. This allowed detailed comparison of the characteristics of patients with community and hospital-acquired influenza, and infection control factors that contributed to influenza spread. METHODS: A surveillance based study was conducted on hospitalised patients with laboratory-confirmed influenza at the Canberra Hospital during April–October 2017. Differences between the hospital-acquired and community-acquired patient characteristics and outcomes were assessed by univariate analysis. Epidemiologic curves were developed and cluster distribution within the hospital was determined. RESULTS: Two hundred and ninety-two patients were included in the study. Twenty-eight (9.6%) acquired influenza in hospital, representing a higher proportion than any of the previous 5 years (range 0.9–5.8%). These patients were more likely to have influenza A (p = 0.021), had higher rates of diabetes (p = 0.015), malignancy (p = 0.046) and chronic liver disease (p = 0.043). Patients acquiring influenza in hospital met clinical criteria for influenza like illness in 25% of cases, compared with 64.4% for community-acquired cases (p < 0.001). Hospital-acquired influenza cases occurred in two distinct clusters. Patients were moved an average of 5 times after diagnosis. Mean length of stay following diagnosis was 13 days compared to 5 days for community-acquired cases (p < 0.001). Of the patients with hospital-acquired influenza, 22 were in shared rooms during their incubation period and 9 were not isolated in single rooms following diagnosis. Treatment was initiated within the recommended 48 h period following symptom onset for 62.5% of hospital-acquired cases compared with 39.8% of community-acquired cases (p = 0.033). CONCLUSIONS: Our results show that clinical presentation differed between patients with hospital-acquired influenza compared with those who acquired influenza in the community. Cases occurred in two clusters suggesting intra-hospital transmission rather than random importation from the community, highlighting the importance of infection control measures to limit influenza spread. Patients with hospital-acquired influenza may present without classical features of an influenza-like illness and this should promote earlier diagnostic testing and isolation to limit spread. Movement of patients after diagnosis is likely to facilitate spread within the hospital. BioMed Central 2019-04-16 /pmc/articles/PMC6469028/ /pubmed/30991976 http://dx.doi.org/10.1186/s12890-019-0842-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Parkash, Nikita Beckingham, Wendy Andersson, Patiyan Kelly, Paul Senanayake, Sanjaya Coatsworth, Nicholas Hospital-acquired influenza in an Australian tertiary Centre 2017: a surveillance based study |
title | Hospital-acquired influenza in an Australian tertiary Centre 2017: a surveillance based study |
title_full | Hospital-acquired influenza in an Australian tertiary Centre 2017: a surveillance based study |
title_fullStr | Hospital-acquired influenza in an Australian tertiary Centre 2017: a surveillance based study |
title_full_unstemmed | Hospital-acquired influenza in an Australian tertiary Centre 2017: a surveillance based study |
title_short | Hospital-acquired influenza in an Australian tertiary Centre 2017: a surveillance based study |
title_sort | hospital-acquired influenza in an australian tertiary centre 2017: a surveillance based study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469028/ https://www.ncbi.nlm.nih.gov/pubmed/30991976 http://dx.doi.org/10.1186/s12890-019-0842-6 |
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