Do hospital pressures change following rotavirus vaccine introduction? A retrospective database analysis in a large paediatric hospital in the UK.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
15 05 2019
Historique:
entrez: 18 5 2019
pubmed: 18 5 2019
medline: 19 5 2020
Statut: epublish

Résumé

Hospitals in the UK are under increasing clinical and financial pressures. Following introduction of childhood rotavirus vaccination in the UK in 2013, rotavirus gastroenteritis (RVGE) hospitalisations reduced significantly. We evaluated changes in 'hospital pressures' (demand on healthcare resources and staff) following rotavirus vaccine introduction in a paediatric setting in the UK. Retrospective hospital database analysis between July 2007 and June 2015. A large paediatric hospital providing primary, secondary and tertiary care in Merseyside, UK. Hospital admissions aged <15 years. Outcomes were calculated for four different patient groups identified through diagnosis coding (International Classification of Disease, 10th edition) and/or laboratory confirmation: all admissions; any infection, acute gastroenteritis and RVGE. Hospital pressures were compared before and after rotavirus vaccine introduction: these included bed occupancy, hospital-acquired infection rate, unplanned readmission rate and outlier rate (medical patients admitted to surgical wards due to lack of medical beds). Interrupted time-series analysis was used to evaluate changes in bed occupancy. There were 116 871 admissions during the study period. Lower bed occupancy in the rotavirus season in the postvaccination period was observed for RVGE (-89%, 95% CI 73% to 95%), acute gastroenteritis (-63%, 95% CI 39% to 78%) and any infection (-23%, 95% CI 15% to 31%). No significant overall reduction in bed occupancy was observed (-4%, 95% CI -1% to 9%). No changes were observed for the other outcomes. Rotavirus vaccine introduction was not associated with reduced hospital pressures. A reduction in RVGE hospitalisation without change in overall bed occupancy suggests that beds available were used for a different patient population, possibly reflecting a previously unmet need. NCT03271593.

Identifiants

pubmed: 31097487
pii: bmjopen-2018-027739
doi: 10.1136/bmjopen-2018-027739
pmc: PMC6530452
doi:

Substances chimiques

Rotavirus Vaccines 0

Banques de données

ClinicalTrials.gov
['NCT03271593']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e027739

Informations de copyright

© Author(s) (or their employer(s)) 2018. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: Rotarix is a trademark of the GSK group of companies. NAC, NF and DH are in receipt of research grant support from the GSK group of companies for the conduct of the present study. NAC has received honoraria for participation in GSK Rotavirus Vaccine Advisory Board Meetings from the GSK group of companies and from Watermark Research Partners for participation in independent data monitoring committee of GSK-sponsored clinical trials of Rotavirus vaccine. The institution of NAC and NF received grant from the GSK group of companies for the conduct of other analysis, not related to the present work. DH received grants from the GSK group of companies and Sanofi Pasteur, and Merck & Co (Kenilworth, New Jersey, USA) outside the submitted work. NB-Z reports grants from the GSK group of companies and from Takeda Pharmaceuticals outside the submitted work. BS and ET are employees of the GSK group of companies. EH, RC, MC and JC have nothing to disclose.

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Auteurs

Ellen Heinsbroek (E)

Centre for Global Vaccine Research, Institute of Infection and Global Health, University of Liverpool, members of Liverpool Health Partners, Liverpool, UK.

Daniel Hungerford (D)

Centre for Global Vaccine Research, Institute of Infection and Global Health, University of Liverpool, members of Liverpool Health Partners, Liverpool, UK.
Field Service-North West, National Infection Service, Public Health England, Liverpool, UK.
NIHR Health Protection Research Unit in Gastrointestinal Infections, Liverpool, UK.

Richard P D Cooke (RPD)

Alder Hey Children's NHS Foundation Trust, members of Liverpool Health Partners, Liverpool, UK.

Margaret Chowdhury (M)

Alder Hey Children's NHS Foundation Trust, members of Liverpool Health Partners, Liverpool, UK.

James S Cargill (JS)

Alder Hey Children's NHS Foundation Trust, members of Liverpool Health Partners, Liverpool, UK.

Naor Bar-Zeev (N)

International Vaccine Access Center, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland, USA.

Neil French (N)

Centre for Global Vaccine Research, Institute of Infection and Global Health, University of Liverpool, members of Liverpool Health Partners, Liverpool, UK.
The Royal Liverpool and Broadgreen University Hospitals NHS Trust, members of Liverpool Health Partners, Liverpool, UK.

Eleni Theodorou (E)

Health Economics, GSK, London, UK.

Baudouin Standaert (B)

Health Economics, GSK, Wavre, Belgium.

Nigel A Cunliffe (NA)

Centre for Global Vaccine Research, Institute of Infection and Global Health, University of Liverpool, members of Liverpool Health Partners, Liverpool, UK.
Alder Hey Children's NHS Foundation Trust, members of Liverpool Health Partners, Liverpool, UK.

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