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. 2019 Jan:147:e246.
doi: 10.1017/S0950268819001377.

Respiratory syncytial virus hospitalisations among young children: a data linkage study

Affiliations

Respiratory syncytial virus hospitalisations among young children: a data linkage study

Namrata Prasad et al. Epidemiol Infect. 2019 Jan.

Erratum in

Abstract

We aimed to provide comprehensive estimates of laboratory-confirmed respiratory syncytial virus (RSV)-associated hospitalisations. Between 2012 and 2015, active surveillance of acute respiratory infection (ARI) hospitalisations during winter seasons was used to estimate the seasonal incidence of laboratory-confirmed RSV hospitalisations in children aged <5 years in Auckland, New Zealand (NZ). Incidence rates were estimated by fine age group, ethnicity and socio-economic status (SES) strata. Additionally, RSV disease estimates determined through active surveillance were compared to rates estimated from hospital discharge codes. There were 5309 ARI hospitalisations among children during the study period, of which 3923 (73.9%) were tested for RSV and 1597 (40.7%) were RSV-positive. The seasonal incidence of RSV-associated ARI hospitalisations, once corrected for non-testing, was 6.1 (95% confidence intervals 5.8-6.4) per 1000 children <5 years old. The highest incidence was among children aged <3 months. Being of indigenous Māori or Pacific ethnicity or living in a neighbourhood with low SES independently increased the risk of an RSV-associated hospitalisation. RSV hospital discharge codes had a sensitivity of 71% for identifying laboratory-confirmed RSV cases. RSV infection is a leading cause of hospitalisation among children in NZ, with significant disparities by ethnicity and SES. Our findings highlight the need for effective RSV vaccines and therapies.

Keywords: Infectious disease epidemiology; paediatrics; respiratory infections; respiratory syncytial virus.

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Conflict of interest statement

NP, ECN, QSH are currently contracted by GlaxoSmithKline on an RSV surveillance project.

Figures

Fig. 1.
Fig. 1.
Weekly counts of acute respiratory infection (ARI) hospitalisations, RSV laboratory-confirmed hospitalisations and RSV ICD-10 coded hospitalisations in Auckland, NZ, 2012–2015. RSV laboratory-confirmed cases include all SARI and non-SARI samples tested via SHIVERS study protocol as well as any samples tested for clinical purposes.
Fig. 2.
Fig. 2.
Flowchart detailing retrospective cohort of children aged <5 years in Auckland, New Zealand in 2012–2015 and number of RSV laboratory confirmed and/or an RSV hospital admissions identified by International Classification of Diseases (ICD), 10th edition (ICD-10) diagnostic codes. aFor incidence rate calculations, correction of non-testing among ARI patients was done using multivariate imputation by chained equations (MICE) method of imputation (MICE Stata). bIncludes both SHIVERS systematic testing results and any results from samples tested for clinical purposes.
Fig. 3.
Fig. 3.
Incidence rate ratios for age group (referent 2 to <5 years old), socio-economic status (referent – quintile 1) and ethnicity (referent – European/other) of RSV-associated ARI hospitalisations among children <5 years of age in Auckland, New Zealand, 2012–2015. *Rate ratios for SES and ethnicity presented in the figure are unadjusted. Adjusted rate ratios are provided in the text. ±SES (socio-economic status) quantified into quintiles using a small-area level measure of household deprivation derived from the national census (NZDep2013) [24].

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