Evidence map›Paper›PMID 34859911›Full record

ArticleJournal of intellectual disability research : JIDR2022

Hospital admissions in infants with Down syndrome: a record-linked population-based cohort study in Wales.

R A Esperanza, A Evans, D Tucker, S Paranjothy, L Hurt

Open access · hybridAbstract read
In one paragraph

Article in Journal of intellectual disability research : JIDR, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 11 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 1 country.

R A EsperanzaSchool of Medicine, Cardiff University, Cardiff, UK.ORCID 0000-0002-2953-5274
A EvansDivision of Population Medicine, School of Medicine, Cardiff University, Cardiff, UK.ORCID 0000-0002-8463-5251
D TuckerCongenital Anomaly Register and Information Service, Public Health Wales, Swansea, UK.ORCID 0000-0003-3077-5918
S ParanjothyDivision of Population Medicine, School of Medicine, Cardiff University, Cardiff, UK.ORCID 0000-0002-0528-3121
L HurtDivision of Population Medicine, School of Medicine, Cardiff University, Cardiff, UK.ORCID 0000-0002-2741-5383
Cardiff University · GBCwm Taf University Health Board · GBPublic Health Wales · GBUniversity of Aberdeen · GB

Funding

Arthritis Research UKBritish Heart FoundationCancer Research UKChief Scientist OfficeDepartment of HealthMedical Research Council MR/K006525/1Wellcome Trust MR/K006525/1
6 · The paper itself

Abstract

backgroundDespite recent advances, mortality in children with Down syndrome remains five times higher than in the general population. This study aims to describe the burden, patterns and causes of hospital admissions in infants with Down syndrome, and compare this with infants without Down syndrome in a population-based cohort.

methodsThis study used data from the Wales Electronic Cohort for Children, a cohort of all children born in Wales between 1990 and 2012. The cohort was generated from routine administrative data, linked to create an anonymised data set within the Secure Anonymised Information Linkage databank. This analysis is based on all infants born between January 2003 and January 2012 who were followed to their first birthday, a move out of Wales, death, or until 31 October 2012 (end of follow-up). Infants with Down syndrome were identified using the Congenital Anomaly Register and Information Service in Wales. Multivariable Cox regression was used to compare the time to first hospital admission. Admission codes were used to identify the commonest indications for hospitalisation and to determine the presence of other congenital anomalies.

resultsWe included 324 060 children, 356 of whom had Down syndrome. Of infants with Down syndrome, 80.3% had at least one hospital inpatient admission during the first year of life, compared with 32.9% of infants without Down syndrome. These first admissions were earlier [median of 6 days interquartile range (IQR) (3, 72) compared with 45 days [IQR 6, 166)] and longer [median of 4 days (IQR 1, 15) compared with 1 day (IQR 0, 3)] than in infants without Down syndrome. The most common causes of admissions were congenital abnormalities, respiratory diseases, conditions originating in the perinatal period and infectious diseases. The presence of other congenital abnormalities increased hospitalisations in all infants, but more so in infants with Down syndrome who spent a median of 21 days in hospital (IQR 11, 47) during their first year of life.

conclusionInfants with Down syndrome are at high risk for early, more frequent and longer hospital admissions. Congenital heart disease and respiratory infections remain a major burden in this population. More research is needed to understand how to better manage these conditions particularly in the first month of life when most admissions occur.

Indexed as

Down SyndromeChildCohort StudiesFemaleHospitalizationHospitalsHumansInfantPregnancyWalesChildrenCo-morbidityDown syndromeHospitalisationsInfants

Identifiers

PMID34859911
PMCPMC9376940
OpenAlexW3213506724

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.