Evidence map›Paper›PMID 31469170›Full record

ArticleDevelopmental medicine and child neurology2020

Health care service for families with children at early risk of developmental delay: an All Our Families cohort study.

Matthew J Russell, Shainur Premji, Sheila Mcdonald, Jennifer D Zwicker, Suzanne Tough

Open access · hybridAbstract read
In one paragraph

Article in Developmental medicine and child neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 8 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 1 institution in 1 country.

Matthew J RussellCommunity Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.ORCID 0000-0002-7749-8586
Shainur PremjiCommunity Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Sheila McdonaldPaediatrics, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Jennifer D ZwickerSchool of Public Policy, University of Calgary, Calgary, AB, Canada.ORCID 0000-0002-0722-5929
Suzanne ToughCommunity Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
University of Calgary · CA

Funding

CIHR
6 · The paper itself

Abstract

aimThis study examined children's health care service use, mothers' workforce participation, and mothers' community engagement based on children's risk of developmental delay.

methodWe used data from the All Our Families study, a prospective pregnancy cohort. Ages and Stages Questionnaire (ASQ) scores at year 2 indicated risk of developmental delay. To investigate the impact of risk of developmental delay when children were not diagnosed, a sensitivity analysis excluded reports of neurodevelopmental disorder (NDD) diagnosis at year 3. Outcomes were maternal reports of children's health and allied health visits (and estimated costs), and maternal workforce participation and community engagement from year 2 to 3.

resultsAmong 1314 mother-child dyads, 209 (16%) children were classified as being at risk of developmental delay by the ASQ, and 42 (3%) had a reported diagnosis of NDD. Risk of developmental delay was related to increased use of allied health care services (incidence risk ratio 5.04 [year 3]; 95% confidence interval 2.49-10.2) and health visits (incidence risk ratio 1.33 [year 3]; 95% confidence interval 1.14-1.54). The average expected allied health costs were greater for children at risk versus not at risk of developmental delay. However, when excluding children with reported diagnoses of an NDD from this analysis, increased service use and costs in the remaining at-risk population were not observed. Community engagement and workplace participation among families did not differ on the basis of risk of developmental delay.

interpretationThese results suggest increased health care service use by families of children at risk of developmental delay is driven by those receiving a diagnosis of an NDD in the subsequent year. WHAT THIS PAPER ADDS: Early developmental delay risk was related to health care service use and costs. Diagnosis of neurodevelopmental disorder drove increased health care service use and costs. Early developmental delay risk did not relate to parental workforce participation. Early developmental delay risk did not relate to community engagement participation.

Indexed as

Health ServicesPatient Acceptance of Health CareChild, PreschoolDevelopmental DisabilitiesFemaleHumansMaleProspective StudiesRisk FactorsSurveys and Questionnaires

Identifiers

PMID31469170
PMCPMC7028137
OpenAlexW2971049984

What OpenQuestion holds

Textmetadata
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.