Evidence map›Paper›PMID 28381208›Full record

ArticleBMC pediatrics2017

Variation in and risk factors for paediatric inpatient all-cause mortality in a low income setting: data from an emerging clinical information network.

David Gathara, Lucas Malla, Philip Ayieko, Stella Karuri, Rachel Nyamai, Grace Irimu, Michael Boele van Hensbroek, Elizabeth Allen, Mike English, Clinical Information Network

Open access · goldAbstract read
In one paragraph

Article in BMC pediatrics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 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

10 authors at 5 institutions in 3 countries.

David GatharaDepartment of Public Health Research, KEMRI Wellcome Trust Research Programme, P.O. Box 43640 00100, Nairobi, Kenya. dgathara@kemri-wellcome.org.
Lucas MallaDepartment of Public Health Research, KEMRI Wellcome Trust Research Programme, P.O. Box 43640 00100, Nairobi, Kenya.
Philip AyiekoDepartment of Public Health Research, KEMRI Wellcome Trust Research Programme, P.O. Box 43640 00100, Nairobi, Kenya.
Stella KaruriDepartment of Public Health Research, KEMRI Wellcome Trust Research Programme, P.O. Box 43640 00100, Nairobi, Kenya.
Rachel NyamaiDivision of Maternal, Newborn, Child and Adolescent Health, Ministry of Health, Nairobi, Kenya.
Grace IrimuDepartment of Public Health Research, KEMRI Wellcome Trust Research Programme, P.O. Box 43640 00100, Nairobi, Kenya.
Michael Boele van HensbroekDepartment of Global Health, Academic Medical Centre, University of Amsterdam, Amsterdam, 22700 1100, DE, The Netherlands.
Elizabeth AllenDepartment of Medical Statistics, London School of Hygiene and Tropical Medicine, London, WC1E 7HT, UK.
Mike EnglishDepartment of Public Health Research, KEMRI Wellcome Trust Research Programme, P.O. Box 43640 00100, Nairobi, Kenya.
Clinical Information Network
Kenya Medical Research Institute · KEMinistry of Health · KEUniversity of Amsterdam · NLUniversity of London · GBUniversity of Oxford · GB

Funding

Wellcome Trust 084538Wellcome Trust 092654Wellcome Trust 097170
6 · The paper itself

Abstract

backgroundHospital mortality data can inform planning for health interventions and may help optimize resource allocation if they are reliable and appropriately interpreted. However such data are often not available in low income countries including Kenya.

methodsData from the Clinical Information Network covering 12 county hospitals' paediatric admissions aged 2-59 months for the periods September 2013 to March 2015 were used to describe mortality across differing contexts and to explore whether simple clinical characteristics used to classify severity of illness in common treatment guidelines are consistently associated with inpatient mortality. Regression models accounting for hospital identity and malaria prevalence (low or high) were used. Multiple imputation for missing data was based on a missing at random assumption with sensitivity analyses based on pattern mixture missing not at random assumptions.

resultsThe overall cluster adjusted crude mortality rate across hospitals was 6 · 2% with an almost 5 fold variation across sites (95% CI 4 · 9 to 7 · 8; range 2 · 1% - 11 · 0%). Hospital identity was significantly associated with mortality. Clinical features included in guidelines for common diseases to assess severity of illness were consistently associated with mortality in multivariable analyses (AROC =0 · 86).

conclusionAll-cause mortality is highly variable across hospitals and associated with clinical risk factors identified in disease specific guidelines. A panel of these clinical features may provide a basic common data framework as part of improved health information systems to support evaluations of quality and outcomes of care at scale and inform health system strengthening efforts.

Indexed as

Health Information SystemsHospital MortalityChild, PreschoolDeveloping CountriesFemaleHealthcare DisparitiesHospitals, CountyHumansInfantKenyaMaleQuality Indicators, Health CareRisk FactorsClinical risk factorsHospitalMortalityPaediatricsQuality of careVariability

Identifiers

PMID28381208
PMCPMC5382487
OpenAlexW2605074433

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.