Evidence map›Paper›PMID 28780500›Full record

ArticleArchives of disease in childhood. Fetal and neonatal edition2018

Perinatal risk factors for neonatal encephalopathy: an unmatched case-control study.

Cally J Tann, Margaret Nakakeeto, Barbara A Willey, Margaret Sewegaba, Emily L Webb, Ibby Oke, Emmanuel Derek Mutuuza, Donald Peebles, Margaret Musoke, Kathryn A Harris and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Archives of disease in childhood. Fetal and neonatal edition, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 3 pooled it
11.8field-weighted citation impact, top 1% 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

38 citing papers in PubMed, 3 syntheses or guidelines pooled it, 75 citations in OpenAlex.

  1. Efficacy of melatonin in term neonatal models of perinatal hypoxia-ischaemia.Annals of clinical and translational neurology · 2022
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  13. Stay cool and keep moving forwards.Pediatric research · 2025
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  14. Evaluating predictive values of umbilical cord arterial lactate for adverse newborn outcomes among term-births in northern Uganda: A cross sectional analytical study.International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics · 2025
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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

15 authors at 8 institutions in 2 countries.

Cally J TannClinical Research Department, London School of Hygiene & Tropical Medicine, London, UK.ORCID http://orcid.org/0000-0003-0131-4952
Margaret NakakeetoNeonatal Medicine, Mulago University Hospital, Kampala, Uganda.
Barbara A WilleyMRC Tropical Epidemiology Group, London School of Hygiene & Tropical Medicine, London, UK.
Margaret SewegabaMRC/UVRI Uganda Research Unit on AIDS, Entebbe, Uganda.
Emily L WebbMRC Tropical Epidemiology Group, London School of Hygiene & Tropical Medicine, London, UK.
Ibby OkeDepartment of Microbiology, Virology and Infection Prevention and Control, Great Ormond Street Hospital For Children NHS Trust, London, UK.
Emmanuel Derek MutuuzaNeonatal Medicine, Mulago University Hospital, Kampala, Uganda.
Donald PeeblesInstitute for Women's Health, University College London, London, UK.
Margaret MusokeNeonatal Medicine, Mulago University Hospital, Kampala, Uganda.
Kathryn A HarrisDepartment of Microbiology, Virology and Infection Prevention and Control, Great Ormond Street Hospital For Children NHS Trust, London, UK.
Neil J SebireInstitute for Child Health, University College London, London, UK.
Nigel KleinInstitute for Child Health, University College London, London, UK.ORCID http://orcid.org/0000-0003-3925-9258
Jennifer J KurinczukNational Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Alison M ElliottClinical Research Department, London School of Hygiene & Tropical Medicine, London, UK.
Nicola J RobertsonInstitute for Women's Health, University College London, London, UK.ORCID http://orcid.org/0000-0002-5783-0828
London School of Hygiene & Tropical Medicine · GBMulago Hospital · UGGreat Ormond Street Hospital · GBLondon Women's Clinic · GBUniversity College London · GBUganda Virus Research Institute · UGUniversity of London · GBUniversity of Oxford · GB

Funding

Medical Research Council MC_UP_1204/9Medical Research Council MC_UU_00027/5Medical Research Council MR/K012126/1Wellcome Trust
6 · The paper itself

Abstract

objectiveNeonatal encephalopathy (NE) is the third leading cause of child mortality. Preclinical studies suggest infection and inflammation can sensitise or precondition the newborn brain to injury. This study examined perinatal risks factor for NE in Uganda.

designUnmatched case-control study.

settingMulago National Referral Hospital, Kampala, Uganda.

methods210 term infants with NE and 409 unaffected term infants as controls were recruited over 13 months. Data were collected on preconception, antepartum and intrapartum exposures. Blood culture, species-specific bacterial real-time PCR, C reactive protein and placental histology for chorioamnionitis and funisitis identified maternal and early newborn infection and inflammation. Multivariable logistic regression examined associations with NE.

resultsNeonatal bacteraemia (adjusted OR (aOR) 8.67 (95% CI 1.51 to 49.74), n=315) and histological funisitis (aOR 11.80 (95% CI 2.19 to 63.45), n=162) but not chorioamnionitis (aOR 3.20 (95% CI 0.66 to 15.52), n=162) were independent risk factors for NE. Among encephalopathic infants, neonatal case fatality was not significantly higher when exposed to early neonatal bacteraemia (OR 1.65 (95% CI 0.62 to 4.39), n=208). Intrapartum antibiotic use did not improve neonatal survival (p=0.826). After regression analysis, other identified perinatal risk factors (n=619) included hypertension in pregnancy (aOR 3.77), male infant (aOR 2.51), non-cephalic presentation (aOR 5.74), lack of fetal monitoring (aOR 2.75), augmentation (aOR 2.23), obstructed labour (aOR 3.8) and an acute intrapartum event (aOR 8.74).

conclusionsPerinatal infection and inflammation are independent risk factors for NE in this low-resource setting, supporting a role in the aetiological pathway of term brain injury. Intrapartum antibiotic administration did not mitigate against adverse outcomes. The importance of intrapartum risk factors in this sub-Saharan African setting is highlighted.

Indexed as

Brain DiseasesCase-Control StudiesFemaleHumansInfantInfant, NewbornInfant, Newborn, DiseasesLogistic ModelsMalePregnancyRisk FactorsTerm BirthUgandaInfectionNeonatal EncephalopathyRisk FactorsUganda

Identifiers

PMID28780500
PMCPMC5916101
OpenAlexW2742187637

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.