Evidence map›Paper›PMID 27057339›Full record

ArticleMaternal health, neonatology and perinatology2015

Risk factors for acute bilirubin encephalopathy on admission to two Myanmar national paediatric hospitals.

G Arnolda, H M Nwe, D Trevisanuto, A A Thin, A A Thein, T Defechereux, D Kumara, L Moccia

Open access · goldAbstract read
In one paragraph

Article in Maternal health, neonatology and perinatology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
6.3field-weighted citation impact, top 4% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

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  11. A neurologic dysfunction scoring protocol for jaundiced neonates requiring exchange transfusion.The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians · 2018
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  15. A decision-making tool for exchange transfusions in infants with severe hyperbilirubinemia in resource-limited settings.Journal of perinatology : official journal of the California Perinatal Association · 2016
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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

8 authors at 6 institutions in 5 countries.

G ArnoldaThrive Networks, Oakland, CA USA ; School of Public Health & Community Medicine, Faculty of Medicine, University of New South Wales, Wales, NSW Australia.ORCID 0000-0003-4948-7633
H M NweDepartment of Paediatrics, University of Medicine (1), Yangon, Myanmar.
D TrevisanutoAmici della Neonatologia Trentina, Trento, Italy ; Children and Women's Health Department, Medical School University of Padua, Padua, Italy.
A A ThinMandalay Children's Hospital (300), Mandalay, Myanmar.
A A TheinDepartment of Neonatology, University of Medicine (1), Yangon, Myanmar.
T DefechereuxDepartment of Surgery, Liege University Hospital, Liege, Belgium.
D KumaraThrive Networks, Oakland, CA USA.
L MocciaThrive Networks, Oakland, CA USA ; Amici della Neonatologia Trentina, Trento, Italy.
University Of Medicine 1 Yangon · MMProvincia Autonoma di Trento · ITThrive · USUniversity of Liège · BEUniversity of Padua · ITUNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundJaundice is the commonest neonatal ailment requiring treatment. Untreated, it can lead to acute bilirubin encephalopathy (ABE), chronic bilirubin encephalopathy (CBE) or death. ABE and CBE have been largely eliminated in industrialised countries, but remain a problem of largely undocumented scale in low resource settings. As part of a quality-improvement intervention in the Neonatal Care Units of two paediatric referral hospitals in Myanmar, hospitals collected de-identified data on each neonate treated on new phototherapy machines over 13-20 months. The information collected included: diagnosis of ABE at hospital presentation; general characteristics such as place of birth, source of referral, and sex; and a selection of suspected causes of jaundice including prematurity, infection, G6PD status, ABO and Rh incompatibility. This information was analysed to identify risk factors for hospital presentation with ABE, using multiple logistic regression.

resultsData on 251 neonates was recorded over 20 months in Hospital A, and 339 neonates over 13 months in Hospital B; the number of outborn neonates presenting with ABE was 32 (12.7 %) and 72 (21.2 %) respectively. In the merged dataset the final multivariate model identified the following independent risk and protective factors: home birth, ORadj = 2.3 (95 % CI: 1.04-5.4); self-referral, ORadj = 2.6 (95 % CI: 1.2-6.0); prematurity, ORadj = 0.40 (95 % CI: 0.18-0.85); and a significant interaction between hospital and screening status because screening positive for G6PD deficiency was a strong and significant risk factor at Hospital B (ORadj = 5.9; 95 % CI: 3.0-11.6), but not Hospital A (ORadj = 1.1; 95 % CI: 0.5-2.5).

conclusionThe study identifies home birth, self-referral and G6PD screening status as important risk factors for presentation with ABE; prematurity was protective, but this is interpreted as an artefact of the study design. As operational research, there is likely to be substantial measurement error in the risk factor data, suggesting that the identified risk factor estimates are robust. Additional interventions are required to ensure prompt referral of jaundiced neonates to treatment facilities, with particular focus on home births and communities with high rates of G6PD deficiency.

Indexed as

Acute Bilirubin EncephalopathyChronic Bilirubin EncephalopathyHyperbilirubinaemiaKernicterusNeonatal jaundice

Identifiers

PMID27057339
PMCPMC4823679
OpenAlexW2128146442

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.