Evidence map›Paper›PMID 35999380›Full record

ArticlePediatric research2023

Adverse short- and long-term outcomes among infants with mild neonatal encephalopathy.

Vishnu-Priya Akula, Achyuth Sriram, Sherian Xu, Eileen Walsh, Krisa Van Meurs, Matthew Cranshaw, Michael W Kuzniewicz

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Pediatric research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Vishnu-Priya AkulaDepartment of Pediatrics, Kaiser Permanente East Bay, Walnut Creek, CA, USA. Vishnu-priya.s.akula@kp.org.
Achyuth SriramKaiser Permanente Northern California Residency Program, Oakland, CA, USA.
Sherian XuDivision of Research, Kaiser Permanente Northern California, Oakland, CA, USA.
Eileen WalshDivision of Research, Kaiser Permanente Northern California, Oakland, CA, USA.
Krisa Van MeursDepartment of Pediatrics, Stanford University School of Medicine, Palo Alto, CA, USA.
Matthew CranshawKaiser Permanente Northern California Residency Program, Oakland, CA, USA.
Michael W KuzniewiczDivision of Research, Kaiser Permanente Northern California, Oakland, CA, USA.
Kaiser Permanente · USKaiser Permanente Walnut Creek Medical Center · USStanford University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStudies in newborns with mild neonatal encephalopathy (mNE) demonstrated normal outcomes, but recent literature suggests otherwise.

methodsThis retrospective cohort study examined inborn infants between 2014 and 2017. Biochemical and clinical characteristics determined the presence of NE and an encephalopathy score categorized infants as Definite or Possible mNE. An Unexposed control group consisted of newborns not meeting the inclusion criteria. Long-term outcomes assessed included cerebral palsy, seizures, developmental disorder, and motor and speech delay. The association of mNE with seizure disorder by 3 years of age was assessed with logistic regression and developmental disorders with Cox proportional hazards models.

resultsOf the 156,501 births, we identified 130 with Definite mNE and 445 with Possible mNE (0.8 and 2.8 per 1000 births, respectively). Both groups had significantly higher rates of any developmental disorder and motor and speech delay when compared to the Unexposed (p < 0.05, except for p = 0.07 for motor delay in the Possible NE group). The Definite mNE group had higher rates of developmental disorder and motor and speech delay when compared to the Unexposed with hazard ratios (95% CI) 2.0 (1.2-3.2), 3.7 (1.5-8.8), and 2.1 (1.3-3.5), respectively.

conclusionsAn estimate of short- and long-term consequences of mNE suggests that there may be a higher risk of adverse outcome. IMPACT: Infants with mild NE are at significant risk for adverse short- and long-term outcomes. The risk of having an abnormal long-term outcome at 3 years of age were doubled in the mild NE group compared to the Unexposed group. Randomized clinical trials are needed as neuroprotective strategies may mitigate these.

Indexed as

Brain DiseasesCerebral PalsyInfant, Newborn, DiseasesLanguage Development DisordersHumansInfantInfant, NewbornInfant, PrematureRetrospective Studies

Identifiers

PMID35999380
OpenAlexW4292836186

What OpenQuestion holds

Textmetadata
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.