Evidence map›Paper›PMID 42509017›Full record

ArticleBMJ paediatrics open2026

Neonatal encephalopathy mortality rate in Aotearoa, New Zealand: review of national data 2010-2020.

Malcolm Battin, Joseph Hii, Wendy Burgess, Jutta van den Boom, Gabrielle McDonald

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Article in BMJ paediatrics open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Malcolm BattinTe Whatu Ora-Te Toka Tumai, Newborn Service, Auckland, New Zealand malcolmb@adhb.govt.nz.ORCID http://orcid.org/0000-0001-9622-0523
Joseph HiiWomen's and Children's Health, University of Otago | Ōtākou Whakaihu Waka, Dunedin, New Zealand.
Wendy BurgessObstetrics and Gynaecology, Te Whatu Ora-Waitematā, Auckland, New Zealand.
Jutta van den BoomNewborn Services, Te Whatu Ora-Waikato, Hamilton, New Zealand.
Gabrielle McDonaldŌtākou Whakaihu Waka, Kōhatu-Centre for Hauora Māori, University of Otago, Dunedin, New Zealand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeonatal encephalopathy (NE) is a condition that affects newborn and can lead to long-term neurological impairments and death. Hypoxic ischaemic encephalopathy is the subset of NE with evidence of a hypoxic ischaemic insult. In Aotearoa New Zealand, national data have been collected for infants ≥37 weeks since 2010 and ≥35 weeks from 2016. Although the mortality rate associated with NE has not been a focus of annual reports, it is an important outcome for counselling whānau (families) and for international comparison.

methodsThe Perinatal and Maternal Mortality Review Committee (PMMRC) dataset was used to calculate mortality rate for cases of moderate/severe NE for two gestational groups, 35 weeks to 36 weeks+6 days (2016-20) and ≥37 weeks (2010-2020). Annual mortality rates in infants ≥37 weeks with NE for the period 2010-20 were calculated overall and by prioritised ethnic group.

resultsIn the PMMRC dataset, there was frequently a history of fetal distress or antenatal sentinel event with the vast majority of included infants having low Apgar scores and requiring resuscitation at birth. The mortality rate was 0.23/1000 births (95% CL 0.17-0.29) for infants ≥37 weeks with no significant change over the study period. The mortality rate for infants with NE between 35 and 36+6 weeks was 0.68/1000 births (95% CL 0.31-1.28), giving a relative risk of 2.99 in preterm compared with term infants with NE. No statistical difference in mortality by prioritised ethnic group was demonstrated.

conclusionsThere has been no improvement in mortality rates for infants with NE despite ongoing efforts to improve early recognition and treatment. Preterm infants were at significantly higher risk of death. The analysis did not demonstrate any ethnic differences in mortality associated with NE.

Indexed as

Hypoxia-Ischemia, BrainInfant MortalityFemaleGestational AgeHumansInfantInfant, NewbornMaleNew ZealandPregnancyEpidemiologyHypoxiaNeonatology

Identifiers

PMID42509017
PMCPMC13409086

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