Evidence map›Paper›PMID 41649815›Full record

ArticleJAMA network open2026

Apgar Score Plus Umbilical Artery pH and Adverse Neonatal Outcomes in Very Preterm Infants.

Harald Ehrhardt, Soodabeh Behboodi, Rolf F Maier, Adrien M Aubert, Ulrika Ådén, Birte Staude, Elizabeth S Draper, Anna Gudmundsdottir, Veronica Siljehav, Heili Varendi and 4 more

Abstract readMulticenter Study
In one paragraph

Article in JAMA network open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

14 authors.

Harald EhrhardtDivision of Neonatology and Pediatric Intensive Care Medicine, Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Ulm, Germany.
Soodabeh BehboodiCentre for Research in Epidemiology and Statistics, Obstetrical, Perinatal and Pediatric Lifecourse Epidemiology, Université Paris Cité, Institut National de la Santé et de la Recherche Médicale, Institut National de la Recherche pour l'Agriculture, l'Alimentation et l'Environnement (INRAE), Paris, France.
Rolf F MaierChildren's Hospital, University Hospital, Philipps University Marburg, Marburg, Germany.
Adrien M AubertCentre for Research in Epidemiology and Statistics, Obstetrical, Perinatal and Pediatric Lifecourse Epidemiology, Université Paris Cité, Institut National de la Santé et de la Recherche Médicale, Institut National de la Recherche pour l'Agriculture, l'Alimentation et l'Environnement (INRAE), Paris, France.
Ulrika ÅdénDepartment of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Birte StaudeDivision of Neonatology and Pediatric Intensive Care Medicine, Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Ulm, Germany.
Elizabeth S DraperDepartment of Health Sciences, University of Leicester, Leicester, United Kingdom.
Anna GudmundsdottirDepartment of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Veronica SiljehavDepartment of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Heili VarendiUniversity of Tartu, Tartu University Hospital, Tartu, Estonia.
Tom WeberUniversity of Copenhagen, Copenhagen, Denmark.
Michael ZemlinHospital for General Pediatrics and Neonatology, Saarland University Medical Center, Homburg, Germany.
Jennifer ZeitlinCentre for Research in Epidemiology and Statistics, Obstetrical, Perinatal and Pediatric Lifecourse Epidemiology, Université Paris Cité, Institut National de la Santé et de la Recherche Médicale, Institut National de la Recherche pour l'Agriculture, l'Alimentation et l'Environnement (INRAE), Paris, France.
EPICE/SHIPS Research Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: The Apgar score, the first clinical assessment to direct measures to stabilize newborn infants, is also used for risk assessment. Its accuracy in estimating outcomes remains poor among very preterm (VPT) infants. Objective: To assess the utility of the combined 5-minute Apgar score and umbilical artery pH (UA-pH) for estimating risks of mortality and severe neonatal morbidity among VPT infants. Design, Setting, and Participants: This cohort study (Effective Perinatal Intensive Care in Europe [EPICE]) analyzed infants born at less than 32 weeks' gestation between April 2011 and September 2012 across 11 European countries. All liveborn VPT infants with Apgar scores and UA-pH data were included. Data were analyzed between February and December 2025. Exposures: Apgar score at 5 minutes and UA-pH. The Apgar score was classified as lower than 7 and 7 or higher, and the UA-pH values were categorized as low (<7.20) and normal (≥7.20). Four groups that combined these 2 measures were defined: Apgar score lower than 7 and low UA-pH; Apgar score lower than 7 and normal UA-pH; Apgar score 7 or higher and low UA-pH; and Apgar score 7 or higher and normal UA-pH. Main Outcomes and Measures: Combined outcome of mortality and/or any adverse morbidity (intraventricular hemorrhage [IVH] >grade 2, cystic periventricular leukomalacia, moderate or severe bronchopulmonary dysplasia [BPD], retinopathy of prematurity ≥stage 2, and necrotizing enterocolitis). Modified Poisson regression was used to estimate relative risks (RRs) between the exposure and the combined mortality and morbidity outcome and 3 individual components: mortality, IVH, and BPD. Models were adjusted for perinatal variables associated with Apgar score and UA-pH and adverse neonatal outcomes. Results: Of 7900 liveborn infants in the EPICE cohort, 4174 (52.8%) had information on Apgar score and UA-pH. These infants included 2249 males (53.9%) and had a median [IQR] gestational age of 29.9 [27.9-31.0] weeks and median [IQR] birth weight of 1240 [960-1520] g. A total of 367 infants (8.8%) had an Apgar score 7 or higher but a low UA-pH, 558 (13.4%) had an Apgar score lower than 7 but a normal UA-pH, and 196 (4.7%) had an Apgar score lower than 7 and a low UA-pH. Infants with an Apgar score lower than 7 had a higher frequency of the combined outcome among those with a normal UA-pH (270 [48.4%] vs 596 [19.5%]) and a low UA-pH (108 [55.1%] vs 596 [19.5%]), with similar adjusted RRs (ARRs; low: 1.4 [95% CI, 1.2-1.7]; normal: 1.4 [95% CI, 1.3-1.6]). For mortality risk, associations were robust for an Apgar score lower than 7 and a low UA-pH (ARR, 2.4; 95% CI, 1.7-3.3) and absent with an Apgar score of 7 or higher and a low UA-pH (ARR, 1.2; 95% CI, 0.8-1.8). IVH risk was increased in all 3 subcategories, including an Apgar score of 7 or higher with a low UA-pH (ARR, 2.0; 95% CI, 1.3-3.0). BPD risk was associated only with an Apgar score lower than 7 and a normal UA-pH (ARR, 1.4; 95% CI, 1.2-1.7). Conclusions and Relevance: In this cohort study of VPT infants, combining information on UA-pH with the 5-minute Apgar score was associated with improved accuracy in estimating the risk of some adverse outcomes-notably mortality and IVH, which occurred soon after birth. These results highlight the importance of exploring the associations of early markers of risk with neonatal mortality and key neonatal morbidities separately.

Indexed as

Apgar ScoreInfant, Extremely PrematureInfant, Premature, DiseasesUmbilical ArteriesCohort StudiesEnterocolitis, NecrotizingEuropeFemaleGestational AgeHumansHydrogen-Ion ConcentrationInfant MortalityInfant, NewbornMaleRisk Assessment

Identifiers

PMID41649815
PMCPMC12881985

What Socratic 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 Socratic graph.