Evidence map›Paper›PMID 42530659›Full record

ArticleEuropean journal of pediatrics2026

Long-term outcomes after previable pPROM: implications for counselling at the limit of viability.

Agnes Grill, Renate Fuiko, Raphaela Pichler, Sophie Jansen, Fanny Mikula, Alex Farr, Angelika Berger, Katharina Goeral

Abstract read
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Article in European journal of pediatrics, 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

What it found

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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

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3 · Its place in the literature

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4 · The record

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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.

Agnes GrillDivision of Neonatology, Intensive Care and Neuropediatrics, Department of Pediatrics and Adolescent Medicine, Comprehensive Center for Pediatrics, Medical University of Vienna, Vienna, Austria.
Renate FuikoDivision of Neonatology, Intensive Care and Neuropediatrics, Department of Pediatrics and Adolescent Medicine, Comprehensive Center for Pediatrics, Medical University of Vienna, Vienna, Austria.
Raphaela PichlerDivision of Neonatology, Intensive Care and Neuropediatrics, Department of Pediatrics and Adolescent Medicine, Comprehensive Center for Pediatrics, Medical University of Vienna, Vienna, Austria.
Sophie JansenDivision of Neonatology, Intensive Care and Neuropediatrics, Department of Pediatrics and Adolescent Medicine, Comprehensive Center for Pediatrics, Medical University of Vienna, Vienna, Austria.
Fanny MikulaDivision of Obstetrics and Feto-Maternal Medicine, Department of Obstetrics and Gynecology, Comprehensive Center for Pediatrics, Medical University of Vienna, Vienna, Austria.
Alex FarrDivision of Obstetrics and Feto-Maternal Medicine, Department of Obstetrics and Gynecology, Comprehensive Center for Pediatrics, Medical University of Vienna, Vienna, Austria.
Angelika BergerDivision of Neonatology, Intensive Care and Neuropediatrics, Department of Pediatrics and Adolescent Medicine, Comprehensive Center for Pediatrics, Medical University of Vienna, Vienna, Austria.
Katharina GoeralDivision of Neonatology, Intensive Care and Neuropediatrics, Department of Pediatrics and Adolescent Medicine, Comprehensive Center for Pediatrics, Medical University of Vienna, Vienna, Austria. katharina.goeral@meduniwien.ac.at.ORCID http://orcid.org/0000-0002-5209-6169

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of this study is to provide institution-specific, contemporary long-term outcome data to improve counselling at the limit of viability after previable preterm prelabour rupture of membranes (pPROM). This is a retrospective cohort study (2009-2022) of infants with pPROM < 23 + 0 weeks' gestation who received active neonatal care. Primary outcome was neurodevelopmental outcome at 24-36 months' corrected age. Among 109 infants, 33 (30.3%) died before discharge. Of 76 survivors, 13 (17.1%) were lost to follow-up and outcome data were available for 63/76 (82.9% follow-up). The mean gestational age was 21.6 weeks at pPROM and 25.7 weeks at delivery. Median Bayley-III scores were 90 (IQR 73-100) for cognition, 81 (IQR 63-97) for language, and 89 (IQR 65-100) for motor function. Cerebral palsy occurred in 11.1%. Survival without moderate or severe neurodevelopmental impairment (NDI) was 72.6%; moderate NDI occurred in 11.0% and severe NDI in 16.4%. Latency duration and gestational age at rupture were not significantly associated with outcome. Severe neonatal morbidity was associated with lower survival without moderate or severe NDI (57.6% vs. 89.7%). In multivariable analysis, gestational age at birth and female sex were associated with favourable outcomes in a perinatal model; after inclusion of major neonatal morbidities, only morbidity burden remained independently associated with outcome (OR 0.39, 95% CI 0.17-0.89).

conclusionA substantial proportion of survivors after pPROM < 23 weeks achieved favourable neurodevelopment at 2-3 years. In this cohort, latency duration and gestational age at membrane rupture were not independently associated with long-term neurodevelopmental outcome. However, any influence of antenatal factors may be mediated through neonatal morbidity. These findings support individualized counselling that considers both antenatal factors and the subsequent postnatal clinical course when discussing long-term prognosis. WHAT IS KNOWN: • Previable preterm prelabour rupture of membranes (pPROM) before 23 weeks' gestation is associated with high perinatal mortality and substantial risk of long-term neurodevelopmental impairment, but available follow-up data remain limited. • Previous studies have suggested that gestational age at membrane rupture and latency duration may influence survival, yet their association with long-term neurodevelopment among survivors remains unclear. WHAT IS NEW: • In this single-centre cohort with standardized Bayley-III follow-up, 72.6% of survivors survived without moderate or severe neurodevelopmental impairment, and 83.6% survived without severe impairment at 2-3 years' corrected age. • Neonatal morbidity burden, rather than gestational age at rupture or latency duration, was more closely associated with later neurodevelopmental outcome, highlighting the importance of the postnatal clinical course for prognostication and counselling.

Indexed as

CounselingNeurodevelopmental DisordersPremature Rupture of Fetal MembranesChild, PreschoolFemaleFetal ViabilityGestational AgeHumansInfantInfant, NewbornInfant, PrematureMalePregnancyRetrospective StudiesExtreme prematurityLimit of viabilityNeurodevelopmental outcomePreterm prelabour rupture of membranesPreviable pPROMSurvival

Identifiers

PMID42530659
PMCPMC13424032

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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 OpenQuestion graph.