Evidence map›Paper›PMID 42472790›Full record

ArticleBMC pediatrics2026

Subclinical cardiac dysfunction in preschool children with a history of bronchopulmonary dysplasia: a pilot cohort study.

Tuğba Kontbay Çetin, Ece Öztarhan, Sultan Kavuncuoğlu, Esin Yıldız Aldemir, Helen Bornaun, Merih Çetinkaya, Müge Payaslı, Sibel Özbek, Kazım Öztarhan

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Article in BMC 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

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Tuğba Kontbay ÇetinPediatric Endocrinology Department, Samsun Research and Training Hospital, Samsun, Turkiye, Turkey. tugbakontbay@gmail.com.
Ece ÖztarhanFaculty of Medicine University, Medical School, Yeditepe University, Istanbul, Turkey.
Sultan KavuncuoğluDepartment of Pediatrics, Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey.
Esin Yıldız AldemirDepartment of Pediatrics, Istanbul Çam and Sakura City Hospital, Istanbul, Turkey.
Helen BornaunDepartment of Pediatric Cardiology, İstanbul Kanuni Sultan Süleyman Research And Traning Hospital, Istanbul, Turkey.
Merih ÇetinkayaDepartment of Neonatalogy, Istanbul Çam and Sakura City Hospital, Istanbul, Turkey.
Müge PayaslıDepartment of Pediatrics, Istanbul Çam and Sakura City Hospital, Istanbul, Turkey.
Sibel ÖzbekDepartment of Neonatalogy, Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey.
Kazım ÖztarhanDepartment of Pediatric Cardiology, Istanbul Faculty of Medicine, Istanbul, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBronchopulmonary dysplasia (BPD) is a prevalent complication of prematurity associated with long-term respiratory and cardiovascular sequelae. While adolescent and adult outcomes have been extensively documented, early childhood cardiac function in BPD survivors remains poorly characterized. This study aimed to evaluate subclinical cardiac alterations in preschool-aged children with a history of BPD using detailed echocardiography and 24-hour Holter monitoring.

methodsIn this prospective cohort study, 122 children were classified into three groups: preschool children with BPD (≤ 32 weeks gestation or < 1500 g; Group 1), gestational age- and birth weight-matched preterm controls without BPD (Group 2), and healthy term controls (Group 3). Perinatal and neonatal data were extracted from medical records. Comprehensive echocardiography including M-mode, Doppler, and tissue Doppler imaging (TDI) assessed right and left ventricular systolic and diastolic function, interventricular septal mechanics, and myocardial performance index. Autonomic regulation was evaluated using 24-hour Holter monitoring. Statistical significance was defined as p < 0.05.

resultsDemographics including age, sex, height, and weight were comparable across groups. Chronic pulmonary changes on chest radiography were present in 31.25% of BPD children, significantly higher than in preterm controls (p = 0.013). Conventional systolic echocardiographic indices (ejection fraction, fractional shortening) were within normal limits in all groups. However, BPD children exhibited right ventricular diastolic dysfunction, with decreased E/A ratio, prolonged isovolumic relaxation time (IVRT), and altered systolic-diastolic timing. TDI revealed subclinical interventricular septal systolic impairment. Left ventricular systolic function was preserved, with mild prolongation of LV diastolic relaxation. No significant differences were observed in heart rate variability or blood pressure percentiles among groups.

conclusionsPreschool children with a history of BPD exhibit subclinical right ventricular and septal dysfunction despite preserved left ventricular systolic performance, normal autonomic regulation, and age-appropriate blood pressure. These findings highlight the early cardiovascular impact of BPD-related pulmonary pathology and underscore the importance of longitudinal cardiac surveillance in this high-risk population to guide preventive interventions.

Indexed as

Bronchopulmonary DysplasiaCase-Control StudiesChild, PreschoolCohort StudiesEchocardiographyElectrocardiography, AmbulatoryFemaleHumansInfant, NewbornMalePilot ProjectsProspective StudiesBronchopulmonary dysplasiaEchocardiographyHeart rate variabilityPrematurityPreschool childrenSubclinical cardiac dysfunction

Identifiers

PMID42472790
PMCPMC13647713

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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.