Evidence map›Paper›PMID 42459567›Full record

ArticleFrontiers in pediatrics2026

Disease-specific quality of life after thoracoscopic repair of esophageal atresia: a single-centre cross-sectional study.

Marcin Łosin, Weronika Lotkowska, Oliwer Sowulewski, Maciej Zagierski, Agnieszka Szlagatys-Sidorkiewicz, Piotr Czauderna

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Article in Frontiers in 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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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

6 authors.

Marcin ŁosinDepartment of Surgery and Urology for Children and Adolescents, Medical University of Gdańsk, Gdańsk, Poland.
Weronika LotkowskaDepartment of Surgery and Urology for Children and Adolescents, Medical University of Gdańsk, Gdańsk, Poland.
Oliwer SowulewskiDepartment of Paediatrics, Gastroenterology, Allergology & Paediatric Nutrition, Medical University of Gdańsk, Gdańsk, Poland.
Maciej ZagierskiDepartment of Paediatrics, Gastroenterology, Allergology & Paediatric Nutrition, Medical University of Gdańsk, Gdańsk, Poland.
Agnieszka Szlagatys-SidorkiewiczDepartment of Paediatrics, Gastroenterology, Allergology & Paediatric Nutrition, Medical University of Gdańsk, Gdańsk, Poland.
Piotr CzaudernaDepartment of Surgery and Urology for Children and Adolescents, Medical University of Gdańsk, Gdańsk, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Survival after esophageal atresia (EA) repair now exceeds 90%, yet little is known about long-term quality of life in patients treated with thoracoscopy as the primary intended approach. Most published cohorts mix open and thoracoscopic approaches, making it difficult to disentangle disease-related impairment from approach-related morbidity. We set out to describe disease-specific health-related quality of life (HRQoL) in a cohort managed by thoracoscopy as the primary intended approach, compare our data with European reference values, and explore child-parent agreement. Methods: Cross-sectional survey of 25 respondents (response rate 56%) from 51 children who underwent EA repair with thoracoscopy as the intended primary approach [7 (14%) required intraoperative conversion to open thoracotomy and were retained under an intention-to-treat principle] at a single Polish centre (2006-2025). The validated Polish EA-QOL questionnaire was administered: parent proxy for children aged 2-7 years ( Results: Overall QoL% ranged from 76% to 79% across age groups. Eating difficulties were the most impaired domain in every questionnaire version (QoL%: 63%-70%), driven largely by problems with food consistency. No domain score differed from reference data after Bonferroni correction, though the Body and Scar domain in older children showed a borderline signal ( Conclusions: In this single-centre cohort managed by thoracoscopy as the primary intended approach, disease-specific HRQoL was generally preserved, with eating-related difficulties as the dominant area of residual impairment. These findings add to the limited literature on approach-specific outcomes in EA and support routine long-term monitoring of food texture tolerance and reflux burden.

Indexed as

EA-QOL questionnaireeating difficultiesesophageal atresia (EA)quality of lifethoracoscopy (VATS)

Identifiers

PMID42459567
PMCPMC13369439

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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.