Follow-up and transition practices in esophageal atresia: a review of European Reference Network on rare Inherited and Congenital Anomalies (ERNICA) centres and affiliates
- PMID: 39521743
- PMCID: PMC11550284
- DOI: 10.1007/s00383-024-05865-z
Follow-up and transition practices in esophageal atresia: a review of European Reference Network on rare Inherited and Congenital Anomalies (ERNICA) centres and affiliates
Abstract
Purpose: The purpose of this study was to understand the provision and distribution of esophageal atresia (EA) follow-up (FU) and transition services across European Reference Network for rare Inherited and Congenital Anomalies (ERNICA) member and affiliate centers.
Methods: A REDCap questionnaire was sent to clinical leads of 18 ERNICA members and 14 affiliate centers.
Results: 29 of 32 centers responded (91%), the majority of which were highly specialized. Two-thirds had a dedicated EA clinic with a specialist multi-disciplinary team (MDT), offered to selected/complex patients only in 40% of centers. ERNICA centers were more likely to offer an MDT FU clinic than affiliates, with lack of resources most cited as a barrier to uptake (67%). Delivery of routine investigations was heterogeneous, particularly provision of three endoscopies over the course of FU (24%). Only 55% had a dedicated transition pathway, more prevalent in ERNICA centers (81% vs. 30%; p < 0.01). Self-reported awareness of ERNICA and European Society for Pediatric Gastroenterology Hepatology and Nutrition (ESPGHAN) guidance for FU and transition was poor (28%).
Conclusion: Despite the existence of European follow-up and transition guidelines, their delivery is not uniform and may be limited by lack of awareness of the guidelines and a lack of resources.
Keywords: Esophageal atresia; European reference networks; Follow-up; Transition.
© 2024. The Author(s).
Conflict of interest statement
The authors declare no competing interests.
Figures
References
-
- Dellenmark-Blom M, Quitmann J, Dingemann C (2020) Health-related quality of life in patients after repair of esophageal atresia: a review of current literature. Eur J Pediatr Surg 30:239–250. 10.1055/s-0040-1710389 - PubMed
-
- Gallo G, van van Tuyll Serooskerken ES, Tytgat S, van der Zee DC, Keyzer-Dekker CMG, Zwaveling S, Hulscher JBF, Groen H, Lindeboom MYA (2021) Quality of life after esophageal replacement in children. J Pediatr Surg 56:239–244. 10.1016/j.jpedsurg.2020.07.014 - PubMed
-
- Svoboda E, Fruithof J, Widenmann-Grolig A, Slater G, Armand F, Warner B, Eaton S, De Coppi P, Hannon E (2018) A patient led, international study of long term outcomes of esophageal atresia: EAT 1. J Pediatr Surg 53:610–615. 10.1016/j.jpedsurg.2017.05.033 - PubMed
-
- Connor MJ, Springford LR, Kapetanakis VV, Giuliani S (2015) Esophageal atresia and transitional care–step 1: a systematic review and meta-analysis of the literature to define the prevalence of chronic long-term problems. Am J Surg 209:747–759. 10.1016/j.amjsurg.2014.09.019 - PubMed
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
