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Conference Paper: Long term functional outcomes and health-related quality of life in patients with esophageal atresia - a tertiary centre experience [Oral presentation]

TitleLong term functional outcomes and health-related quality of life in patients with esophageal atresia - a tertiary centre experience [Oral presentation]
Authors
Issue Date14-Apr-2025
Abstract

Purpose: This study evaluates the clinical outcomes and compares the quality of life in esophageal atresia patients over the past two decades. 

Method: Medical records of all esophageal atresia patients who received surgical repair between 1997-2021 in a tertiary center were reviewed to assess for associated anomalies and complications. Both patients and parents were invited to participate in health-related quality of life (HRQOL) studies either in person, via phone or online. The Pediatric Quality of Life Inventory Generic (Peds-QL) Core Scale Version 4.0 and Gastrointestinal Quality of Life Index (GIQLI) were used as generic and system-specific assessment tools respectively. Numeric values were expressed in medians (interquartile range).

Results: A total of 31 patients were eligible for the study. The median birth weight was 2470g (1935g-3075g). The smallest patient had a birth weight of 1360g. Primary repair was performed in 28 (90%) patients. Anastomotic leak was reported in two (6.5%) patients, both of them requiring revision surgery. Repeated endoscopic dilatation was required in 12 (38.7%) patients and seven (22.6%) required anti-reflux procedures. No statistically significant risk factor was found to be associated with the above complications. 

For the HRQOL assessment, our cohort of patients showed an overall score of 82.6 (60.5-94.6), physical score of 93.8 (71.9-100) and psychosocial score of 73.3 (54.6-95.8) when using the generic Peds-QL questionnaire. When using the system-specific GIQLI, they scored 83.7 (78.7-89.8). Both questionnaires do not show significant difference between survivors of esophageal atresia and the normal population matched for age and gender. 

Conclusion: Long term survivors of esophageal atresia demonstrated satisfactory HRQOL which is comparable to normal population in both generic and system-specific assessment tools. Post-operative complications which were treated did not appear to have a great impact on subsequent HRQOL. However, these patients may have psychosocial concerns that should be addressed. 


Persistent Identifierhttp://hdl.handle.net/10722/356037

 

DC FieldValueLanguage
dc.contributor.authorKum, VTL-
dc.contributor.authorWong, CWY-
dc.contributor.authorWong, KKY-
dc.date.accessioned2025-05-22T00:35:17Z-
dc.date.available2025-05-22T00:35:17Z-
dc.date.issued2025-04-14-
dc.identifier.urihttp://hdl.handle.net/10722/356037-
dc.description.abstract<div><p>Purpose: This study evaluates the clinical outcomes and compares the quality of life in esophageal atresia patients over the past two decades. </p><p>Method: Medical records of all esophageal atresia patients who received surgical repair between 1997-2021 in a tertiary center were reviewed to assess for associated anomalies and complications. Both patients and parents were invited to participate in health-related quality of life (HRQOL) studies either in person, via phone or online. The Pediatric Quality of Life Inventory Generic (Peds-QL) Core Scale Version 4.0 and Gastrointestinal Quality of Life Index (GIQLI) were used as generic and system-specific assessment tools respectively. Numeric values were expressed in medians (interquartile range).</p><p>Results: A total of 31 patients were eligible for the study. The median birth weight was 2470g (1935g-3075g). The smallest patient had a birth weight of 1360g. Primary repair was performed in 28 (90%) patients. Anastomotic leak was reported in two (6.5%) patients, both of them requiring revision surgery. Repeated endoscopic dilatation was required in 12 (38.7%) patients and seven (22.6%) required anti-reflux procedures. No statistically significant risk factor was found to be associated with the above complications. </p><p>For the HRQOL assessment, our cohort of patients showed an overall score of 82.6 (60.5-94.6), physical score of 93.8 (71.9-100) and psychosocial score of 73.3 (54.6-95.8) when using the generic Peds-QL questionnaire. When using the system-specific GIQLI, they scored 83.7 (78.7-89.8). Both questionnaires do not show significant difference between survivors of esophageal atresia and the normal population matched for age and gender. </p><p>Conclusion: Long term survivors of esophageal atresia demonstrated satisfactory HRQOL which is comparable to normal population in both generic and system-specific assessment tools. Post-operative complications which were treated did not appear to have a great impact on subsequent HRQOL. However, these patients may have psychosocial concerns that should be addressed. </p></div>-
dc.languageeng-
dc.relation.ispartof58th Annual Meeting of the Pacific Association of Pediatric Surgeons (13/04/2025-17/04/2025, Melbourne, Australia)-
dc.titleLong term functional outcomes and health-related quality of life in patients with esophageal atresia - a tertiary centre experience [Oral presentation]-
dc.typeConference_Paper-

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