Establishment of a condition-specific ...
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Title :
Establishment of a condition-specific quality-of-life questionnaire for children born with esophageal atresia aged 2–7 across 14 countries
Author(s) :
Dellenmark Blom, Michaela [Auteur]
Witt, Stefanie [Auteur]
Universitaetsklinikum Hamburg-Eppendorf = University Medical Center Hamburg-Eppendorf [Hamburg] [UKE]
Zendejas, Benjamin [Auteur]
Sabolić, Ivana [Auteur]
University Hospital Centre Zagreb
Porras-Hernandez, Juan Domingo [Auteur]
Durkin, Natalie [Auteur]
Eaton, Simon [Auteur]
Birketvedt, Kjersti [Auteur]
Sánchez Galán, Alba [Auteur]
Eszter Müller, Katalin [Auteur]
Rozensztrauch, Anna [Auteur]
Soyer, Tutku [Auteur]
LI, Siqi [Auteur]
Capital University of Medical Sciences [Beijing] [CUMS]
Fourtaka, Anastasia [Auteur]
Centre Hospitalier Régional Universitaire [CHU Lille] [CHRU Lille]
de Vos, Corne [Auteur]
Slater, Graham [Auteur]
Špoljarić, Ana [Auteur]
Bennett, John [Auteur]
Emblem, Ragnhild [Auteur]
Andrásdi, Zita [Auteur]
Smigiel, Robert [Auteur]
Patkowski, Dariusz [Auteur]
Ulukaya Durakbaşa, Çiğdem [Auteur]
Stilinovic, Marina [Auteur]
gottrand, Fréderic [Auteur]
Lille Inflammation Research International Center (LIRIC) - U995
Škrljak Šoša, Dora [Auteur]
Luetić, Tomislav [Auteur]
Gerus, Sylwester [Auteur]
yang, Shen [Auteur]
Zhao, Yong [Auteur]
Gu, Yichao [Auteur]
Li, Shuangshuang [Auteur]
Rodriguez-Alvirde, Diego [Auteur]
Kadenczki, Orsolya [Auteur]
Pasini, Miram [Auteur]
Vuokko, Wallace [Auteur]
Widenmann, Anke [Auteur]
Milagres Sikwete, Feliciana [Auteur]
Huang, Jinshi [Auteur]
Martínez Martínez, Leopoldo [Auteur]
Abrahamsson, Kate [Auteur]
Izadi, Shawn [Auteur]
M Ure, Benno [Auteur]
Sidler, Daniel [Auteur]
H Quitmann, Julia [Auteur]
Dingemann, Jens [Auteur]
Medizinische Hochschule Hannover = Hannover Medical School [MHH]
Witt, Stefanie [Auteur]
Universitaetsklinikum Hamburg-Eppendorf = University Medical Center Hamburg-Eppendorf [Hamburg] [UKE]
Zendejas, Benjamin [Auteur]
Sabolić, Ivana [Auteur]
University Hospital Centre Zagreb
Porras-Hernandez, Juan Domingo [Auteur]
Durkin, Natalie [Auteur]
Eaton, Simon [Auteur]
Birketvedt, Kjersti [Auteur]
Sánchez Galán, Alba [Auteur]
Eszter Müller, Katalin [Auteur]
Rozensztrauch, Anna [Auteur]
Soyer, Tutku [Auteur]
LI, Siqi [Auteur]
Capital University of Medical Sciences [Beijing] [CUMS]
Fourtaka, Anastasia [Auteur]
Centre Hospitalier Régional Universitaire [CHU Lille] [CHRU Lille]
de Vos, Corne [Auteur]
Slater, Graham [Auteur]
Špoljarić, Ana [Auteur]
Bennett, John [Auteur]
Emblem, Ragnhild [Auteur]
Andrásdi, Zita [Auteur]
Smigiel, Robert [Auteur]
Patkowski, Dariusz [Auteur]
Ulukaya Durakbaşa, Çiğdem [Auteur]
Stilinovic, Marina [Auteur]
gottrand, Fréderic [Auteur]

Lille Inflammation Research International Center (LIRIC) - U995
Škrljak Šoša, Dora [Auteur]
Luetić, Tomislav [Auteur]
Gerus, Sylwester [Auteur]
yang, Shen [Auteur]
Zhao, Yong [Auteur]
Gu, Yichao [Auteur]
Li, Shuangshuang [Auteur]
Rodriguez-Alvirde, Diego [Auteur]
Kadenczki, Orsolya [Auteur]
Pasini, Miram [Auteur]
Vuokko, Wallace [Auteur]
Widenmann, Anke [Auteur]
Milagres Sikwete, Feliciana [Auteur]
Huang, Jinshi [Auteur]
Martínez Martínez, Leopoldo [Auteur]
Abrahamsson, Kate [Auteur]
Izadi, Shawn [Auteur]
M Ure, Benno [Auteur]
Sidler, Daniel [Auteur]
H Quitmann, Julia [Auteur]
Dingemann, Jens [Auteur]
Medizinische Hochschule Hannover = Hannover Medical School [MHH]
Journal title :
Frontiers in Pediatrics
Abbreviated title :
Front. Pediatr.
Volume number :
11
Publisher :
Frontiers Media SA
Publication date :
2023-10-23
ISSN :
2296-2360
HAL domain(s) :
Sciences cognitives
English abstract : [en]
Esophageal atresia (EA) is a rare congenital anomaly characterized by a discontinuity of the esophagus. Following surgical repair, survival rates have improved dramatically the past decenniums and today exceed 90%, but the ...
Show more >Esophageal atresia (EA) is a rare congenital anomaly characterized by a discontinuity of the esophagus. Following surgical repair, survival rates have improved dramatically the past decenniums and today exceed 90%, but the children commonly present with esophageal and respiratory morbidity. In 2018, a condition-specific quality-of-life questionnaire for children with esophageal atresia (EA) aged 2–7 in Sweden-Germany was finalized (The EA-QOL questionnaire). The study aim was to describe the evaluation of the new translations across 12 new countries in Europe, Asia, Africa, Central-and North America.MethodsFollowing forward-backward translation into the new languages, the 17-item EA-QOL questionnaire was tested in cognitive debriefing interviews with parents of children with EA aged 2–7. Parents rated if each item was easy to understand (clarity) and sensitive to answer (interference with personal integrity). They could skip responding to a non-applicable/problematic item and give open comments. Predefined psychometric criteria were used; item clarity ≥80%/item sensitive to answer ≤20%/item feasibility ≤5% missing item responses. The decision to modify the translation was based on native expert, patient stakeholder, and instrument developer review, and the need for harmonization between translations.ResultsSimilar to findings in the Swedish-German cognitive debriefing, the cross-cultural analysis of input from 116 parents from 12 new countries (4–14 parents, median 9 parents/country) showed that all items in the EA-QOL questionnaire fulfilled the criteria for item clarity ≥80% and sensitive to answer (ranging from 1%-4.5%), although results varied between countries. Four items had missing responses between 5.2% and 13.4%, three within the same domain and were in line with parents’ explanations. Poor translations and feasibility were improved.ConclusionsBased on parent input, the collaboration between native experts, patient stakeholders, and instrument developers, a linguistic version of the EA-QOL questionnaire for children aged 2–7 for use in and across 14 countries has been established. These efforts have set the conditions for a cross-cultural field test of the EA-QOL questionnaire and will open the doors for a new chapter in outcome research, registries, and clinical practice concerning children with EA. In the long-term, this will help increase knowledge of the disease's burden, promote patient-centeredness, exchange of information between nations, and strengthen evidence-based treatments for children born with EA.Show less >
Show more >Esophageal atresia (EA) is a rare congenital anomaly characterized by a discontinuity of the esophagus. Following surgical repair, survival rates have improved dramatically the past decenniums and today exceed 90%, but the children commonly present with esophageal and respiratory morbidity. In 2018, a condition-specific quality-of-life questionnaire for children with esophageal atresia (EA) aged 2–7 in Sweden-Germany was finalized (The EA-QOL questionnaire). The study aim was to describe the evaluation of the new translations across 12 new countries in Europe, Asia, Africa, Central-and North America.MethodsFollowing forward-backward translation into the new languages, the 17-item EA-QOL questionnaire was tested in cognitive debriefing interviews with parents of children with EA aged 2–7. Parents rated if each item was easy to understand (clarity) and sensitive to answer (interference with personal integrity). They could skip responding to a non-applicable/problematic item and give open comments. Predefined psychometric criteria were used; item clarity ≥80%/item sensitive to answer ≤20%/item feasibility ≤5% missing item responses. The decision to modify the translation was based on native expert, patient stakeholder, and instrument developer review, and the need for harmonization between translations.ResultsSimilar to findings in the Swedish-German cognitive debriefing, the cross-cultural analysis of input from 116 parents from 12 new countries (4–14 parents, median 9 parents/country) showed that all items in the EA-QOL questionnaire fulfilled the criteria for item clarity ≥80% and sensitive to answer (ranging from 1%-4.5%), although results varied between countries. Four items had missing responses between 5.2% and 13.4%, three within the same domain and were in line with parents’ explanations. Poor translations and feasibility were improved.ConclusionsBased on parent input, the collaboration between native experts, patient stakeholders, and instrument developers, a linguistic version of the EA-QOL questionnaire for children aged 2–7 for use in and across 14 countries has been established. These efforts have set the conditions for a cross-cultural field test of the EA-QOL questionnaire and will open the doors for a new chapter in outcome research, registries, and clinical practice concerning children with EA. In the long-term, this will help increase knowledge of the disease's burden, promote patient-centeredness, exchange of information between nations, and strengthen evidence-based treatments for children born with EA.Show less >
Language :
Anglais
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
CHU Lille
Inserm
Université de Lille
Inserm
Université de Lille
Submission date :
2023-11-21T10:21:12Z
2023-11-24T07:36:07Z
2023-11-24T07:36:07Z
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