Literature DB >> 23689265

Development and validation of a celiac disease quality of life instrument for North American children.

Nicole E Jordan1, Yuelin Li, Danielle Magrini, Suzanne Simpson, Norelle Rizkalla Reilly, Amy R Defelice, Robbyn Sockolow, Peter H R Green.   

Abstract

OBJECTIVE: Given the social constraints imposed by a gluten-free diet, it can be hypothesized that children with celiac disease (CD) living in the United States have a reduced health-related quality of life (HRQOL); however, there is no validated CD-specific HRQOL instrument for children living in the United States. The goals of this study were to develop and validate a CD-specific HRQOL instrument for children 8 to 18 years of age with CD and to report HRQOL in these children using both generic- and disease-specific instruments.
METHODS: This was a prospective study using focus group methodology to develop a CD-specific HRQOL instrument that was then administered to children 8 to 18 years of age with CD living throughout the United States. Instrument validation methods included construct, convergent, and divergent validities.
RESULTS: Two instruments were developed: CD-specific pediatric HRQOL instrument (CDPQOL) 8 to 12 and CDPQOL 13 to 18. A total of 181 children with CD completed the CDPQOL as well as a comparator generic instrument. Exploratory factor analysis restructured the CDPQOL and reduced the total number of items. The CDPQOL showed a moderate agreement with the Psychosocial dimensions of the generic instrument confirming convergent validity and low-to-moderate agreement with the Physical Health Summary dimension of the generic instrument confirming divergent validity.
CONCLUSIONS: The CDPQOL, consisting of 13 to 17 questions, is a validated instrument for the measurement of HRQOL in children 8 to 18 years of age with CD living in the United States.

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Year:  2013        PMID: 23689265     DOI: 10.1097/MPG.0b013e31829b68a1

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   2.839


  10 in total

1.  Hypervigilance to a Gluten-Free Diet and Decreased Quality of Life in Teenagers and Adults with Celiac Disease.

Authors:  Randi L Wolf; Benjamin Lebwohl; Anne R Lee; Patricia Zybert; Norelle R Reilly; Jennifer Cadenhead; Chelsea Amengual; Peter H R Green
Journal:  Dig Dis Sci       Date:  2018-01-31       Impact factor: 3.199

Review 2.  Psychological morbidity of celiac disease: A review of the literature.

Authors:  Fabiana Zingone; Gillian L Swift; Timothy R Card; David S Sanders; Jonas F Ludvigsson; Julio C Bai
Journal:  United European Gastroenterol J       Date:  2015-04       Impact factor: 4.623

3.  A comprehensive questionnaire for the assessment of health-related quality of life in coeliac disease (CDQL).

Authors:  Halfdan Skjerning; Jonathan Hourihane; Steffen Husby; Audrey DunnGalvin
Journal:  Qual Life Res       Date:  2017-07-05       Impact factor: 4.147

4.  Diminished quality of life among adolescents with coeliac disease using maladaptive eating behaviours to manage a gluten-free diet: a cross-sectional, mixed-methods study.

Authors:  J W Cadenhead; R L Wolf; B Lebwohl; A R Lee; P Zybert; N R Reilly; J Schebendach; R Satherley; P H R Green
Journal:  J Hum Nutr Diet       Date:  2019-03-05       Impact factor: 3.089

5.  Turkish Validity-Reliability Study of the Celiac Disease-Specific Pediatric Quality of Life Scale.

Authors:  Cemal Koçak; Semih Sandal; Meltem Çöl; Aydan Kansu Tanca; Zarife Kuloğlu; Ceyda Tuna Kırsaçlıoğlu
Journal:  Turk J Gastroenterol       Date:  2022-03       Impact factor: 1.555

Review 6.  Activities, Participation and Quality of Life Concepts in Children and Adolescents with Celiac Disease: A Scoping Review.

Authors:  Sonya Meyer; Sara Rosenblum
Journal:  Nutrients       Date:  2017-08-24       Impact factor: 5.717

7.  Development and Validation of the Celiac Disease-Children's Activities Report (CD-Chart) for Promoting Self-Management among Children and Adolescents.

Authors:  Sonya Meyer; Sara Rosenblum
Journal:  Nutrients       Date:  2017-10-17       Impact factor: 5.717

8.  Health-related quality of life using specific and generic questionnaires in Spanish coeliac children.

Authors:  Josefa Barrio; Maria Luz Cilleruelo; Enriqueta Román; Cristina Fernández
Journal:  Health Qual Life Outcomes       Date:  2020-07-25       Impact factor: 3.186

9.  Outcome measures in coeliac disease trials: the Tampere recommendations.

Authors:  Jonas F Ludvigsson; Carolina Ciacci; Peter Hr Green; Katri Kaukinen; Ilma R Korponay-Szabo; Kalle Kurppa; Joseph A Murray; Knut Erik Aslaksen Lundin; Markku J Maki; Alina Popp; Norelle R Reilly; Alfonso Rodriguez-Herrera; David S Sanders; Detlef Schuppan; Sarah Sleet; Juha Taavela; Kristin Voorhees; Marjorie M Walker; Daniel A Leffler
Journal:  Gut       Date:  2018-02-13       Impact factor: 23.059

10.  Assessing Health-Related Quality of Life in Children with Coeliac Disease: The Italian Version of CDDUX.

Authors:  Marco Crocco; Angela Calvi; Paolo Gandullia; Federica Malerba; Anthea Mariani; Sonia Di Profio; Barbara Tappino; Stefano Bonassi
Journal:  Nutrients       Date:  2021-02-02       Impact factor: 5.717

  10 in total

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