Literature DB >> 22357782

Measuring knowledge of patients with congenital heart disease and their parents: validity of the 'Leuven Knowledge Questionnaire for Congenital Heart Disease'.

Hsiao-Ling Yang1, Yueh-Chih Chen, Jou-Kou Wang, Bih-Shya Gau, Chi-Wen Chen, Philip Moons.   

Abstract

BACKGROUND: Patients with congenital heart disease (CHD) and their parents need to have sufficient knowledge on their condition, treatment, medication, and preventive measures. The Leuven Knowledge Questionnaire for Congenital Heart Disease (LKQCHD) was developed to comprehensively measure the level of knowledge in patients with CHD. AIMS: This study aimed to translate the LKQCHD into Chinese and to test its validity to be used in patients with CHD and their parents.
METHOD: Questionnaire translation was guided by a three-step linguistic validation method. Evidence based on test content and on relation with other variables was obtained. For test content, we included five experts in CHD and research methods. Furthermore, the instrument was tested in 89 pairs of adolescents with CHD and their parents.
RESULTS: We found a high item-level content validity index (>0.78 in all except two items), high scale-level content validity index (>0.90), high free-marginal multirater Kappa (>0.75), and low average proportion of missing values (0.49% in adolescents; 0.51% in parents), showing an excellent content validity. The hypothesized positive correlations between parental knowledge and parental educational level and between patient's knowledge and patient's age, as well as the hypothesis that parents have more knowledge than their children, were confirmed. This provides validity evidence based on relation with other variables.
CONCLUSIONS: The Chinese version of the LKQCHD is valid to assess the level of knowledge in patients with CHD and their parents.

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Year:  2012        PMID: 22357782     DOI: 10.1177/1474515111429662

Source DB:  PubMed          Journal:  Eur J Cardiovasc Nurs        ISSN: 1474-5151            Impact factor:   3.908


  9 in total

1.  Disease knowledge, perceived risk, and health behavior engagement among adolescents and adults with congenital heart disease.

Authors:  Jamie L Jackson; Kelly Tierney; Curt J Daniels; Kathryn Vannatta
Journal:  Heart Lung       Date:  2014-09-30       Impact factor: 2.210

2.  The role of illness uncertainty in the relationship between disease knowledge and patient-reported outcomes among adolescents and adults with congenital heart disease.

Authors:  Steven E Schiele; Charles F Emery; Jamie L Jackson
Journal:  Heart Lung       Date:  2018-11-22       Impact factor: 2.210

3.  Antecedents of self-care in adults with congenital heart defects.

Authors:  Nancy McCabe; Sandra B Dunbar; Javed Butler; Melinda Higgins; Wendy Book; Carolyn Reilly
Journal:  Int J Cardiol       Date:  2015-08-16       Impact factor: 4.164

4.  Person-centred transition programme to empower adolescents with congenital heart disease in the transition to adulthood: a study protocol for a hybrid randomised controlled trial (STEPSTONES project).

Authors:  Mariela Acuña Mora; Carina Sparud-Lundin; Ewa-Lena Bratt; Philip Moons
Journal:  BMJ Open       Date:  2017-04-17       Impact factor: 2.692

5.  Development of an Online, Evidence-Based Patient Information Portal for Congenital Heart Disease: A Pilot Study.

Authors:  Jonathan R G Etnel; Arie P J van Dijk; Jolanda Kluin; Robin A Bertels; Elisabeth M W J Utens; Eugene van Galen; Ad J J C Bogers; Johanna J M Takkenberg
Journal:  Front Cardiovasc Med       Date:  2017-05-01

6.  Impact of a transition education program on health-related quality of life in pediatric patients with congenital heart disease: study design for a randomised controlled trial.

Authors:  Oscar Werner; Charlene Bredy; Kathleen Lavastre; Sophie Guillaumont; Gregoire De La Villeon; Marie Vincenti; Cristelle Gerl; Yves Dulac; Nathalie Souletie; Philippe Acar; Laurence Pages; Marie-Christine Picot; Gerard Bourrel; Agnes Oude Engberink; Elodie Million; Hamouda Abassi; Pascal Amedro
Journal:  Health Qual Life Outcomes       Date:  2021-01-19       Impact factor: 3.186

Review 7.  Advances in Managing Transition to Adulthood for Adolescents With Congenital Heart Disease: A Practical Approach to Transition Program Design: A Scientific Statement From the American Heart Association.

Authors:  Anitha S John; Jamie L Jackson; Philip Moons; Karen Uzark; Andrew S Mackie; Susan Timmins; Keila N Lopez; Adrienne H Kovacs; Michelle Gurvitz
Journal:  J Am Heart Assoc       Date:  2022-03-17       Impact factor: 6.106

8.  Patient and physician view on patient information and decision-making in congenital aortic and pulmonary valve surgery.

Authors:  Jonathan R G Etnel; Willem A Helbing; Jolien W Roos-Hesselink; Regina The; Ad J J C Bogers; Johanna J M Takkenberg
Journal:  Open Heart       Date:  2018-11-10

9.  Translation, cross-cultural adaptation, and validation of the Leuven Knowledge Questionnaire for congenital heart disease instrument into Brazilian Portuguese.

Authors:  Fátima Helena Cecchetto; Giuseppe Dick Bonato; Thaís Sena Mombach Barreto; Fernando Riegel; Lúcia Campos Pellanda
Journal:  J Pediatr (Rio J)       Date:  2020-08-09       Impact factor: 2.990

  9 in total

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