Literature DB >> 22964588

An evaluation of disease knowledge in dyads of parents and their adolescent children with congenital heart disease.

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

Abstract

BACKGROUND: Congenital heart disease (CGHD) can be considered a chronic disease for many patients. To adopt a healthy lifestyle and to avoid complications, patients with CGHD and their parents need to have good knowledge of the heart defect and its consequences.
OBJECTIVE: The aims of this study were to evaluate patient and parental knowledge of CGHD and to explore the related factors of their respective disease knowledge.
METHODS: This study included 116 dyads of adolescents with CGHD (43.1% male adolescents; aged 12-18 years) and one of their parents (79.3% mothers; median age, 46 years). All participants completed the Leuven Knowledge Questionnaire for Congenital Heart Disease, and then we calculated a correct rate score to determine the overall disease knowledge of the respondents.
RESULTS: The correct rate score was 38.8% for adolescents with CGHD and 51.4% for parents (t = 7.69; P < .001). The only determinant of knowledge in parents was their educational level (standardized estimate = 6.160, P < .001). In adolescents, knowledge was determined by age (standardized estimate = 2.242, P = .002) and parental knowledge (standardized estimate = 0.311, P < .001).
CONCLUSIONS: Although parents have significantly greater disease knowledge than their children do, the level of knowledge in both parents and adolescents is suboptimal. Because parents' knowledge influenced their adolescents' knowledge, educational interventions should target both adolescent patients and parents. Transition programs can play a pivotal role in this respect.

Entities:  

Mesh:

Year:  2013        PMID: 22964588     DOI: 10.1097/JCN.0b013e318260c308

Source DB:  PubMed          Journal:  J Cardiovasc Nurs        ISSN: 0889-4655            Impact factor:   2.083


  9 in total

1.  Readiness for Transition to Adult Health Care for Young Adolescents with Congenital Heart Disease.

Authors:  Kimberly T Stewart; Nita Chahal; Adrienne H Kovacs; Cedric Manlhiot; Ahlexxi Jelen; Tanveer Collins; Brian W McCrindle
Journal:  Pediatr Cardiol       Date:  2017-02-10       Impact factor: 1.655

2.  Adolescent Women with Congenital Heart Disease: Self-Reported Reproductive Health Discussions with Health Care Providers.

Authors:  Amy J Katz; Shannon Lyon; Anne G Farrell; Nayan Srivastava; Tracey A Wilkinson; Marcia L Shew
Journal:  J Pediatr Adolesc Gynecol       Date:  2022-01-06       Impact factor: 2.046

3.  Effectiveness of a decision aid for patients with depression: A randomized controlled trial.

Authors:  Lilisbeth Perestelo-Perez; Amado Rivero-Santana; Juan Antonio Sanchez-Afonso; Jeanette Perez-Ramos; Carmen Luisa Castellano-Fuentes; Karen Sepucha; Pedro Serrano-Aguilar
Journal:  Health Expect       Date:  2017-03-10       Impact factor: 3.377

4.  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

5.  Improving Transitions of Care for Young Adults With Congenital Heart Disease: Mobile App Development Using Formative Research.

Authors:  Keila N Lopez; Michael O'Connor; Jason King; James Alexander; Melissa Challman; Donna K Lovick; Nicole Goodly; Amelia Smith; Elliott Fawcett; Courtney Mulligan; Debbe Thompson; Michael Fordis
Journal:  JMIR Form Res       Date:  2018-01-29

6.  Efficacy of a Transitional Support Program Among Adolescent Patients With Childhood-Onset Chronic Diseases: A Randomized Controlled Trial.

Authors:  Mayumi Morisaki-Nakamura; Seigo Suzuki; Asuka Kobayashi; Sachiko Kita; Iori Sato; Miwa Iwasaki; Yoichiro Hirata; Atsushi Sato; Akira Oka; Kiyoko Kamibeppu
Journal:  Front Pediatr       Date:  2022-03-31       Impact factor: 3.418

7.  The process of transition from pediatric to adult healthcare services for nephrological patients: Recommendations vs. reality-A single center experience.

Authors:  Dorella Scarponi; Gabriella Cangini; Andrea Pasini; Claudio La Scola; Francesca Mencarelli; Cristina Bertulli; Domenico Amabile; Marco Busutti; Gaetano La Manna; Andrea Pession
Journal:  Front Pediatr       Date:  2022-08-23       Impact factor: 3.569

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

北京卡尤迪生物科技股份有限公司 © 2022-2023.