Literature DB >> 27055357

Psychosocial needs of children undergoing an invasive procedure for a CHD and their parents.

Eveline M Levert1, Willem A Helbing2, Karolijn Dulfer1, Ron T van Domburg3, Elisabeth M W J Utens1.   

Abstract

OBJECTIVE: The aim of this study was to investigate the psychosocial needs of both parents of children with CHD (aged 0-18 years) and patients themselves (aged 8-18 years) in the week before cardiac surgery or a catheter intervention. Patients Eligible participants included all consecutive patients (0-18 years) scheduled to undergo cardiac surgery or a catheter intervention in our hospital between March, 2012 and July, 2013. Psychosocial needs were assessed using a disease-specific questionnaire designed for this study, consisting of a 83-item parent version and a 59-item child version (for children ⩾8 years), each covering five domains: physical/medical, emotional, social, educational/occupational, and health behaviour; two items assessed from whom and in what format psychosocial care was preferred. Quality of life was also assessed. Interventions If parents/patients reported a need for psychosocial care, referral to adequate mental health-care professionals was arranged.
RESULTS: More than 40% of participating parents and >50% of participating children reported a need for psychosocial care on each of the five domains. Needs for psychosocial care for parents themselves were highest for those with children aged 0-12 years. Parents and patients report clear preferences when asked from whom and in what format they would like to receive psychosocial care. Quality of life was relatively high for both parents and patients. Psychosocial care interventions in our hospital increased significantly after the implementation of this study.
CONCLUSIONS: Results show that psychosocial care is rated as (very) important by both parents and children during an extremely stressful period of their life.

Entities:  

Keywords:  Children; congenital; heart; parents; psychosocial

Mesh:

Year:  2016        PMID: 27055357     DOI: 10.1017/S1047951116000391

Source DB:  PubMed          Journal:  Cardiol Young        ISSN: 1047-9511            Impact factor:   1.093


  9 in total

1.  Parents of Very Young Children with Congenital Heart Defects Report Good Quality of Life for Their Children and Families Regardless of Defect Severity.

Authors:  J S Lee; N Cinanni; N Di Cristofaro; S Lee; R Dillenburg; K B Adamo; T Mondal; N Barrowman; G Shanmugam; B W Timmons; P W Longmuir
Journal:  Pediatr Cardiol       Date:  2019-11-07       Impact factor: 1.655

Review 2.  Quality of life of parents with children with congenital abnormalities: a systematic review with meta-analysis of assessment methods and levels of quality of life.

Authors:  Marisa Garcia Rodrigues; Matilde Monteiro Soares; José Daniel Rodrigues; Luís Filipe Azevedo; Pedro Pereira Rodrigues; José Carlos Areias; Maria Emília Areias
Journal:  Qual Life Res       Date:  2021-09-05       Impact factor: 4.147

Review 3.  Mental Health Problems in Parents of Children with Congenital Heart Disease.

Authors:  Gerasimos A Kolaitis; Maya G Meentken; Elisabeth M W J Utens
Journal:  Front Pediatr       Date:  2017-05-08       Impact factor: 3.418

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.  Termination of pregnancy for fetal anomalies: Parents' preferences for psychosocial care.

Authors:  Frederike H W Dekkers; Attie T J I Go; Luuk Stapersma; Alex J Eggink; Elisabeth M W J Utens
Journal:  Prenat Diagn       Date:  2019-05-21       Impact factor: 3.050

6.  Patient information portal for congenital aortic and pulmonary valve disease: a stepped-wedge cluster randomised trial.

Authors:  Jonathan R G Etnel; Lidia R Bons; Frederiek De Heer; Daniëlle Robbers-Visser; Ingrid M Van Beynum; Bart Straver; Monique Rm Jongbloed; Philippine Kiès; Martijn G Slieker; Arie P J Van Dijk; Jolanda Kluin; Robin A Bertels; Elisabeth M W J Utens; Regina The; Eugene Van Galen; Barbara J M Mulder; Nico A Blom; Mark G Hazekamp; Jolien W Roos-Hesselink; Willem A Helbing; Ad J J C Bogers; Johanna J M Takkenberg
Journal:  Open Heart       Date:  2021-03

7.  The Role of Clinical Psychology and Peer to Peer Support in the Management of Chronic Medical Conditions - A Practical Example With Adults With Congenital Heart Disease.

Authors:  Edward Callus; Gabriella Pravettoni
Journal:  Front Psychol       Date:  2018-05-30

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.  The CHIP-Family study to improve the psychosocial wellbeing of young children with congenital heart disease and their families: design of a randomized controlled trial.

Authors:  Malindi van der Mheen; Ingrid M van Beynum; Karolijn Dulfer; Jan van der Ende; Eugène van Galen; Jorieke Duvekot; Lisette E Rots; Tabitha P L van den Adel; Ad J J C Bogers; Christopher G McCusker; Frank A Casey; Willem A Helbing; Elisabeth M W J Utens
Journal:  BMC Pediatr       Date:  2018-07-12       Impact factor: 2.125

  9 in total

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