Literature DB >> 20804952

The meaning of cost for families of children with congenital heart disease.

Jean Anne Connor1, Nancy E Kline, Sandra Mott, Sion Kim Harris, Kathy J Jenkins.   

Abstract

INTRODUCTION: The purpose of this study was to describe the cost burden of congenital heart disease (CHD) and the associated social impact as experienced by families.
METHOD: Qualitative methods were used to collect and interpret data. Semi-structured interviews were conducted with parents of children with various degrees of CHD complexity and socioeconomic status currently admitted for congenital heart surgery at a large tertiary care regional center.
RESULTS: The meaning of cost burden as defined by participants resulted in the emergence of two major categories, lifestyle change and uncertainty. Cost was described beyond monetary terms and as a result, data in each category were further clustered into three underlying subcategories labeled financial, emotional, and family burden. The child's disease complexity and parent's socioeconomic status seem to be linked to higher levels of stress experienced in terms of finances, emotional drain, and family member burden. Prenatal diagnosis was noted to trigger early discussion of financial uncertainty, often resulting in altered personal spending prior to birth. DISCUSSION: The cost experienced by parents of children with complex CHD was described as both life-changing and uncertain. Informing families of these types of additional stressors may allow issues of finances to be considered early in the overall preparation of caring for a child with complex CHD. Copyright 2010 National Association of Pediatric Nurse Practitioners. Published by Mosby, Inc. All rights reserved.

Entities:  

Mesh:

Year:  2010        PMID: 20804952     DOI: 10.1016/j.pedhc.2009.09.002

Source DB:  PubMed          Journal:  J Pediatr Health Care        ISSN: 0891-5245            Impact factor:   1.812


  21 in total

1.  Financial burdens and mental health needs in families of children with congenital heart disease.

Authors:  Nancy McClung; Jill Glidewell; Sherry L Farr
Journal:  Congenit Heart Dis       Date:  2018-04-06       Impact factor: 2.007

2.  Motivations and Features of Co-Parenting an Infant With Complex Congenital Heart Disease.

Authors:  Karen Pridham; Tondi M Harrison; Anne Chevalier McKechnie; Roger Brown
Journal:  West J Nurs Res       Date:  2017-06-09       Impact factor: 1.967

3.  Border Medicine: The Pediatric Cardiology Perspective.

Authors:  Ashutosh Agrawal; Sethuraman Swaminathan; Suvarna L Guvvala; Sudheer R Gorla
Journal:  Pediatr Cardiol       Date:  2019-07-25       Impact factor: 1.655

4.  Elevated hsa-miR-99a levels in maternal plasma may indicate congenital heart defects.

Authors:  Lars Kehler; Orsolya Biro; Levente Lazar; Janos Rigo; Balint Nagy
Journal:  Biomed Rep       Date:  2015-08-27

Review 5.  Familial impact and coping with child heart disease: a systematic review.

Authors:  Alun C Jackson; Erica Frydenberg; Rachel P-T Liang; Rosemary O Higgins; Barbara M Murphy
Journal:  Pediatr Cardiol       Date:  2015-01-25       Impact factor: 1.655

6.  Analysis of the psychosocial impact of caretaking on the parents of an infant with severe congenital heart defect.

Authors:  Jessica Lazar; Mark Justin Hylarides
Journal:  BMJ Case Rep       Date:  2017-03-16

Review 7.  What is Known About Critical Congenital Heart Disease Diagnosis and Management Experiences from the Perspectives of Family and Healthcare Providers? A Systematic Integrative Literature Review.

Authors:  S Watkins; O Isichei; T L Gentles; R Brown; T Percival; L Sadler; R Gorinski; S Crengle; E Cloete; M W M de Laat; F H Bloomfield; K Ward
Journal:  Pediatr Cardiol       Date:  2022-09-20       Impact factor: 1.838

8.  Social Risk Factors Impact Hospital Readmission and Outpatient Appointment Adherence for Children with Congenital Heart Disease.

Authors:  Abigail C Demianczyk; Shashank P Behere; Deepika Thacker; Maia Noeder; Emily A Delaplane; Christian Pizarro; Erica Sood
Journal:  J Pediatr       Date:  2018-10-23       Impact factor: 4.406

9.  Parent mental health and family functioning following diagnosis of CHD: a research agenda and recommendations from the Cardiac Neurodevelopmental Outcome Collaborative.

Authors:  Erica Sood; Amy Jo Lisanti; Sarah E Woolf-King; Jo Wray; Nadine Kasparian; Emily Jackson; Mary R Gregory; Keila N Lopez; Bradley S Marino; Trent Neely; Amy Randall; Sinai C Zyblewski; Cheryl L Brosig
Journal:  Cardiol Young       Date:  2021-06-04       Impact factor: 1.093

10.  Caregiving Strategies in Families of Children with Congenital Heart Disease: A Qualitative Study.

Authors:  Zahra Dalir; Zahra-Sadat Manzari; Hossein Kareshki; Abbas Heydari
Journal:  Iran J Nurs Midwifery Res       Date:  2021-01-18
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