Literature DB >> 28302658

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

Jessica Lazar1, Mark Justin Hylarides1.   

Abstract

This case report considers the psychosocial burden of caring for an infant with a severe congenital heart defect (CHD) on parents. Improved prenatal diagnostics and postnatal surgical intervention have created a new and increasing demographic of children and adults with CHDs that require lifelong medical care. For this reason, primary caregivers spend excessive amounts of time in hospitals and medical facilities, and must regularly decipher vast amounts of unfamiliar medical terminology and concepts with varying levels of assistance from medical personnel. This often leads to marked psychological morbidities in parental caregivers, such as stress, anxiety and depression. The financial cost of caring for infants with CHD, including loss of employment opportunities, is another important factor that impacts the quality of life of caregivers. Frequent and extended travel to seek specialised medical care, often at distant medical centres, represents an additional burden. 2017 BMJ Publishing Group Ltd.

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Mesh:

Year:  2017        PMID: 28302658      PMCID: PMC5372187          DOI: 10.1136/bcr-2016-218351

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  26 in total

1.  THE PATHOLOGIC ANATOMY OF TETRALOGY OF FALLOT AND ITS VARIATIONS.

Authors:  M LEV; F A ECKNER
Journal:  Dis Chest       Date:  1964-03

2.  Values parents apply to decision-making regarding delivery room resuscitation for high-risk newborns.

Authors:  Renee D Boss; Nancy Hutton; Leslie J Sulpar; Anna M West; Pamela K Donohue
Journal:  Pediatrics       Date:  2008-09       Impact factor: 7.124

3.  Psychosocial morbidity among parents of children with congenital heart disease: a prospective longitudinal study.

Authors:  Stephen Lawoko; Joaquim J F Soares
Journal:  Heart Lung       Date:  2006 Sep-Oct       Impact factor: 2.210

4.  Use of the Internet by parents of paediatric patients.

Authors:  Brynn K Wainstein; Katy Sterling-Levis; Sally A Baker; Jonathan Taitz; Michael Brydon
Journal:  J Paediatr Child Health       Date:  2006-09       Impact factor: 1.954

5.  Distress and hopelessness among parents of children with congenital heart disease, parents of children with other diseases, and parents of healthy children.

Authors:  Stephen Lawoko; Joaquim J F Soares
Journal:  J Psychosom Res       Date:  2002-04       Impact factor: 3.006

6.  Quality of life among parents of children with congenital heart disease, parents of children with other diseases and parents of healthy children.

Authors:  S Lawoko; J J F Soares
Journal:  Qual Life Res       Date:  2003-09       Impact factor: 4.147

Review 7.  Parent education after newborn congenital heart surgery.

Authors:  Sherry Pye; Angela Green
Journal:  Adv Neonatal Care       Date:  2003-06       Impact factor: 1.968

8.  Maternal experiences making a decision about heart surgery for their young children with congenital heart disease.

Authors:  Shu-Fan Lan; Pei-Fan Mu; Kai-Sheng Hsieh
Journal:  J Clin Nurs       Date:  2007-12       Impact factor: 3.036

9.  Children subjected to cardiac surgery for congenital heart disease. Part 2 - parental emotional experiences.

Authors:  Samuel Menahem; Zeffie Poulakis; Margot Prior
Journal:  Interact Cardiovasc Thorac Surg       Date:  2008-05-19

10.  Effects of nonlocal geographically separated hospitalizations upon families.

Authors:  Janice B Agazio; Paula Ephraim; Norma J Flaherty; Cynthia A Gurney
Journal:  Mil Med       Date:  2003-10       Impact factor: 1.437

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