Literature DB >> 22825406

Parental needs among children with birth defects: defining a parent-to-parent support network.

A M Mathiesen1, C J Frost, K M Dent, M L Feldkamp.   

Abstract

The objective of this study was to explore how a parent-to-parent support network could impact parents of a child with a structural birth defect by specifically looking at parents' continued needs, aspects influencing their participation in support networks, and their recommendations. Structural birth defects occur in approximately 3 % of all infants, representing a significant public health issue. For many reasons, parents are uniquely qualified to provide support to each other. Data were collected retrospectively through a qualitative approach of focus groups or one-on-one interviews. Thirty one parents of infants registered in the Utah Birth Defect Network participated in the study. Three themes emerged, "current sources and inconsistencies in parent-to-parent-support," "aspects that influence participation in parent-to-parent network," and "recommendations for a parent-to-parent program." Health care providers need to be aware of the services and inform parents about these options. A statewide parent-to-parent network integrated into all hospitals would be a valuable resource to facilitate sharing of issues related to caring for an infant or child with a birth defect.

Entities:  

Mesh:

Year:  2012        PMID: 22825406     DOI: 10.1007/s10897-012-9518-6

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  28 in total

1.  Rural/urban differences in access to and utilization of services among people in Alabama with sickle cell disease.

Authors:  Joseph Telfair; Akhlaque Haque; Marc Etienne; Shenghui Tang; Sheryl Strasser
Journal:  Public Health Rep       Date:  2003 Jan-Feb       Impact factor: 2.792

2.  What parents of seriously ill children value: parent-to-parent connection and mentorship.

Authors:  Shelley Cohen Konrad
Journal:  Omega (Westport)       Date:  2007

3.  A qualitative study of Parent to Parent support for parents of children with special needs. Consortium to evaluate Parent to Parent.

Authors:  J G Ainbinder; L W Blanchard; G H Singer; M E Sullivan; L K Powers; J G Marquis; B Santelli
Journal:  J Pediatr Psychol       Date:  1998-04

4.  Sex differences in help-seeking for alcohol problems--1. The barriers to help-seeking.

Authors:  B Thom
Journal:  Br J Addict       Date:  1986-12

5.  Children with special health care needs program: urban/rural comparisons.

Authors:  R M Saywell; T W Zollinger; M E Schafer; T M Schmit; J K Ladd
Journal:  J Rural Health       Date:  1993       Impact factor: 4.333

6.  Psychological distress in parents of children with severe congenital heart disease: the impact of prenatal versus postnatal diagnosis.

Authors:  C L Brosig; B N Whitstone; M A Frommelt; S J Frisbee; S R Leuthner
Journal:  J Perinatol       Date:  2007-08-23       Impact factor: 2.521

7.  Proximity of pediatric genetic services to children with birth defects in Texas.

Authors:  Amy P Case; Mark A Canfield; Ann Barnett; Patricia Raimondo; Margaret Drummond-Borg; Judith Livingston; Jenifer Kowalik
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2008-11

8.  Age-related parenting stress differences in mothers of children with spina bifida.

Authors:  Michelle M Macias; Conway F Saylor; Brandy P Rowe; Nancy L Bell
Journal:  Psychol Rep       Date:  2003-12

9.  Social support networks among families of children with craniofacial anomalies.

Authors:  B A Benson; A M Gross; S C Messer; G Kellum; L A Passmore
Journal:  Health Psychol       Date:  1991       Impact factor: 4.267

Review 10.  Parents' psychological adjustment in families of children with spina bifida: a meta-analysis.

Authors:  Ignace P R Vermaes; Jan M A M Janssens; Anna M T Bosman; Jan R M Gerris
Journal:  BMC Pediatr       Date:  2005-08-25       Impact factor: 2.125

View more
  4 in total

1.  Opinions of youngsters with congenital below-elbow deficiency, and those of their parents and professionals concerning prosthetic use and rehabilitation treatment.

Authors:  Ecaterina Vasluian; Ingrid G M de Jong; Wim G M Janssen; Margriet J Poelma; Iris van Wijk; Heleen A Reinders-Messelink; Corry K van der Sluis
Journal:  PLoS One       Date:  2013-06-24       Impact factor: 3.240

2.  The supportive care needs of parents with a child with a rare disease: results of an online survey.

Authors:  Lemuel J Pelentsov; Andrea L Fielder; Thomas A Laws; Adrian J Esterman
Journal:  BMC Fam Pract       Date:  2016-07-21       Impact factor: 2.497

3.  Caudal Duplication Syndrome Systematic Review-A Need for Better Multidisciplinary Surgical Approach and Follow-Up.

Authors:  Spătaru Radu-Iulian; Avino Adelaida; Iozsa Dan-Alexandru; Ivanov Monica; Serban Dragos; Tomescu Luminiţa Florentina; Cirstoveanu Cătălin
Journal:  Medicina (Kaunas)       Date:  2020-11-27       Impact factor: 2.430

4.  Insights from parents about caring for a child with birth defects.

Authors:  Jodi Lemacks; Kristin Fowles; Amanda Mateus; Kayte Thomas
Journal:  Int J Environ Res Public Health       Date:  2013-08-07       Impact factor: 3.390

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.