Literature DB >> 20384476

Exploring parent-sibling communication in families of children with sickle cell disease.

J Carolyn Graff1, Jane S Hankins, Belinda T Hardy, Heather R Hall, Ruth J Roberts, Susan L Neely-Barnes.   

Abstract

BACKGROUND: Communication within families of children with sickle cell disease is important yet has not been adequately investigated.
METHODS: Focus group interviews were conducted with parents of children with sickle cell disease to explore parent-sibling communication about sickle cell disease.
RESULTS: Communication was influenced by attributes and behaviors of the parent, the child with sickle cell disease, and the sibling; extended family, neighbors, friends, and church members or social networks; and available, accessible resources related to the child's health, child's school, and parent employment. Outcomes that influenced and were influenced by factors within and outside the parent-sibling dyad and nuclear family included parent satisfaction, parent roles, family intactness, and status attainment.
CONCLUSIONS: These findings support previous research with African-American families and expand our views of the importance of educating parents, family members, and others about sickle cell disease. The findings suggest a need to explore sibling perception of this communication, parent and sibling perception of the impact of frequent hospitalizations and clinic visits on the sibling and family, and variations within families of children with sickle cell disease.

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Mesh:

Year:  2010        PMID: 20384476      PMCID: PMC3171801          DOI: 10.3109/01460861003663987

Source DB:  PubMed          Journal:  Issues Compr Pediatr Nurs        ISSN: 0146-0862


  10 in total

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Review 5.  Suggested guidelines for the treatment of children with sickle cell anemia.

Authors:  E Vichinsky; B H Lubin
Journal:  Hematol Oncol Clin North Am       Date:  1987-09       Impact factor: 3.722

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Authors:  A Ashley-Koch; Q Yang; R S Olney
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7.  Silent infarction as a risk factor for overt stroke in children with sickle cell anemia: a report from the Cooperative Study of Sickle Cell Disease.

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8.  Sib understanding of genetics and attitudes toward carrier testing for X-linked severe combined immunodeficiency.

Authors:  J H Fanos; J Davis; J M Puck
Journal:  Am J Med Genet       Date:  2001-01-01

9.  Child, parent and family factors as predictors of adjustment for siblings of children with a disability.

Authors:  R Giallo; S Gavidia-Payne
Journal:  J Intellect Disabil Res       Date:  2006-12

10.  An expanded Transactional Stress and Coping Model for siblings of children with sickle cell disease: family functioning and sibling coping, self-efficacy and perceived social support.

Authors:  J I Gold; M Treadwell; L Weissman; E Vichinsky
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  10 in total
  4 in total

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2.  Parental Communication and Experiences and Knowledge of Adolescent Siblings of Children with 22q11.2 Deletion Syndrome.

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4.  Quality of life among caregivers of sickle cell disease patients: a cross sectional study.

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  4 in total

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