Document Detail


Balanced information about Down syndrome: What is essential?
MedLine Citation:
PMID:  21548127     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
The purpose of this study was to explore the perspectives of genetic counselors and parents of children with Down syndrome to define essential information for the initial discussion of a new diagnosis. We compared information given in both prenatal and postnatal settings, and also aimed to distinguish differences between the informational needs of parents and the information genetic counselors provide. Online surveys were distributed to members of the National Down Syndrome Congress, National Down Syndrome Society, and National Society of Genetic Counselors. Participants included 993 parents of children with Down syndrome and 389 genetic counselors. Participants rated 100 informational features about Down syndrome as Essential, Important, or Not Too Important for inclusion in the first discussion of the diagnosis. Responses identified 34 essential informational items for the initial discussion of Down syndrome, including clinical features, developmental abilities, a range of prognostications, and informational resources. Healthcare providers should consider incorporating these items in their initial discussion of a diagnosis in both prenatal and postnatal settings. Statistically significant differences between parent and genetic counselor responses illustrate that information is valued differently and that parents appreciate information about the abilities and potential of people with Down syndrome, as opposed to clinical details. Balancing clinical information with other aspects of the condition, as well as a better understanding of the information parents consider most important, may enable healthcare professionals to more effectively satisfy families' informational needs following a new diagnosis of Down syndrome. © 2011 Wiley-Liss, Inc.
Authors:
Kathryn B Sheets; Robert G Best; Campbell K Brasington; Madeleine C Will
Related Documents :
21463277 - Cognitive and behavioral characteristics of children with dravet syndrome: an overview.
2289317 - Emery-dreifuss syndrome in three generations of females, including identical twins.
20963467 - Tako-tsubo cardiomyopathy in a patient with bilateral lesions in the dorsal medulla.
9090407 - Large vestibular aqueduct syndrome with high ct density and high mr signal intensity.
12270797 - Neurocutaneous syndromes.
2717687 - The complex nature of the mechanism of toxicity of antibiotic dithiacyclohexadiene poly...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2011-5-5
Journal Detail:
Title:  American journal of medical genetics. Part A     Volume:  -     ISSN:  1552-4833     ISO Abbreviation:  -     Publication Date:  2011 May 
Date Detail:
Created Date:  2011-5-6     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101235741     Medline TA:  Am J Med Genet A     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Copyright Information:
Copyright © 2011 Wiley-Liss, Inc.
Affiliation:
Division of Medical Genetics, Duke University Medical Center, Durham, North Carolina. katie.sheets@duke.edu.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Is autosomal recessive Silver-Russel syndrome a separate entity or is it part of the 3-M syndrome sp...
Next Document:  Distinctive phenotype in 9 patients with deletion of chromosome 1q24-q25.