Document Detail


Clinical implications of the ethics of informed consent for first-trimester risk assessment for trisomy 21.
MedLine Citation:
PMID:  16104682     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
OBJECTIVE: We identify the clinical implications of the ethics of informed consent for risk assessment for trisomy 21. FINDING: Based on the ethics of informed consent, we find that routinely offering first-trimester risk assessment in centers qualified to provide it is ethically obligatory, and routinely withholding the results of first-trimester risk assessment is ethically unjustified. CONCLUSION: The ethics of informed consent is an essential dimension of first-trimester risk assessment for trisomy 21.
Authors:
Frank A Chervenak; Laurence B McCullough; Stephen T Chasen
Publication Detail:
Type:  Journal Article; Review    
Journal Detail:
Title:  Seminars in perinatology     Volume:  29     ISSN:  0146-0005     ISO Abbreviation:  Semin. Perinatol.     Publication Date:  2005 Aug 
Date Detail:
Created Date:  2005-08-17     Completed Date:  2005-12-22     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7801132     Medline TA:  Semin Perinatol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  277-9     Citation Subset:  IM    
Affiliation:
Department of Obstetrics and Gynecology, Weill Medical College of Cornell University, New York, NY 10021, USA. fac2001@med.cornell.edu
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MeSH Terms
Descriptor/Qualifier:
Down Syndrome / diagnosis*
Ethics, Medical*
Female
Fetal Diseases / diagnosis*
Humans
Informed Consent / ethics*,  psychology
Nuchal Translucency Measurement / ethics
Pregnancy
Pregnancy Trimester, First
Prenatal Diagnosis / ethics*

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


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