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Semiconductor Sequencing for Preimplantation Genetic Testing for Aneuploidy
Published on: August 25, 2019
Clinical implications of the ethics of informed consent for first-trimester risk assessment for trisomy 21
Frank A Chervenak1, Laurence B McCullough, Stephen T Chasen
1Department of Obstetrics and Gynecology, Weill Medical College of Cornell University, New York, NY 10021, USA. fac2001@med.cornell.edu
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.
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