Recommendations to improve the patient experience and avoid bias when prenatal screening/testing
Author:
Funder
US Department of Health and Human Services Administration for Community Living
Publisher
Elsevier BV
Subject
Public Health, Environmental and Occupational Health,General Medicine
Reference26 articles.
1. Receiving the initial Down syndrome diagnosis: a comparison of prenatal and postnatal parent group experiences;Nelson Goff;Intellect Dev Disabil,2013
2. New insights into the formation and duration of flashbulb memories: evidence from medical diagnosis memories;May;Appl Cogn Psychol,2020
3. Physicians' perceptions of people with disability and their health care: study reports the results of a survey of physicians' perceptions of people with disability;Iezzoni;Health Aff (Millwood),2021
4. Parental experiences after prenatal diagnosis of fetal abnormality;Hodgson;Semin Fetal Neonatal Med,2018
5. Evaluation of patient education materials: the example of circulating cell free DNA testing for aneuploidy;Kloza;J Genet Couns,2015
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1. Parent‐reported genetic counselor adherence to the NSGC practice resource for communicating a potential prenatal diagnosis: Impact on the Down syndrome diagnosis experience;Journal of Genetic Counseling;2024-07-19
2. Supporting patient decision-making in non-invasive prenatal testing: a comparative study of professional values and practices in England and France;BMC Medical Ethics;2024-03-21
3. NICU Language, Everyday Ethics, and Giving Better News: Optimizing Discussions about Disability with Families;Children;2024-02-15
4. The impact of implicit and explicit bias about disabilities on parent experiences and information provided during prenatal screening and testing;Disability and Health Journal;2024-01
5. Ethical challenges in autism genomics: Recommendations for researchers;European Journal of Medical Genetics;2023-09
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