Abstract
Prenatal screening for genetic disease and developmental disabilities is rapidly becoming a routine part of the management of low-risk pregnancies. Yet research on how to best inform pregnant women about these tests and their special ethical entailments remains sparse. We asked 130 low-risk pregnant women of diverse ethnic and social class backgrounds a series of questions about a prenatal test they had been offered within the previous 3 months. All had been given an informational booklet about the test at the time it was offered; about half also saw a video. We found that neither group of women retained much of the information they had received about the prenatal screening but that those who saw the video remembered more. Information-retention also varied significantly by ethnicity and level of education.
Original language | English (US) |
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Pages (from-to) | 135-146 |
Number of pages | 12 |
Journal | Patient Education and Counseling |
Volume | 27 |
Issue number | 2 |
DOIs | |
State | Published - Mar 1996 |
Externally published | Yes |
Keywords
- Ethnicity and medical care
- Prenatal diagnostic screening
- Video instruction
ASJC Scopus subject areas
- Medicine(all)