Women's preference for non‐invasive prenatal DNA testing versus chromosomal microarray after screening for Down syndrome: a prospective study. (14th January 2018)
- Record Type:
- Journal Article
- Title:
- Women's preference for non‐invasive prenatal DNA testing versus chromosomal microarray after screening for Down syndrome: a prospective study. (14th January 2018)
- Main Title:
- Women's preference for non‐invasive prenatal DNA testing versus chromosomal microarray after screening for Down syndrome: a prospective study
- Authors:
- Cheng, YKY
Leung, WC
Leung, TY
Choy, KW
Chiu, RWK
Lo, T‐K
Kwok, KY
Sahota, DS - Abstract:
- Abstract : Objective: To examine preferences for follow‐up testing in women screened with high or intermediate risk for Down syndrome in the first or second trimester. Design: Prospective cohort study. Setting: Three public hospitals in Hong Kong, China. Sample: Women with pregnancies termed as high risk (≥1:250; HR) or intermediate risk (1:251–1200; IR) for Down syndrome. Methods: Women with pregnancies screened as HR were offered the choices of: (1) an invasive test plus chromosomal microarray (CMA) to obtain more detailed fetal genetic information; (2) non‐invasive cell‐free prenatal DNA screening (NIPT) to detect trisomies 13, 18 and 21, and to avoid procedure‐related miscarriage; and (3) to decline any further testing. Women received standardised counselling informing them that the reporting times were identical, the procedure miscarriage risk was 0.1–0.2% and that there was no charge for screening. Women with IR pregnancies (1:251–1200) were offered NIPT as a secondary screening test. Main outcome measures: Uptake rate for NIPT. Results: Three hundred and forty‐seven women had pregnancies deemed as HR; 344 (99.1%) women opted for follow‐up testing, 216 (62.2%) of whom chose NIPT. Five hundred and seven of 614 women (82.6%) with IR risk chose NIPT. Seven (21%) of 34 women with nuchal translucency ≥3.5 mm opted for NIPT. Conclusion: In a setting where reporting times are similar and there is no cost difference between options, approximately 60% of women with pregnanciesAbstract : Objective: To examine preferences for follow‐up testing in women screened with high or intermediate risk for Down syndrome in the first or second trimester. Design: Prospective cohort study. Setting: Three public hospitals in Hong Kong, China. Sample: Women with pregnancies termed as high risk (≥1:250; HR) or intermediate risk (1:251–1200; IR) for Down syndrome. Methods: Women with pregnancies screened as HR were offered the choices of: (1) an invasive test plus chromosomal microarray (CMA) to obtain more detailed fetal genetic information; (2) non‐invasive cell‐free prenatal DNA screening (NIPT) to detect trisomies 13, 18 and 21, and to avoid procedure‐related miscarriage; and (3) to decline any further testing. Women received standardised counselling informing them that the reporting times were identical, the procedure miscarriage risk was 0.1–0.2% and that there was no charge for screening. Women with IR pregnancies (1:251–1200) were offered NIPT as a secondary screening test. Main outcome measures: Uptake rate for NIPT. Results: Three hundred and forty‐seven women had pregnancies deemed as HR; 344 (99.1%) women opted for follow‐up testing, 216 (62.2%) of whom chose NIPT. Five hundred and seven of 614 women (82.6%) with IR risk chose NIPT. Seven (21%) of 34 women with nuchal translucency ≥3.5 mm opted for NIPT. Conclusion: In a setting where reporting times are similar and there is no cost difference between options, approximately 60% of women with pregnancies classed as HR would opt for NIPT, offering simple but limited aneuploidy assessment, over a diagnostic procedure with comprehensive and more detailed assessment. Tweetable abstract: 60% of pregnant Chinese women prefer NIPT over CMA when screened as high risk for Down syndrome. Tweetable abstract: 60% of pregnant Chinese women prefer NIPT over CMA when screened as high risk for Down syndrome. … (more)
- Is Part Of:
- BJOG. Volume 125:Number 4(2018)
- Journal:
- BJOG
- Issue:
- Volume 125:Number 4(2018)
- Issue Display:
- Volume 125, Issue 4 (2018)
- Year:
- 2018
- Volume:
- 125
- Issue:
- 4
- Issue Sort Value:
- 2018-0125-0004-0000
- Page Start:
- 451
- Page End:
- 459
- Publication Date:
- 2018-01-14
- Subjects:
- Cell‐free DNA -- chromosomal microarray -- Down syndrome screening -- non‐invasive prenatal DNA testing -- trisomy
Obstetrics -- Periodicals
Gynecology -- Periodicals
618 - Journal URLs:
- http://www.blackwellpublishing.com/journal.asp?ref=1470-0328&site=1 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/1471-0528.15022 ↗
- Languages:
- English
- ISSNs:
- 1470-0328
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2105.748000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 8967.xml