Second-tier non-invasive prenatal screening for Down syndrome in a public obstetric unit: the first 12 months

Authors

  • Horace HC CHEUNG
  • Lai-Yin TONG
  • William WK TO

DOI:

https://doi.org/10.12809/hkjgom.22.1.02

Keywords:

Down syndrome, Noninvasive prenatal testing

Abstract

Objective: To review the uptake rate of non-invasive prenatal testing (NIPT) in the first 12 months of implementation in the obstetric unit of United Christian Hospital.
Methods: Between December 2019 and November 2020, women with a fetal Down syndrome (DS) risk ratio of ≥1:250 after first-trimester DS screening (using maternal serum markers and nuchal translucency thickness on ultrasonography) or second-trimester DS screening (using maternal serum markers) were offered free-of-charge second-tier NIPT or invasive testing. Results of NIPT and invasive testing and pregnancy outcome of these women were reviewed. Characteristics of those opting for NIPT versus invasive testing were compared. Univariate and
logistic regression analyses were used to determine significant factors associated with opting for NIPT.

Results: During the study period, 2182 women underwent first-trimester DS screening (n=2086) or second-trimester DS screening (n=96). 117 women were screen positive, with a DS risk ratio of <1:250. The screen-positive rate was 5.36% overall and 5.23% for first trimester and 8.33% for second trimester. Of the 117 women, 26 had NIPT in private settings before or after being screened positive, 89 opted for NIPT (n=65) or invasive testing (n=24) in our hospital, and two did not have further testing owing to spontaneous miscarriage (n=1) or termination of pregnancy
(n=1). Of 91 women with NIPT, 84 (92.3%) were at low risk for common aneuploidies, four were at high risk for T21 (n=2) or T18 (n=2), and three had abnormalities other than common aneuploidies. Six of the high-risk women underwent invasive testing and abnormalities were confirmed. Of the 24 women who opted for invasive testing, 14 had normal results and 10 had abnormal results. In logistic regression analysis, predictors for opting for invasive
testing (rather than NIPT) were presence of abnormalities on ultrasonography (odds ratio (OR)=13.9, p=0.01), a nuchal translucency thickness of ≥3 mm (OR=7.62, p=0.01), and education level below tertiary level (OR=7.14, p=0.02).
Conclusion: In the first 12 months of implementation in United Christian Hospital, the uptake rate of NIPT as a second-tier test after positive DS screening was 77.8%, which is higher than that reported in previous studies when NIPT was a self-financed test.

References

Sahota DS, Leung WC, Chan WP, To WW, Lau ET, Leung TY. Prospective assessment of the Hong Kong Hospital Authority universal Down syndrome screening programme. Hong Kong Med J 2013;19:101-8.

Chiu RW, Chan KC, Gao Y, et al. Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massive parallel genomic sequencing of DNA in maternal plasma. Proc Natl Acad Sci U S A 2008;105:20458-63.

Palomaki GE, Kloza EM, Lambert-Messerlian GM, et al. DNA sequencing of maternal plasma to detect down syndrome an international clinical validation study. Genet Med 2011;13:913-20.

Gil MM, Quezada M, Revello R, Akolekar R, Nicolaides KH. Analysis of cell free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis. Ultrasound Obstet Gynecol 2015;45:249-66.

Norton ME, Jacobsson B, Swamy GK, et al. Cell-free DNA analysis for noninvasive examination of trisomy. N Engl J Med 2015;372:1589-97.

Akolekar R, Beta J, Picciarelli G, Ogilvie C, D’Antonio F. Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and metaanalysis. Ultrasound Obstet Gynecol 2015;45:16-26.

Wang Y, Zhu J, Chen Y, et al. Two cases of placental T21 mosaicism: challenging the detection limits of non-invasive prenatal testing. Prenat Diagn 2013;33:1207-10.

Benn P, Borrell A, Chiu R, et al. Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis. Prenat Diagn 2015;35:725-34.

Committee Opinion No. 640: Cell-Free DNA Screening For Fetal Aneuploidy. Obstet Gynecol 2015;126:e31-e37.

Chiu RW, Akolekar R, Zheng YW, et al. Noninvasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study. BMJ 2011;342:c7401.

Ng VKS, Chan AL, Lau WL, Leung WC. Second tier noninvasive prenatal testing in a regional prenatal diagnosis prenatal service unit: a retrospective analysis and literature review. Hong Kong Med J 2020;26:10-8.

Poon CF, Tse WC, Kou KO, Leung KY. Uptake of noninvasive prenatal testing in Chinese women following positive down syndrome screening. Fetal Diagn Ther 2015;37:141-7.

Chan YM, Leung WC, Chan WP, Leung TY, Cheng YKY, Sahota DS. Women’s uptake of non-invasive DNA testing following a high-risk screening test for trisomy 21 within a publicly funded healthcare system: findings from a retrospective review. Prenat Diagn 2015;35:342-7.

Kou KO, Poon CF, Tse WC, Mak SK, Leung KY. Knowledge and future preference of Chinese women in a major public hospital in Hong Kong after undergoing non-invasive prenatal testing for positive aneuploidy screening: a questionnaire survey. BMC Pregnancy Childbirth 2015;15:199.

Cheng Y, Leung WC, Leung TY, et al. Women’s preference for non-invasive prenatal DNA testing versus chromosomal microarray after screening for Down syndrome: a prospective study. BJOG 2018;125:451-9.

Lo TK, Chan KY, Kan AS, et al. Decision outcomes in women offered noninvasive prenatal test (NIPT) for positive Down screening results. J Matern Fetal Neonatal Med 2019;32:348-50.

Han J, Zhen L, Pan M, et al. Uptake of non-invasive prenatal testing in Chinese women: money matters. Eur J Obstet Gynecol Reprod Biol 2015;195:100-2.

Bakkeren IM, Kater-Kuipers A, Bunnik EM, et al. Implementing non-invasive prenatal testing (NIPT) in the Netherlands: an interview study exploring opinions about and experiences with societal pressure, reimbursement, and an expanding scope. J Genet Couns 2020;29:112-21.

Maxwell S, O’Leary P. Public funding for non-invasive prenatal testing for fetal aneuploidy – It’s time. Aust N Z J Obstet Gynaecol 2018;58:385-7.

Lau JY, Yi H, Ahmed S. Decision making for non-invasive prenatal testing for Down syndrome: Hong Kong Chinese women’s preferences for individual vs relational autonomy. Clin Genet 2016;89:550-6.

Gregg AR, Skotko GB, Benkendorf JL, et al. Non-invasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics. Genet Med 2016;18:1056-65.

Lo TK, Chan KY, Kan AS, et al. Study of the extent of information desired by women undergoing non-invasive prenatal testing following positive prenatal Down-syndrome screening test results. Int J Gynaecol Obstet 2017;137:338-9.

Christiaens L, Chitty LS, Langlois S. Current controversies in prenatal diagnosis: expanded NIPT that includes conditions other than trisomies 13, 18, and 21 should be offered. Prenat Diagn 2021;41:1316-23.

Yin L, Tang Y, Lu Q, Pan A, Shi MF. Application value of NIPT for uncommon fetal chromosomal abnormalities. Mol Cytogenet 2020;13:39.

Lo TK, Chan KY, Kan AS, et al. Effect of knowledge on women’s likely uptake of and willingness to pay for noninvasive test (NIPT). Eur J Obstet Gynecol Reprod Biol 2018;222:183-4.

Taylor JB, Chock VY, Hudgins L. NIPT in a clinical setting: an analysis of uptake in the first months of clinical availability. J Genet Couns 2014;23:72-8.

Montgomery S, Thayer ZM. The influence of experiential knowledge and societal perceptions on decision-making regarding non-invasive prenatal testing (NIPT). BMC Pregnancy Childbirth 2020;20:630.

Petersen OB, Smith E, Van Opstal D, et al. Nuchal translucency of 3.0-3.4 mm an indication for NIPT or microarray? Cohort analysis and literature review. Acta Obstet Gynecol Scand 2020;99:765-74.

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Published

2023-04-06

How to Cite

1.
CHEUNG HH, TONG L-Y, TO WW. Second-tier non-invasive prenatal screening for Down syndrome in a public obstetric unit: the first 12 months. Hong Kong J Gynaecol Obstet Midwifery [Internet]. 2023 Apr. 6 [cited 2024 May 8];22(1). Available from: https://hkjgom.org/home/article/view/307

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