The impact of prenatal screening tests on prenatal diagnosis in Taiwan from 2006 to 2019: a regional cohort study

BMC Pregnancy Childbirth. 2022 Jan 9;22(1):23. doi: 10.1186/s12884-021-04360-w.

Abstract

Background: The purpose of this study is to evaluate the impact of prenatal screening tests on prenatal diagnosis in Taiwan's 14 years from 2006 to 2019.

Methods: The prenatal screening methods evolved from the second-trimester serum screening to combined first-trimester screening (cFTS) and then followed by the non-invasive cell-free DNA prenatal test (NIPT). The data used by the Department of Statistics, the Ministry of Health and Welfare and Department of Household Registration, Ministry of the Interior public website.

Results: This regional registry-based cohort retrospective study examined a total of 2,775,792 births from January 2006 to December 2019. The proportion of advanced maternal age (AMA) pregnancies increased from 11.63% in 2006 to 30.94% in 2019. Overall, invasive diagnostic testing was used in 87.22% of AMA pregnancies. The prenatal detection rate of trisomy 21 and 18 increased from 74.1% and 83.3% in 2006 to 96.9% and 98.8% in 2019, respectively.

Conclusion: During the second-trimester and cFTS periods, the percentage of AMA pregnancies increased every year and the number of invasive procedures also accompany with increased percentage of AMA. However, during the period that NIPT were implemented, the percentage of invasive procedures decreased.

Keywords: Combined first-trimester screening (cFTS); Non-invasive prenatal test (NIPT); Prenatal cytogenetic diagnosis; Second-trimester serum screening.

MeSH terms

  • Cohort Studies
  • Cytodiagnosis / trends*
  • Down Syndrome / diagnosis
  • Female
  • Humans
  • Maternal Age
  • Maternal Serum Screening Tests / trends*
  • Noninvasive Prenatal Testing / trends*
  • Pregnancy
  • Pregnancy Trimesters
  • Prenatal Diagnosis / methods*
  • Prenatal Diagnosis / trends*
  • Registries
  • Retrospective Studies
  • Taiwan
  • Trisomy 13 Syndrome / diagnosis
  • Trisomy 18 Syndrome / diagnosis