The Influence of the Introduction of Fetal Anomaly Scans on Pregnancy Terminations in Cases of Upper Limb Anomalies: A Retrospective Cohort Study From 2000 to 2023.
Arda Arduç, Eline Huiberts, Margriet H M van Doesburg, Ingeborg H Linskens, Elisabeth van Leeuwen, Merel C Van Maarle, Eva Pajkrt
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引用次数: 0
Abstract
Objective: To examine the association between the introduction of the fetal anomaly scans in the Netherlands and termination of pregnancy (TOP) in cases of prenatally detected upper limb anomalies.
Methods: We conducted a retrospective study among prenatally detected upper limb anomalies between 2000 and 2023. Anomalies were categorized as reduction defects, syndactyly, or polydactyly, and classified as isolated or non-isolated. We analyzed TOP rates across three periods (2000-2006, 2007-August 2021, September 2021-2023), including an interrupted time series (ITS) analysis to assess the impact of introducing second- and first-trimester anomaly scans (STAS, FTAS).
Results: We included 300 pregnancies, of which 133 (44.3%) were isolated. Overall TOP rates did not differ significantly between periods, except for isolated reduction defects, where a significant increase was observed (p = 0.032). TOP rates over time did not increase for syndactyly and polydactyly. Median gestational age at diagnosis decreased across the three periods: from 20.4 to 19.4 weeks and then to 14.9 weeks. Similarly, the timing of termination of pregnancy decreased from 20.5 to 16.8 weeks and then to 15.0 weeks.
Conclusion: Earlier prenatal detection followed the introduction of STAS and FTAS. Despite this shift in timing, no consistent changes in termination rates were observed across the study periods. While overall TOP rates remained stable, a trend towards higher termination rates was observed for isolated reduction defects.
期刊介绍:
Prenatal Diagnosis welcomes submissions in all aspects of prenatal diagnosis with a particular focus on areas in which molecular biology and genetics interface with prenatal care and therapy, encompassing: all aspects of fetal imaging, including sonography and magnetic resonance imaging; prenatal cytogenetics, including molecular studies and array CGH; prenatal screening studies; fetal cells and cell-free nucleic acids in maternal blood and other fluids; preimplantation genetic diagnosis (PGD); prenatal diagnosis of single gene disorders, including metabolic disorders; fetal therapy; fetal and placental development and pathology; development and evaluation of laboratory services for prenatal diagnosis; psychosocial, legal, ethical and economic aspects of prenatal diagnosis; prenatal genetic counseling