Literature DB >> 29845619

Trends in invasive prenatal diagnostic testing at a single institution.

Adeola Awomolo1, Kristy Palomares1, Guadalupe Herrera Garcia1, Todd Rosen1, Christina Duzyj1, Elena Ashkinadze1.   

Abstract

OBJECTIVE: As diagnostic methodologies evolve, we sought to determine whether invasive testing rates would decline, whether there would be a shift in indications for invasive testing, and whether the diagnostic yield would increase.
METHODS: We conducted a retrospective, observational study from 2006 through 2015. We quantified the number of invasive procedures per year and examined what percentage of these procedures yielded abnormal results. We also examined the indications for testing and determined the trend of these indications during the study period.
RESULTS: The number of amniocenteses showed a steady decline (P < .05). The number of CVS procedures has increased and was recently equivalent to amniocentesis. The percentage of abnormal results steadily increased from 11.4% to 27.0% (P < .001). The abnormal aneuploidy screening indication remained constant over time. Advanced maternal age (AMA) as the sole indication substantially declined from 42.3% to 15.52% (P < .001). Testing for a known single gene disorder steadily increased from 3.0% to 9.20% (P = .018).
CONCLUSION: Our study showed a significant decline in the number of amniocenteses, a steady increase in the percentage of abnormal results from invasive testing, and a decline in AMA as the sole indication for invasive testing.
© 2018 John Wiley & Sons, Ltd.

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Year:  2018        PMID: 29845619     DOI: 10.1002/pd.5290

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  2 in total

1.  Comparison of indications and results of prenatal invasive diagnostic tests before and after the implementation of the use of cell-free fetal DNA: a tertiary referral center experience.

Authors:  Firat Okmen; Huseyin Ekici; Ismet Hortu; Metehan Imamoglu; Duygu Arican; Haluk Akın; Sermet Sagol
Journal:  J Assist Reprod Genet       Date:  2020-05-21       Impact factor: 3.412

2.  In-house genetic counseling increases the detection of abnormal karyotypes-a 26-year experience in prenatal diagnosis in a single tertiary referral hospital in Poland.

Authors:  Julia Bijok; Anna Kucińska-Chahwan; Diana Massalska; Alicja Ilnicka; Grzegorz Panek; Tomasz Roszkowski
Journal:  J Assist Reprod Genet       Date:  2020-05-19       Impact factor: 3.412

  2 in total

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