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Managing risks for genetic conditions in donor sperm treatment: current practices in Belgian fertility clinics. | LitMetric

Managing risks for genetic conditions in donor sperm treatment: current practices in Belgian fertility clinics.

Reprod Biomed Online

Department of Philosophy and Moral Sciences, Ghent University, Ghent, Belgium; Department of Public Health and Primary Care, Ghent University, Ghent, Belgium.

Published: November 2024

AI Article Synopsis

  • The study explored how Belgian fertility clinics approach the management of genetic risks in treatments using donor sperm.
  • An electronic survey sent to clinics revealed that while all assessed donor risks, a significant lack of consistent communication about adverse genetic events existed between clinics, donors, and recipients.
  • Findings indicated that although genetic conditions were often suspected or identified in donor sperm treatments, clinics varied in their protocols for informing affected parties and deciding on the future use of donor sperm linked to adverse events.

Article Abstract

Research Question: How do fertility clinics in Belgium manage risks for genetic conditions in donor sperm treatment?

Design: An electronic questionnaire was distributed to all fertility clinics in Belgium in June 2023, focusing on treatments with anonymous sperm donors from 2018 to 2022. Responses from 15 clinics were analysed anonymously using IBM SPSS statistics.

Results: All clinics assessed donor risks, including a personal and family history, conventional karyotyping and (for 83.3% of the clinics) carrier screening for common autosomal recessive conditions. For recipients, 58.3% of the clinics relied only on a personal and family history. Despite efforts, the suspicion or detection of genetic conditions in donor sperm treatment was prevalent, with 9.4 adverse events reported per 100 children born. When adverse events occurred, most clinics (58.3%) would not inform the donor if no additional genetic testing was needed. Around 1 in 4 (26.7%) clinics always informed recipients about an adverse event possibly related to their donor. An equal number (26.7%) categorically ruled out the use of spermatozoa from a donor after an adverse event was traced back to his DNA, and 53.3% would not consider using the donor when the adverse event was not genetically confirmed. For the other clinics, deciding when to disclose new genetic risk information or when to allow the use of a donor linked to an adverse event was a complex matter involving different considerations.

Conclusion: Although suspected or detected genetic conditions linked to donor treatments were common, there was wide variation in how Belgian clinics prevented and managed these situations.

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Source
http://dx.doi.org/10.1016/j.rbmo.2024.104352DOI Listing

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