The Human Fertilisation and Embryology Authority (HFEA) has informed the Department that it does not require clinics to submit the information requested as part of its routine data collection. However, incidents involving loss, damage or accidental destruction of embryos should be notified to the HFEA in accordance with the requirement to report adverse incidents that occur in licensed establishments.
The HFEA uses the adverse incident reporting system to help clinics learn from mistakes and to develop control measures to reduce the risk of incidents reoccurring. Information about risk control measures is issued to clinics in the form of HFEA alerts and patient safety notices. Past alerts have included guidance on transportation of embryos and associated risks and risks involving power supply and critical equipment. The HFEA’s Code of Practice also makes clear that where adverse incidents occur, clinics are expected to review relevant procedures to minimise the risk of any reoccurrence of the incident and inform the HFEA of the revised procedures.
The HFEA has advised the Department that it intends to continue the development of its systems for improving risk management in clinics and dissemination of critical information in response to individual incidents.
The information requested is shown in the following table.
IVF2 Donor insemination3 2002 9,760 889 2003 10,076 821 2004 10,190 749 20051 11,268 645 Notes: 1. 2005 are the most recent year for which information is currently available. 2. Data include all IVF treatment cycles including use of donated eggs, frozen embryo transfers and treatment cycles involving the use of micromanipulation techniques. 3. Data include treatment cycles involving artificial insemination and Gamete Intrafallopian Transfer. Source: Human Fertilisation and Embryology Authority (HFEA), A long term analysis of the HFEA register data 1991-2006, revised February 2008.