英文摘要 |
Objectives: A national registry and public data reporting have together become an important strategy for health surveillance of assisted reproductive technologies (ARTs). We have analyzed the development of registry systems, the tendency to highlight maternal and infant health risk, and the formats for public reporting based on a cross-national comparison. Methods: We selected the UK, US, Sweden, Japan, and Taiwan as countries for comparison. Archival data, secondary literature, and in-depth interviews of relevant policy-makers in Japan and Taiwan were included. Results: The UK, US, Sweden, and Taiwan have achieved compulsory registry through legal requirement. The Japan Society of Obstetrics and Gynecology has adopted a voluntary reporting system, and has recently achieved a 100% reporting rate. Most countries gradually focus on the health risk for mothers and infants, rather than merely display the technical competence by calculating success rates. The number of multiple embryos transferred during IVF, and multiple pregnancy and live birth rates were shown to serve as important indicators of health risk surveillance. Some countries report new indicators, such as "elective single embryo transfer rate" and "term, normal weight, and singleton" live birth rate. The UK, US, and Sweden provide innovative formats to make reporting data accessible, readable, and useful for the general public. Taiwan and Japan limit its readership to professionals and lack efforts for broader public communication. Conclusions: Taiwan has one of the most complete ART registry systems in the world, but the surveillance on maternal and infant health and the quality of public reporting remains inadequate. To build evidence-based policy-making and to improve ART safety, surveillance reporting in Taiwan needs to meet the global standard. |