P512: Multidisciplinary team patterns in Prader-Willi syndrome (MDT-PWS): Analysis of medical geneticists and specialists outpatient visits from a single US payer

Conclusion:In summary, across 12 HRN sites, GC uptake among patients with positive CDCT1 results was moderate, with about half completing a session.This is consistent with prior genetic counseling uptake rates in a population genomic screening setting.Most individuals who declined GC were already aware of their result or had previously received counseling, suggesting prior awareness and perceived redundancy as key drivers of non-participation.Practical barriers, such as time constraints, played a smaller role.Overall, genetic counseling uptake was moderate and consistent across conditions, with higher participation among females and individuals aged 49-58 years.These findings highlight the need to reduce barriers and support access to GC for all patients, ensuring they understand their results and care options.