Panel 2:
Research questions regarding fertility, infertility risk and Assisted Reproductive Technology in sickle cell disease
| • Define effects of sickle cell disease pathophysiology and treatments on oocyte quality, blastocyst development and miscarriage |
| • Establish infertility rates and risks in people with sickle cell disease; include all genotypes |
| • Define gonadoprotection or gonadotoxicity of hydroxyurea, chronic transfusion, and other sickle cell disease therapies in chronically exposed people with attention to dose and duration of treatment |
| • Establish ideal timing of fertility preserving interventions and study protocols to optimize outcomes and minimize complications |
| • Identify which sickle cell disease treatments need to be discontinued, and for what time period, before gamete cryopreservation |
| • Define pregnancy outcomes when cryopreserved gametes are used |
| • Measure barriers to fertility preservation |