![]()
A global collaborative registry dedicated to understanding outcomes after liver transplantation in patients with Sickle Cell Disease.
Patient and centre recruitment will open soon
Why This Registry Matters
Liver transplantation in patients with Sickle Cell Disease remains rare and complex.
Outcomes are influenced by hematologic phenotype, transfusion strategies, vaso-occlusive risk, iron overload, cardiopulmonary comorbidity, and perioperative management variability.
Current evidence is limited to small series and isolated reports.
The SCDLT Registry aims to generate high-quality, international data to improve:
Who Can Participate
How to Get Involved
What the Registry Collects
Governance and Data Security
The SCDLTregistry.org Team