Register
Community
Overview
Experts
Editors
Fellows
Code of conduct
AI Guidelines for Physicians
Company
About Us
FAQs
Privacy Policy
Terms of Use
Careers
Programs
News
News Releases
Press Coverage
Publications
Blog
Contact Us
Sign in
Please select the option that best describes you:
Topics:
Hematology
•
Sickle Cell
•
Benign Hematology
How would you manage iron overload in sickle cell patients with cirrhosis?
How does your management change if the patient has concurrent renal insufficiency?
Related Questions
How would you manage a patient with HbSS and severe pulmonary hypertension on home oxygen?
How do you counsel sickle cell patients on the use of G-CSF to treat neutropenia from other causes, like malignancy?
What unique work up or management would you offer for stroke in patients with sickle cell trait, beyond standard stroke management?
How long would you continue chronic transfusion therapy for adult sickle cell patients who have had a stroke?
Is there specific data on using luspatercept for sickle beta+ thalassemia with transfusion-dependent anemia?
What hydroxyurea dose do you target for HbSC disease?
Would you consider long term avatrombopag use in patients with cirrhosis requiring higher platelet counts for medical therapy?
Is there benefit to aggressively treating hemochromatosis in a patient who has already progressed to cirrhosis at the time of diagnosis?
How would you manage aplastic anemia refractory to multiple agents?
How do you manage a subchorionic hematoma in type 1 von Willebrand disease, with borderline normal levels of vWF?