Changes in the quality of life of adults with sickle cell disease following allogeneic stem cell transplantation: A mixed‐methods, prospective cohort study

Changes in the quality of life of adults with sickle cell disease following allogeneic stem cell transplantation: A mixed‐methods, prospective cohort study

Abstract Advances in conditioning regimens have made non‐myeloablative allogeneic hematopoietic stem cell transplantation (HSCT) a viable curative option for adults with sickle cell disease (SCD). However, prospective studies comparing pre‐ and post‐transplant patient‐reported health outcomes are sc...

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Bibliographic Details
Main Authors:	Elisabeth Dovern, Sterre J. A. M. Nijland, Annemarie M. J. Braamse, Maud M. vanMuilekom, Elisabeth M. J. Suijk, Gerianne M. Hoogendoorn, Charlotte F. J. vanTuijn, Michael R. DeBaun, Bart J. Biemond, Lotte Haverman, Erfan Nur
Format:	Article
Language:	English
Published:	Wiley 2025-03-01
Series:	HemaSphere
Online Access:	https://doi.org/10.1002/hem3.70100
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