Gaps in the diagnosis and management of iron overload in sickle cell disease: a ‘real‐world’ report from the GRNDaD registry

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Bibliographic Details
Published inBritish journal of haematology Vol. 195; no. 5; pp. e157 - e160
Main Authors Wilson, Samuel R., Sears, Matthew, Williams, Elizabeth, Drapekin, Jesse, Sivakumar, Ishwarya, Padrino, Susan, Desai, Payal C., Hager, Ward, Manwani, Deepa, Clay, Leila J., Field, Joshua J., Kanter, Julie, Cohen, Alice J., Saif Ur Rehman, Sana, Lanzkron, Sophie, Little, Jane A.
Format Journal Article
LanguageEnglish
Published England Blackwell Publishing Ltd 01.12.2021
Subjects
Adolescent
Adult
Anemia, Sickle Cell - blood
Anemia, Sickle Cell - complications
Anemia, Sickle Cell - therapy
Child
Child, Preschool
chronic transfusion
Cross-Sectional Studies
Disease Management
Erythrocyte Transfusion - adverse effects
Female
Ferritins - blood
Hematology
Humans
Infant
iron chelation
Iron Overload - blood
Iron Overload - diagnosis
Iron Overload - etiology
Iron Overload - therapy
liver iron concentration
Male
Middle Aged
serum ferritin
Sickle cell anemia
Sickle cell disease
Young Adult
iron chelation
serum ferritin
chronic transfusion
liver iron concentration
Sickle cell disease
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Bibliography:SourceType-Other Sources-1
ObjectType-Article-1
content type line 63
ObjectType-Correspondence-2
ISSN:0007-1048
1365-2141
DOI:10.1111/bjh.17762