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Posttransfusion hyperhemolysis syndrome in beta thalassemia major: Postulation of various mechanisms
  • Ganesh Kasinathan,
  • Jameela Sathar
Ganesh Kasinathan
Ampang Hospital
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Jameela Sathar
Ampang Hospital.
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Abstract

Hyperhemolysis syndrome (HS) should be considered in a multiply transfused thalassemia patient. HS in this patient was attributed to a combination of factors including multiple transfusions, presence of anti-Cw, macrophage hyperactivity, hypersplenism and suppression of erythropoiesis.

Peer review status:ACCEPTED

20 Jan 2021Submitted to Clinical Case Reports
21 Jan 2021Submission Checks Completed
21 Jan 2021Assigned to Editor
30 Jan 2021Reviewer(s) Assigned
03 Mar 2021Review(s) Completed, Editorial Evaluation Pending
03 Mar 2021Editorial Decision: Revise Minor
02 Apr 20211st Revision Received
02 Apr 2021Submission Checks Completed
02 Apr 2021Assigned to Editor
02 Apr 2021Review(s) Completed, Editorial Evaluation Pending
14 Apr 2021Editorial Decision: Accept