Optimal Manual Exchange Transfusion Protocol for Sickle Cell Disease: A Retrospective Comparison of Two Comprehensive Care Centers in the United Kingdom and Canada-Reference-Cited by-同舟云学术

Optimal Manual Exchange Transfusion Protocol for Sickle Cell Disease: A Retrospective Comparison of Two Comprehensive Care Centers in the United Kingdom and Canada

Published:2015-06-26 Issue:5 Volume:39 Page:310-315
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Mian Hira S.,Ward Richard,Telfer Paul,Kaya Banu,Kuo Kevin H.M.

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2015.1057734

Reference20 articles.

1. Stroke Prevention Trial in Sickle Cell Anemia (STOP): extended follow-up and final results

2. Stroke with transfusions changing to hydroxyurea (SWiTCH): A phase III randomized clinical trial for treatment of children with sickle cell anemia, stroke, and iron overload

3. Discontinuing prophylactic transfusions increases the risk of silent brain infarction in children with sickle cell disease: data from STOP II

4. Prevention of a First Stroke by Transfusions in Children with Sickle Cell Anemia and Abnormal Results on Transcranial Doppler Ultrasonography

5. Discontinuing Prophylactic Transfusions Used to Prevent Stroke in Sickle Cell Disease

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1. Manual red cell exchange (RBCXm) in acute sickle cell crisis: A feasible modality in resource limited settings;Transfusion Clinique et Biologique;2024-05

2. Manual erythroexchange in sickle cell disease: multicenter validation of a protocol predictive of volume to exchange and hemoglobin values;Annals of Hematology;2020-07-21

3. How I manage sickle cell patients with high transcranial doppler results;British Journal of Haematology;2017-08-02

4. Efficacy and Safety of Manual Partial Red Cell Exchange in the Management of Severe Complications of Sickle Cell Disease in a Developing Country;Advances in Hematology;2017

5. Sickle cell disease: when and how to transfuse;Hematology;2016-12-02