Safety, tolerability, and outcomes of regular automated red cell exchange transfusion in the management of sickle cell disease-Reference-Cited by-同舟云学术

Safety, tolerability, and outcomes of regular automated red cell exchange transfusion in the management of sickle cell disease

Published:2016-02-16 Issue:6 Volume:31 Page:545-550
ISSN:0733-2459
Container-title:Journal of Clinical Apheresis
language:en
Short-container-title:J. Clin. Apheresis

Author:

Tsitsikas Dimitris A.¹,Sirigireddy Bala¹,Nzouakou Ruben¹,Calvey Alexander¹,Quinn Joanne¹,Collins Janine¹,Orebayo Funmilayo¹,Lewis Natasha¹,Todd Sophie¹,Amos Roger J.¹

Affiliation:

1. Heamoglobinopathy Service, Department of Haematology, Homerton University Hospital NHS Foundation Trust; London United Kingdom

Publisher

Wiley

Subject

Hematology,General Medicine

Reference19 articles.

1. Red cell exchange in sickle cell disease;Swerdlow;Hematology Am Soc Hematol Educ Program,2006

2. Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography;Adams;N Engl J Med,1998

3. Causes and outcomes of the acute chest syndrome in sickle cell disease. National Acute Chest Syndrome Study Group;Vichinsky;N Engl J Med,2000

4. STOP Investigators. Impact of chronic transfusion on incidence of pain and acute chest syndrome during the Stroke Prevention Trial (STOP) in sickle-cell anemia;Miller;J Pediatr,2001

5. A comparison of chronic manual and automated red blood cell exchange transfusion in sickle cell disease patients;Kuo;Br J Haematol,2015

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