Comparison of automated erythrocytapheresis versus manual exchange transfusion to treat cerebral macrovasculopathy in sickle cell anemia

Transfusion

Volumn 56, Issue 5, 2016, Pages 1121-1128

  Koehl, Bérengère ^a,b   Sommet, Julie ^a,b,c   Holvoet, Laurent ^a   Abdoul, Hendy ^a   Boizeau, Priscilla ^a   Ithier, Ghislaine ^a   Missud, Florence ^a   Couque, Nathalie ^a   Verlhac, Suzanne ^a   Voultoury, Pauline ^a   Sellami, Fatiha ^a   Baruchel, André ^a,b   Benkerrou, Malika ^a,c  

^a HÔPITAL ROBERT DEBRÉ   (France)

^b UNIVERSITÉ PARIS DESCARTES   (France)

^c Paris Diderot University   (France)

Author keywords

[No Author keywords available]

Indexed keywords

FERRITIN; HEMOGLOBIN S;

ADOLESCENT; ALLOIMMUNIZATION; APHERESIS DEVICE; ARTICLE; AUTOMATED ERYTHROCYTAPHERESIS; BLOOD TRANSFUSION REACTION; BONE MARROW TRANSPLANTATION; CEREBRAL MACROVASCULOPATHY; CEREBROVASCULAR ACCIDENT; CHELATION THERAPY; CHILD; CLINICAL ARTICLE; COMPARATIVE EFFECTIVENESS; CONTROLLED STUDY; CYTAPHERESIS; DISPOSABLE EQUIPMENT; ERYTHROCYTE TRANSFUSION; EXCHANGE BLOOD TRANSFUSION; FAINTNESS; FEMALE; FOLLOW UP; HEALTH CARE COST; HEMATOLOGIC DISEASE; HEMATOLOGY EQUIPMENT; HUMAN; IRON OVERLOAD; MALE; OUTCOME ASSESSMENT; PHLEBOTOMY; PRESCHOOL CHILD; PRIMARY PREVENTION; RETROSPECTIVE STUDY; SCHOOL CHILD; SICKLE CELL ANEMIA; VASCULAR ACCESS; ANEMIA, SICKLE CELL; AUTOMATION; BLOOD; CEREBROVASCULAR DISORDERS; COMPARATIVE STUDY; COMPLICATION; DEVICES; ECONOMICS; ERYTHROCYTE; PROCEDURES; STROKE;

ADOLESCENT; ANEMIA, SICKLE CELL; AUTOMATION; CEREBROVASCULAR DISORDERS; CHILD; CHILD, PRESCHOOL; CYTAPHERESIS; ERYTHROCYTES; EXCHANGE TRANSFUSION, WHOLE BLOOD; FEMALE; FERRITINS; HEMOGLOBIN, SICKLE; HUMANS; IRON OVERLOAD; MALE; RETROSPECTIVE STUDIES; STROKE;

EID: 84962248860     PISSN: 00411132     EISSN: 15372995     Source Type: Journal    
DOI: 10.1111/trf.13548     Document Type: Article

References (16)

1. Stuart MJ, Nagel RL., Sickle-cell disease. Lancet 2004; 364: 1343-60.
2. Aygun B, Wruck LM, Schultz WH, et al., Chronic transfusion practices for prevention of primary stroke in children with sickle cell anemia and abnormal TCD velocities. Am J Hematol 2012; 87: 428-30.
3. Ohene-Frempong K, Weiner SJ, Sleeper LA, et al., Cerebrovascular accidents in sickle cell disease: rates and risk factors. Blood 1998; 91: 288-94.
4. Adams RJ, Nichols FT, Figueroa R, et al., Transcranial Doppler correlation with cerebral angiography in sickle cell disease. Stroke 1992; 23: 1073-7.
5. Adams RJ, McKie VC, Brambilla D, et al., Stroke prevention trial in sickle cell anemia. Control Clin Trials 1998; 19: 110-29.
6. Scothorn DJ, Price C, Schwartz D, et al., Risk of recurrent stroke in children with sickle cell disease receiving blood transfusion therapy for at least five years after initial stroke. J Pediatr 2002; 140: 348-54.
7. Lee MT, Piomelli S, Granger S, et al., Stroke prevention trial in sickle cell anemia (STOP): extended follow-up and final results. Blood 2006; 108: 847-52.
8. Bader-Meunier B, Verlhac S, Elmaleh-Berges M, et al., Effect of transfusion therapy on cerebral vasculopathy in children with sickle-cell anemia. Haematologica 2009; 94: 123-6.
9. Kuo KH, Ward R, Kaya B, et al., A comparison of chronic manual and automated red blood cell exchange transfusion in sickle cell disease patients. Br J Haematol 2015; 170: 425-8.
10. Cohen AR, Martin MB, Silber JH, et al., A modified transfusion program for prevention of stroke in sickle cell disease. Blood 1992; 79: 1657-61.
11. Michot JM, Driss F, Guitton C, et al., Immunohematologic tolerance of chronic transfusion exchanges with erythrocytapheresis in sickle cell disease. Transfusion 2015;55:357-63.
12. Wahl SK, Garcia A, Hagar W, et al., Lower alloimmunization rates in pediatric sickle cell patients on chronic erythrocytapheresis compared to chronic simple transfusions. Transfusion 2012; 52: 2671-6.
13. Kim HC, Dugan NP, Silber JH, et al., Erythrocytapheresis therapy to reduce iron overload in chronically transfused patients with sickle cell disease. Blood 1994; 83: 1136-42.
14. Adamkiewicz TV, Abboud MR, Paley C, et al., Serum ferritin level changes in children with sickle cell disease on chronic blood transfusion are nonlinear and are associated with iron load and liver injury. Blood 2009; 114: 4632-8.
15. Raghupathy R, Manwani D, Little JA., Iron overload in sickle cell disease. Adv Hematol 2010; 2010: 272940.
16. Porter JB, Evangeli M, El-Beshlawy A., Challenges of adherence and persistence with iron chelation therapy. Int J Hematol 2011; 94: 453-60.