ANTIGEN-MATCHED DONOR BLOOD IN THE TRANSFUSION MANAGEMENT OF PATIENTS WITH SICKLE-CELL DISEASE

被引:117
作者
TAHHAN, HR
HOLBROOK, CT
BRADDY, LR
BREWER, LD
CHRISTIE, JD
机构
[1] E CAROLINA UNIV, PITT CTY MEM HOSP,SCH MED,DEPT PATHOL & LAB MED, TRANSFUS SERV, GREENVILLE, NC 27834 USA
[2] E CAROLINA UNIV, PITT CTY MEM HOSP, CHILDRENS HOSP EASTERN N CAROLINA,SCH MED, DEPT PEDIAT, GREENVILLE, NC USA
关键词
D O I
10.1046/j.1537-2995.1994.34794330008.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Alloimmunization to red cell antigens is a significant risk in chronically transfused patients with sickle cell disease. Antigen matching, by decreasing the likelihood of alloantibody development, may significantly facilitate long-term management while decreasing morbidity. Study Design and Methods: The transfusion records of 86 patients who underwent chronic transfusion for sickle cell disease at a tertiary-care medical center were reviewed retrospectively to determine the efficacy of an antigen-matching program in the prevention of alloimmunization to clinically significant red cell antigens. Recipients were phenotyped and given units matched for the K, C, E, S, and Fy(a) or Fy(b) antigens. Results: None (0%) of the 40 patients who received antigen-matched transfusions showed any evidence of alloimmunization, while 16 (34.8%) of the 46 patients who received both antigen-matched and non-antigen-matched transfusions developed clinically significant alloantibodies. The cost was 1.8 to 1.5 times that for a standard transfusion protocol. Conclusion: On the basis of this experience, it is recommended that transfusion centers engaged in the management of chronically transfused sickle cell anemia patients consider providing antigen-matched units for such patients. This is recommended not only because it prevents alloimmunization but also because such a program provides additional clinical benefits to the patient that may outweigh the higher costs of the process.
引用
收藏
页码:562 / 569
页数:8
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