Prolonged isolated red blood cell transfusion requirement after allogeneic blood stem cell transplantation: identification of patients at risk

被引:12
作者
Dahl, Daphne
Hahn, Andreas
Koenecke, Christian
Heuft, Hans-Gert
Dammann, Elke
Stadler, Michael
Buchholz, Stefanie
Krauter, Juergen
Eder, Matthias
Sykora, Karl-Walter
Klein, Christoph
Ganser, Arnold
Sauer, Martin
机构
[1] Hannover Med Sch, Dept Pediat Hematol Oncol, D-30625 Hannover, Germany
[2] Hannover Med Sch, Dept Biometr, D-30625 Hannover, Germany
[3] Hannover Med Sch, Dept Med Hematol Oncol Hemostasis & Stem Cell Tra, D-30625 Hannover, Germany
[4] Hannover Med Sch, Dept Transfus Med, D-30625 Hannover, Germany
关键词
BONE-MARROW-TRANSPLANTATION; AUTOIMMUNE HEMOLYTIC-ANEMIA; APLASIA FOLLOWING MAJOR; ERYTHROPOIESIS; DEFICIENCY; PREVENTION; CHIMERISM; LEUKEMIA; ORIGIN;
D O I
10.1111/j.1537-2995.2009.02461.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Delayed donor red blood cell chimerism (DRCC), pure red blood cell aplasia (PRCA), and autoimmune hemolytic anemia (AIHA) are poorly documented complications after hematopoietic cell transplantation (HCT). The clinical variable "prolonged isolated red blood cell transfusion requirement" (PRTR) was evaluated as a trigger for an extended diagnostic workup. STUDY DESIGN AND METHODS: PRTR was defined as the need for red blood cell (RBC) transfusions beyond Day 60 after HCT. We analyzed 487 patients transplanted between 2000 and 2006. Median age was 37 years (range, 0-70 years). Peripheral blood stem cells (n = 344), marrow (n = 138), and cord blood (n = 5) from 278 unrelated and 209 family donors were used. RESULTS: Univariate analysis identified age (incidence of 18.3% among elderly patients, 10.5% in adults, and 2.0% among children [p = 0.002]), ABO incompatibility (16.4% after major incompatible, 2.9% after minor incompatible, and 9.4% after ABO-compatible transplantations [p = 0.003]), conditioning (15.2% after reduced-intensity regimens vs. 7.3% after myeloablative conditioning; p = 0.006), donor type (13.2% after HLA-matched unrelated, 13.6% after mismatched unrelated, 5.7% after matched related, and 0.0% after mismatched related grafts; p = 0.026), and acute graft-versus-host disease (aGVHD; 7.1% with aGVHD vs. 12.5% without aGVHD; p = 0.046) as predisposing factors. In multivariate analysis minor ABO incompatibility (odds ratio [OR] = 0.2, p = 0.01), younger age (OR = 0.1, p = 0.02), and matched related HCT (OR = 0.4, p = 0.02) remained independent protective factors. CONCLUSIONS: PRTR could serve as a trigger for a standardized screening for DRCC, PRCA, and AIHA after HCT.
引用
收藏
页码:649 / 655
页数:7
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