Factors influencing post-transfusional platelet increment in pediatric patients given hematopoietic stem cell transplantation

被引:21
作者
Balduini, CL [1 ]
Salvanesch, L
Klersy, C
Noris, P
Mazzucco, M
Rizzuto, F
Giorgiani, G
Perotti, C
Stroppa, P
Di Pumpo, M
Nobili, B
Locatelli, F
机构
[1] Policlin San Matteo, IRCCS, I-27100 Pavia, Italy
[2] Univ Pavia, IRCCS San Matteo, Dept Internal Med, I-27100 Pavia, Italy
[3] IRCCS San Matteo, Ctr Blood Transfus, Pavia, Italy
[4] Univ Pavia, IRCCS San Matteo, Dept Pediat, I-27100 Pavia, Italy
[5] Univ Naples Federico II, Policlin 2, Osped 1, Dept Pediat, I-80138 Naples, Italy
关键词
bone marrow transplantation; platelet transfusion; human platelet antigens; alloantibodies;
D O I
10.1038/sj.leu.2402307
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Patients undergoing allogeneic hematopoietic stem cell transplantation (HSCT) always require platelet transfusions, but the increase in platelet count is often less than expected. Since factors responsible for poor response to platelet transfusions in this clinical setting are largely unknown, we performed a prospective study in 87 consecutive children transplanted in a single institution. The mean 16-h corrected count increment (CCI) of 598 platelet transfusions was 5.76 +/- 8.32 x 10(9)/l. Both before and after HSCT, 13.8% of patients had antibodies against HLA and/or platelet-specific antigens. Univariate analysis identified 12 factors significantly associated with a lower post-transfusion CCI, but only four reached statistical significance in the multivariate analysis. These four factors were concomitant therapy with vancomycin, alloimmunization, use of an Autopheresis cell separator for preparation of platelet concentrates and cytomegalovirus infection. We, therefore, suggest that a better response to platelet transfusions could be obtained by choosing a suitable cell separator, by avoiding the use of vancomycin and by adopting measures that reduce alloimmunization and CMV infection. Moreover, screening patients for HLA and platelet-specific antibodies before HSCT would identify the majority of subjects who will develop alloimmune refractoriness after transplantation and would allow the search for a compatible donor in advance.
引用
收藏
页码:1885 / 1891
页数:7
相关论文
共 35 条
[1]   Clinical and laboratory factors associated with platelet transfusion refractoriness: A case-control study [J].
Alcorta, I ;
Pereira, A ;
Ordinas, A .
BRITISH JOURNAL OF HAEMATOLOGY, 1996, 93 (01) :220-224
[2]   Incompatibility for CD31 and human platelet antigens and acute graft-versus-host disease after bone marrow transplantation [J].
Balduini, CL ;
Noris, P ;
Giorgiani, G ;
Martinetti, M ;
Klersy, C ;
Spedini, P ;
Belletti, S ;
Maccario, R ;
Gusberti, L ;
Locatelli, F .
BRITISH JOURNAL OF HAEMATOLOGY, 1999, 106 (03) :723-729
[3]  
BISHOP JF, 1988, BLOOD, V71, P383
[4]   Influence of antibiotics on posttransfusion platelet increment [J].
Bock, M ;
Muggenthaler, KH ;
Schmidt, U ;
Heim, MU .
TRANSFUSION, 1996, 36 (11-12) :952-954
[5]   Benefit of prestorage leukocyte depletion of single-donor platelet concentrates [J].
Chalandon, Y ;
Mermillod, B ;
Beris, P ;
Doucet, A ;
Chapuis, B ;
Roux-Lombard, P ;
Dayer, JM .
VOX SANGUINIS, 1999, 76 (01) :27-37
[6]   RELATIVE IMPORTANCE OF IMMUNE AND NONIMMUNE CAUSES OF PLATELET REFRACTORINESS [J].
DOUGHTY, HA ;
MURPHY, MF ;
METCALFE, P ;
ROHATINER, AZS ;
LISTER, TA ;
WATERS, AH .
VOX SANGUINIS, 1994, 66 (03) :200-205
[7]  
Friedberg R C, 1995, Curr Opin Hematol, V2, P493
[8]   Alloimmunization to platelets in heavily transfused patients with sickle cell disease [J].
Friedman, DF ;
Lukas, MB ;
Jawad, A ;
Larson, PJ ;
OheneFrempong, K ;
Manno, CS .
BLOOD, 1996, 88 (08) :3216-3222
[9]   CLINICAL MANIFESTATIONS OF GRAFT VERSUS HOST DISEASE IN HUMAN RECIPIENTS OF MARROW FROM HL-A-MATCHED SIBLING DONORS [J].
GLUCKSBERG, H ;
STORB, R ;
FEFER, A ;
BUCKNER, CD ;
NEIMAN, PE ;
CLIFT, RA ;
LERNER, KG ;
THOMAS, ED .
TRANSPLANTATION, 1974, 18 (04) :295-304
[10]  
Govindarajan R, 1999, AM J HEMATOL, V62, P122, DOI 10.1002/(SICI)1096-8652(199910)62:2<122::AID-AJH14>3.3.CO