Clinical and laboratory factors underlying refractoriness to platelet transfusions

Of the spectrum of clinical and laboratory factors responsible for refractoriness to platelet transfusions, some are amenable to intervention, some to circumvention, and others only to acceptance and support for complications. Identification of the likely reason for refractoriness in a given individual patient is critical to determine the optimum management strategy. The blood bank or transfusion service can and perhaps should play a direct role in that strategy through the provision of single donor platelets collected by apheresis. Single donor platelets offer a number of real and theoretical advantages over random donor platelets, including the potential for crossmatching, reduction in net donor exposures, maintenance of ABO‐compatibility, improved inventory management, and perhaps diminished rate of alloimmunization. The sole perceived benefits of random donor platelets are cost and availability. The cost differential, however, needs to take into account a variety of factors beyond the immediate concern of platelet collection and distribution, including many highly dependent upon local factors. The optimum management of the platelet refractory patient requires more appropriate use of single donor apheresis platelets coupled with platelet crossmatching when necessary. Data from outcomes studies presented indicates that increased reliance upon single donor apheresis platelets at the expense of pooled random donor units can improve the overall quality of transfusion practice by decreasing platelet utilization, resource consumption, donor exposures, and platelet wastage. © 1996 Wiley‐Liss, Inc.

[1]  E. Gluckman Umbilical cord blood biology and transplantation , 1995, Current opinion in hematology.

[2]  K. Oksanen Leukocyte‐depleted blood components prevent platelet refractoriness in patients with acute myeloid leukemia , 1994, European journal of haematology.

[3]  L. Williamson,et al.  Bedside filtration of blood products in the prevention of HLA alloimmunization--a prospective randomized study. Alloimmunisation Study Group , 1994 .

[4]  K. Yuen,et al.  Clinical factors influencing the efficacy of pooled platelet transfusions , 1988 .

[5]  G. Andreu,et al.  Prevention of HLA immunization with leukocyte-poor packed red cells and platelet concentrates obtained by filtration. , 1988, Blood.

[6]  J. Akkerman,et al.  Use of leukocyte-depleted platelet concentrates for the prevention of refractoriness and primary HLA alloimmunization: a prospective, randomized trial. , 1991, Blood.

[7]  J. Rowe,et al.  Selection of platelets for refractory patients by HLA matching and prospective crossmatching , 1992, Transfusion.

[8]  F. Claas,et al.  Occurrence of Allogeneic HLA and Non-HLA Antibodies After Transfusion of Prestorage Filtered Platelets and Red Blood Cells: A Prospective Study , 1995 .

[9]  K. Anderson,et al.  Prophylactic versus therapeutic platelet transfusion practices in hematology and/or oncology patients , 1995, Transfusion.

[10]  J. Szer,et al.  Factors influencing 20‐hour increments after platelet transfusion , 1991, Transfusion.

[11]  K. Oksanen,et al.  Prevention of alloimmunization in patients with acute leukemia by use of white cell‐reduced blood components—a randomized trial , 1991, Transfusion.

[12]  J. Fehr,et al.  Safety of stringent prophylactic platelet transfusion policy for patients with acute leukaemia , 1991, The Lancet.

[13]  P. Mintz,et al.  Clinical and blood bank factors in the management of platelet refractoriness and alloimmunization. , 1993, Blood.

[14]  L. R. Hill,et al.  Prevention of refractoriness and HLA-alloimmunization using filtered blood products. , 1988, Blood.

[15]  S. Self,et al.  Refractoriness to random donor platelet transfusions in patients with aplastic anaemia: a multivariate analysis of data from 264 cases , 1987, British journal of haematology.

[16]  E. Beutler Platelet transfusions: the 20,000/microL trigger [see comments] , 1993 .

[17]  S. Slichter,et al.  A model to determine required pool size for HLA‐typed community donor apheresis programs , 1989, Transfusion.

[18]  T. Lister,et al.  Relative Importance of Immune and Non‐Immune Causes of Platelet Refractoriness , 1994, Vox sanguinis.

[19]  L. Skibsted,et al.  The frequency of platelet alloantibodies in pregnant women and the occurrence and management of neonatal alloimmune thrombocytopenic purpura. , 1990, Obstetrical & gynecological survey.

[20]  D. Brubaker,et al.  Relationship of HLA and platelet‐reactive antibodies in alloimmunized patients refractory to platelet therapy , 1987, American journal of hematology.