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Single-Donor Platelets:Arguments for Preferential Use
Paul M. Ness, MD
Transfusion Medicine Division
Johns Hopkins Medical Institutions
TRANSFUSION PRACTICESPlatelets
• Prepared as a byproduct of whole blood collections or by apheresis
• Major use for (1) acute hemorrhage due to thrombocytopenia or (2)prophylaxis during periods of bone marrow aplasia
• Effectiveness limited by alloimmunization during chronic therapy or septic reactions until recently
APHERESIS PLATELETSPOTENTIAL ADVANTAGES
• Reduction in infectious complications
• Reduction in transfusion reactions
• Ease of leukodepletion
• Reduction in transfusion frequency
• Treatment of alloimmunized recipients
• Prevention of alloimmunization
SPTRJOHNS HOPKINS (1987-1990)
• Incidence of 1:4200 transfusions in oncology patients
• Septic reactions were more common with random donor platelet concentrates (RDP)
• Reactions were more common with longer periods of storage
• Source was skin contaminant in 4/7 cases; bacteremic donor in 3/7 cases
Conclusions
• Single donor platelets substantially reduce but do not eliminate SPTR.
• Pretransfusion screening has substantially reduced SPTR, but pathogen redcution will be required to eliminate all SPTR.
• Although current risks of viral infections are miniscule, SDP may be of value to prevent emerging infections
Platelet Transfusion Reactions
• Febrile reactions due to white cells or cytokines produced during storage
• Allergic reactions
• TRALI
Moderate to Severe ReactionsTRAP Study
• Temperature increase > 2 degrees C
• Chills with rigors
• Extensive urticarial eruptions
• Dyspnea
• Cyanosis
• Bronchospasm
• Anaphylaxis
Reduction in Transfusion Reactions
• Premedication is often prescribed but convincing data of efficacy are lacking
• Washing platelets reduces allergic reactions but increments and survival are compromised
• Limiting donor exposure should reduce reactions from contaminating elements
• ULR reduces febrile reactions
Ease of Leukodepletion
• Ongoing debate in the US about universal versus selective leukoreduction
• Current apheresis equipment produces SDP which routinely meet ULR requirements
• Filtration of PC to meet leukoreduction requirements is cumbersome
PLATELET TRANSFUSIONSNorol et al, BLOOD 1998
• Higher platelet dosages increase the transfusion interval from 2 to 4 days
• Higher doses facilitate outpatient therapy.
• Importance of dose is controversial for prevention of bleeding in patients with hematologic malignancies; dose trial to be initiated by TMH Network
PLATELET ALLOIMMUNIZATION
• Most important long term complication of platelet transfusion therapy
• Incidence depends upon patients under study, previous transfusions or pregnancies, and intensity of therapy
• About 1/3 of patients with AML become alloimmunized and refractory to random platelets
PLATELET ALLOIMMUNIZATION
• About 50% of HLA “matched” transfusions are failures
• Alloimmunized recipients remain at risk for hemorrhage when transfusions fail
• Therapy for refractory patients is expensive
SELECTION OF COMPATIBLE DONORS
• Define antibody specificity and avoid incompatible antigens
• HLA matching ( family or volunteer)
• Platelet crossmatching
• Obtain compatible platelets by apheresis
ALLOIMMUNIZATION Therapy Prevention
• HLA matching• Platelet crossmatching• Experimental
therapies
• Leukodepletion• UV irradiation• Reducing donor
exposure with SDP is not effective
APHERESIS PLATELETSPOTENTIAL ADVANTAGES
• Reduction in infectious complications• Reduction in transfusion reactions• Ease of leukodepletion• Reduction in transfusion frequency• Treatment of alloimmunized recipients• Prevention of alloimmunization (UNPROVEN)• Platelet quality
Summary
• We switched to SDP primarily because of the problem with SPTR; even with bacterial detection, we still believe that patient care is enhanced by using SDP.
• Avoiding pooling was a large motivation for the laboratory to move to SDP; with pool and store at the blood center now permissible, we might re-evaluate our position, depending upon the cost.