Source, dose, benefits, risks, and prophylactic transfusion triggers
The goal of platelet transfusion is to stop or prevent bleeding in thrombocytopenic patients or those with platelet dysfunction [1
]. Bleeding is a relatively uncommon cause of death in non-trauma patients but can be a significant morbid event at worst and, at best, quite upsetting for patients, families, and providers. Thus, traditionally, with the view that platelet transfusion is essentially benign, the impetus has been to transfuse platelets aggressively to prevent rather than treat bleeding. There are two types of platelet products for transfusion. Whole blood platelets, which are derived from four to five whole blood donations, pooled, leukoreduced, bacterially tested, and irradiated, used to be the standard transfusion product but now are less frequently used in the US. Apheresis platelets derived from donors who spend a couple of hours on a cell separator have become the most commonly used product in the US. The usual doses have been in the range of 3 × 1011
to 5 × 1011
platelets per transfusion but one-quarter to one-half of these doses has been shown to be equivalent in preventing bleeding in a recent but as yet unpublished large national randomized trial (Prophylactic Platelet Dose on Transfusion Outcomes, or PLADO) [4
]. Whole blood pooled and apheresis platelets are considered by most experts to be interchangeable in terms of efficacy and safety.
Patients receiving pheresis platelets are likely to have a higher risk of hemolytic reactions if they are ABO-mismatched [5
] and a higher risk of acute lung injury (transfusion-related acute lung injury) due to having larger amounts of plasma from a single donor, but carry a lower risk of infectious disease transmission due to fewer donor exposures. Earlier studies have demonstrated that alloimmunization and refractoriness to transfusion (inability to raise the platelet count with transfusion) are common in recipients of non-leukoreduced transfusions [8
] and ABO-mismatched platelet transfusions [9
]. Thus, almost everyone agrees that platelet transfusions should always be leukoreduced and that every effort should be made to use only ABO-identical platelets whenever possible.
For patients who have severe or repeated fever, rigors, or allergic or pulmonary complications with transfusion (about 1-5% of patients; mostly fever, rigors, and/or urticaria), saline-washed platelets are available in some hospitals [10
]. These require about 2 hours of additional preparation time and contain about 20% fewer platelets than unwashed platelets. One study suggests that clinical outcomes (survival) are improved with the use of washed platelets in adult patients with acute leukemia and that post-transfusion fever, rigors, and urticaria can be almost completely eliminated [11
Traditionally, platelet transfusions in hematology-oncology have been given prophylactically as serious bleeding is fortunately uncommon in these patients. The safe threshold for prophylactic transfusion in a clinically stable patient who does not have serious bleeding (e.g., that requiring red cell transfusion or representing serious or life-threatening morbidity) is considered to be a platelet count of 10,000/µL [12
]. There is reasonable consensus that for patients who are bleeding, septic, or hemodynamically unstable, the threshold for transfusion should be raised to 15,000-20,000/µL. Patients with life-threatening bleeding in the chest or head are usually transfused at higher platelet count thresholds (30,000-50,000/µL). Despite the evidence that a platelet count of more than 10,000/µL is adequate to prevent spontaneous hemorrhage and that serious bleeding is quite rare at counts above 20,000/µL, many interventionalists and surgeons nonetheless insist on platelet counts of at least 25,000/µL for multi-lumen catheter insertion and 50,000/µL for invasive procedures such as major surgery or liver or lung biopsy. The evidence in support of these practices is nil, but traditional practices do not change without convincing evidence demonstrating that they are unnecessary or even counterproductive, and these practices may well be both.
An uncommon indication for platelet transfusion is a platelet dysfunction (due to disease or a commonly employed drug such as aspirin) that is associated with serious bleeding or that accompanies the need for major surgery or another high-risk invasive procedure such as liver biopsy.
One reason that strategies for platelet transfusion have been difficult to study and change is that the effectiveness of platelet transfusion is not easily evaluated. If the transfusion is therapeutic, then the amount and rate of bleeding are the only really important measures of response. Quantitation of these is not easily achieved. There are no laboratory tests that adequately measure the efficacy of platelet transfusion, thus clinical evaluation is the only appropriate approach. In the case of prophylactic platelet transfusions, the situation is even more difficult. The increase in platelet count is the only available response measure other than the absence of bleeding. The general goal has been to achieve a platelet count above 20,000/µL, but the post-transfusion platelet count is usually not measured except in hematology-oncology patients and, in any case, platelet count correlates very poorly with bleeding. Typically, platelet counts are performed each morning and if the count is below 10,000/µL, a platelet transfusion is given. In patients with bleeding or requiring invasive procedures, post-transfusion platelet counts can be performed at any time after the transfusion, from a few minutes to a few hours. Because increments are often transient in acutely ill patients, the transfusion should be performed just prior to any invasive procedure, not the day before or several hours before. A common practice, albeit one based on common sense rather than data, is to infuse platelets during the procedure to ensure that additional platelets are present during the time of maximal challenge to hemostasis.
Platelet transfusion refractoriness
If refractoriness to platelet transfusion (poor post-transfusion platelet count increments) is suspected, this is evaluated primarily by immediate post-transfusion count increments (approximately 10-60 minutes after completion of the transfusion). HLA antibody-mediated immune refractoriness is further differentiated from other causes such as sepsis, hypersplenism, and drug-related causes by measurement of anti-platelet/anti-HLA antibodies and failure to raise the platelet count post-transfusion. In other causes, there is often a short-lived (a few hours) rise in count but poor platelet survival post-transfusion. The most common cause of severe refractoriness is allosensitization, the formation of IgG antibodies to HLA-A,B (class I major histocompatibility complex) antigens in the transfusion recipient due to prior pregnancy or transfusion or both. Donor alloimmunization to HLA class I and II or granulocyte antigens (i.e., antibody in the platelet product) can be an etiology for transfusion-related acute lung injury in the recipient. Recipient alloimmunization to HLA class I in previous non-sensitized patients is almost entirely prevented by using leukoreduced red cells from which the platelets and white cells have been removed by filtration and leukoreduced platelets from which the white cells have been removed [8
]. Universal leukoreduction is standard procedure at almost all European hospitals. Unfortunately, not all hospitals in the US practice universal leukoreduction of blood components, thus patients may come to referral centers with recent prior transfusion sensitization. Women, particularly those with multiple pregnancies, are more likely to experience this complication than men are. Unfortunately, once refractoriness has developed, it portends a poor overall prognosis [15
In the refractory patient, anti-HLA class I antibody tests using panel reactivity that employs a cytotoxicity method are often used. An enzyme-linked immunosorbent assay or immunofluorescent assay that detects anti-platelet-specific antibodies (very rare) and HLA class I antibodies is also used in some instances. If specificities can be determined, selecting platelet donors who lack the class I HLA antigens to which the recipient has antibody is the simplest and fastest approach to dealing with immune refractoriness. Two other strategies have some success: HLA-A,B-matched platelets and crossmatched platelets. Both strategies have a good but not great success rate of about 50-75% if a grade A or B HLA match or crossmatched platelet apheresis unit is available. A grade A or B HLA match is when the donor platelets carry no HLA-A,B antigens that are not identical with or serologically cross-reactive with those of the recipient. Sometimes, a family member, particularly an HLA-matched sibling who served as the donor for a stem cell transplant, can be the best donor as they tend to be closely matched. Many cases of clinical refractoriness currently are due to drug-related anti-platelet antibodies, with common offending drugs being vancomycin, amphotericin, and other anti-microbials (rarely quinidine or other drugs). Tests for drug-related antibodies are not routinely available, and the primary approach is discontinuing the drug and observing whether transfusion responsiveness returns within a few days to a week of continuing platelet transfusion.