Platelet transfusion refractoriness

Platelet transfusion refractoriness is the failure to achieve the desired level of blood platelets in a patient following a platelet transfusion. The cause of refractoriness may be either immune or nonimmune based. Among immune-related refractoriness, antibodies against HLA antigens are the primary cause. Non-immune causes include splenomegaly (enlargement of the spleen), fever, and recent chemotherapy.[1]

Diagnosis

Platelet transfusion refractoriness is typically diagnosed using the corrected count increment, which requires 4 items of information:

  1. Pre-transfusion platelet count
  2. Post-transfusion platelet count: the post-transfusion blood sample for this measurement should be collected 10โ€“60 minutes after the transfusion has been completed
  3. Body surface area
  4. Number of platelets transfused: the blood bank maintains records of the estimated number of platelets in each unit. Current requirements in the US stipulate that a unit of apheresis platelets must contain at least 3.0 x1011 platelets.[2]

The CCI is calculated as follows: CCI= (Post-transfusion platelet count - Pre-transfusion platelet count)(BSA) รท (number of platelets transfused).

A CCI greater than 7500 indicates a sufficient post-transfusion increment, whereas a CCI less than 7500 is considered diagnostic of platelet refractoriness.

Immune-mediated refractoriness usually shows little or no increment in the immediate post-transfusion platelet count. Non-immune refractoriness may show an initial rise in platelet count, but a subsequent 8-hour or 12-hour post-transfusion sample shows a return to the baseline platelet count.

References

  1. โ†‘ Colman, Robert W.; Marder, Victor J.; Clowes, Alexander W.; George, James N.; Goldhaber, Samuel Z. (2005), Hemostasis and Thrombosis: Basic Principles and Clinical Practice (5th ed.), Lippincott Williams & Wilkins, p. 1195, ISBN 0-7817-4996-4
  2. โ†‘ AABB (2014). Standards for Blood Banks and Transfusion Services. AABB. ISBN 9781563958878.


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