Medicine:Platelet transfusion refractoriness

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Short description: Platelet reduction following transfusion

Platelet transfusion refractoriness is the repeated 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 non-immune. Among immune-related refractoriness, antibodies against HLA antigens are the primary cause. Non-immune causes include splenomegaly (enlargement of the spleen), fever, and sepsis.[1][2]

Cause

Platelet refractoriness can be due to immune causes or non-immune causes.[3] Non-immune causes account for over 80% of cases of platelet refractoriness, and sepsis is one of the most common non-immune causes.[2][3][4][5] HLA alloimmunization is the commonest immune cause of platelet refractoriness.[2][3][4][5]

Non-immune causes

Patient-related

Platelet component-related

  • Age of platelet component[6][7]
  • ABO mismatch between platelet component and recipient[6][7]
  • Number of platelets within the component if platelet increment (PI) is used to calculate platelet refractoriness[6]
  • Pathogen-reduced platelet component[8]

Immune causes

Diagnosis

Platelet transfusion refractoriness can be defined in several different ways. All measures of platelet refractoriness are defined by the timing of the post-transfusion platelet count, usually 1 hour post transfusion or 24 hours post transfusion or both.[2][9]

Platelet increment (PI)

This is the simplest method, and only requires data on the platelet count before and after the transfusion.[9] The platelet increment is also known as the absolute count increment and count increment.[5][10]

PI = post-transfusion platelet count - pre-transfusion platelet count

However, it is affected by the number of platelets given in the transfusion (platelet dose) and the patient's blood volume. Larger patients and smaller platelet doses decrease the platelet increment.[2][9] These factors are adjusted for in the other methods of defining platelet refractoriness.[2][3][9]

A 1-hour post-transfusion PI of less than 5 to 10 x 109/l is considered evidence of platelet refractoriness.[5][10] Due to lack of data on platelet dose this is often the only measure of platelet refractoriness that can be performed in routine clinical practice.[5]

Percentage platelet recovery (PPR)

Requires data on the platelet increment (PI), the patient's total blood volume (TBV) - estimated using the patient's weight multiplied by 0.075, and the number of platelets transfused (platelet dose)[10][11]

PPR = ((PI x TBV)/PD) x 100

At 1 hour post-transfusion, a PPR < 20% is considered evidence of platelet refractoriness.[5][10] At 16 hours post-transfusion a PPR < 10% is considered evidence of platelet refractoriness.[10]

Percentage platelet increment (PPI)

PPI is very similar to the percentage platelet recovery (PPR) but there has been an additional adjustment for splenic pooling of platelets (PPR multiplied by 2/3)[5][11]

PPI = PPR/0.67 = ((PI / 0.67) x TBV)/PD x 100

Corrected count increment (CCI)

This requires data on the platelet increment (PI, in platelets/µl), the patient's Body surface area (BSA, in m2), and the number of platelets transfused (PD, in 1011).[5][10][11]

[math]\displaystyle{ {CCI} = PI * \frac{BSA}{PD} }[/math]

For example, a PI of 25,000 platelets/µl, a BSA of 1.8m2 and a PD of 4x1011 gives a CCI of 11,250 platelets*m2/1011µl

At 1 hour post-transfusion a CCI greater than 7500 indicates a sufficient post-transfusion increment, whereas a CCI less than 7500 is considered diagnostic of platelet refractoriness.[10] At 24 hours post transfusion a CCI less than 5000 suggests platelet refractoriness.[10]

Platelet dose

Some blood banks maintain records of the estimated number of platelets in each unit.[5] Current requirements in the US stipulate that a unit of apheresis platelets must contain at least 3.0 x1011 platelets.[12] In England only 1% of adult platelet components are tested to check the number of platelets meet the minimum required standard of 2.4 x 1011 platelets.[13][14] Only components that contain fewer than 1.6 x 1011 platelets are discarded.[13][14] This means that there can be a lot of variability in the number of platelets contained within each transfusion.[5]

Treatment

Treatment depends on the underlying cause.[citation needed]

Non-immune causes are usually treated by treating the underlying cause e.g. sepsis.[3][15]

If there is no obvious non-immune cause, a first step can be to use platelet components that are likely to produce the greatest platelet increment (less than 3 days old and ABO-matched), while further investigations are performed (testing for HLA antibodies).[3][4]

If an immune cause is suspected and HLA antibodies are detected, then HLA-selected platelet components can be used.[3][4] Although HLA-selected platelets lead to improved platelet increments at 1 hour post-transfusion,[16] there is currently insufficient evidence to demonstrate their clinical effectiveness at preventing bleeding.[16]

If HLA antibodies are not detected, and HPA antibodies are detected, then HPA-selected or crossmatched platelet components can be used.[3][7][15]

HLA and HPA-selected components should not be used if no HLA or HPA antibodies are detected.[15]

References

  1. ↑ 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 978-0-7817-4996-1 
  2. ↑ 2.0 2.1 2.2 2.3 2.4 2.5 Stanworth, Simon J.; Navarrete, Cristina; Estcourt, Lise; Marsh, Judith (2015). "Platelet refractoriness – practical approaches and ongoing dilemmas in patient management" (in en). British Journal of Haematology 171 (3): 297–305. doi:10.1111/bjh.13597. ISSN 1365-2141. PMID 26194869. 
  3. ↑ 3.0 3.1 3.2 3.3 3.4 3.5 3.6 3.7 "Guidelines for the management of platelet transfusion refractoriness". http://hospital.blood.co.uk/media/2130/d5795605-7d36-40ce-8fb9-8c77254e24c6.pdf. 
  4. ↑ 4.0 4.1 4.2 4.3 "transfusion.com.au" (in en). https://transfusion.com.au/transfusion_practice/platelet_refractoriness. 
  5. ↑ 5.0 5.1 5.2 5.3 5.4 5.5 5.6 5.7 5.8 5.9 Hod, Eldad; Schwartz, Joseph (2008). "Platelet transfusion refractoriness" (in en). British Journal of Haematology 142 (3): 348–360. doi:10.1111/j.1365-2141.2008.07189.x. ISSN 1365-2141. PMID 18510692. 
  6. ↑ 6.0 6.1 6.2 Slichter, Sherrill J.; Granger, Suzanne; Kaufman, Richard M.; Hess, John R.; Ness, P. M.; Strauss, Ronald G.; Assmann, Susan F.; Triulzi, Darrell J. (2012-06-07). "The impact of platelet transfusion characteristics on posttransfusion platelet increments and clinical bleeding in patients with hypoproliferative thrombocytopenia" (in en). Blood 119 (23): 5553–5562. doi:10.1182/blood-2011-11-393165. ISSN 1528-0020. PMID 22496156. 
  7. ↑ 7.0 7.1 7.2 Petraszko, Tanya; Zeller, Michelle (2018). Chapter 18: Platelet Transfusion, Alloimmunization and Management of Platelet Refractoriness. Canadian Blood Services. https://professionaleducation.blood.ca/en/transfusion/guide-clinique/platelet-transfusion-alloimmunization-and-management-platelet. 
  8. ↑ Estcourt, Lise J; Malouf, Reem; Hopewell, Sally; Trivella, Marialena; Doree, Carolyn; Stanworth, Simon J; Murphy, Michael F (2017-07-30). "Pathogen-reduced platelets for the prevention of bleeding". Cochrane Database of Systematic Reviews 7 (9): CD009072. doi:10.1002/14651858.cd009072.pub3. ISSN 1465-1858. PMID 28756627. 
  9. ↑ 9.0 9.1 9.2 9.3 Rebulla, Paolo (2005). "A mini-review on platelet refractoriness". Haematologica 90 (2): 247–253. ISSN 1592-8721. PMID 15710579. 
  10. ↑ 10.0 10.1 10.2 10.3 10.4 10.5 10.6 10.7 Pavenski, Katerina; Freedman, John; Semple, J. W. (2012). "HLA alloimmunization against platelet transfusions: pathophysiology, significance, prevention and management". Tissue Antigens 79 (4): 237–245. doi:10.1111/j.1399-0039.2012.01852.x. ISSN 1399-0039. PMID 22385314. 
  11. ↑ 11.0 11.1 11.2 Rebulla, P. (1993). "Formulae for the definition of refractoriness to platelet transfusion" (in en). Transfusion Medicine 3 (1): 91–92. doi:10.1111/j.1365-3148.1993.tb00108.x. ISSN 1365-3148. PMID 8038900. 
  12. ↑ AABB (2014). Standards for Blood Banks and Transfusion Services. AABB. ISBN 9781563958878. 
  13. ↑ 13.0 13.1 "Platelets, Apheresis, Leucocyte Depleted". https://www.transfusionguidelines.org/red-book/chapter-7-specifications-for-blood-components/7-10-platelets-apheresis-leucocyte-depleted. 
  14. ↑ 14.0 14.1 "Platelets, Pooled, Buffy Coat Derived, in Additive Solution and Plasma, Leucocyte Depleted". https://www.transfusionguidelines.org/red-book/chapter-7-specifications-for-blood-components/7-11-platelets-in-additive-solution-and-plasma-leucocyte-depleted. 
  15. ↑ 15.0 15.1 15.2 Nahirniak, Susan; Slichter, Sherrill J.; Tanael, Susano; Rebulla, Paolo; Pavenski, Katerina; Vassallo, Ralph; Fung, Mark; Duquesnoy, Rene et al. (2015). "Guidance on platelet transfusion for patients with hypoproliferative thrombocytopenia". Transfusion Medicine Reviews 29 (1): 3–13. doi:10.1016/j.tmrv.2014.11.004. ISSN 1532-9496. PMID 25537844. 
  16. ↑ 16.0 16.1 Pavenski, Katerina; Rebulla, Paolo; Duquesnoy, Rene; Saw, Chee Loong; Slichter, Sherrill J.; Tanael, Susano; Shehata, Nadine (2013). "Efficacy of HLA-matched platelet transfusions for patients with hypoproliferative thrombocytopenia: a systematic review" (in en). Transfusion 53 (10): 2230–2242. doi:10.1111/trf.12175. ISSN 1537-2995. PMID 23550773. 



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