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Therapeutic plasma exchange in the treatment of thrombotic microangiopathies


Authors: M. Lánská 1;  Z. Kořístek 2;  P. Žák 1
Authors‘ workplace: IV. interní hematologická klinika LF UK a FN Hradec Králové 1;  Klinika hematoonkologie LF OU a FN Ostrava 2
Published in: Transfuze Hematol. dnes,30, 2024, No. S1, p. 7-15.
Category:
doi: https://doi.org/10.48095/cctahd2024suppl1S7

Overview

Therapeutic plasma exchange (TPE) has an irreplaceable place in the treatment of some types of thrombotic microangiopathies. In TTP, it has become the standard of care. TPE is defined by the American Society for Apheresis (ASFA) as a therapeutic extracorporeal procedure in which the patient‘s plasma is separated from other blood components. Although it is an invasive technique requiring high-quality venous access, TPE is quite safe, and when performed correctly, complications are rare. It can be started within tens of minutes if necessary, and it has essentially no real contraindications. Separation of plasma from other blood components is ensured by centrifugation or membrane filtration. Crystalloids, 5% albumin solution and freshly frozen donor plasma are used as a replacement solution in various proportions and combinations and nowadays, solvent-detergent-treated plasma is used increasingly. At least one total plasma volume (TPV) of the patient should be replaced in one procedure, with less than 70% of the TPV being replaced. It is important to remember to collect blood samples for ADAMTS13 and other tests, or preserve plasma samples, before starting TPE treatment, as interpretation of results from samples collected after TPE may be erroneous. The efficacy of TPE is determined by two mechanisms: 1) removal of the disease mediator or plasma components contributing to the pathogenesis of the condition; 2) delivery of the missing or dysfunctional plasma component when plasma is used as a replacement solution. The efficacy of TPE varies between the various forms of thrombotic microangiopathies, ranging from a clear and prompt effect in TTP to no effect at all in some forms of atypical haemolytic uraemic syndrome.

Keywords:

thrombotic thrombocytopenic purpura – therapeutic plasma exchange – thrombotic microangiopathy – plasma


Sources
1. Novotný J, Penka M. Trombotické mikroangiopatie. Transfuze Hematol Dnes. 2020; 26 (2): 80–90.
2. Moschcowitz E. An acute febrile pleiochromic anemia with hyaline thrombosis of the terminal arterioles and capillaries. An undescribed disease. Arch Intern Med. 1925; 6 (1): 89–93.
3. Gasser C, Gauthier E, Steck A, Siebenmann RE, Oechslin R. Hämolytisch-urämische syndrome bilaterale nierenrindennekrosen bei akuten erworbenchen hämolytischen anämien. Schweiz Med Wschr. 1955; 85: 905–909.
4. Rubenstein MA, Kagan BM, MacGillviray MH, Merliss R, Sacks H. Unusual remission in a case of thrombotic thrombocytopenia purpura syndrome following fresh blood exchange transfusions. Ann InternMed. 1959; 51: 1409–1419.
5. Bukowski RM, Hewlett JS, Harris JW, et al. Exchange transfusions in the treatment of thrombotic thrombocytopenic purpura. Semin Hematol. 1976; 13: 219–232.
6. Garthwaite T, Laurie A, Aster RH, Kaminskas E, Pisciotta AV. Remission in thrombotic thrombocytopenic purpura apparently induced by exchange transfusion [abstract]. Clin Res. 1976; 24: 570A.
7. Bukowski RM, King JW, Hewlett JS. Plasmapheresis in the treatment of thrombotic thrombocytopenic purpura. Blood. 1977; 50 (3): 413–417.
8. Byrnes JJ, Khurana M. Treatment of thrombotic thrombocytopenic purpura with plasma. N Engl J Med. 1977; 297 (25): 1386–1389.
9. Rock GA, Shumak KH, Buskard NA, et al. Comparison of plasma exchange with plasma infusion in the treatment of thrombotic thrombocytopenic purpura. N Engl J Med. 1991; 325 (6): 393–397.
10. Furlan M, Robles R, Lammle B. Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis. Blood. 1996; 87: 4223–4234.
11. Tsai H-M. Physiologic cleavage of von Willebrand factor by a plasma protease is dependent on its conformation and requires calcium ion. Blood. 1996; 87: 4235–4244.
12. Furlan M, Robles R, Solenthaler M, Wassmer M, Sandoz P, Lammle B. Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura. Blood. 1997; 89: 3097–3103.
13. Clark WF. Thrombotic microangiopathy: current knowledge and outcomes with plasma exchange. Semin Dialysis. 2012; 25 (2): 214–219.
14. Keklik M, Çelik S, Yıldızhan E. Comparison of centrifugal and membrane filtration modalities on therapeutic plasma exchange. J Clin Apher. 2022; 37 (3): 217–222.
15. Hafer C, Golla P, Gericke M, et al. Membrane versus centrifuge-based therapeutic plasma exchange: a randomized prospective crossover study. Int Urol Nephrol. 2016; 48: 133–138.
16. Kes P, Janssens ME, Bašić-Jukić N, Kljak M. A randomized crossover study comparing membrane and centrifugal therapeutic plasma exchange procedures. Transfusion. 2016; 56: 3065–3072.
17. Ward DM. Conventional apheresis therapies: a review. J Clin Apher. 2011; 26 (5): 230–238.
18. Winters JL. Hematology Am Soc Hematol Educ Program. 2017; 2017 (1): 632–638. doi: 10.1182/asheducation-2017.1.632.
19. Reeves HM, Winters JL. The mechanisms of action of plasma exchange. Br J Haematol. 2014; 164 (3): 342–351. doi: 10.1111/bjh.12629.
20. Ipe TS, Marques MB. Vascular access for therapeutic plasma exchange. Transfusion. 2018; 58 (Suppl 1): 580–589.
21. Cheng CW, Hendrickson JE, Tormey CA, Sidhu D. Therapeutic plasma exchange and its impact on drug levels: an ACLPS critical review. Am J Clin Pathol. 2017; 148 (3): 190–198.
22. Piedrafita A, Ribes D, Cointault O, Chauveau D, Faguer S, Huart A. Plasma exchange and thrombotic microangiopathies: from pathophysiology to clinical practice. Transfusion Apheresis Sci. 2020; 59 (6): 102990.
23. Lee LJ, Roland KJ, Sreenivasan GM, Zypchen LN, Ambler KL, Yenson PR. Solvent-detergent plasma for the treatment of thrombotic microangiopathies: a Canadian tertiary care centre experience. Transfusion Apheresis Sci. 2018; 57 (2): 233–235.
24. Bauer PR, Ostermann M, Russell L, et al. Plasma exchange in the intensive care unit: a narrative review. Intensive Care Med. 2022; 48: 1382–1396.
25. Rizvi MA, Vesely SK, George JN, et al. Complications of plasma exchange in 71 consecutive patients treated for clinically suspected thrombotic thrombocytopenic purpura-hemolytic-uremic syndrome. Transfusion. 2000; 40: 896–901.
26. Som S, Deford CC, Kaiser ML, et al. Decreasing frequency of plasma exchange complications in patients treated for thrombotic thrombocytopenic purpura-hemolytic uremic syndrome, 1996 to 2011. Transfusion. 2012; 52: 2525–2532.
27. McClain RS, Terrell DR, Vesely SK, George JN. Plasma exchange complications in patients treated for thrombotic thrombocytopenia purpura–hemolytic uremic syndrome: 2011 to 2014. Transfusion. 2014; 54 (12): 3257–3259.
28. Som S, Deford CC, Kaiser ML, et al. Decreasing frequency of plasma exchange complications in patients treated for thrombotic thrombocytopenic purpura-hemolytic uremic syndrome, 1996 to 2011. Transfusion. 2012; 52: 2525–2532.
29. Connelly‐Smith L, Alquist CR, Aqui NA, et al. Guidelines on the use of therapeutic apheresis in clinical practice – evidence‐based approach from the Writing Committee of the American Society for Apheresis: the ninth special issue. J Clin Apher. 2023; 38 (2): 77–278.
30. Bandarenko N, Brecher ME. United States thrombotic thrombocytopenic purpura apheresis study group (US TTP ASG): multicenter survey and retrospective analysis of current efficacy of therapeutic plasma exchange. J Clin Apher. 1998; 13: 133–141.
31. Chae P, Raval JS, Liles D, Park YS, Mazepa MA. Plasma exchange taper for acquired TTP is protective against recurrence at both 30 days and 6 months: a retrospective study from 2 academic medical centers. Blood. 2015; 126 (23): 1046.
32. Raval JS, Mazepa MA, Rollins‐Raval MA, Kasthuri RS. Therapeutic plasma exchange taper does not decrease exacerbations in immune thrombotic thrombocytopenic purpura patients. Transfusion. 2020; 60 (8): 1676–1680.
33. Patriquin CJ, Clark WF, Pavenski K, et al. How we treat thrombotic thrombocytopenic purpura: results of a Canadian TTP practice survey. J Clin Apher. 2017; 32: 246–256.
34. Mazepa MA, Raval JS, Brecher ME, et al. Treatment of acquired thrombotic thrombocytopenic purpura in the U.S. remains heterogeneous: current and future points of clinical equipoise. J Clin Apher. 2018; 33: 291–296.
35. Peyvandi F, Scully M, Kremer Hovinga JA, et al. Caplacizumab for acquired thrombotic thrombocytopenic purpura. N Engl J Med. 2016; 374 (6): 511–522.
36. Hrdličková R, Blahutová Š, Kovářová P, Čermáková Z. Vrozená trombotická trombocytopenická purpura. Transfuze Hematol Dnes. 2023; 29 (Suppl 3): 3S34–3S37.
37. Menne J, Nitschke M, Stingele R, et al. Validation of treatment strategies for enterohaemorrhagic Escherichia coli O104: H4 induced haemolytic uraemic syndrome: case-control study. Br Med J. 2012; 345: e4565.
38. Nathanson S, Kwon T, Elmaleh M, et al. Acute neurological involve-ment in diarrhea associated hemolytic uremic syndrome. Clin J AmSoc Nephrol. 2010; 5: 1218–1228.
39. Michael M, Bagga A, Sartain SE, Smith RJ. Haemolytic uraemic syndrome. The Lancet. 2022; 400 (10364): 1722–1740.
40. Fakhouri F, Schwotzer N, Frémeaux-Bacchi V. How I diagnose and treat atypical haemolytic uremic syndrome. Blood. 2023; 141 (9): 984–995.
41. Winters JL. Plasma exchange in thrombotic microangiopathies (TMAs) other than thrombotic thrombocytopenic purpura (TTP). Hematology 2017, Am Soc Hematol Educ Program Book. 2017; 2017 (1): 632–638.
42. Yang LP, Zhao P, Wu YJ, et al. Treatment outcome and efficacy of therapeutic plasma exchange for transplant-associated thrombotic microangiopathy in a large real-world cohort study. Bone Marrow Transplant. 2022; 57: 554–561.
43. Young JA, Pallas CR, Knovich MA. Transplant-associated thrombotic microangiopathy: theoretical considerations and a practical approach to an unrefined diagnosis. Bone Marrow Transplant. 2021; 56 (8): 1805–1817.
44. Bennett CL, Jacob S, Dunn BL, et al. Ticlopidine-associated ADAMTS13 activity deficient thrombotic thrombocytopenic purpura in 22 persons in Japan: a report from the Southern Network on Adverse Reactions (SONAR). Br J Haematol. 2013; 161: 896–898.
45. Simetka O, Klat J, Gumulec J, Dolezalkova E, Salounova D, Kacerovsky M. Early identification of women with HELLP syndrome who need plasma exchange after delivery. Transfus Apher Sci. 2015; 52: 54–59.
46. Colpo A, Marson P, Pavanello F, et al. Therapeutic apheresis during pregnancy: A single center experience. Transfusion Apher Sci. 2019; 58 (5): 652–658.
47. Wind M, Gaasbeek AG, Oosten LE, et al. Therapeutic plasma exchange in pregnancy: A literature review. Eur J Obst Gynecol Reprod Biol. 2021; 260: 29–36.
48. Li A, Makar RS, Hurwitz S, et al. Treatment with or without plasma exchange for patients with acquired thrombotic microangiopathy not associated with severe ADAMTS13 deficiency: a propensity score-matched study. Transfusion. 2016; 56 (8): 2069–2077.
PODÍL AUTORŮ NA RUKOPISU
ML – příprava rukopisu
ZK, PZ – korekce a revize rukopisu
PROHLÁŠENÍ AUTORŮ
Autoři práce prohlašují, že v souvislosti s tématem, vznikem a publikací tohoto článku nejsou ve střetu zájmů a vznik ani publikace článku nebyly podpořeny žádnou farmaceutickou firmou.
Do redakce doručeno dne: 6. 12. 2023.
Přijato po recenzi dne: 20. 5. 2024.
MUDr. Miriam Lánská, Ph.D.
IV. interní hematologická klinika
FN Hradec Králové
Sokolská 581
e-mail: miriam.lanska@fnhk.cz
Labels
Haematology Internal medicine Clinical oncology
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