Literature DB >> 2363411

Effectiveness of the cryosupernatant fraction of plasma in the treatment of refractory thrombotic thrombocytopenic purpura.

J J Byrnes1, J L Moake, P Klug, P Periman.   

Abstract

Many patients with thrombotic thrombocytopenic purpura (TTP) satisfactorily respond to plasma therapy (plasmapheresis and/or plasma infusion). Some, however, respond either not at all or only transiently and incompletely. Evidence indicates that platelets and endothelial cell-derived unusually large von Willebrand factor (ULvWF) multimers, as well as the largest vWF multimers in plasma, form thrombi which are deposited in the microvascular circulation. Accordingly, platelet transfusions are avoided unless there is intra-cranial or other life-threatening hemorrhage. The largest plasma multimers of vWF are, however, replenished by the infusion of large volumes of whole plasma. We postulated that under conditions of massive plasma replacement, plasma depleted of the largest multimers of vWF might be preferable for the treatment of TTP episodes. The largest vWF multimers sediment in the cryoprecipitate, and the cryoprecipitate-poor fraction of plasma (cryosupernatant) is depleted of these forms. Seven patients responding inadequately to intensive plasma therapy were switched to receive cryosupernatant in place of whole plasma. All patients improved quickly following this change in therapy, and the TTP syndrome resolved in all seven.

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Year:  1990        PMID: 2363411     DOI: 10.1002/ajh.2830340303

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  9 in total

Review 1.  Current concepts in thrombotic thrombocytopenic purpura.

Authors:  Han-Mou Tsai
Journal:  Annu Rev Med       Date:  2006       Impact factor: 13.739

2.  Diagnosis and management of atypical hemolytic uremic syndrome in children: single centre experience.

Authors:  Rashmi D Patel; Aruna V Vanikar; Manoj R Gumber; Kamal V Kanodia; Kamlesh S Suthar; Himanshu V Patel; Hargovind L Trivedi
Journal:  Indian J Hematol Blood Transfus       Date:  2013-06-08       Impact factor: 0.900

Review 3.  Renal function following hematological stem cell transplantation in childhood.

Authors:  Ludwig Patzer; Karim Kentouche; Felix Ringelmann; Joachim Misselwitz
Journal:  Pediatr Nephrol       Date:  2003-04-29       Impact factor: 3.714

Review 4.  Translational mini-review series on complement factor H: therapies of renal diseases associated with complement factor H abnormalities: atypical haemolytic uraemic syndrome and membranoproliferative glomerulonephritis.

Authors:  M Noris; G Remuzzi
Journal:  Clin Exp Immunol       Date:  2007-12-07       Impact factor: 4.330

Review 5.  Thrombotic thrombocytopenic purpura: a thrombotic disorder caused by ADAMTS13 deficiency.

Authors:  Han-Mou Tsai
Journal:  Hematol Oncol Clin North Am       Date:  2007-08       Impact factor: 3.722

Review 6.  The thrombocytopenic purpuras. Recognition and management.

Authors:  S Gillis
Journal:  Drugs       Date:  1996-06       Impact factor: 9.546

7.  Thrombotic thrombocytopenic purpura/hemolytic uremic syndrome: a multivariate analysis of factors predicting the response to plasma exchange.

Authors:  A Pereira; R Mazzara; J Monteagudo; C Sanz; L Puig; A Martínez; A Ordinas; R Castillo
Journal:  Ann Hematol       Date:  1995-06       Impact factor: 3.673

Review 8.  Beyond plasma exchange: novel therapies for thrombotic thrombocytopenic purpura.

Authors:  Kathryn Dane; Shruti Chaturvedi
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2018-11-30

9.  Management of pregnancy-associated thrombotic thrombocytopenia purpura.

Authors:  Ashley Fyfe-Brown; Gwen Clarke; Kara Nerenberg; Sujata Chandra; Venu Jain
Journal:  AJP Rep       Date:  2012-12-19
  9 in total

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