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10.1097/MD.0000000000003712

http://scihub22266oqcxt.onion/10.1097/MD.0000000000003712
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C4998437!4998437 !27310951
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suck abstract from ncbi


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pmid27310951
      Medicine+(Baltimore) 2016 ; 95 (24 ): e3712
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  • Recombinant thrombomodulin for secondary thrombotic thrombocytopenic purpura #MMPMID27310951
  • Nakamura K ; Inokuchi R ; Hiruma T ; Ohshima K ; Sonoo T ; Tokunaga K ; Doi K ; Nakajima S
  • Medicine (Baltimore) 2016[Jun]; 95 (24 ): e3712 PMID27310951 show ga
  • In the pathogenesis of thrombotic thrombocytopenic purpura (TTP), reductions in the enzyme activity of ADAMTS13, which cuts ultralarge von Willebrand multimers, generates shear stress on the microvascular endothelium, leading to platelet aggregation and the formation of a thrombus. ADAMTS13 activity is markedly decreased in typical TTP, but is only mildly reduced in secondary TTP, which concomitantly develops with primary disease. The latter develops with septic disseminated intravascular coagulation (DIC) and often causes organ failure. Recombinant thrombomodulin (rTM) is a drug that is used to treat DIC and may also remit TTP because it improves vascular endothelial dysfunction. Therefore, we herein investigated the efficacy of rTM in patients treated for the pathology of secondary TTP. Patients who were admitted to the Emergency and Critical Care Center of our hospital and met the following conditions were extracted and retrospectively analyzed: hemolytic anemia accompanied by fragmented red blood cells (Hb?
  • |ADAMTS13 Protein/*blood [MESH]
  • |Aged [MESH]
  • |Dose-Response Relationship, Drug [MESH]
  • |Female [MESH]
  • |Follow-Up Studies [MESH]
  • |Humans [MESH]
  • |Male [MESH]
  • |Purpura, Thrombotic Thrombocytopenic/*drug therapy/enzymology [MESH]
  • |Recombinant Proteins [MESH]
  • |Retrospective Studies [MESH]
  • |Thrombomodulin/*administration & dosage [MESH]


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