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2264           Part XII:  Hemostasis and Thrombosis                                                                                                                        Chapter 132:  Thrombotic Microangiopathies            2265




                 37.  Camous L, Veyradier A, Darmon M, et al: Macrovascular thrombosis in critically ill     68.  Rizvi MA, Vesely SK, George JN, et al: Complications of plasma exchange in 71
                  patients with thrombotic micro-angiopathies. Intern Emerg Med 9:267, 2014.  consecutive patients treated for clinically suspected thrombotic thrombocytopenic
                 38.  Hawkins BM, Abu-Fadel M, Vesely SK, George JN: Clinical cardiac involvement in   purpura-hemolytic-uremic syndrome. Transfusion 40:896, 2000.
                  thrombotic thrombocytopenic purpura: A systematic review. Transfusion 48:382, 2008.    69.  Lim W, Vesely SK, George JN: The role of rituximab in the management of patients with
                 39.  Hughes C, McEwan JR, Longair I, et al: Cardiac involvement in acute thrombotic   acquired thrombotic thrombocytopenic purpura. Blood 125:1526, 2015.
                  thrombocytopenic purpura: Association with troponin T and IgG antibodies to     70.  Westwood JP, Webster H, McGuckin S, et al: Rituximab for thrombotic thrombocy-
                  ADAMTS 13. J Thromb Haemost 7:529, 2009.               topenic purpura: Benefit of early administration during acute episodes and use of pro-
                 40.  Benhamou Y, Assie C, Boelle PY, et al: Development and validation of a predictive   phylaxis to prevent relapse. J Thromb Haemost 11:481, 2013.
                  model for death in acquired severe ADAMTS13 deficiency-associated idiopathic     71.  Hie M, Gay J, Galicier L, et al: Preemptive rituximab infusions after remission efficiently
                  thrombotic thrombocytopenic purpura: The French TMA Reference Center experi-  prevent relapses in acquired thrombotic thrombocytopenic purpura. Blood 124:204,
                  ence. Haematologica 97:1181, 2012.                     2014.
                 41.  Zini G, d’Onofrio G, Briggs C, et al: ICSH recommendations for identification, diagnos-    72.  Carson KR, Evens AM, Richey EA, et al: Progressive multifocal leukoencephalopa-
                  tic value, and quantitation of schistocytes. Int J Lab Hematol 34:107, 2012.  thy after rituximab therapy in HIV-negative patients: A report of 57 cases from the
                 42.  Burns ER, Lou Y, Pathak A: Morphologic diagnosis of thrombotic thrombocytopenic   Research on Adverse Drug Event and Reports project. Blood 113:4834, 2009.
                  purpura. Am J Hematol 75:18, 2004.                    73.  Bharat A, Xie F, Baddley JW, et al: Incidence and risk factors for progressive multifocal
                 43.  Veyradier A, Obert B, Houllier A, et al: Specific von Willebrand factor-cleaving     leukoencephalopathy among patients with selected rheumatic diseases. Arthritis Care
                  protease in thrombotic microangiopathies: A study of 111 cases. Blood 98:1765, 2001.  Res (Hoboken) 64:612, 2012.
                 44.  Bianchi V, Robles R, Alberio L, et al: Von Willebrand factor-cleaving protease     74.  Lunel-Fabiani F, Masson C, Ducancelle A: Systemic diseases and biotherapies: Under-
                  (ADAMTS13) in thrombocytopenic disorders: A severely deficient activity is specific   standing, evaluating, and preventing the risk of hepatitis B reactivation.  Joint Bone
                  for thrombotic thrombocytopenic purpura. Blood 100:710, 2002.  Spine 81:478, 2014.
                 45.  Tsai HM: Is severe deficiency of ADAMTS-13 specific for thrombotic thrombocy-    75.  Aqui NA, Stein SH, Konkle BA, et al: Role of splenectomy in patients with refractory or
                  topenic purpura? Yes. J Thromb Haemost 1:625, 2003.    relapsed thrombotic thrombocytopenic purpura. J Clin Apher 18:51, 2003.
                 46.  Asada Y, Sumiyoshi A, Hayashi T, et al: Immunohistochemistry of vascular lesion in     76.  Kappers-Klunne MC, Wijermans P, Fijnheer R, et al: Splenectomy for the treatment of
                  thrombotic thrombocytopenic purpura, with special reference to factor VIII related   thrombotic thrombocytopenic purpura. Br J Haematol 130:768, 2005.
                  antigen. Thromb Res 38:469, 1985.                     77.  Katkhouda N, Hurwitz MB, Rivera RT, et al: Laparoscopic splenectomy: Outcome and
                 47.  Hosler GA, Cusumano AM, Hutchins GM: Thrombotic thrombocytopenic purpura   efficacy in 103 consecutive patients. Ann Surg 228:568, 1998.
                  and hemolytic uremic syndrome are distinct pathologic entities. A review of 56 autopsy     78.  Ferrara F, Annunziata M, Pollio F, et al: Vincristine as treatment for recurrent episodes
                  cases. Arch Pathol Lab Med 127:834, 2003.              of thrombotic thrombocytopenic purpura. Ann Hematol 81:7, 2002.
                 48.  Zomas A, Saso R, Powles R, et al: Red cell fragmentation (schistocytosis) after bone     79.  Bobbio-Pallavicini E, Porta C, Centurioni R, et al: Vincristine sulfate for the treatment
                  marrow transplantation. Bone Marrow Transplant 22:777, 1998.  of thrombotic thrombocytopenic purpura refractory to plasma-exchange. The Italian
                 49.  Kanamori H, Takaishi Y, Takabayashi M, et al: Clinical significance of fragmented red   Cooperative Group for TTP. Eur J Haematol 52:222, 1994.
                  cells after allogeneic bone marrow transplantation. Int J Hematol 77:180, 2003.    80.  Bobbio-Pallavicini E, Porta C, Tacconi F, et al: Intravenous prostacyclin (as epopros-
                 50.  Mannucci PM, Canciani MT, Forza I, et al: Changes in health and disease of the metal-  tenol) infusion in thrombotic thrombocytopenic purpura. Four case reports and
                  loprotease that cleaves von Willebrand factor. Blood 98:2730, 2001.  review of the literature. Italian Cooperative Group for Thrombotic Thrombocytopenic
                 51.  Kremer Hovinga JA, Zeerleder S, Kessler P, et al: ADAMTS-13, von Willebrand factor   Purpura. Haematologica 79:429, 1994.
                  and related parameters in severe sepsis and septic shock. J Thromb Haemost 5:2284,     81.  Sagripanti A, Carpi A, Rosaia B, et al: Iloprost in the treatment of thrombotic microan-
                  2007.                                                  giopathy: Report of thirteen cases. Biomed Pharmacother 50:350, 1996.
                 52.  Uemura M, Fujimura Y, Matsumoto M, et al: Comprehensive analysis of ADAMTS13     82.  Dervenoulas J, Tsirigotis P, Bollas G, et al: Efficacy of intravenous immunoglobulin in
                  in patients with liver cirrhosis. Thromb Haemost 99:1019, 2008.  the treatment of thrombotic thrombocytopaenic purpura. A study of 44 cases. Acta
                 53.  Park YD, Yoshioka A, Kawa K, et al: Impaired activity of plasma von Willebrand factor-  Haematol 105:204, 2001.
                  cleaving protease may predict the occurrence of hepatic veno-occlusive disease after     83.  Anderson D, Ali K, Blanchette V, et al: Guidelines on the use of intravenous immune
                  stem cell transplantation. Bone Marrow Transplant 29:789, 2002.  globulin for hematologic conditions. Transfus Med Rev 21:S9, 2007.
                 54.  Nguyen L, Li X, Duvall D, et al: Twice-daily plasma exchange for patients with refrac-    84.  Cataland SR, Jin M, Lin S, et al: Cyclosporin and plasma exchange in thrombotic
                  tory thrombotic thrombocytopenic purpura: The experience of the Oklahoma Registry,   thrombocytopenic purpura: Long-term follow-up with serial analysis of ADAMTS13
                  1989 through 2006. Transfusion 48:349, 2008.           activity. Br J Haematol 139:486, 2007.
                 55.  Scully M, Hunt BJ, Benjamin S, et al: Guidelines on the diagnosis and management     85.  Shortt J, Oh DH, Opat SS: ADAMTS13 antibody depletion by bortezomib in throm-
                  of thrombotic thrombocytopenic purpura and other thrombotic microangiopathies.     botic thrombocytopenic purpura. N Engl J Med 368:90, 2013.
                  Br J Haematol 158:323, 2012.                          86.  Ahmad HN, Thomas-Dewing RR, Hunt BJ: Mycophenolate mofetil in a case of relapsed,
                 56.  Zeigler ZR, Shadduck RK, Gryn JF, et al: Cryoprecipitate poor plasma does not improve   refractory thrombotic thrombocytopenic purpura. Eur J Haematol 78:449, 2007.
                  early response in primary adult thrombotic thrombocytopenic purpura (TTP). J Clin     87.  Li GW, Rambally S, Kamboj J, et al: Treatment of refractory thrombotic thrombocy-
                  Apher 16:19, 2001.                                     topenic purpura with N-acetylcysteine: A case report. Transfusion 54:1221, 2014.
                 57.  Rock G, Anderson D, Clark W, et al: Does cryosupernatant plasma improve outcome in     88.  Spiekermann K, Wormann B, Rumpf KW, Hiddemann W: Combination chemother-
                  thrombotic thrombocytopenic purpura? No answer yet. Br J Haematol 129:79, 2005.  apy with CHOP for recurrent thrombotic thrombocytopenic purpura. Br J Haematol
                 58.  Michael M, Elliott EJ, Craig JC, et al: Interventions for hemolytic uremic syndrome and   97:544, 1997.
                  thrombotic thrombocytopenic purpura: A systematic review of randomized controlled     89.  Passweg JR, Rabusin M, Musso M, et al: Haematopoetic stem cell transplantation for
                  trials. Am J Kidney Dis 53:259, 2009.                  refractory autoimmune cytopenia. Br J Haematol 125:749, 2004.
                 59.  Prowse C: Properties of pathogen-inactivated plasma components. Transfus Med Rev     90.  Callewaert F, Roodt J, Ulrichts H, et al: Evaluation of efficacy and safety of the anti-
                  23:124, 2009.                                          VWF Nanobody ALX-0681 in  a preclinical  baboon model of acquired thrombotic
                 60.  McCarthy LJ: Evidence-based medicine for apheresis: An ongoing challenge.  Ther   thrombocytopenic purpura. Blood 120:3603, 2012.
                  Apher Dial 8:112, 2004.                               91.  Cataland SR, Peyvandi F, Mannucci PM, et al: Initial experience from a double-blind,
                 61.  Yarranton H, Cohen H, Pavord SR, et al: Venous thromboembolism associated with the   placebo-controlled, clinical outcome study of ARC1779 in patients with thrombotic
                  management of acute thrombotic thrombocytopenic purpura. Br J Haematol 121:778,   thrombocytopenic purpura. Am J Hematol 87:430, 2012.
                  2003.                                                 92.  O’Brien KL, Price TH, Howell C, Delaney M: The use of 50% albumin/plasma replace-
                 62.  Allford SL, Harrison P, Lawrie AS, et al: Von Willebrand factor—Cleaving protease   ment fluid in therapeutic plasma exchange for thrombotic thrombocytopenic purpura.
                  activity in congenital thrombotic thrombocytopenic purpura. Br J Haematol 111:1215,   J Clin Apher 28:416, 2013.
                  2000.                                                 93.  Zhan H, Streiff MB, King KE, Segal JB: Thrombotic thrombocytopenic purpura at
                 63.  del Rio-Garma J, Alvarez-Larran A, Martinez C, et al: Methylene blue-photoinacti-  the Johns Hopkins Hospital from 1992 to 2008: Clinical outcomes and risk factors for
                  vated plasma versus quarantine fresh frozen plasma in thrombotic thrombocytopenic    relapse. Transfusion 50:868, 2010.
                  purpura: A multicentric, prospective cohort study. Br J Haematol 143:39, 2008.    94.  Bandarenko N, Brecher ME: United States Thrombotic Thrombocytopenic Purpura
                 64.  Bobbio-Pallavicini E, Gugliotta L, Centurioni R, et al: Antiplatelet agents in thrombotic   Apheresis Study Group (US TTP ASG): Multicenter survey and retrospective analysis
                  thrombocytopenic purpura (TTP). Results of a randomized multicenter trial by the   of current efficacy of therapeutic plasma exchange. J Clin Apher 13:133, 1998.
                  Italian Cooperative Group for TTP. Haematologica 82:429, 1997.    95.  Tsai H-M, Shulman K: Rituximab induces remission of cerebral ischemia caused by
                 65.  Coppo P, Lassoued K, Mariette X, et al: Effectiveness of platelet transfusions after   thrombotic thrombocytopenic purpura. Eur J Haematol 70:183, 2003.
                  plasma exchange in adult thrombotic thrombocytopenic purpura: A report of two     96.  Sadler JE: Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic
                  cases. Am J Hematol 68:198, 2001.                      purpura. Blood 112:11, 2008.
                 66.  Goel R, Ness PM, Takemoto CM, et al: Platelet transfusions in platelet consumptive     97.  McClain RS, Terrell DR, Vesely SK, George JN: Plasma exchange complications
                  disorders are associated with arterial thrombosis and in-hospital mortality.  Blood   in patients treated for thrombotic thrombocytopenia purpura-hemolytic uremic
                  125:1470, 2015.                                        syndrome: 2011 to 2014. Transfusion 54:3257, 2014.
                 67.  Doerfler ME, Kaufman B, Goldenberg AS: Central venous catheter  placement in     98.  Kennedy AS, Lewis QF, Scott JG, et al: Cognitive deficits after recovery from throm-
                  patients with disorders of hemostasis. Chest 110:185, 1996.  botic thrombocytopenic purpura. Transfusion 49:1092, 2009.







          Kaushansky_chapter 132_p2253-2266.indd   2264                                                                 17/09/15   3:48 pm
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