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DOI: 10.1055/s-0040-1708541
Immune-Mediated Thrombotic Thrombocytopenic Purpura: A Narrative Review of Diagnosis and Treatment in Adults

Abstract
Immune-mediated thrombotic thrombocytopenic purpura (iTTP) is a rare and potentially lethal disease characterized by fragmentary hemolysis, moderate-to-severe thrombocytopenia, end-organ dysfunction, and severely reduced ADAMTS13 levels (< 10%). Survival in iTTP has improved significantly since the introduction of plasma exchange as standard therapy combined with immune suppression to address the underlying pathophysiology. A host of challenges remain including prompt recognition of the disease, treatment of the end-organ effects of the disease, improving the early mortality rate, significantly reducing the relapse rate as well as addressing refractory disease. Discussed in this narrative review of iTTP are the recent measures aimed at addressing these issues, including improvements in clinical prediction models, postremission maintenance approaches with early retreatment as well as the development of novel therapies.
Publication History
Publication Date:
07 April 2020 (online)
© 2020. Thieme. All rights reserved.
Thieme Medical Publishers, Inc.
333 Seventh Avenue, 18th Floor, New York, NY 10001, USA
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References
- 1
Scully M,
Cataland S,
Coppo P.
et al;
International Working Group for Thrombotic Thrombocytopenic Purpura.
Consensus on the standardization of terminology in thrombotic thrombocytopenic purpura
and related thrombotic microangiopathies. J Thromb Haemost 2017; 15 (02) 312-322
MissingFormLabel
- 2
Moschcowitz E.
An acute febrile pleiochromic anemia with hyaline thrombosis of the terminal arterioles
and capillaries; an undescribed disease. JAMA Intern Med 1925; 36 (01) 89-93
MissingFormLabel
- 3
Rubinstein MA,
Kagan BM,
MacGillviray MH,
Merliss R,
Sacks H.
Unusual remission in a case of thrombotic thrombocytopenic purpura syndrome following
fresh blood exchange transfusions. Ann Intern Med 1959; 51 (06) 1409-1419
MissingFormLabel
- 4
Marcus AJ.
Moschcowitz revisited. N Engl J Med 1982; 307 (23) 1447-1448
MissingFormLabel
- 5
Bell WR,
Braine HG,
Ness PM,
Kickler TS.
Improved survival in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome.
Clinical experience in 108 patients. N Engl J Med 1991; 325 (06) 398-403
MissingFormLabel
- 6
Rock GA,
Shumak KH,
Buskard NA.
et al;
Canadian Apheresis Study Group.
Comparison of plasma exchange with plasma infusion in the treatment of thrombotic
thrombocytopenic purpura. N Engl J Med 1991; 325 (06) 393-397
MissingFormLabel
- 7
Tsai H-M,
Lian EC-Y.
Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic
purpura. N Engl J Med 1998; 339 (22) 1585-1594
MissingFormLabel
- 8
Levy GG,
Nichols WC,
Lian EC.
et al.
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic
purpura. Nature 2001; 413 (6855): 488-494
MissingFormLabel
- 9
Crawley JT,
de Groot R,
Xiang Y,
Luken BM,
Lane DA.
Unraveling the scissile bond: how ADAMTS13 recognizes and cleaves von Willebrand factor.
Blood 2011; 118 (12) 3212-3221
MissingFormLabel
- 10
Joly BS,
Coppo P,
Veyradier A.
An update on pathogenesis and diagnosis of thrombotic thrombocytopenic purpura. Expert
Rev Hematol 2019; 12 (06) 383-395
MissingFormLabel
- 11
Moake JL,
Rudy CK,
Troll JH.
et al.
Unusually large plasma factor VIII:von Willebrand factor multimers in chronic relapsing
thrombotic thrombocytopenic purpura. N Engl J Med 1982; 307 (23) 1432-1435
MissingFormLabel
- 12
Dent JA,
Berkowitz SD,
Ware J,
Kasper CK,
Ruggeri ZM.
Identification of a cleavage site directing the immunochemical detection of molecular
abnormalities in type IIA von Willebrand factor. Proc Natl Acad Sci U S A 1990; 87
(16) 6306-6310
MissingFormLabel
- 13
Fujikawa K,
Suzuki H,
McMullen B,
Chung D.
Purification of human von Willebrand factor-cleaving protease and its identification
as a new member of the metalloproteinase family. Blood 2001; 98 (06) 1662-1666
MissingFormLabel
- 14
Furlan M,
Robles R,
Morselli B,
Sandoz P,
Lämmle B.
Recovery and half-life of von Willebrand factor-cleaving protease after plasma therapy
in patients with thrombotic thrombocytopenic purpura. Thromb Haemost 1999; 81 (01)
8-13
MissingFormLabel
- 15
Zheng XL.
Structure-function and regulation of ADAMTS-13 protease. J Thromb Haemost 2013; 11
(Suppl. 01) 11-23
MissingFormLabel
- 16
Arya M,
Anvari B,
Romo GM.
et al.
Ultralarge multimers of von Willebrand factor form spontaneous high-strength bonds
with the platelet glycoprotein Ib-IX complex: studies using optical tweezers. Blood
2002; 99 (11) 3971-3977
MissingFormLabel
- 17
Roose E,
Schelpe AS,
Joly BS.
et al.
An open conformation of ADAMTS-13 is a hallmark of acute acquired thrombotic thrombocytopenic
purpura. J Thromb Haemost 2018; 16 (02) 378-388
MissingFormLabel
- 18
Amorosi EL,
Ultmann JE.
Thrombotic thrombocytopenic purpura: report of 16 cases and review of the literature.
Medicine (Baltimore) 1966; 45 (02) 139-160
MissingFormLabel
- 19
Alwan F,
Vendramin C,
Vanhoorelbeke K.
et al.
Presenting ADAMTS13 antibody and antigen levels predict prognosis in immune-mediated
thrombotic thrombocytopenic purpura. Blood 2017; 130 (04) 466-471
MissingFormLabel
- 20
Matsumoto M,
Bennett CL,
Isonishi A.
et al.
Acquired idiopathic ADAMTS13 activity deficient thrombotic thrombocytopenic purpura
in a population from Japan. PLoS One 2012; 7 (03) e33029
MissingFormLabel
- 21
Page EE,
Kremer Hovinga JA,
Terrell DR,
Vesely SK,
George JN.
Thrombotic thrombocytopenic purpura: diagnostic criteria, clinical features, and long-term
outcomes from 1995 through 2015. Blood Adv 2017; 1 (10) 590-600
MissingFormLabel
- 22
Scully M,
Yarranton H,
Liesner R.
et al.
Regional UK TTP registry: correlation with laboratory ADAMTS 13 analysis and clinical
features. Br J Haematol 2008; 142 (05) 819-826
MissingFormLabel
- 23
Mariotte E,
Azoulay E,
Galicier L.
et al;
French Reference Center for Thrombotic Microangiopathies.
Epidemiology and pathophysiology of adulthood-onset thrombotic microangiopathy with
severe ADAMTS13 deficiency (thrombotic thrombocytopenic purpura): a cross-sectional
analysis of the French national registry for thrombotic microangiopathy. Lancet Haematol
2016; 3 (05) e237-e245
MissingFormLabel
- 24
Coppo P,
Schwarzinger M,
Buffet M.
et al;
French Reference Center for Thrombotic Microangiopathies.
Predictive features of severe acquired ADAMTS13 deficiency in idiopathic thrombotic
microangiopathies: the French TMA reference center experience. PLoS One 2010; 5 (04)
e10208
MissingFormLabel
- 25
Bendapudi PK,
Li A,
Hamdan A.
et al.
Derivation and prospective validation of a predictive score for the rapid diagnosis
of thrombotic thrombocytopenic purpura: the plasmic score. Blood 2014; 124 (21) 231-231
MissingFormLabel
- 26
Bentley MJ,
Wilson AR,
Rodgers GM.
Performance of a clinical prediction score for thrombotic thrombocytopenic purpura
in an independent cohort. Vox Sang 2013; 105 (04) 313-318
MissingFormLabel
- 27
Bendapudi PK,
Hurwitz S,
Fry A.
et al.
Derivation and external validation of the PLASMIC score for rapid assessment of adults
with thrombotic microangiopathies: a cohort study. Lancet Haematol 2017; 4 (04) e157-e164
MissingFormLabel
- 28
Kokame K,
Nobe Y,
Kokubo Y,
Okayama A,
Miyata T.
FRETS-VWF73, a first fluorogenic substrate for ADAMTS13 assay. Br J Haematol 2005;
129 (01) 93-100
MissingFormLabel
- 29
Favaloro EJ,
Grispo L,
Exner T,
Koutts J.
Development of a simple collagen based ELISA assay aids in the diagnosis of, and permits
sensitive discrimination between type I and type II, von Willebrand's disease. Blood
Coagul Fibrinolysis 1991; 2 (02) 285-291
MissingFormLabel
- 30
Starke R,
Machin S,
Scully M,
Purdy G,
Mackie I.
The clinical utility of ADAMTS13 activity, antigen and autoantibody assays in thrombotic
thrombocytopenic purpura. Br J Haematol 2007; 136 (04) 649-655
MissingFormLabel
- 31
Meyer SC,
Sulzer I,
Lämmle B,
Kremer Hovinga JA.
Hyperbilirubinemia interferes with ADAMTS-13 activity measurement by FRETS-VWF73 assay:
diagnostic relevance in patients suffering from acute thrombotic microangiopathies.
J Thromb Haemost 2007; 5 (04) 866-867
MissingFormLabel
- 32
Muia J,
Gao W,
Haberichter SL.
et al.
An optimized fluorogenic ADAMTS13 assay with increased sensitivity for the investigation
of patients with thrombotic thrombocytopenic purpura. J Thromb Haemost 2013; 11 (08)
1511-1518
MissingFormLabel
- 33
Kato S,
Matsumoto M,
Matsuyama T,
Isonishi A,
Hiura H,
Fujimura Y.
Novel monoclonal antibody-based enzyme immunoassay for determining plasma levels of
ADAMTS13 activity. Transfusion 2006; 46 (08) 1444-1452
MissingFormLabel
- 34
Jin M,
Cataland S,
Bissell M,
Wu HM.
A rapid test for the diagnosis of thrombotic thrombocytopenic purpura using surface
enhanced laser desorption/ionization time-of-flight (SELDI-TOF)-mass spectrometry.
J Thromb Haemost 2006; 4 (02) 333-338
MissingFormLabel
- 35
Binder NB,
Griffiths M,
Vetr H.
A rapid and simple assay for the determination of Adamts-13 activity. Blood 2016;
128 (22) 1399-1399
MissingFormLabel
- 36
Favresse J,
Lardinois B,
Chatelain B,
Jacqmin H,
Mullier F.
Evaluation of the fully automated HemosIL Acustar ADAMTS13 activity assay. Thromb
Haemost 2018; 118 (05) 942-944
MissingFormLabel
- 37
Ferrari S,
Scheiflinger F,
Rieger M.
et al;
French Clinical and Biological Network on Adult Thrombotic Microangiopathies.
Prognostic value of anti-ADAMTS 13 antibody features (Ig isotype, titer, and inhibitory
effect) in a cohort of 35 adult French patients undergoing a first episode of thrombotic
microangiopathy with undetectable ADAMTS 13 activity. Blood 2007; 109 (07) 2815-2822
MissingFormLabel
- 38
Thomas MR,
de Groot R,
Scully MA,
Crawley JTB.
Pathogenicity of anti-ADAMTS13 autoantibodies in acquired thrombotic thrombocytopenic
purpura. EBioMedicine 2015; 2 (08) 942-952
MissingFormLabel
- 39
Rieger M,
Mannucci PM,
Kremer Hovinga JA.
et al.
ADAMTS13 autoantibodies in patients with thrombotic microangiopathies and other immunomediated
diseases. Blood 2005; 106 (04) 1262-1267
MissingFormLabel
- 40
Thomas MR,
Robinson S,
Scully MA.
How we manage thrombotic microangiopathies in pregnancy. Br J Haematol 2016; 173 (06)
821-830
MissingFormLabel
- 41
Scully M,
Hunt BJ,
Benjamin S.
et al;
British Committee for Standards in Haematology.
Guidelines on the diagnosis and management of thrombotic thrombocytopenic purpura
and other thrombotic microangiopathies. Br J Haematol 2012; 158 (03) 323-335
MissingFormLabel
- 42
Joly BS,
Coppo P,
Veyradier A.
Thrombotic thrombocytopenic purpura. Blood 2017; 129 (21) 2836-2846
MissingFormLabel
- 43
Fox LC,
Cohney SJ,
Kausman JY.
et al.
Consensus opinion on diagnosis and management of thrombotic microangiopathy in Australia
and New Zealand. Intern Med J 2018; 48 (06) 624-636
MissingFormLabel
- 44
Dervenoulas J,
Tsirigotis P,
Bollas G.
et al.
Thrombotic thrombocytopenic purpura/hemolytic uremic syndrome (TTP/HUS): treatment
outcome, relapses, prognostic factors. A single-center experience of 48 cases. Ann
Hematol 2000; 79 (02) 66-72
MissingFormLabel
- 45
Kremer Hovinga JA,
Vesely SK,
Terrell DR,
Lämmle B,
George JN.
Survival and relapse in patients with thrombotic thrombocytopenic purpura. Blood 2010;
115 (08) 1500-1511 , quiz 1662
MissingFormLabel
- 46
Toussaint-Hacquard M,
Coppo P,
Soudant M.
et al.
Type of plasma preparation used for plasma exchange and clinical outcome of adult
patients with acquired idiopathic thrombotic thrombocytopenic purpura: a French retrospective
multicenter cohort study. Transfusion 2015; 55 (10) 2445-2451
MissingFormLabel
- 47
Zeigler ZR,
Shadduck RK,
Gryn JF.
et al;
North American TTP Group.
Cryoprecipitate poor plasma does not improve early response in primary adult thrombotic
thrombocytopenic purpura (TTP). J Clin Apher 2001; 16 (01) 19-22
MissingFormLabel
- 48
Rock G,
Anderson D,
Clark W.
et al;
Canadian Apheresis Group; Canadian Association of Apheresis Nurses.
Does cryosupernatant plasma improve outcome in thrombotic thrombocytopenic purpura?
No answer yet. Br J Haematol 2005; 129 (01) 79-86
MissingFormLabel
- 49
Rock G,
Yousef H,
Neurath D,
Lu M.
ADAMTS-13 in fresh, stored, and solvent/detergent-treated plasma. Transfusion 2006;
46 (07) 1261-1262
MissingFormLabel
- 50
Scott EA,
Puca KE,
Pietz BC,
Duchateau BK,
Friedman KD.
Comparison and stability of ADAMTS13 activity in therapeutic plasma products. Transfusion
2007; 47 (01) 120-125
MissingFormLabel
- 51
Howard MA,
Williams LA,
Terrell DR,
Duvall D,
Vesely SK,
George JN.
Complications of plasma exchange in patients treated for clinically suspected thrombotic
thrombocytopenic purpura-hemolytic uremic syndrome. Transfusion 2006; 46 (01) 154-156
MissingFormLabel
- 52
Cataland SR,
Kourlas PJ,
Yang S.
et al.
Cyclosporine or steroids as an adjunct to plasma exchange in the treatment of immune-mediated
thrombotic thrombocytopenic purpura. Blood Adv 2017; 1 (23) 2075-2082
MissingFormLabel
- 53
Scully M,
McDonald V,
Cavenagh J.
et al.
A phase 2 study of the safety and efficacy of rituximab with plasma exchange in acute
acquired thrombotic thrombocytopenic purpura. Blood 2011; 118 (07) 1746-1753
MissingFormLabel
- 54
Froissart A,
Veyradier A,
Hié M,
Benhamou Y,
Coppo P.
French Reference Center for Thrombotic Microangiopathies.
Rituximab in autoimmune thrombotic thrombocytopenic purpura: a success story. Eur
J Intern Med 2015; 26 (09) 659-665
MissingFormLabel
- 55
Scully M,
Cohen H,
Cavenagh J.
et al.
Remission in acute refractory and relapsing thrombotic thrombocytopenic purpura following
rituximab is associated with a reduction in IgG antibodies to ADAMTS-13. Br J Haematol
2007; 136 (03) 451-461
MissingFormLabel
- 56
Froissart A,
Buffet M,
Veyradier A.
et al;
French Thrombotic Microangiopathies Reference Center; Experience of the French Thrombotic
Microangiopathies Reference Center.
Efficacy and safety of first-line rituximab in severe, acquired thrombotic thrombocytopenic
purpura with a suboptimal response to plasma exchange. Crit Care Med 2012; 40 (01)
104-111
MissingFormLabel
- 57
Lim W,
Vesely SK,
George JN.
The role of rituximab in the management of patients with acquired thrombotic thrombocytopenic
purpura. Blood 2015; 125 (10) 1526-1531
MissingFormLabel
- 58
Westwood JP,
Webster H,
McGuckin S,
McDonald V,
Machin SJ,
Scully M.
Rituximab for thrombotic thrombocytopenic purpura: benefit of early administration
during acute episodes and use of prophylaxis to prevent relapse. J Thromb Haemost
2013; 11 (03) 481-490
MissingFormLabel
- 59
Page EE,
Kremer Hovinga JA,
Terrell DR,
Vesely SK,
George JN.
Rituximab reduces risk for relapse in patients with thrombotic thrombocytopenic purpura.
Blood 2016; 127 (24) 3092-3094
MissingFormLabel
- 60
Sun L,
Mack J,
Li A.
et al.
Predictors of relapse and efficacy of rituximab in immune thrombotic thrombocytopenic
purpura. Blood Adv 2019; 3 (09) 1512-1518
MissingFormLabel
- 61
Benhamou Y,
Paintaud G,
Azoulay E.
et al;
French Reference Center for Thrombotic Microangiopathies.
Efficacy of a rituximab regimen based on B cell depletion in thrombotic thrombocytopenic
purpura with suboptimal response to standard treatment: results of a phase II, multicenter
noncomparative study. Am J Hematol 2016; 91 (12) 1246-1251
MissingFormLabel
- 62
Zaja F,
Battista ML,
Pirrotta MT.
et al.
Lower dose rituximab is active in adults patients with idiopathic thrombocytopenic
purpura. Haematologica 2008; 93 (06) 930-933
MissingFormLabel
- 63
McDonald V,
Manns K,
Mackie IJ,
Machin SJ,
Scully MA.
Rituximab pharmacokinetics during the management of acute idiopathic thrombotic thrombocytopenic
purpura. J Thromb Haemost 2010; 8 (06) 1201-1208
MissingFormLabel
- 64
Kremer Hovinga JA,
Studt JD,
Demarmels Biasiutti F.
et al.
Splenectomy in relapsing and plasma-refractory acquired thrombotic thrombocytopenic
purpura. Haematologica 2004; 89 (03) 320-324
MissingFormLabel
- 65
Dubois L,
Gray DK.
Case series: splenectomy: does it still play a role in the management of thrombotic
thrombocytopenic purpura?. Can J Surg 2010; 53 (05) 349-355
MissingFormLabel
- 66
Lombardi AM,
Pasquale ID,
Businaro MA.
et al.
Relapsing thrombotic thrombocytopenic purpura with low ADAMTS13 antigen levels: an
indication for splenectomy?. Hematol Rep 2019; 11 (01) 7904
MissingFormLabel
- 67
Coppo P,
Cuker A,
George JN.
Thrombotic thrombocytopenic purpura: toward targeted therapy and precision medicine.
Res Pract Thromb Haemost 2018; 3 (01) 26-37
MissingFormLabel
- 68
Bartunek J,
Barbato E,
Heyndrickx G,
Vanderheyden M,
Wijns W,
Holz JB.
Novel antiplatelet agents: ALX-0081, a nanobody directed towards von Willebrand factor.
J Cardiovasc Transl Res 2013; 6 (03) 355-363
MissingFormLabel
- 69
Callewaert F,
Roodt J,
Ulrichts H.
et al.
Evaluation of efficacy and safety of the anti-VWF nanobody ALX-0681 in a preclinical
baboon model of acquired thrombotic thrombocytopenic purpura. Blood 2012; 120 (17)
3603-3610
MissingFormLabel
- 70
Peyvandi F,
Scully M,
Kremer Hovinga JA.
et al;
TITAN Investigators.
Caplacizumab for acquired thrombotic thrombocytopenic purpura. N Engl J Med 2016;
374 (06) 511-522
MissingFormLabel
- 71
Scully M,
Cataland SR,
Peyvandi F.
et al;
HERCULES Investigators.
Caplacizumab treatment for acquired thrombotic thrombocytopenic purpura. N Engl J
Med 2019; 380 (04) 335-346
MissingFormLabel
- 72 FDA approved caplacizumab-yhdp. Accessed: January 6, 2019 at: https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approved-caplacizumab-yhdp
MissingFormLabel
- 73
Chen J,
Reheman A,
Gushiken FC.
et al.
N-acetylcysteine reduces the size and activity of von Willebrand factor in human plasma
and mice. J Clin Invest 2011; 121 (02) 593-603
MissingFormLabel
- 74
Rottenstreich A,
Hochberg-Klein S,
Rund D,
Kalish Y.
The role of N-acetylcysteine in the treatment of thrombotic thrombocytopenic purpura.
J Thromb Thrombolysis 2016; 41 (04) 678-683
MissingFormLabel
- 75
Coppo P.
French Reference Center for Thrombotic Microangiopathies.
Treatment of autoimmune thrombotic thrombocytopenic purpura in the more severe forms.
Transfus Apheresis Sci 2017; 56 (01) 52-56
MissingFormLabel
- 76
Patriquin CJ,
Thomas MR,
Dutt T.
et al.
Bortezomib in the treatment of refractory thrombotic thrombocytopenic purpura. Br
J Haematol 2016; 173 (05) 779-785
MissingFormLabel
- 77
Pandey MR,
Vachhani P,
Ontiveros EP.
Remission of severe, relapsed, and refractory TTP after multiple cycles of bortezomib.
Case Rep Hematol 2017; 2017: 9681832
MissingFormLabel
- 78
Shortt J,
Oh DH,
Opat SS.
ADAMTS13 antibody depletion by bortezomib in thrombotic thrombocytopenic purpura.
N Engl J Med 2013; 368 (01) 90-92
MissingFormLabel
- 79
van Balen T,
Schreuder MF,
de Jong H,
van de Kar NC.
Refractory thrombotic thrombocytopenic purpura in a 16-year-old girl: successful treatment
with bortezomib. Eur J Haematol 2014; 92 (01) 80-82
MissingFormLabel
- 80
Scully M,
Knöbl P,
Kentouche K.
et al.
Recombinant ADAMTS-13: first-in-human pharmacokinetics and safety in congenital thrombotic
thrombocytopenic purpura. Blood 2017; 130 (19) 2055-2063
MissingFormLabel
- 81
Plaimauer B,
Kremer Hovinga JA,
Juno C.
et al.
Recombinant ADAMTS13 normalizes von Willebrand factor-cleaving activity in plasma
of acquired TTP patients by overriding inhibitory antibodies. J Thromb Haemost 2011;
9 (05) 936-944
MissingFormLabel
- 82
Jestin M,
Benhamou Y,
Schelpe AS.
et al;
French Thrombotic Microangiopathies Reference Center.
Preemptive rituximab prevents long-term relapses in immune-mediated thrombotic thrombocytopenic
purpura. Blood 2018; 132 (20) 2143-2153
MissingFormLabel
- 83
Hie M,
Gay J,
Galicier L.
et al;
French Thrombotic Microangiopathies Reference Centre.
Preemptive rituximab infusions after remission efficiently prevent relapses in acquired
thrombotic thrombocytopenic purpura. Blood 2014; 124 (02) 204-210
MissingFormLabel
- 84
Mariani S,
Trisolini SM,
Capria S.
et al.
Acquired thrombotic thrombocytopenic purpura in a child: rituximab to prevent relapse.
A pediatric report and literature review. Haematologica 2018; 103 (03) e138-e140
MissingFormLabel
- 85
Westwood JP,
Thomas M,
Alwan F.
et al.
Rituximab prophylaxis to prevent thrombotic thrombocytopenic purpura relapse: outcome
and evaluation of dosing regimens. Blood Adv 2017; 1 (15) 1159-1166
MissingFormLabel
- 86
Saleem R,
Rogers ZR,
Neunert C,
George JN.
Maintenance rituximab for relapsing thrombotic thrombocytopenic purpura: a case report.
Transfusion 2019; 59 (03) 921-926
MissingFormLabel
- 87
Bresin E,
Gastoldi S,
Daina E.
et al.
Rituximab as pre-emptive treatment in patients with thrombotic thrombocytopenic purpura
and evidence of anti-ADAMTS13 autoantibodies. Thromb Haemost 2009; 101 (02) 233-238
MissingFormLabel
- 88
Tate C,
Mollee P.
Intravenous OxyContin-associated thrombotic microangiopathy treated successfully without
plasma exchange. Med J Aust 2015; 202 (06) 330-331
MissingFormLabel
- 89
Balduini CL,
Gugliotta L,
Luppi M.
et al;
Italian TTP Study Group.
High versus standard dose methylprednisolone in the acute phase of idiopathic thrombotic
thrombocytopenic purpura: a randomized study. Ann Hematol 2010; 89 (06) 591-596
MissingFormLabel
- 90
Nguyen L,
Li X,
Duvall D,
Terrell DR,
Vesely SK,
George JN.
Twice-daily plasma exchange for patients with refractory thrombotic thrombocytopenic
purpura: the experience of the Oklahoma Registry, 1989 through 2006. Transfusion 2008;
48 (02) 349-357
MissingFormLabel
- 91
Kremer Hovinga JA,
Coppo P,
Lämmle B,
Moake JL,
Miyata T,
Vanhoorelbeke K.
Thrombotic thrombocytopenic purpura. Nat Rev Dis Primers 2017; 3: 17020
MissingFormLabel
- 92
Beloncle F,
Buffet M,
Coindre JP.
et al;
Thrombotic Microangiopathies Reference Center.
Splenectomy and/or cyclophosphamide as salvage therapies in thrombotic thrombocytopenic
purpura: the French TMA Reference Center experience. Transfusion 2012; 52 (11) 2436-2444
MissingFormLabel