TY - JOUR
T1 - Diagnostic and treatment guidelines for thrombotic thrombocytopenic purpura (TTP) 2017 in Japan
AU - For Ttp Group Of Blood Coagulation Abnormalities Research Team, Research On Rare And Intractable Disease Supported By Health, Labour, And Welfare Sciences Research Grants
AU - Matsumoto, Masanori
AU - Fujimura, Yoshihiro
AU - Wada, Hideo
AU - Kokame, Koichi
AU - Miyakawa, Yoshitaka
AU - Ueda, Yasunori
AU - Higasa, Satoshi
AU - Moriki, Takanori
AU - Yagi, Hideo
AU - Miyata, Toshiyuki
AU - Murata, Mitsuru
N1 - Publisher Copyright:
© 2017, The Japanese Society of Hematology.
PY - 2017/7/1
Y1 - 2017/7/1
N2 - Thrombotic thrombocytopenic purpura (TTP) can rapidly progress into a life-threatening condition, thus the importance of appropriate diagnosis and treatment cannot be overstated. Until recently, TTP has mainly been diagnosed by clinical findings such as thrombocytopenia and non-immune hemolytic anemia. In addition to these clinical findings, however, reduced activity of a disintegrin-like and metalloprotease with thrombospondin type 1 motif 13 (ADAMTS13) below 10% has been accepted internationally as a diagnostic criterion for TTP. In the present guidelines, we have taken all of these criteria into consideration. TTP is classified as acquired if the patient is positive for anti-ADAMTS13 autoantibodies, and as congenital if ADAMTS13 gene abnormalities are detected. Fresh-frozen plasma (FFP) transfusion is performed in patients with congenital TTP to supplement ADAMTS13. Plasma exchange therapy using FFP is conducted in patients with acquired TTP to supplement ADAMTS13 and remove anti-ADAMTS13 autoantibodies. To suppress autoantibody production, corticosteroid therapy may be administered in conjunction with plasma exchange. Recent reports show that the monoclonal anti-CD-20 antibody rituximab is effective in patients with refractory or relapsed TTP.
AB - Thrombotic thrombocytopenic purpura (TTP) can rapidly progress into a life-threatening condition, thus the importance of appropriate diagnosis and treatment cannot be overstated. Until recently, TTP has mainly been diagnosed by clinical findings such as thrombocytopenia and non-immune hemolytic anemia. In addition to these clinical findings, however, reduced activity of a disintegrin-like and metalloprotease with thrombospondin type 1 motif 13 (ADAMTS13) below 10% has been accepted internationally as a diagnostic criterion for TTP. In the present guidelines, we have taken all of these criteria into consideration. TTP is classified as acquired if the patient is positive for anti-ADAMTS13 autoantibodies, and as congenital if ADAMTS13 gene abnormalities are detected. Fresh-frozen plasma (FFP) transfusion is performed in patients with congenital TTP to supplement ADAMTS13. Plasma exchange therapy using FFP is conducted in patients with acquired TTP to supplement ADAMTS13 and remove anti-ADAMTS13 autoantibodies. To suppress autoantibody production, corticosteroid therapy may be administered in conjunction with plasma exchange. Recent reports show that the monoclonal anti-CD-20 antibody rituximab is effective in patients with refractory or relapsed TTP.
KW - ADAMTS13
KW - TMA
KW - TTP
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U2 - 10.1007/s12185-017-2264-7
DO - 10.1007/s12185-017-2264-7
M3 - Article
C2 - 28550351
AN - SCOPUS:85019695457
SN - 0925-5710
VL - 106
SP - 3
EP - 15
JO - International journal of hematology
JF - International journal of hematology
IS - 1
ER -