ISTH guidelines for the diagnosis of thrombotic thrombocytopenic purpura

被引:203
作者
Zheng, X. Long [1 ]
Vesely, Sara K. [2 ]
Cataland, Spero R. [3 ]
Coppo, Paul [4 ]
Geldziler, Brian [5 ]
Iorio, Alfonso [6 ]
Matsumoto, Masanori [7 ]
Mustafa, Reem A. [8 ]
Pai, Menaka [6 ]
Rock, Gail [9 ]
Russell, Lene [10 ]
Tarawneh, Rawan [11 ]
Valdes, Julie
Peyvandi, Flora [12 ,13 ,14 ]
机构
[1] Univ Kansas, Med Ctr, Dept Pathol & Lab Med, 3901 Rainbow Blvd,5016 Delp, Kansas City, KS 66160 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Hudson Coll Publ Hlth, Oklahoma City, OK USA
[3] Ohio State Univ, Dept Med, Columbus, OH 43210 USA
[4] Sorbonne Univ, Hop St Antoine, AP HP, Ct Reference Microangiopathies Thrombot,Serv Hema, Paris, France
[5] McMaster Univ, Dept Hlth Res Methods Res & Impact, Hamilton, ON, Canada
[6] McMaster Univ, Dept Med, Hamilton, ON, Canada
[7] Nara Med Univ, Dept Blood Transfus Med, Kashihara, Nara, Japan
[8] Univ Kansas, Med Ctr, Dept Med, Kansas City, KS 66103 USA
[9] Univ Ottawa, Ottawa, CA USA
[10] Copenhagen Univ Hosp, Dept Intens Care, Copenhagen, Denmark
[11] Ohio State Univ, Dept Neurol, Wexner Med Ctr, Columbus, OH 43210 USA
[12] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Angelo Bianchi Bonomi Hemophilia & Thrombosis Ctr, Milan, Italy
[13] Fdn Luigi Villa, Milan, Italy
[14] Univ Studi Milano, Dept Pathophysiol & Transplantat, Milan, Italy
关键词
ADAMTS13; diagnosis; guidelines; thrombosis; TTP; HEMOLYTIC-UREMIC SYNDROME; FACTOR-CLEAVING PROTEASE; SEVERE ADAMTS13 DEFICIENCY; COMPLEMENT INHIBITOR ECULIZUMAB; ESCHERICHIA-COLI; PLASMA-EXCHANGE; MICROANGIOPATHIES; FRETS-VWF73; ASSAY; EPIDEMIOLOGY;
D O I
10.1111/jth.15006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Despite an increase in our understandings of pathogenesis of thrombotic thrombocytopenic purpura (TTP), the approaches for initial diagnosis and management of TTP vary significantly. Objective The evidence-based guidelines of the International Society on Thrombosis and Haemostasis (ISTH) are intended to support patients, clinicians, and other health care professionals in their decisions about the initial diagnosis and management of acute TTP. Methods In June 2018, ISTH formed a multidisciplinary panel that included hematologists, an intensive care physician, nephrologist, clinical pathologist, biostatistician, and patient representatives, as well as a methodology team from McMaster University. The panel composition was designed to minimize the potential conflicts of interests. The panel used the Grading of Recommendations Assessment, Development, and Evaluation approach and the Population, Intervention, Comparison, Outcome framework to develop and grade their recommendations. Public comments were sought and incorporated in the final document. Results The panel agreed on three recommendations covering the initial diagnosis with emphasis on the importance of ADAMTS13 testing (eg, activity, anti-ADAMTS13 IgG or inhibitor) and assessment of the pretest probability of TTP by clinical assessment and/or the risk assessment models like the PLASMIC or French score. The panel noted how availability and turnaround time of ADAMTS13 test results might affect early diagnosis and management, in particular the use of caplacizumab. Conclusions There is a lack of high-quality evidence to support strong recommendations for the initial diagnosis and management of a suspected TTP. The panel emphasized the importance of obtaining ADAMTS13 testing in a proper clinical context. Future research should focus on how to monitor and act on ADAMTS13 levels during remission.
引用
收藏
页码:2486 / 2495
页数:10
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