Literature DB >> 27476033

How we treat thrombotic thrombocytopenic purpura: Results of a Canadian TTP practice survey.

Christopher J Patriquin1, William F Clark2, Katerina Pavenski3, Donald M Arnold4, Gail Rock5, Stephen R Foley4.   

Abstract

BACKGROUND: Thrombotic thrombocytopenic purpura (TTP) is a rare disease with 90% mortality if untreated. Since the Canadian Apheresis Group (CAG) trial showed greater survival with therapeutic plasma exchange (TPE) versus plasma infusion, there has been widespread adoption of TPE. Beyond TPE, there is significant practice variation. To characterize this, we developed a survey sent to physicians who might be directly involved in TTP management.
METHODS: The survey was sent to CAG members as well as hematologists and nephrologists nationwide and addressed areas of controversy or recognized practice heterogeneity. Descriptive statistics were used to summarize responses, and the χ2 test was used to compare respondents who were and were not CAG physicians. We also compared responses by estimated frequency of TTP cases per year.
RESULTS: The CAG response rate was 31% (13 of 42). The survey was sent to 665 non-CAG physicians, of whom 41 responded (6.1%). Though not statistically different, CAG and non-CAG respondents varied regarding use of corticosteroids, aspirin, and venous thromboembolism (VTE) prophylaxis. Significant differences were found between CAG and non-CAG groups regarding cryosupernatant as fluid choice (69.2% vs. 22.5%, P = .004) and the use of TPE tapering (84.6% vs. 51.3%, P = .034), respectively.
CONCLUSION: TTP treatment is variable across centres in Canada. Areas of significant variation include the choice of replacement fluid for TPE and whether or not and how to taper TPE. Our survey highlights the practice heterogeneity that exists and identifies areas where more evidence is needed and perhaps where trials should be performed.
© 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  TTP; practice survey; therapeutic apheresis; thrombotic microangiopathy; thrombotic thrombocytopenic purpura

Mesh:

Year:  2016        PMID: 27476033     DOI: 10.1002/jca.21489

Source DB:  PubMed          Journal:  J Clin Apher        ISSN: 0733-2459            Impact factor:   2.821


  4 in total

Review 1.  Beyond plasma exchange: novel therapies for thrombotic thrombocytopenic purpura.

Authors:  Kathryn Dane; Shruti Chaturvedi
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2018-11-30

2.  Real-world data confirm the effectiveness of caplacizumab in acquired thrombotic thrombocytopenic purpura.

Authors:  Linus A Völker; Jessica Kaufeld; Wolfgang Miesbach; Sebastian Brähler; Martin Reinhardt; Lucas Kühne; Anja Mühlfeld; Adrian Schreiber; Jens Gaedeke; Markus Tölle; Wolfram J Jabs; Fedai Özcan; Silke Markau; Matthias Girndt; Frederic Bauer; Timm H Westhoff; Helmut Felten; Martin Hausberg; Marcus Brand; Jens Gerth; Markus Bieringer; Martin Bommer; Stefan Zschiedrich; Johanna Schneider; Saban Elitok; Alexander Gawlik; Anja Gäckler; Andreas Kribben; Vedat Schwenger; Ulf Schoenermarck; Maximilian Roeder; Jörg Radermacher; Jörn Bramstedt; Anke Morgner; Regina Herbst; Ana Harth; Sebastian A Potthoff; Charis von Auer; Ralph Wendt; Hildegard Christ; Paul T Brinkkoetter; Jan Menne
Journal:  Blood Adv       Date:  2020-07-14

3.  Successful Management of Thrombotic Thrombocytopenic Purpura in a Jehovah's Witness: An Individualized Approach With Joint Decision-Making.

Authors:  Ming Y Lim; Charles S Greenberg
Journal:  J Patient Exp       Date:  2019-02-14

4.  Combination of Fresh Frozen Plasma and Cryosupernatant Plasma for Therapeutic Plasma Exchange in Thrombotic Thrombocytopenic Purpura: A Single Institution Experience.

Authors:  Qiuyan Lin; Liping Fan; Haobo Huang; Feng Zeng; Danhui Fu; Shijin Wei
Journal:  Biomed Res Int       Date:  2019-01-30       Impact factor: 3.411

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.