Antiphospholipid Syndrome Clinical Research Task Force Report

被引:33
作者
Erkan, D. [1 ]
Derksen, R. [2 ]
Levy, R. [3 ]
Machin, S. [4 ]
Ortel, T. [5 ]
Pierangeli, S. [6 ]
Roubey, R. [7 ]
Lockshin, M.
机构
[1] Cornell Univ, Hosp Special Surg, Weill Med Coll, Barbara Volcker Ctr Women & Rheumat Dis, New York, NY 10021 USA
[2] Univ Med Ctr, Utrecht, Netherlands
[3] Univ Estado Rio de Janeiro, Rio De Janeiro, Brazil
[4] Univ Coll London Hosp, London, England
[5] Duke Univ Hlth Syst, Durham, NC USA
[6] Univ Texas Med Branch, Galveston, TX USA
[7] Univ N Carolina, Chapel Hill, NC USA
关键词
anticardiolipin antibodies; antiphospholipid syndrome; lupus anticoagulant; RISK-FACTORS; THROMBOSIS; UPDATE;
D O I
10.1177/0961203310395053
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Antiphospholipid Syndrome (APS) Clinical Research Task Force (CRTF) was one of six Task Forces developed by the 13(th) International Congress on Antiphospholipid Antibodies (aPL) organization committee with the purpose of: a) evaluating the limitations of APS clinical research and developing guidelines for researchers to help improve the quality of APS research; and b) prioritizing the ideas for a well-designed multicenter clinical trial and discussing the pragmatics of getting such a trial done. Following a systematic working algorithm, the Task Force identified five major issues that impede APS clinical research and the ability to develop evidence-based recommendations for the management of aPL-positive patients: (1) aPL detection has been based on partially or non-standardized tests, and clinical (and basic) APS research studies have included patients with heterogeneous aPL profiles with different clinical event risks; (2) clinical (and basic) APS research studies have included a heterogeneous group of patients with different aPL-related manifestations (some controversial); (3) thrombosis and/or pregnancy risk stratification and quantification are rarely incorporated in APS clinical research; (4) most APS clinical studies include patients with single positive aPL results and/or low-titer aPL ELISA results; furthermore, study designs are mostly retrospective and not population based, with limited number of prospective and/or controlled population studies; and (5) lack of the understanding the particular mechanisms of aPL-mediated clinical events limits the optimal clinical study design. The Task Force recommended that there is an urgent need for a truly international collaborative approach to design and conduct well-designed prospective large-scale multi-center clinical trials of patients with persistent and clinically significant aPL profiles. An international collaborative meeting to formulate a good research question using 'FINER' (Feasible; Interesting; Novel; Ethical; and Relevant) criteria took place in November 2010. Lupus (2011) 20, 219 224.
引用
收藏
页码:219 / 224
页数:6
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