Stroke and the antiphospholipid syndrome: consensus meeting Taormina 2002

被引:61
作者
Brey, RL
Chapman, J
Levine, SR
Ruiz-Irastorza, G
Derksen, RHWM
Khamashta, M
Shoenfeld, Y
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Med, Div Neurol, San Antonio, TX 78229 USA
[2] Tel Aviv Univ, Dept Neurol, Chaim Sheba Med Ctr, Sackler Fac Med, IL-69978 Tel Aviv, Israel
[3] Mt Sinai Sch Med, Stroke Program, Dept Neurol, New York, NY USA
[4] Univ Basque Country, Serv Internal Med, Hosp Cruces, Dept Med, Bizkaia 48903, Spain
[5] Univ Med Ctr, Dept Rheumatol & Clin Immunol, Utrecht, Netherlands
[6] St Thomas Hosp, Rayne Inst, Lupus Unit, London SE1 7EH, England
[7] Sheba Med Ctr, Dept Med B, Tel Hashomer, Israel
[8] Sheba Med Ctr, Ctr Autoimmune Dis, Tel Hashomer, Israel
[9] Tel Aviv Univ, Sackler Fac Med, IL-69978 Tel Aviv, Israel
关键词
anticoagulant therapy; antiphospholipid antibodies; antiphospholipid syndrome; cerebrovascular disorders; lupus anticoagulant; stroke;
D O I
10.1191/0961203303lu390oa
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ischaemic stroke is the only neurological manifestation accepted as a clinical diagnostic criterion for the antiphospholipidsyndrome (APS). This association is reasonably well established in patients first diagnosed with APS but is less clear in randomly selected stroke patients who test positive on one occasion for antiphospholipid antibodies and who have no other evidence of systemic autoimmune disease. We propose a grading system that posits stroke to be definitely, likely or possibly associated with antiphospholipid antibodies (aPL). Further, there are limited prospective data to determine appropriate treatment. There is controversy as to whether the presence of aPL even increases risk of a recurrent stroke or other thromboembolic event, although data point to persistent medium-high titre aCL and/or LA as risk factors for recurrence. In the absence of data to guide clinicians on the best treatment, we cannot make strong recommendations as to optimal therapy, nor can we propose clear consensus treatment guidelines.
引用
收藏
页码:508 / 513
页数:6
相关论文
共 66 条
[1]   CEREBROVASCULAR-DISEASE AND ANTIPHOSPHOLIPID ANTIBODIES IN SYSTEMIC LUPUS-ERYTHEMATOSUS, LUPUS-LIKE DISEASE, AND THE PRIMARY ANTIPHOSPHOLIPID SYNDROME [J].
ASHERSON, RA ;
KHAMASHTA, MA ;
GIL, A ;
VAZQUEZ, JJ ;
CHAN, O ;
BAGULEY, E ;
HUGHES, GRV .
AMERICAN JOURNAL OF MEDICINE, 1989, 86 (04) :391-399
[2]  
BABIKIAN VL, 1990, STROKE, V21, P1268
[3]   ANTICARDIOLIPIN ANTIBODY AND STROKE - POSSIBLE RELATION OF VALVULAR HEART-DISEASE AND EMBOLIC EVENTS [J].
BARBUT, D ;
BORER, JS ;
WALLERSON, D ;
AMEISEN, O ;
LOCKSHIN, M .
CARDIOLOGY, 1991, 79 (02) :99-109
[4]  
BorowskaLehman J, 1995, FOLIA NEUROPATHOL, V33, P231
[5]   Detection of cerebral microembolic signals by transcranial Doppler may be a useful part of the equation in determining stroke risk in patients with antiphospholipid antibody syndrome [J].
Brey, RL ;
Carolin, MK .
LUPUS, 1997, 6 (08) :621-624
[6]   Antiphospholipid antibodies and stroke in young women [J].
Brey, RL ;
Stallworth, CL ;
McGlasson, DL ;
Wozniak, MA ;
Wityk, RJ ;
Stern, BJ ;
Sloan, MA ;
Sherwin, R ;
Price, TR ;
Macko, RF ;
Johnson, CJ ;
Earley, CJ ;
Buchholz, DW ;
Hebel, JR ;
Kittner, SJ .
STROKE, 2002, 33 (10) :2396-2400
[7]   ANTIPHOSPHOLIPID ANTIBODIES AND CEREBRAL-ISCHEMIA IN YOUNG-PEOPLE [J].
BREY, RL ;
HART, RG ;
SHERMAN, DG ;
TEGELER, CH .
NEUROLOGY, 1990, 40 (08) :1190-1196
[8]  
Brey RL, 1999, STROKE, V30, P252
[9]  
CAMERLINGO M, 1995, ACTA NEUROL SCAND, V92, P69
[10]  
CAMPBELL AL, 1995, THROMB HAEMOSTASIS, V73, P529