Antiphospholipid Syndrome in the Elderly: Caution
Author(s) -
JeanCharles Piette,
P. Cacoub
Publication year - 1998
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/01.cir.97.22.2195
Subject(s) - medicine , antiphospholipid syndrome , intensive care medicine , thrombosis
Ten years after its identification, thousands of articles and 2 books have made the APS popular. Subsequently, the diagnosis of a possible APS is now frequently considered in daily practice, not only by subspecialists but also by general practitioners, in patients with thrombosis, sometimes whatever their age at the time of the first vascular event. We wish to emphasize here the potential hazards associated with a diagnosis of APS in elderly patients.Historically, APS was first identified as a subset of patients with SLE because of the strong association observed in this disorder between the occurrence of thrombosis, either arterial or venous, and/or miscarriages and the presence of aPL (ie, Lupus anticoagulant) and/or aCL. Later, APS was also recognized in patients who had no features of SLE, leading to the concept of a “primary APS.”1 A set of criteria has been proposed to discriminate primary from SLE-related APS.2 Although aPL may be encountered in multiple circumstances, primary and SLE-related appear to be the 2 major variants of APS.2 3 4 APS usually affects young patients. This is obviously true for SLE-related APS, given that …
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