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[Catastrophic antiphospholipid syndrome].
- Source :
-
La Revue de medecine interne [Rev Med Interne] 2012 Apr; Vol. 33 (4), pp. 194-9. Date of Electronic Publication: 2012 Feb 16. - Publication Year :
- 2012
-
Abstract
- The catastrophic antiphospholipid syndrome (CAPS) is a life-threatening condition resulting from rapidly progressive widespread thromboses mainly affecting the microvasculature in the presence of antiphospholipid antibodies. Within a few days, the patients develop multiorgan failure with pulmonary distress, renal failure with severe hypertension, cerebral, cardiac, digestive or cutaneous involvement. CAPS develops in less than 1% of patients with antiphospholipid syndrome, either primary or associated with systemic lupus erythematosus. CAPS reveals the antiphospholipid syndrome in about 50% of cases. CAPS may be precipitated by infectious diseases, surgical procedures or discontinuation of anticoagulation. CAPS overall mortality rate has decreased in the past decade and is now around 30%. Within our hospital, it has been reduced to 10%. The main differential diagnoses are other thrombotic microangiopathies, and heparin-induced thrombocytopenia. The treatment of CAPS consists of the empirical association of anticoagulation and corticosteroids, plus plasma exchange or intravenous immunoglobulins. Cyclophosphamide is added in patients with systemic lupus erythematosus. The prevention of CAPS is based upon the adequate management of the perioperative period when surgery cannot be avoided, the prompt treatment of infections and the education of patients with antiphospholipid syndrome.<br /> (Copyright © 2012 Société nationale Française de médecine interne (SNFMI). Published by Elsevier SAS. All rights reserved.)
- Subjects :
- Antibodies, Antiphospholipid blood
Antiphospholipid Syndrome diagnosis
Antiphospholipid Syndrome immunology
Antiphospholipid Syndrome mortality
Biomarkers blood
Catastrophic Illness therapy
Diagnosis, Differential
Drug Therapy, Combination
Evidence-Based Medicine
Humans
Hypertension etiology
Hypertension therapy
Immunoglobulins, Intravenous
Immunologic Factors blood
Lupus Erythematosus, Systemic diagnosis
Lupus Erythematosus, Systemic immunology
Lupus Erythematosus, Systemic mortality
Multiple Organ Failure etiology
Multiple Organ Failure therapy
Plasma Exchange
Renal Insufficiency etiology
Renal Insufficiency therapy
Respiratory Insufficiency etiology
Respiratory Insufficiency therapy
Risk Assessment
Risk Factors
Severity of Illness Index
Treatment Outcome
Anticoagulants therapeutic use
Antiphospholipid Syndrome complications
Antiphospholipid Syndrome therapy
Glucocorticoids therapeutic use
Lupus Erythematosus, Systemic complications
Lupus Erythematosus, Systemic therapy
Subjects
Details
- Language :
- French
- ISSN :
- 1768-3122
- Volume :
- 33
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- La Revue de medecine interne
- Publication Type :
- Academic Journal
- Accession number :
- 22341856
- Full Text :
- https://doi.org/10.1016/j.revmed.2012.01.005