Treatment in thrombotic antiphospholipid syndrome: a review.
T S VadgamaA SmithMaria Laura BertolacciniPublished in: Lupus (2019)
Antiphospholipid syndrome an autoimmune disease characterized by thrombosis and/or pregnancy morbidity alongside the presence of antiphospholipid antibodies (aPL). This review evaluates primary and secondary thromboprophylaxis in patients with aPL and thrombotic events. In primary thromboprophylaxis a risk-stratified approach is needed based on aPL, comorbidity with other autoimmune conditions and cardiovascular vascular risk factors. In primary thromboprophylaxis, the efficacy of low-dose aspirin is debatable and requires better-designed controlled studies. So far warfarin has not been shown to improve venous and/or arterial thrombosis incidence in aPL carriers and instead increased safety concerns. The benefit of hydroxychloroquine is inconclusive despite promising data, requiring large, controlled trials. For secondary thromboprophylaxis warfarin seems to be the best option with potential in renal transplant recipients and better efficacy at high intensity, although maintenance of target international normalized ratio needs careful monitoring. Aspirin has not shown to be beneficial, and data on rivaroxaban are limited and contradictory. Despite all data being informative, there are limitations that need to be addressed with robust clinical trials.
Keyphrases
- venous thromboembolism
- direct oral anticoagulants
- low dose
- high intensity
- risk factors
- atrial fibrillation
- electronic health record
- clinical trial
- pulmonary embolism
- big data
- multiple sclerosis
- systemic lupus erythematosus
- high dose
- cardiovascular events
- antiplatelet therapy
- resistance training
- preterm birth
- data analysis
- deep learning
- combination therapy
- pregnant women
- artificial intelligence
- coronary artery disease
- oral anticoagulants
- replacement therapy