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diagnosis syndrome treatment aps hematology arteritis classification disease eular2019 fungal gca giantcell signs symptoms acr2021 adultonset algorithm anesthesia anesthesiology anticoagulation
2019 EULAR recommendations for thrombosis in (Antiphospholipid Syndrome) APS Venous Thrombosis - Arterial Thrombosis INR Target Duration Recurrence Dr. Laurent ARNAUD
2019 EULAR recommendations ... thrombosis in (Antiphospholipid ... Syndrome #APS #management ... #EULAR2019 #guidelines ... #rheumatology #
2019 EULAR Recommendations - Obstetrics Management in (Antiphospholipid Syndrome) APS Previous Thrombosis? Previous Pregnancy Complications? Dr. Laurent ARNAUD @Lupusreference #obstetrics
2019 EULAR Recommendations ... - Obstetrics Management ... in (Antiphospholipid ... #EULAR2019 #guidelines ... #rheumatology #
Antiphospholipid Syndrome (APS) APS is a rare autoimmune disorder characterized by recurring blood clots resulting from antibodies
at least: • 1 clinical ... presence of 1 clinical ... present Treatment (EULAR ... Guidelines): • ... APS #diagnosis #management
Candidemia Workup and Management - IDSA Guidelines 1) Antibiotics • Empiric: Echinocandins (e.g. micafungin) for most patients
Candidemia Workup and Management ... - IDSA Guidelines ... Complications • Ocular ... week to assess ocular ... or TEE unless clinical
Giant Cell Arteritis (GCA) - Vasculitis Management Algorithm - ACR/VF 2021 Guidelines • Visual Symptoms/Loss or
) - Vasculitis Management ... - ACR/VF 2021 Guidelines ... GCA #Vasculitis #Management ... Treatment #ACR2021 #Guidelines ... #algorithm #rheumatology
EULAR/ACR Classification Criteria for Systemic Lupus Erythematosus Clinical Domains: • Constitutional domain: Fever • Cutaneous domain: Non-scarring
EULAR/ACR Classification ... Erythematosus Clinical ... Immunologic domains: • Antiphospholipid ... Erythematosus #diagnosis #rheumatology
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Still's Disease Clinical ... • Ocular: uveitis ... Disease #diagnosis #management ... #treatment #rheumatology
Cryofibrinogenemia Summary Cryofibrinogenemia Epidemiology: • 40-70 years with a modest female predominance Cryofibrinogenemia: • The precipitation of a
Cryofibrinogenemia Clinical ... pulmonary emboli, and ocular ... Diagnosis: • + Clinical ... HUS and HIT • Antiphospholipid ... Cryofibrinogenemia #diagnosis #rheumatology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... ulceration • Ocular ... Behcet syndrome (Clinical ... Syndrome #diagnosis #management ... signs #symptoms #rheumatology
Myasthenia Gravis Overview Myasthenia Gravis is an autoimmune disorder of the postsynaptic neuromuscular junction. Ab to
Clinical Picture ... Ocular- 50%: Ptosis ... Clinical DX: - ... Bedside: ice pack ... Gravis #diagnosis #management
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