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management diagnosis erythematosus hematology sle systemic activation acute anemia aplastic chronic differential druginduced macrophage mas oncology pharmacology risk syndrome
Medications for Treatment of Acute Gout - NSAIDs - Colchicine (Colcrys) - Corticosteroids #Acute #Gout #Medications #Treatment
Medications for ... Gout - NSAIDs ... #Medications #Treatment ... #Management #AAFP ... #Rheumatology
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 Approach to Gout Diagnosis: r/o septic arthritis! Needle-shaped, negative birefringent crystals Treatment: • Weight loss, diet, d/c culprit
Approach to Gout ... diet, d/c culprit medications ... Lowering Therapy (ULT ... ): 1) 2+ flares ... #ULT #rheumatology
Medications for Prevention of Chronic Gout Colchicine (Colcrys) Pegloticase (Krystexxa) Probenecid Xanthine oxidase inhibitors: - Allopurinol (Zyloprim) - Febuxostat (Uloric) #Chronic
Medications for ... Prevention of Chronic Gout ... #Medications #Treatment ... #Management #AAFP ... #Rheumatology
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 Gout - Management Acute Gout Flare 1) colchicine, NSAIDs, glucocorticoids 2) Anakinra (IL-1 inhibitor) When to Start Urate
Gout - Management ... Lowering Therapy (ULT ... 3) 2+ gout flares ... #Management #treatment ... #rheumatology
SLE (Systemic Lupus Erythematosus) Suspect: Clinical evidence of (fatigue, rash, photosensitivity, inflammatory arthritis, weight loss, and fever) and
Non-autoimmune rheumatologic ... lymphopenia, low PLT ... extremities Drug ... • Antihistone: Drug ... activation and/or medications
Drug Induced Systemic Lupus Erythematosus > 100 drugs have been associated with drug-induced SLE High risk (>5%): •
Lupus Erythematosus ... for 1 year of treatment ... SLE #Systemic #Lupus ... Erythematosus #medications ... differential #diagnosis #rheumatology
Gout - Diagnosis and Management Summary 3 Conditions for Gout to Manifest: 1. Hyperuricemia 2. Monosodium urate deposition in
Metabolic syndrome • Medications ... treatment; consider ... comorbidities/drug ... • Oral drug failure ... #rheumatology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
SJIA], systemic lupus ... ) • Sepsis • Drug-induced ... tests ↑ AST ↑ ALT ... Treatment: • Corticosteroids ... #Rheumatology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Dyskeratosis congenita • Drugs ... - Cytotoxic drugs ... - Antithyroid medications ... • ↓ WBC • ↓ PLT ... aplastic anemia Treatment
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