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diagnosis algorithm hemeonc hit induced oncology anemia aplastic causes chronic cll coagulation decisionaid dic disseminated dosing hemophagocytic hlh intravascular leukemia
Heparin Induced Thrombocytopenia (HIT) - Diagnosis and Management - GrepMed Handbook Presentation: • Plts ↓50% (nadir
Thrombocytopenia ... Diagnosis and Management ... ♀, ↑Age, ESRD Pathophysiology ... Management: • ... #Treatment #Hematology
Disseminated Intravascular Coagulation (DIC) Overview Increased Clotting and Consumption of Clotting Factors Findings: • Bleeding • Recent history
Coagulation (DIC) Overview ... protein C and S Pathophysiology ... + Bleeding Treatment ... diagnosis #causes #treatment ... #management #hematology
Managing warfarin INR Warfarin dosage must be individualized according to the patient's response to the drug, and
#management #algorithm ... #pharmacology #treatment ... #medications #table ... #decisionaid #cardiology ... #hematology #warfarin
Our approach to the diagnosis and initial management of patients with suspected HIT. Our approach is
diagnosis and initial management ... and to adjust treatment ... #Hematology #HIT ... #Heparin #Induced ... #Thrombocytopenia
Chronic Lymphocytic Leukemia (CLL) - Summary Overview: • Most common leukemia in adults • Disorder of
CLL) - Summary Overview ... Symptoms of anemia or thrombocytopenia ... with anemia or thrombocytopenia ... Leukemia #oncology #hematology ... hemeonc #diagnosis #management
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Aplastic Anemia - Overview ... - Antithyroid medications ... aplastic anemia Treatment ... Anemia #oncology #hematology ... #diagnosis #management
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
Lymphohistiocytosis (HLH) Pathophysiology ... +++ (Plt, Hb), Hepatic ... Lymphohistiocytosis #diagnosis #management ... #treatment #summary ... #rheumatology
TAFRO TAFRO syndrome was first described in 2010, standing for: - Thrombocytopenia - Anasarca - Fever - Reticulin fibrosis - Organomegaly TAFRO syndrome
syndrome - IGG4 - Hepatic ... cell lymphoma Pathophysiology ... Hypoalbuminemia Treatment ... TAFRO #diagnosis #management ... #rheumatology #
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