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diagnosis syndrome teg coagulation hemophagocytic hlh lymphohistiocytosis acr2021 algorithm behcet behcets calcium capillary clarksons classification coagulopathy cppd criticalcare deposition dermatology
Learning about thromboelastography (TEG). - Tom Fadial @thame #Diagnosis #Hematology #Coagulation #Pharmacology #Thromboelastogram #TEG #Interpretation #Thromboelastography #Laboratory
#Diagnosis #Hematology ... #Coagulation #Pharmacology ... #Thromboelastogram ... #TEG #Interpretation ... #Thromboelastography
Thromboelastogram Interpretation Reaction Time (R Value): - Time till initiation of fibrin clot - Treatment: FFP, protamine K
Thromboelastogram ... Interpretation ... #TEG #Interpretation ... #Thromboelastography ... #coagulation #hematology
Thromboelastography (TEG) based therapy and Management If r time prolonged -> FFP If MA low -> plts/cryoprecipitate (if
Thromboelastography ... #TEG #Management ... #Diagnosis #Hematology ... #Thromboelastogram ... #Treatment
Thromboelastogram (TEG) Interpretation • R-time (R) - Time to first deviation from baseline • K-time (K)
Thromboelastogram ... (TEG) Interpretation ... #TEG #thromboelastography ... #diagnosis #management ... #hematology #coagulopathy
THROMBOELASTOGRAPHY (TEG) General Principle • A small cuvette is rotated to simulate sluggish venous flow and stimulate clot
THROMBOELASTOGRAPHY ... nickmmark #TEG #Thromboelastogram ... #Diagnosis #Management ... #CriticalCare #Hematology ... #Interpretation
Polyarteritis Nodosa (PAN) - Vasculitis Management Algorithm - ACR/VF 2021 Guidelines • Severe Disease → Remission
) - Vasculitis Management ... Guidelines • Severe Disease ... • Non-Severe Disease ... #Treatment #ACR2021 ... Guidelines #algorithm #rheumatology
Behcet's Syndrome - Treatment Ulcers: • Treatment: Topical steroids • Prevention: Colchicine • Azathioprine for refractory disease Arthritis:
Behcet's Syndrome - Treatment ... Ulcers: • Treatment ... #Syndrome #Treatment ... #management #pharmacology ... #rheumatology
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
→Activation of CD8 ... IFN-y) → Excessive activation ... Lymphohistiocytosis #diagnosis #management ... #treatment #summary ... #rheumatology
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
excessive macrophage activation ... age, however the disease ... agent are the main ... Lymphohistiocytosis #diagnosis #management ... #treatment #hematology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Macrophage Activation ... • Fever is the main ... Treatment: • Corticosteroids ... Syndrome #Diagnosis #Management ... #Hematology #Rheumatology
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