12 results
treatment rheumatology algorithm disease hepatology hit induced syndrome thrombocytopenia behcet causes cirrhosis classification coagulation complications dermatology dic disseminated gastroenterology hemeonc
Management and Complications of Cirrhosis and Ascites Ascites Workup Algorithm Ascites Management Refractory Ascites Hyponatremia Spontaneous Bacterial Peritonitis (SBP) Hepatic Hydrothorax AKI in
Management and Complications ... Ascites Workup ... Peritonitis (SBP) Hepatic ... Complications #diagnosis ... #hepatology
Ascites - Diagnostic Approach and Differential Diagnosis The most common causes: cirrhosis, malignancy and heart failure. Approx
Ascites - Diagnostic ... bilirubin 2) Routine tests ... 3) Optional tests ... #workup #Differential ... #Diagnosis #hepatology
Our approach to the diagnosis and initial management of patients with suspected HIT. Our approach is
results of HIT laboratory ... tests, which are ... #Diagnosis #Management ... #Hematology #HIT ... #Heparin #Induced
Approach to Thrombotic Microangiopathy (TMA) - Differential Diagnosis and Management Algorithm Suspected TMA: Unexplained thrombocytopenia + MAHA
Diagnosis and Management ... hemoglobin/hemosiderin, Hepatic ... Direct antiglobulin test ... #Diagnosis #Management ... #Algorithm #hematology
Heparin Induced Thrombocytopenia (HIT) - Diagnosis and Management - GrepMed Handbook Presentation: • Plts ↓50% (nadir
and Management ... (at injection sites ... approach for post-test ... : Confirmatory test ... #Hematology #HemeOnc
Disseminated Intravascular Coagulation (DIC) Overview Increased Clotting and Consumption of Clotting Factors Findings: • Bleeding • Recent history
or venipuncture sites ... Laboratory Findings ... #Coagulation #diagnosis ... causes #treatment #management ... #hematology
TTP - Laboratory Evaluation for Thrombotic Thrombocytopenic Purpura Activity of von Willebrand factor-cleaving protease activity - A
TTP - Laboratory ... value is low, tests ... indirect antiglobulin tests ... WBC count and differential ... #Workup #Hematology
IgG4-Related Disease Clinical history: Man, 60 years, multiorgan involvement, unique or multiple inflammatory pseudotumor 4 phenotypes: •
relapse No specific laboratory ... tests: • IgG4 ... #management #phenotypes ... #workup #treatment ... #rheumatology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
pathognomonic laboratory ... tests in Behcet ... Behcet disease) Differential ... #management #signs ... #symptoms #rheumatology
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
other etiology • Laboratory ... characteristic sites ... blockers had the best ... #diagnosis #management ... #Dermatology
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