32 results
Summary of Coagulation Deficiencies
Inherited:
 • Hemophilia A - Deficiency of Factor VIII
 • Hemophilia B -
Summary of Coagulation ... of Factor IX Acquired ... Advanced Liver Disease ... Acute DIC - Septic shock ... table #comparison #diagnosis
Classification of Diabetes Insipidus

Central or neurogenic diabetes insipidus:
 - Congenital - Structural malformations affecting the hypothalamus
AQP-2 gene - Acquired ... insipidus: - Acquired ... Treatment is aimed ... Classification #Types #Nephrology ... #Diagnosis #Differential
Shock - Diagnosis and Management Summary
 • Hypotension: SBP<90, SBP drop >40, MAP<65 (Normotension, HTN possible
Shock - Diagnosis ... and Management Summary ... Tamponade - Pulmonary ... #Diagnosis #Management ... #treatment #workup
Shock - Differential Diagnosis Framework
 - MAP <65. SBP <90, drop in SBP > 40
 -
Diagnosis Framework ... , Severe Valve Disease ... • Obstructive: Pulmonary ... Treatment Goals ... #Differential #Diagnosis
Polycythemia Vera (PV) - Diagnosis and Management Summary
Diagnostic Criteria:
 • Elevated hemoglobin and/or hematocrit AND
 •
and Management Summary ... Diagnostic Criteria ... with evidence of acquired ... von Willebrand disease ... #Management #Summary
Blastomycosis (Blastomyces): Gilchrist’s disease, Chicago disease - Summary Sheet
 • Morphology
 • Geography, Reservoir and Mode
- Summary Sheet ... resembles community-acquired ... blastomycosis • Diagnosis ... #Blastomyces #diagnosis ... #management #summary
Approach to Undifferentiated Shock - OnePager Summary
Shock occurs when there is inadequate blood flow (CO) &
- OnePager Summary ... Shock occurs when ... essential to determine treatment ... Cardiac Tamponade, Pulmonary ... #diagnosis #differential
Myasthenia Gravis - Summary
 • an autoimmune disease of the postsynaptic neuromuscular junction associated with antibodies
Myasthenia Gravis - Summary ... 50 years in men Diagnosis ... immunosuppressive therapy is required ... within 3 years of diagnosis ... #management #neurology
Hemophagocytic Lymphohistiocytosis (HLH)
Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
Purtilo (XLP) Acquired ... • Autoimmune diseases ... Unknown cause Treatment ... #management #treatment ... #summary #rheumatology
Pulmonary Renal Syndromes - OnePager Summary
Autoimmune ANCA vasculitis (AAV): GPA (granulomatous with polyangiitis), EGPA (eosinophilic granulomatosis
Syndromes - OnePager Summary ... life-threatening diseases ... Inflammatory eye disease ... #differential #diagnosis ... #management #treatment