17 results
Assessment and management of cirrhosis in people older than 16 years: summary of NICE guidance
#cirrhosis #assessment
Assessment and management ... than 16 years: summary ... guidance #cirrhosis #assessment ... #management #hepatitis ... #NICE #hepatology
Lipid Management 2018 Summary
- Stephen D. Sisson MD FACP 

#Management #PrimaryCare #Lipids #Statins #Reassessment #Initiation #Algorithm
Lipid Management ... 2018 Summary - ... Lipids #Statins #Reassessment ... #Initiation #Algorithm ... #Intensity #Summary
Hypereosinophilia (HE) Summary

 • Definition
 • When to Suspect?
 • A Partial Classification of Hypereosinophilia
 •
Hypereosinophilia (HE) Summary ... • A Partial Classification ... Hypereosinophilia #HE #hematology ... #diagnosis #management
Summary of types of haemolytic anaemia. Visit gramproject.com for more medical diagrams, tables and flowcharts for
Summary of types ... diagnosis #clinical #management ... #differential #algorithm ... #anaemia #haematology
Our approach to the diagnosis and initial management of patients with suspected HIT. Our approach is
diagnosis and initial management ... primarily on clinical assessment ... imprecise, and complemented ... #Hematology #HIT ... Thrombocytopenia #Algorithm
A priority in this project was to appropriately stratify participants into a low, medium, or high-intensity
The classification ... for Fall Risk Assessment ... The algorithm is ... STEADI) #Diagnosis #Management ... Risk #Screening #Assessment
Systemic Lupus Erythematosus (SLE) - Diagnosis and Management Summary
 • Epidemiology: 10-180/100,000, Typically Age 20-40, F:M
Diagnosis and Management ... Summary • Epidemiology ... 80% - Low complement ... Usual therapeutic management ... #Summary #rheumatology
Vasculitis and Vasculitides - Differential Diagnosis Framework

When to Consider Vasculitis:
 • Purpura, ischemic skin lesions
 •
often involved • Hypocomplementemic ... Urticaria and hypocomplementemia ... against MPO • Complement ... differential #diagnosis #rheumatology ... #classification
Hemophagocytic Lymphohistiocytosis (HLH)
Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
+ Etiological Assessment ... for etiological assessment ... Lymphohistiocytosis #diagnosis #management ... #treatment #summary ... #rheumatology
Cryoglobulinemia Summary

Cryoglobulins:
 • Cryoglobulins are Igs in the serum that precipitate in vitro at temperatures below
Cryoglobulinemia Summary ... • Low serum C4 complement ... diagnosis #types #classification ... #rheumatology #