15 results
Algorithm for the Evaluation of Pediatric Head Trauma (PECARN) - Need for Head CT #Diagnosis #Management
Algorithm for the Evaluation ... of Pediatric Head ... Need for Head CT #Diagnosis ... #Management #EM ... PECARN #Algorithm #Ddxof
Evaluation and Management of Pediatric Fever #Diagnosis #Management #EM #Peds #Fever #Workup #Evaluation #Discharge #Admission #Algorithm
Evaluation and Management ... of Pediatric Fever ... #Diagnosis #Management ... #EM #Peds #Fever ... Admission #Algorithm #Ddxof
Septic Arthritis - Diagnosis and Management Summary
Clinical Exam: hot, swollen, pain with passive AND active ROM
active ROM +/- fever ... necrosis, Lyme disease ... count, and crystal evaluation ... MH/CCF/CWRU EM ... #Diagnosis #Management
Kawasaki Disease (KD) - Diagnosis and Management Summary

Kawasaki Disease (KD) is the most common vasculitis of
Presentation: • Fever ... , Tachycardia, Arthritis ... Criteria - Fever ... #rheumatology #pediatrics ... #diagnossi #management
Algorithm for the Evaluation of Kawasaki and Incomplete Kawasaki Disease:
Diagnosis
* Fever >5d
* Criteria (4/5)
  -
Algorithm for the Evaluation ... Fever >5d * Criteria ... #Pediatrics #Kawasaki ... #Disease #Criteria ... Workup #Algorithm #Ddxof
Clinical Algorithm for Emergency Department Evaluation and Management of UTI in Febrile Infants and Young Children

Urinary
Emergency Department Evaluation ... and Management ... Guidelines are based ... UTI #Algorithm #Diagnosis ... #Fever
Adult Onset Still's Disease
Systemic inflammation with urticarial rash.
Rash: 
 • Nonpruritic, evanescent (correlates with time of
Onset Still's Disease ... early evening • Arthritis ... - Yamaguchi criteria ... Arthralgias or arthritis ... #rheumatology #management
Evaluation of suspected incomplete Kawasaki Disease

1. AHA consensus recommendations
2. Infants ≤6 months old on day ≥7
Evaluation of suspected ... incomplete Kawasaki Disease ... old on day ≥7 of fever ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
Macrophage Activation Syndrome (MAS)
Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH)

What?
A subset of
juvenile idiopathic arthritis ... juvenile idiopathic arthritis ... Histopathologic criteria ... Activation #Syndrome #Diagnosis ... #Management #Hematology
Hemophagocytic Lymphohistiocytosis (HLH)
Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
• Clinical: fever ... • Autoimmune diseases ... Adult-onset Still disease ... inhibitors under evaluation ... #management #treatment