20 results
Validation of the Step-By-Step Approach to Febrile Infants

#Diagnosis #Management #Pediatrics #Peds #Febrile #Infant #StepByStep #Algorithm #LP
#Diagnosis #Management ... #Pediatrics #Peds ... #Febrile #Infant ... #StepByStep #Algorithm ... Stratification #Fever
Step by Step Algorithmic Approach to Pediatric Fever

Age < 21 days old (or 28 days for
Fever Age < 21 ... #Peds #Diagnosis ... #Management #StepByStep ... #Algorithm #Infant ... #Fever
“Step by Step” – the new kid on the block – aims to risk stratify this
with fever without ... CRP < 20 mg/L #Diagnosis ... #Management #Pediatrics ... #Peds #Febrile ... #Infant #StepByStep
The Febrile Child - some diagnostic clues to evaluating the febrile child.

#Febrile #Fever #Evaluation #Assessment #Signs
#Febrile #Fever ... Evaluation #Assessment #Signs ... #Symptoms #PhysicalExam ... #Diagnosis #Peds ... #Pediatrics
Clinical Algorithm for Emergency Department Evaluation and Management of UTI in Febrile Infants and Young Children

Urinary
department with fever ... This algorithm was ... UTI #Algorithm #Diagnosis ... #Peds #UrinaryTract ... #Pediatrics #Fever
Practical Pediatric Viral Rash Algorithm

Child presenting with rash and current/ recent symptoms of viral illness but
Practical Pediatric ... but is well with fever ... five days and no signs ... / symptoms of sepsis ... #Peds #Diagnosis
The Febrile Infant Step-by-Step Algorithm
This is an algorithm developed by European emergency physicians to identify low-risk
92.0% and 46.9% #Diagnosis ... EBM #Management #Pediatrics ... #Peds #Febrile ... #Infant #StepByStep ... Stratification #Fever
Kernig's Sign in Meningitis

Kernig's sign is present if the patient, in the supine position with the
In this video, the ... infant cries as ... Meningitis #Clinical #Video ... #PhysicalExam #Pediatrics ... #Peds #neurology
Croup Diagnosis and Management Pearls
Common childhood illness, usually viral and self limiting. Characterised by a seal-like
Croup Diagnosis ... hoarse voice +/- fever ... rhinorrhea, and fever ... #Management #pediatrics ... #peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
occur in utero as ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics