11 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 #LP ... Antibiotics #Risk #Stratification
Validation of the “Step-by-Step” Approach in the Management of Young Febrile Infants
Visual Abstract by Dr. Kirsty
Young Febrile Infants ... 27382134 #EBM #Peds ... #Pediatrics #VisualAbstract ... #StepByStep #Algorithm ... #Risk #Stratification
Clinical features of shock from dehydration in an infant

Decreased level of consciousness 
Sunken fontanelle 
Dry mucous
dehydration in an infant ... Decreased level ... #PhysicalExam #Signs ... #Dehydration #Peds ... #Pediatrics
gestational diabetes algorithm
#Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes algorithm ... #Infant #Diabetic ... #Mother #Pediatrics ... OBGYN #Diagnosis #Pathophysiology ... Complications #Peds
Pediatric SVT - Management Algorithm
Identify SVT:
 • HR not variable
 • Abrupt rate changes
 • Infants:
Pediatric SVT - ... Management Algorithm ... rate changes • Infants ... Signs of shock or ... #peds #Pediatric
“Step by Step” – the new kid on the block – aims to risk stratify this
“low risk” an infant ... Diagnosis #Management #Pediatrics ... #Peds #Febrile ... #Algorithm #LP ... Antibiotics #Risk #Stratification
The Febrile Infant Step-by-Step Algorithm
This is an algorithm developed by European emergency physicians to identify low-risk
The Febrile Infant ... This is an algorithm ... EBM #Management #Pediatrics ... #Peds #Febrile ... Antibiotics #Risk #Stratification
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm
Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic Infant ... Differential Diagnosis Algorithm ... Nervous System - Decreased ... #Causes #Peds # ... Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
Evaluation of suspected incomplete Kawasaki Disease

1. AHA consensus recommendations
2. Infants ≤6 months old on day ≥7
Infants ≤6 months ... lack of tapering, decreased ... clinical and lab signs ... #Diagnosis #Peds ... #Pediatrics #Kawasaki