11 results
NRP Neonatal Resuscitation Algorithm 

#Neonatal #NRP #Resuscitation #Algorithm #Algorithm #Ddxof #Management #Peds #Assessment #Pediatrics
NRP Neonatal Resuscitation ... Algorithm #Neonatal ... Management #Peds #Assessment ... #Pediatrics
Hypoxic-ischemic encephalopathy (HIE) 

#HypoxicIschemic #encephalopathy #HIE #Neonatal #Peds #Pediatrics #Pathophysiology
encephalopathy #HIE #Neonatal ... #Peds #Pediatrics ... #Pathophysiology
Initial assessment and management of coma in pediatric population.

Airway - is it secure? 
Breathing — is
Initial assessment ... management of coma in pediatric ... treatable: - hypoglycaemia ... care unit #Assessment ... #Coma #Pediatrics
Rapid Assessment of the Neonate With Sonography (RANS) Scan

Recommended algorithm for RANS scan. 
* Abnormal vital
Rapid Assessment ... of the Neonate ... POCUS #Sonography #Neonate ... #Peds #Pediatrics
Causes of Pediatric Seizures - Differential Diagnosis Algorithm
Infantile:
 • Benign Focal Epilepsy of Infancy
 • West
Causes of Pediatric ... Metabolic: • Hypoglycemia ... • Hyperglycemia ... Sturge-Weber Syndrome Neonates ... #Causes #Peds #Pediatrics
CRIES is a 10-point scale, using a physiologic basis similar to APGAR: Crying; Requires increased oxygen
construct in assessing neonatal ... Diagnosis #Peds #Pediatrics ... #PainScale #Neonatal ... PostOperative #Assessment
Ebstein Anomaly
 • Prevalence
 • Pathophysiology
 • Presentation
 • Physical Examination Findings
 • Initial Management
 •
Prevalence • Pathophysiology ... • Surgery in Neonates ... management #cardiology #pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Poor suckling -> Neonatal ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Assessment of diabetic control:
 - Any episodes of hypoglycaemia, diabetic ketoacidosis, hospital admission? 
 - Is
Assessment of diabetic ... Any episodes of hypoglycaemia ... still awareness of hypoglycaemia ... primarycare #DM1 #Peds #Pediatrics ... #Assessment
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Hyperkalemia, Hypoglycemia ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics