23 results
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm
Congenital Anomaly / Disorder:
 •
Causes of Sudden ... Arrhythmia • Neurologic ... #Diagnosis #Algorithm ... #Causes #Peds # ... Pediatrics
Kernig's Sign in Meningitis

Kernig's sign is present if the patient, in the supine position with the
Kernig's Sign in ... Meningitis Kernig's sign ... this video, the infant ... Prakash #Kernigs #Sign ... #Peds #neurology
Pediatric SVT - Management Algorithm
Identify SVT:
 • HR not variable
 • Abrupt rate changes
 • Infants:
Pediatric SVT - ... rate changes • Infants ... : HR > 180bpm ECG ... Signs of shock or ... #peds #Pediatric
Epiglottitis - Swollen inflamed epiglottis 
Clinical (Rapid onset) 
 • Fever 
 • Sore throat
inflamed epiglottis Clinical ... #Epiglottitis #Signs ... #Causes #Diagnosis ... #Differential #Peds ... #Pediatrics
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm
Cardiac:
 • Congenital Heart Disease
 •
Causes of Apparent ... Disturbances Neurologic ... Breathing • Apnea of Infancy ... #Algorithm #Causes ... #Peds #Pediatrics
CATCH Predictors for Clinically Significant TBI 
 - GCS Less than 15 at 2 hours post
Predictors for Clinically ... exam - Any Sign ... Predictors #Traumatic #Brain ... #Injury #Diagnosis ... #Peds #Pediatrics
Peri-operative Hyperthermia - Guidelines for Crises in Anaesthesia
If prolonged or ≥ 39 C this is a
39 C this is a clinical ... devices, especially infants ... hyperthermia crisis (late sign ... Phaeochromocytoma Neurologic ... • Traumatic brain
Acute Kidney Injury - AKI Workup Algorithm and Differential Diagnosis
Baseline Investigations: full blood count with differential,
Injury - AKI Workup Algorithm ... and Differential Diagnosis ... investigations depending on clinical ... context and signs ... #nephrology #causes
Differentiating NBTE from Infective Endocarditis
No pathognomonic signs/symptoms or echo features that are specific to NBTE, and
pathognomonic signs ... valves • MRI brain ... in up to 30% of cases ... often seen • MRI brain ... territory large infarct
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics