17 results
Clinical features of shock from dehydration in an infant

Decreased level of consciousness 
Sunken fontanelle 
Dry mucous
Clinical features of shock ... dehydration in an infant ... Decreased level ... #PhysicalExam #Signs ... #Peds #Pediatrics
Pediatric SVT - Management Algorithm
Identify SVT:
 • HR not variable
 • Abrupt rate changes
 • Infants:
Pediatric SVT - Management ... Algorithm Identify ... rate changes • Infants ... Signs of shock or ... #Algorithm #peds
Infant UTI Algorithm (<8 weeks of age)

Emergency Medicine Cases @EMCases

#Infant #Pediatric #UTI #Algorithm #Diagnosis #Management #UrinaryTractInfection
Infant UTI Algorithm ... Emergency Medicine Cases ... @EMCases #Infant ... #Diagnosis #Management ... UrinaryTractInfection #Peds
American College of Critical Care Medicine algorithm for time-sensitive, goal-directed stepwise management of hemodynamic support in
Care Medicine algorithm ... goal-directed stepwise management ... hemodynamic support in infants ... #Shock #Algorithm ... #CriticalCare #Peds
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm
Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Infant (Floppy ... Differential Diagnosis Algorithm ... Nervous System - Decreased ... #Causes #Peds #
Shock Overview
A state of tissue hypoxia due to decreased or dysregulated oxygen delivery or extraction, resulting
hypoxia due to decreased ... - Decreased SVR ... anaphylaxis, toxins/meds ... Classification #diagnosis #management ... #differential #causes
Shock Overview
A state of tissue hypoxia due to decreased or dysregulated oxygen delivery or extraction, resulting
hypoxia due to decreased ... - Decreased SVR ... anaphylaxis, toxins/meds ... Classification #diagnosis #management ... #differential #causes
Bradycardia
1) First Steps: IV, O2, Monitors, ECG, Pads on patient, Crash Cart in room. Is patient
worsening brady, Signs ... of Shock, SBP < ... Increase by 5mA/ ... Then increase to ... #differential #management
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... deficiencies present in infants ... Signs/Symptoms/Complications ... vomiting • Late (shock ... endocrinology #peds
Evaluation of suspected incomplete Kawasaki Disease

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