13 results
Clinical features of shock from dehydration in an infant

Decreased level of consciousness 
Sunken fontanelle 
Dry mucous
Clinical features ... in an infant ... Decreased level ... #PhysicalExam #Signs ... #Peds #Pediatrics
Pediatric SVT - Management Algorithm
Identify SVT:
 • HR not variable
 • Abrupt rate changes
 • Infants:
SVT - Management Algorithm ... rate changes • Infants ... Signs of shock or ... tachycardia #Management #Algorithm ... #peds #Pediatric
American College of Critical Care Medicine algorithm for time-sensitive, goal-directed stepwise management of hemodynamic support in
American College of Critical ... Care Medicine algorithm ... 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 Newborn) - Differential ... Diagnosis Algorithm ... Nervous System - Decreased ... #Causes #Peds #
Erythematous Rashes - THE ALGORITHMIC APPROACH

Characterized by diffuse redness of the skin due to
capillary congestion, erythematous
Erythematous Rashes - THE ALGORITHMIC ... syndrome (SSS) in infants ... , the differential ... fever, and toxic shock ... Febrile #Fever #Differential
Shock Overview
A state of tissue hypoxia due to decreased or dysregulated oxygen delivery or extraction, resulting
hypoxia due to decreased ... death Common Clinical ... - Decreased SVR ... anaphylaxis, toxins/meds ... #criticalcare #differential
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 ... bradycardia #diagnosis #differential
Shock Overview
A state of tissue hypoxia due to decreased or dysregulated oxygen delivery or extraction, resulting
hypoxia due to decreased ... death Common Clinical ... - Decreased SVR ... anaphylaxis, toxins/meds ... #criticalcare #differential
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... 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 ... if they have no clinical ... lack of tapering, decreased ... and lab signs ( ... #Diagnosis #Peds