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comparison diagnosis peds cardiogenic criticalcare differential findings pathophysiology sign 21hydroxylasedeficiency 21ohd abcdes algorithm cardiology dehydration diabetes distributive features genetics hypovolemic
Types of Shock - Comparison, Signs and Symptoms #Shock #Types #Comparison #Table #Signs #Symptoms #Classification
Types of Shock - ... Comparison, Signs ... and Symptoms ... #Table #Signs # ... Symptoms #Classification
Shock - Findings, Signs and Symptoms by Classification - Hypovolemic (Intravascular volume depletion) - Distributive (Vasodilation)
Shock - Findings ... , Signs and Symptoms ... by Classification ... #Table #CriticalCare ... #Sign #Symptoms
Syncope - Findings, Signs and Symptoms by Classification - Reflex Syncope - Cardiogenic Syncope
Syncope - Findings, Signs ... and Symptoms by ... Classification ... #Table #CriticalCare ... #Sign #Symptoms
Diabetes Insipidus vs Syndrome of Inappropriate ADH (SIADH) - Comparison Table Diabetes Insipidus - Inadequate ADH SIADH -
) - Comparison Table ... SIADH #Comparison #Table ... Pathophysiology #Signs ... #Symptoms #Diagnosis ... #Endocrinology
Bedside Classification of Shock Hypovolemic shock - Vomiting, diarrhea, overdiuresis - Hemorrhage (GI, peritoneal, RP) Distributive shock
Bedside Classification ... shock - Vomiting ... #Classification ... Cardiogenic #Comparison #Table ... Diagnosis #Features #Signs
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features of shock ... #PhysicalExam #Signs ... #Symptoms #Shock ... Dehydration #Peds #Pediatrics
SCAI Pyramid of Cardiogenic Shock Classification E - Extremis - A patient experiencing cardiac arrest with ongoing
of Cardiogenic Shock ... Classification ... currently experiencing signs ... or symptoms of ... #Classification
Pediatric SVT - Management Algorithm Identify SVT: • HR not variable • Abrupt rate changes • Infants:
Pediatric SVT - ... Monitors, Pads AP Stable ... Signs of shock or ... Algorithm #peds #Pediatric
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... vomiting • Late (shock ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
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