14 results
diagnosis algorithm pathophysiology assessment genetics physicalexam timeline treatment 21hydroxylasedeficiency 21ohd abcs cardiology chf cirrhosis clinical coma cries cthead decisionaid dehydration
Initial assessment and management of coma in pediatric population. Airway - is it secure? Breathing — is
assessment and management ... of coma in pediatric ... necessary, transfer to paediatric ... Assessment #Coma #Pediatrics ... #Peds #ABCs #CriticalCare
Pediatric SVT - Management Algorithm Identify SVT: • HR not variable • Abrupt rate changes • Infants:
Pediatric SVT - ... Management Algorithm ... AP Stable? ... Signs of shock or ... #Pediatric #treatment
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Dehydration #Peds ... #Pediatrics
American College of Critical Care Medicine algorithm for time-sensitive, goal-directed stepwise management of hemodynamic support in
goal-directed stepwise management ... to next step if shock ... #CriticalCare # ... Peds #Pediatrics ... #Sepsis #Management
Clinical Features and Complications of Measles Rash: Spreads downwards, from behind the ears to the whole Of the
Clinical Features ... Kopliks KoplikSpots #Peds ... #Pediatrics #Timeline ... #Signs #Symptoms
PECARN Head CT Decision Aid The Head CT Choice decision aid was developed in Rochester, Minnesota. Full
observation, and signs ... and symptoms that ... (Figure 2) #Management ... #PatientInfo #Peds ... #Pediatrics #DecisionAid
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... /Symptoms/Complications ... pathophysiology #peds ... #pediatrics
CRIES is a 10-point scale, using a physiologic basis similar to APGAR: Crying; Requires increased oxygen
Increased vital signs ... 1995) CRIES (Table ... in the ED, the clinician ... #Diagnosis #Peds ... #Pediatrics #PainScale
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... vomiting • Late (shock ... endocrinology #peds ... #pediatrics
Clinical features of Liver Disease in Children #Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology **
Clinical features ... #LiverFailure #Signs ... #Symptoms #PhysicalExam ... Findings #Diagnosis #Peds ... #Pediatrics #Hepatology
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