5 results
genetics pathophysiology 21hydroxylasedeficiency abcs algorithm cabcde cardiology chf cpap diagnosis differential endocrinology foamed heartfailure icu neonate pharmacology praderwilli primary survey
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
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... sleep apnea, cor pulmonale ... pathophysiology #peds ... #pediatrics
Pediatric Trauma Primary Survey: C-ABCDE C - Catastrophic Bleeding - Life-threatening hemorrhage • Apply direct pressure/compression bandage
Primary Survey: C-ABCDE ... Apnea/poor effort, Signs ... ↓ BP is a late sign ... normalized vital signs ... #management
Continuous Positive Airway Pressure in the Neonate WHY CPAP? • Maintain airway patency • Helps avoid alveoli
auscultate for signs ... - Note baby's tone ... CPAP #Neonate #Management ... #ABCs #ABCDE #Peds ... #Pediatrics
It is important to recognize Acute Decompensated Heart Failure (ADHF) as more than just simply a
Signs of poor perfusion ... Signs of congestion ... with presence of pulmonary ... essentially Cardiogenic Shock ... heartfailure #chf #criticalcare
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