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diagnosis management peds differential algorithm criticalcare genetics pathophysiology pneumonia 21hydroxylasedeficiency 21ohd acquired adult aspirin biphasic bronchiectasis cap cardiology causes chagas
Signs and Symptoms of Respiratory Distress Through the Years. #signs #symptoms #diagnosis #differential #neonatal #pediatrics #adult
Signs and Symptoms ... #signs #symptoms ... differential #neonatal #pediatrics ... #adult #peds #pulmonary
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
Extrapulmonary manifestations of COVID-19 • Neurologic: Headaches, Dizziness, Encephalopathy, Guillain-Barré, Ageusia, Myalgia, Anosmia, Stroke • Renal:
vein thrombosis, Pulmonary ... arrhythmias, Cardiogenic shock ... ischemia, Acute cor pulmonale ... Extrapulmonary #Diagnosis #Signs ... #Symptoms #SARSCOV2
Pediatric SVT - Management Algorithm Identify SVT: • HR not variable • Abrupt rate changes • Infants:
Pediatric SVT - ... Signs of shock or ... Algorithm #peds #Pediatric ... #treatment
Shock - Diagnosis and Management Summary • Hypotension: SBP<90, SBP drop >40, MAP<65 (Normotension, HTN possible
Shock - Diagnosis ... possible w/ early shock ... Full Set of Vital Signs ... Tamponade - Pulmonary ... #criticalcare #treatment
Biphasic Illness of Leptospirosis Some patients do not progress to severe disease. Others, rapidly develop severe disease
brief interval symptom ... dysfunction) • Pulmonary ... hemorrhage • ARDS • Shock ... Diagnosis #Illness #Signs
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... sleep apnea, cor pulmonale ... pathophysiology #peds #pediatrics
Salicylate Toxicity - Diagnosis and Management Consider if: 1) Patient is hot and altered 2) You see tachypnea with
ingestion/exposure Symptoms ... , Diaphoresis, Pulmonary ... edema, Shock Labs ... diagnosis #management #Treatment
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 ... endocrinology #peds #pediatrics
Pheochromocytoma - Diagnosis and Management Summary 10 percent rule = 10% of pheochromocytomas are extra-adrenal, multiple, bilateral,
bilateral, malignant, pediatric ... life • M=F Symptoms ... and Signs: 50% ... and signs: • ... may present with pulmonary
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