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diagnosis 21hydroxylasedeficiency 21ohd antiarrhythmics cardiomyopathy classification endocrinology evaluation genetics management pediatrics perioperative peripartum pharmacology phases preop preoperative risk stratification treatment
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... enzyme 21-OHase causes ... • Early: decr feeding ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
Antiarrhythmics Pharmacology Summary Cardiac Conduction Phases: Phase 0 - Ventricular Depolarization: • Na+ channels open leading to a
Transient K+ efflux moving ... inotropy) ACCP Cardiology ... Classification #Classes ... #pathophysiology ... #phases #cardiology
Preoperative Risk Evaluation Major Pre-Op Questions: 1. Does the patient have any modifiable risk factors that could be
ASA class If ... event, follow ACC algorithm ... Cataract Plan for Meds ... - what is the bleeding ... one post op Cardiology
Peripartum Cardiomyopathy - Summary 1. Definition • Towards the end of pregnancy to 5 months postpartum
exclude other causes ... during Delivery • Stable ... Period • Breast-feeding ... teratogenic GDMT meds ... diagnosis #management #cardiology
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