10 results
Pacemaker Coding Terminology
#Diagnosis #Cardiology #PPM #Pacemaker #LetterCode #Coding #Classification #Table #CoreEM
Pacemaker Coding ... Diagnosis #Cardiology #PPM ... Pacemaker #LetterCode #Coding ... #Classification ... #Table #CoreEM
The first three letters refer to chamber paced, chamber sensed, and response to sensed events. The
#Cardiology #PPM ... Pacemaker #LetterCode #Coding ... #Classification ... #Table
Causes of Iron Deficiency - Differential Diagnosis Algorithm
 • Blood loss: GI (cancer, ulcer, IBD), GU
Causes of Iron Deficiency ... Differential Diagnosis Algorithm ... achlorhydria: PPI ... #Deficiency #Differential ... #Fe #algorithm
Causes of Anemia by Mean Corpuscular Volume (MCV) - Differential Diagnosis Algorithm
Low Mean Corpuscular Volume (<80
Causes of Anemia ... Differential Diagnosis Algorithm ... Volume (<80 fL) • Iron ... #Anemia #MCV #Classification ... Differential #Diagnosis #Algorithm
Overall Approach to Anemia - Differential Diagnosis Algorithm

Blood Loss
 • Acute Bleed - Normocytic / Normochromic
MCH, MCHC, Serum Iron ... Deficiency • ... B12/Folate Deficiency ... Non-lmmune #Anemia #Classification ... #Causes #Hematology
Causes of Hyponatremia - Differential Diagnosis Algorithm
Hypovolemia, UNa > 20: 
 • Renal losses, Diuretic excess,
Differential Diagnosis Algorithm ... Mineral corticoid deficiency ... , Salt-losing deficiency ... Glucocorticoid deficiency ... Differential #Diagnosis #Algorithm
Classification, Differential Diagnosis, and Features of Hyponatremia According to Volume Status 

Hypervolemic hypernatremia 
 - CHF
Classification, ... deficit - Salt-losing ... #Hyponatremia #Classification ... Differential #Diagnosis #Table ... #Causes
Causes of Copper Deficiency - Differential Diagnosis
Hereditary: 
 - Menkes disease, familial hypoceruloplasminemia
Decreased / Inadequate Intake:
Causes of Copper ... Deficiency - Differential ... diarrhea, protein-losing ... supplementation) or iron ... supplements #Copper #Deficiency
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-Hydroxylase Deficiency ... mutation in CYP21A2 coding ... enzyme 21-OHase causes ... maintains appropriate ion ... amount of enzyme deficiency
Antiarrhythmics Pharmacology Summary
Cardiac Conduction Phases:
Phase 0 - Ventricular Depolarization:
 • Na+ channels open leading to a
Transient K+ efflux moving ... Vaughan Williams Classification ... : CLASS 1 - Sodium ... reduce speed of ion ... #Pharmacology #Classification