16 results
Pacemaker Coding Terminology
#Diagnosis #Cardiology #PPM #Pacemaker #LetterCode #Coding #Classification #Table #CoreEM
Pacemaker Coding ... 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
Classification, Differential Diagnosis, and Features of Hyponatremia According to Volume Status 

Hypervolemic hypernatremia 
 - CHF
Classification, ... deficit - Salt-losing ... #Hyponatremia #Classification ... Differential #Diagnosis #Table
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... the lab values table ... #Diagnosis #Algorithm ... #Neonatology #Peds ... #Pediatrics #Table
Lab patterns seen in Inborn Errors of Metabolism

A table of lab values compiled from UpToDate and
Metabolism A table ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... #Neonatology #Peds ... #Pediatrics #Table
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm
Cardiac:
 • Congenital Heart Disease
 •
Differential Diagnosis Algorithm ... Aspiration • Breath-holding ... Hernia Witnessed Choking ... Differential #Diagnosis #Algorithm ... #Causes #Peds #
Causes of Pediatric Spells - Differential Diagnosis Algorithm
Neonates and Infant Spells:
 • Benign Sleep Myoclonus
 •
Differential Diagnosis Algorithm ... Spells: • Breath-holding ... Differential #Diagnosis #Algorithm ... #Causes #Peds #
CRIES is a 10-point scale, using a physiologic basis similar to APGAR: Crying; Requires increased oxygen
similar to APGAR: Crying ... distress and breath-holding ... 1995) CRIES (Table ... #Diagnosis #Peds
Disc Herniations - Pathogenesis and Complications
• 90% of Lumbar disc herniations happen at L4/5 and L5/S1
•
-> Disc less able ... -> Mechanical loading ... complications #msk #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds