27 results
Pacemaker Coding Terminology
#Diagnosis #Cardiology #PPM #Pacemaker #LetterCode #Coding #Classification #Table #CoreEM
Pacemaker Coding ... Pacemaker #LetterCode #Coding ... #Classification ... #Table #CoreEM
The first three letters refer to chamber paced, chamber sensed, and response to sensed events. The
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 ... #Causes
Classification of Jaundice
Unconjugated hyperbilirubinemia (predominantly indirect bilirubin)
 • Increased bilirubin production (eg, hemolytic anemias, hemolytic reactions,
Classification of ... mutation in genes coding ... miscellaneous causes ... #Jaundice #Classification ... #differential #causes
REBEL Review 99: Serotonin Syndrome via Yosuf Alam, MSIV

Presentation: Altered mentd status, Seizures, Myoclonus, Hypertension, Hyperthermia
Hyperthermia (most common cause ... Diagnosis: Clinical ... rhabdomyolysis • External cooling
Malignant Hyperthermia Crisis - Guidelines for Crises in Anaesthesia
Unexplained increase in ETCO2 AND tachycardia AND increased
other, more common causes ... ❾ Begin active cooling ... • Cooling jackets ... Plan admission to critical ... Myoglobinaemia: forced
Duchenne Muscular Dystrophy (DMD)
The term "Muscular dystrophy" refers to a group of inherited progressive muscle disorders.
Muscular Dystrophy is named ... defects in the gene coding ... brain. 1 in 3 cases
Mild-to-Moderate Ulcerative Colitis - Management Algorithm
Curcumin:
 • Natural phytochemical from turmeric
 • 2g/day divided in 2-3
Colitis - Management Algorithm ... Nissle • VSL#3: ↑ clinical ... • Budesonide Foam ... suppository or foam ... 5-ASA brands Algorithm
Positive Varus Stress Test in LCL Injury

Interesting knee injury in a young basketball player who landed
landed awkwardly coming ... injury, we are able ... Injury #Positive #Clinical
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21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... mutation in CYP21A2 coding ... enzyme 21-OHase causes