16 results
Anterior ischemic optic neuropathy (AION) - Recognition of giant cell arteritis (GCA)

1) Is visual loss caused
optic neuropathy (AION ... loss caused by AION ... Doppler US : halo sign ... PET/CT: aortitis ... Ophthalmology #Diagnosis #Algorithm
Algorithm for the Evaluation of Pediatric Head Trauma (PECARN) - Need for Head CT #Diagnosis #Management
Algorithm for the ... Need for Head CT ... Management #EM #Peds ... HeadCT #PECARN #Algorithm
Causes of Chronic Pediatric Cough - Differential Diagnosis Algorithm
Poor Growth
 - Non-Specific CXR
Differential Diagnosis Algorithm ... Abnormal CXR / CT ... Abnormal CXR / CT ... Differential #Diagnosis #Algorithm ... #Causes #Peds #
PECARN Head CT Decision Aid

The Head CT Choice decision aid was developed in Rochester, Minnesota. Full
PECARN Head CT Decision ... Aid The Head CT ... disadvantages of cranial CT ... observation, and signs ... #PatientInfo #Peds
Standardized Physical Abuse Guideline
<6 months of age
 • Social work consult
 • Skeletal survey
 • Head
survey • Head CT ... • Abdominal CT ... AST or ALT> 80, signs ... Guidelines #Workup #Peds
Pediatric SVT - Management Algorithm
Identify SVT:
 • HR not variable
 • Abrupt rate changes
 • Infants:
SVT - Management Algorithm ... ECG, Monitors, Pads ... Signs of shock or ... tachycardia #Management #Algorithm ... #peds #Pediatric
Practical Pediatric Viral Rash Algorithm

Child presenting with rash and current/ recent symptoms of viral illness but
Pediatric Viral Rash Algorithm ... five days and no signs ... #Rash #Viral #Algorithm ... #Pediatrics #Peds
Rapid Assessment of the Neonate With Sonography (RANS) Scan

Recommended algorithm for RANS scan. 
* Abnormal vital
Recommended algorithm ... Abnormal vital signs ... Sonography #Neonate #Peds
Hypochloremia - Differential Diagnosis Algorithm

Cause - Decreased Intake:
 • Low salt in diet
 • Exclusive D5W
Differential Diagnosis Algorithm ... - Gitelman SIGNS ... extracellular anion ... Differential #Diagnosis #Algorithm
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
maintains appropriate ion ... Signs/Symptoms/Complications ... endocrinology #peds