18 results
Adrenal Insufficiency Algorithm - Cosyntropin Stimulation Test
T-1m: Baseline cortisol drawn
T0: 250 µg cosyntropin given IV
T30m: Repeat
Insufficiency Algorithm ... level drawn BCM IM ... Insufficiency #Testing #Algorithm ... #Stimulation #endocrinology
Steroid Synthesis Pathway

Dr. Caoimhe Costigan @CaoimheCostigan

#Steroid #Synthesis #pathophysiology #algorithm #endocrinology
Steroid #Synthesis #pathophysiology ... #algorithm #endocrinology
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Adrenal Insufficiency Diagnosis Algorithm
Test 1: Baseline AM Cortisol 
 - Beware of major normal value
 -
Insufficiency Diagnosis Algorithm ... response BCM IM ... Insufficiency #Diagnosis #Algorithm ... #endocrinology
Erythroderma - Diagnostic Algorithm. Pathophysiology: 1) Extensive cutaneous capillary dilation, results in widespread exfoliation of the
Erythroderma - Diagnostic Algorithm ... Pathophysiology: ... epidermal turnover rate ... accelerated mitotic rate ... Erythroderma #Nikolsky #Algorithm
Growth Hormone Excess - Pathogenesis and clinical findings
 • Acromegaly and gigantism share the same pathophysiology
share the same pathophysiology ... prior to growth plate ... excess after growth plate ... signs #symptoms #endocrinology ... #pathophysiology
A good approach when dealing with hypotension at the bedside includes using the following systematic four
Heart Rate 2. ... Management #EM #IM ... Hypotension #Approach #Algorithm
Short Stature - Differential Diagnosis Algorithm
Normal Variant, Normal Puberty Onset (BA = CA)
 • Familial Short
Differential Diagnosis Algorithm ... Short Stature (Late ... Differential #Diagnosis #Algorithm ... #endocrinology
Anaphylaxis: Treatments (Acute)
Additional Info:
 • IV steroids may be considered for prevention of late phase reactions.
prevention of late ... treatment) 1:1000 IM ... Treatments #Management #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
, vomiting • Late ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology