02b: Adrenal HT Flashcards
Adrenal mechanisms for HT can be caused by excess:
- Glucocorticoids (ZF)
- Mineralocorticoids (ZG)
- Catecholamines (medulla)
90% of all congenital adrenal hyperplasia is due to (X) deficiency. Is HT a symptom?
X = 21-a hydroxylase
No (but other enzyme deficiencies causing CAH do have HT)
List the causes of primary aldosteronism. Star the most common. Double-star the severe causes.
- Bilateral hyperplasia*
- Adrenal adenoma/carcinoma**
- Glucocorticoid-remediable
Pt with treatment-resistant BP makes you suspicious for (X), especially if (Y) serum levels are (low/high).
X = hyperaldosteronism
Y = K
Low
Screening for hyperaldosteronism via which test/lab?
Plasma aldo:renin ratio (aka aldo:PRA ratio)
Aldo:PRA ratio cutoff greater than (X) as well as plasma (Y) greater than 10 suggests diagnosis of…
X = 30
Y = aldosterone
Hyperaldosteronism
List the guidelines for screening with aldo:PRA ratio
- BP over 150/100 despite 3 BP meds
- Low K
- Adrenal incidentaloma
Pt has high serum aldosterone and a high aldo:PRA ratio. What’s the next step?
Confirm diagnosis of hyperaldosteronism by V-loading maneuver (oral salt loading, saline infusion); normal response is to lower aldosterone
Hyperaldosteronism: (X) is the most reliable test to distinguish unilateral adenoma from bilateral hyperplasia
Venous aldosterone and cortisol samples from adrenal veins
Hyperaldosteronism from adenoma: what’s the Rx?
Surg (often curative) and maybe medical therapy (K-sparing diuretics)
Hyperaldosteronism from bilateral hyperplasia: what’s the Rx?
- K sparing diuretics
- Ca channel blockers
- ACEi
T/F: Pheochromocytomas make up only 1% of hypertensive cases
True
Patient has spike in BP during surgery. What should he/she be screened for?
Pheo
T/F: FHx of Pheo is reason to screen patient
True
Which familial syndromes put patient at risk for Pheo?
- Familial Pheo
- MEN-2
- Neurofibromatosis
- VHL syndrome