Endocrine Hypertension Flashcards

1
Q

What is the definition of hypertension?

A

Systolic BP: >140, Diastolic >90

In two or more visits after the initial screen

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2
Q

At what age do we stop using 95% percentile as the definition of hypertension in children? What is this definition?

A

Children aged 13+

> 130 systolic or >80 diastolic is HTN

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3
Q

What is primary vs secondary hypertension and what are the three endocrine causes of hypertension?

A

Primary - 85%, also known as essential hypertension, no known etiology

Secondary - 15%

  1. Renovascular hypertension
  2. Pheochromocytoma
  3. Primary aldosteronism
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4
Q

What are presentations of hypertension which make you lean more towards an endocrine cause than primary / essential hypertension?

A
  1. Severe / resistant HTN (refractory after 3+ meds)
  2. Young onset (<30), or rapid old onset
  3. Hypertension with spontaenous hypokalemia (hyperaldosteronism)
  4. Episodic HTN - pheochromocytoma
  5. Characteristic physical exam findings
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5
Q

What are characteristic physical exam findings for primary aldosteronism causing hypertension?

A

Often due to hypokalemia, there are characteristic physical exam findings:

  1. Neuromuscular irritability
  2. Muscular weakness (inability to increase blood flow to muscles)
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6
Q

What physical exam findings are associated with pheochromocytoma?

A
  1. Cold, clammy hands - peripheral vasoconstriction

2. Cafe au lait spots - if associated with NF-1

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7
Q

What physical exam finding is associated with renovascular hypertension?

A

Abdominal bruit -> if HTN is caused by renal artery stenosis

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8
Q

What is the most common cause of secondary hypertension? What is the threshold at which this occurs and what are the two subtypes?

A

Renal artery stenosis
-> occurs at greater than 75% stenosis

  1. Atherosclerotic - usually elderly patients, 2/3
  2. Fibromuscular dysplasia - usually young women, 1/3
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9
Q

What are the two types of fibromuscular dysplasia and which is more common? Where in the renal artery does this occur?

A
  1. Medial fibroplasia -> much more common (80%)
  2. Intimal fibroplasia

Occurs usually in distal renal arteries -> string of beads appearance

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10
Q

When will renin be high vs not in renovascular hypertension?

A

Unilateral - can be high or normal, as contralateral kidney will decrease renin production -> choose to treat via clinical index of suspicion

Bilateral - will be high, along with increased BUN / creatinine

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11
Q

What is the gold standard of renovascular hypertension diagnosis and what is done to treat? Is it effective?

A

Gold standard: Renal angiography

  • > treat with angioplasty with stent placement
  • > very effective in fibromuscular dysplasia, moderately effective in atherosclerosis (restonosis occurs)
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12
Q

Where in the renal artery is fibromuscular dysplasia vs atherosclerotic stenosis?

A

Fibromuscular dysplasia - distal renal artery segments

Atherosclerotic disease - proximal segments (near branch points from aorta)

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13
Q

What is the medical therapy for renovascular hypertension?

A

ACE inhibitors (except in bilateral renal artery stenosis)
or
ARBs (i.e. valsartan)

mainstay due to pathogenic mechanism

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14
Q

When is surgery preferred over medical therapy for renovascular HTN?

A

Recent onset HTN (<5 years), particularly younger patients

Intolerant to medical therapy

Recurrent flash pulmonary edema or refractory heart failure

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15
Q

Is hypokalemia required for primary aldosteronism? What can precipitate it?

A

No! In fact, most patients are not hypokalemic because of the body’s potassium conservation mechanism

Diuretics can precipitate it however -> diuretic-induced hypokalemia is a common way of diagnosing

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16
Q

Does primary aldosteronism present with peripheral edema? How?

A

No -> aldosterone escape mechanism.

Spontaneous diuresis occurs to excrete sodium to normal levels and limit expansion of extracellular volume by release of atrial natriuretic peptide (ANP) -> released in response to distention

17
Q

What is typically used as the screening test for primary aldosteronism?

A

PAC/PRA ratio
Plasma aldosterone concentration / plasma renin activity

If ratio >20, it has 100% sensitivity, because aldosterone will be very high compared to renin.

18
Q

How is definitive diagnosis of primary aldosteronism made? What should be done if this test is positive?

A

Salt-loading. Salt load for 3 days
-> urinary sodium will be high, but aldosterone will be non-suppressed.

If test is positive -> order CT scan of adrenal to look for abnormality

19
Q

What should be done for patients with a normal adrenal CT following a positive test for primary aldosteronism? How about if you are over age 40 and CT is positive?

A

Same test for both: adrenal vein aldosterone sampling -> see which adrenal gland is overproducing.

Over age 40, non-functioning adenomas are common -> need to sample adrenal vein to be sure gland is overproducing

20
Q

What drugs are used for medical treatment of primary aldosteronism and which is preferred?

A

Spironolactone and Eplerenone

Spironolactone is preferred -> longer halflife and greater antagonist activity

Eplerenone - fewer anti-androgen side effects, but more expensive

21
Q

What is the classic triad of pheochromocytoma?

A

Headache
Sweating
Palpitations

22
Q

Does pheochromocytoma always present with hypertension? What is the patternof HTN?

A

95% of people will have hypertension

50% will have intermittent (episodic) HTN, but 50% have sustained HTN as well.

5% of people remain normotensive due to adrenoceptor downregulation.

23
Q

What defines a low vs high risk patient for pheochromocytoma?

A

Low - resistant HTN with hyperadrenergic spells, and adrenal mass w/o characteristics of pheo

High - Previously resect pheo, FHx of pheo, genetic syndrome related to pheo (i.e. MEN2), adrenal mass with high suspicion on MRI/CT

24
Q

What testing should be done for pheochromocytoma in low and high risk patients? Which one should children have done?

A

Low risk - Urinary fractional metanephrines -> higher specificity, lower sensitivity (i.e. patients with minimal acute symptoms unlikely to have major problems)

High risk - Plasma fractional metanephrines -> higher sensitivity for when it matters, but lower specificity (many false positives)

Children -> do plasma metanephrines since much easier

25
Q

What is the imaging study of choice for pheochromocytoma?

A

MRI - increased brightness on T2 MRI, best overall test

CT - can be used, but high rate of misdiagnosis of incidentaloma

MIBG radionucleotide scan -> used only for extra-adrenal localization

26
Q

What is the treatment sequence for pheochromocytoma?

A
  1. Alpha blockade - irreversible, i.e. phenoxybenzamine

followed by:

  1. Beta blockade
    - > reversing this order could cause hypertensive crisis

then

  1. Tumor resection
27
Q

When should germline screening for pheochromocytoma be done?

A

Young age
Bilateral pheos
Unilateral pheo with FHx
Paraganglioma present

28
Q

What germ lie mutations are associated with pheochromocytoma?

A

NF-1 -> neurofibromatosis 1
VHL -> von Hippel Lindau
RET -> MEN2A and 2B

29
Q

What is pseudopheochromocytoma, and what must be ruled out?

A

Disease of paroxysmal hypertension caused by increased sympathetic tone

Rule out:
Labile HTN
Panic Disorder