Endocrine Flashcards

1
Q

Macular edema treatment

A

Anti VEGF intravitreal injections
Monthly for 12 months then followed by intermittent injections to prevent recurrence

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2
Q

Asymptomatic patients with primary hyperparathyroid are surgical candidates if they have any of the following:

A
  1. serum calcium level >1 mg/dL (0.25 mmol/L) above the upper limit of normal
  2. creatinine clearance <60 mL/min
  3. T-score <−2.5 or vertebral fracture
  4. age <50 years
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3
Q

The diagnosis of Familial hypocalciuric hypercalcemia, if ca / creat ratio

A

< 0.01

IF > 0.02, FHH is excluded

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4
Q

Sclerosis inhibitors Romosozumab ( evenity) contraindication

A

It increases risk of CVA, MI, CV death

It’s should be followed by bisphosphonate or denosumab

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5
Q

Bisphosphante contraindicated in

A

GFR < 35
Vit D or Hypocalcemia until corrected

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6
Q

Denosumab side effects

A

Cellulitis
Bronchitis
Osteonecrosis of the jew and femur

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7
Q

Paget disease assessment

A
  1. Serum ca
  2. Vit D
  3. Whole body radionuclide bone scan
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8
Q

Treatment of Paget disease

A

Single dose of 5 mg iv zoledronic acid

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9
Q

Morning cortisol level suggests AI

A

< 82.8

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10
Q

Morning cortisol level unlikely to be AI

A

> 414

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11
Q

Synacthen test

A

=< 496.8 ; AI

> 496.8 ; unlikely

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12
Q

Adrenal insufficiency diagnosis steps

A
  1. Morning cortisol
  2. If in green zone ; Synacthen
  3. If confirmed AI ; do ACTH to see if it’s 1ry or 2 ry
  4. If 1 ry AI ; do 21 hydroxylase antibody
  5. If antibody-ve ; do CT adrenal
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13
Q

To diagnose primary aldosteronism

PAC/PRA should be……?

A

A PAC/PRA > 20 with a PAC of at least 15 ng/dL (414 pmol/L) is considered a positive result

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14
Q

How to diagnose primary aldosteronism In patients taking an ACEi or or ARBs?

A

renin should be elevated and testing may start with PRA measurement.

If the PRA is suppressed, the likelihood of primary aldosteronism is high

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15
Q

How to diagnose primary aldosteronism in patients taking Mineralocorticoid receptor antagonists (spironolactone and eplerenone) and high doses of amiloride ?

A

These medications can significantly interfere with interpretation of PAC/PRA and

should be discontinued 4 to 6 weeks before evaluation if possible.

However, if testing while a patient is taking a mineralocorticoid receptor antagonist reveals suppressed PRA, further testing can be done without stopping the medication.

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16
Q

The localization study of choice for primary aldosteronism

A

-CT adrenal

  • Most patients with primary aldosteronism should undergo adrenal vein sampling to confirm the source.
17
Q

Treatment of primary aldosteronism

A
  1. adrenalectomy ( Serum potassium levels should be monitored weekly for the first month postoperatively)
  2. Spironolactone if not candidates or refuse surgery
18
Q

Initial tests in pheochromocytoma

A

Initial tests include measurement of

  1. plasma free metanephrine collected in a supine position or
  2. 24-hour urine fractionated metanephrine and catecholamine levels.

*medications should be discontinued at least 2 weeks before testing if possible.

mild elevations may require repeat testing.
Levels >4 times the upper limit of normal, in the absence of acute stress or illness, are consistent with a catecholamine-secreting tumor.

Plasma free-metanephrine is a more convenient test and is often chosen if the index of suspicion is high.

If suspicion is low, urine fractionated metanephrine and catecholamines may be a better option.

19
Q

tumor localization in pheochromocytoma ?

A

tumor localization should only occur after establishing the biochemical diagnosis of catecholamine excess to avoid misdiagnosing an incidental nonfunctioning adrenal mass as a pheochromocytoma.

-abdominal and pelvic contrast-enhanced CT
If the CT scan is negative, and suspicion of a catecholamine-secreting tumor is high,

-the next step is advanced
imaging, including the iodine 123-metaiodobenzylguanidine, octreotide, or gallium-68 DOTATATE scans.

Advanced imaging may also be indicated in patients with very large pheochromocytomas (>10 cm) to detect
metastatic disease or paragangliomas to detect several tumors.

20
Q

The definitive treatment for pheochromocytoma/paraganglioma ?

A
  • surgical resection.
  • Preoperative α-receptor blockade with phenoxybenzamine for 10 to 14 days before surgery is essential to prevent hypertensive crises during surgery.

The dose is progressively increased to achieve
1. BP 130/80 mm Hg or less and pulse of 60 to 70/min seated,

  1. and SBP >/= 90 with pulse of 70 - 80/min standing.
21
Q

α-blockade & β-blocker in pheochromocytoma?

A

A β-blocker is added after α-blockade is achieved to manage reflex tachycardia, but it should never be started before adequate α-blockade, because unopposed α-adrenergic vasoconstriction can result in a hypertensive crisis.

22
Q

Pheochromocytomas may occur in familial syndromes including …?

A
  1. MEN type 2,
  2. von Hippel-Lindau syndrome, and
  3. neurofibromatosis type 1.

Therefore, all patients with catecholamine-secreting tumors should be offered genetic counseling.

23
Q

All patients with an adrenal incidentaloma should undergo testing for

A

Cushing syndrome and pheochromocytoma if the unenhanced CT attenuation is > 10 HU

In selected patient:
- HTN + Hyper K ; PAC/PRC ration

  • androgens , who suspected; DHEA, testosterone and androstenedione
24
Q

Target TSH in papillary thyroid cancer

A

To reduce cancer recurrence, a sufficient dose of levothyroxine is administered to suppress the serum TSH below normal

25
Q

Primary ovarian insufficiency

A

High FSH & LH in amenorrheic woman < 40 years of age

26
Q

Menopausal ovarian failure

A

High FSH & LH in amenorrheic woman > 40 years of age

27
Q

Drug holiday in Osteoporosis

A

Can be initiated in a patient who is not at high risk of # after 3 years (IV) to 5 years (oral) of bisphosphonate treatment

If patient remaining at high risk of # may be continue bisphosphonate or switch to alternative medication

28
Q

(Low ) 24-hour urine calcium excretion in

A

1.FHH

  1. Malnutrition or malabsorption of vitamin D and/or calcium
29
Q

Osteomalacia
Mineral abnormalities?

A

High Alk.phos

Low ca
Low phos