Drugs for Hypothalamic and Pituitary Disorders Flashcards

1
Q

what are the clinical indications of somatotropin? (2)

A

recombinant human growth hormone, SC administered 6-7x/ week

  1. GH deficiency
  2. pediatric patients with short stature caused by factors other than GH deficiency (Prader-Willi, Turner, Noonan Syndromes, Idiopathic Short Stature)
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2
Q

what toxicities are associated with somatotropin in children and adults, respectively?

A

recombinant human growth hormone, SC administered 6-7x/ week

children - adverse effects rare, include intracranial pressure, scoliosis, edema, hyperglycemia (induced insulin resistance)

adults - peripheral edema, myalgias, arthralgia of hands/wrists, carpal tunnel

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3
Q

what is the clinical indication of mecasermin?

A

recombinant form of human IGF-1 approved for severe IGF-1 deficiency (not responsive to exogenous growth hormone)

adverse effect - hypoglycemia (related to activation of insulin receptors), requires consumption of carbohydrates with drug

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4
Q

octreotide vs pegvisomant

A

octreotide (also lanreotide): somatostatin agonist (GH antagonist)

pegvisomant: growth hormone receptor antagonist

used to treat smaller GH-secreting adenomas (larger adenomas treated with surgery/ radiation)

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5
Q

what toxicities are associated with octreotide?

A

long-acting somatostatin agonist —> reduces growth hormone production, SC injections every 8 hours

adverse effects: GI disturbance, gallstones, sinus bradycardia, conduction disturbances

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6
Q

what toxicities are associated with pegvisomant?

A

competitive growth hormone receptor antagonist, used to treat acromegaly, SC administration daily

adverse effects - flu symptoms, nausea, diarrhea, altered liver function tests (LFTs), contraindicated in patients with liver disease

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7
Q

what is the clinical indication of cabergoline and bromocriptine?

A

dopamine (DA) agonists, standard pharmacological treatment for hyperprolactinemia

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8
Q

what is considered complete vs partial success of cabergoline in women with anovulation?

A

dopamine agonist, used to treat hyperprolactinemia

complete success = pregnancy or 2 consecutive menses with evidence of ovulation

partial success = 2 menstrual cycles without evidence of ovulation or 1 ovulatory cycle

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9
Q

what toxicities are associated with cabergoline or bromocriptine?

A

dopamine agonists, used to treat hyperprolactinemia

adverse effects (most common reasons for therapy discontinuation) - nausea, headache, orthostatic hypotension, fatigue, delusions/hallucinations, contraindicated in patients with valvular heart disease

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10
Q

what are the clinical indications of Pitocin?

A

synthetic oxytocin, used to induce labor for conditions requiring early vaginal delivery

ex - uncontrolled maternal diabetes, worsening preeclampsia, intrauterine infection

also used for controlling uterine hemorrhage due to uterine atony (failure to contract) in immediate postpartum period

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11
Q

what toxicities are associated with synthetic oxytocin (Pitocin)?

A

serious toxicity is rare when used judiciously

toxicity due to excessive stimulation of uterine contractions (—> fetal distress, uterine rupture) or inadvertent activation of ADH (—> fluid retention, hyponatremia, seizures)

therefore, contraindicated in fetal distress, abnormal fetal presentation, or predispositions for uterine rupture

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12
Q

what is the effect of ADH (vasopressin) binding V1 vs V2 receptors?

A

V1 —> vasoconstriction (vasopressor action)

V2 —> renal fluid reabsorption (antidiuretic action)

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13
Q

does desmopressin act preferentially on V1 or V2 receptors?

A

long-acting ADH analog, preferentially binds V2

V1 —> vasoconstriction
V2 —> renal fluid reabsorption

used to treat central diabetes insipidus

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14
Q

what is the clinical indication of tolvaptan and conivaptan?

A

“-vaptans” = ADH receptor antagonists

preferentially bind V2 receptors (mediates antidiuretic actions), used to treat SIADH —> promote excretion of free water

note tolvaptan has risk of hepatotoxicity, limited to 30 day use

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