Which of the following drugs would be most appropriate for postcoital contraception in this patient?

Questions 88

ATI RN

ATI RN Test Bank

Endocrine Pharmacology Quizlet Questions

Question 1 of 5

Which of the following drugs would be most appropriate for postcoital contraception in this patient?

Correct Answer: C

Rationale: The correct answer is C: Levonorgestrel. Levonorgestrel is a progestin commonly used for emergency contraception due to its effectiveness in preventing pregnancy when taken shortly after unprotected intercourse. It works by inhibiting ovulation and fertilization. Clomiphene (A) is used to induce ovulation, not for emergency contraception. Leuprolide (B) is a gonadotropin-releasing hormone agonist used for conditions like endometriosis or prostate cancer, not for emergency contraception. Fulvestrant (D) is a selective estrogen receptor degrader used in breast cancer treatment, not for emergency contraception.

Question 2 of 5

Which of the following actions most likely mediated the therapeutic efficacy of calcitriol in a patient with diffuse demineralization of bone?

Correct Answer: D

Rationale: The correct answer is D because calcitriol, the active form of vitamin D, increases intestinal calcium absorption by enhancing the expression of calcium-binding proteins and transporters. This helps in the treatment of diffuse demineralization of bone by ensuring an adequate supply of calcium for bone mineralization. Stimulation of liver hydroxylation of cholecalciferol (choice A) and renal α hydroxylase (choice B) are not directly related to the therapeutic efficacy of calcitriol. Decreased intestinal phosphate absorption (choice C) would not address the demineralization of bone because phosphate is not the primary mineral component of bone.

Question 3 of 5

Which of the following drugs would be appropriate to include in the therapeutic management of this patient?

Correct Answer: A

Rationale: The correct answer is A: Calcitriol. This patient likely has a calcium deficiency, as calcitriol is the active form of vitamin D that helps regulate calcium levels in the body. It would be appropriate for managing this condition. B: Hydrochlorothiazide is a diuretic used to treat high blood pressure and edema, not calcium deficiency. C: Sodium fluoride is used to prevent tooth decay, not for treating calcium deficiency. D: Triamterene is a diuretic that works by increasing potassium excretion, not relevant for treating a calcium deficiency.

Question 4 of 5

A 27-year-old woman with amenorrhea, infertility, and galactorrhea was treated with a drug that successful restored ovulation and menstruation. Before being given the drug, the woman was carefully questioned about previous mental health problems, which she did not have. She was advised to take the drug orally. The drug used to treat this patient was probably.

Correct Answer: A

Rationale: The correct answer is A) Bromocriptine. Bromocriptine is a dopamine agonist that inhibits prolactin secretion. In this case, the woman presented with symptoms of hyperprolactinemia (amenorrhea, infertility, and galactorrhea), which can be effectively treated by reducing prolactin levels with bromocriptine. By restoring ovulation and menstruation, bromocriptine addresses the underlying cause of her symptoms. Option B) Desmopressin is a synthetic form of vasopressin used to treat conditions like diabetes insipidus, not hyperprolactinemia. Option C) Human gonadotropin hormone is used in fertility treatments to stimulate ovulation but does not address the underlying cause of hyperprolactinemia. Option D) Leuprolide is a gonadotropin-releasing hormone agonist used to treat conditions like endometriosis and prostate cancer, not hyperprolactinemia. In an educational context, understanding the pharmacological treatment of endocrine disorders is crucial for healthcare professionals. This case highlights the importance of recognizing the symptoms of hyperprolactinemia and knowing the appropriate pharmacological intervention to restore hormonal balance and fertility in patients. By grasping the mechanism of action of drugs like bromocriptine, healthcare providers can effectively manage endocrine disorders and improve patient outcomes.

Question 5 of 5

Which of the following drugs is least likely to be used as part of a controlled ovarian hyperstimulation protocol?

Correct Answer: D

Rationale: In the context of controlled ovarian hyperstimulation protocols, the drug least likely to be used is Pergolide (Option D). Pergolide is a dopamine agonist primarily used in the management of Parkinson's disease and has limited to no role in ovarian stimulation protocols. Human chorionic gonadotropin (Option A) is commonly used to trigger ovulation in assisted reproductive technologies. Leuprolide (Option B) is a GnRH agonist that can help prevent premature ovulation during ovarian stimulation. Menotropins (Option C) are a combination of FSH and LH hormones used to stimulate follicle development in the ovaries. Educationally, understanding the specific roles of different drugs in controlled ovarian hyperstimulation is crucial for healthcare professionals working in reproductive endocrinology and infertility. By knowing which drugs are commonly used and their mechanisms of action, practitioners can optimize treatment protocols for patients undergoing fertility treatments.

Access More Questions!

ATI RN Basic


$89/ 30 days

ATI RN Premium


$150/ 90 days

Similar Questions