Lecture 7: MHT/SERMS Flashcards

1
Q

What is the primary therapy for menopausal symptoms?

A

Estrogen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

How does a women with an intact uterus affect the type of pharmacologic treatment used for menopause?

A

In addition to estrogen they MUST be on progestin!

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are the 4 estrogens available for use in menopausal hormone therapy?

A

1) Estradiol
2) Conjugated estrogens (CE)
3) Esterified estrogens (EE)
4) Estropipate: estrone solubilized w/ sulfate and stabilized w/ piperazne

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What are the 3 progestin drugs available for menopausal hormone therapy?

A

1) Medroxyprogesterone (MPA alone or with CE)
2) Methyltestosterone (alone or with EE)
3) Progesterone (alone)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Why must progestins be given along side estrogens in a women with an intact uterus?

A
  • Estrogen will cause unopposed endometrial proliferation
  • Progestin’s oppose effects of estrogen’s.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are 3 things that estrogen therapy causes a decreased production/activity of?

A
  • ↓ cholesterol (TC/LDL-C)
  • ↓ anti-thrombin III
  • ↓ osteoclast activity (bone turnover)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are 5 things that estrogen therapy causes increased production/activity of?

A
  • ↑ TAG’s and HDL-C
  • ↑ clotting factors
  • ↑ platelet aggregation
  • ↑ Sodium and fluid retention
  • ↑ Thyroid Binding Globulin (TBG)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

List 7 potential AE’s associated with a combo of estrogen + progestin used for treatment of postmenopausal women.

A
  • Breast cancer
  • CHD
  • Dementia (aged 65 y/o +)
  • GB disease
  • Stroke
  • Venous thromboembolism
  • Urinary incontinence
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

List 3 potential benefits associated with a combo of estrogen + progestin used for treatment of postmenopausal women.

A
  • Improvement of diabetes
  • Less risk of all fractures
  • Less risk of colorectal cancer
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

List 5 potential AE’s associated with estrogen used for treatment of postmenopausal women.

A
  • Dementia (aged 65 y/o +)
  • GB disease
  • Stroke
  • Venous thromboembolism
  • Urinary incontinence
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

List 3 potential benefits associated with estrogen thrapy used for treatment of postmenopausal women.

A
  • ↓ risk of breast cancer (invasive)
  • ↓ risk of all fractures
  • Improvement of diabetes
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

The women’s health initiative study found that MHT is very effective for what?

A
  • Minimize/treat vasomotor sx’s and vaginal changes (and their associated complications)
  • Do NOT use for prevention of CVD or dementia and do NOT use solely for benefit on bone or colorectal cancer
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is the recommendation/agreement for using MHT therapy in younger women?

A

MHT is an acceptable option for tx of moderate-severe menopausal sx’s in relatively young (up to age 59 or within 10 years of menopause)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is the recommendation/agreement for MHT therapy in women with vaginal sx’s only?

A

Preferred tx are low doses of vaginal estrogen (topical)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Which age group has less risk of blood clots/stroke from MHT therapy?

A

50-59 y/o group

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

There is an increased risk of breast cancer with MHT seen within how long of treatment?

A
  • 3-5 years of continous estrogen + progestin
  • Use it at the lowest dose possible for the shortest amount of time.
17
Q

What are the 2 SERM’s we need to know for this exam?

A
  • Ospemifene
  • Clomiphene
18
Q

What is the tissue selective estrogen complexes (TSECs) we need to know for this exam?

A

Bazedoxifene

19
Q

What is the clinical indication for the SERM, Ospemifene?

A
  • Tx of moderate-to-severe dyspareunia (painful intercourse)
  • A sx of vulvar and vagnal atrophy (VVA) of menopause
20
Q

Explain the MOA of the SERM, Ospemifene.

A
  • Estrogen agonist at ER’s of the vagina –> ↑ superficial cell growth, ↑ vaginal secretions, ↓ vaginal pH, ↓ pain/discomfort during intercourse
  • Estrogen antagonist at ER’s in the breast
21
Q

What are the AE’s associated with the SERM, Ospemifene?

A
  • Worsening of hot flashes/sweating
  • Estrogenic-similar effects on coagulation (↑ risk of stroke/VTE; but at lower rate than estrogens alone)
  • Endometrial thickening (proliferation) and even hyperplasia —> concern for malignancy, but no cases in clinical trials yet
22
Q

What are the contraindications for using the SERM, Ospemifene?

A
  • Unusual/abnormal vaginal bleeding
  • Thromboembolic diseases: CVA or MI or VTE or PE or DVT
  • Caution with use in smokers
  • Estrogen-related neoplasia’s: uterine or ovarian or breast
23
Q

What is the clinical indication for using the SERM, Clomiphene?

A

Infertility in anovulatory women

24
Q

What is the MOA of the SERM, Clomiphene?

A
  • Primarily blocks inhibitory actions of estrogen on hypothalamus GnRH and pituitary gonadotropin release (anti-estrogen)
  • ↑ gonadotropin (FSH, LH) secretion thereby stimulating the ovaries to develop oocyte follicles
25
Q

Which patients are the most significant effects seen in when treated with the SERM, Clomiphene?

A

Induction of ovulation in women w/ amenorrhea, PCOS,anddysfunctional bleedingw/anovulatory cycles

26
Q

What are the 2 clinical indications for the use of the TSEC, Bazedoxifene (w/ CE)?

A
  1. Tx of moderate-to-severe vasomotor sx’s assoc. w/ menopause in women with a uterus
  2. Prevention of post-menopausal osteoporosis (along w/ Ca2+ and Vit D) in women with a uterus
27
Q

What is the MOA of the TSEC, Bazedoxifene?

A
  • Antagonist activity in endometrium (replaces progestin-concept in women with an intact uterus) and in breast tissue
  • Has estrogenic agonist effects, especially in bone (CE agent)
28
Q

How does Bazedoxifene differ from the 1st gen. SERMS as far as effects and utility?

A
  • Does NOT stimulate endometrial proliferation
  • Has been shown (lab) to destroy HER2 malignant cells (SERDs), including cells resisten to Tamoxifen, similar to anti-estrogen drug Fluvestrant)
  • Less vaginal bleeding than CE w/ progestin therapy
29
Q

What are the AE’s associated with the TSEC, Bazedoxifene?

A
  • ALL estrogen-related effects (due to CE component)
  • Bazedoxifene-specific: has the potential of worsening hot flashes/sweating (similar to Tamoxifen, Raloxifene and Ospemifene)
30
Q

What are the 4 AE’s associated with the SERM, Clomiphene?

A
  • Multiple births
  • Ovarian cysts —> ovarian cancer w/ prolonged use (limit use to 3 cycles)
  • Hot flashes
  • Luteal-phase dysfunction –> inadequate progesterone prod.