Sweatman: Drugs to Treat Menopause Flashcards

1
Q

symptoms of menopause are brought about via

A

loss of endogenous production of estrogen

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2
Q

what is no longer being used to treat symptoms of menopause

A

HRT–> too many CV bone dz., and Cancer risks

*though this treatment is very effective

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3
Q

CEE + MPA increases risks for

A
>Coronary Heart Dz
>Invasive Breast cancer
>stroke
>PE
>gall bladder dz
>Dememtnia
>urinary incontinence
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4
Q

CEE and MPA decrease the risk for

A

> hip fractures
Diabetes
Vasomotor Syptoms

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5
Q

CEE alone shows what

A

more balanced risks vs benefits

>Dec risk of breast cancer

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6
Q

Side effects after therapy stopped

*neither regimine affected all cause mortality

A

except for risk of breast cancer..the other side effects do away

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7
Q

absolute risks of adverse affects are much lower in

A

younger women as opposed to odler women

*time since menopause influences absolute risk

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8
Q

guidelines for HRT

A

currently remains the appropriate management for moderate to severe menopausal symptoms–> but not rcommended E +P of E alone for long term management of chronic disease prevention

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9
Q

deciding if patient should get HT

A
  1. determine if they have mod-severe menopausal symptoms
  2. determine if contraindications to HT and h/o CHD, CVA, TIA
  3. assess CHD risk and years since last menstrual period
    ( OK: 6-10 no unless VL risk: >10 years AVOID)
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10
Q

E and oteoprosis

A

recommended to treat women at HIGH risk for fracture who cannot tolerate alternative OP therapies

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11
Q

Women with genitourianry symptoms in the absence of vasomotor symptoms should receive

A

low dose, vaginal estrogen

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12
Q

women on HT follow up

A

reassess each steo every 6-12 months

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13
Q

never give woman HT if

A

unexplained vaginal bleeding, liver disease, DVT hx, clotting disorder, breast or endometrial cancer,

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14
Q

who is not a good cancidate overall (regqrdless of CHD risk score)

A

women who have been post menopausal for over 10 years

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15
Q

Vasomotor symptoms most common in

A

Africn Americans

–> peaking in the late perimenopause

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16
Q

before treatment of perimenopausal VMS explore

A

secondary causes of flushing_carcinoid, hyperthyroidism, alchohol, emotional flushoing, CCB;, pheochromocytoma

17
Q

non-pharm tx of VMS (small-moderate improvement of symptoms)

A

aerobic exercise, avoid smoking, moderate etoh, dressing in layers, low ambient temperature, consuming cool drinks, paced respiration (requires training), clinical hypnosis, cognitive behavioral therapy

18
Q

pharmicological treatment of VMS

*all others are off label

A
Paroxetine
fluoxetine
escitalopram
venlafaxine
clonidine
gabapentin
19
Q

SE’s of Paroxetine, Fluoxetine, and Escitalopram (all the same)

A

N, HA, Insomnia, Possible Sexual Dysfunction

20
Q

SE’s of Venlafaxine

A

Nausea OR Vomiting, Dry mouth, anorexia, possible sexual dysfunction

21
Q

Clonidine SE’s

A

dry mouth, insomnia, drowsiness, skin reactions to transdermal patch

22
Q

SE’s for gabapentin

A

dizziness
unsteadiness
drowsiness

23
Q

qualifications of the drigs to treat VMS

A
  • MOA unknown
  • lower doses than for depression/pain
  • affects are more rapid in onset
24
Q

MOA for clonidine

A

raises sweating threshold in thermoregulatory center and in the periphery it lowers vascular reactivity

25
Q

Name the oral estrogens approved for treatment of Menopause

A

> 17 beta estradiol
ethinyl estradiol
conjugated estrogen

26
Q

name the oral progesterones available to treat menopausal symptoms

A

Medoxyprogesterone actate
Norethindrone acetate
Drospirenone
micronized progesterone

27
Q

transdermal estrogen treatment in Menopausal symptoms

A

estradiol patch/gel/spray/emulsion

28
Q

vaginal estrogen treatment in menopausal

A

estradiol cream/tablet/ring

29
Q

transdermal progesterones

A

norethindrone acetate

levonorgestril

30
Q

the most effective treatment regimine for V<A and Urogenital atrophy

A

Estrogem +/- progesterone

31
Q

relief of treatment with E+/- P occurs within

A

one month

32
Q

Side effects of HT (dose related)

A

breast tenderness and uterine bleeding

less commonly: Vomiting, headaches, weight change, rash pruritis, cholecystitis

33
Q

route of administration preferred

A

transdermal –> no first pass metabolism

34
Q

benefit of transdermal route

A

first pass metabolism (transdermal avoids)–> promotes prothrombotic hemostatic changes oin factor IX, activated protein C resistance and TPA

35
Q

name the conjugated estrogen

A

Bazedoxifene

36
Q

Bazedoxifene makeup and MOA

A

combo of Estrogens and a SERM–>agonist in some E-sensitive tissues and an antagonist is others
–> in OM women it helps prevent endometrial overgrowth

37
Q

help prevent endometrial overgrowth in Post menopausal women taking estrogens

A

bazedoxifene (e + SERM)

38
Q

risk of VWS recurring when drug is stopped

A

50%

*independent of duration of sue

39
Q

what happens with VMS is stopped

A
  • ->VMS recurs in 50%
  • ->bone resoprtion worsens, –>vulvovaginal atrophy recurs
  • ->other risks and benefits return to baseline rather quickly with exception of breast cancer