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62 Cards in this Set

  • Front
  • Back
describe the events during premenopause
-decline in ovarian fx and increase of anovulatory cycles
-absence of ovulation, decrease levels of ovarian hormones(estradiol, progesterone)
-loss of negative feedback; increased levels of gonadotropic hormones (FSH, LH)
-menstrual cycle length increases
-increased menstrual irregularity
what is the pathophysiology of decreasing ovarian fx and weight with age
-decreased number of ovarian follicles which undergo ovulation
-without maturation, estradiol production, ovulation, and progesterone secretion do not occur
what are the clinical manifestations of approaching menopause?
-menstrual irregularity, lengthening menstrual intervals, and anovulation
-vasomotor Sx: hot flushes
-urogenital atrophy
clinical manifestations of approaching menopause are related to the decline in ______
estradiol
Levels of ___&______ continually increase to a maximum at 2-3 yrs after menopause (these levels are higher than premenopausal)
FSH & LH
residual ovarian follicles become refractory to the________, produce less __________, and exert less ___________.
1. gonadotropins
2. estradiol
3. negative feedback on the hypothalamic-pituitary-gonadal axis
after menopause, the primary estrogen is _________, which is derived from androgens produced in the __________,
1. estrone
2. adrenal cortex
Androgen produced in the adrenal cortex undergo peripheral conversion (aromatization) mostly in the ___________
adipose tissue
__________ production is also diminished during the climacteric
progesterone
perimenopause consists of three stages which are?
premenopause, menopause, and postmenopause
postmenopausal progesterone levels are ________to premenopausal concentrations occurring in the follicular phase of the ovarian cycle
equal
acute perimenopausal Sx
-vasomotor Sx
-genitourinary atrophy
-psychogenic effects: mood changes/irritability
osteoporosis is a major consequence of __________
long-term estrogen deficiency
after premenopausal bilateral oophorectomy, 37-50% pts experience_________
vasomotor Sx: hot flushes
what are the characteristics of hot flushes?
-episodic, rather than continuous
-due to estrogen deficiency in the CNS or estrogen withdrawal
-downward resetting of the thermoregulatory center set point
-occur as core temp decreases
vasomotor Sx of perimenopause
-hot flushes
-HA
-night sweats (hot flushes at night)
-insomnia
__________is highly effective at relieving these symptoms
MHT
S & Sx of genitourinary atrophy
-thinning and drying of the urinary tract and vaginal tissues
-dryness due to decreased vaginal secretions; easily traumatized tissues or bleeding
-atrophic changes in genitourinary organs
-vaginal pH changes
-
vaginal pH changes in genitourinary atrophy predispose pts to ____________
increased bacterial colonization and infectious vaginitis
discuss the forms of administering intravaginal estrogen
-conjugated estrogen vaginal cream
-vaginal ring sustained release delivery system (ring inserted near cervix and estradiol is slowly released over 3 mo to exert local effects)
intravaginal estrogen is insufficient amt for relief of ____________
vasomotor Sx
The National Menopause Society recommends that estrogen-progestin therapy be prescribed at ________dose for _________time to relieve menopausal Sx such as vasomotor instability and atrophic vaginitis
1.the lowest effective dose
2.the shortest possible time
Endocrine Society states that:
1. _________relieves Sx and normalize vaginal atrophy
2._________ reduces Sx of overactive
3._________reduces incidence of recurrent UTI's
1. very low doses of vaginal estradiol
2. vaginal or systemic estrogen
3. vaginal estrogen
What are the goals of MHT?
-tx acute perimenopausal Sx
-estrogen combined with a progestin to suppress estrogen-induced endometrial hyperplasia and and cancer in pts with an intact uterus (estrogen alone if no uterus)
long-term MHT is NOT USED for what three purposes?
-primary and secondary prevention of CV dz
-osteoporosis
-Alzheimer's Dz
what is an endogenous estrogen product used for MHT?
estradiol transdermal patches
what is a naturally-occurring estrogens used for MHT?
conjugated equine estrogens
-oral products (Premarin)
actions of transdermal estrogen patches
-moderate to severe vasomotor Sx associated with menopause
-atrophic conditions caused by deficient endogenous estrogen production
-prevention of postmenopausal osteoporosis
____is used only in hysterectomized women (women without an intact uterus)
Estrogen Therapy
Why are oral progestins used with MHT?
to decrease the risk of endometrial hyperplasia and CA associated with unopposed estrogen in women with an intact uterus
describe the recommendations for progestin admin during MHT
-medroxyprogesterone acetate for at least 12 days a month in cyclical regimens
-daily in continuous regimens
indications of estrogen/progestin combined products
-moderate to severe vasomotor Sx associated with menopause
-vulvar and vaginal atrophy
-prevention of osteoporosis
dosing schedule for cyclic sequential MHT
-estrogen daily for days 1-25 of each month
-progestin daily added for 12 days (days 13-25) each month
-days 25-30 are hormone free
97% incidenceof _____________ starting on day 25 of cyclic sequential MHT. Some pts may experience ________during the period of estrogen therapy
1. withdrawal bleeding (usually light and painless)
2. return of Sx
In cyclic sequential MHT, endometrial CA is avoided if ___________________.
-progestin component is adequately dosed and of sufficient duration
what is an advantage of continuous sequential MHT?
-prevents Sx of estrogen deficiency in pts who experience those Sx on hormone-free days
what are the characteristics of continuous combined MHT?
-both estrogen and progestin on all days of the month
-designed to produce amenorrhea (d/c of menses)
-after 6 mo, 60-65% are amenorrheic
low dose ET/MHT vs standard dose?
-decreased severity of hot flushes
-improved vaginal maturation index
-osteoporosis prevention post menopause when combined with progestin and calcium supplement
MHT and Alzheimer's dz?
-MHT increases the risk of probable dementia in postmenopausal women >/=65yrs
-in studies failed to prevent mild cognitive impairment
MHT and endometrial CA?
--progestin should be added to ET in women with and intact uterus to prevent endometrial hyperplasia and decrease the risk
-hysterectomized women should receive unopposed ET
MHT and breast CA?
-increased risk after 5yrs of use(can be 2-3)
-short courses of MHT for tx of Sx of menopause should be safe(2-3yrs)
-women with intact uterus should use other methods to prevent osteoporosis and CAD
analysis showed that MHT puts postmenopausal women at increased risk for ______, _________, __________, and a _______
1. breast CA (26%)
2. stroke (41%)
3. MI (29%)
4. >/= 2-fold increase in PE
What benefits did analysis show with MHT use?
-decreased incidence of hip fracture (33%)
-decreased colorectal CA (37%)
short term use of MHT still viewed as safe and effective to a duration of?
<5yrs
(risks do not outweigh benefits after 5yrs)
decision to stop estrogen only trial was based on?
-increased risk of stroke similar to that in EEP study
-trend toward an increased risk of probable dementia and/or mild cognitive impairment
-reduction in hip fxs
-no increases in breast CA
neither primary nor secondary prevention of _____are achieved with long term MHT
-CV dz
increased risk of demetia in postmenopausal women was evident after___and persisted for _____ shown in one study
1. 1st year
2. the duration of the trial
MHT _________the risk for dementia
doubles
Neither MHT nor ET increase the risk of __________ in women 50-59
MI
lack of benefit or increase in CHD risk with MHT use thought to be due to ________
harmful effects of MHT in older women starting therapy many years after onset of menopause
MHT may increase risk of ____________ in postmenopausal women by 64% and the magnitude of the increase is related to _________
1. gallbladder dz
2. dosing route
summary of estrogen + progestin MHT advantages
-decreased risk of colorectal CA
- decreased risk of fx
summary of estrogen + progestin MHT disadvantages
-increased risk of stroke, blood clots,breast CA, dementia
-no protection against mild cognitive impairment
- increased risk of AMI (not for 50-59yr olds)
estrogen alone MHT increases risk of?
stroke
Mgmt for breast tenderness associated with hormone replacement therapy
-reduce estrogen dose
Mgmt for vasomotor Sx associated with hormone replacement therapy
-increase estrogen dose
Mgmt for heavy withdrawal bleeding associated with hormone replacement therapy
- decrease estrogen dose
-switch to a continuous progestin dosing regimen
Mgmt for HAs associated with hormone replacement therapy
-if migraine-like consider d/c
-switch to continuous estrogen therapy
Mgmt for bloating associated with hormone replacement therapy
-switch to a different progestin
Mgmt for mood alterations associated with hormone replacement therapy
-decrease progestin dose
Mgmt for decreased libido associated with hormone replacement therapy
-add estrogen to regimen
absolute contraindications to postmenopausal estrogen therapy
- presence of estrogen-related CA
- undiagnosed abnormal vaginal bleeding
-active lever dz or chronic severe liver dysfunction
-active thrombophlebitis or thromboembolic d/o
- prior complications form estrogen therapy