What are the options we have in our hand to counteract endocrine deficiencies partly induced such changes in
reproductive organs , Brain, Mood
changes , Somatic changes( asthenia, sarcopenia
)?? Can we have any one safe drug which will take care of all the activities of diminished endogenous oestrogens
and (??) decreased androgens . No single agent till date is available though Tibolone
as a monotherapy will replenish most of the deficiencies in different organs induced by endogenous hypoestrogenism . :
Clonidine is treated
like migrant labour!!!! The forgotten antihypertensives!!!!
Evolution of antihypertensives since early sixties. The supportive drugs in menopause
which are nonhormonal but reasonably effective are 3) Raloxifene for osteoprirtection
4) Clonidine- an antihypertensive (brand
names are Arkamin –Unichem 100 mcg per tab or
Brand name Catapres –Zydus 150
mcg tab for hot flushes. Extremely effective. Start slowly increase the dose
and taper off slowly. . Arkamin(Clonidine) reduces alpha 2 receptors in brain stem. One can
add hydrochlorothiazide in the same Tab (brand name is Arkamin-H , Catapres –DUO)
-to add such drug if she is hypertensive as well . Additionally
in to counteract Meno sym and skeletal changes
, sarcopenia in particular 5) Stretching
exercises, Yoga, Fiber diet , engaging in NGO/Social activities will go a long
way if husband can’t afford much time with meno woman.
Mourn for three antihypertensives
e .g. Aldomet, Clonidine, and Esidrex)
are dead. : Evolution
of antihypertnses: Once Clonidine which was a very popular antihypertensive
agent when we were Medical students in early
sixties . On those days(Fifty five yrs back) 1) Clonidine 2) alpha Dopa (Aldomet) ,3) Prazosin (Minipress XL –Pfizer) all were
sympatholytic agents were the chief agents to control HTN and Chlorothiazide (brand
Esidrex ) were also liberally used
eiethr singly or with chlorothiazide ( Esidrex) . Of such four agents only Prazosin is still alive
(not in HDU even) , other are dead. Such , three
agents are Alpha Dopa-Aldomet, Clonidine, and Esidrex are dead. However with progress of vascular
physiology and cardiology .
.such four drugs were replaced
by 5) Beta Blockers. 6) Ca Channel Blockers, 7) ARB, 8) ACE inhibitors 9)newer agents for
hypertensive crisis to be used with the help of syringe pump. Nitrites and
Coronary dilators are separate class as is lipid lowering agents which is now
used in our discipline of PCO
. Why we the clinicians
are afraid of long term Oestrogen replacement therapy? What
did WHI warned us??
Ans:-While most clinicians agree the
short term estrogen replacement
therapy is currently the best treatment for the vasomotor symptoms and to prevent osteoporosis scientific data raises concerns about the risks of this
therapy particularly for long period
. How safe is short term E therapy ?? Ans:-It should be noted that there is no
evidence of adverse effects from short term estrogen therapy for the acute relief
of menopausal symptoms. Currently, hormone replacement therapy is indicated for vasomotor symptoms and should be used
for short a duration as short as possible in the smallest
dose. For women who cannot or
choose not to take estrogen , the antihypertensive agent Clonidine
may help to ameliorate the
vasomotor symptoms
The Women’s Health Initiative Study
of continuous estrogen - progestin treatment reported a small but significant Risk A) increased risk of breast cancer, and risk of “continuous
Estrogen & progesterone therapy”
is heart disease,: Risk B
of “continuous Estrogen &
progesterone therapy”—may cause
pulmonary embolism and Risk 3 of “continuous Estrogen & progesterone therapy” :-- stroke. But, the advantage enjoyed by the concerned women on hormone replacement therapy that they had fewer fractures and Advantage 2 :- a lower
incidence of colon cancer.
. A selective estrogen receptor modulator such as raloxifene is helpful
in preventing bone loss , but does not alter the hot flushes. Weight bearing exercise,
calcium and vitamin D
supplementation and estrogen replacement are important cornerstones in maintaing bone mass.
Because the FSH release from pit responds
to the inhibin and not to estrogen, the FSH
level cannot be used to titrate the estrogen replacement dose. In
other words, the FSH
concentration is still elevated even though the estrogen
replacement may be sufficient.
Other diseases that are important to consider in
the perimenopausal woman include hypothyroidism , diabetes mellitus ,
hypertension, and breast cancer.
What
about Depression in menopause? Ans: Women in this
stage of life may also experience
depression whether spontaneous
in its onset or situational due to grief or middle adjustments(Midlife
crisis).The practitioner should
advocate aerobic exercise at least
three time a week, again, with weight
bearing exercise being advantageous for
the prevention of osteoporosis. Bone
mineral density testing such as by dual energy X-ray absorptiometry is useful in the early identification of osteoporosis and osteopenia . BMD testing is indicated for all postmenopausal women aged 65 years
or older and postmenopausal
women at risk for osteoporosis and presenting with a bone
fracture. Alcohol abuse , may increase in this age due to family crisis
and depression which have to enquired upon and managed by proper counseling.
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