Vaginal dryness and vaginal atrophy facts
- Vaginal atrophy is the medical term that refers to the thinning of the wall
of the vagina that occurs during the menopause (the time when menstrual periods
have ceased) in women.
- Vaginal atrophy occurs due to falling estrogen levels.
- Vaginal atrophy may be associated with vaginal dryness, itching,
irritation, and/or pain during sexual intercourse.
- Hormone therapy can be effective in treating vaginal atrophy and other
menopausal symptoms, but hormone therapy carries its own risks.
- Local vaginal hormone creams or vaginal lubricants are alternatives to
systemic hormone therapy.
What causes vaginal dryness and vaginal atrophy?
Vaginal atrophy is the medical term that refers to the thinning of the wall
of the vagina that occurs during menopause (the time when menstrual periods have
ceased) in women. Prior to menopause, the vaginal lining appears plump, bright
red, and moist. As estrogen levels decline, the lining of the vagina becomes
thinner, drier, light pink to bluish in color, and less elastic. This is a
normal change that is noticed by many postmenopausal and postmenopausal women.
Estrogen levels begin to fall as the menopause approaches. Estrogens are
mainly produced by the ovaries. Estrogens control the development of female body
characteristics such as the breasts, body shape, and body hair. Estrogens also
play a significant role in the regulation of the
menstrual cycle and pregnancy.
Most women reach menopause between the ages of 45 and 55, but it can occur
earlier or later in life. The menopause average age is 51 years old. Every
woman is different, and there is no definitive way to predict when an individual
woman will enter menopause. Also, women in the menopausal transition experience
symptoms with varying degrees of severity. Not all postmenopausal and
postmenopausal women will have the same symptoms or experience the same levels
of severity.
What symptoms can be associated with vaginal dryness and vaginal atrophy?
Other vaginal symptoms that are commonly associated with vaginal atrophy
include vaginal dryness, itching, irritation, and/or pain with sexual
intercourse (known as dyspareunia). The vaginal changes also lead to an
increased risk of vaginal infections.
In addition to the vaginal symptoms, women may experience other symptoms of
the menopausal transition. Hot flashes, night sweats, mood changes, fatigue,
urinary tract infections, urinary incontinence, acne, memory problems, and
unwanted hair growth.
How is vaginal dryness and vaginal atrophy diagnosed?
Vaginal symptoms such as itching, dryness, or pain with sexual intercourse is
typically sufficient to assume that a women is suffering from vaginal dryness
and vaginal atrophy if she is experiencing other symptoms consistent with
the menopausal transition. Of course, a careful physical examination, including
a pelvic examination, is necessary to rule out other conditions (such as
infections) that may be causing vaginal symptoms.
There are no specific tests available to determine whether the vaginal wall
has become thinner or less elastic.
What treatments are available for vaginal dryness and vaginal atrophy?
Vaginal dryness and atrophy do not need to be treated unless they cause
symptoms or discomfort. Women who experience symptoms have several treatment
options.
Hormone therapy
Hormone therapy (HT) is effective in treating vaginal dryness/vaginal
atrophy. HT has also been referred to as hormone replacement therapy (HRT) or
postmenopausal hormone therapy (PHT). HT has been shown to effectively reduce
vaginal dryness as well as help control hot flashes associated with menopause.
However, HT is not without its risks. Long-term studies (the NIH-sponsored
Women's Health Initiative, or WHI) of women who took oral combined hormone
therapy containing both estrogen and progesterone showed that these women had an
increased risk for heart attack, stroke, and breast cancer when compared with
women who did not receive it.
Women taking oral estrogen alone had an increased
risk for stroke, but not for heart attack or breast cancer. Estrogen therapy
alone, however, is associated with an increased risk of developing
endometrial
cancer (cancer of the lining of the uterus) in postmenopausal women who have not
had their uterus surgically removed.
HT may be administered in pill form or transdermally (patches or sprays from which the
medication is absorbed through the skin). Transdermal hormone products are
already in their active form without the need for "first pass" metabolism in the
liver to be converted to an active form. Since transdermal hormone products do
not have effects on the liver, this route of administration has become the
preferred form for most women. A number of preparations are available for oral
and transdermal forms of HT, varying in the both type and amount of hormones in
the products.
So-called "bioidentical" hormone therapy for perimenopausal women has been a
source of much attention in recent years. Bioidentical hormone preparations are
hormones with the same chemical formula as those made naturally in the body but
which are produced in a laboratory by altering compounds derived from
naturally-occurring plant products. While some of these preparations are U.S.
FDA-approved and manufactured by drug companies, others are made at special
pharmacies called compounding pharmacies, which make the preparations on a
case-by-case basis for each patient. Since individually compounded products
cannot be standardized, these individual preparations are not regulated by the
FDA. There is no evidence that bioidentical preparations provide superior
symptom relief. Studies to establish the long-term safety and effectiveness of
these products have not yet been carried out.
No matter what form of therapy is used, the decision about hormone therapy
should take into account the inherent risks and benefits of the treatment along
with each woman's own medical history and the severity of her symptoms. Current
recommendations state that if hormone therapy is used, it should be used at the
smallest effective dose for the shortest possible time.
Vaginal treatments
There are also local, topical (meaning applied directly to the vagina) low-dose
hormonal treatments for the symptoms of vaginal dryness and vaginal atrophy.
Local treatments include the vaginal estrogen ring, vaginal estrogen cream, or
vaginal estrogen tablets. Local (vaginal) estrogen treatments can be very
effective in reducing vaginal dryness while having a minimal effect on other
tissues in the body.
Vaginal moisturizing agents such as creams or lotions (for example, K-Y
Silk-E Vaginal Moisturizer or KY Liquibeads Vaginal Moisturizer) as well as the
use of lubricants during sexual intercourse are non-hormonal options for managing the
discomfort of vaginal dryness.
Applying Betadine topically on the outer vaginal area, and soaking in a sitz
bath or soaking in a bathtub of warm water may be helpful for relieving symptoms
of burning and vaginal pain after intercourse.
What is the outlook for vaginal dryness and vaginal atrophy?
Vaginal dryness and vaginal atrophy are common complaints in postmenopausal
women. While these conditions do not produce serious consequences, they are a source of
significant discomfort for many women. Hormone treatments are available that are
very effective in reducing vaginal dryness, but whether or not to use hormone
therapy is an individual decision that must consider the inherent risks and
benefits of the treatment along with each woman's own medical history. Women
with only mild symptoms may experience relief by using vaginal moisturizing
agents and/or lubricants during sexual intercourse.
Medically reviewed by Mikio Nihira, M.D; American Board of Obstetrics and Gynecology
REFERENCES:
Rossouw J.E; Anderson G.L; Prentice R.L (2008) Risks and
benefits of estrogen plus progestin in healthy postmenopausal women:
principal results From the Women's Health Initiative randomized
controlled trial.
Utian W.H; Archer D.F; Bachmann (2008) Estrogen and progestogen use in
postmenopausal women: July 2008 position statement of The North
American Menopause Society. Menopause. 4(1):584-602.
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