ORAL
CONTRACEPTIVE AND ACNE TREATMENT IN ONE:
DIANE-35 |
Adolf E. Schindler
Dept. Obstetrics and Gynecology, University of Essen, Germany
The clinical use of cyproterone acetate (CPA) - the most potent
antiandrogenic progestin - was initiated 1970 in combination with
ethinylestradiol (EE). Starting with the reversed biphasic regimen
gradually a very effective hormonal tool for the treatment of
sions of androuenisation in women and a most effective contraceptive
has emerged using 2 mg of CPA and 0.035 mg of EE (Diane-350).
Since ovulation inhibition is already accomplished with 1 mg CPA/day,
Diane-35 suppresses the hypothalamic-pituitary-ovarian-axis reliable,
which results in a very low Pearl index (0.1). This also leads
to an excellent cycle control and bleeding pattern. In addition,
Diane-35 has multifactorial antiandrogenic effects: 1. Competition
at the cellular androgen receptor level. 2. Increasing androgen
metabolic clearance at the hepatic level and reducing the activity
of 5-alpha reductase at the skin level. 3. Being antigonadotropic
leads to suppression of ovarian androgen secretion. 4. Increasing
SHBG and decreasing free testosterone. This causes the desired
clinical effects after 6 months of treatment: 1. Normalisation
of acne 73%, seborrhoea 73.4%, after 12 months: acne 90.6%, seborrhoea
87.4%. The strong long-term positive metabolic effects need to
be taken into account: 1. Favourable effects on carbohydrate metabolism.
2. Favourable effects on lipid metabolism. Long-term use of Diane-35
has no negative effect on liver function and does not increase
the risk of liver cancer.
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| INTRODUCING
THE NEW OC YASMIN WITH THE NOVEL PROGOESTOGEN THE SPECIAL ADVANTAGES
OF A CONTRACEPTIVE WITH ANTIMINERALOCORTICOID AND ANTIANDROGENIC ACTIVITIES |
J.M. Foidart MD, PhD
Dept. of Gynecology, University of Liège, LIEGE, BELGIUM
Drospirenone is a novel progestogen which differs in important
ways from other currently available progestogens. It has a pharmacological
profile that is very similar to natural progesterone. Drospirenone
is not only strongly progestogenic but it also has antimineralocorticoid
and antiandrogenic activities. An OC containing Drospirenone ha
therefore the potential to counteract fluid retention resulting
from the mineralocorticoid activity of ethinylestradiol, and therefore
avoid or reduce any problems associated with fluid retention such
as weight gain.
Two large, randomized, multicenter, open-label. clinical studies
investigated the contraceptive efficacy and tolerance of Yasmin,
a new oral contraceptive containing 30 μg ethinylestradiol
plus 3 mg Drospirenone (28,000 cycles. Both preparations provided
effective contraception excellent Pearl indexes and cycle control.
Their influences on haemostasis parameters, lipid and carbohydrate
metabolism was minimal. Pre-existing acne and seborrhea were improved
and blood pressure was essentially unchanged. Yasmin provided
effective contraception, (0.09 corrected Pearl Index), excellent
cycle control and tolerance.
However, Yasmin had a more favorable effect on body weight than
Marvelon, with the mean body weight remaining lower than baseline
throughout the study, the difference between the two preparations
being statistically significant.
In conclusion, Yasmin provides effective contraception, excellent
cycle control, good tolerability and a weight loss that confers
a significant beneficial effect on compliance in women with tendency
to weight gain due to water retention.
In order to quantify the effect on well-being, a quality of life
(QOL) survey was carried out (Yasmin n= 180). The respondents
who had taken Yasmin during the trial rated their weight their
disposition before and during menstruation, as well as their skin
and hair conditions better with Yasmin than without this innovative
OC.
This perception of Yasmin as having a positive effect on overall
well-being is likely to reflec the antimineralocorticoid and antiandrogenic
activities of Drospirenone. In consequence, it can be anticipated
that general satisfaction with oral contraception, and therefore
compliance may be enhanced.
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| THE
INTRAUTERINE SYSTEM (IUS) MIRENA: LONG-ACTING CONTRACEPTION WITH ADDED
BENEFITS |
Pekka
Lähteenmäki, MD, PhD
The
levonorgestrel intrauterine system (LNG IUS, Mirena®) is a long‑acting
hormonal method, which releases 20 pg/24 h of LNG into uterine
cavity. It provides highly effective contraception for 5 years
with a Pearl rate of 0. 1. In addition to postmenstrual insertion
the LNG IUS can be inserted also directly after first trimester
abortion or six weeks after delivery. The incidence of ectopic
pregnancies is only one in 5.000 users annually. Only very low
blood concentrations of LNG are measured. Therefore, the hormonal
side effects are relatively rare. The LNG IUS is completely reversible
method of contraception. The high degree of satisfaction is reflected
by high first year continuation rates of 80 %. The LNG IUS reduces
menstrual blood loss by inactivating the growth of endometrium.
It can be used effectively as a treatment for menorrhagia. The
studies show it reducing the need for hysterectomy due to menorrhagia.
Total local amenorrhea is successful in 20 % of the users after
12 months. The reduction in the number of days of menstrual bleeding
increases the quality of life. The LNG IUS has been shown to decrease
dysmenorrhea. As with oral contraceptives, LNG IUS decreases the
incidence of pelvic inflammatory disease. One large study demonstrates
a decrease in the development of fibroids in LNG IUS users.
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| PATIENT
COUNSELLING ON JUS - A LOCAL EXPERIENCE |
Dr. Sue ST Lo, MBBS, MRCOG
The Family Planning Association of Hong Kong
The levonorgestrel - releasing intrauterine system (IUS) had
been used in many countries in the past 30 years. Clinical trials
had shown that the device is a highly effective contraceptive
and severe complications are rare. Despite its high clinical efficacy,
the IUS is not a popular contraceptive. In Hong Kong, less than
5% of women who had ever practiced contraception had used intrauterine
contraceptive device (IUCD). The proportion of women using IUS
was even lower. There is a general fear about putting a foreign
object in the uterus and myths about IUCD were still prevalent.
For the IUS, there were additional concerns for menstrual disturbance.
Great difficulties had been encountered during the recruitment
for an acceptability study on IUS. In the initial 6 months of
recruitment, we had approached 57 eligible women, only 19 women
agreed to use the IUS. The reasons for rejecting IUS were: disliked
irregular spotting (40.5%), preferred other IUCD (19%), disliked
amenorrhea (16.7%) and preferred other methods (16.7%). Among
48 successful insertion of IUS, 2 subjects had their IUS expulsed
on day 26 and 3 months, both said they would wanted a re-insertion
if given the opportunity. Four subjects requested removal, none
was for spotting or amenorrhoea. The acceptability and continuation
rate were high if subjects had been thoroughly counseled on the
effects of IUS and they accepted the method.
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