Fertility Control COPY Flashcards
Female Reproductive Endocrinology - Fertility Control
- GnRH released from the …
- Works on … pituitary to release LH and FSH
- These stimulate the ovary to make the egg and also make oestrogen and progesterone
- These hormones work in a … feedback mechanism on GnRH and pituitary to … LH and FSH production
- These stimulate the ovary to make the egg and also make oestrogen and progesterone
- Hormonal contraception with high levels of oestrogen and/or progesterone will have the same … feedback effect - … production of LH and FSH - … stimulation of developing follicles and make implantation … likely
- GnRH released from the hypothalamus
- Works on anterior pituitary to release LH and FSH
- These stimulate the ovary to make the egg and also make oestrogen and progesterone
- These hormones work in a negative feedback mechanism on GnRH and pituitary to reduce LH and FSH production
- These stimulate the ovary to make the egg and also make oestrogen and progesterone
- Hormonal contraception with high levels of oestrogen and/or progesterone then this will have the same negative feedback effect - decreasing production of LH and FSH - decreasing stimulation of developing follicles and make implantation less likely
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Combined Hormonal Contraceptives (CHC)
- Available as … (COC), … patches (CTP), and vaginal … (CVR).
- Highly …-dependant methods where the failure rate if used perfectly (i.e. correctly and consistently) is less than …%.
- Certain factors such as the person’s …, … including diarrhoea and vomiting (COC only), and drug … (enzyme inducing drugs) may contribute to contraceptive failure.
- Prescriptions of up to … months’ supply for CHC initiation or continuation may be appropriate to avoid unwanted discontinuation and increased risk of pregnancy.
- Should not be continued beyond … years of age as safer alternatives exist.
- Available as tablets (COC), transdermal patches (CTP), and vaginal rings (CVR).
- Highly user-dependant methods where the failure rate if used perfectly (i.e. correctly and consistently) is less than 1%.
- Certain factors such as the person’s weight, malabsorption including diarrhoea and vomiting (COC only), and drug interactions (enzyme inducing drugs) may contribute to contraceptive failure.
- Prescriptions of up to 12 months’ supply for CHC initiation or continuation may be appropriate to avoid unwanted discontinuation and increased risk of pregnancy.
- Should not be continued beyond 50 years of age as safer alternatives exist.
Benefits of Combined Hormonal Contraceptives
- Reduced risk of …, … and … cancer;
- … bleeding patterns
- Reduced dys… and men…;
- Management of symptoms of p…, e… and … syndrome;
- Improvement of …;
- Reduced … symptoms;
- Maintaining … … density in peri-menopausal females under the age of … years.
- Reduced risk of ovarian, endometrial and colorectal cancer;
- Predictable bleeding patterns
- Reduced dysmenorrhoea and menorrhagia;
- Management of symptoms of polycystic ovary syndrome (PCOS), endometriosis and premenstrual syndrome;
- Improvement of acne;
- Reduced menopausal symptoms;
- Maintaining bone mineral density in peri-menopausal females under the age of 50 years.
Risks with Combined Hormonal Contraceptives
- … cancer and … cancer associated with current or recent use of CHC issmall, but is greater than that with progestogen-only or non-hormonal contraception.
- Venous and arterial …
- CHC is associated with a …-…-fold increase in VTE risk compared with non-use of CHC.
- Absolute risk of VTE during use of CHC is estimated by the European Medicines Agency to be between 5 and 12 per 10 000 women per year of use compared to 2 per 10 000 non-CHC users per year.
- NB VTE risk is lower during CHC use than during … and the … period.
- By reducing rates of … pregnancy, CHC use lowers the overall rate of VTE in the population in comparison to populations without access to effective contraception.
- CHC is associated with a …-…-fold increase in VTE risk compared with non-use of CHC.
- VTE events that do occur during use of CHC, approximately …% are fatal
- … (LNG), … (NET) and Nor… COC are associated with a lower risk of venous thromboembolic events than COC containing newer progestogens, the combined transdermal patch and the combined vaginal ring.
- COC containing higher EE (…) doses may be associated with greater risk of arterial thrombotic events than lower EE doses.
- Breast cancer and cervical cancer associated with current or recent use of CHC is
- small, but is greater than that with progestogen-only or non-hormonal contraception.
-
Venous and arterial thromboembolism
- CHC is associated with a 3- to 3.5-fold increase in VTE risk compared with non-use of CHC.
- Absolute risk of VTE during use of CHC is estimated by the European Medicines Agency to be between 5 and 12 per 10 000 women per year of use compared to 2 per 10 000 non-CHC users per year.
- NB VTE risk is lower during CHC use than during pregnancy and the postpartum period.
- By reducing rates of unplanned pregnancy, CHC use lowers the overall rate of VTE in the population in comparison to populations without access to effective contraception.
- CHC is associated with a 3- to 3.5-fold increase in VTE risk compared with non-use of CHC.
- VTE events that do occur during use of CHC, approximately 1% are fatal
- Levonorgestrel (LNG), norethisterone (NET) and norgestimate COC are associated with a lower risk of venous thromboembolic events than COC containing newer progestogens, the combined transdermal patch and the combined vaginal ring.
- COC containing higher EE (ethinylestradiol) doses may be associated with greater risk of arterial thrombotic events than lower EE doses.
What does this table show?
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Risks with combined hormonal contraceptives
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Options for how to use Combined Hormonal Contraception
- Standard use: How many days for pill/ how many rings/patch and what break?
- Shortened hormone-free interval: How many days for pill/ how many rings/patch and what break?
- Extended use: How many days for pill/ how many rings/patch and what break?
- Flexible extended use: How many days for pill/ how many rings/patch and what break?
- Continuous use: How many days for pill/ how many rings/patch and what break?
- Standard use: 21 days (21 active pills or 1 ring, or 3 patches) break of 7 days
- Tailored Use
- Shortened hormone-free interval: 21 days (21 active pills or 1 ring, or 3 patches) break of 4 days
- Extended use: 9 weeks ( 3 x 21 active pills or 3 rings, or 9 patches used consecutively) break = 4 or 7 days
- Flexible extended use: Continuous use (>21 days) of active pills, patches or rings until breakthrough bleeding occurs for 3-4 days. Break = 4 days
- Continuous use: Continuous use of active pills, patches or rings - no break
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Oral progestogen-only contraceptives
- Alter … … to prevent … and may inhibit … in some women;
- … desogestrel-only preparations consistently inhibit ovulation and this is their … mechanism of action.
- Progestogen-only contraceptives offer a suitable alternative to combined hormonal contraceptives when oestrogens are …
- Alter cervical mucus to prevent sperm penetration and may inhibit ovulation in some women;
- Oral desogestrel-only preparations consistently inhibit ovulation and this is their primary mechanism of action.
- Progestogen-only contraceptives offer a suitable alternative to combined hormonal contraceptives when oestrogens are contra- indicated.
Parenteral Progestogen-only contraceptives
- Medroxyprogesterone acetate (Depo-Provera®, SAYANA PRESS®) is a …-acting progestogen given by …;
- At least as effective as the … preparations
- … action, it may be used as a short-term or long-term contraceptive for women
- … return of … and … cycles may occur after discontinuation of treatment but there is no evidence of …
- Norethisterone enantate (Noristerat®) is a long-acting progestogen given as an oily injection which provides contraception for …; it is used as short-term interim contraception e.g. before vasectomy becomes effective.
- E…-releasing implant (Nexplanon®) is also available.
- Highly effective long-acting contraceptive, consisting of a single flexible rod that is inserted subdermally into the lower surface of the upper arm and provides contraception for up to … Local reactions such as bruising and itching can occur at the insertion site. The contraceptive effect of etonogestrel is rapidly reversed on removal of the implant.
- Medroxyprogesterone acetate (Depo-Provera®, SAYANA PRESS®) is a long-acting progestogen given by injection;
- At least as effective as the combined oral preparations
- Prolonged action, it may be used as a short-term or long-term contraceptive for women
- Delayed return of fertility and irregular cycles may occur after discontinuation of treatment but there is no evidence of permanent infertility.
- Norethisterone enantate (Noristerat®) is a long-acting progestogen given as an oily injection which provides contraception for 8 weeks; it is used as short-term interim contraception e.g. before vasectomy becomes effective.
-
Etonogestrel-releasing implant (Nexplanon®) is also available.
- Highly effective long-acting contraceptive, consisting of a single flexible rod that is inserted subdermally into the lower surface of the upper arm and provides contraception for up to 3 years. Local reactions such as bruising and itching can occur at the insertion site. The contraceptive effect of etonogestrel is rapidly reversed on removal of the implant
Intra-uterine progestogen-only device
- Mirena®, Jaydess® and Levosert® release … directly into the uterine cavity.
- Licensed for contraception and some licensed for the treatment of …
- Effects - prevention of endometrial …, thickening of cervical …, and suppression of … in some women (in some cycles), the intra-uterine system itself may contribute slightly to the contraceptive effect.
- Return of … after removal is rapid and appears to be complete.
- Advantages over … intra-uterine devices - improvement in any … and a reduction in blood loss; possible reduced pelvic … disease
- Mirena®, Jaydess® and Levosert® release levonorgestrel directly into the uterine cavity.
- Licensed for contraception and some licensed for the treatment of menorrhagia
- Effects - prevention of endometrial proliferation, thickening of cervical mucus, and suppression of ovulation in some women (in some cycles), the intra-uterine system itself may contribute slightly to the contraceptive effect.
- Return of fertility after removal is rapid and appears to be complete.
- Advantages over copper intra-uterine devices - improvement in any dysmenorrhoea and a reduction in blood loss; possible reduced pelvic inflammatory disease
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Comparative contraceptive success rates
- Perfect use of CHC - …% failure rate compared to …% typical use
- Perfect use of Progestogen-only injectable - …% failure rate compared to …% typical use
- Progestogen-only implant - …% failure rate
- Which is best in terms of success rates?
- Perfect use of CHC - 0.3% failure rate compared to 9% typical use
- Perfect use of Progestogen-only injectable - 0.2% failure rate compared to 6% typical use
- Progestogen-only implant - 0.05% failure rate
- Progestogen-only implant - best in terms of success rates
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Emergency Contraception
- Hormonal emergency contraceptives (includes levonorgestrel and ulipristal acetate) should be offered as soon as possible after unprotected intercourse if a … intra-uterine device is not appropriate or is not acceptable to the patient; either drug should be taken as soon as possible after unprotected intercourse to increase ….
- Hormonal emergency contraception administered after … is ineffective.
- Levonorgestrel is effective if taken within … hours (…) of unprotected intercourse and may also be used between … and … hours after unprotected intercourse [unlicensed use], but efficacy decreases with time.
- Ulipristal acetate is effective if taken within … hours (… days) of unprotected intercourse.
- Ulipristal acetate has been demonstrated to be … effective than levonorgestrel for emergency contraception.
- It is possible that a… could reduce the effectiveness of oral emergency contraception, particularly levonorgestrel; if BMI is greater than … g/m2 or body-weight is greater than … kg, it is recommended that either ulipristal acetate or a double dose of levonorgestrel [unlicensed indication] (see Emergency contraception under levonorgestrel) is given. It is unknown which is more effective.
- … should be considered as the first-line hormonal emergency contraceptive for a woman who has had unprotected intercourse 96–120 hours ago (even if she has also had unprotected intercourse within the last 96 hours). It should also be considered first line for a woman who has had unprotected sexual intercourse within the last 5 days if it is likely to have taken place during the 5 days before the estimated day of ovulation.
- Hormonal emergency contraceptives (includes levonorgestrel and ulipristal acetate) should be offered as soon as possible after unprotected intercourse if a copper intra-uterine device is not appropriate or is not acceptable to the patient; either drug should be taken as soon as possible after unprotected intercourse to increase efficacy.
- Hormonal emergency contraception administered after ovulation is ineffective.
- Levonorgestrel is effective if taken within 72 hours (3 days) of unprotected intercourse and may also be used between 72 and 96 hours after unprotected intercourse [unlicensed use], but efficacy decreases with time.
- Ulipristal acetate is effective if taken within 120 hours (5 days) of unprotected intercourse.
- Ulipristal acetate has been demonstrated to be more effective than levonorgestrel for emergency contraception.
- It is possible that a higher body-weight or BMI could reduce the effectiveness of oral emergency contraception, particularly levonorgestrel; if BMI is greater than 26 g/m2 or body-weight is greater than 70 kg, it is recommended that either ulipristal acetate or a double dose of levonorgestrel [unlicensed indication] (see Emergency contraception under levonorgestrel) is given. It is unknown which is more effective.
- Ulipristal acetate should be considered as the first-line hormonal emergency contraceptive for a woman who has had unprotected intercourse 96–120 hours ago (even if she has also had unprotected intercourse within the last 96 hours). It should also be considered first line for a woman who has had unprotected sexual intercourse within the last 5 days if it is likely to have taken place during the 5 days before the estimated day of ovulation.
Male Reproductive Endocrinology - Female Control
- GnRH released from hypothalamus
- Stimulates production LH and FSH from pituitary
- LH stimulates production of testosterone in Leydig Cells - negative feedback on GnRH and LH
- Male hormonal contraception - focus on increasing testosterone levels which exploits this loop - reduction of GnRH - decreases FSH and sperm production
- GnRH released from hypothalamus
- Stimulates production LH and FSH from pituitary
- LH stimulates production of testosterone in Leydig Cells - negative feedback on GnRH and LH
- Male hormonal contraception - focus on increasing testosterone levels which exploits this loop - reduction of GnRH - decreases FSH and sperm production
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Update on male hormonal contraception
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Update on male hormonal contraception
Giulia Gava and Maria Cristina Meriggiola Ther Adv Endocrinol Metab 2019, Vol. 10: 1–9
- … testosterone a week is an option (TE)
- Or long lasting testosterone (…)
- Or depot with TU and … combined
- 200mg testosterone a week is an option (TE)
- Or long lasting testosterone (TU)
- Or depot with TU and NETE combined
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Side Effects of Male Hormonal Contraceptives
- Testosterone-only regimens: a…, altered …, night …, … weight, and … changes.
- The combination of testosterone with a … allowed a reduction of testosterone dose minimizing … side effects.
- Progestins derived from …, which retain their androgenic activity, more often caused androgen-related adverse side effects such as …, … or decreased … …
- Interestingly, adverse side events reported by 93% of men on active treatment were also reported by 81% of men on placebo treatment.
- Testosterone-only regimens: acne, altered libido, night sweats, increased weight, and mood changes.
- The combination of testosterone with a progestin allowed a reduction of testosterone dose minimizing androgenic side effects.
- Progestins derived from nortestosterone, which retain their androgenic activity, more often caused androgen-related adverse side effects such as weight gain, acne, or decreased HDL- cholesterol.
- Interestingly, adverse side events reported by 93% of men on active treatment were also reported by 81% of men on placebo treatment.