Fertility Control Flashcards

1
Q

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
  • 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
A
  • 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
  • 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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2
Q

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.
A
  • 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.
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3
Q

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.
A
  • 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.
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4
Q

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.
  • 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.
A
  • 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.
  • 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.
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5
Q

What does this table show?

A

Risks with combined hormonal contraceptives

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6
Q

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?
A
  • 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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7
Q

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 …
A
  • 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.
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8
Q

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.
A
  • 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
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9
Q

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
A
  • 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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10
Q

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?
A
  • 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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11
Q

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.
A
  • 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.
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12
Q

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
A
  • 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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13
Q

Update on male hormonal contraception

A
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14
Q

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
A
  • 200mg testosterone a week is an option (TE)
  • Or long lasting testosterone (TU)
  • Or depot with TU and NETE combined
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15
Q

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.
A
  • 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.
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