Subfertility Flashcards

1
Q

CONCEPTION

what percentage of women will conceive within 1 year?

A
  • 80% couples will conceive within 1 year if; the woman is under 40, they do not use contraception and have regular intercourse
  • Of those that do not conceive in the first year about half will conceive in the second year
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2
Q

CONCEPTION

what factors will affect a womans ability to convceive?

A

alcohol
smoking
weight

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3
Q

CONCEPTION

alcohol

A
  • Women – drinking no more than 1 or 2 units of alcohol once or twice a week and avoiding episodes of intoxication reduces risk of harming the developing fetus
  • Men – alcohol consumption within DoH reccomdendation won’t affect semen quality. Excessive alcohol detrimental to sperm
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4
Q

CONCEPTION

smoking

A
  • Women – reduce fertility/ passive smoking can affect their chance of conceiving
  • Men – association with smoking and reduced semen quality (impact on male fertility is uncertain
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5
Q

CONCEPTION

weight

A
  • BIM >30 likely to take longer to conciver
  • Women with BMI <19 with amenorrhoea/oligomehorrhoea, increasing body weight improves chance of conception
  • Men with BMI >30 have reduced fertility
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6
Q

list some causes of female infertility

A
  • Tubal pathology
  • Ovulatory disorder
  • Uterine factor
  • Unexplained
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7
Q

FEMALE INFERTILITY

tubal pathology

A
  • Pelvic inflammatory disease, endometriosis and previous ectopic pregnancy can result in tubal pathology
  • PID is infection of upper part of female reproductive tract (uterus, fallopian tubes and ovaries). It is caused by bacteria spreading from vagina and cervix, most commonly as a result of unprotected intercourse. Most common bacteria is chlamydia
  • Women without these comorbidities should be offered hysterosalpingography or hysterosalpingo-contrast-ultrasonography to screen for tubal occlusion
  • Women who have comorbidities should be offered laparoscopy and dye test so other pelvic pathology can be assessed
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8
Q

FEMALE INFERTILITY

chlamydia

A
  • Chlamydia trachomatis – obligate intracellular parasite, weakly gram negative
  • 3x as many women as men diagnosed with chlamydia
  • Mainly asymptomatic
  • Women 15-39 have highest prevelance, followed by women aged 20-24
  • Infection can spread to upper genital tract I women causing pelvic inflammatory disease and can result in future infertility or ectopic pregnancy
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9
Q

FEMALE INFERTILITY

endometriosis

A
  • Cells similar to those in endometrium grows outside of it. Most often this is on ovaries, fallopian tube, peritoneum, pelvic side in rare cases, may occur in parts of body such as lungs
  • Main symptoms are dysparinurea, pelvic pain, infertility and dysmenorrhea
  • Nearly half of those affected have chronic pelvic pain, 70% pain occurs during menstruation
  • 40% infertile
  • Less common symptoms – urinary or bowel symptoms
  • 25% have no symptoms
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10
Q

FEMALE INFERTILITY
endometrioma
1. pathogenesis
2. surgical treatment

A
  1. 1) invagination and subsequent collection of menstrual debris from endometriotic implants, which are located on the ovarian surface and
    2) adherent peritoneum and colonization of functional ovarian cysts by endometriotic cells.
  2. Surgery aims to eliminate endometriotic tissue and to provide sufficient tissue for histological assessment, and to preserve a maximum amount of normal ovarian tissue (where fertility is desired and/or risk of menopause is to be avoided). It has been shown that surgical treatment of endometriotic cysts is associated with the unintentional removal or destruction of ovarian follicles
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11
Q

tests for tubal patency

A
  • hysterosalpingography
  • Hysterosalpingo-contrast-ultrasonography
  • laparoscopy and dye
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12
Q

FEMALE INFERTILITY

what are uterine factors

A

Uterine fibroids (leiomyomas) are benign smooth muscle tumours of the uterus and grow anywhere in the womb and vary in size considerably

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13
Q

FEMALE INFERTILITY

what are the main types of uterine fibroids

A
  • Intramural fibroids – most common, develop in musce wall of the womb
  • subserosal fibroids – fibroids that develop outside the wall of the womb into the pelvis and can become very large
  • submucosal fibroids – fibroids that develop in the muscle layer beneath the womb’s inner lining and grow into the cavity of the womb
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14
Q

FEMALE INFERTILITY

how should uterine fibroids me managed in infertile couples

A
  • In infertile women, appropriate evaluation and classification of fibroids, particularly those involving or suspected to be involving the endometrial cavity is essential.
  • Submucosal fibroids (should be treated hysteroscopically or laparoscopic for large L2) to improve conception rates.
  • The management of intramural fibroids should be individualised on a case to case basis subserosal fibroid are unlikely to have any major impact on fertility
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15
Q

FEMALE INFERTILITY

uterine polyps

A
  • Overgrowth of endometrial cells (cells in the lining of the uterus) can lead to the formation of uterine polyps, also known as endometrial polyps. These polyps are usually noncancerous (benign), although some can be cancerous
  • Uterine polyps range in size from a few millimeters to several centimeters. They attach to the uterine wall by a large base or a thin stalk.
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16
Q

FEMALE INFERTILITY

uterine polyps signs and symptoms

A
  • Irregular menstrual bleeding
  • Bleeding between menstrual periods
  • Excessively heavy menstrual periods
  • Vaginal bleeding after menopause
  • Infertility - Polyps can cause infertility by disrupting the lining of the uterus, thus interfering with implantation of a fertilized embryo.
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17
Q

FEMALE INFERTILITY

anovulation

A
  • when the ovaries do not release an oocyte during a menstrual cycle and thus a common cause of infertility
  • Oligomenorrhoea is infrequent menstruation. Usually with menstrual periods occurring at intervals of greater than 35 days, with only four to nine periods in a year.
  • Amenorrhea is the absence of a menstrual period in a woman of reproductive age. Physiological states of amenorrhoea are seen, most commonly, during pregnancy and lactation
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18
Q

anovulation

WHO classification

A
  • WHO1 (15%) – Hypothalamic-pituitary failure. (hypogonadotrophic hypogonadism)
  • WHO2 (80%) – Hypothalamic-pituitaryovarian dysfunction (predominately PCOS)
  • WHO3 (5%) – Ovarian failure (hyper-gonadotropic, hypo-estrogenic)
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19
Q

anovulation

describe hypothalamic pituitary failure (WHO 1)

A
  • Results from gonadal failure due to abnormal pituitary gonadotropin levels from either – absenct or inadequate hypothalamic GnRH secretion or failure of pituitary gonadotropin secretion
  • tumor of the hypothalamic pituitary region
  • Functional forms of Hypothalamicpituitary failure are characterized by a transient defect in GnRH secretion, and are relatively common in women, in response to significant weight loss, exercise, or stress leading to hypothalamic amenorrhea.
  • characterized by low circulating sexual steroids associated with low or inappropriately normal gonadotropin levels. Low
  • LH/FSH. Low oestrogen
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20
Q

PCOS

  1. symptoms
  2. diagnosis
  3. other differentials
A
  1. menstrual irregularities, hirsutism (increased body and facial hair), acne and infertility.
  2. • Revised Rotterdam Criteria
    •Two of the following three criteria are required:
    1: oligo/anovulation
    2: hyperandrogenism - clinical (hirsutism) or biochemical (raised FAI or free testosterone)
    3: polycystic ovaries on ultrasound
  3. Other aetiologies must be excluded such as congenital adrenal hyperplasia, androgen secreting tumours, Cushing syndrome, thyroid dysfunction and hyperprolactinaemia
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21
Q

OVARIAN FAILURE

  1. what is it
  2. causes
A

1.Namely Premature Ovarian Failure. The loss of function of the ovaries before the age 40. Associated: Amenorrhea, hypergonadotropism, and hypoestrogenism.

2. • Usually idiopathic 
• Genetic include Turners syndrome and Fragile X Syndrome
• Smoking Radiation/chemotherapy 
• Autoimmune disease 
• High FSH/LH, low oestrogen
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22
Q

MALE INFERTILITY

ageing man

A
  • Oxidative damage to sperm DNA – most sensitive is chromosome 15
  • Increase in
    • Complex neurological conditions; autism, bipolar disease, schizophrenia, severe epilepsy
    • Dominant genetic disorders
    • Cleft palate, diaphragmatic hernia, cardiac malformations
    • Miscarriages
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23
Q

MALE INFERTILITY

WHO reference values for sperm

A
  • Semen volume: 1.5 ml or more
  • Sperm concentration: 15 million spermatozoa per ml or more
  • Total sperm number: 39 million spermatozoa per ejaculate or more
  • Total motility (percentage of progressive motility and non-progressive motility): 40% or more motile or 32% or more with progressive motility
  • Vitality: 58% or more live spermatozoa
  • Sperm morphology (percentage of normal forms): 4% or more
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24
Q

MALE INFERTILITY

when should semen analysis be repeated?

A
  • If the result of the first semen analysis is abnormal, a repeat confirmatory test should be offered.
  • Repeat confirmatory tests should ideally be undertaken 3 months after the initial analysis to allow time for the cycle of spermatozoa formation to be completed. However, if a gross spermatozoa deficiency (azoospermia or severe oligozoospermia) has been detected the repeat test should be undertaken as soon as possible
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25
Q
  1. aspermia
  2. azoospermia
  3. oligozospermia
  4. asthenozoospermia
  5. teratozoospermia
  6. necrozoospermia
A
  1. absence of semen
  2. absence sperm
  3. very low sperm count
  4. poor sperm motility
  5. sperm carry more morphological defects than usual
  6. all sperm in the ejaculate are dead
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26
Q

causes of male factor infertility

A
  • hypothalamus/pituitary malfunction and consequently an inadequate stimulation of otherwise normal genital tract and testicles
  • tumors (craniopharynioma, pituitary adenomas, metastases),
  • irradiation
  • head injury
  • debilitating illness(hemochromatosis, sarcoidosis, tuberculosis),
  • syndroms:Kallmann’s, Prader-Willi, Laurence- Moon-Biedl idiopathic
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27
Q

investigations for male factor infertility

A
  • specific history

* low levels of follicle stimulating hormone(FSH) and luteinizing stimulating hormone (LH) modern pulsatile pump

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28
Q

treatment for male factor infertility

A
  • pulsatile replacement of gonadotropin releasing hormone(GnRH)
  • injections of gonadotropins(FSH/LH) usually hCG or hMG ( human chorionic or menopausal gonadotropin )
29
Q

what should not be offered to men with male factor infertility

A
  • Men with idiopathic semen abnormalities should not be offered antioestrogens, gonadotrophins, androgens, bromocriptine or kininenhancing drugs because they have not been shown to be effective.
  • Men should be informed that the significance of antisperm antibodies is unclear and the effectiveness of systemic corticosteroids is uncertain.
  • Men with leucocytes in their semen should not be offered antibiotic treatment unless there is an identified infection because there is no evidence that this improves pregnancy rates.
30
Q

non obstructive azoospermia (hypergonadotropic testicular failure)

A
  • Causes: atrophic or absent testes
  • Anorchism: loss of testes (trauma, torsion, tumor-chemo/radiotherapy)
  • Infections; mumps, orchitis Immunisation!!!, treat !
  • Gonadal dysgenesis-defective Y chromosome you may still get some sperm
  • Klinefelter’s Syndrome
  • Cryptorchidism Operate early
31
Q

obstructive azoospermia (post testicular)

A
  • Causes: Male reproductive tract obstruction. Sperm are still produced, but not
  • ejaculated FSH,LH usually normal.
  • Consider genetic testing for microdeletion of Y Chromosome and cystic fibrosis

• Causes of post-testicular azoospermia:

  • Congenital absence of the vas deferens.
  • Cystic fibroisis (CF) gene mutation analysis should performed prior to treatment, because these men are at a higher risk for carrying CF gene mutation.
  • Unilateral renal agenesis (URA)
  • Acquired due to vasectomy, infection or other injury to the male reproductive Tract.
32
Q

surgical management of male infertility

A
  • Where appropriate expertise is available, men with obstructive azoospermia should be offered surgical correction of epididymal blockage because it is likely to restore patency of the duct and improve fertility. Surgical correction should be considered as an alternative to surgical sperm recovery and IVF(NICE 2014).
  • Men should not be offered surgery for varicoceles as a form of fertility treatment because it does not improve pregnancy rates
33
Q

assisted conception treatment strategies

A
  • IVF - own and/or donor sperm
  • intracytoplasmic sperm injections (ICSI)
  • intrauterine insemination donor sperm
34
Q

intracytoplasmic sperm injection (ICSI)

A

own sperm or in combination with:
• MESA – Microsurgical Epididymal Sperm Aspiration
• PESA – Percutaneous Epididymal Sperm Aspiration
• TESE – Testicular Sperm Extraction
• TESA -Percutaneous Testicular Sperm Aspiration

35
Q

intrauterine insemination donor sperm

A
  • Minimally invasive techniques of obtaining sperm from either the epididymis or testis can be performed under local anesthetic
  • With limited frozen sperm specimen ICSI is treatment of choice
36
Q

INVESTIGATING FERTILITY PROBLEMS

history

A

history of pelvic infections, chlamydia, pregnancies with another partner, Terminations of pregnancies. Medical conditions, leisure activities, occupation, as they can all help in a diagnosis.

37
Q

INVESTIGATING FEMALE INFERTILITY

menstruation

A

frequency and regularity of their menstrual cycles. Serum progesterone in the mid-luteal phase of their cycle (day 21 of a 28-day cycle) to confirm ovulation even if they have regular menstrual cycles

38
Q

INVESTIGATING FEMALE INFERTILITY

women with prolonged irregular menstrual cycles

A

should be offered a blood test to measure serum progesterone. Depending upon the timing of menstrual periods, this test may need to be conducted later in the cycle (for example day 28 of a 35-day cycle) and repeated weekly thereafter until the next menstrual cycle starts.

39
Q

INVESTIGATING FEMALE INFERTILITY

women with irregular menstrual cycles

A

should be offered a blood test to measure serum gonadotrophins (follicle-stimulating hormone and luteinising hormone)

40
Q

INVESTIGATING FEMALE INFERTILITY

who should be offered prolactin test?

A

This test should only be offered to women who have an ovulatory disorder, galactorrhoea or a pituitary tumour.

41
Q

INVESTIGATING FEMALE INFERTILITY

when should thyroid function be tested?

A

Women with possible fertility problems are no more likely than the general population to have thyroid disease. Testing of thyroid function should be confined to women with symptoms of thyroid disease.

42
Q

INVESTIGATING FEMALE INFERTILITY

what should be offered to women who are not known to have comorbidities such as PID, ectopics, endometriosis?

A

hysterosalpingo-contrastultrasonography or hysterosalpingography to screen for tubal occlusion because this is a reliable test for ruling out tubal occlusion, and it is less invasive and makes more efficient use of resources than laparoscopy.

43
Q

INVESTIGATING FEMALE INFERTILITY

what should be offered to women with comorbidities such as PID, ectopics, endometriosis?

A

offered laparoscopy and dye so that tubal and other pelvic pathology can be assessed at the same time

44
Q

INVESTIGATING FEMALE INFERTILITY

what is ovarian reserve?

A

A term that is used to determine the capacity of the ovary to provide eggs that are capable of fertilisation resulting in a healthy and successful pregnancy.

45
Q

INVESTIGATING FEMALE INFERTILITY
ovarian reserve
pathophysiology and main contributing factor

A
  • FSH is produced by the pituitary and travels through the blood to the ovaries where it stimulates the growth of follicles. A normal FSH level is somewhere between 2-8.9: this is enough to support the growth of one follicle. Measure day 2-5 of the cycle
  • AMH is produced by the growing follicles and is a direct marker of the number of follicles. AMH varies with age but normal levels are somewhere between 3 and 35. Lower levels are indicative of poor reserve and higher levels associated with, but not diagnostic of, polycystic ovaries. AMH varies less through the cycle and so can be measured at any time
  • Antral follicle count is performed via USS to count the number of follicles measuring 2 to 10 mm in greatest diameter to predict response IVF
  • Age is, however, the ultimate marker of ovarian reserve. In general, older women with good reserve are likely to do less well in IVF than younger women with poor reserve.
46
Q

MANAGEMENT OF FEMALE INFERTILITY

for unexplained fertility

A
  • NO ovarian stimulation agents (such as clomifene citrate,or letrozole)
  • clomifene citrate as a standalone treatment does not increase the chances of a pregnancy or a live birth
  • Advise women who are having regular unprotected sexual intercourse to try to conceive for a total of 2 years (this can include up to 1 year before their fertility investigations) before IVF will be considered.
  • Offer IVF treatment to women with unexplained infertility who have not conceived after 2 years (this can include up to 1 year before their fertility investigations) of regular unprotected sexual intercourse.
47
Q

MANAGEMENT OF FEMALE INFERTILITY

for women with proximal tubal obstruction

A

selective salpingography plus tubal catheterisation, or hysteroscopic tubal cannulation, may be treatment options because these treatments improve the chance of pregnancy.

48
Q

MANAGEMENT OF FEMALE INFERTILITY

for women with hydrosalpinges

A

offered salpingectomy, preferably by laparoscopy, before IVF treatment because this improves the chance of a live birth.

49
Q

MANAGEMENT OF FEMALE INFERTILITY

for women with amenorrhoea found to have intrauterine adhesions?

A

offered hysteroscopic adhesiolysis because this is likely to restore menstruation and improve the chance of pregnancy.

50
Q

MANAGEMENT OF FEMALE INFERTILITY

women with suspected polyp

A

Most doctors advise hysteroscopy and polyp removal if a polyp is suspected before stimulation for IVF. However, the clinical evidence and benefit of different management options during assisted reproduction technology cycles are conflicting. Currently, there is insufficient evidence to recommend one particular option over others when a polyp is suspected during stimulation for in vitro fertilisation.

51
Q

MANAGEMENT OF FEMALE INFERTILITY

women with hypothalamic pituitary ovarian dysfunction (mainly PCOS)

A
  • Advise women with WHO Group II anovulatory infertility who have a BMI of 30 or over to lose weight.
  • This alone may restore ovulation, improve their response to ovulation induction agents, and have a positive impact on pregnancy outcomes.
52
Q

MANAGEMENT OF FEMALE INFERTILITY

women with ovarian failure

A

IVF with donor eggs/adoption

53
Q
MANAGEMENT OF FEMALE INFERTILITY
ovulatory disorders (most commonly PCOS)
A

Ovulation Induction
• This is the process of stimulating ovulation (of a single follicle) by use of oral agents e.g
• Clomiphene citrate:-blocking the action of oestrogen in an area of the brain called the hypothalamus
• Metformin
• or combination of both
• Either way, the hypothalamus responds by sending a stronger signal to the pituitary, which then releases increased amounts of FSH and LH – the two hormones responsible for egg growth and, ultimately, ovulation.

54
Q

MANAGEMENT OF FEMALE INFERTILITY

what are the risks of ovulation induction

A
  • Multiple pregnancy
  • Metformin should be informed of the side effects associated with its use (such as nausea, vomiting and other gastrointestinal disturbances).
55
Q

MANAGEMENT OF FEMALE INFERTILITY

managing super ovulation/controlled ovarian hyperstimulation

A
  • Also known as controlled ovarian hyperstimulation, is the process of inducing a woman to release more than one egg in a month.
  • This treatment is for women with Hypogonadotrophic Hypogonadism or PCOS or PCOS with failed clomiphene Rx.
  • The treatment is started between days 3 - 5 of the cycle, by daily injection with the follicle stimulating drug. The treatment is monitored by ultrasound scans and blood tests as necessary to reduce risk of overstimulation/multiple pregnancy.
  • When the biggest follicle reaches 17mm in diameter, with no more than 2 others of this size, an injection of a different hormone (Human Chorionic Gonadotrophin - HCG) is given to induce ovulation with planned intercourse.
56
Q

MANAGEMENT OF FEMALE INFERTILITY

management of PCOS women resistant to clomiphene

A

Laparoscopic ovarian drilling
• This is a surgical treatment that can trigger ovulation in women with PCOS , trying to get pregnant but you have not been able to ovulate despite losing weight and using clomiphene, with or without metformin.
• Approximately 80% of patients who undergo ovarian drilling resume ovulation, while nearly 50% were able to become pregnant within a year.
• Less likely to have twins or triplets compared to other fertility treatments (which are as high as 10%).

57
Q

MANAGEMENT OF FEMALE INFERTILITY

IVF fertilisation - describe the process

A

Fertilisation of an egg with sperm outside the body, in vitro (“in glass”). The process involves monitoring and stimulating a woman’s ovulatory process, removing an ovum or ova (egg or eggs) from the woman’s ovaries and letting sperm fertilise them in a liquid in a laboratory. The fertilised egg (zygote) undergoes embryo culture for 2–6 days, and is then transferred to the same or another woman’s uterus, with the intention of establishing a successful pregnancy

58
Q

IVF FERTILISATION

egg retrieval

A

Under ultrasound guidance, the operator inserts a needle through the vaginal wall and into an ovarian follicle, taking care not to injure organs located between the vaginal wall and the ovary. The other end of the needle is attached to a suction device. Once the follicle is entered, suction is gently applied to aspirate follicular fluid and with it, hopefully, cellular material including the oocyte.

59
Q

IVF FERTILSATION

embryo transfer

A

Embryo transfer is performed either at the cleavage stage (day 2 to 4) or the blastocyst stage (day 5 or 6). A soft transfer catheter is loaded with the embryo. The catheter is inserted through the cervical canal and advanced into the uterine cavity. Correct placement, which is 1–2 cm from the uterine fundus. Anaesthesia is generally not required. After withdrawal, the catheter is handed to the embryologist, who inspects it for retained embryos.

60
Q

IVF FERTILSATION

embryo number

A
  • The appropriate number of embryos to be transferred depends on the age of the woman, whether it is the first, second or third full IVF cycle attempt and whether there are top-quality embryos available. The technique of selecting only one embryo to transfer to the woman is called elective-single embryo transfer (eSET) or, when embryos are at the blastocyst stage, elective single blastocyst transfer (e-SBT).
  • This significantly lowers the risk of multiple pregnancies, e-SET twin rate 3.5% vs 38% with 2 embryos transferred. e–SBT twin rate 2% vs 25% with 2 blastocysts transferred. At the same time, pregnancy rates are not significantly less with e-SBT compared to transferring 2 blastocysts.
61
Q

CONTRACEPTION
condoms
1. method
2. useful info

A
  1. physical barrier

2. relatively low success rate, especially in young people, protects against STI

62
Q

CONTRACEPTION
combined oral contraceptive pill
1. method
2. what does it increase the risk of?

A
  1. inhibits ovulation

2. increases risk of VTE, increases risk of breast and cervical cancer

63
Q

CONTRACEPTION
progesteron only pill (excluding desogestrel)
1. method
2. common side effect

A
  1. thicken cervical mucus

2. irregular bleeding

64
Q

CONTRACEPTION
injectable contraceptive (medroxyprogesterone acetate)
1. method
2. how long does it last

A
  1. inhibits ovulation and thickens cervical mucus

2. 12 weeks

65
Q
CONTRACEPTION
implantable contraceptive (etongestrel)
1. method
2. common side effect
3. how long does it last?
A
  1. inhibits ovulation and thickens cervical mucus
  2. irregular bleeding
  3. 3 years
66
Q

CONTRACEPTION
intrauterine contraceptive device
method

A

decreases sperm motility and survival

67
Q

CONTRACEPTION
intrauterine system (levonorgestrel)
1. method
2. common side effect

A
  1. prevents endometrial proliferation and thickens cervical mucus
  2. irregular bleeding
68
Q

CONTRACEPTION

methods of emergency contraception and mode of action

A

levonorgestrel - inhibit ovulation
ulipristal - inhibits ovulation
intrauterine contraceptive device - toxic to sperm and ovum and also inhibits implantation