Menstrual disorders Flashcards

1
Q

What is dysmenorrhoea?

A

Painful lower abdominal cramping which occurs before or during menstruation and affects QoL.

There are two types:
- Primary = absence of underlying pelvic pathology, occurs in young females. All secondary causes must be excluded.
- Secondary = underlying pelvic pathology e,.g. endometriosis, fibroids, PID, IUD insertion.

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2
Q

Causes of secondary dysmenorrohea

A
  • Endometriosis/adenomyosis = cyclic pain + prior menses
  • Fibroids = menorrohage + mass
  • PID
  • Ovarian Ca
  • Cervical Ca
  • IUD insertion, usually 3-6m after insertion
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3
Q

Investigations for dysmenorrhoea

A
  • abdo ex
  • pelvic ex +/- speculum
  • pregnancy test
  • HVS + ECS
  • cervical smear if due
  • USS
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4
Q

Dx criteria for primary dysmenorrhoea (6)

A

Primary dx is likely if:
1. Pain starts 6-12m after menarche, once cycles are regular.
2. Crampy lower abdo pain may radiate.
3. Pain starts before menstruation and lasts <72hrs, improves as menses progresses.
4. Non-gynae syx: N+V, diarrhoea, fatigue, irritability, dizziness, bloating, headache, lower back pain, emotional syx, are present.
5. Other gynae syx are NOT present.
6. Pelvic ex is normal.

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5
Q

Dx for secondary dysmenorrhoea (4)

A
  1. Pain starts after several years of painless periods.
  2. Pain is not consistently related to menstruation alone and may persist after menstruation finishes or may be present throughout + exacerbated by menstruation.
  3. Other syx present:
    - Gynae Syx = dyspareunia, PV discharge, menorrhagia, IMB, PCB
    - Non-Gynae Syx = rectal pain, bleeding etc
  4. Abnormal pelvic although absence of findings does not exclude dx.
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6
Q

Management of primary + secondary dysmenorrhoea

A

Primary
(1.) Non-pharm: heat pack, TENS
(2.) simple analgesia
(3.) mefenamic acid (NSAID)
(4.) Mirena. Note: Copper IUD not used as can cause heavier and painful periods
- Refer if syx are severe and not responded to Rx for 3-6m.

Secondary
(1.) manage depending on underlying cause
(2.) 2ww if ascites, pelvic or abdo mass OR abnormal cervix o/e OR persistent OMB, PCB with no features of infection/PID OR USS suggestive of cancer

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7
Q

What is Premenstrual Syndrome (PMS)? Presentation?

A

(1.) PMS refers to distressing psychological, emotional and physical syx that occurs prior to menstruation (luteal phase of menstrual cycle i.e. straight after ovulation).
- Syx can impact QoL
- Syx resolve once menstruation begins
- Syx not present before menarche, during pregnancy or after menopause.
(2.) When features are severe + significant effect on QoL = premenstrual dysphoric disorder.

Presentation can vary within individuals
(1.) psychological syx: Low mood, Anxiety, Mood swings, Irritability, loss of libido
(2.) physical syx: breast tenderness, bloating, clumsiness, headache

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8
Q

Dx of PMS

A

(1.) Syx Diary
- Spans two menstrual cycles.
- Demonstrates cyclical syx that occur before, and resolve after, onset of menstruation

(2.) GnRH analogue initiated by specialist:
- this halts menstrual cycle and temporarily induce menopause, to see if the syx resolve.
- this confirms dx

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9
Q

Management of PMS

A

(1.) Healthy lifestyle, exercise, diet, smoking cessation, sleep, stress etc.
(2.) Analgesia
(3.) COCP with no pill free interval - this suppresses ovulation + syx. For moderate PMS.
(4.) SSRI non-stop or during luteal phase e.g. day 15-28. For severe PMS.
(5.) Consider CBT
(6.) Hysterectomy + oophorectomy - pt must not want children

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10
Q

What is primary amenorrhoea?

A

Defined as not starting menstruation:
- By 13y when there is no other evidence of pubertal development
- By 15y where there are other signs of puberty, such as breast bud development

Puberty starts age 8-14 in girls. In girls, puberty starts with the development of breast buds, then pubic hair, and finally menstrual periods about two years from the start of puberty.

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11
Q

Causes of Primary Amenorrhoea

A

Normal secondary sexual characteristics present
- structural pathology e.g. imperforated hymen, absent uterus, vaginal agenesis, female genital mutilation

No secondary sexual characteristics
- turner’s - ovaries fail to develop
- kallman syndrome (delayed puberty + loss of smell)
- hypothalamic-pituitary dysfunction - e.g. stress, wt loss, and/or excessive exercise

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12
Q

Investigations of Primary Amenorrhoea

A

(1.) Assess evidence of puberty
(2.) Bloods
- baseline
- hormonal: FSH, LH, IGF1, prolactin, testosterone
(3.) Genetic testing for Turner’s
(4.) Imaging

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13
Q

Management of Primary Amenorrhoea

A

(1.) Replacement hormones - induce menstruation
- e.g. pulsatile GnRH in hypogonadotrophic hypogonadism (hypopituitarism or Kallman syndrome) to induce ovulation
- e.g. COCP in ovarian cause such as PCOS, absent ovaries

(2.) Manage stress, heathy weight gain if this is the cause

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14
Q

What is secondary amenorrhoea?

A

Defined as no menstruation for >3m after previous regular menstrual periods.

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15
Q

Causes of secondary amenorrhoea? (4Ps)

A

4P’s = Pregnancy, PCOS, prolactinoma, premature ovarian insufficiency

Gynae
- Pregnancy (most common)
- Menopause + premature ovarian failure
- Hormonal contraception
- Ovarian causes e.g. PCOS
- Uterine pathology e.g. Asherman’s syndrome

Non-gynae
- hypopituitarism or pituitary pathology
- Thyroid pathology
- Hyperprolactinaemia

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16
Q

Investigations for secondary amenorrhoea

A

(1.) Pelvic ex + speculum
(2.) Pregnancy test
(3.) Bloods: FSH, LH, testosterone, prolactin, TFT
- FSH, LH: primary ovarian failure (hi FSH), PCOS (hi LH), hypothalamic/pituitary problem (lo)
- Testosterone -> PCOS (hi), androgen tumour
- Prolactin, MRI if tumour suspected
- TSH -> hypo or hyperthyroidism
(4.) USS

17
Q

Management for secondary amenorrhoea

A

(1.) Establish Cause (PCOS, hypothyroidism, menopause, preg, wt loss, excessive exercise etc)
- gynae referral if premature ovarian insufficiency, asheman’s syndrome suspected
- endo referral if hyperprolactinoma, hi testerone not due to PCOS

(2.) Manage osteoporosis risk if amenorrhoea for >12m:
- Vit D, Ca, HRT or COCP

18
Q

What is Polycystic ovarian syndrome? Complications? Presentation?

A
  • Metabolic and reproductive condition.
  • Complications: T2DM, CVD, infertility, endometrial ca, OSA, anxiety + depression

Clinical features include:
- Oligomenorrhoea or amenorrhoea
- Infertility
- Obesity
- Hirsutism
- Acne

19
Q

Dx of Polycystic ovarian syndrome

A

Rotterdam Criteria - used for making a Dx, requires at least two of three key features:
1. Oligoovulation/anovulation - irregular or absent menstrual periods
2. Hyperandrogenism - hirsutism and acne
3. Polycystic ovaries on USS (>12 cysts per ovary)

20
Q

Investigations of Polycystic ovarian syndrome

A

(1.) Bloods:
- raised LH
- raised testosterone
- normal/raised oestrogen
- normal or low sex hormone-binding globulin (SHBG)
- raised insulin
- prolactin
- TSH

(2.) Calculate free androgen index (using SHBG + testosterone)

(3.) TV USS
- Follicles arranged around periphery of ovary - “string of pearls”
- Dx criteria either: 12 or more developing follicle in one ovary OR Ovarian volume >10cm

(4.) OGTT - screening for DM

21
Q

Management of Polycystic ovarian syndrome

A

(1.) Mx DM/obesity/CVD risk= wt loss, diet, exercise, smoking cessation, stain if QRISK >10%

(2.) Ameno/oligmenorrhoea = cyclic progesterones or low dose COCP

(3.) TVUS: if ET >7-10mm -> refer

Managing infertility
(1.) Wt loss
(2.) Refer for clomifene (1st line) or metformin. Laparoscopic ovarian drilling or IVF may be considered too.

22
Q

What is menopause? Postmenopause? Perimenopause? Premature menopause?

A

(1.) Menopause is the point at which menstruation stops. Average age is 51y. It is caused by lack of ovarian follicular function causing the following:
- Low oestrogen + progesterone levels
- hi LH + FSH due to absence of negative feedback from oestrogen

(2.) Postmenopause = 12m after final menstrual period

(3.) Perimenopause = time around menopause (time leading up to + 12m after), may experience vasomotor syx and irregular periods.

(4.) Premature menopause = menopause <40y (premature ovarian insufficiency)

23
Q

Perimenopausal syx?

A

Caused by lack of oestrogen:
- PMS
- irregular menstrual periods
- secondary amenorrhea
- hot flushes, night sweats, vaginal dryness.

24
Q

Risks associated with menopause?

A
  • CVD + Stroke
  • Osteoporosis
  • Pelvic organ prolapse
  • Urinary incontinence
25
Q

Dx of menopause?

A

DX can be made in >45y with typical syx, without performing any investigations.

Consider FSH blood test in following:
- <40y with suspected premature menopause
- 40-45y with syx or change in menstrual cycle

Blood results:
- High FSH + LH
- Low progesterone + oestrogen

26
Q

Management of menopause?

A

Contraception for:
- 2y after LMP in <50y
- 1y after LMP in >50y
- until 51y if premature ovarian insufficiency
- note: it does not affect menopause but may mask syx which can make dx hard.

Consider Rx if interfering with life:
(1.) No Rx, syx resolves after 2-5y. Advise healthy lifestyle.
(2.) HRT - cyclic in peri, continous in postmenopausal.
(3.) SSRI (FLuoxetine for FLUshes)
(4.) Topical oestrogen = vaginal dryness and atrophy (can be used alongside systemic HRT)
(5.) CBT

27
Q

What is Premature Ovarian Failure? Causes?

A
  • Menopause <40y
  • Hi risk of CVD, stroke, osteoporosis, cognitive impairment due to lack of oestrogen
  • Characterised by hypergonadotropic hypogonadism
  • Cause is idiopathic (50%), iatrogenic, AI, genetic, infection e.g. mumps, TB, CMV.
28
Q

Dx of Premature Ovarian Failure

A

<40y with
- menopausal syx PLUS
- elevated FSH (must be raised on TWO consecutive samples >4w apart)

29
Q

Management of Premature Ovarian Failure

A

HRT + contraception until 51y

30
Q

When would you give cyclic and continuous HRT

A
  • Cyclic Rx = perimenopausal women (had a period within <1y)
  • Continuous Rx = postmenopausal women (no period for 1y or more)
31
Q

When would you give oestrogen only HRT

A

Oestrogen only HRT is indicated in those with no uterus only

32
Q

Menopausal women - should they still be using contraceptives?

A

Yes!

  • 2y after LMP in <50y
  • 1y after LMP in >50y
  • until 51y if premature ovarian insufficiency