NM701 - Module 5 - AUB (abnormal uterine bleeding) and Pelvic Pain

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113 Terms

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Common causes of anovulation include:

PATHOLOGIC:

thyroid/pituitary disorders - (if too little or too much)

hyperprolactinemia

iatrogenic (radiation/meds)

PCOS - (one of the hallmarks of PCOS is oligo-ovulation)--- that may stretch out into long enough time periods that we call it anovulation)

PHYSIOLOGIC:

pregnancy (most common)

lacation

perimenarche (immature HPO axis)

perimenopause (not as sensitive to FSH and cycles space out)

low/high BMI

excessive exercise

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Estrogen levels will

increase the thickness of the endometrium

high estrogen = heaviest bleeding

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Explain why excessive uterine bleeding may be a sign of endometrial hyperplasia or cancer

Although rare, long periods of anovulation in the presence of unopposed estrogen can predispose to developing endometrial cancer.

Hyperplasia can mutate the cells of the lining that can become cancerous.

hyperplasia or cancer always a possible cause of heavy or irregular uterine bleeding, especially when a woman has been anovulatory for a long time

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What methods can rule out endometrial cancer?

Start with TVUS and move to biopsy only if imaging findings are suspicious.

A thin endometrium on TVUS can rule out endometrial cancer (less invasive)

Timing of the ultrasound is important to avoid false positives

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Age of onset for endometriosis

adolescent to early adulthood

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Age of onset for PCOS, adenomyosis, PMS, endometrial hyperplasia

middle to late reproductive years

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Age of onset for ovarian/breast cancer

post menopausal

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Intense itching of the vulva may be associated with:

lichen sclerosis, yeast vaginitis, contact dermatitis

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What is the origin of most chronic pelvic pain?

About 2/3 of chronic pelvic pain has a GI or GU origin

other causes:

abortion

ectopic

PID

ovarian pain

adrenal tension

fibroids

dyspareunia

endometriosis

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What are the most encountered diagnoses in gynecologic care?

amenorrhea

abnormal uterine bleeding

hyper androgenic disorders

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Amenorrhea

NO pd x 3mos OR

6mos if cycles are irregular

this and anovulation can occur when estrogen is present or absent

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How can we effectively rule out endometrial hyperplasia or cancer?

via TVUS and if they endometrial lining is less than 4mm thick

endometrial sampling is indicated if lining is large

**for many perimenopausal women, lining will be thick UNLESS ORDERED WITHIN THE FIRST 5 DAYS OF THE PD**

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dysmennorhea

painful menstrual cramps

primary in young people is normal with high prostaglandins

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Anovulation in a rich environment means the body gets stuck in

LACK OF PROGESTERONE - the luteal phase leading to hyperplasia and random painless disorganized bleeding

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causes of Intermenstrual periods

fragile or inflamed tissue on the cervix, vagina or higher in the reproductive tract

cervical polyps

cervical cx

STI's

ectropion

irregularly sloughing hyperplastic endometrium

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When does intermenstrual bleeding occur?

either with regular or irregular periods

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Causes of prolonged bleeding

pelvic pathology

endometriosis

hypo androgenic disroders

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A change in the TIMING of the period is caused by

a hormonal change such as:

GNRH

release patterns of FSH, LH

no progesterone

Examples:

Thyroid disorder

PCOS

endometrial hyperplasia

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A change in the BLEEDING is caused by

a structural or systemic change (mostly structural)

Leiomyomas (Fibroids)

adenomyosis

Examples:

polyps (spotting)

blood dyscrasias

rarely von willebrands disease

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NO BLEEDING (amenorrhea) can be caused by

EITHER hormonal or structural changes

Ex:

Outflow obstruction

elevated prolactin

pregnancy

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F. is a 24-year-old woman who reports that her last period was 5 months ago. Her periods have always been irregular, with 7-8 periods per year. She is sexually active and uses condoms for contraception. F. has never been pregnant. She has had screening Paps since age 21 and both have been normal. F's prior medical history is uncomplicated. Her past surgical history includes repair of an ankle ligament in high school. She is training for a marathon and has intentionally lost 15 pounds in the last few months.

Review of systems:

increasing acne and hair growth on her chin

more frequent headaches, some with nausea and vomiting.

Based on F's history, the clinician can safely conclude that F has:

secondary ammenorrhea

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Based on F's history and review of systems, EXPECTED history and exam findings would be:

hirsutism

acanthosis nigricans

lack of PMS

dysmenorrhea

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What lab tests are necessary in someone with secondary amenorrhea?

Pregnancy test (always R/O first!)

TSH

Prolactin

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Which is true regarding making a diagnosis of polycystic ovary syndrome (PCOS)

oligo-ovulation and clinical signs of hyperandrogenism

According to the Rotterdam criteria, these 2 criteria are sufficient for diagnosis once other conditions are excluded.

*DIAGNOSIS OF EXCLUSION*

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with PCOS, what is true about a progestogen test?

likely to bleed after the PCT because her estrogen levels are adequate to develop an endometrium

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with PCOS considering differential diagnosis?

Pituitary tumors or dysfunction are possible considering bleeding pattern and symptoms.

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If lab testing confirms PCOS, management should include:

incorporating reproductive life goals in the plan.

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What is true regarding using combined oral contraceptives (COCs) to manage PCOS?

COCs raise sex hormone binding globulin because they are administered orally, which may help bind free androgens and reduce new hair growth.

COCs typically improve acne as well.

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B. is a 46-year-old woman who presents with "period problems." She reports that her periods have been getting progressively heavier for about 3 years, but it's getting to the point now that she has a hard time leaving the house the first 3 days of her period because they are so heavy. Her periods are generally regular, with a 26-day cycle length. Her husband had a vasectomy 10 years ago. She had three normal vaginal deliveries without pregnancy or birth complications. Surgical history includes only an appendectomy at age 25. B. is a 1 pack per day smoker. A review of systems is significant for headaches, recent constipation, and dry skin. Her BMI is 31.

___________________________________________________

Possible differential diagnoses for B currently include:

anemia

AUB-E

perimenopause

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abnormal bleeding patterns are associated with

a large, tender uterus

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Which diagnsotic tests to order if you think the patient has prolactinemia?

An endometrial biopsy or transvaginal ultrasound early in the cycle to evaluate the endometrium.

Yes, endometrial hyperplasia and endometrial cancer are don't-miss-it diagnoses. This woman's endometrium must be evaluated in some way because she is experiencing progressively worsening heavy menstrual bleeding

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If a patient is dx with AUB, a safe option is

MONOPHASIC birth control

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B asks about a hysterectomy to address her heavy menstrual bleeding. An appropriate response from the clinician is:

Hysterectomy does work to solve this problem, but there are significant risks from surgery.

Most people find their heavy bleeding is adequately controlled by a Mirena IUD.

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What may commonly cause secondary amenorrhea?

prolonged anovulation with low or no estrogen

prolonged anovulation with normal or high estrogen

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secondary amenorrhea

no period for 3 mos in women with previously normal periods AND for nine months in women with previous oligomenorrhea (infrequent periods, more than 35 days)

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In one pathway to secondary amenorrhea, a pituitary tumor causes

PROLACTIN to rise which suppresses

GNRH, resulting in very low levels of

ESTROGEN

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Prolactin may increase because of:

frequent breast stimulation

breastfeeding

prolactinoma (bening pituitary tumor)

medications (such as mood stabiliziers)

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What are causes of secondary amenorrhea?

PREGNANCY

asherman syndrome

cervical stenosis

contraception

thyroid issue

pituitary tumor

PCOS

cns/hypothalmic disorders (anorexia, chronic disease, stress, athleticism)

obesity

prolactinoma

menopause

ovarian insufficiency

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causes of primary amenorrhea

pregnancy, imperforate hymen, gonadal dysgenesis (turner's syndrome), HPO axis abnormalities (anorexia, bulimia, weight loss, excessive exercise), FSH greater than 40

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what is the hormonal state for PCOS and obesity?

normal to high estrogen

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What is the hormonal state for menopause and ovarian insufficiency?

HIGH FSH/LH with LOW estrogen

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What is the hormonal state for chronic disease, anorexia and prolactinoma?

LOW estrogen

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Expected Progestogen challenge test results for galactorrhea,

prolactinemia, ovarian insufficiency

NO bleed due to insufficient estrogen (negative)

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Expected Progestogen challenge test results for PCOS and obesity

WITHDRAWAL BLEED (positive)

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ss of adenomyosis

Enlarged uterus on bimanual exam

Usually in older women

Caused by endometrial tissue implanted in the myometrium

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SS of endometriosis

Uterus may be fixed to pelvis or other structures

pelvic pain, dysmenorrhea, dyspareneuia, abnormal bleeding

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SS of both Endometriosis OR adenomyosis

Tender uterus on bimanual exam

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what type of woman is more likely to have adenomyosis?

40+ who is multip

HX of miscarriage, curettage, endometrial resection, csection or tamoxifen use

previously normal menses

no pelvic pain until recently

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what type of woman is more likely to have endometriosis?

dysmenorrhea, painful defecation, and infertility

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most common cause of anovulation

pregnancy

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What are differential diagnosis for heavy bleeding?

endometriosis

adenomyosis

hyperplasia

perimenopause

fibroids (if they have SS - leiomyomatas)

polyps

PID

adhesions

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what is the hallmark of endometriosis?

Cyclical pelvic pain worse at 1 to 2 days before menses and WITH PERIODS

may or may not involve bleeding changes

may progress to pain in between periods

pain with intercourse

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what some less common causes of AUB?

copper IUD

miscarriage

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What does ACOG recommend if 45 and up with AUB or risk factors?

must ensure its not hyperplasia prior to treating

do a pelvic US or endometrial biopsy

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risk factors for hyperplasia

AUB

postmenopausal bleeding

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most common causes of amenorrhea in general?

pregnancy

menopause

PCOS

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fibroids (leiomyomas)

most commonly have NO SX

can cause pain

benign estrogen-dependent uterine muscle tumors --> menorrhagia (heavy period) most common presentation

Surgical Indications = cause anemia, severe pelvic pain, uterine size > 12 wks, urinary symptoms, growth after menopause, recurrent miscarriage or infertility, rapid increase in size

-- Complications = recurrence in 50%, adhesions

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waht is the first line tx for AUB-E?

LNG - IUD

IUD will assist with long term bleeding but to stop acute bleeding, estrogen therapy or tranexamic acid is used

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what medication is helpful for adenomysis and dysmenorrhea?

NSAIDS

helpful when pain severe and medication resistant because they reduce pain by reducing prostaglandins

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Adenomyosis

benign invasive growth of the myometrium that may cause heavy, painful menstrual bleeding

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What are all the risks for unopposed estrogen/endometrial hyperplasia?

PCOS,

obesity,

estrogen therapy w/o progesterone

lynch syndrome (hereditary nonpolyposis colorectal cancer (HNPCC) - high risk for colon cancer and endo cancer

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What does the PCT require?

requires estrogen to be present (and the outflow tract has to be patent) for there to be a withdrawal bleed.

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SS of uterine fibroid

enlarged uterus, asymmterical, painless, usually associated with AUB

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SS of adenomyosis

benign invasive growth of the myometrium that may cause heavy, painful menstrual bleeding

ENLARGED uterus, symmetrical, moderate tenderness, increases menses

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SS of cervical polyps

bright red PAINLESS bleeding after sex

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SS of nabothian cysts

white, firm, painless nodules visible on cervix

<p>white, firm, painless nodules visible on cervix</p>
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differential diagnosis for secondary amennorhea

hypothyroidism

hyperprolactinemia

outflow tract obstruction and hyperandrogenic chronic anovulation.

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Regularity of periods by age

18- 29 and 42+ = 9 days or less

30-41 = 7 days or less

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AUB-PALM

related to structural abnormalities

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AUB - COEIN

UNrelated to structural abnormalities

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What physiologic processes explain why irregular menses are common during adolescence and perimenopause?

due to life cycle changes

in first 2 yrs of pd and 3 yrs before menopause

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Consider the differences between evaluating and managing a YOUNG person's abnormal uterine bleeding and an OLDER person's abnormal uterine bleeding. How is the investigation different? Why? What are the special concerns of a perimenopausal person with AUB

Adolescence- don’t require as much, if any, investigation, if during the first 2 years of menses

1. Assess for eating disorders, iron/folic acid deficiency anemia

2. Assess for sexual function, need for BC

3. Pelvic exam only if specific indication

·Perimenopausal- incidence of AUB increases within 3 years of menopause

1. Associated w/ menopause or ovulatory s/s: PMS, dyspareunia or irregular bleeding

2.Provide education r/t health risks: diet/exercise for osteoporosis, quit smoking, etc.

3. r/o endometrial hyperplasia/endometrial cancer (45yo+)

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What conditions cause heavy, irregular and/or intermenstrual bleeding?

If childbearing age w/ previously normal cycle -

most likely cause is a complication of pregnancy → rule that out, then begin down PALM-COEIN:

- Polyps (bleed easy)

- Adenomyosis – menorrhagia (abnormal heavy bleeding during menstruation)

- Leiomyoma-fibroids- if submucosal- then interfere with endometrium and is more likely to cause AUB

-Malignancy/hyperplasia - postmenopausal bleeding

-Coagulopathy - heavy, usually first sign in teen yrs of bleeding disorder

-Ovulatory dysfunction

-Heavy - secondary to high/sustained unopposed estrogen

-PCOS - estrogen-related breakthrough bleeding

-Endocrine - thyroid, pituitary, increased prolactin

-Heavy & irregular - POPs, progestin-only contraception

-Irregular - post-menarche or perimenopausal

-Heavy and often prolonged - pelvic pathology

-Uterine fibroids/leiomyomas

-Adenomyosis

- Endometrial polyps

-Heavy and intermenstrual - endometrial is often predictable and cyclical and can also be intermenstrual or prolonged

- Intermenstrual - chlamydia

-Irregular - gonorrhea and endometritis or iatrogenic often characterized by breakthrough bleeding

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What are likely and unlikely causes of different types of AUB:

New-onset vs. long-standing bleeding abnormalities

1. Regular: structural or systemic cause e.g.: fibroids, polyps (spotting), blood dyscrasias

2. Irregular: Hormonal change/cause e.g. thyroid problems, PCOS, endometrial hyperplasia (UNLIKELY)

3. Amenorrhea: either- outflow tract obstruction, elevated prolactin, pregnancy

1. Irregular and/or regular:

1. Ovulatory dysfunction

2. Fibroids- heavy, clots, “pelvic fullness” (UNLIKELY)

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Describe the assessment (history, physical examination, and diagnostic testing) and management options for individuals presenting with abnormal uterine bleeding. Include patient education.

1.HX: a detailed menstrual hx

2. PE:

General PE for signs of systemic illness such as fever, ecchymoses, enlarged thyroid, or evidence of

hyperandrogenism (hirsutism, acne, clitoromegaly, or male pattern baldness.

Acanthosis nigricans (darkening of the skin in folds and creases) may be seen in people with PCOS

3. DX TESTING:

A pelvic examination is essential for a person of any age who is (or has been) sexually active or has abdominal pain, anemia, or bleeding that results in hemodynamic instability.

A pelvic examination is most likely not necessary if the patient is an adolescent who is not sexually active, recent menarche, and normal hematocrit.

A pelvic examination is helpful for identifying normal genital anatomy, outflow tract patency, and if estrogen depletion is present.

4. Labs and dx:

2. Pregnancy test

3. CBC if indicated or if anemia is suspected

4. Thyroid-stimulating hormone (TSH), especially if thyroid abnormality is suspected

5. Prolactin level if they have headaches, has galactorrhea and/or peripheral vision changes

6. Pap test

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AUB-C

Coagulopathies

13% of ppl with AUB present with a clotting disorder

von willebrand is the most common

TX: referral

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Anovulatory cycles are characterized by:

lack of PROGESTERONE in the LUTEAL phase that leads to an unstable, excessively vascular endometrium

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One of the most concerning causes of AUB is endometrial hyperplasia, a precursor to endometrial cancer. How may endometrial hyperplasia present clinically? How (and in whom) should we rule it out?

Clinical presentation: *most common s/s of endometrial cancer is AUB and postmenopausal bleeding

-Should r/o: If a person is experiencing AUB-O (ovulatory dysfunction) and 45+, endometrial biopsy and pelvic sonography are recommended OR if they are

younger than age 45 (35-45) and have a history of unopposed estrogen exposure, failed medical management (and neg preg test), and persistent AUB, - anendometrial biopsy should be performed

*Transvaginal ultrasound (TVUS) of the endometrial thickness can effectively rule out endometrial hyperplasia in postmenopausal women; if the thickness of the endometrial lining or "stripe" on ultrasound is less than 4 mm, it's extremely unlikely that the woman has hyperplasia.

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What medications or therapies are used to treat heavy or prolonged menstrual bleeding (for example, tranexamic acid and CHC)? What are their contraindications? What do patients need to know about how to use them

1. Estrogen (ACUTE)

Contraindicated: hx of thrombosis or other coagulopathies

-progesterone needs to be taken after COCs - monophasic

-if flow does not stop w/in 48 hours of tx- return for evaluation

-use antiemetic since high estrogen cancause nausea

2. POP,CHC, IUD, Cyclic MPA, NSAIDS, Tranexamic acid (CHRONIC/LONG TERM)

-Contraindicated: pregnancy, ulcers (nsaids), blood clots (TXA), fibroid (IUD)

3. GnRH agonists - used when awaiting surgery for HMB

NOT FOR LONG TERM BLEEDING due to S/E and its expensive

4. estrogen/progesterone (ACUTE PROLONGED BLEEDING)

5. NSAIDS - used ideally for IDIOPATHIC HMB

6. TXA - 2nd line option for NONHORMONAL use

effective in combination with von willebrand disease

VTE CONCERN

S/E rare but include nausea and leg cramps

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management goals for HMB

normalize bleeding

correct anemia

prevent cancer

restore quality of life

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progesterone vs estrogen in resolving acute bleeding

progestogens are not as effective as estrogen in stopping acute bleeding but they are effective long term AFTER acute bleeding has been resolved

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How can the levonorgestrel IUD be used for women with AUB?

After acute bleeding is under control, may initiate levonorgestrel IUD for long-term txt, causes chronic anovulation.

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What other treatments are available for individuals diagnosed with AUB-E?

1. COCs, progestin therapy (depo, Nexplanon, mini pill), if testing shows anemia d/t

bleeding, iron therapy is recommended2. If medical therapy fails- surgical options: d&c, endometrial ablation, uterine artery

embolization, hysterectomy3. AUB-E dx of exclusion

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How can COCs be used to stop prolonged or heavy bleeding?

1. monophasic COC admin 3x/daily should result in the ↓ of bleeding w/in 24 (up tp 48) hours.

2. COC is typically tapered to 2x/daily for 2 days, then 1 pill daily for 21 days of active pills followed by 7 days of placebo pills or no pills.

3. An alternative to the 21/7 cycle is an extended regimen of 84 days of monophasic COC followed by a 7 day pill-free interval.

4. When the bleeding stops, 2.5 mg of conjugated equine estrogen (Premarin) can be admin daily, followed by the addition of 10 mg of medroxyprogesterone acetate (Provera) during the last 10 days of therapy to initiate withdrawal bleeding.

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Know the difference between primary amenorrhea & secondary amenorrhea

Primary amenorrhea is the failure to begin menses by age 16-but has normal secondary sexual characteristics. Any girl who has not reached menarche by age 15 or

who has not had a menses within 3 years of menarche should be evaluated

Secondary amenorrhea is defined as 3 months without a period with previously normal periods

AND for nine months in women with previous oligomenorrhea (infrequent periods, more than 35 days

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What are the special assessment and diagnostic concerns of each type of amenorrhea including INITIAL WORKUP?

For Primary Amenorrhea

Initial workup:

1. No period by 15 - maybe no uterus or intact hymen, no ovaries, no vagina

2B.IF Secondary sex characteristics are present-

U/S first (see if they have a uterus), preg test as

indicated, refer to endocrinology

2A.If no secondary sex characteristics- HPOA is not working, =

draw an FSH/LH and refer

For Secondary Amenorrhea

1. May be caused by outflow tract obstruction, surgery on endometrium (ashmans syndrome)

or hormonal problem interfering with HPO axis at ANY LEVEL:

more cmmmon prolactinemia and tsh

less common hpo issue

NORMAL/HIGH estrogen w/ PROLONGED unopposed

exposure (this is VERY BAD)

1A.check TSH and prolactin first

1B.If normal, order a PCT

If normal prolactin but ABNORMAL TSH = thyroid disease

If normal TSH but ABNORMAL prolactin = refer to determine

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Describe the assessment (history, physical examination, and diagnostic testing) and management options for women presenting with amenorrhea. Include patient education

1. History - lifestyle, exercise, meds, drug use, eating habits, s/s eating disorders, family hx of anatomic or genetic abnormalities.

- Other symptoms r/t differential

-Pregnancy - breast tenderness, nausea, vomiting

-Prolactinoma - headaches, visual field defects

-Thyroid problems - dry skin, constipation, etc.

2. Primary

-Physical exam - focus on

-Identifying maturation of secondary sex - tanner staging

-Establishing outflow tract patency - any bleeding from vagina

-Outflow tract abnormalities d/t abnormal development are rare - still consider

-If cervix not visible or vagina not patent → imperforate hymen-Obstructed bimanual exam → referral and f/u for possible vaginal septum or blind pouch

3. Secondary - check TSH and prolactin - if normal → PCT

4. Lab tests

1. Estrogen production - reliable measure of ovarian function

2. Serum estradiol: >40 = functioning ovaries, low may = ovarian failure or hypothalamic

amenorrhea

3. Progestogen challenge test

4. Endometrial thickness measurement

5. Serum FSH concentration - indirect measurement, lower level = normal function

6. If these tests = ovaries are producing estrogen and FSH normal = dx of chronic

anovulation

7. Serum prolactin -for dx of hyperprolactinemia w/ amenorrhea

8. Hyperprolactinemia

9. Serum prolactin

1. Not always w/ galactorrhea (nipple discharge)

10. Some meds can → elevated level (antidepressants, opiates, CCBs, and estrogens),

ask about meds

11. If w/ amenorrhea - more evaluation needed to r/o pituitary tumors and hypothalamic

mass lesions

5. Tx of choice is dopamine agonist

6. PCT +, no galactorrhea, and prolactin level normal = possibility of pituitary tumors

ruled out =dx is anovulation

1. Tx - progestogen for first 10 days each month or CHC

2. Evaluate for PCOS

7. Anovulation - management necessary, if not treated

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What particular information does a progestin challenge test provide? What conditions would cause a person to be amenorrheic and then have a positive or negative progestin challenge test? (For instance: an amenorrheic woman has a NEGATIVE PCT but does not have an outflow tract problem…what can we deduce about the probable estrogen level?)

1. PCT+ (positive) 1. Withdrawal bleeding = functioning ovaries b/c bleeding only occurs if sufficient circulating estrogen is present *ANY amount of bleeding is a POSITIVE result*

-Withdrawal bleeding should occur w/in 7-10 days after d/c of progesterone and if outflow tract is patent

-Positive tests with: PCOS, Obesity

-A positive progestin challenge test: if their lack of menstruation is due to anovulation (lack of ovulation), meaning their body is producing sufficient estrogen but not releasing an egg

2. PCT - (negative)

1. Minimal/no estrogen → no endometrium → no flow

-Negative tests with: galactorrhea (milk unrelated to preg), prolactinemia, ovarian insufficiency

A negative progestin challenge test would indicate a problem with the uterine lining or outflow tract, like Asherman's syndrome, where the endometrium isn't adequately estrogenized, usually due to low estrogen levels from conditions like hypothalamic amenorrhea or premature ovarian failure

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What conditions cause clinical hyperandrogenism?

PCOS-most common

Adrenal hyperplasia/tumor

Hyperthecosis

Androgen producing tumors

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What are the clinical manifestations and health consequences of hyperandrogenic disorders? How will you tell these disorders apart in practice?

Clinical manifestations:

Gradual onset with slow progression

Symptoms such as- acne, alopecia, hirsutism, maybe over wt/obese (50%), “apple-shaped”, insulin resistance, polycystic ovaries, menstrual irregularity (HALLMARK feature) can lead to amenorrhea and/or prolonged anovulatory bleeding, difficulty achieving pregnancy is common

Tell apart: history, PE, and labs

i.e. negative TSH/Prolactin, higher free testosterone with s/s of hirsutism- PCOS (r/o all other causes)

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What are the health consequences of hyperandrogenic disorders?

*Dyslipidemia- may result in metabolic syndrome (lipid level, fasting glucose for labs)

*Metabolic syndrome

*CVD

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How do the cycles with hyper androgenic disorders differ from normal menstrual cycles?

Irregularity is a hallmark feature of PCOS-

Oligomenorrhea (infrequent periods) - most common presentation of overt menstrual dysfunction - cycle length 35-199 days

Amenorrhea - cycle >199 days

More significant endocrinopathies including more severe hyperandrogenemia, ↑ serum LH and cortisol and incidence of hyperinsulinemia

Polymenorrhea (frequent periods) - more rarely, may be iron def. anemia

Bleeding generally unpredictable. Can be heavy

Regular menses can occur w/ oligo-anovulation → subclinical menstrual dysfunction w/ regular menses but chronic anovulation

Either type may have unpredictable menses before bleeding d/t lack of premenstrual s/s = clinical indication of anovulation

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What are the assessment, diagnostic, management considerations, and special risks faced by individuals with hyperandrogenic disorders?

1. Assess:

1. age of onset (Tanner stages, etc)

2. menstrual pattern, preg hx, miscarriage

3. obesity, hirsutism, seborrhea, acne, alopecia

4. complete medication hx

5. s/s of hirsutism and virilization- libido, muscle bulk, voice deepening, breast atrophy,

clitoromegaly

6. polydipsia or polyuria (glucose intolerance)

7. s/s hyperprolactinemia/pit tumor (galactorrhea, visual disturbances, HA)

8. s/s cushing syndrome (striae, mood chages, easy bruising or wt gain)

9. CVD and metabolic risk factors (smoking, hx HTN, dislipidemia, DM, CVD)

10. Fam hx

2. PE:

1. ht, wt, BMI, obesity degree, distribution of body fat (wt circumference of >35*)

2. VS esp BP

3. Skin- hirsutism, acne, alopecia, acanthosis

4. Thyroid

5. Breast (galactorrhea)

6. Cushings (moon face, hump)

7. Pelvic-clitoris, bimanual for uterine size, ovaries, and mass presence

3. Labs:

1. prolactin (mild elevations of prolactin are common in women with PCOS, may also identify women with prolactinoma-extremely rare)

2. TSH

3. lipids

4. 2-h OGTT

5. Progesterone days 20-24 of menstrual cycle

6. Serum 17-OHP- low-levels r/o congenital adrenal hyperplasia

7. Imaging: pelvic US, TVUS

endometrial biopsy (d/t risk of hyperplasia w/ unchecked estrogen), avoid routine adrenal

imaging

Special risks: endometrial cancer, metabolic syndrome, higher rate of CVD

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How will you assess and diagnose PCOS?

Dx of EXCLUSION;

Rotterdam Criteria: must have 2/3 of following with no other cause identified:

1. Irregular menses (d/t irregular ovulation)

2. Multiple cysts in the ovaries (d/t unruptured dominant follicle)

3. Clinical hyperandrogenism (hirsutism, acne, alopecia, virilization)

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FIRST LINE management for PCOS.

1.lifestyle modifications- weight loss, and exercise, metformin, hirsutism management- hair removal in women with PCOS who are not trying to conceive

COC is the best medical maintenance therapy to treat menstrual disorders and manage symptoms

progestin may be used for endometrial protection

letrozole should be considered as 1st line therapy compared with clomiphene

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What red flags indicate the need for immediate referral in hyperandrogenic individuals?

Virilization: enlarged clitoris, deepening voice, increase in muscle mass, breast atrophy, increased aggression/libido -RED FLAG if they happen SUDDENLY.

Virilizing tumors: sudden onset of advanced PCOS symptoms concerning for adrenal or ovarian tumors

*should see endocrinologist immediately- virilization effects can be permanent

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What should the assessment (history, physical examination, and diagnostic testing) of an individual with vulvar skin changes include?

Hx:

1. OLDCARTS

2. Prior self or prescribed txt and their outcomes

3. Concomitant systemic changes (ie lymphadenopathy of skin, perianal or oral mucosal disease)

4. Ask about all products used on the vulva and vagina

5. Increased risk of malignancy should be considered when women report a prior hx of high-risk HPV or close fam hx of skin malignancies

2. PE:

1. Conduct a thorough exam of vulva, beginning with keratinized skin areas (inguinal folds, mons

pubis, and labia majora), followed by partially keratinized (labia minora, clitoral hood, and posterior fourchette)

2. Palpation for lymphadenopathy

3. inspection of scalp, eyes, nasal mucosa, and oral mucosa

4. Examination of the skin folds

5. Spec exam to identify involvement of vaginal mucosa

3. Dx: 1. Selective testing may aid dx- ex: tests for candida, STIs, microscopy for scabies or vaginal

pathogens

2. Microscopy in all women with symptoms

3. Biopsy with any atypical, nonresponsive findings

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How is lichen sclerosis managed?

lichen sclerosis: chronic mucocutaneous disorder that is characterized by inflammation, epithelial thinning, and depigmentation, and dermal changes-often include agglutination of labia minora, can be progressive or relapsing and remitting.

Most often genital, occasionally identified in other body areas, including trunk neck, forearms, axillae, and under the breasts, most often occurring on tissue that has undergone trauma

Dull, nonspecific vulvar irritation, whereas progressive disease often manifests with severe pruritus, burning, and associated dyspareunia; perianal symptoms, including pruritus ani, painful defecation, and anal fissures may also occur

Goals of tx: s/s relief, reversal of agglutination, prevention of further architectural distortion w/ loss of function, and prevention of potential malignant changes

First line tx - high or very high potency topical steroid ointment - clobetasol propionate 0.05%; 3 month tapered dosing common

Yearly vulvar exam

Atypical or nonresponsive to tx - referral to specialist

<p>lichen sclerosis: chronic mucocutaneous disorder that is characterized by inflammation, epithelial thinning, and depigmentation, and dermal changes-often include agglutination of labia minora, can be progressive or relapsing and remitting.</p><p>Most often genital, occasionally identified in other body areas, including trunk neck, forearms, axillae, and under the breasts, most often occurring on tissue that has undergone trauma</p><p>Dull, nonspecific vulvar irritation, whereas progressive disease often manifests with severe pruritus, burning, and associated dyspareunia; perianal symptoms, including pruritus ani, painful defecation, and anal fissures may also occur</p><p>Goals of tx: s/s relief, reversal of agglutination, prevention of further architectural distortion w/ loss of function, and prevention of potential malignant changes</p><p>First line tx - high or very high potency topical steroid ointment - clobetasol propionate 0.05%; 3 month tapered dosing common</p><p>Yearly vulvar exam</p><p>Atypical or nonresponsive to tx - referral to specialist</p>
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How would you recognize and manage Cervical polyps?

Cervical polyps:

may be single or multiple, usually <3cm in diameter

lobular/pear-shaped, stalk arises from cervical canal and size varies

1. Often asymptomatic and incidentally dx

2. postcoital or intermenstrual bleeding

Management:

1. SDM- observation (education to report irregular or postcoital bleeding) or removal for histology (indications are symptoms such as irregular or postcoital bleeding, increased discharge, larger than 3cm, necrotic, friable, irregular

color)

2. if stalk is clearly visible, removal is simple and in office. GRab polyp, clamp and apply pressure for 3-5 minutes, twist forceps to remove polyp. May bleed-can cauterize

<p>Cervical polyps: </p><p>may be single or multiple, usually &lt;3cm in diameter</p><p>lobular/pear-shaped, stalk arises from cervical canal and size varies</p><p>1. Often asymptomatic and incidentally dx</p><p>2. postcoital or intermenstrual bleeding </p><p>Management:</p><p>1. SDM- observation (education to report irregular or postcoital bleeding) or removal for histology (indications are symptoms such as irregular or postcoital bleeding, increased discharge, larger than 3cm, necrotic, friable, irregular</p><p>color)</p><p>2. if stalk is clearly visible, removal is simple and in office. GRab polyp, clamp and apply pressure for 3-5 minutes, twist forceps to remove polyp. May bleed-can cauterize</p>
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How would you recognize and manage Nabothian cysts?

small white/yellow raised areas

retention cysts of endocervical glands are a normal variation

leave them alone - harmless