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Fifth stage 

Gynecology 

Lec-5

 

  اسماء

13/4/2016

 

 

Polycystic ovary syndrome

 

 

The student at the end of this lecture  should be able to: 

  Enumerate the diagnostic criteria for PCOS. 
  Describe it’s clinical presentation. 
  Describe the underlying hormonal changes . 
  Describe the ultrasounic features diagnosing PCOS. 
  Predict the life long risk for PCOS. 
  Differentiate PCO from PCOS. 
  Describe the available options for treating the presenting problems. 

 

Poly cystic ovary syndrome: 

Is a heterogeneous collection of symptoms and signs . 
It's diagnosed by the presensce of two out of the following three criteria: 
 oligo and /or anovulation. 
 Hyperandrogenism clinically or biochemically. 
 Polycystic ovaries by transvaginal ultrasound. 

 

Incidence: 

In general,1-4% of women in the reproductive age suffer from PCO. 

It’s the commonest endocrine disorder in women, prevalence(15-20%). 

 

Inheritance: 

It runs in families and affect approximately 50% of 1

st

  degree relatives suggest dominant 

inheritance 

  

Clinical presentations of PCOS: 

-no symptoms 

-menstrual irregularities and dysfunction ranging from 


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oligomenorrhoea to amenorrhoea , about 30% have normal cycle,50%have 
oligomenorrhoea and 20% have amenorrhoea. Even in patient with regular cycle with 
hyperandrogenism the rate of anovulation is 21%. 

-hyperandrogenism : hirsutism ,acne ,alopecia ,but not virilism. 

-obesity (10-65%):central type with higher waist to hip ratio .     

-recurrent miscarrige:its relation to PCOS has been recently questioned. 

-insulin resistance and hyperinsulinemia . 

-impaired glucose tolerance test(1/3 of obese PCOS patient have impaired glucose 
tolerance test and 7.5% to 10% have type 2 diabetes. 

-abnormal lipoprotein are common in PCOS(elevated total cholesterol, triglyceride, LDL, 
and low level of HDL.   

 

Pathophysiology and labrotory finding: 

Hyperandrogenism and anovulation in PCOS is caused by endocrine abnormality mainly in 
the ovary  with the total testosterone level is usually not more than twice the upper normal 
range(20-80 ng/dl). 

High intraovarian androgen concentration inhibit follicular maturation. 

E1 level is increased as a result of peripheral aromatization of hyperandrogenisim . 

There is abnormal estrogen feed back at the hypothalamic pituitary gland result in elevated 
LH and LH:FSH ratio and exhibit elevated prolactin level in 25% of patients. 

 

PCOS patient insulin resistance and compensatory hyperinsulinaemia as a result of PCOS 
and obesity. Insulin is a potent stimulus for insuline secretion of androgen by the ovary by 
the presence of different type of receptor doesn’t exhibit insulin resistance also it suppress 
the synthesis of SHBG by the liver thus elevate the free androgen index. Patient are at 
increased risk of glucose intolerance or frank diabetes.   

 

Long term risk for patients with PCOS: 

Persistently elevated level of estrogen uninterrupted by progesterone increase the risk of 
endometrial cancer, breast cancer and ovarian cancer. 

Obesity  and metabolic abnormality  and increase of plasminogen activator inhibitor cause 
reduced fibrinolysis all are risk factors for the development of ischemic heart disease (7 fold 
increase in MI) ,hypertention and dyslipidaemia . 


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Insulin resistance and hyperinsulinaemia make the patient at risk of diabetes and 
gestational diabetes later on in life. 

During subsequent pregnancy there is increased risk of abortion ,gestational diabetes ,and 
pre-eclampsia. 
There is also increased morbidity in obese PCOS who fails to reduce their weight. 

 

Diagnostic investigation: 

Ultrasound: increased stromal thickness and increased ovarian volume (>10 cm3)(specific 
for PCOS),and the presence of 12 or more follicles measured 2-9 mm in diameter. 

Serum endocrinology: 

Increase serum LH 

Increase serum LH : FSH ratio 

Increase serum androgen (testosterone and androstenedione) 

Decrease SHBG 

Increase estradiol and estrone (not measured routinely as Very wide rang of values). 

Increase serum prolactin. 

Increase serum insulin level. 

Impaired glucose tolerance . 

 

Management of PCOS: 

The clinical management of PCOS should be focused on the individual problems  

Obesity : obesity worsen the symptoms and the endocrine profile so obese women (BMI 
>30 kg/m2) should reduce their weight and modify their life style by diet modification , 
increase exercise , stop smoking. 

  

Menstrual irregularities:     

 low dose combined oral contraceptive preparation.  

 Progesterone as medroxy progesterone  acetate (provera) Or dydrogesterone 
(duphastone) for 12 days every 1-3 months to induce withdrawal bleeding. 

 

 


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Hyperandrogenism and hirsutism : 

A standirized scoring system as the modified Ferriman and Gallway score  may be used  to 
evaluate the degree of hirsutism before and during treatment . 

Physical treatment : electrolysis, waxing and bleaching, Laser and photothermolysis may be 
helpful while waiting the effect of medical treatment. 

Medical treatment : stop further progression and decrease the rate of hair growth. 
Adequate contraception is important during treatment as antiandrogen disturb the 
development of male genital tract: 

First line is diane (ethinylestradiol 30 Mg with cyproterone acetate 2mg.CPA may cause 
liver damage 

So require regular checking  and once response is achieved we should be switched to COCP 
because diane can increase the risk of thromboembolism. 

Spironolactone is a weak diuretic with antiandrogenic properities  can be used at a daily 
dose of 25-100 mg . 

Other antiandrogen as Ketoconazole ,Finasteride and Flutamide (not used because their 
side effect and they are no more effective thane CPA 

 

Treatment of infertility in PCOS: 

1. life style modification including diet reduction and exercise. A loss of 5-10% of body 
weight in obese PCOS patients improve the prospect of both spontaneous and drug induced 
ovulation   

2.Medical Induction of ovulation in PCOS patient     

by a. antioestrogen :      - clomiphene citrate . 
                                          - Tamoxifene.  

Clomiphene citrate : is an orally active synthetic non steroidal   compound with oestrogenic 
and non oestrogenic properties. 

It displace the oestrogen from it’s receptor at the hypo-thalamic pituitary axis reduce it’s 
negative feed back  and encourage GnRH secretion. 

It’s administered at 50 mg daily dose on day 2-6 of a spontaneous and induced menstrual 
cycle (increased by 50 mg /day till ovulation occur for a max.  Dose. 

A course of 6-12 cycles can be used in women who respond to treatment with monitoring 
by ultrasound for follicular response. 

Ovulation is expected in 80% and pregnancy in 40% . 


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Adverse reaction to such treatment: 

-Antioestrogenic side effect including thickening of the cervical mucos and hot flushes in 
10% of women. 

-abdominal pain ,nausea , vomiting . 

-headache and visual disturbance. 

-breast tenderness. 

-reversible hair loss. 

-ovarian enlargement, and ovarian hyperstimulation syndrome is rare in <1%. 

-Multiple pregnancy in 10%. 

-Ovarian cancer described in women receive treatment for more than 12 cycles. 

Tamoxifen: 
has structure similar to clomiphene .the recommended dose is 20- 40 mg per day from day 
3 for 5 days  it have the same pregnancy rate as clomiphene with less potent 
antioestrogenic action on the cervical mucos. 

 

b. Medical induction by gonadotrophin :  

Gonadotrophin are used when the patient do not respond to clomifene or fails to conceive 
after 6-12 ovulatory cycles. 

Preperation in common use include recombinant FSH or purified urinary human 
menopausal gonadotrophin (FSH and LH). Gonadotrophin treatment result in cumulative  

Pregnancy rates of 40-50% and  1-2% rate of OHSS. 

 
 c. GnRH analogues in ovulation induction : it’s used 
in conjunction with gonadotrophin to achieve pituitary down regulation to facilitate cycle 
control 

 

d. Metformin : this is an oral biguanide inhibits the production of hepatic glucose ,enhance 
the sensitivity of peripheral tissue to insulin thus decrease the secretion of insulin and treat 
hyperinsulinaemia. 

Metformin is shown to decrease hyperandrogenism and abnormalities of gonadotrophin 
secretion and can restore menstrual  cyclicity and fertility. 

The usual dose is 850 mg bid or 500 mg t.d.s. taken Before meal . 

 


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Side effect of metformin: nausea ,vomiting , flatulance and diarrhoea . (these can be 
reduced by taking the drug before the meal and by gradually increasing the dose  start with 
850 mg  nocturnal then 850 mg bid for the next week. 

Metformin is not usually cause Lactic acidosis in non diabetic patient with PCOS with 
normal liver and renal Function. 

Regular checking of renal and liver function, metformin should discontinued for 3 days after 
iodine containing compound and should be discontinued during pregnancy (although there 
is no evidence of Teratogenesis). 

                                                                                                    

3. Surgical method of ovulation induction

 

Laparoscopic ovarian diathermy LOD: by diathermy or Laser, it appear to be more 
successful in a slim patient with high LH level. A unipolar coagulating current is used to 
deliver four punctures to a depth of 4 mm in each ovary .The principle advantage of ovarian 
drilling is monofollicular ovulation resulting in fewer multiple pregnancy rate with the 
cumulative  pregnancy  rate similar to those obtained with 3-6 cycle of gonadotrophin. 

LOD has replaces the wedge resection of the ovaries as it result into extensive peri-ovarian 
and peritubal adhesion. 

 




رفعت المحاضرة من قبل: Abdalmalik Abdullateef
المشاهدات: لقد قام 30 عضواً و 186 زائراً بقراءة هذه المحاضرة








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