Professional Documents
Culture Documents
METHODICAL GUIDELINES
for practical lesson
4 course
II. Aim:
A student should be know to:
- The principles of organization and provision of obstetric care in Ukraine (order
№41,7620);
- The function of the family doctor to provide obstetric care
- Clinical anatomy of the female genital organs.
- Physiological changes in the female genital organs in different age periods.
- Regulation of neuroendocrine function of the reproductive system.
- The collection features special gynecological history.
- Basic examination methods in gynecology: an overview of the external genitalia, studies
using mirrors, bimanual examination.
- Methods diagnostics of functional ovaries.
- Ray diagnostic techniques in gynecology: MRI, CT, MSH.
- Ultrasonic methods in gynecology.
- Instrumental methods of inspection: probing the uterus, uterus curettage, biopsy, puncture
of the abdominal cavity through the rear arch.
- Endoscopic methods: colposcopy, hysteroscopy, laparoscopy. Laboratory diagnosis:
oncocytology, bacterioscopy, bacteriology, ELISA, PCR, pathologic study.
- General gynecological diseases symptomatology (pain, discharges, menstrual cycle and
bleeding, infertility, sexual disorders, disorders of adjacent organs).
A student should be able to:
- Familiarity with the work gynecological department;
- Registration of medical records, on receipt of gynecological patients to hospital.
- Introduction to the provision of gynecological care for women according to the order of
Ministry of Health of Ukraine № 620 and 417
Bivalve speculum is introduced into vagina with closed values. With thumb and index fingers
of the left hand labia are drawn and speculum is inserted into vagina, placing blades parallel to
pudendal cleft. After insertion speculum is turned on 90°. The speculum is inserted as far as it
goes which in most women means insertion of the entire speculum length. The speculum is then
opened in a smooth delicate way with slight tilting of the speculum, the cervix slides into space
between the blades of the speculum. The speculum is then locked into the opened position using
the thumb screw (fig. 22).
Sims speculum is inserted into vagina in such a way: with left hand labia major and minor are
drawn laterally and with right one the speculum turned, slantwise to pudendal cleft is inserted into
vagina, slightly pressing on perineum. Flat anterior speculum (lateral) should be inserted parallely,
lifting up anterior wall of vagina (fig. 23). Flat speculum should be inserted additionally in case if
vagina is wide and its lateral walls are hanging.
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finger if vagina is narrow. Fingers during insertion into vagina should be gently pushed
downwards to avoid unpleasant feelings of irritation of the most sensible areas such as anterior
wall, clitoris, region of urethra. During introducing fingers into vagina following signs are
estimated: presence or absence of pain, outer width (in women, which live sexual life, two fingers
enter easily). Determination of the muscles tone and perineum state is performed with pressing on
the muscles of the pelvic floor. During gradual moving of fingers into vagina its length, width,
ability to tension, rugosity, humidity degree, septums presence, tumors, scars, constrictions are
determined. An attention to vaults depth, presence or absence of pain, hanging, shortening should
be paid. After palpation cervical form (cylindrical, conic, deformed), its size (underdeveloped,
normal size or hypertrophied), presence or absence of ruptures, state of external os (opened, closed,
deformed), consistence (dense, sclerosed, softened, of heterogeneous consistence), tumors
presence are determined. Cervical attitude to pelvis axis is also estimated. Then fingers are placed
into anterior vault and cervix is pushed to back. With abdominal hand one should cautiously press
on the front abdominal wall towards fingers those are inserted into vagina. So, uterus is found
between fingers of the abdominal and vaginal hands. If uterus is retroflected, then vaginal fingers
are placed into the posterior fornix.
Uterus is situated in pelvis in such a way that its body and cervix form an angle, opened frontally
(anteflexio), and the whole uterus is flexed forward (ante-versio). It is sufficiently mobile at
displacement attempt. Overmobility of the uterus is observed at its descent and prolapses due to
incompetence of ligament system. Limited movability is common at adhesions and infiltrates
presence in true pelvis.
During uterus examination its size (in nonparous women it is smaller than in parous
ones) is determined. Diminish of the uterus size is observed at genital infantilism and
menopause. Enlarged uterus can be found at pregnancy and tumors presence. Uterine shape
normally is pear-like, flattened in front-back direction, at pregnancy it can be asymmetric
due to protrusion of implantation place, at subserous fibromyoma it is tuberous. Uterine
consistency is tightly-elastic and painless.
Bimanual examination of the adnexa begins with placing the vaginal fingers to the side
of the cervix deep in the lateral fornix. It is important to note that the fallopian tubes are not
palpable. Ovaries can be palpated as elastic painless structures. They are mobile and rather
sensitive. Normal uterine and ovarian ligaments could not determined. Normally there is no
pain and infiltration in paramethrium.
Recto-abdominal examination. In girls, or in case of athresia or stenosis of vagina
recto-abdominal examination is made. This method should be used for more detailed
inspection of pelvic organs tumors. The examination is made by introducing index finger
into rectum. As at previous examination external hand is placed on the anterior abdominal
wall over pubis. Vaginal part of cervix which directly adjoins to the anterior wall of rectum is
palpated. Its size, mobility, uterine and adnexa sizes, sacral-uterine ligaments and
parametriums are palpated.
Additional methods of examination
They are: bacterioscopy examination (smear for purity degree), cytologic investigation
of vaginal smears, bacteriological checkup, methods of functional diagnostics, colposcopy,
biopsy, uterine sounding, fractional diagnostic curettage of cervical canal and uterine cavity
with the following histological research, culdocentesis, pertubation and hydrotubation. X-
ray examination methods such as hysterosalpingography, pelviography and bicontrast
pelviography are also used. Colposcopy, hysteroscopy, laparoscopy and culdoscopy are
endoscopic methods in gynecology. Ultrasonic examination is wide-spreaded nowadays.
These methods are used for verification of the diagnosis. Cytologic investigation is obligatory
for women who undergo monitoring.
Nurse or midwife prepares the woman and necessary instruments (specula, sets for
abrasion, spoons or brushes for smear taking) for carrying out additional examinations. Nurse
must prepare a bottle with 10 % formalin solution for tissual fixation of the biopsy tissue
after curettage. Proper assignment registration on research is of great importance.
Smears from vagina are taken for purity degree, gonorrhea, oncocytologic investigation,
"hormonal mirror".
Following instruments are necessary for material taking:
• vaginal specula
• Folkman's spoon or gynecological spatula or brush
• forceps
• glass slide
• cotton swab
• antiseptic solution
• registration form for laboratory
Patient's preparation:
• to place the patient on examining table
• to make desinfection of external genitalia
• to insert gynecological speculum into vagina, dispose cervix in speculums
Bacterioscopic investigation of vaginal discharge gives possibility to determine vaginal
purity degree, bacterial flora, presence of contraindications to different diagnostic manipulations.
This method gives possibility to diagnose inflammatory process.
Technique of smear taking for examination on vaginal purity degree:
• to insert a gynecological speculum into vagina
• to take some discharge from the posterior vaginal fornix with gynecologic forceps, spatula,
gutter sound, or Folkman's spoon and by stroking motions to drift it on a glass slide
• withdraw a speculum from vagina
• write out an order to laboratory
Laboratory assistant quantifies epithelium cells, leukocyte number, microflora character
(Doderlein's bacillus, pathogenic flora — gram-negative bacillus, cocci, fungi, trichomonades,
gonococci) and also reaction of vaginal discharge.
There are 4 stages of vaginal discharge purity.
Smear on gonorrhea presence. Material for research is taken just from the cervical canal,
urethra (before urination after light massage of the posterior urethra wall) and rectum drift on a glass
slide as separate strokes.
Bacteriological research is taken to find the pathogene and its sensitiveness to antibiotics.
Material for research is a content of cervical canal, vagina, urethra and puncture material. This
material should be sent into bacteriological laboratory. It is necessary to indicate the date and time
when the material was taken.
Oncocytologic research (Pap smear) is made for the early diagnostics of oncologic diseases.
Smear taking technique for oncocytologic research:
• speculum insertion
• carefully taking the discharge from the cervix by cotton swab which is clutched in forceps
• material for investigation is taken by gynecological disposable wooden spatula from the anterior
and lateral vaults of vagina, external cervical os, vaginal part of cervix and from pathologically
altered parts which are revealed during colposcopy. Material is taken by brush or gutter probe
(fig. 26 a, b)
• drift it on the glass slide (fig. 27)
• withdraw a speculum
• write an order to the laboratory
Cytological investigation gives a possibility to reveal women who need more detailed
examination (biopsy, diagnostic curretage, etc).
There are 5 Pap smear types:
• I type — unaltered epithelium
• II-а type — inflammatory process
• Il-b type — proliferation, metaplasia, hyperkeratosis (at corresponding clinical picture they
are interpreted as polyp, simple leukoplakia, endocervicosis
• Ill-a type — light, moderate, dysplasia on the background of benign processes on unaltered
epithelium
References:
1. Obstetrics – edited by Professor I.B. Ventskivska, Kyiv “Medicine”, 2008.
2. Gynecology – Stephan Khmil - Ternopil, 2003.
3. Danforth's Obstetrics and gynaecology. - Seventh edition.- 1994. - P. 201-225.
4. Basic Gynecology and Obstetrics. - Norman F. Gant, F. Gary Cunningham. -1993. -- P. 406-
412.
5. Obstetrics and gynecology. - Pamela S.Miles, William F.Rayburn, J.Christopher Carey. -
Springer-Verlag New York, 1994. - P. 62-64.
METHODICAL GUIDELINES
for practical lesson
4 course
DISCIPLINE “OBSTETRICS AND GYNECOLOGY”
Basal temperature
In the beginning of this phase follicle consists of ovum which is surrounded by the thick
membrane. It is 2-2,5 mm in diameter. An ovum increases in its sizes and has brilliante
membrane in the surface that is called zona pellucida. An ovum is packed with biochemicals that
new organism will use until its own genes begin to function. These biochemicals include proteins,
RNA, ribosomes, lipids and the molecules that influence cell specialization in the early embryo. An
ovum can be an impressive storehouse and it becomes maturate after two-cell divisions in meiosis I,
the primary oocyte is divided to form a small polar body and a large haploid secondary oocyte. In
meiosis II, reductional secondary oocyte is divided to yield another small polar body and a
mature ovum.
Polar bodies are absorbed by the woman's body and normally play no further role in the
development. Follicle granulosa membrane forms as a result of follicle cells proliferation. By that
time in the central part of these cells the cavity is formed. The last one contains follicular liquid.
Granulosa cells those form corona radiata surround an ovum. It is situated in the numerous cells
which have been situated near the follicle. This number of cells is called a cumulus oophorus. The
follicular fluid contains follicular or estrogenic hormones.
The dominant follicle reaches a diameter of 12-20 mm. As the dominant follicle enlarges
and follicular fluid accumulates in it, it grows and rupture. It is the final stage of the follicular
phase, which is called ovulation. Ovulation is the process when the membrane of mature follicle is
ruptured and oocyte is expelled from the follicle.
Oocyte gets into abdominal cavity and is taken by the uterine tube fimbrias. Process of
fertilization takes place in the uterine tubes. After ovulation the dominant follicle transform into
the corpus luteum. The second luteal phase of the reproductive cycle begins. There is
luteinization — the conversion of granulosa and theca cells to luteal cells with the acquinisation
of LH receptors. After this luteal cells can synthesize and secrete large amount of progesterone,
that is protein hormone inhibiting FSH secretion.
The corpus luteum has a fixed life term during 14 days, since 15-th to 28-th days of menstrual
cycle. There are following processes in corpus luteum: 1) vascularization 2) blossoming 3)
involution — in case when pregnancy doesn't occur corpus luteum is called corpus luteum of
menstruation. Regression of corpus luteum lasts for 2 months and is over with the formation of
white body. If oocyte becomes fertilized and implants within the endometrium, the early
pregnancy begins secreting human chorionic gonadotropin (hCG), which sustains the corpus
luteum for the following 10-12 weeks. Corpus luteum of pregnancy produces such hormone as
relaxin which has tocolytic effect on the uterus.
/ level — target organs (uterus, vagina and breasts).
Uterine cycle
The endometrial lining of the uterus undergoes dramatic histologic changes during the
reproductive cycle. There are cyclic changes in the uterus as well as in the ovaries. They are the
most considerable in the functional layer of endometrium and are composed of such phases as
desquamation, regeneration, proliferation and secretion.
Desquamation (mensis) lasts from the first to the second or fifth day of the reproductive
cycle. During menstruation, the endometrium is sloughed out both with blood.
Functional layer of the endometrium is supplied with blood by spiral arteries. The spiral arteries
extend from the arteries of the basal layer. Estrogen is a mitogenic hormone, which stimulates cell
growth. With rising estradiol production during the follicular phase of the cycle, there is growth of
the spiral arteries those extend into the surface of endometrium only at the end of the proliferative
phase. There is an excessive growth of the spiral arteries in the secretory phase. They become
most twisty and look like tangles. The capillaries those are situated in the superficial layer of
endometrium enlarge in their sizes and look like sinusoids. Spiral arteries of the functional layer
contracts before the beginning of menstruation. It causes blood stasis, thrombosis, increasing
vessel's permeability and their destroying. The necrosis and sloughing of the tissue occurs. It
finishes on the third or fourth day of the menstrual cycle.
At the same time there is an inverse development of corpus luteum in ovaries, progesterone
level decreases, hypothalamus produces foliberin and pituitary folitropin which stimulates the
maturation of the new follicle in the ovary.
Regeneration phase takes place simultaneously with desquamation and is finally completed
up to the 6-7th day of menstrual cycle. The thickness of the endometrium at this moment is 2-5
mm. There is maturing of follicle in the ovary at this time (fig. 17).
Proliferation phase lasts from the 7th to the 14th days of the cycle. The endometrium
continues to thicken and the endometrial glands continue to elongate under the estrogens influence.
The endometrium thickness is 20 mm, but its glands don't function. Endometrial glands are straight
or somewhat twisted. There is a network of argyrophile fibers inside of the endometrial strome. At
the final stage of proliferation the endometrial glands become tortuous and spiral arteries reach the
surface of endometrium (fig. 15, 18).
There is a completion of the follicle maturation in the ovary, the production of estrogens is
peak on the 14th day until the end of proliferative phase. Pituitary stops the FSH-secretion,
hypothalamus starts production of luliberin which
Cervical cycle
Uterine cervix is an important biological valve that controles the flow of biological
substances into the uterine cavity and from it. Besides, it protects the uterine cavity from the
infective agents' penetration. It provides menstrual blood outflow and excretion from the uterine
cavity. Endocervix is covered by a simple columnar epithelium which contains secretory crypts.
Secretory crypts produce cervical mucus. All uterine cervix structures are very sensitive to the
steroid influence. Secretory cells of the endocervix constantly produce sticky transparent liquid,
which is called cervical mucus. The quantity and composition of the mucus are regulated by the
ovarian hormones secretion and they change during the reproductive cycle. In periovulation
period the quantity of the mucus increases up to 600 mg per day, but in luteal phase the mucus
quantity is only 50 mg per day.
Hydrated gel is the main component of the mucus that contains hydrocarbo-nates and
glycoproteins. Such endocervical mucus characteristics as quantity, water contents and viscosity
are maximal at the time of ovulation when the estradiol production is increased. All these
changes create the most favourable conditions for fertilization.
Mucus flows down from the internal os to the external one. Epithelial cell microvilli
oscillations direct the mucus flow into periphery of the endocervix. It favors the movement of
active spermatocytes into the uterine cavity, which are able to overcome cervical mucus flow.
Defective spermatocytes move away from the uterine cavity.
Prostaglandines and relaxin also can influence on the uterine cervix. These hormones
promote dilation of the cervix in pre-ovulatory period.
Under the. influence of estradiol, the endocervical glands secrete large quantity of thin transparent
mucus. Pure watery endocervical mucus contains the increased number of mucin,
glycoproteides, salts and decreased quantity of cellular elements. An external os of the cervical
canal is more dilated in the ovulation; microfibrils of endocervix are situated parallely. The last
one creates the microcanals which promote the migration of spermatocytes. Under the influence
of progesterone in post-ovulatory period the cervical canal is closed, the quantity of mucus is
decreased, microfibriles are situated as network which is non permeable for spermatocytes.
Vaginal cycle
Estradiol stimulates vaginal thickening and maturation of the surface epithelial cells of the
vaginal mucous in the follicular phase. Estradiol also facilitates vaginal transudation during the
sexual excitement, creating a moist lubricated vagina for sexual intercourse. During the luteal
phase of the cycle the vaginal epithelium stops its thickness but the secretory changes are
diminished. The thickness of epithelium becomes twice less. In the result of this desquamation
occurs. The superficial layer of vaginal epithelium is desquamated in this phase.
Cellular composition of vaginal contents is a biological test of sexual glands' hormonal activity.
Superficial, intermediate, parabasal and basal cells ratio depends on the vaginal hormonal state.
The quantity of superficial cells are correlated with the estradiol saturation of organism. The
more estradiol production results in more superficial cells. During the luteal phase of the cycle the
quantity of intermediate cells predominates. Parabasal and basal cells appear during ovarian
hypofunction and menopause. They are absent during the normal ovary function in the
reproductive women.
Breast cycle
The ductal elements in the breasts, nipples and areolae respond to estradiol ;cretion. After
ovulation, progesterone stimulates the acinar (milk producing) ds. Because the acinar glands are
located in the tissue of breasts, it gives the ~ts a more rounded configuration. Moreover,
progesterone makes the venous m on the surface of the breasts and it appears more prominent and
accentuates В small Montgomery glands contained within the areolae. These dynamic changes
can be observed during the reproductive cycle.
BIOLOGICAL ACTION OF THE OVARIAN SEX STEROIDS AND
GONADOTROPINS
Estrogens
Estrogens are produced by the follicular internal membrane cells and in less quantity by the
adrenal cortex. Estradiol, estron and estriol are the main estrogenic hormones. Estradiol is the
most active. Estrogenic hormones are circulated in the blood in free state and binding together
with proteins. The last one is biological inactive form.
Cholesterol that has been created from lipoproteids is the main structural compound for all
the steroid hormones. Steroid hormone secretion is stimulated by FSH and LH and by some
enzyme systems, for example aromatases.
The quantity of estrogens predominates in blood plasma. Estrogens enter the liver, then
they go into the intestine. Estrogenic hormones are destroyed in the liver and excreted with urine
via kidneys. Uterus (endometrium and myometrium), vagina and breasts are target organs for this
group of hormones.
The main biological effects of estrogenic hormones:
• provoke the growing and development of uterus and breasts during puberty
• stimulate hypertrophy and hyperplasia of myometrium during pregnancy
• cause the proliferative phase of endometrium
• uterine-placental blood circulation regulation, increase blood supply of uterus
• stimulate vaginal mucus epithelial cells maturation and differentiation
• myometrium sensibilizing to contractile drugs, thus increasing uterine tension, excitability
and contractivity
• increase uterine tubes peristalsis during ovulation that accelerates sperm migration
• endocervical stimulation to mucus production, increase mucus plug permeability for sperm
• nitrogen, sodium and fluid retention in the organism; calcium and phosphorus retention in the
bones
• decrease the level of blood cholesterol
• reticuloendothelial system stimulation in physiologic quantities, phagocytes activity that
respond for antibacterial immunity
Thus, in general, estrogenic hormones promote fertilization, interm onse' and normal duration of
labor. Menopausal estrogenic deficiency leads to the bone's calcium and phosphorus loss,
increases quantity of cholesterol. These factors provoke bones' fractures and cardiac diseases.
Estrogenic action inti organism depends on the doses: small or average doses stimulate ovaries,
follicul lar development and maturation; large doses depress ovulation; too large dosei lead to
atrophic processes in the ovaries.
I. Scientific and methodical grounds of the theme: disorders of the menstrual cycle constitute
20% in the structure of gynecological diseases. Various kinds of disoderes of the menstrual
function lead to a high loss of ability to work development of neuropsychic complications,
disability of women. These complications require complex approach and combined treatment of
doctors of several specialities- gynecologists, endocrinologists, neuropathologists, etc. That’s
why,study of this pathology is of a great importance for doctors of any speciality.
II. Aim:
A student should be able to Know:
1. Regulation of neuroendocrine function of the reproductive system.
2. Methods diagnostics of functional ovaries.
3. Classification of functional disorders of the reproductive system.
4. Amenorrhea: classification, diagnosis.
5. Abnormal uterine bleeding. Clinic, modern methods of diagnosis and treatment
principles.
1. Topicality: Early and active detection of benign tumours and precancer disorders of the female
reproductive organs and mammary glands, their timely and correct treatment –are the guarantee
to solve the problem of malignant diseases. Annumerated causes make this topic rather
important.
2. Educational objectives: to acquaint the students with frequency, structure, risk factors of
development of benign formations of the female reproductive organs and mammary gland.
Discuss clinical manifestation, methods of diagnostics and treatment of benign tumours of the
external genitals, ovaries, uterus and mammary gland.
3. 3.1 To know:
1. Pathogenetical variants of development of uterine myoma.
2. Classification of uterine myoma.
3. The main clinical symptoms peculiar for uterine fibromyoma.
4. Examination methods to diagnose uterine myoma.
5. Conservative methods of treatment.
6. Indications for surgical treatment of myoma.
7. Methods of surgical treatment of myoma.
8. Classification of benign ovarian tumours.
9. Complications of ovarian tumours.
10. Peculiarities of examination and treatment of ovarian cystoma.
11. Gynecological preconditions of diseases of the mammary gland.
3.2 To be able to:
1. Diagnose benign tumours of the external genitals, uterine and adnexa.
2. Make up a proper plan of examination to diagnose benign uterine tumours.
3. Make up a proper plan of examination to diagnose benign ovarian tumours.
4. Prepare a set of instruments to perform diagnostic scrapping of the uterine wall.
5. Make a target biopsy of the uterine cervix.
6. Perform speculum examination, vaginal examination, make the initial diagnostics.
8. Make up an individual plan of treatment.
3.3 Master the practical skills = a III.
1. Speculum examination of the uterine cervix.
2. Take smears for the cytological examination.
3. Bimanual gynecological examination.
4. Perform differentation diagnostics of intramural band submucous uterine myoma, cyst and
cystoma.
5. Determine indications for surgical treatment in patients with ovarian tumours and their
complications (torture of tumour peduncle, rupture and malignization).
Bartholinitis
Bartholinitis is an inflammation of Bartholin's gland (large gland of vaginal vestibule). It
may be caused by Staphylococcus, E.coli and N. gonorrhea. Any type of the pathogen initiates
ductal inflammation and obstruction that can lead to Bartholin's abscess. There can be serous, serous-
purulent, or purulent inflammation.
Obstruction of the opening of the main duct into the vestibule leads to abscess formation.
Infection of Bartholin's glands can lead to secondary infections, abscess or cyst formation (fig
85). When the gland becomes full and painful, incision and drainage is appropriate. Patients with
abscess usually require abscess incision with insertion of the catheter in abscess cavity. Recurrent
infection from vaginal flora and mucous cyst formation are common sequelae of bartholinitis. If
the infection of gland is caused by N. gonorrhea specific antibacterial treatment is prescribed.
Vulvitis
Vulvitis is a vulvar inflammation. It may be primary and secondary. Primary vulvitis is
caused by local irritants (including feminine hygiene sprays, deodorants, tight-fitting synthetic
undergarments in women with obesity or diabetes mellitus. Secondary vulvitis are caused by
accompanying discharge from vagina. Reduced estrogens levels in reproductive age women, and
more frequent in girls and menopause women may lead to vulvitis.
Clinic. Erythema, edema of vulva and skin ulcers are all indices of the infection.
Patient's complains are itching or burning. Excoriation caused by the patient's scratching
of the skin of vulva are often seen in vulvar irritation.
To relieve inflammation and itching the main suspected cause must be removed. The
therapy includes local application of boric acid solution or KMn04 solution. Candidasis is
treated with Gyno-paveril 150mg in suppositories — 3 days, or Orungal lOOmg twice a day
during 6-7 days orally, and then one capsule per day every first day of menstrual cycle during
3-6 cycles. Treatment with local antibiotics and steroids is successful.
Vaginitis (colpitis)
Vaginitis (colpitis) is an inflammation of vagina. It is the most frequent cause of visits
to gynecologists. It may be caused by Staphylococcus, Streptococcus, E.coli and other.
Excessive vaginal discharge is associated with an identifiable microbiologic cause in 80%
to 90%of cases. Hormonal or chemical causes account for most of the remaining cases. Vaginitis
may be acute, subacute and chronic. There are two forms of vulvitis: purulent and granulosa-
diffusional.
The main symptom is the increased, gray-white or yellow discharge generally serous or
purulent with rancid odour. The patients complain of dysuria, vulvar itching, burning and
dyspareunia. Examination may reveal edema or erythema of vulva and vagina, petechia or
patches in the upper vagina or on the cervix. In case of chronic vaginitis all these signs are not so
expressed.The cultures from vagina, cervix,urethra, ductus of Bartholin's gland should be
microscopically examined.
Treatment of nonspecific vaginitis is comlex:
• using of antiinflammatory medicines
• treatment of neuroendocrinologic and immunodificiency conditions
• treating of male sexual partner; patients should avoid sexual contacts while therapy
Local treatment includes using of syringing with antiseptic fluid (KMn04, furacilin,
chlorhexidin) no more than 3-4 days. In case of acute or chronic vaginitis laser therapy may be
used.
Metronidazol (vaginal suppositories), chlorhinaldin, terginan, betadin, gyno-paveril may be
prescribed. For normalization of vaginal ecosystem solkotry-chovac, vagilak, Lactobacterin and
Bifidumbacterin are used.
Bacterial Vaginosis
10-25% of all gynecologic patients have this disease. Among sexually transmitted diseases,
bacterial vaginosis is diagnosed in 60-65%> of women. Bacterial vaginosis is a result of an
overgrowth of both anaerobic bacteria and the aerobic bacteria Gardnerella vaginalis. Anaerobes
and G. vaginalis are normal inhabitants of vagina, but these bacteria overgrowth dominant of the
normal Lactobacillus flora results in the appearance of a thin, fishy odor, gray vaginal discharge
that adheres to the vaginal walls.
A small amount of vaginal discharge may be normal (2ml) particularly at the midcycle.
Bacterial vaginosis causes an increased vaginal discharge (15-20ml), vulvar irritation, pruritus,
dysuria and foul odour.
The diagnosis of bacterial vaginosis is based on the presence of the following
characteristics of the discharge:
• pH is higher than 4,5
• a homogeneous thin appearance
• a fishy amine odour produced by anaerobes when 10% KOH is added
presence of clue cells (vaginal epithelial cells to which organisms are attached).
Cultures aren't helpful because anaerobes and Gardnerella vaginalis can be recovered
from normal flora of healthy women, but the concentration of both bacteria is higher in
patients with bacterial vaginosis (fig. 86). Factors that lead to overgrowth of G.vaginalis and
anaerobes have not been identified.
Endocervicitis
Endocervicitis is the inflammation of mucosa layer of the endocervix. Bacteria cause
infection of the columnar epithelium. Chlamidia trachomatis, Mycoplasma, Trichomonada
vaginalis, N. Gonorrhoeae, viruses, Candida, E.coli, Staphylococci cause endocervicitis.
Cervix is constantly exposed to trauma during childbirth, abortion.The abundant
mucus secretion of the endocervical glands both with the bacterial ascend from the vagina
creates a situation that is advantaging to infection.
The inflammatory process is chiefly confined to the endocervical glands. The squamous
epithelium of the exocervix may be involved into the process called acute exocervicitis. The
extent of endocervical involvement as compared with exocervical one appears to have some
relation to the infecting agent.
Chronic cervicitis manifestation is cervical erosion. Erosion indicates the presence
around the cervical os a zone of infected tissue that has a granular appearance. It implies the loss
of superficial layers of the stratified squamous epithelium of the cervix and overgrowth of
infected endocervical tissues.
The inflammatory process stimulates a reparative attempt in the form of an upward
growth of squamous epithelium, causing some of the ducts of the endocervical glands to be
obstructed. Retention of mucus and other fluid within these glands results in the formation of
Nabothian cycts. These cysts are endocervical glands filled with infected secretion. Their ducts
become secondarily included into the inflammation and reparative processes.
The most important in the diagnosis of chronic cervitis is the exclusion of the malignant
process. Before the begining of treatment, examination with colposcope should be carried out.
The cervicitis may appear as a reddish granulation raised above the surrounding surface, giving
the impression of being papillary.
A Papanicolaou smear should be obtained and suspicious areas should undergo biopsy.
Treatment Acute cervicitis is treated with appropriate antibiotics (it depends on bacterial
agent). Local treatment of acute phase is a real danger of dissemination of infection. Laser therapy is
used in treatment of acute and chronic cervicitis.
Electocautherization is the traditional treatment of chronic cervicitis, especially with
erosion, cervical ulcers or ectropion. Nowadays cryosurgery or laser surgery has replaced
electrocautherization.
Acute endometritis
Acute endometritis is an inflammation of endometrium (mucus layer of uterine). It may
occur in such cases as: endometritis after uterine curettage or suction and puerperal endometritis.
Endometritis is caused by bacterias, viruses, mycoplasmas. The most frequent the associations of
3-4 anaerobic bacteria and 1-2 aerobic are the main reason of endometritis.
Anaerobic bacteria compose apart of the normal cervicogenital flora. There are two known
mechanisms which cause anaerobic infection: antibiotic selection that preferentially inhibits
aerobic bacteria and tissual trauma that occurs after surgery which reduces the redox potencial.
Anaerobes produce odorous metabolic products.
Uterus has endometrium factors of local immunity. There are T-lymphocytes and other
factors of cellular imunity in endometrial stroma. Lymphocytes and :utrophiels normally appear
in the endometrium in the second half of menstrual 'cle; their presence does not necessarily
constitute endometritis. The appearing 'plasma cells represents immune response, usually to
foreign bacterial antigen. The organism should be cultured before applying of antimicrobal
therapy, s anaerobes compose a part of normal flora, deep tissual cultures not mtaminated by
surface bacteria are required. Forty eight or more hours are quired for anaerobe recovery, and
treatment usually is based on clinical signs, here are nonspecific and specific endometritis.
Specific endometritis is caused у М. Tuberculosis, N. Gonorrhea, Chlamidia trachomatis,
Actinomyces.
Chronic endometritis
Chronic endometritis is a sequale of untreated acute endometritis or nona-dequate
treatment of postabortion or purperal endometritis. The chronic endometritis sometimes is
associated with the use of intrauterine device (IUD). In some cases it may occur without acute
stage.
Clinic. The chronic endometritis results from organisms that are normally in lower
genital tract (Protei, E. Coli, Staphylococcus, Mycoplasma). Bacteria that can be recovered are
usually of low pathogenicity, but more virulent intrauterine bacteria occasionally cause the
serous purulent' discharge, abnormal uterine bleeding and moderate uterine tenderness.
Diagnosis is based on anamnesis and clinical manifestation. It could not be diagnosed unless
plasma cells are found in the endometrium. Ultrasonography can identify gas vesicules in uterine
cavity, hyperechogenic places (local fibrosis, sclerosis) in basal layer of endometrium.
Treatment. A complex treatment is used. It includes a medicines for curing of
accompaning deseases, desensibilisative medicines and additional general health measures,
vitamines.
Physiotherapy has an important role. It improves pelvic hemodynamics. Diathermy on
lower abdomen, electrophoresis with copper, zinc, ultrasound, inductothermy, laser radiation are
used. If during physiotherapy the process becomes strained antibiotic therapy is recomended.
While remission antibiotic using is not proved.
Physiotherapy promotes to activation of hormonal ovarian function. If effect is not enouph
than a hormonal therapy is used (taking into account the patient's age, term of deseases, degree
of ovarian hypofunction). Health resort treatment is effective (balneologic therapy, mudcure
resort).
Salpingoophoritis
Salpingoophoritis is the inflammation of the uterine tubes and the ovaries.
Salpingoophoritis is the most frequent among all pelvic inflammatory deseases. Most cases of
oophoritis are secondary to salpingitis. The ovaries become infected by the purulent material that
escapes from fallopian tube. If the tubal fimbriae are adherent to the ovary, the tube and ovary
together may form a large retort-shaped tubo-ovarian abscess.
Most patients with salpingoophoritis have lower abdominal, adnexal tenderness
(unilateral or bilateral) purulent cervical exudate or purulent vaginal discharge (fig. 88).
Clinic. There are four stages of salpingoophoritis. The first — salpingitis without
irritation (inflammation), of the peritoneum, the second—with signs of peritonitis, the third with
occlusion of uterine tubes and tuboovarian abscess and the fourth is the rupture of tuboovarian
abscess. During bimanual examination adnexal inflammatory mass is revealed.
The diagnosis of salpingoophoritis is based on the history, physical examination and
laboratory tests. Besides that additional ultrasonography and laparoscopy can be used.
Laparoscopy provides the most accurate way to diagnose the inflammatory process and its
stage. It should be used in cases when the diagnosis is unclear, especially in patients with severe
peritonitis, to exclude a ruptured abscess and
Tuboovarian abscess
Tuboovarian abscess (TOA) may occur as a complication of salpingoopho-ritis. It
begins from acute purulent salpingitis when all layers of uterine tubes are involved into the
process. The tubes characteristically become swollen and redde is the muscularis and serosa are
inflamed. If exudate drips from the fimbriated mds of the tubes a pelvic peritonitis is produced
then it can give rise to peritoneal idhesions. The swollen and congested fimbriaes may adhere
to one another and produce tubal occlusion. The fimbriae may occlude tubes producing
permanent ubal infertility. The swollen and congested fimbriae may adhere to ovary, trapping he
exudate in the tube and giving rise to pyosalpinx or if the ovary becomes nfected, a
tuboovarian abscess (fig. 90). The mucosal folds may adhere to one mother forming gland-
like spaces that are filled with exudate. If the infection subsides after agglutination of the
fimbria and closure of the peripheral end of he tube, secretion accumulates and distends the
tube, forming pyosalpinx. Each •ecidive of chronic salpingoophoritis has more clinical
manifestation and is treated vith difficulty. TOA is associated with IUD, microbe association,
chronic salpingoophoritis.
Intoxication in case of TOA leads to liver disorders. Decreasing of albumin-globulin
index is observed while the level of general proteins is normal for a ong time. The degree of
these disorders depends on the time of duration of the process.
Clinic. Clinic of TOA depends on the volume of purulent damage of adnexa, duration of the
process, disorders of adjacent organs. There are some syndromes vhich are divided into local
syndrome (pain, purulent discharge, peritoneal symptoms and palpation of tuboovarian mass).
uterine body
tuboovarian abscesses
Peritonitis
Pelvioperitonitis is an inflammation of pelvic peritoneum.The polymicrobial infection
such as Escherichia coli and other aerobic, enteric, gramnegative rods, group of p-hemolytic
staphylococci, anaerobic, streptococci, Bacteroides species, aphylococci, mycoplasms cause
the process. Pelvioperitonitis occurs secon-ary. Primary process is in uterine tubes, ovaries,
uterus and parametrium. In lost cases purulent damage of uterine adnexa lasts with
pelvioperitonitis. lfection can be spread by limphogenic or blood vessels, and from uterine
tubes l case of salpingitis, especially gonococcial infection.
Clinic characterizes the acute inflammation. High temperature, severe lower bdominal
pain, fever or chills, tachycardia are common. There can be nausea nd sometimes vomiting.
Muscular defence and rebound tenderness are the ymptoms of peritoneal irritation. Anterior
abdomen wall takes part in breathing ct.Tender adnexa are present at bimanual examination.
Cervical motion causes ain. Posterior fornix is painfull.
Laboratory tests reveal increasing of white blood cell count and erythrocyte
edimentation rate. C-reactive protein levels may appear. Generall blood test hould be done 4-
5 times per day to diagnose transformation of pelvioperitonitis о peritonitis.
Treatment All the patients should be hospitalized. Ideally, the antibiotic hould be
selected according to the organism present in the fallopian tube or items, but in most cases
empiric therapy must be used. Treatment includes intravenous doxycycline and either cefoxitin
or cefotetan or intravenous clindamycin ind gentamicin for at least 4 days followed by oral
clindamicin or tetracyclin for [0-14 days. Hospitalized patients who have peritonitis but do
not have adnexal ibscess usually respond rapidly to the regimens. In the presence of an
adnexal ibscess, even if the systemic manifestations are mild, antibiotics which eliminate
3.fragilis should be selected because most pelvic abscesses contain this organism. Clindamycin,
Metronidazol, Cefoxitin, or Impinem should be used to treat pelvic ibscess. If there is an
intrauterine device it should be removed as soon as therapy s started. Surgery is indicated in
the case of ruptured pyosalpinx or ovarian ibscess. Colpotomy drainage usually is preferable
when unruptured midline cul-de-sac abscess is present. Laparotomy is required for such
problems as unresolved abscess or adnexal mass that does not subside, surgery should be
limited to the most conservative procedures that will be effective. Unilateral abscess respond
to unilateral salpingoophorectomy.
Septic shock
Septic shock is associated with infection caused gram-negative aerobic coliform
organisms those are producing endotoxins. In gynecological practice it may occur in case of septic
abortion, localized or spreading peritonitis, thrombophlebitis. Septic shock is a special organism
reaction that is expressed in development of severe systemic disorders. It may be caused by using of
broad spectrum antibiotic in high doses, that results in releasing of great amount of endotoxin.
Endotoxin, a complex cell wall-associated lipopolysaccharide, is released into the circulation
at the time of bacterial death, resulting in multiple hemodynamic effects. The subsequent activation
of lymphocytic T-cells and mass cells results in histamine and kinin activation as well as the
activation of kallikrenin and decrease in kallikreinogen and kallikrein inhibitor. These changes
result in the release of bradykinin, a potent arterial dilator. Early septic shock is a classic example
of distributive shock, related to a systemic maldistribution of relatively normal or even increased
cardiac output. Clinical findings include hypotension, fever and chills. Initial hemodynamic findings
include decreased systemic vascular resistance and high normal or elevated cardiac output. The
continued maldistribution of cardiac output leads to local tissue hypoxia and to the development of
lactic acidosis and organ dysfunction. This decrease in systemic vascular resistance is caused by the
release of vasoactive substances, as well as by vascular endothelial cell injury, which promotes
capillary plugging secondary to complement induced leukocyte aggregation. These factors lead to
increased arteriovenous shunting.
If the process continues a second hemodynamic phase of septic shock is developed. The
primary importance in this late phase is the development and progression of myocardial
dysfunction leading to ventricular failure. Studies assessing stroke work index and ventricular
ejection fraction have demonstrated depressed intrinsic ventricular function even in the early
stage of septic shock. Pulmonary hypertension, another important hemodynamic alteration is
often associated with septic shock, may have additional profound hemodynamic consequences.
As the sequalae of renal kidneys filtration disorders — the shock kidney is formed and acute
renal insufficiency is developed. Signs of liver disorders are hyperbilirubinemia, lipid
metabolism abnormalities.
Patients who recover from the initial hemodynamic instability of septic shock may suffer
prolonged morbidity secondary to endotoxin-mediated pulmonary capillary injury and
noncardiogenic pulmonary edema. Such lung failure is a major cause of death in patients whose
hypotension was prolonged and may experience acute tubular necrosis. Endotoxin mediated
endothelial cell injury and associated thromboplastine-like activity as well as prolonged shock
from any other cause may also lead to activation of the coagulation cascade and a clinical
picture of disseminated intravascular clotting syndrome (DIC).
Clinic and diagnosis. The clinical manifestation develops just after surgical operation on
infected organs. The body temperature rises till 39-40°C and is high during 1-3 days. Then the
temperature decreases, chills is a characteristic feature of the septic shock.
Among clinical findings there are hypotension without bleeding or nonade-quete to it,
tachycardia, 120-140 per minute. Decreasing of blood circulative volume leads to rising of
shock index till 1,5 (normally 0,5). Skin is pale and wet because of perspiration, later
akrocyanosis can appear. Breath disorders, like tachypnoe till 30-60 per minute, is the sign of
shock lungs. Skin may be colored in yellow, there may be blood vomiting.
The most dangerous complication of septic shock is kidney insufficiency. Clinical
manifestation at the beginning is oligouria — less than 30 ml per hour. Later anuria is
developed. All these changes in organism appear in very short time in 6-8 or sometimes 10-
12 hours.
Diagnosis is based on the following signs:
• septic organ
• low blood pressure, nonadequate to blood loss
• nervoues system disorders
• pain of different parts of body
• decreasing of diuresis
• rash on the skin
The blood temperature should be taken every 3 hours, blood pressure is measured
every 30 minutes, urine quantity must be measured. Bacterial culture from infected organ,
blood analysis, coagulogram and biochemical tests are performed.
Treatment of septic shock. The treatment of septic shock involves optimising preload relative
intravascular volume with crystalloid infusion as well as treating of the underlying infection.
Although some authorities advocate the use of colloid solutions for volume replacement, there is
noconvincing evidence that using of such solutions decreases the incidence of pulmonary edema
or adult respiratory distress syndrome. In most cases the infection is polymicrobial and broad
spectrum coverage for gram-negative and gram-positive aerobic and anaerobic organisms is most
appropriate. If an abscess is involved, promt surgical drainage after initial resuscitation is
mandatory. Patients in septic shock should be treated with dopamine hydrochloride. This agent in
doses of less than 5mg/kg/minute improves renal blood flow by means of dopaminergic
mesenteric vasodilatation; in doses of 5 to 30 mg/kg/minute, a positive inotropic effect is also
seen. The hemodynamic manipulation of patients whose hypotension fails to respond rapidly to
volume infusion may be assisted by pulmonary artery catheterization, allowing the clinician to
achieve optimal preload before the institution of inotropic or vasoconstrictive therapy. High-dose
corticosteroids are advocated (60-120 mg of prednizolone or 8-16 mg of dexamethazone). To
renew Ph balance lactosol or bicarbonate natrii are indicated.
SPECIFIC INFLAMMATORY DISEASES
(Sexually transmitted diseases)
To specific inflammatory diseases of the female reproductive organs belong tuberculosis
and sexually transmitted diseases. According to the WHO's classification, there are 21 such
diseases. Their frequency has been risen for the last years.
SEXUALLY TRANSMITTED DISEASES
(the WHO's classification)
Classic venereal diseases
Nosology Microorganism
1. Syphilis Treponema pallidum
2. Gonorrhea Neisseria gonorrhoeae
3. Chancroid Hemophilus ducrei
4. Lymphogranuloma venereum Chlamydia trachomatis
5. Donovanosis, or granuloma Callimmantobacteriumgranul
inguinale omatis
3,4,5 are mostly in tropic countries
Other sexually transmitted infections
Nosology Microorganism
A — that affect mostly genital tract
1. Syphilis Treponema pallidum
1. Urogenital chlamydiasis Chlamydia trachomatis
2. Urogenital trichomoniasis Trichomonas vaginalis
3. Urogenital mycoplasmosis Mykoplasma hominis
4. Candidosis vulvovaginitis Candida albicans
5. Genital herpes Herpes simplex virus
6. Genital warts Papillomavirus hominis
7. Molluscum contagiosum Molluscoviras hominis
8. Bacterial vaginosis Gardnerella vaginalis та mini
9. Urogenital shigellosis of збудники
Shigella species
10. Pediculosis pubis
homosexualists Phthyrus pubis
11. Scabies Sarcoptes scabiei
В — With mostly affection of other organs
1. Infection, caused by HIV Human immunodeficiency
2. Hepatitis В virus Hepatitis В virus
3. Cytomegalovirus infection Cytomegalovirus hominis
4. Amebiasis Entamoeba hystolytica
5. Lambliosis Giardia lamblia
Gonorrhea
Gonorrhea is a contagious disease caused by Neisseria gonorrhoeae. Among the
specific inflammatory diseases of the female genital tract gonorrhea takes the second place
and is in 5-25% of cases of all STDs.
Etiology and pathogenesis. Gonorrhea is caused by Neisseria gonorrhea (fig. 92).
The causative agent was found in 1879 by A. Neisser. Gram-negative N. gonorrhea is not
stable in the outer surrounding and dies quickly at the influence of antiseptic solutions, boiling,
drying, but it is rather stabile in human organism. In uncomfortable conditions they transform
into L-forms, which can transform into the usual form in the favourable conditions. In case of
chronic gonorrhea, N. gonorrhoeae are situated mostly in leukocytes and out of the cells, in
case of the acutening of the process they are found in the leukocytes.
Fig. 92. An agent of gonorrhea —
gonococus
N. gonorrhea affects mostly those parts of urogenital tract, that are covered with cylindric
epithelium: mucosa of urethra, cervical canal, Bartholin's glands ducts, mucosa of uterine cavity,
uterine tubes, ovarian epithelium, peritoneum. During the pregnancy, childhood and menopausal
period there can be gonorrheal vaginitis.
The source of infection is a person with gonorrhea.
Ways of infecting:
• the disease is sexually transmitted
• homosexual contacts, orogenital contacts
• very rarely through sponges, towels, underwear
• during labour from mother (infected eyes, vagina in girls)
Incubational period lasts for 3-7 days, sometimes for 2-3 weeks.
According to the stage of spreading the process the gonorrhea of lowei part of genital
organs (gonorrheal urethritis, endocervicitis, Bartholinitis, vulvovaginitis) and gonorrhea of upper
parts — gonorrhea ascendens (endometritis, salpingitis, pelvioperitonitis) is classified.
According to duration there are such forms of gonorrhea:
• fresh gonorrheal infection with acute, subacute, torpid passing, which lasts less than two
months
• chronic gonorrheal infection, lasting more than two months
• latent gonorrheal infection
In women the clinic of gonorrhea depends on the localization of the process, virulency of
causative agent, age of woman, organism's reactivity, stage of the disease (chronic, acute).
Fresh gonorrhea in acute forms has expressed clinical manifestations. Subacute form is
characterized by subfebrile condition, sometimes by expressed clinical symptoms, which
appeared two weeks before. Torpid gonorrhea in acute form has mild clinical manifestations or is
asymptomatic, but N. gonorrhoeae are found in the patient. Latent form is diagnosed when there
is no bacteriologic and bacterioscopic confirment, no symptoms, but person is a source of
infection. Chronic gonorrhea lasts for more than 2 months, or without establishing of the
beginning.
Gonococcal urethritis. Clinical manifestation appears within 3-5 days after infection and is
characterized by dysuria. Variable degrees of edema and erythema of the urethral meatus, purulent
or mucopurulent discharge are present.
Gonococcal Bartholinitis. It may occur when N. gonorrhea with vaginal discharge
infects the Bartholin's gland. It is manifested by edema, erythema around the duct's os. When
the occlusion occurs, pseudoabscess or Bartholin's abscess which are accompanied by purulent
process symptoms can develop.
Gonococcal endocervicitis. Inflammatory process develops in mucosal layer of the cervical
canal. Examination reveals edema and erythema of vagina and part of the cervix. There is a red
crown around the cervical os and a mucopurulent cervical discharge.
Gonococcal proctitis occurs very rarely. Rectum is involved into the process in the result of
contamination with the infected genital discharge. Clinic includes tenesmus and rectal pain.
Gonococcal endometritis is the first stage of the ascendant gonorrhea with infection of
basal and functional layer of endometrium. It is manifested by lower abdominal pain, high body
temperature, sometimes nausea, vomiting. Pain often has spasmatic character. Discharge is
sanguine-purulent or mucopurulent. Uterus is painful at palpation. Chronic endometritis is
characterized by menstrual disorders.
Gonococcal salpingitis is the infection of the fallopian tubes, mostly bilateral. In acute
stage the pain in lower part of abdomen is common. It becomes stronger, motion, nausea,
vomiting. Menstrual disorders can occur.
Smears must be taken on the 2-4th day of the menstrual cycle and after provocation in
24, 48, 72 hours, that allows to reveal N. gonorrhea.
Treatment is provided in special clinic. Sometimes the patient is treated by the
venerologist in ambulatory.
To reveal another sexually transmitted diseases clinical and laboratory examination must
be performed. While prescribing medicines the clinical form, complications and severity of the
process should be taken into consideration.
The main medicines in gonorrhea treatment are antibiotics. Gonococcal infection very often
is accompanied with trichomoniasis, chlamidiasis, candidiasis, mycoplasmosis.
Antibiotics that have influence on the following agents such as: Ciprofloxacin,
Doxycyclin, Trobicyn, Sumamed, Cephtriaxon, Afloxacin in combination with Metronidazol,
Tiberal, Naxogyn should be prescribed. The dose of antibiotics is taken according to the methodical
instructions of the Ukraine МНР and annotation of medicines.
Gonovaccine is used after ineffective antibiotic treatment and relapse in the latent fresh
torpid and chronic form of the disease (200-300 mln. of microbe bodies, in 2-3 days
intramuscularly). During pregnancy immunotherapy and antibiotics with negative influence on a
fetus are not used.
For toilet of external genital organs 0,002% solution of Chlorhexidine, Re-cutan, Baliz-2
are prescribed. Local treatment of chronic gonorrhea is conducted after disappearing of the signs
of acute inflammation. In chronic and subacute stages physiotherapeutic methods are used: laser
radiation, paraffinotherapy, mud-cure, diathermy, inductothermy, U.H.F-therapy.
The control of the results of treatment: disappearing of subjective signs and microbe
agents in all the infected organs and discharge. On the 7-10th day after medical therapy the
bacterioscopic and bacteriologic methods are used to confirm the results of treatment. If there is
no N. gonorrhea in the material, then the combined provocation is conducted: injection of
Gonovaccine (500 mln. of microbe bodies), instillation of 1% Lugol's solution in urethra, 0,5%
solution of Argentum Nitrate into cervical canal. Discharge from this organ should be examined
during 3 days. Smears are taken during menstruation and then after provocation in 24, 48, 72
hours. Such examinations are provided during 2-3 menstrual cycles. Women which have
contacts or work with children are not allowed to work.
Prophylaxis. Using of condom is the most effective prevention method. If the sexual
intercourse has happened without it, then the external genital organs should be washed with water
and soap, and after urination syringing with 0,05% Chlorhexidin solution should be performed.
Urogenital trichomoniasis
Urogenital trichomoniasis is caused by Trichomonas vaginalis and is a result f their
invasion into the lower part of genital tract and urethra.
Ethiology. Trichomonas vaginalis is a flagellate protozoan (fig. 93, 94) and t is transmitted
by sexual intercourse. It is not stable in outer environment, dies n few seconds under the influence
of antiseptic solutions, in water it dies during 5-45 minutes, and also when they wash hands with
soap, it is sensitive to drying, n human organism Trichomonas vaginalis can exist in 3 forms:
common one pear-shape form), amebiform with the expressed phagocytosis action (it can
ihagocytise mycoplasmas, N. gonorrhea and other bacteria that caused the recur-ence of
mycoplasmas or gonorrhea. This is the most spread disease among all he sexually transmitted
ones. Its frequency rate reaches 50-70% of sexually ictive women. According to the WHO
statistics, 10% of world population suffer rom trichomoniasis. Non-sexual transmission is very
seldom: when they use ;ponges, underwear, towels.
Incubation period lasts for 5-15 days, the main places of trichomonas >arasitizing are
mucose membranes of vagina, cervical canal, uterus cavity, uterine ubes, Bartholin gland's duct,
urethra, urinary bladder.
Inflammatory process develops in the infected mucous membrane: edema, lyperemia,
exudation, desquamation affects epithelial cells.
Clinical manifestations. Vaginitis, urethritis, endocervicitis, proctitis are he most
common manifestations, ascendant infection meets rarely.
Urogenital mycoplasmosis
Ethiology. Microbal agents are Mycoplasma hominis, Mycoplasma genita-loum,
Ureaplasma urealiticum.
In the etiology of the inflammatory diseases of female genital organs the associaton of
mycoplasmosis with trichomoniasis, N. gonorrhea, Chlamidia trachomatis, anaerobes is of great
importance.
Mycoplasmas are transmitted sexually and they are highly spread among the population.
Clinic. Mycoplasmas infection can occur in acute and chronic form, and has no
symptoms, which are specific for this agent. It is often found in healthy women. Mycoplasmosis
is characterized by torpid course, sometimes the latent forms of the reproductive system
inflammation are observed. The agents may be activated under the influence of menstruation, oral
contraceptives, pregnancy, delivery. Ureaplasma is identified in the patients with vaginitis,
cervicitis, urethritis, in association with other bacteria the symptoms are typically and described in
the part "Nonspecific inflammatory diseases of the female genital organs".
Diagnosis. To reveal ureaplasmas the bacteriological method is used. Material is taken
from the purulent discharge of Bartholin's glands, from uterine tubes at salpingitis, tuboovatian
tumors at pelvic inflammatory disease. Test on the urease is done (colour index). It is based on
the property of ureaplasms to product urease, that changes the pH and the colour of indicator.
Serological diagnosis is also used. Immunogram in diagnosis of mycoplasmosis and other infection
(Chlamidia, gonorrhea, trochomoniases, herpes simplex virus) is indicated.
Treatment. Using of antimicrobal medicines from macrolid group (Erythromycin,
Sumamed, Roxitromycin), Tetracyclin group (Tetracyclin, Doxycyclin), Fluorochinolones
(Ciprofloxacin) is etiotropic treatment. They are prescribed for not less than 10-14 days with the
following laboratory control. Another course of treatment is immunity stimulation
(Immunoglobulin, Levamizol, T-activin, Ginseng Tincture).
Prophylaxis. Examination of the risk group (prostitutes, women with infertility,
inflammatory processes of genital organs), and keeping to the same measures for preventing sexually
transmitted diseases are used.
Syphilis
Syphilis is an infective disease, that is transmitted sexually.
Etiology. The pathogene is Treponema pallidum. In microscopic examination it has spiral
shape and is movable. Optional temperature for reproduction of Treponema is 37°C. It is very
sensitive to different external conditions. It dies during boiling, drying, under the influence of
different chemical agents and 90% ethanol. While working with the infected persons hands are
cleaned with ethanol. It prevents from infection at contact with syphilitic rash having Treponema
pallidum on its surface. At 40°C (temperature for keeping blood for transfusion in refrigerator)
Treponema pallidum dies in 24 hours.
The source of infection is the infected person.
Ways of transmission:
• sexual perversion (oro-genital, homosexual contacts)
• transplacental — congenital syphilis, when a child is infected by transplacental
transmission
• professional — while examining the ill person with wet surfaced rash
• transfusion (very rarely) — as a sequale of blood transfusion from the ill person
Clinical manifestations. 3-4 weeks pass from the moment of agent penetration into
organism and till the first manifestations of the disease. This is the so-caled incubational period.
The microbe is already in human organism, but there are no complications and signs of the
disease.
After finishing of incubational period the first signs appear only in the area of agent
inoculation. This is the so-called primary lesion (ulcerated shancre) (fig. 96). It appears as a
painless indurated papula on skin or mucos with erosion or necrosis of the surface. Is a hard-
based, well-
Fig. 96. Ulcerated shancre of labia major
circumscribed lesion. There is no inflammation around it and it has smooth surface with
serous discharge. Its
size is from several mm to few cm, and it can be coated with whitish discharge like old
fat. On mucos of genital organs or anus it is like fissure. Sometimes shancre can gangrenize.
Indurative edema belongs to the atypical forms of shancres. Labia major enlarges in size, they
are firm and painless. Chancre on pubis, thighs and cervix can occur rarely.
If the shancre is situated on the genital organs, then after nearly 7 days the inguinal
lymphatic nodes enlarge on one side (scleradenitis, bubo), rarely on both sides. They are
firm, movable, painless. They are not connected with skin and have no suppuration. This is
the primary syphilis, that lasts for 6-8 weeks from the appearing of the shancre (the first 3-4
weeks is primary seronegative period, when Wassermann reaction is negative, and next 3-4
weeks, when Wassermann test is positive). Diagnosis in this period is based on the history
taking (sexual contact, incubation period, examination of sexual partner, revealing of Treponema
pallidum on shancre surface, positive serological reactions (Wasser-mann's,
immunofluorescence).
Without identification of the agent or positive serological reactions diagnosis of syphilis
is not proved.
After 6-8 weeks of shancre development, the body temperature may rise, there is the
night headache, bone pain can appear. This is the so-called/?ro<iroma/ period. During this time
the agents are reproducted intensively, they appear in blood (treponems sepsis) and there is
disseminated rash on skin and mucosal layer. There appear the signs of secondary syphilis.
Firstly roseolas (little red macula 0,5-1 cm in size) appear on body skin. They disappear for a
while after the finger pressure, don't protuberate over the skin level. After some period
papulas, very rarely pustulas or hair shedding appear. In this time on skin and mucos of the
female genitals papula (erosion nodes) can appear. They are firm, without inflammation, up to
1 cm in diameter, with moist surface, rich in microbal agents (Treponema pallidum), that make
them very infectious. There are no subjective feelings. As a result of irritation these nodes
enlarge, indurate and transform into the so-called condyloma lata, 0,5-1 cm and more in
diameter, indurated, prominating above skin level, without signs of acute inflammation,
painless, with smooth or tuberous, sometimes with moist surface.
There are plenty of agents on the surface of condyloma lata and they are very
contagious. They should differ it from viral pointed condylomas (soft, on the pedicle, with
lobular, like cauli-flower structure).
Diagnosis is confirmed by presenting erosional papulas and condyloma lata, positive
serological reactions (Wassermann's reaction, reaction of immobilization of Treponems).
Treatment of syphilis is provided by penicillin antibiotics (bicillin, retarpen, extencillin)
in venerologic dispensary, according to the instructions of the Ukrainian Ministry of Health
Care.
Prophylactic measures: avoiding of extramarital relationships, using of condom. If
coitus was without condom or it has been torn, then the external genital organs should be
washed with soap and warm water, and during the first 2 hours the cleaning of genitals should
be performed.
AIDS
Agent of AIDS is retrovirus, which affect immune system of organism.There are two types
of Human immunodeficiency virus, that caused acguired immunodeficiency syndrome (AIDS):
HIV-1 and HIV-2.
HIV-1 is spread in all the countries of the world. HIV (human immunodeficiency virus)
is very sensitive to heating, while at boiling it dies immediately, as well as after applying of 70%
Ethanol, 0,2% solution of Natrii hypochlorate and other desinfective solution. But this virus
survives in its dried form during 4-6 days in 22°C temperature, in lower temperature even more.
The source of infection is the ill person or viral carrier. People with AIDS are infective all over the
life.The quantity of people with HIV in many times prevalents the quantity of ill person with
AIDS. Infected person becomes contagious in a very short time — 1 -2 weeks after infection.
The ways of infection:
• sexual, which insures natural viral transport from one person to another, as well as
sequel of homosexual contacts
• parenteral way of infection occurs when they break the sanitary rules making injections,
especially intravenous, when injections are made with one syringe, with changing only the needle
• professional way of infection of medical personnel occurs when blood of the person
with AIDS contacts with lesioned skin (microtrauma, fissure etc) or mucosal layer during
manipulations (injections and others)
• transfusional way occurs very rarely, when the infected blood is transfused to the
healthy person
• transplacental — from the infected mother to the child
So, HIV infection can be transmitted from people to people in direct contact: "blood to
blood" or "blood to sperm". Transmission of virus through saline during kissing is less possible.
The virus isn't transmitted by insect stings.
Clinical manifestations of AIDS: Incubation period can last from 1 month to 10
months or even to years. Clinical manifestations may vary, they can be divided into some
periods. In 30-50% of the inspected persons in 2-4 weeks an acute period can be observed:
fever, tonsillitis, enlarging of neck lymphatic nodes, liver, spleen. This lasts for 7-10 days, and
then the disease becomes latent. The only sign of illness at this time may be the enlarged
peripheral lymphatic nodes. They are movable, not connected with tissues, some of them are
painful at palpation. Such enlarging of the nodes can indicate to the AIDS, if it lasts for more
than 1,5-2 months. Later the so-called AIDS-associated or premorbid complex of symptoms
is developed. It can last from 1 to 6 months during some years. In this time many different
symptoms and diseases which are not specific for AIDS (up to 200) are developed. That is
the long-term fever, generalized enlarging of peripheral lymphatic nodes, periodical diarrhea,
weight loosing (more than 10%), oral cavity candidiasis, leukoplakia of tongue, folliculitis,
different skin lesions.
This period lasts wave-likely while health becomes better till the clinic remission,
when person considers himself absolutely healthy.
The last period is AIDS. In such persons different infectious diseases occur (up to 170)
on the base of immunodeficiency, caused by HIV-infection. Nervous system is damaged (in
30-90% of patients), poor orientation, bad memory and demention are develops.
Pneumocystic pneumonia (lung inflammation) occurs up to 60% with severe, sometimes with
fulminant passing. In 60% of cases severe and long-termed diarrhea is observed. Kaposhi's
sarcoma very often progresses and becomes the reason of death at young age In significant
part of patients having AIDS, malignant processes like lymphoma and others are developed as
a result of virus influence on immune mechanism of human being. Skin and mucosa are damaged
with Candida fungi (candidiasis, Herpes simplex and Circular herpes virus with severe, relapsing
duration, they don't undergo to usual methods of treatment.
Diagnosis. In AIDS the following diagnosis are mentioned:
• epidemiological history (homosexualism, drug abuse, prostitution, intravenous
injections etc.)
• a long-term enlargening of peripheral lymphatic nodes, loosing of body weight, long-
term fever and diarrhea
• revealing of antibodies to HIV in blood by immunofluorescent analysis and others. 5 ml
of venous blood is taken, and it is kept in refrigerator at the tempreature of+2 — +4°C. Serum is
taken out after appearing of the blood the clot and sent to the laboratory not later than in 1-3 days
Treatment. There are no medicines for treating AIDS. But remedies, that
inhibit development of the disease are used. Nowadays there is an effective
preparation for treatment of HIV infection and AIDS — Krixivan (protease inhibitor). Triple
therapy of Krixivan base (Krixivan+AZT+ZTS) has high effectiveness, decreases quantity of
viruses in blood to lower level. Immunostimu-lators, immunomodulators, symptomatic
therapy depending on the pathology is used.
Prophylaxis:
• sanitary and educational work among inhabits
• avoiding of pre- and extramatrial relationships
• using of condoms (decrease the transmission in 200-500 times)
• prophylaxis of drug abuse, parenteral (subcutaneous or intravenous) injectons of medicines
proper sterilization of medical instruments, using syringes and needles of single use
• using special defence agents by medical workers contacting with patients' blood and
other biological substances (special closes, double gloves, goggles, masks)
• control of donor blood
VIRAL DISEASES
The quantity of viral diseases of genital organs has been significantly inc-increasing for
the last time, especially among young people.
Viral infections can occur in latent form, with less symptoms and with expressed clinical
manifestation. That's why it is very difficult to diagnose them. These diseases have especially
negative influence on the pregnancy. There is a risk of viral transmission to fetus.
They can cause fetus diseases or defects of development, leading to fetus death or
miscarriage." Every pregnant woman with miscarried fetus must be examined on these
infections presence, because in the majority of such women Cytomegalovirus, Gripp virus,
Hepatitis A and В virus, Papillomavirus are revealed. Besides the influence on fetus, according to
the recent investigations, viral infection causes malignant growth in the female genital organs.
Herpesvirus infection
Herpesvirus diseases of genital organs are caused by Herpes simplex virus, mostly of the
second type (HSV-2). Source of the infection are infected persons and carriers. It may be
revealed in young sexually active women. It can be transmitted during orogenital contact. The
virus is located mostly in mucos membranes of urogenital tract in men and cervical canal in
women, also in the nervous ganglions of lumbar and sacral parts of sympathetic nervous system.
Genital herpes is transmitted sexually. During pregnancy it may cause miscarriage and
malformations.
Genital herpes is considered to be all-life persistant infection, that's why it has a relapsing
passing.
Clinical manifestations. According to the clinical signs, the disease duration is divided into
typical, non-typical, and asymptomatic one (viral carrier).
Typical passing of the disease is characterized by genital and extragenital signs.
Extragenital signs: rising tempreature, mialgias, headache, nausea, viral rash on face, bad
sleep. Genital signs are present on the lower parts of genital system — vulva, vagina, cervix,
near urethra os perineum. Single or plural vesicles up to 2-3 mm in size, with erythema and
edema, which exist for 2-3 days appear in mucous membranes. After vesicle rupture erosion
with incorrect form, covered with yellow discharge appears. The erosion re-epitheliazes
without scars in 2-4 weeks.
Patients complain of pain, irritation, itching in area with viral lesions.
Clinical manifestations are in three forms:
• I — acute primary
• II — chronic recurrent
• III — atypic
Depending on the localization, genital herpes is divided into three stages:
• the first one — herpes lesions of external genital organs
• the second — herpes lesions of the vagina, cervix, urethra
• the third — herpes lesions of the uterus, adnexa, bladder
Diagnosis is based on history taking, complaints, objective examination, revealing of
HSV-2 or its antibodies in the patient's serum.
The most informative method of identification is isolation of the virus from discharge
of the cervix, vagina, uterine cavity, urethra. For express-diagnosis a method of fluoriscine
antibodies and immunoperoxydase method are used. There is electro-microscopic method of
HSV-2 identification and the method of viruses inoculation on tissue culture with the
following studying of their properties.
Treatment is difficult because of the relapses of the disease and possibility of
reinfection.
Antiviral medicines belong to three main groups (according to the action
mechanism):
• replication inhibitors of viral nucleic acid
• interferon and compounds, that have interferon-inductive action
• compounds with other antiviral action
Difficulties of treatment are caused by virus peculiarities (they are obligate
intracellular parasites).
As a result of investigation of virus nature on molecular level, new medicines were
created. They have the influence on viral growth and development of the virus. They are
Zovirax (Acyclovir, Valacyclovir), Alpizarin, Foscarnet, Valtrex, Herpevir. Acyclovir is used
in dose of 600-1200 mg per day, orally or intravenously.
Local therapy by 3% Megasin ointment, 3% Bonaphton or 3% Alpizarin is also used.
For treatment of the recurrent herpes antiviral medicines, herpal vaccines, antirecidive
immunotherapy are used.
Condylomas acuminata
Ethiology. Condylomas acuminata are caused by Human Papillomavirus of 16 and 18
types. They are transmitted sexually (fig. 98). Resistant to disinfective agents viruses may be killed
by high temperature during sterilization. Incubational period of condyloma acuminata lasts from 1 to
9 months. The disease often occurs in sexually active persons. Papillomavirus causes genital
cancer. These patients have in 1-2 thousands times more chances to acquire a malignant process,
than healthy people. Condylomas acuminata can transform into cancer in 6-26% of cases.
Clinical manifestations: On the onset of disease single pink, sometimes grey warts,
with thin pedicle, rarely with wide base appears on skin surface of labia majora, perineal area
and mucosal layer of urethra, anus, vagina, cervix. Condylomas acuminatum can grow
significantly and fuse (fig. 99). They looks like cauliflower, with lobular structure, and have
long-term duration. Some patients with long-term duration of the process can have big
condylomas, like tumor. They can be complicated by abnormal vaginal discharge, due to the
secondary vaginal infection. Condylomas may cause some difficulties at walking, intercourse.
During pregnancy and delivery they can cause bleeding. In 15-17% of patients regression
may occur, especially during pregnancy.
Clinical diagnosis. Lobular surface, soft consistency, thin pedicle should be taken
into consideration.
Differential diagnosis for genital warts includes condylomata latum, which have wide
base, brown or red colour, and no lobular structure. Also other manifestations of syphilis are
present there.
Treatment If genital warts are large, laser vaporization is performed. It is more
effective, than criodestruction or surgical diathermy. For treatment of small condylomas 30%
solution of Podophyllin, Condilin or Resorcin are used. Modern effective remedy is Solcoderm.
Molluscum contagiosum
Ethiology. Molluscum contagiosum is caused by virus, that is transmitted by contact
with the ill persons or during using their things. In adults the main way of transmission is
sexual contact. Children are infected more often. Incubation period lasts from 2 till 9 months.
Clinical manifestations. On skin the small firm dome-shaped papules 5-7 mm in
diameter, occasionally enlarging to 1-3 cm conglomerates is appeared. The flesh-colored
papules have specific central umbilication (fig. 100). Lesions are located on the external
genital organs, perineum, pubis, hips, face.
Molluscum contagiosum can persist for a long time.
Clinical diagnosis. After direct pressure by forceps white caseous material can be got.
Treatment. The lesions are pressed by forceps and cleaned by Iodine solution or
Betadine, garlic juice or cryotherapy.
Cytomegalovirus infection
Infectional agent is Human cytomegalovirus. The percentage of the infected women
according to the world literature is very high. In Western Europe it is from 50 to 85%. Among
pregnant women with usual miscarriage 70% are infected.
of Izonicotine acid (Izoniazide, Saluzid) and PASA. The last one has not only
bacteriostatic action, but also prevents from development of microorganisms resistention to
antibiotics and preparations of izonicotine acid, that's why they can be used for a long time.
Treatment lasts for 1,5-2 years, during the first 3-6 months the combination of 3 medicines is
used, and later on for 6-8 months 2 agents are taken. After that supportive therapy is performed
till 2 years.
Intramuscular and oral usage of medicines are combined with injection of some dose of
medicine in focus of lesion. Lidase with antibiotics and hydrocortisone are used for this purpose
by means of colpocentesis to the damaged organ. These medicines may be used during
hydrotubations. 1 % solution of chimo-tripsin is used through posterior fornix and by
electrophoresis. In some cases surgical treatment is used. In spring and autumn antirecidive therapy
is performed.
Rehabilitation of such patients is provided in specialized health resorts (Odessa,
Alupka). For resolvation of residual affects after tuberculosis physiotherapy and pelotherapy are
used.
PYOSALPINX RUPTURE
An abscess rupture takes place spontaneously or in the result of physical trauma.
Clinic. Before abscess perforation there is always patient's health change to the worse -
pain reinforces, temperature rises, peritoneum irritation symptoms are intensifying. Just after
rupture there appears an acute pain which has a cutting character through the abdomen, collapse,
nausea, vomiting, stomach is strained and strongly painful. General patient's state becomes
worse, the face features sharpen, breathing becomes frequent and superficial. In the result of
bowels paresis abdomen becomes flatulent, peristalsis disappears and meteorism develops.
Diagnosis. During stomach percussion one can find blunting of sound in lateral
departments because of exudate presence in abdominal cavity.
During bimanual examination uterus and ovaries palpation is impossible because of acute
pain and tension of front abdominal wall and vaginal fornixes bulgeng. Pelvic peritonitis may
develop in the result of pyosalpinx rupture. Specification of the diagnosis can be made by means
of ultrasonic research and culdocentesis.
Treatment. Cure of patients with purulent process in abdominal cavity is a complicated
problem, successful solving of which needs fast and decisive actions. Operative cure with
ablating of altered ovaries and following drainage of abdominal cavity is necessary. Laparotomy
should be made by lower-middle incision, because this access gives a possibility to make a
revision of abdominal cavity organs and its wide drainage, and if it is necessary - peritoneal
dialysis. During the operation it is necessary examine appendix because its frequent involving in
pathological process. If pathological changes are found appendectomy is done. Removal of
purulent mass is technically difficult and needs caution and carefulness, but ablating of purulent
formation is obligatory, because drainage, without ablating causes formation of purulent fistulas,
those do not heal for a long time. A conservative care of such patients (antibiotics, vitamin
therapy, cold on umbilicus) can give a temporary state improvement, but not a convalescence.
Disease acquires chronic recidivate character with frequent acutenings. Operative intervention is
inevitable anyways, however before operation it is necessary to make out suitable patient's
preparation with stimulation of immune system and detoxicaton.
Torsion of tumor crus
Cystoma cms torsion can happen more often, but sometimes the eras of subserous fibrous
myoma can also happen. Quick motions, pregnancy, labor, stormy bowel peristalsis can cause
torsion. In the result of torsion trophies of tumor tissue disturb, degenerative changes and
necrosis with wall rupture appear in it
Clinic. Complete and incomplete eras torsion may occur. Clinically at eras torsion the
symptoms of "acute abdomen" appear. Muscles of anterior abdominal wall tension is expressed
on the part of process localization. In case of a big tumor its contours are available for palpation
through abdominal wall, and during bimanual examination one can reach a lower tumor pole.
Examination is very painful. In incomplete torsion the clinical picture is poor less and all
phenomena can temporally vanish if blood supply of the tumor will be renewed.
Treatment. Torsion of tumor'eras needs immediate operation. Protraction with
laparotomy gives rise to tumor necrosis, infection, beginning of adhesion's process and accretion
of tumor to adjacent organs, that will create additional complications during the operation. An
operation volume depends on ovarian tumor type: at benign tumor it is removed; in suspicion of
malignization total hysterectomy with omentum resection is indicated.
There is a peculiarity in the operation: clench is laid more proximally from the place of
torsion and the tumor is cut off without twisting its crus. It is forbidden to twist the crus because
the thrombs those are in crus and also substances of necrotic destruction of the tumor can get into
woman's blood.
IV. Control questions and tasks
1. Etiology, pathogenesis and classification of extrauterine pregnancy.
2. Clinical signs of progressing extrauterine pregnancy and the methods of its
diagnostics.
3. Clinical signs of interrupted extrauterine pregnancy and the methods of its
diagnostics.
4. Clinical differences of extrauterine pregnancy interrupted by the rupture of the
uterine tube and tubular abortion.
5. Differentiation diagnostics of extrauterine pregnancy and acute appendicitis.
6. Methods of surgical treatment of extrauterine pregnancy.
7. Indications for concervative treatment of tubular pregnancy.
8. Methods of concervative treatment of tubular pregnancy.
9. Cervical pregnancy. Diagnostics and treatment.
1. A 31- year- old patient is admitted in the gynecological department
complaining of severe blood discharge from the genitals, weakness, and dizziness. She
experienced measles, parotitis flu, frequent quinsy. Menstrual cycle is not regular,
starting from the age of 12. She became sick 15 days ago, when blood discharge
appeared from the genitals after 2 months of delay. The following days intensity of
bleeding increased, weakness and dizziness developed. A general condition is of
moderate severity. Pulse is 90. BP- 80/70, mercury. The tongue is moist and clean. The
patient is of an average fatness, the mammary glands are poorly developed. Heart or lung
pathology is not found. Blood analysis: haemolobin- 50g/l, erythrocytes- 2200000.
Rectal-abdominal examination: smooth and conical cervix, uterine body is in the normal
position, small, mobile, painless. The adnexa are not detected on the both sides. Blood
discharge with clots.
Diagnosis. Plan of treatment. Measures concerning prevention of uterine
bleeding.
The term infertility is generally used to indicate that a couple has a reduced capacity to
conceive as compared with the mean capacity of the general population. In a group of normal
fertile couples, the monthly conception rate, or fecundability, is about 20%. This figure is
important for all couples seeking fertility to know, because it will alleviate unrealistic
expectations of immediate success with various therapies, which can only approach 20% per
cycle (with the exception of in vitro fertilization/embryo transfer [IVF-ET]). For most couples
the correct term should be subfertility, suggesting a decreased capacity for pregnancy but not an
impossible feat.
KEY POINTS
• In 1995 about 10% of all U.S. couples with women in the reproductive age group were
infertile—6.2 million women.
• The incidence of infertility steadily increases in women after age 30.
• Among fertile couples who have coitus in the week before ovulation, there is only
about a 20% (monthly fecundability of 0.2) chance of developing a clinical pregnancy
in each ovulatory cycle.
• In about half of fertile couples attempting to conceive the woman will become
pregnant in 3 months, 75% in 6 months, and 90% at the end of 1 year.
• Infertile couples who conceive do not have higher rates of spontaneous abortion or
perinatal mortality than age-matched control subjects.
• In the United States approximately 10% to 15% of cases of infertility are caused by
anovulation, 30% to 40% by an abnormality of semen production, 30% to 40% by
pelvic disease, and 10% to 15% by abnormalities of sperm transport through the
cervical canal. About 10% to 20% of cases are unexplained.
• The primary diagnostic tests for infertility are documentation of ovulation, semen
analysis, and hysterosalpingogram (HSG).
• The basal body temperature (BBT) increases when circulating levels of progesterone
increase, and a sustained increase of BBT occurs following ovulation.
• A sustained rise in BBT or a serum progesterone level greater than 5 ng/mL is
presumptive evidence of ovulation.
• A midluteal-phase serum progesterone level above 10 ng/mL is an indication of
adequate luteal function.
• A high percentage of fertile men will have at least one abnormal parameter in their
semen analysis.
• In women with a normal HSG, a hysteroscopy is unnecessary because it will not detect
additional abnormality.
• Other diagnostic tests for infertility, including (1) measurement of serum prolactin and
TSH in ovulatory women, (2) a late luteal-phase endometrial biopsy, (3) immunologic
tests to detect sperm antibodies, and (4) bacterial culture of cervical mucus and semen.
• There is no evidence that treatment of an abnormality in the tests just listed
significantly improves pregnancy rates compared with withholding therapy.
• Of all the causes of infertility, treatment of anovulation results in the greatest success.
• When ovulation is induced with clomiphene citrate and no other causes of infertility
are present, conception rates over time are similar to those of a normal fertile
population.
• Discontinuation of therapy is the major reason for the reported difference in ovulation
and conception rates in anovulatory women treated with clomiphene.
• More than 90% of women with oligomenorrhea and 66% with secondary amenorrhea
and E2 levels of 40 pg/mL or higher will have presumptive evidence of ovulation
following clomiphene therapy.
• When conception occurs after clomiphene treatment in anovulatory women, the
incidence of multiple gestation is increased to about 8%, nearly all of them being twin
gestations. The incidences of clinical spontaneous abortion, ectopic gestation,
intrauterine fetal death, and congenital malformation are not significantly increased.
• Formation of ovarian cysts is the major side effect of clomiphene treatment.
• About 5% to 10% of women treated with the individualized, graduated, sequential
regimen of clomiphene citrate fail to ovulate with the highest dosage.
• Treatment of anovulation with gonadotropin effects an ovulatory rate of about 100%.
• The pregnancy rate per cycle with gonadotropins is similar to that following
clomiphene therapy (22%).
• The incidence of spontaneous abortion after HMG therapy is high (25% to 35%), and
clinically detectable ovarian enlargement occurs in about 5% to 10% of treatment
cycles.
• If GnRH is used for ovulation induction it needs to be administered in a pulsatile
manner at intervals of 1 to 2 hours.
• For women with polycystic ovaries who do not ovulate following administration of
clomiphene citrate, partial ovarian destruction by electrocautery or laser through the
laparoscope is effective in inducing ovulation.
• Pregnancy rates for oligospermia following intrauterine insemination are in the 25% to
35% range.
• Semen donors need to be carefully screened to be certain that they are in good health,
do not have a potentially inherited disorder, and will not transmit an infectious agent in
the semen.
• Because antibodies to HIV may not develop for several months after infection, it is
recommended that all donor insemination be performed with frozen sperm that has
been stored for at least 6 months at which time negative antibodies to HIV should be
observed in the donor before the sperm is used for insemination.
• The prognosis for fertility after tubal reconstruction depends on the amount of damage
to the oviduct as well as the location of the obstruction.
• If both proximal and distal obstructions of the oviduct exist, intrauterine pregnancy is
uncommon, and operative reconstruction should not be performed, IVF is the best
therapy.
• Women with pelvic tuberculosis should be considered sterile, and no tubal
reconstructive procedures should be attempted. IVF may be attempted if the
endometrial cavity is not infected.
• Overall conception rates following salpingostomy are in the 30% range, with a high
percentage (about one fourth) being tubal pregnancies.
• The pregnancy rate after salpingolysis and fimbrioplasty for partial distal obstruction
is about 65%.
• Unlike the results of distal tubal reconstruction, the use of microsurgery has improved
intrauterine pregnancy rates for proximal tubal disease.
• Proximal tubal obstruction is now usually treated by cannulation of the oviducts with
catheters or balloons placed under hysteroscopic visualization.
• The benefit of second-look laparoscopy after tubal surgery has not been established.
• No medical therapy for endometriosis has proved to increase pregnancy rates
compared with no treatment.
• Pregnancy rates for women with mild endometriosis can be increased with the use of
controlled ovarian hyperstimulation and intrauterine insemination but not with
danazol.
• About 65% of women with mild endometriosis and no other cause of infertility
conceive without treatment. With moderate or severe disease, pregnancy rates with
expectant management are 25% and 0%, respectively.
• Conception rates for women treated surgically have been reported to be in the 50% to
60% range for those with moderate endometriosis and 30% to 40% for those with
severe endometriosis.
• About half of infertile women with myomas conceive after myomectomy.
• Luteal-phase deficiency, as currently diagnosed histologically, is probably a normal
biologic variant and not a true cause of infertility.
• No data conclusively demonstrate that the finding of antisperm antibodies in either
member of the couple is a cause of infertility.
• In women with unexplained infertility the use of controlled ovarian hyperstimulation
(COH) and intrauterine insemination (IUI) yields monthly fecundity rates of 10% to
15%. Therefore COH and IUI should be the initial treatment for women who ovulate,
have patent oviducts, and whose male partner has at least 5 million motile sperm in the
ejaculate.
• For IVF with and without ICSI the delivery rate per cycle in which ova are retrieved is
as high as 40% depending on the age of the woman.
• The rate of pregnancy following IVF is directly related to the number of embryos
placed in the uterine cavity.
• The pregnancy rate per cycle of IVF remains relatively constant for about six cycles
after which it declines. After six cycles the cumulative pregnancy rate is about 60%.
• There is a high spontaneous abortion rate (about 30%) for pregnancies after IVF.
• If an infertile couple fails to conceive after 2 years of therapy, they should be informed
the chances for conception are remote.
• The optimal treatment for all causes of sperm abnormalities is ICSI. With this
technique, pregnancy rates per cycle are similar to that of IVF performed for other
causes of infertility.
KEY POINTS
• In 2002, of the 62 million women in the United States ages 15 to 44 years,
approximately one third were not at risk for pregnancy, and 62%, 38 million, were
using a method of contraception. About 7% of women of reproductive age were
sexually active and not using any contraceptive.
• In 2001, there were about 6.4 million pregnancies in the United States. There were 4
million births and about 1.3 million elective abortions. Half of all pregnancies were
unintended. About 20% of all pregnancies were electively terminated.
• Of women ages 15 to 44 in the United States in 2002, male and female sterilization
were used by 22%, oral contraceptives by 19%, male condom by 11%, the progestin
injection by 3%, and the IUD by 1.3%.
• Typical and perfect use failure rates in the first year of use range between 5% and 27%
for coitus-related methods beween 0.3% and 8% for oral contraceptives (OCs) and
0.3% to 3% for the injection. The IUD and implants have typical use failure rates less
than 1%.
• Contraceptive failure rates are increased in inverse relation to the user's age, level of
education, and socioeconomic class.
• Pregnancy results from failure of spermicide use are not associated with an increased
risk of fetal malformations.
• The active ingredient in spermicides is a surfactant, usually nonoxynol 9, which
immobilizes or kills sperm on contact.
• Barrier techniques reduce the rate of transmission of sexually transmitted diseases,
both bacterial and viral.
• The most effective type of periodic abstinence is the symptothermal method.
• OC formulations in the United States consist of varying dosages of one of the
following progestins: estranes: norethindrone, norethindrone acetate, ethynodiol
diacetate, or gonanes: norgestrel (or its active isomer, levonorgestrel), desogestrel,
norgestimate, or a spironolactone derivative, drosperinone and either of two estrogens,
ethinyl estradiol or ethinyl estradiol-3-methyl ether, also called mestranol.
• A given weight of norgestrel or the other gonanes has 5 to 10 times more
progestational activity than the equivalent weight of norethindrone, whereas
norethindrone acetate and ethynodiol diacetate are similar in potency to norethindrone.
• Metabolic effects of the estrogen component of OCs include an increase in serum
globulins that have a thrombophilic effect and altering of the lipid profile to increase
triglycerides and HDL cholesterol and lower LDL cholesterol.
• Metabolic effects of the progestin component of OCs include peripheral insulin
resistance and lowering HDL cholesterol and raising LDL cholesterol.
• Ethinyl estradiol is approximately 1.7 times as potent as an equivalent weight of
mestranol.
• No significantly increased risk of breast cancer occurs among current or former users
of OC or in various high-risk subgroups of OC users.
• OC users have an increased risk of developing invasive cervical cancer, particularly
adenocarcinoma, compared with users of no contraception, but a causal relation has
not been established.
• The rate of return of fertility after stopping OCs is delayed, but eventually the
percentage of women who conceive after stopping all methods of contraception,
including OCs, is the same.
• Babies born to women who discontinue OCs or who conceive while ingesting OCs
have no greater incidence of any type of birth defect.
• All OC formulations with less than 50 μg of estrogen increase the risk of venous
thrombosis and embolism three- to fourfold.
• A significantly increased risk of developing MI occurs only in current OC users older
than age 35 who smoke.
• Users of low-dose OCs do not have a significantly increased risk of developing
ischemic or hemorrhagic stroke if they do not smoke or have hypertension.
• The cause of MI in older OC users who smoke is arterial thrombosis.
• Adverse effects produced by the estrogenic component of OCs include nausea, breast
tenderness, fluid retention, temporary increase in blood pressure, thrombosis, changes
in mood, and chloasma. Progestins produce certain androgenic adverse effects,
including weight gain, nervousness, depression, tiredness, and acne, as well as failure
of withdrawal bleeding or amenorrhea.
• In an ovulatory cycle the mean blood loss during menstruation is approximately 35
mL, compared with 20 mL for women ingesting OCs.
• OC users are about half as likely to develop iron deficiency anemia as are control
subjects.
• OC users are significantly less likely to develop menor-rhagia, irregular menstruation,
or intermenstrual bleeding than nonusers.
• The risk of developing endometrial cancer, as well as ovarian cancer, in OC users and
former users is only half that in control subjects. OC users also have a 50% reduction
in the incidence of benign breast disease.
• OC users have approximately 50% less dysmenorrhea and about 40% less
premenstrual disorders than do control subjects.
• Functional ovarian cysts occur less frequently in OC users than in nonusers if they use
monophasic, but not multiphasic, formulations.
• Prior use of OCs does not affect mortality rates in women.
• OCs reduce the clinical development of salpingitis (PID) in women infected with
gonorrhea or Chlamydia by 50%, and the overall incidence of PID in OC users is
reduced by 50%.
• OCs reduce the risk of ectopic pregnancy by more than 90% in women currently using
them.
• There are three types of injectable contraception: depomedroxyprogesterone acetate
(DMPA), norethindrone enanthate, and several progestin–estrogen combinations. All
are very effective.
• Women using injectable DMPA (150 mg every 3 months) intramuscularly or 104 mg
subcutaneously have a first-year pregnancy rate of 0.1%.
• Injectable DMPA is associated with loss of bone density that recovers after DMPA is
stopped.
• Women treated with injectable progestins for contraception have complete disruption
of the normal menstrual cycle and an irregular bleeding pattern that is usually followed
by amenorrhea.
• The most effective method of emergency contraception is ingestion of two tablets of
750 μg of levonorgestrel taken 12 hours apart with a failure rate about 1%.
• The contraceptive patch is applied to the skin for seven days. Effectiveness and
adverse effects are similar to OCs.
• The contraceptive vaginal ring is placed in the vagina for 3 weeks. Effectiveness and
adverse effects are similar to OCs.
• The cumulative incidence of accidental pregnancy with the copper T 380A IUD is
1.6% after 7 years of use and 1.7% after 12 years of use. This IUD is approved for 10
years' use.
• The incidence of adverse events with IUDs steadily decreases with increasing age of
the woman.
• The main mechanism of contraceptive action of the copper IUD is production of a
local sterile inflammatory reaction of leukocytes, which destroys sperm and prevents
fertilization.
• Resumption of fertility after IUD removal is not delayed and occurs at the same rate as
resumption after discontinuation of use of mechanical contraceptive methods.
• A copper or progesterone-releasing IUD can be removed and a new one reinserted
immediately afterward. The IUD can be safely inserted on any day of the cycle.
• In the first year of use, the copper T 380 IUD has approximately a 0.5% pregnancy
rate, a 10% expulsion rate, and a 15% rate of removal for medical reasons, and the
incidence of each of these events diminishes steadily in subsequent years.
• In women wearing a copper T IUD, 50 to 60 mL of blood is lost per cycle; with the
levonorgestrel-releasing IUS, the amount of blood loss is about 5 mL per cycle.
• Mefenamic acid, 500 mg twice daily during menses, significantly reduces menstrual
blood loss in IUD users.
• The fundal perforation rate with the copper T 380 IUD is about 1 per 3000 insertions.
• The incidence of congenital anomalies is not increased in infants born with any type of
IUD in utero.
• If a woman conceives with an IUD in place and the IUD is not removed, the incidence
of spontaneous abortion is about 55%, approximately three times greater than would
occur without an IUD. If, after conception, the IUD is removed, the incidence of
spontaneous abortion is reduced to about 20%.
• If a woman conceives with a copper IUD in place, her chances of having an ectopic
pregnancy is about 5%, approximately 10 times greater than occurs in conceptions
without an IUD.
• Women using a copper T 380 IUD have approximately a 90% lower overall risk of
having an ectopic pregnancy than women using no method of contraception.
• The rate of prematurity among live births occurring with an IUD in utero is increased
about two to four times.
• The overall risk of PID in users of IUDs with a monofilament tail string is increased
only during the first 3 weeks after insertion.
• Pregnancy rates after reanastomosis of the vas range from 45% to 60%, whereas those
after oviduct reanastomosis range from 50% to 80%.
• About 1% of sterilized women request reversal. In the United States approximately
7000 women request reversal each year.
• Usually about 15 to 20 ejaculations are required after vasectomy before a man is
sterile.
• After vasectomy, two aspermic ejaculates are required before the male is considered
sterile.
• After sterilization by tubal interruption, the 1-year failure rate is 0.55 per 100 women,
the 5-year failure rate is 1.31 per 100 women, and the 10-year failure rate is 1.85 per
100 women. About one third of the pregnancies are ectopic.
• Complication rates are three to four times higher for second-trimester abortions than
for first-trimester abortions.
• The most effective medical means to terminate pregnancies less than 8 weeks'
gestation is the combination of mifepristone followed by misoprostol, with a failure
rate less than 5%.
• A single subdermally placed implant containing etonogestrel provides excellent
contraceptive effectiveness for 3 years.
• A microinsert placed into the oviducts transcervically provides very effective
permanent pregnancy prevention.