basic mekanisme of menstruasi
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MENSTRUAL CYCLEPHYSIOLOGY ND P THOPHYSIOLOGY
Dr. Supriyatiningsih, M.Kes, SpOG
Department of Obstetrics & GynecologyFaculty of Medicine Muhammadiyah University
Yogyakarta Indonesia
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THE NORMAL MENSTRUAL CYCLES ISDETERMINED B Y A COMPL EX INTERA CTION
B ETWEEN REPRODUCTIVE ENDOCRINE ORGA N
HYPOTHALAMUS ANTERIOR PITUITARY GLAND
OVARYENDOMETRIUM
But the main regulation isintraovarian
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The Menstruation Cycle
3 activity during Menstrual Cycle :
Hypothalamus and Pituitary activity
Ovarian activity
Uterine activity
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Uterus
Menses
Ovary
Anterior pituitary
Hypothalamus
CNS
Environment
Compartemen I
Compartemen II
Compartemen III
Compartemen IV
Estrogen Progesterone
FSH LH
GnRH
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To survive, the follicle must be exposed to a waveof gonadotropic hormone release
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Ovulasi
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Number of oocytes at different ages
Age # of cells
3-6 weeks ofgestation
Endoderm of theyolk sac
10,000
8 weeks Proliferation bymitosis
600,000
8-20 Mitosis, meiosis,atresia
6-7,000,000
20-40 weeks 80% loss 1-2,000,000Birth to puberty Loss to atresia 300,000
Reproductiveyears
Ovulation 400-500
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Membran sel
LISOSOM
Asam fosfataseEnzim litik
Prostaglandin
Penurunanaliran darah
Vasokonstriksia. spiralis
Iskemia
VEGF & FGFRegenerasi endometrium
Makrofag
PMN
LImfosit granulasi
Sel Mast
Sekresi danaktivasi sitokin
Upregulated MMP
DegranulasiTriptase &kimase
Menstruasi
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Norm al m ens t rual b leed ing
Occurs approximately once a month(every 26 to 35 days).
Lasts a limited period of time (3 to 7 days). May be heavy for part of the period, but
usually does not involve passage of clots. Often is preceded by menstrual cramps,
bloating and breast tenderness, althoughnot all women experience thesepremenstrual symptoms.
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DefinitionsNormal:
Mean interval is 28 days+/- 7 days.
Mean duration is 4 days.More than 7 days is
abnormal.
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A bn orm al Bleed ing
Abnormal bleeding (DUB or dysfunctionaluterine bleeding) includes:
Too frequent periods (more often than every 26
days). Heavy periods (with passage of large, egg-sizedclots).
Any bleeding at the wrong time, including
spotting or pink-tinged vaginal discharge Any bleeding lasting longer than 7 days. Extremely light periods or no periods at all
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Dysfunctional Uterine Bleeding(DUB)
Most common menstrual disorder. Can affect any women from menarche to
menopause. Often the first clinical diagnosis for any
excessive menstrual bleedings.
Diagnosis has to be confirmed by aprocess of exclusion of pathologicalcauses.
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Term Definition Pattern
Amenorrhea No uterine bleeding for at least 6 monthsMenorrhagia Excessive amount (>80 mL/cycle) or
prolonged duration >7days, also calledhypermenorrhea
Occurs atirregularintervals
Metrorrhagia Uterine bleeding occuring at irregular but
frequent interval, amount variesirregular
Menometrorrhagi
Irregular, heavy, and prolonged menstrualbleeding
irregular
Oligomenorrhea
Decreased, scanty flow, the termhypomenorrhea is used for regular timingwith scanty amount.
Interval > 36-40days
Polymenorrhea Regular, frequent menstruation Interval
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Average blood loss with
menstruation is 35-50cc.
95% of women lose
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DefinitionsMenorrhagia:
Prolonged > 7 days or > 80 ccoccurring at regular intervals.
Synonymous with
hypermenorrhea
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Menorrhagia occurs in 9-14% of healthy women.
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DefinitionsMetrorrhagia:
Uterine bleeding occurringat irregular but frequent
intervals.
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Etiologies AUB Organic
Systemic Reproductive
tract disease Iatrogenic
Dysfunctional Ovulatory
Anovulatory
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Reproductive TractCauses of Benign Origin
Atrophy Leiomyoma Polyps Cervical lesions Infection
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60% of women with PMBwill be found to haveatrophy. 10% will have
polyps and 10% will havehyperplasia.
Karlsson, et al ., 1995
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Incidence of Endometrial Cancer
in Premenopausal Women
2.3/100,000 in 30-34 yr old6.1/100,000 in 35-39 yr old36/100,000 in 40-49 yr old
ACOG Practice Bulletin #14, 2000
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DUB Abnormal uterine bleeding
for which an organicetiology has been excluded.
It is either ovulatory oranovulatory in origin.
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PUD
Perdarahan dari uterus yang didasari oleh gangguan hormonal porosHipotamus-hipofisis-ovarium semata, tanpa dijumpai kelainan organik,sistemik, metabolik, keganasan maupun gangguan kehamilan dini
elainan Organik
Sistemik Metabolik
Keganasan Ggn kehamilan dini
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Premenstrual Syndrome
Premenstrual Syndrome (PMS) is defined as the cyclicrecurrence in the luteal phase of the menstrual cycle of acombination of distressing physical, psychological,and/or behavioral changes of sufficient severity to resultin deterioration of interpersonal relationships and/orinterference with normal activities. Nearly 200symptoms have been associated with this definition andit is the clustering of these signs and symptoms that isthe hallmark of PMS.
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Catamenial
The term catamenial is derived from the Greek
and signifies around menses. In general aninstance where a single recognized medicalcondition presented in the premenstruum wasreferred to as a catamenial disorder while a
cluster of symptoms was referred to as PMS.
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Premenstrual Magnification
Many patients with psychiatric disorders also complain ofworsening of their symptoms around the premenstrualphase, called premenstrual magnification (PMM).
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PMS
Milder symptoms are believed to occur in about 30% to80% of reproductive-age women, while severesymptoms are estimated to occur in 3% to 5% ofmenstruating women.
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Concordance Rate
The concordance rate (if both twins have PMS)was found to be significantly higher in
monozygous twins (93%) than dizygous twins(44%) and in non-twin control women (31%).
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Common Symptoms of PMS
Women with PMSSymptom Showing Symptoms (%)Behavioral
Fatigue 92
Irritability 91Labile mood with alternating
sadness and anger 81Depression 80Oversensitivity 69Crying spells 65Social withdrawal 65Forgetfulness 56Difficulty concentrating 47
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Common Symptoms of PMS(Continued)
Physical Abdominal bloating 90Breast tenderness 85
Acne 71 Appetite changes and
food cravings 70Swelling of the extremities 67
Headache 60Gastrointestinal upset 48
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Differences Between PMS and PMDD
Dia nostic criteria Tenth Revision of the International Classification of
Disease (ICD-10)
Diagnostic and Statistical Manual of Mental
Disorders, 4 th ed.(DSM-IV)
Providers usingthese criteria
Obstetrician/gynecologists, primary
care physicians
Psychiatrists, other mental health care
providersNumber of symptomsrequired
One 5 of 11 symptoms
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Differences Between PMS and PMDD(Continued)
Functionalimpairment
Prospectivecharting of symptoms
Not required
Not required
Interference withsocial or rolefunctioningrequired
Prospectivedaily charting of symptomsrequired for twocycles
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Patterns of PMS
Premenstrual symptoms can begin at ovulation withgradual worsening of symptoms during the luteal phase(pattern 1).
PMS can begin during the second week of the lutealphase (pattern 2).
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Patterns of PMS(Continued)
Some women experience a brief, time-limited episode ofsymptoms at ovulation, followed by symptom-free daysand a recurrence of premenstrual symptoms late in theluteal phase (pattern 3).
The most severely affected women have symptoms thatat ovulation worsen across the luteal phase and remitonly after menses cease (pattern 4). These women
describe having only one week a month that is symptom-free.
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Differential Diagnosis
Psychiatric disorders Major depression Dysthymia
Generalized anxiety Panic disorder Bipolar illness (mood
irritability)
Other
Medical disorders Anemia Autoimmune disorders Hypothyroidism
Diabetes Seizure disorders Endometriosis Chronic fatigue syndrome Collagen vascular
disease
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Differential Diagnosis(Continued)
Premenstrualexacerbation
Of psychiatric disorders Of seizure disorders Of endocrine disorders Of cancer Of systemic lupus
erythematosus Of anemia Of endometriosis
Psychosocial spectrum Past history of sexual
abuse Past, present, or current
domestic violence
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Diagnosis of PMS
PMSA. Does not meet DSM-IV criteria
but does meet ICD-10 criteriafor PMS
B. Symptoms occur only in theluteal phase, peak shortlybefore menses, and ceasewith menstrual flow or soonafter
C. Presence of one or more ofthe following symptoms
Mild psychological discomfort Bloating and weight gain Breast tenderness Swelling of hands and feet Aches and pains Poor concentration Sleep disturbance Change in appetite
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PMDD (DMS-IV Criteria)
A. At least five of the symptoms below, with at leastone being a core symptom, are present a weekbefore menses and remit a few days after onset ofmenses:
Depressed mood or dysphoria (core symptom) Anxiety or tension (core symptom) Affective lability (core symptom) Irritability (core symptom) Decreased interest in usual activities
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PMDD (DMS-IV Criteria)(Continued)
Concentration difficulties Marked lack of energy Marked change in appetite, overeating, or food
cravings Hypersomnia or insomnia Feeling overwhelmed Other physical symptoms (e.g., breast
tenderness, bloating, headache, joint or musclepain)
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Treatment of PMS
Oral contraceptives Vitamin B 6 Bromocriptine Monoamine oxidase inhibitors Synthetic progestational agents Spironolactone Massage therapy Chiropractic therapy Calcium
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MENOPAUSE
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Gejolak panas
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Osteoporosis
Tulang keropos Ngilu-ngilu Patah tulang Bungkuk Tambah pendek
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Kerusakan bag tulang NORMAL
The good ne s
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The good newsMenopause and
postmenopauseosteoporosis
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Kulit keriput
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Sukar tidur
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Jantung berdebar
PusingMudah pingsan
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Gangguan fungsi seks
Vagina kering Hub. Seks sakit Lendir sedikit Nafsu sek turun
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Libido menurun
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Gangguan berkemih
InkontinensiaNgompol
Some benefits of estrogen replacement
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Some benefits of estrogen replacementtherapy (ERT) for treating menopausal
related health problem Estrogen replacement therapy (ERT) results in the relief
of menopausal symptoms such as hot flushes andatrophy of genital tract
ERT halts postmenopausal bone loss, increases bonemineral density (BMD) and reduces the incidence offractures
ERT reduces levels of total cholesterol and low-densitylipoprotein (LDL) cholesterol
Nelson H. JAMA 2004;291:1610-20
B fi f l i i
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Benefits of estrogen plus progestin inpostmenopausal women
WHI study. JAMA 2002;288:321-33
Estrogen + progestin
Plasebo
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Weight gain during traditionalHRT has been one of the main
reasons for discontinuation
Although it may not be the onlyreason, it contributes to poor
compliance
Van Seumeren I. Maturitas 2000;34(Suppl 1):3 8
LIVER ESTROGEN
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Na+ / water retention(= weight gain)K+ elimination
Aldosterone
KIDNEY ADRENAL GLAND
LIVER ESTROGEN
HRT
Increased edema
Increased body weight
Changes in body weight with
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Changes in body weight with Angeliq and estradiol alone
1.5
1.0
0.5
0
0
-0.5
0
-1.5
Mean weightchange (kg)
Angeliq (n = 224)
Estradiol (n = 225)
1 2 3 4 5 6 7 8 9 10 11 12 13
-1.0
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The end