Evaluation and Management of Abnormal Uterine Bleeding in Premenopausal Women
Evaluation and Management of Abnormal Uterine Bleeding in Premenopausal Women
Evaluation and Management of Abnormal Uterine Bleeding in Premenopausal Women
R1.
Introduction
9 to 14 percent of women between menarche and menopause.
Pituitary follicle-stimulating hormone estrogen proliferation of the endometrium luteinizing hormone surge ovulation corpus luteum progesterone. In the absence of pregnancy, estrogen and progesterone levels decline withdrawal bleeding (13 to 15 day postovulation) Disruption of normal physiology, anatomic changes in the endometrium, or endometrial cancer may result in abnormal uterine bleeding.
Anovulatory bleeding - irregular or infrequent periods, with flow ranging from light to excessively heavy.
Ovulatory bleeding (menorrhagia) - regular intervals (every 24 to 35 days, excessive volume or duration of more than seven days.
Anovulatory bleeding
Menarche (the immature hypothalamic-pituitary-ovarian axis), Up to eight years before menopause Ovulation does not occur no corpus luteum forms to produce progesterone prolonged estrogenic stimulation excessive proliferation, endometrial instability, and erratic bleeding. Underlying disease - Polycystic ovary syndrome Uncontrolled diabetes mellitus Hypo or hyperthyroidism Hyperprolactinemia Drug - Antiepileptics (valproic acid) , antipsychotics (haloperidol, chlorpromazine, thiothixene), atypical antipsychotics (clozapine, risperidone)
Recurrent anovulation causes an increased risk of endometrial cancer. About 14 percent of premenopausal women with recurrent anovulatory cycles develop endometrial cancer or its precursor, hyperplasia with atypia. 30 percent of cases of hyperplasia with atypia progress to cancer, and 42.6 percent of women with this pathology have undiagnosed, concurrent endometrial adenocarcinoma. High risk - advanced age, obesity, nulliparity, infertility, diabetes, family history of colon cancer, long-term unopposed estrogen therapy, or a history of tamoxifen use.
Office endometrial biopsy - inexpensive, convenient, low risk of complications. (82.3% sensitive for hyperplasia with atypia and 91 % sensitive for endometrial cancer 98 % specificity for both) Hysteroscopy structual abnormality
Progestin therapy and oral contraceptives routine withdrawal bleeding decrease the risk of hyperplasia or cancer correct any related excessive menstrual bleeding
Oral contraceptives - 35 mcg or less of ethinyl estradiol Cyclic oral medroxyprogesterone acetate (Provera) - 10 mg /day for 10~14 days per month
Hyperplasia without atypia - cyclic medroxyprogesterone acetate + continuous megestrol (Megace) at 40 mg/day or levonorgestrel-releasing intrauterine system (Mirena) F/U Endometrial biopsy - in three to six months
Hysterectomy - adenocarcinoma
Ovulatory bleeding
Ovulatory abnormal uterine bleeding(menorrhagia) regular intervals , excessive volume or duration. Underlying disease - Hypothyroidism, late-stage liver disease, bleeding disorders (vWD), structural changes(submucosal fibroids or endometrial polyps) Ovulatory bleeding progesterone slough the endometrium regularly minimal risk of developing cancer.
Transvaginal ultrasonography Saline infusion sonohysterography - enhanced views of the endometrium endometrial biopsy hysteroscopy
<Nonhormonal Therapies>
Nonsteroidal anti-inflammatory drugs (NSAIDs) - decrease prostaglandin levels, reducing menstrual bleeding.
In one small study, naproxen sodium (Anaprox) and mefenamic acid (Ponstel) decreased flow volume by 46 and 47 percent, respectively. There is no evidence that one NSAID is more effective than another Tranexamic acid (Lysteda), - an antifibrinolytic, more effect than NSAID - bleeding disorders (fertility or contraindications to oral contraceptives.
<Surgery>
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