Publications by authors named "Milim S"

Study Objective: To determine whether isotonic 5.0% mannitol is superior to 1.5% glycine in preventing development of hyponatremic encephalopathy.

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Study Objectives: To evaluate the experiences of women who underwent laparoscopic leiomyoma coagulation (myolysis) alone and those who had myolysis in conjunction with transcervical endomyometrial resection (TEMR), transcervical electrosurgical resection of submucous leiomyomas (TSR), or both.

Design: Continuing, prospective observational study with mean (+/- SEM) follow-up of 36.0 +/- 1.

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Objective: To assess the force needed to mechanically dilate the cervix of a nonpregnant woman after intracervically injecting dilute (0.05 U/mL) vasopressin solution.

Methods: In a randomized, double-blind study, equal amounts of either a dilute vasopressin solution or placebo (normal saline) were injected into the intracervical stroma at 4- and 8-o'clock positions, just beneath the mucosal surface, in 52 women immediately before cervical dilatation in preparation for operative hysteroscopy.

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Study Objectives: To assess the relationship of menstrual timing of administration of gonadotropin-releasing hormone (GnRH) agonist on the effectiveness of endometrial thinning and unwanted uterine bleeding.

Design: Prospective observational study.

Setting: Gynecology department of a community hospital.

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Study Objective: To assess the effectiveness of treating adenomyomata with laparoscopic bipolar coagulation.

Design: Prospective, observational study. Setting.

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Objective: To assess the effect of intracervical injection of dilute (0.05 U/mL) vasopressin solution on blood loss during operative hysteroscopy.

Methods: In a randomized, double-blind study, dilute vasopressin solution or placebo (normal saline) was injected into the cervical stroma of 106 women before dilation of the cervix in preparation for operative hysteroscopy.

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From February 1992 through March 1995, 167 women (mean ± SEM age 44.7 ± 0.3 yrs, range 22-52 yrs) with symptomatic leiomyomata underwent laparoscopic leiomyoma bipolar coagulation.

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We assessed the effectiveness of laparoscopic bipolar coagulation in 20 women with severe dysmenorrhea, chronic menorrhagia, and a magnetic resonance imaging diagnosis of adenomyomata. In addition, nine women underwent transcervical endomyometrial resection; three (33.3%) of these women underwent concomitant submucous leiomyoma resection.

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We assessed the force necessary for mechanical cervical dilatation on a nonpregnant uterus after intracervical administration of dilute vasopressin solution 0.05 U/ml. In a prospective, double-blind, randomized study, vasopressin or placebo was injected into the cervical stroma before dilating the cervix in preparation for resectoscopy.

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A study was designed to assess the effect of intracervical injection of dilute vasopressin solution 0.05 U/ml on intraoperative blood loss during operative hysteroscopy. In a prospective, computer-randomized, double-blind study, vasopressin or placebo (normal saline) was injected into the cervical stroma of 108 women before dilatation of the cervix.

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This study compared the changes in blood chemistry that occur during operative hysteroscopy when either 5.0% mannitol or 1.5% glycine is used as a distention medium.

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Study Objectives: To evaluate the accuracy of magnetic resonance imaging (MRI) for diagnosing nodular adenomyosis by percutaneous myometrial biopsies.

Design: Prospective observational study.

Setting: Gynecology department of community hospitals.

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Study Objective: To evaluate 100 laparoscopic hysterectomies and their variations in private practice and visiting professorship programs.

Design: A prospective observational study.

Setting: Gynecology departments of 17 teaching, community, and proprietary hospitals in the northeastern United States.

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Study Objective: To evaluate the effectiveness and safety of transcervical electrosurgical resection (TSR) of submucous leiomyomas with or without concomitant transcervical endomyometrial resection (TEMR) for chronic menorrhagia.

Design: Prospective observational study, with 6-month follow-up of all 208 women and up to 6-year follow-up of 185 (88.9%).

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