Methods to Reduce Blood Loss in Abdominal Myomectomy

Blood Loss Clinical Trial

Official title: Comparing Preoperative Vaginal Misoprostol, Intraoperative Oxytocin Infusion, Intravenous Carbetocin and Pericervical Hemostatic Tourniquet in Reducing Blood Loss During Abdominal Myomectomy, a Randomized Controlled Trial

Status Not yet recruiting

Clinical Trial Summary

The aim of the study is to compare the effectiveness of a single preoperative dose of vaginal misoprostol, intraoperative oxytocin infusion, IV carbetocin and pericervical tourniquet for the reduction of blood loss during of abdominal myomectomy.

Clinical Trial Description

Uterine leiomyomas (fibroids) are the most common benign tumours among women. Fibroids are found in approximately 20% of women over 35 years of age. They are mostly asymptomatic, but in 20-50% of patients, fibroids may cause problems such as heavy menstrual bleeding, anaemia, pelvic pain and pressure,symptoms from extrinsic compression of the colorectal and urinary tract,recurrent abortion and infertility. Surgery is indicated for symptomatic uterine leiomyomas; hysterectomy for women who have completed childbearing (women > 40 years old), and myomectomy for women <40 years old who wish to preserve uterine and fertility .Myomectomy can be accomplished by laparotomy, laparoscopy, or hysteroscopy (transvaginal) approaches.

Uterine fibroids have a rich blood supply which may result in intensive bleeding during the myomectomy procedure.This surgical procedure may be associated with substantial morbidity, in particular major blood loss especially in abdominal myomectomy. Fletcher reported that 23% patients undergoing open myomectomy lost over 1000ml of blood. Other studies reported the operative blood loss range between 100 ml and 3000 mls. Blood transfusion can be required in up to 20% of the women during abdominal myomectomy and may require hysterectomy in up to 2% of patient undergoing abdominal myomectomy.

A number of interventions have been introduced to reduce bleeding rate during myomectomy:

1. interventions on uterine arteries as peri cervical mechanical tourniquet, preoperative clamping or embolization of bilateral uterine and/or ovarian arteries (UAE)

2. uterotonics as ergometrine, oxytocin, misoprostol, peri-operative injection of ascorbic acid, or intraoperative vasopressin or terlipressin injection (hormonal tourniquet) into myometrium , or intra-myometrial infiltration of bupivacaine plus epinephrine,

3. myoma dissection techniques as use of laser, electrosurgery and chemical dissectors such as mesna.

4. GnRH analogues reduce haemorrhage during surgery if used for 2-4 months preoperatively. GnRH analogues are expensive and may make removing fibroids difficult because of reduced distinction between capsule and myometrium.

However, these strategies may be associated with some complications, and some of these are ineffective or expensive or require extra steps before the actual procedure.

The Foley catheter, often used as a tourniquet in low resource countries, is cheap and readily available;however, they require intermittent release intraoperatively to prevent the build-up of toxins and tissue ischemia, and may be impracticable to apply sometimes. Once the tourniquet is removed, there is bleeding from the raw myometrium and cavities with the possibility of increased blood loss and blood transfusion. Tourniquet occlusion of uterine and ovarian vessels prior to myomectomy was reported by Kongenyuy et al to have higher efficacy in reducing intraoperative blood loss when compared to other interventions. Mechanical vascular occlusion techniques such as tourniquet or uterine artery embolization, though popular in recent years have significant disadvantages as (i) require additional interventions or a separate procedure during the operation (ii) difficulty of access to the uterine artery with large and laterally placed myomas and (iii) difficulty of placing the tourniquet. In practice,there are instances when application of the tourniquet is impracticable and another method is indicated as in case of significant pelvic adhesions and leiomyoma in the broad ligament, uterine isthmus or cervix.

Medical agents are always an attractive option to arrest haemorrhage. Preoperative Misoprostol, a prostaglandin E1 analogue, was registered in many countries for use in gynaecology and obstetrics. Its popularity in developing countries is accounted by its advantages over other interventions as being inexpensive choice with thermal and light stability and shelf life of several years in tropical conditions. It acts by promoting myometrial contractions and reducing uterine artery blood flow significantly and thus reducing bleeding during myomectomy . Reports on misoprostol use to control blood loss in abdominal myomectomy showed a reduction in intra and post-operative blood loss, surgical time, and post-operative blood transfusion . Misoprostol has advantage of multiple routes of administration as sublingual, oral, rectal or vaginal. The bioavailability curve of rectal and vaginal misoprostol is qualitatively similar although rectal route has longer half-life with lesser side effects than oral route. The peak plasma level of 400 μg of vaginal misoprostol is reached one to two hours after administration and is sustained for four hours, and the side effects are self-limiting . Another advantage of Misoprostol is that it is much cheaper than GnRH analogues; the most popular method for reducing bleeding in myomectomy operation. Another advantage over GnRH analogues is that the effect of GnRH analogues achieved only after an average time of 3 months while misoprostol can be administered an hour before the operation and significantly reduces intra-operative blood loss. Side effects of misoprostol appear within 90 minutes of administration, i.e., while patient is under anaesthesia and are less disturbing in nature such as nausea, vomiting, diarrhea, abdominal pain, fever and chills. Single dose of misoprostol is associated with lower incidence of shivering and hyperpyrexia and with no serious systemic side effects.

Oxytocin is a hormone secreted mainly from the pituitary gland. Its main function is uterine contraction during labour and delivery. Oxytocin is the agent of choice in the prevention of postpartum uterine atony and bleeding. Oxytocin acts directly on the myometrium through the oxytocin receptor(OXTR) and stimulates contractions. Oxytocin affects oxytocin receptors in the myometrium and fibroid tissue, which stimulates synthesis and release of contractile prostaglandins. Increased uterine contractility directly affects uterine vascular structures, decreasing blood supply to the arteries and fibroids. Decreased blood volume in the uterus and constricted uterine vasculature due to uterine contraction and vaso-constrictive effect of oxytocin results in reducing intraoperative blood loss. Oxytocin receptors also exist in the nonpregnant uterus with a 50-100 times lower concentration than in pregnant uterus.The expression of oxytocin receptors have been identified in the endometrium as well as in the microvascular endothelial cells of the myometrium. Further, oxytocin receptors were found to be higher in fibroids than in normal myometrium. Main side effects caused by oxytocin are tachycardia, hyponatremia and hypotension but usually these side effects don't occur with low doses but it should be used cautiously because an intravenous bolus of 10 IU oxytocin could be detrimental to women with heart disease or to women who are hypovolemic.

Nevertheless, oxytocin has a short half-life (4-10 minutes), necessitating continuous intravenous infusion. Moreover, saturation of myometrial oxytocin receptors could reduce its effectiveness, and excessive dosing can lead to coronary-artery contraction and hypotension; additionally, water intoxication can occur owing to its anti-diuretic effects.

Carbetocin is a long-acting synthetic octapeptide analogue of oxytocin(which is a nonapeptide) with agonist properties at the oxytocin receptor. The molecular changes give Carbetocin more stability and avoid early decomposition .Originally, it is an obstetric drug used to control postpartum hemorrhage . In recent times, it has been studied in the reduction of bleeding during myomectomy, but the available data are limited. The pharmacodynamic properties of Carbetocin are comparable to those of endogenous oxytocin.

Carbetocin selectively binds to oxytocin receptors in the smooth muscle of the uterus resulting in rhythmic uterine contractions, increased frequency of existing contractions, and increased uterine tone. During surgery, addition of carbetocin will lead to strong muscle contractions that makes myometrium pale with less bleeding and myoma will become more protruding.

It can be administered as a single-dose injection, either intravenously or intramuscularly or can be given intramyometrial. Intravenously administered Carbetocin has a half-life of approximately 40 minutes, around 4-10 times longer than that reported for oxytocin. Following intramuscular injection, Carbetocin reaches peak plasma concentrations in less than 30 minutes and has 80% bioavailability. Carbetocin onset of action is rapid irrespective of administration route, but duration of action is longer following intramuscular injection as contractions continue for 60 minutes after the intravenous injection and for 120 minutes after the intramuscular administration. The optimal Carbetocin dose (intravenous or intramuscular) is100 μg.

Other methods:

Preoperative uterine embolization decreases blood loss during a myomectomy, however, this option is limited by the accessibility of equipment and by having trained physicians to complete the procedure .

Vasopressin is not a cost-effective choice and there can be associated pulmonary oedema, temporary increase in blood pressure and myocardial infarction with it.

In this study, we will compare the effectiveness of a single preoperative dose of vaginal misoprostol ,intraoperative oxy¬tocin infusion, IV carbetocin and pericervical tourniquet for the reduction of blood loss at the time of abdominal myomectomy. ;

Related Conditions & MeSH terms

• Abdominal Myomectomy
• Blood Loss
• Hemorrhage

• NCT number: NCT04595812
• Study type: Interventional
• Source: Cairo University
• Contact: Reham Hany Mohamed Elkhalifa
• Phone: +201158778007
• Email: reham_khalifa1990@yahoo.com
• Status: Not yet recruiting
• Phase: Phase 4
• Start date: November 1, 2020
• Completion date: September 15, 2022