术前米索前列醇与术中颈周止血止血带减少子宫肌瘤切除术出血量的比较研究

Asraa Ahmed Alhameedi, Amal Aboseef, Doaa Efaat
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The intraoperative comments on type, site, size of fibroid, operation time, amount of blood loss, and blood transfusion need were recorded. The main outcome measures were as follows: primary outcome included the estimated blood loss and postoperative hemoglobin (Hb) and hematocrit (HCT) level, and secondary outcome included the possibility of blood transfusion and operative time. Results There was a significantly shorter duration of operation in tourniquet group (47.5±4.7) compared with misoprostol group (53.0±6.9) (P=0.001). There was significant less blood loss in the tourniquet group compared with the misoprostol group (375.0±96.3 and 440±78, respectively) (P=0.006). There was a statistically significant difference between the studied groups regarding blood transfusion, as eight patients (26.7%) of misoprostol group received blood transfusion, whereas only two patients (6.7%) of tourniquet group received blood transfusion (P=0.038). 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引用次数: 1

摘要

目的比较术前阴道米索前列醇与术中宫颈止血止血带在子宫肌瘤切除术中减少出血量的效果。患者和方法本前瞻性随机对照研究于2020年8月至2021年2月在Al-Zahraa大学医院妇产科进行了60例有症状的子宫肌瘤和腹部子宫肌瘤切除术的患者。患者分为两组:A组(米索前列醇组)包括30名妇女,她们在子宫肌瘤切除术前1小时阴道接受400 mg米索前列醇;B组(止血带组)包括30名妇女,她们在子宫肌瘤切除术期间接受术中经宫颈婴儿喂养管形式的止血带。记录术中对肌瘤的类型、部位、大小、手术时间、出血量、输血需水量的评价。主要观察指标如下:主要观察指标包括估计失血量和术后血红蛋白(Hb)和红细胞压积(HCT)水平,次要观察指标包括输血可能性和手术时间。结果止血带组手术时间(47.5±4.7)明显短于米索前列醇组(53.0±6.9)(P=0.001)。止血带组出血量明显少于米索前列醇组(分别为375.0±96.3和440±78)(P=0.006)。两组输血比较差异有统计学意义,米索前列醇组输血8例(26.7%),止血带组输血2例(6.7%),差异有统计学意义(P=0.038)。各组间基线(术前)Hb和HCT水平差异不显著。然而,两组术后Hb和HCT差异有统计学意义,止血带组高于米索前列醇组(分别为33.7±2.6和32.2±2.4);P = 0.033)。结论与术前使用米索前列醇相比,在子宫肌瘤切除术中经颈处系上止血带可显著减少术中出血量,缩短手术时间,降低输血风险。
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Comparative study of preoperative misoprostol versus intraoperative pericervical hemostatic tourniquet in reducing blood loss in cases of myomectomy
Objective The aim was to compare preoperative vaginal misoprostol versus intraoperative per-cervical hemostatic tourniquet in reducing blood loss during myomectomy. Patients and methods This prospective randomized control study was conducted on 60 patients who were experiencing symptomatic uterine myoma and underwent abdominal myomectomy at the Obstetrics and Gynecology Department of Al-Zahraa University Hospital from August 2020 to February 2021. The patients were divided into two groups: group A (misoprostol group) included 30 women who received 400 mg misoprostol vaginally 1 h before myomectomy operation, and group B (tourniquet group) included 30 women who underwent intraoperative per-cervical infant feeding tube form of tourniquet, during myomectomy. The intraoperative comments on type, site, size of fibroid, operation time, amount of blood loss, and blood transfusion need were recorded. The main outcome measures were as follows: primary outcome included the estimated blood loss and postoperative hemoglobin (Hb) and hematocrit (HCT) level, and secondary outcome included the possibility of blood transfusion and operative time. Results There was a significantly shorter duration of operation in tourniquet group (47.5±4.7) compared with misoprostol group (53.0±6.9) (P=0.001). There was significant less blood loss in the tourniquet group compared with the misoprostol group (375.0±96.3 and 440±78, respectively) (P=0.006). There was a statistically significant difference between the studied groups regarding blood transfusion, as eight patients (26.7%) of misoprostol group received blood transfusion, whereas only two patients (6.7%) of tourniquet group received blood transfusion (P=0.038). There was insignificant difference in baseline (preoperative) Hb and HCT levels between the study groups. However, there was a statistically significant difference between the study groups regarding the postoperative Hb and HCT, which were higher in the tourniquet group compared with the misoprostol group (33.7±2.6 and 32.2±2.4, respectively; P=0.033). Conclusion Fastening a tourniquet at per-cervical area during abdominal myomectomy reduced the intraoperative blood loss significantly compared with preoperative misoprostol, with shorter operative time with decreased incidence of risk of blood transfusion.
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