Tamer E El-Ghazaly, Ibrahim A Abdelazim, A Elshabrawy
{"title":"Intrauterine Levobupivacaine Instillation for Pain Control in Women Undergoing Diagnostic Hysteroscopy.","authors":"Tamer E El-Ghazaly, Ibrahim A Abdelazim, A Elshabrawy","doi":"10.4103/gmit.gmit_48_21","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Many women experience pain and discomfort after hysteroscopic procedure. Pain and discomfort after hysteroscopic procedures can be explained by the cervical dilatation, intrauterine manipulation, and/or hydrodistension. This study designed to evaluate the efficacy of intrauterine levobupivacaine instillation for pain control in women undergoing diagnostic hysteroscopy.</p><p><strong>Materials and methods: </strong>One hundred and twenty (120) women scheduled for diagnostic hysteroscopy and endometrial biopsy due to uterine bleeding were included in this study and randomized either to levobupivacaine group or controls. At the end of hysteroscopy, 5 mL of 0.5% levobupivacaine was instilled intrauterine in levobupivacaine group, while 5 mL of 0.9% saline was instilled intrauterine in controls. Participants were kept in the hospital for 12 h after diagnostic hysteroscopy to detect the postoperative (PO) pain intensity using visual analog scale (VAS), and PO required analgesics.</p><p><strong>Results: </strong>The VAS was significantly lower in levobupivacaine group compared to controls 3 h. PO (1.31 ± 1.02 vs. 1.62 ± 0.76, respectively), (<i>P</i> = 0.01), 6 h. PO (0.81 ± 1.24 vs. 1.53 ± 0.88, respectively), (<i>P</i> = 0.004), and 9 h. PO (0.55 ± 1.25 vs. 1.12 ± 0.95, respectively), (<i>P</i> = 0.01). The total PO required analgesics were significantly lower in levobupivacaine group compared to controls (<i>P</i> = 0.005).</p><p><strong>Conclusion: </strong>The intrauterine levobupivacaine instillation was simple, and effective for pain relief after diagnostic hysteroscopy, it significantly decreased pain score assessed by VAS at 3, 6, and 9 h., PO, and it significantly decreased PO required analgesics.</p>","PeriodicalId":45272,"journal":{"name":"Gynecology and Minimally Invasive Therapy-GMIT","volume":"11 4","pages":"209-214"},"PeriodicalIF":1.4000,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/2d/32/GMIT-11-209.PMC9844048.pdf","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gynecology and Minimally Invasive Therapy-GMIT","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/gmit.gmit_48_21","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 4
Abstract
Objectives: Many women experience pain and discomfort after hysteroscopic procedure. Pain and discomfort after hysteroscopic procedures can be explained by the cervical dilatation, intrauterine manipulation, and/or hydrodistension. This study designed to evaluate the efficacy of intrauterine levobupivacaine instillation for pain control in women undergoing diagnostic hysteroscopy.
Materials and methods: One hundred and twenty (120) women scheduled for diagnostic hysteroscopy and endometrial biopsy due to uterine bleeding were included in this study and randomized either to levobupivacaine group or controls. At the end of hysteroscopy, 5 mL of 0.5% levobupivacaine was instilled intrauterine in levobupivacaine group, while 5 mL of 0.9% saline was instilled intrauterine in controls. Participants were kept in the hospital for 12 h after diagnostic hysteroscopy to detect the postoperative (PO) pain intensity using visual analog scale (VAS), and PO required analgesics.
Results: The VAS was significantly lower in levobupivacaine group compared to controls 3 h. PO (1.31 ± 1.02 vs. 1.62 ± 0.76, respectively), (P = 0.01), 6 h. PO (0.81 ± 1.24 vs. 1.53 ± 0.88, respectively), (P = 0.004), and 9 h. PO (0.55 ± 1.25 vs. 1.12 ± 0.95, respectively), (P = 0.01). The total PO required analgesics were significantly lower in levobupivacaine group compared to controls (P = 0.005).
Conclusion: The intrauterine levobupivacaine instillation was simple, and effective for pain relief after diagnostic hysteroscopy, it significantly decreased pain score assessed by VAS at 3, 6, and 9 h., PO, and it significantly decreased PO required analgesics.
目的:许多妇女在宫腔镜手术后感到疼痛和不适。宫腔镜手术后的疼痛和不适可由宫颈扩张、宫内操作和/或水膨胀来解释。本研究旨在评估子宫内左旋布比卡因对诊断性宫腔镜检查妇女疼痛控制的疗效。材料与方法:本研究纳入120例因子宫出血而行诊断性宫腔镜检查和子宫内膜活检的妇女,随机分为左布比卡因组和对照组。宫腔镜检查结束时,左旋布比卡因组宫腔内灌注0.5%左布比卡因5 mL,对照组宫腔内灌注0.9%生理盐水5 mL。诊断性宫腔镜检查后住院12小时,采用视觉模拟评分法(VAS)检测术后疼痛强度,并对术后疼痛进行镇痛。结果:左布比卡因组VAS评分3 h PO(1.31±1.02∶1.62±0.76)、6 h PO(0.81±1.24∶1.53±0.88)、9 h PO(0.55±1.25∶1.12±0.95)显著低于对照组(P = 0.01)。左布比卡因组总PO用量明显低于对照组(P = 0.005)。结论:宫腔内左旋布比卡因对诊断性宫腔镜术后疼痛缓解简单有效,可显著降低术后3、6、9 h VAS疼痛评分,并显著降低术后所需镇痛药物。