Mina Yadollahi, K. Sadegi, M. Afshari, Batool Shahraki Mojahed
{"title":"Effect of spinal anesthesia with sufentanil on length of stages I and II of labor in singleton pregnant women: a randomized controlled trial","authors":"Mina Yadollahi, K. Sadegi, M. Afshari, Batool Shahraki Mojahed","doi":"10.18051/univmed.2023.v42.94-100","DOIUrl":null,"url":null,"abstract":"BackgroundLabor pain is one of the most painful experiences in a women's life. One of the methods of pain relief is spinal anesthesia. The purpose of this study was to evaluate the effect of spinal anesthesia with sufentanil on the length of the first and second stages of labor in singleton pregnant women.\nMethodsA randomized clinical trial was conducted involving 56 women who had to be at least 37 weeks pregnant with a singleton pregnancy and 20 to 35 years of age, as well as seeking a spontaneous natural delivery. They were randomized into an intervention group (spinal anesthesia with sufentanil) of 28 subjects and a control group (no spinal anesthesia) of 28 subjects. Statistical analysis was performed using SPSS software program 20.0.\nResultsMean duration of stage I of labor was 152.32 ± 92.01 and 187.68 ± 121.01 minutes in the intervention and control groups, respectively (p=0.34), whereas mean duration of stage II of labor in the 2 groups was 15.96 ± 14.26 and 26.43 ± 20.90 minutes, respectively (p=0.06). Twenty five percent of women in the intervention group and 35.71% of women in the control group experienced a long stage I, whereas 21.43% of women in the intervention group and 35.71% of women in the control group experienced a long stage II (p>0.05).\nConclusionThis study suggests that spinal anesthesia with sufentanil does not increase the duration of labor stages. It is recommended that more studies be performed in the future using larger sample sizes to allow for the drawing of solid conclusions.","PeriodicalId":42578,"journal":{"name":"Universa Medicina","volume":" ","pages":""},"PeriodicalIF":0.2000,"publicationDate":"2023-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Universa Medicina","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18051/univmed.2023.v42.94-100","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 1
Abstract
BackgroundLabor pain is one of the most painful experiences in a women's life. One of the methods of pain relief is spinal anesthesia. The purpose of this study was to evaluate the effect of spinal anesthesia with sufentanil on the length of the first and second stages of labor in singleton pregnant women.
MethodsA randomized clinical trial was conducted involving 56 women who had to be at least 37 weeks pregnant with a singleton pregnancy and 20 to 35 years of age, as well as seeking a spontaneous natural delivery. They were randomized into an intervention group (spinal anesthesia with sufentanil) of 28 subjects and a control group (no spinal anesthesia) of 28 subjects. Statistical analysis was performed using SPSS software program 20.0.
ResultsMean duration of stage I of labor was 152.32 ± 92.01 and 187.68 ± 121.01 minutes in the intervention and control groups, respectively (p=0.34), whereas mean duration of stage II of labor in the 2 groups was 15.96 ± 14.26 and 26.43 ± 20.90 minutes, respectively (p=0.06). Twenty five percent of women in the intervention group and 35.71% of women in the control group experienced a long stage I, whereas 21.43% of women in the intervention group and 35.71% of women in the control group experienced a long stage II (p>0.05).
ConclusionThis study suggests that spinal anesthesia with sufentanil does not increase the duration of labor stages. It is recommended that more studies be performed in the future using larger sample sizes to allow for the drawing of solid conclusions.
分娩疼痛是女性一生中最痛苦的经历之一。减轻疼痛的方法之一是脊髓麻醉。本研究的目的是评价舒芬太尼脊髓麻醉对单胎孕妇第一、二产程长度的影响。方法对56名年龄在20 ~ 35岁、孕37周以上、单胎妊娠且寻求自然分娩的妇女进行随机临床试验。随机分为干预组(舒芬太尼脊髓麻醉)28例,对照组(非脊髓麻醉)28例。采用SPSS 20.0软件进行统计学分析。结果干预组和对照组第一产程平均时间分别为152.32±92.01、187.68±121.01 min (p=0.34),两组第二产程平均时间分别为15.96±14.26、26.43±20.90 min (p=0.06)。干预组有25%的女性和对照组有35.71%的女性经历了较长的I期,而干预组有21.43%的女性和对照组有35.71%的女性经历了较长的II期(p>0.05)。结论舒芬太尼脊髓麻醉不会增加产程时间。建议将来使用更大的样本量进行更多的研究,以便得出可靠的结论。