M. Chanzá , M. Núñez , M.C. Velasco , C. Rodríguez-Cosmen , A.C. Carpintero , L. Gallart
{"title":"在腹腔镜妇科手术中,皮下碳纤维接触加热与皮下强制空气加热预防体温过低:一项随机试验","authors":"M. Chanzá , M. Núñez , M.C. Velasco , C. Rodríguez-Cosmen , A.C. Carpintero , L. Gallart","doi":"10.1016/j.redare.2025.501689","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Studies comparing intraoperative warming devices report discordant or out-of-date results. This trial compared two underbody warming devices.</div></div><div><h3>Methods</h3><div>Thirty patients undergoing elective prolonged laparoscopic gynecologic surgery were randomized to underbody warming by forced air (n = 15) or contact with a carbon fibre blanket (n = 15). The main outcome was esophageal temperature at the end of surgery. We also compared temperature throughout surgery and need for rescue warming, blood loss, fluids infused, urine output, and adverse events. Outcomes were compared with χ² or Fisher exact tests, t-tests, and mixed effects models as appropriate.</div></div><div><h3>Results</h3><div>No median (interquartile range) differences between forced-air and contact warming were found in initial or final temperatures (36.2 °C [36.0, 36.2] <em>vs</em> 36.3 °C [35.9, 36.6] and 36.6 °C [36.2, 36.8] <em>vs</em> 36.3 °C [35.6, 36.5]). Temperature slightly increased over time in the forced-air group and slightly decreased in contact group (0.11 °C/h (0.02, 0.19) <em>vs</em> −0.05 °C/h (−0.13, 0.03), <em>p</em> = 0.008). A single patient required rescue warming (in contact group after 4.75 h). Surgery took longer in the contact group (3.2 h [2.5, 3.8] <em>vs</em> 4.0 h [2.9, 5.6] h, <em>p</em> = 0.042). Two surgeons complained of dizziness related to ambient heat in the forced-air group. No differences were found in the remaining variables.</div></div><div><h3>Conclusions</h3><div>During use of the underbody forced-air and carbon-fibre warming devices tested, we recorded only very slight differences in temperature changes over the course of surgery. The variations can be considered clinically unimportant as no significant difference was evident at the end of surgery.</div></div>","PeriodicalId":94196,"journal":{"name":"Revista espanola de anestesiologia y reanimacion","volume":"72 5","pages":"Article 501689"},"PeriodicalIF":0.0000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Underbody carbon-fiber contact warming versus underbody forced-air warming to prevent hypothermia during laparoscopic gynecologic surgery: A randomized trial\",\"authors\":\"M. Chanzá , M. Núñez , M.C. Velasco , C. Rodríguez-Cosmen , A.C. Carpintero , L. Gallart\",\"doi\":\"10.1016/j.redare.2025.501689\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>Studies comparing intraoperative warming devices report discordant or out-of-date results. This trial compared two underbody warming devices.</div></div><div><h3>Methods</h3><div>Thirty patients undergoing elective prolonged laparoscopic gynecologic surgery were randomized to underbody warming by forced air (n = 15) or contact with a carbon fibre blanket (n = 15). The main outcome was esophageal temperature at the end of surgery. We also compared temperature throughout surgery and need for rescue warming, blood loss, fluids infused, urine output, and adverse events. Outcomes were compared with χ² or Fisher exact tests, t-tests, and mixed effects models as appropriate.</div></div><div><h3>Results</h3><div>No median (interquartile range) differences between forced-air and contact warming were found in initial or final temperatures (36.2 °C [36.0, 36.2] <em>vs</em> 36.3 °C [35.9, 36.6] and 36.6 °C [36.2, 36.8] <em>vs</em> 36.3 °C [35.6, 36.5]). Temperature slightly increased over time in the forced-air group and slightly decreased in contact group (0.11 °C/h (0.02, 0.19) <em>vs</em> −0.05 °C/h (−0.13, 0.03), <em>p</em> = 0.008). A single patient required rescue warming (in contact group after 4.75 h). Surgery took longer in the contact group (3.2 h [2.5, 3.8] <em>vs</em> 4.0 h [2.9, 5.6] h, <em>p</em> = 0.042). Two surgeons complained of dizziness related to ambient heat in the forced-air group. No differences were found in the remaining variables.</div></div><div><h3>Conclusions</h3><div>During use of the underbody forced-air and carbon-fibre warming devices tested, we recorded only very slight differences in temperature changes over the course of surgery. The variations can be considered clinically unimportant as no significant difference was evident at the end of surgery.</div></div>\",\"PeriodicalId\":94196,\"journal\":{\"name\":\"Revista espanola de anestesiologia y reanimacion\",\"volume\":\"72 5\",\"pages\":\"Article 501689\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Revista espanola de anestesiologia y reanimacion\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2341192925000848\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista espanola de anestesiologia y reanimacion","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2341192925000848","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
背景:比较术中加热装置的研究报告了不一致或过时的结果。该试验比较了两种人体下暖装置。方法:30例选择性长时间腹腔镜妇科手术患者随机分为强制空气加热组(n = 15)和接触碳纤维毯组(n = 15)。主要观察指标为手术结束时食管温度。我们还比较了整个手术过程中的温度和急救温度、失血量、输液量、尿量和不良事件。采用χ 2或Fisher精确检验、t检验和混合效应模型对结果进行比较。结果:在初始或最终温度(36.2°C [36.0, 36.2] vs 36.3°C[35.9, 36.6]和36.6°C [36.2, 36.8] vs 36.3°C[35.6, 36.5])中,强制空气加热和接触加热之间没有中位数(四分位数范围)差异。加压空气组的温度随时间略有升高,接触组的温度略有下降(0.11°C/h (0.02, 0.19) vs -0.05°C/h (-0.13, 0.03), p = 0.008)。1例患者需要急救加热(接触组为4.75 h),接触组手术时间更长(3.2 h [2.5, 3.8] vs 4.0 h [2.9, 5.6] h, p = 0.042)。在强制空气组中,两名外科医生抱怨与环境高温有关的头晕。其余变量没有发现差异。结论:在使用体底加压空气和碳纤维加热装置的过程中,我们在手术过程中记录到的温度变化只有非常微小的差异。这些差异在临床上不重要,因为在手术结束时没有明显的差异。
Underbody carbon-fiber contact warming versus underbody forced-air warming to prevent hypothermia during laparoscopic gynecologic surgery: A randomized trial
Background
Studies comparing intraoperative warming devices report discordant or out-of-date results. This trial compared two underbody warming devices.
Methods
Thirty patients undergoing elective prolonged laparoscopic gynecologic surgery were randomized to underbody warming by forced air (n = 15) or contact with a carbon fibre blanket (n = 15). The main outcome was esophageal temperature at the end of surgery. We also compared temperature throughout surgery and need for rescue warming, blood loss, fluids infused, urine output, and adverse events. Outcomes were compared with χ² or Fisher exact tests, t-tests, and mixed effects models as appropriate.
Results
No median (interquartile range) differences between forced-air and contact warming were found in initial or final temperatures (36.2 °C [36.0, 36.2] vs 36.3 °C [35.9, 36.6] and 36.6 °C [36.2, 36.8] vs 36.3 °C [35.6, 36.5]). Temperature slightly increased over time in the forced-air group and slightly decreased in contact group (0.11 °C/h (0.02, 0.19) vs −0.05 °C/h (−0.13, 0.03), p = 0.008). A single patient required rescue warming (in contact group after 4.75 h). Surgery took longer in the contact group (3.2 h [2.5, 3.8] vs 4.0 h [2.9, 5.6] h, p = 0.042). Two surgeons complained of dizziness related to ambient heat in the forced-air group. No differences were found in the remaining variables.
Conclusions
During use of the underbody forced-air and carbon-fibre warming devices tested, we recorded only very slight differences in temperature changes over the course of surgery. The variations can be considered clinically unimportant as no significant difference was evident at the end of surgery.