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find Keyword "寒战" 4 results
  • Efficacy of Granisetron in Preventing Postanesthesia Shivering

    目的:探讨同哌替啶和曲马多比较,格拉斯琼预防全麻后寒战的临床效果。方法:120例ASA I~II级,在全麻下拟行择期手术患者,随机分为四组,每组30例:T组(曲马多1mg/kg),G组(格拉斯琼40 μg/kg),M组(哌替啶0.4mg/kg)和P组(0.9%生理盐水)。各组药物在手术结束时通过静脉给予。记录术后寒战评分和麻醉恢复时间及镇静程度。结果:同对照组比较,格拉斯琼明显减少麻醉后寒战的发生(Plt;0.01),但同哌替啶和曲马多组比较无统计学差异(Pgt;0.05)。哌替啶组和曲马多组的麻醉恢复时间(20.58±3.56和16.45±4.13 min)较对照组(12.61±3.31 min)和格拉斯琼组(13.58±3.41 min)明显延长(Plt;0.05)。结论:使用40 μg/kg格拉司琼同使用曲马多1mg/kg和哌替啶0.4mg/kg一样可有效地预防麻醉后寒战。

    Release date:2016-09-08 10:04 Export PDF Favorites Scan
  • Efficacy of Granisetron in Preventing Postanesthetic Shivering

    目的:探讨同哌替啶和曲马多比较,格拉斯琼预防全麻后寒战的临床效果。方法:120例ASA I~II级,在全麻下拟行择期手术患者,随机分为四组,每组30例:T组(曲马多1 mg/kg),G组(格拉斯琼40 μg/kg),M组(哌替啶0.4 mg/kg)和P组(0.9%生理盐水)。各组药物在手术结束时通过静脉给予。记录术后寒战评分和麻醉恢复时间及镇静程度。结果:同对照组比较,格拉斯琼明显减少麻醉后寒战的发生(P<0.01),但同哌替啶和曲马多组比较无统计学差异(P >0.05)。哌替啶组和曲马多组的麻醉恢复时间(20.58±3.56和16.45 ±4.13 min)较对照组(12.61 ± 3.31 min)和格拉斯琼组(13.58 ± 3.41 min)明显延长(P<0.05)。结论:使用40 μg/kg格拉司琼同使用曲马多1 mg/kg和哌替啶0.4 mg/kg一样可有效地预防麻醉后寒战。

    Release date:2016-09-08 10:12 Export PDF Favorites Scan
  • Clinical Effect and Safety of Prophylactic Ondansetron for the Prevention of Postoperative Shivering: A Meta-analysis

    ObjectiveTo evaluate the effectiveness and safety of prophylactic ondansetron for the prevention of postoperative shivering. MethodsAccording to the Cochrane Handbook, we searched such databases as Cochrane Library, PubMed, OVID, EMbase, CNKI, CBM, and VIP (From January 1999 to September 2013) to collect the literature about ondansetron for the prevention of postoperative shivering. According to the predefined inclusion and exclusion criteria, we screened randomized controlled trials (RCTs). The included studies were evaluated and analyzed by meta-analysis with RevMan 5.0 software. ResultsNine RCTs involving 655 patients were included. The results of meta-analysis showed that there was a significant difference in incidence of postoperative shivering between group ondansetron and the controls [RR=0.32, 95%CI (0.24, 0.42), P<0.05]. There was a significant difference in incidence of postoperative nausea and vomiting between the ondansetron group and the control group [RR=0.30, 95%CI (0.14, 0.63), P<0.05]. There was no significant difference in the 1 min and 5 min neonate born Apgar score between the ondansetron group and the control group [WMD=0.03, 95%CI (-0.02, 0.09), P=0.26; WMD=-0.02, 95%CI (-0.12, 0.08), P=0.68]. ConclusionIntravenous ondansetron before surgery can significantly reduce postoperative shivering without any increment of adverse effects.

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  • Efficacy of Maternal Body Temperature Preservation during Caesarean Section: A Systematic Review

    Objective To systematically review the efficacy of maternal body temperature preservation during caesarean section. Methods Databases including PubMed, EMbase, The Cochrane Library (Issue 2, 2015), WanFang Data, CBM and CNKI were searched from inception to July 2015 to collect randomized controlled trials (RCTs) of body temperature preservation in patients with caesarean delivery. Two reviewers independently screened literature, extracted data and assessed the risk of bias of included studies. Then, meta-analysis was performed using RevMan5.3 software. Results A total of 15 RCTs involving 1 331 patients were included. The results of meta-analysis showed that patients in the temperature preservation group had a smaller body temperature variation (MD= –0.22, 95%CI –0.32 to –0.13, P < 0.000 01) and a lower incidence of shivering (RR=0.53, 95%CI 0.42 to 0.67, P < 0.000 01) than patients in the control group. There were no statistical differences between the two groups in blood loss (MD= –13.77, 95%CI –33.95 to 6.42, P=0.18) and newborn Apgar score (MD=0.12, 95%CI –0.37 to 0.6, P=0.64). Conclusions Current evidence shows that body temperature preservation measures can better protect patients with caesarean delivery. Specifically, body temperature preservation measures could reduce patients’ body temperature variation and incidence of shivering but had no effect on blood loss and newborn Apgar score. Due to limited quality and quantity of the included studies, more high quality studies are needed to verify the above conclusion.

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