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首页> 外文期刊>Canadian journal of anesthesia: Journal canadien d'anesthesie >A randomized trial of phenylephrine infusion versus bolus dosing for nausea and vomiting during Cesarean delivery in obese women
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A randomized trial of phenylephrine infusion versus bolus dosing for nausea and vomiting during Cesarean delivery in obese women

机译:肥胖女性剖腹产肾上腺素输注对恶臭和呕吐的随机试验

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Abstract Purpose Hypotension is common after spinal anesthesia for Cesarean delivery. It is associated with nausea, vomiting, and fetal acidosis. Previous research on phenylephrine excluded obese subjects. We compared the incidence of intraoperative nausea and vomiting (IONV) in obese patients who received a prophylactic phenylephrine infusion vs those who received bolus dosing for the treatment of spinal-induced hypotension. Methods In this multicentre, double-blinded randomized controlled trial, 160 obese women undergoing elective Cesarean delivery under spinal anesthesia were randomized to receive a prophylactic phenylephrine infusion initiated at 50 μg·min ?1 (and titrated according to a predefined algorithm) or 100 μg phenylephrine boluses to treat hypotension. Maternal systolic blood pressure was maintained within 20% of baseline. The primary study outcome was the incidence of IONV. Results Intraoperative nausea and vomiting were significantly reduced in the infusion group compared to the bolus group (46% vs 75%, respectively; relative risk [RR], 0.61; 95% confidence interval [CI], 0.47 to 0.80; P vs 42%, respectively; RR, 0.62; 95% CI, 0.40 to 0.97; P = 0.04), but no difference in the incidence of vomiting. Postoperative vomiting at two hours was reduced in the infusion group (11% vs 25%; RR, 0.44; 95% CI, 0.21 to 0.90; P = 0.02);however, there were no differences in the incidence or severity of postoperative nausea, need for rescue antiemetics at two hours and 24 hr, or the incidence of postoperative vomiting at 24 hr. Conclusion In obese women undergoing Cesarean delivery with spinal anesthesia, prophylactic phenylephrine infusion was associated with less intraoperative nausea, less need for rescue antiemetics, and reduced early postoperative vomiting. Trial registration www.clinicaltrials.gov ( NCT01481740). Registered 22 July 2011.
机译:摘要目的的低血压是脊髓麻醉后循环分娩后常见。它与恶心,呕吐和胎儿酸中毒有关。以前关于苯妥的研究排除了肥胖的主题。我们比较了接受预防脱脂肾上肾上腺素输注的肥胖患者的术中恶心和呕吐(IONV)的发病率与那些接受脊柱诱导的低血压治疗的推注给药的人。方法在这种多期式,双盲随机对照试验中,在脊髓麻醉下进行选修剖宫产的160名肥胖妇女随机接受在50μg·min·1(并根据预定算法滴定)或100μg滴定的预防脱脂肾上肾上腺素输注。去妥妥肾上腺素治疗低血压。母体收缩压在基线的20%以内保持。初级研究结果是IONV的发生率。结果与推注组(分别为46%vs 75%;相对风险[rr],0.61; 95%置信区间[ci],0.47至0.80; p与0.47至0.80; p与0.47至0.80; p vs 42%(相对风险)显着减少了术中恶心和呕吐。分别; RR,0.62; 95%CI,0.40至0.97; p = 0.04),但呕吐的发生率没有差异。输液组术后呕吐在两个小时(11%vs 25%; RR,0.44; 95%CI,0.21至0.90; P = 0.02);然而,术后恶心的发病率或严重程度没有差异,需要在两小时和24小时的救援止血,或24小时术后呕吐的发生率。结论在肥胖妇女接受脊髓麻醉中进行剖宫产的妇女,预防脱脂肾上肾上腺素输注与术中恶心较少,不太需要抢救止血,降低术后呕吐。试用注册www.clinicaltrials.gov(nct01481740)。 2011年7月22日注册。

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