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首页> 外文期刊>BMC Anesthesiology >Haloperidol dose combined with dexamethasone for PONV prophylaxis in high-risk patients undergoing gynecological laparoscopic surgery: a prospective, randomized, double-blind, dose-response and placebo-controlled study
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Haloperidol dose combined with dexamethasone for PONV prophylaxis in high-risk patients undergoing gynecological laparoscopic surgery: a prospective, randomized, double-blind, dose-response and placebo-controlled study

机译:氟哌啶醇联合地塞米松预防妇科腹腔镜手术高危患者的PONV:一项前瞻性,随机,双盲,剂量反应和安慰剂对照研究

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Background Low-dose haloperidol is known to be effective for the prevention of postoperative nausea and vomiting (PONV). However, precise dose-response studies have not been completed, especially in patients at high risk for PONV who require combination therapy. This study sought to identify which dose of haloperidol 1mg or 2mg could be combined with dexamethasone without adverse effects in high-risk patients undergoing gynecological laparoscopic surgery. Methods Female adults (n?=?150) with three established PONV risk factors based on Apfel’s score were randomized into one of three study groups. At the end of anesthesia, groups H0, H1, and H2 were given intravenous (IV) saline, haloperidol 1 mg, and haloperidol 2 mg, respectively. All patients were given dexamethasone 5 mg during the induction of anesthesia. The overall early (0–2 h) and late (2–24 h) incidences of nausea, vomiting, rescue anti-emetic administration, pain, and adverse effects (cardiac arrhythmias and extrapyramidal effects) were assessed postoperatively. The sedation score was recorded in the postanesthesia care unit (PACU). Results The total incidence of PONV over 24 h was significantly lower in groups H1 (29?%) and H2 (24?%) than in group H0 (54?%; P?=?0.003), but there was no significant difference between groups H1 and H2. In the PACU, group H2 had a higher sedation score than groups H1 and H0 (P? Conclusions For high-risk PONV patients undergoing gynecological laparoscopic surgery, when used with dexamethasone, 1-mg haloperidol was equally effective as 2 mg in terms of preventing PONV with the less sedative effect. Trial Registration ClinicalTrials.gov ( NCT01639599 ).
机译:背景技术已知小剂量氟哌啶醇可有效预防术后恶心和呕吐(PONV)。但是,尚未完成精确的剂量反应研究,尤其是在需要联合治疗的PONV高危患者中。这项研究试图确定在妇科腹腔镜手术的高危患者中,哪种剂量的氟哌啶醇1mg或2mg可以与地塞米松联合使用而不会产生不良影响。方法将根据Apfel评分建立了三个PONV危险因素的成年女性(n?=?150)随机分为三个研究组之一。麻醉结束时,分别给组H0,H1和H2静脉注射(IV)盐水,氟哌啶醇1 mg和氟哌啶醇2 mg。在麻醉诱导期间,所有患者均给予地塞米松5 mg。术后评估恶心,呕吐,抗呕吐的急救,疼痛和不良反应(心律失常和锥体外系反应)的总体早期(0–2 h)和晚期(2–24 h)发生率。镇静分数记录在麻醉后护理单元(PACU)中。结果H1组(29%)和H2组(24 %%)在24小时内PONV的总发生率显着低于H0组(54 %%; P <= 0.003),但两者之间无显着差异。组H1和H2。在PACU中,H2组的镇静分数高于H1和H0组(P?结论)对于接受妇科腹腔镜手术的高危PONV患者,当与地塞米松一起使用时,在预防方面,1-mg氟哌啶醇等效于2 mg镇静作用较小的PONV,临床注册ClinicalTrials.gov(NCT01639599)。

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