Eberhart L H, Morin A M, Seeling W, Bothner U, Georgieff M
Klinik für Anästhesiologie, Universität Ulm.
Anasthesiol Intensivmed Notfallmed Schmerzther. 1999 Sep;34(9):528-36. doi: 10.1055/s-1999-207.
Randomised, controlled trials using prophylactic droperidol to prevent postoperative nausea and vomiting (PONV) were included in a meta-analysis to estimate efficiency and dose-response of treatment.
Studies were systematically extracted from Medline, the manufacturer's database, and a supplemental search of references lists and current issues of locally available anaesthesia journals. Complete prevention of PONV defined as absence of nausea, retching, and vomiting within 6 hours (early PONV) and within 48 hours (late PONV) was chosen as the main end point. Additional information such as dose of droperidol, time and way of administration, and biometric data of the patients were extracted from each study. The pooled relative risk and the number-needed-to treat (NNT) were calculated.
A total of 72 studies with 107 comparative subgroups were accepted for analysis according to the prospectively defined criteria. Of these sixty-nine trials reported a lower incidence of PONV with droperidol. The incidence of early and late PONV among the 5370 patients receiving droperidol was 23.4% and 38.2%, respectively. The corresponding incidence among the 3954 control patients was 40.7% and 53.9%. The relative risk for patients receiving prophylactic droperidol of suffering from early PONV was 0.58 and 0.71 for late PONV. The NNT for preventing one patient from PONV was 5.8 and 6.4 for early and late PONV, respectively. Treatment with droperidol was more effective when the baseline risk for PONV was higher than 25% for early PONV and 35% for late PONV. Under these circumstances the NNT was between 2.6 and 5.6. There was no dose response relationship for droperidol when the drug was applied in doses ranging from 0.5 to 300 micrograms.kg-1 body weight. It was not possible to derive reliable information about the incidence of side-effects of the droperidol administration.
Droperidol is an effective antiemetic drug. The drug can be administered to patients with an increased risk of suffering from PONV without antiemetic prophylaxis. Since a positive dose response is lacking, droperidol should only be administered in doses of 1 mg or less.
将使用预防性氟哌利多预防术后恶心呕吐(PONV)的随机对照试验纳入一项荟萃分析,以评估治疗的有效性和剂量反应。
从医学文献数据库(Medline)、制造商数据库以及对参考文献列表和当地可用麻醉学杂志当期进行的补充检索中系统提取研究。将完全预防PONV定义为在6小时内(早期PONV)和48小时内(晚期PONV)无恶心、干呕和呕吐,以此作为主要终点。从每项研究中提取氟哌利多剂量、给药时间和方式以及患者生物特征数据等其他信息。计算合并相对风险和需治疗人数(NNT)。
根据预先确定的标准,共纳入72项研究中的107个比较亚组进行分析。其中69项试验报告使用氟哌利多时PONV发生率较低。5370例接受氟哌利多治疗的患者中,早期和晚期PONV发生率分别为23.4%和38.2%。3954例对照患者中的相应发生率分别为40.7%和53.9%。接受预防性氟哌利多治疗的患者发生早期PONV的相对风险为0.58,晚期PONV为0.71。预防一例患者发生PONV的NNT,早期PONV为5.8,晚期PONV为6.4。当早期PONV的基线风险高于25%且晚期PONV高于35%时,氟哌利多治疗更有效。在这些情况下,NNT在2.6至5.6之间。当氟哌利多以0.5至300微克·千克体重的剂量应用时,不存在剂量反应关系。无法得出关于氟哌利多给药副作用发生率的可靠信息。
氟哌利多是一种有效的止吐药物。对于PONV风险增加的患者,在无预防性止吐治疗的情况下也可使用该药物。由于缺乏阳性剂量反应,氟哌利多仅应以1毫克或更低剂量给药。