地塞米松治疗术后恶心呕吐的随机剂量发现试验。

Dexamethasone for the treatment of established postoperative nausea and vomiting: A randomised dose finding trial.

机构信息

From the Division of Anaesthesiology, Department of Anaesthesiology, Pharmacology, Intensive Care and Emergency Medicine, Geneva University Hospitals, Geneva (CC, MRT), Division of Anaesthesiology, Department of Anaesthesiology, Intensive Care and Emergency Medicine, Ospedale Regionale di Lugano, EOC, Lugano, Switzerland (CC), Division of Clinical Pharmacology and Toxicology, Department of Anaesthesiology, Pharmacology, Intensive Care and Emergency Medicine, Geneva University Hospitals (JD), Division of Anaesthesiology, University Hospitals of Lausanne (EA, CK), Department of Clinical Epidemiology and Medical Technology Assessment, Maastricht University Medical Centre, Maastricht, the Netherlands (SMJvK), Division of Anaesthesiology, Réseau Hospitalier Neuchatelois, Neuchatel (J-BC), Division of Anaesthesiology, Etablissements Hospitaliers du Nord Vaudois, Yverdon les Bains et Saint Loup (SG), Faculty of Medicine, University of Geneva, Geneva (CC, JD, MRT) and Faculty of Biology and Medicine, University of Lausanne, Lausanne, Switzerland (EA, CK).

出版信息

Eur J Anaesthesiol. 2022 Jun 1;39(6):549-557. doi: 10.1097/EJA.0000000000001636. Epub 2021 Nov 16.

DOI:10.1097/EJA.0000000000001636

PMID:34799501

Abstract

BACKGROUND

Dexamethasone is widely used for the prevention of postoperative nausea and vomiting (PONV) but little is known about its efficacy for the treatment of established PONV.

OBJECTIVE

To test the antiemetic efficacy of intravenous dexamethasone for the treatment of established PONV in adults undergoing surgery under general anaesthesia and to determine whether there is dose-responsiveness.

DESIGN

The DexPonv trial is a multicentre, placebo-controlled, randomised, double-blind, dose-finding study. Inclusion of patients was between September 2012 and November 2017. Follow-up for PONV symptoms was for 24 h. Thirty days postoperatively, patients were contacted by study nurses for any information on postoperative bleeding and infection.

SETTING

Four public hospitals in Switzerland.

PATIENTS

A total of 803 adults scheduled for elective surgery without any antiemetic prophylaxis signed the consent form; 714 were included. Among those, 319 had PONV and 281 patients were eventually randomised (intention to treat population and safety set). The per protocol set consisted of 260 patients.

INTERVENTIONS

Patients with PONV symptoms (including retching) were randomised to a single intravenous dose of dexamethasone 3, 6 or 12 mg or matching placebo.

MAIN OUTCOME MEASURES

The primary endpoint was the absence of further nausea or vomiting (including retching), within 24 h after administration of the study drug.

RESULTS

Dexamethasone was ineffective during the first 24 h, whatever the dosage, compared to placebo, even when the model was adjusted for known risk factors (P = 0.170). There were no differences in the time to treatment failure or the quality of sleep during the first night. There was a positive correlation between the dose of dexamethasone and blood glucose concentrations (P < 0.001), but not with bleeding risk, wound infections or other adverse effects.

CONCLUSION

This randomised trial failed to show anti-emetic efficacy of any of the tested intravenous regimens of dexamethasone for the treatment of established PONV in adults undergoing surgery under general anaesthesia.