Dexamethasone and clinically significant postoperative nausea and vomiting: a prespecified substudy of the randomised perioperative administration of dexamethasone and infection (PADDI) trial

被引:10
|
作者
Corcoran, Tomas B. [1 ,2 ,3 ]
Martin, Catherine [3 ]
O'Loughlin, Edmond [2 ,4 ]
Ho, Kwok M. [1 ,2 ,4 ,5 ]
Coutts, Pauline [1 ]
Chan, Matthew T. [6 ]
Forbes, Andrew [3 ]
Leslie, Kate [3 ,7 ,8 ]
Myles, Paul [3 ,9 ]
机构
[1] Royal Perth Hosp, Dept Anaesthesia & Pain Med, Perth, WA, Australia
[2] Univ Western Australia, Sch Med & Pharmacol, Perth, WA, Australia
[3] Monash Univ, Sch Publ Hlth & Prevent Med, Melbourne, Vic, Australia
[4] Fiona Stanley Hosp, Perth, WA, Australia
[5] Murdoch Univ, Perth, WA, Australia
[6] Chinese Univ Hong Kong, Dept Anaesthesia & Intens Care, Hong Kong, Peoples R China
[7] Univ Melbourne, Melbourne, Vic, Australia
[8] Royal Melbourne Hosp, Dept Anaesthesia & Pain Management, Melbourne, Vic, Australia
[9] Alfred Hosp, Dept Anaesthesia & Perioperat Med, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
antiemetic; complication; dexamethasone; glucocorticoid; patient-centred outcome; postoperative nausea and vomiting; AMBULATORY SURGERY; ADMISSION; OUTCOMES; AUDIT;
D O I
10.1016/j.bja.2022.05.018
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: Clinically significant postoperative nausea and vomiting (PONV) is a patient-reported outcome which reflects patient experience. Although dexamethasone prevents PONV, it is unknown what impact it has on this experience. Methods: In this prespecified embedded superiority substudy of the randomised Perioperative Administration of Dexamethasone and Infection (PADDI) trial, patients undergoing non-urgent noncardiac surgery received dexamethasone 8 mg or placebo intravenously after induction of anaesthesia, and completed a validated PONV questionnaire. The primary outcome was the incidence of clinically significant PONV on day 1 or day 2 postoperatively. Secondary outcomes included the incidence of clinically significant PONV and severe PONV on days 1 and 2 considered separately. Results: A total of 1466 participants were included, with 733 patients allocated to the dexamethasone arm and 733 to matched placebo. The primary outcome occurred in 52 patients (7.1%) in the dexamethasone arm and 66 (9%) patients in the placebo arm (relative risk [RR]1/4 0.79; 95% confidence interval [CI], 0.56e1.11; P 1/4 0.18). Severe PONV occurred on day 2 in 27 patients (3.9%) in the dexamethasone arm and 47 patients (6.7%) in the placebo arm (RR 1/4 0.58; 95% CI, 0.37e0.92; P 1/4 0.02; number needed-to-treat (NNT)1/4 36.7; 95% CI, 20e202). In the entire cohort of 8880 PADDI patients, lower nausea scores, less frequent administration of antiemetics, and fewer vomiting events were recorded by patients in the dexamethasone arm up to day 2 after surgery. Conclusions: Administration of dexamethasone 8 mg i.v. did not influence clinically significant PONV. Dexamethasone administration did, however, decrease the incidence and severity of PONV, and was associated with less frequent administration of antiemetic agents. Clinical trial registration: ACTRN12614001226695.
引用
收藏
页码:327 / 335
页数:9
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