Meta-analysis of the safety of 5-HT3 antagonists with dexamethasone or droperidol for prevention of PONV

被引:23
|
作者
Leslie, JB [1 ]
Gan, TJ
机构
[1] Mayo Clin, Coll Med, Scottsdale, AZ 85259 USA
[2] Mayo Clin, Mayo Clin Hosp, Scottsdale, AZ 85259 USA
[3] Duke Univ, Med Ctr, Dept Anesthesiol, Durham, NC 27710 USA
关键词
dexamethasone; dolasetron; droperidol; 5-HT3; granisetron; ondansetron; PONV;
D O I
10.1345/aph.1G381
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BACKGROUND: Antiemetic guidelines recommend a combination of serotonin (5-HT3) with a second agent such as droperidol or dexamethasone. Physicians have been reluctant to employ these guidelines due to concerns over the black-box warning of droperidol and safety concerns with a steroid. OBJECTIVE: To assess the safety profiles of 5-HT3 receptor antagonist (5-HT(3)RA) monotherapy and combination therapy with a steroid or droperidol for prophylaxis of postoperative nausea and vomiting (PONV). METHODS: A MEDLINE search of English-language reports of randomized controlled trials (RCTs) was conducted (1966-September 2005) using the key terms 5-HT3, granisetron, ondansetron, dolasetron, tropisetron, PONV, postoperative, vomiting, emesis, and nausea. RCTs with treatment arms comparing 5-HT(3)RA monotherapy (granisetron, ondansetron, dolasetron, or tropisetron) with dexamethasone or droperidol or 5-HT3RA combinations and providing incidence data on adverse events were identified and reviewed. Within-study odds ratios with 95% confidence intervals were calculated to determine the incidence rates of all adverse events in RCTs using 5-HT(3)RA monotherapy and combination therapies. Overall effect sizes for frequently reported adverse events were estimated by pooling ORs using fixed- and random-effect models. RESULTS: Pooled ORs (ORPpooled) for adverse events with 5-HT(3)RA/dexamethasone versus 5-HT(3)RA for PONV prophylaxis were not significant for any reported adverse events or the overall incidence of adverse events; 5-HT(3)RA/droperidol versus 5-HT(3)RA was significant only for decreased headache incidence (fixed model: ORpooled 0.35; 95% CI 0.18 to 0.69). The ORpooled for 5HT(3)RA/dexamethasone versus dexamethasone was not significant for any reported adverse events except headaches (fixed model ORpooled 1.75; 95% CI 1.01 to 3.03), none of which was serious. ORpooled for 5-HT(3)RA/droperidol versus droperidol was not significant for any reported adverse events. Avascular necrosis, occult infection, and delayed wound healing were not observed with either combination therapy. Cardiac abnormalities were observed with 5-HT(3)RA/droperidol therapy. CONCLUSIONS: This meta-analysis indicates that either therapy has a safety profile similar to that of dexamethasone, droperidol, or 5-HT(3)RA.
引用
收藏
页码:856 / 872
页数:17
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