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  • Impact of perioperative dexamethasone on postoperative analgesia and side-effects: systematic review and meta-analysis.

Impact of perioperative dexamethasone on postoperative analgesia and side-effects: systematic review and meta-analysis.

British journal of anaesthesia (2012-12-12)
N H Waldron, C A Jones, T J Gan, T K Allen, A S Habib
要旨

The analgesic efficacy and adverse effects of a single perioperative dose of dexamethasone are unclear. We performed a systematic review to evaluate the impact of a single i.v. dose of dexamethasone on postoperative pain and explore adverse events associated with this treatment. MEDLINE, EMBASE, CINAHL, and the Cochrane Register were searched for randomized, controlled studies that compared dexamethasone vs placebo or an antiemetic in adult patients undergoing general anaesthesia and reported pain outcomes. Forty-five studies involving 5796 patients receiving dexamethasone 1.25-20 mg were included. Patients receiving dexamethasone had lower pain scores at 2 h {mean difference (MD) -0.49 [95% confidence interval (CI): -0.83, -0.15]} and 24 h [MD -0.48 (95% CI: -0.62, -0.35)] after surgery. Dexamethasone-treated patients used less opioids at 2 h [MD -0.87 mg morphine equivalents (95% CI: -1.40 to -0.33)] and 24 h [MD -2.33 mg morphine equivalents (95% CI: -4.39, -0.26)], required less rescue analgesia for intolerable pain [relative risk 0.80 (95% CI: 0.69, 0.93)], had longer time to first dose of analgesic [MD 12.06 min (95% CI: 0.80, 23.32)], and shorter stays in the post-anaesthesia care unit [MD -5.32 min (95% CI: -10.49 to -0.15)]. There was no dose-response with regard to the opioid-sparing effect. There was no increase in infection or delayed wound healing with dexamethasone, but blood glucose levels were higher at 24 h [MD 0.39 mmol litre(-1) (95% CI: 0.04, 0.74)]. A single i.v. perioperative dose of dexamethasone had small but statistically significant analgesic benefits.

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製品内容

Sigma-Aldrich
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デキサメタゾン, ≥98% (HPLC), powder
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デキサメタゾン, powder, γ-irradiated, BioXtra, suitable for cell culture, ≥80% (HPLC)
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デキサメタゾン 溶液, 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®
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デキサメタゾン, meets USP testing specifications
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デキサメタゾン, Pharmaceutical Secondary Standard; Certified Reference Material
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デキサメタゾン, tested according to Ph. Eur.
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デキサメタゾン, VETRANAL®, analytical standard
デキサメタゾン, European Pharmacopoeia (EP) Reference Standard
システム適合性用デキサメタゾン, European Pharmacopoeia (EP) Reference Standard
デキサメタゾン, European Pharmacopoeia (EP) Reference Standard