论文已发表
注册即可获取德孚的最新动态
IF 收录期刊
Authors Gottlieb IJ, Tunick DR, Mack RJ, McCallum SW, Howard CP, Freyer A, Du W
Received 31 August 2017
Accepted for publication 10 November 2017
Published 16 February 2018 Volume 2018:11 Pages 383—393
DOI https://doi.org/10.2147/JPR.S149879
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Minal Joshi
Peer reviewer comments 2
Editor who approved publication: Dr Katherine Hanlon
Objective: This randomized, double-blind, placebo-controlled study evaluated
the safety and efficacy of an intravenous (IV) nanocrystal formulation of
meloxicam in subjects with moderate-to-severe pain following a standardized
unilateral bunionectomy.
Methods: Fifty-nine subjects aged 18–72 years were
randomized to receive doses of either 30 mg (n=20) or 60 mg (n=20) meloxicam IV
or placebo (n=19), administered once daily as bolus IV injections over 15–30
seconds (two or three doses). Safety, the primary objective, was assessed by physical
examination, clinical laboratory tests, and the incidence of adverse events
(AEs). Efficacy was evaluated by examining summed pain intensity differences
over the first 48 hours (SPID48) using analysis
of covariance models. Use of opioid rescue analgesic agents was evaluated.
Results: Generally, AEs were mild-to-moderate in
intensity, and their incidence was similar across the three treatment groups.
No serious AEs were reported; there were no withdrawals due to AEs, including
injection-related AEs. The estimated effect size for SPID48 versus placebo was 1.15 and 1.01 for
meloxicam IV doses 30 mg and 60 mg, respectively (P ≤0.01).
Both doses produced significantly greater pain reductions versus placebo (P ≤0.05) at all evaluated
times/intervals during the 48-hour period. The proportions of subjects with
≥30% and ≥50% overall reduction in pain from baseline after 6 and 24 hours were
significantly higher with meloxicam IV 30 mg doses versus placebo, but not with
meloxicam IV 60 mg doses. The time to first use of rescue medication was
significantly longer versus placebo with meloxicam IV 60 mg (P <0.05), but not with meloxicam
IV 30 mg doses.
Conclusion: Meloxicam IV was generally safe and well
tolerated in subjects with moderate-to-severe post-bunionectomy pain.
Once-daily administration of meloxicam IV 30 mg and 60 mg exhibited rapid onset
of analgesia (as early as 15 minutes) with maintenance of analgesic effect for
two consecutive 24-hour periods.
Keywords: bunionectomy,
postoperative pain, meloxicam IV, COX-2 inhibitor, safety, efficacy
摘要视频链接:Intravenous meloxicam for
post-bunionectomy pain