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Effects of ibuprofen on sleep quality as measured using polysomnography and subjective measures in healthy adults.

机译:使用多导睡眠图和主观措施对健康成年人的布洛芬对睡眠质量的影响。

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BACKGROUND: Although some literature has suggested that NSAIDs may affect sleep physiology, this observation is not consistent with clinical use of these drugs and has not been verified using standard sleep-research methodologies. OBJECTIVE: This study was undertaken to determine whether ibuprofen 400 mg administered at 3, 7, and 11 pm (total daily dose, 1200 mg) produced any significant alterations in the character and quality of night-time sleep as measured by standard sleep laboratory polysomnography (PSG) and subjective measures. METHODS: This 4-day, multiple-dose, double-blind, randomized, placebo-controlled trial was conducted in a hospital-based, sleep laboratory in the United States (DENT Neurological Institute at Millard Fillmore Hospital, Buffalo, New York). Healthy subjects aged > or = 18 years spent 3 consecutive nights in a sleep laboratory. Day 1ight 1 was for acclimation; day 2ight 2, for baseline PSG and subjective sleep assessments; and day 3ight 3, for treatment effects on sleepcharacter and quality. All subjects received placebo on days 1 and 2. On day 3, subjects received ibuprofen 400 mg or placebo TID. RESULTS: All 30 subjects (15 per group) completed the study (18 men, 12 women; all white). The mean age (SD) was 28.6 years and mean body weight was 71.4 kg. In both groups, mean values for sleep efficiency and quality of sleep were significantly higher on night 3 compared with baseline; the mean (SD) changes from baseline were not significantly different between the ibuprofen and control groups (sleep efficiency, 0.4 [6.3] and 0.3 [6.2]; quality of sleep, 8.6 [26.8] and 3.3 [21.3]). Mean night-3 sleep efficiency in the ibuprofen group was 88.6%--substantially higher than the minimally acceptable sleep efficiency of 75% stated in the protocol. Three mild adverse events were reported in 2 subjects. CONCLUSION: This study found that in these subjects a total daily dose of 1200 mg ibuprofen did not produce any clinically or statistically significant alterations in the character and quality of nighttime sleep as measured using standard sleep laboratory PSF and subjective measures.
机译:背景:尽管一些文献表明,非甾体抗炎药可能会影响睡眠生理,但这一观察结果与这些药物的临床使用不一致,并且尚未使用标准的睡眠研究方法进行验证。目的:进行这项研究是为了确定布洛芬400 mg在下午3点,7点和11点(每日总剂量1200 mg)在夜间睡眠的特征和质量方面是否产生了任何显着变化,如通过标准睡眠实验室多导睡眠监测仪所测量的(PSG)和主观措施。方法:这项为期4天,多剂量,双盲,随机,安慰剂对照的试验在美国一家医院的睡眠实验室(纽约州布法罗市Millard Fillmore医院的DENT神经病学研究所)进行。年龄大于或等于18岁的健康受试者在睡眠实验室连续住了3个晚上。第1天/第1天是适应环境;第2天/晚上2,用于基线PSG和主观睡眠评估;第3天/第3晚,以治疗对睡眠特征和质量的影响。所有受试者在第1天和第2天接受安慰剂。在第3天,受试者接受布洛芬400 mg或安慰剂TID。结果:所有30名受试者(每组15名)完成了研究(男18名,女12名;全白人)。平均年龄(SD)为28.6岁,平均体重为71.4 kg。两组中,第3晚的睡眠效率和睡眠质量的平均值均比基线高。布洛芬组和对照组之间的平均(SD)变化与基线无显着差异(睡眠效率分别为0.4 [6.3]和0.3 [6.2];睡眠质量分别为8.6 [26.8]和3.3 [21.3])。布洛芬组的平均Night-3睡眠效率为88.6%-大大高于协议中规定的最低可接受的75%的睡眠效率。在2名受试者中报告了3次轻度不良事件。结论:这项研究发现,在这些受试者中,每日总剂量1200 mg布洛芬在使用标准睡眠实验室PSF和主观测量方法测得的夜间睡眠特征和质量上没有产生任何临床或统计学上的显着变化。

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