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预防性芬太尼口颊片对发作性运动性呼吸困难的影响:一项先导性双盲随机对照试验。

Effect of Prophylactic Fentanyl Buccal Tablet on Episodic Exertional Dyspnea: A Pilot Double-Blind Randomized Controlled Trial.

机构信息

Department of Palliative Care, Rehabilitation and Integrative Medicine, MD Anderson Cancer Center, Houston, Texas, USA.

Department of Palliative Care, Rehabilitation and Integrative Medicine, MD Anderson Cancer Center, Houston, Texas, USA.

出版信息

J Pain Symptom Manage. 2017 Dec;54(6):798-805. doi: 10.1016/j.jpainsymman.2017.08.001. Epub 2017 Aug 10.

Abstract

CONTEXT

Episodic dyspnea is one of the most common, debilitating, and difficult-to-treat symptoms.

OBJECTIVE

We conducted a pilot study to examine the effect of prophylactic fentanyl buccal tablet (FBT) on exercise-induced dyspnea.

METHODS

In this parallel, double-blind randomized placebo-controlled trial, opioid-tolerant patients were asked to complete a six-minute walk test (6MWT) at baseline and then a second 6MWT 30 minutes after a single dose of FBT (equivalent to 20-50% of their total opioid dose) or matching placebo. We compared dyspnea Numeric Rating Scale (NRS, 0-10, primary outcome), walk distance, vital signs, neurocognitive function, and adverse events between the two 6MWTs.

RESULTS

Among 22 patients enrolled, 20 (91%) completed the study. FBT was associated with a significant within-arm reduction in dyspnea NRS between 0 and six minutes (mean change -2.4, 95% CI -3.5, -1.3) and respiratory rate (mean change -2.6, 95% CI -4.7, -0.4). Placebo was also associated with a nonstatistically significant decrease in dyspnea (mean change -1.1). Between-arm comparison of dyspnea scores in the second 6MWT favored FBT, albeit not statistically significant (estimate -0.25, P = 0.068). Global impression revealed more patients in the FBT group than placebo group reporting their dyspnea was at least "somewhat better" in the second 6MWT (4 of 9 vs. 0 of 11, P = 0.03). The other secondary outcomes did not differ significantly between arms.

CONCLUSIONS

This study supports that prophylactic FBT was associated with a reduction of exertional dyspnea and was well tolerated. Our findings support the need for larger trials to confirm the therapeutic potential of rapid-onset opioids.

摘要

背景

发作性呼吸困难是最常见、最使人虚弱和最难治疗的症状之一。

目的

我们进行了一项试点研究,以检验预防性丁丙诺啡颊片剂(FBT)对运动诱发的呼吸困难的影响。

方法

在这项平行、双盲、随机安慰剂对照试验中,阿片类药物耐受患者在基线时完成了 6 分钟步行测试(6MWT),然后在单次给予 FBT(相当于其总阿片类药物剂量的 20-50%)或匹配安慰剂后 30 分钟进行第二次 6MWT。我们比较了两次 6MWT 之间呼吸困难数字评定量表(NRS,0-10,主要结局)、步行距离、生命体征、神经认知功能和不良事件。

结果

在纳入的 22 名患者中,有 20 名(91%)完成了研究。FBT 与 0 至 6 分钟时呼吸困难 NRS 显著降低(平均变化-2.4,95%CI-3.5,-1.3)和呼吸频率(平均变化-2.6,95%CI-4.7,-0.4)相关。安慰剂也与呼吸困难的非统计学上显著降低相关(平均变化-1.1)。第二次 6MWT 时,两组之间的呼吸困难评分比较有利于 FBT,但无统计学意义(估计值-0.25,P=0.068)。总体印象显示,在第二次 6MWT 中,FBT 组比安慰剂组报告呼吸困难至少“有所改善”的患者更多(9 例中有 4 例,11 例中有 0 例,P=0.03)。其他次要结局在两组之间无显著差异。

结论

本研究支持预防性 FBT 与运动性呼吸困难的减轻有关,且耐受性良好。我们的研究结果支持需要更大规模的试验来确认快速起效阿片类药物的治疗潜力。

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