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Opioids in patients with COPD and refractory dyspnea: literature review and design of a multicenter double blind study of low dosed morphine and fentanyl (MoreFoRCOPD)

机译:患有COPD和难治性呼吸困难患者的阿片类药物:文献综述和低诱剂吗啡和芬太尼的多中心双盲研究(Moreforcopd)

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Refractory dyspnea or breathlessness is a common symptom in patients with advanced chronic obstructive pulmonary disease (COPD), with a high negative impact on quality of life (QoL). Low dosed opioids have been investigated for refractory dyspnea in COPD and other life-limiting conditions, and some positive effects were demonstrated. However, upon first assessment of the literature, the quality of evidence in COPD seemed low or inconclusive, and focused mainly on morphine which may have more side effects than other opioids such as fentanyl. For the current publication we performed a systematic literature search. We searched for placebo-controlled randomized clinical trials investigating opioids for refractory dyspnea caused by COPD. We included trials reporting on dyspnea, health status and/or QoL. Three of fifteen trials demonstrated a significant positive effect of opioids on dyspnea. Only one of four trials reporting on QoL or health status, demonstrated a significant positive effect. Two-thirds of included trials investigated morphine. We found no placebo-controlled RCT on transdermal fentanyl. Subsequently, we hypothesized that both fentanyl and morphine provide a greater reduction of dyspnea than placebo, and that fentanyl has less side effects than morphine. We describe the design of a robust, multi-center, double blind, double-dummy, cross-over, randomized, placebo-controlled clinical trial with three study arms investigating transdermal fentanyl 12 mcg/h and morphine sustained-release 10?mg b.i.d. The primary endpoint is change in daily mean dyspnea sensation measured on a numeric rating scale. Secondary endpoints are change in daily worst dyspnea, QoL, anxiety, sleep quality, hypercapnia, side effects, patient preference, and continued opioid use. Sixty patients with severe stable COPD and refractory dyspnea (FEV1??50%, mMRC?≥?3, on optimal standard therapy) will be included. Evidence for opioids for refractory dyspnea in COPD is not as robust as usually appreciated. We designed a study comparing both the more commonly used opioid morphine, and transdermal fentanyl to placebo. The cross-over design will help to get a better impression of patient preferences. We believe our study design to investigate both sustained-release morphine and transdermal fentanyl for refractory dyspnea will provide valuable information for better treatment of refractory dyspnea in COPD. Trial registration NCT03834363 (ClinicalTrials.gov), registred at 7 Feb 2019, https://clinicaltrials.gov/ct2/show/NCT03834363 .
机译:难治性呼吸困难或呼吸困难是晚期慢性阻塞性肺病(COPD)患者的常见症状,对生活质量(QOL)具有高负面影响。已经研究了低剂量的阿片类药物在COPD中的难治性呼吸困难以及其他寿命条件下,并证明了一些积极影响。然而,在第一次评估文献时,COPD的证据质量似乎低或不确定,主要集中在吗啡上,这可能比其他阿片西等其他阿片类药物更副作用。对于当前发布,我们执行了系统的文献搜索。我们搜索了安慰剂控制的随机临床试验,研究由COPD引起的难治性呼吸污染物的阿片类药物。我们包括报告呼吸困难,健康状况和/或QOL的试验。十五次试验中的三种展示了阿片类药物对呼吸缺陷的显着积极作用。只有四项试验中的一个报告QOL或健康状况中的一个,表明了显着的积极效果。三分之二的含有试验调查吗啡。我们发现在透皮芬太尼上没有发现安慰剂控制的RCT。随后,我们假设芬太尼和吗啡均比安慰剂的呼吸困难减少,并且芬太尼具有比吗啡的副作用较少。我们描述了具有三个研究臂调查透皮芬太尼12mcg / h和吗啡持续的10毫克持久的安慰剂对照的安慰剂对照,安慰剂对照的安慰剂控制的临床试验的设计。主终点是在数值评级测量中测量的每日平均呼吸困难感应的变化。次要终点是每日最糟糕的呼吸困难,QOL,焦虑,睡眠质量,Hypercapnia,副作用,患者偏好以及持续的阿片类药物的变化。将包括六十患者严重稳定的COPD和难治性呼吸困难(FEV1?50%,最佳标准治疗的50%,MMRC?≥≤3)。 COPD中难治性呼吸困难的阿片类药物的证据不如通常欣赏的那样强大。我们设计了一种比较更常用的阿片类药物和透皮芬太尼来安慰剂的研究。交叉设计将有助于获得更好的患者偏好印象。我们认为,我们的研究设计探讨了持续释放的吗啡和透皮芬太尼,用于难治性呼吸困难将提供有价值的信息,以便更好地治疗COPD中的难治性呼吸困难。试验登记NCT03834363(ClinicalTrials.gov),2019年2月7日注册,https://clinicaltrials.gov/ct2/show/nct03834363。

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