Hull York Medical School, University of Hull, Scarborough, North Yorkshire, United Kingdom.
J Palliat Med. 2013 Mar;16(3):250-5. doi: 10.1089/jpm.2012.0270. Epub 2013 Jan 31.
The longer-term effects of opioids for breathlessness are not known in people with chronic heart failure (CHF).
Our aim was to assess the longer-term effect of oral opioids on breathlessness due to CHF.
We conducted a 3-month open-label extension to a crossover randomized controlled trial (RCT) comparing 4 days of morphine, oxycodone, and placebo. Thirty-five participants from a tertiary cardiology clinic completed the RCT. Thirty-three were followed for 3 months, continuing open-label opioids if they wished. Thirteen participants continued an opioid; 20 did not. Four measures of breathlessness intensity (0-10 numerical rating scale [NRS] and modified Borg score, each recording worst and average breathlessness during 24 hours) were combined using principal component analysis to give a single measure for the primary analysis. Groups were compared using analysis of covariance. Secondary measures included quality of life (SF-12(®) Health Survey), cardiorespiratory, and global impression of change in breathlessness at 3 months.
At 3 months, the composite breathlessness measure improved to a greater extent in the opioid group (p=0.017). The opioid group had an improvement in global impression of change (mean 2.62 [opioids] versus -0.65 [nonopioids]; p=0.0009). The SF-12 physical component improved more in the opioid group (p=0.014). Cardiorespiratory variables were unchanged.
Opioids given for 3 months were well tolerated and safe. Opioid-related improvement in breathlessness in people with CHF might not be seen until longer-term administration. We cannot conclude from these data that they are effective and a longer-term RCT is needed.
慢性心力衰竭(CHF)患者使用阿片类药物缓解呼吸困难的长期效果尚不清楚。
我们旨在评估口服阿片类药物对 CHF 所致呼吸困难的长期影响。
我们对一项交叉随机对照试验(RCT)进行了 3 个月的开放性扩展研究,该 RCT 比较了吗啡、羟考酮和安慰剂的 4 天疗程。35 名来自三级心脏病学诊所的参与者完成了 RCT。33 名参与者继续进行 3 个月的开放性标签阿片类药物治疗,如果愿意的话。13 名参与者继续使用阿片类药物;20 名参与者未继续使用。使用主成分分析将 4 种呼吸困难强度测量方法(0-10 数字评分量表[NRS]和改良 Borg 评分,分别记录 24 小时内的最差和平均呼吸困难)进行组合,得到主要分析的单一测量值。使用协方差分析比较两组。次要措施包括 3 个月时的生活质量(SF-12(®)健康调查)、心肺功能和呼吸困难改善的总体印象。
在 3 个月时,阿片类药物组的复合呼吸困难测量值有更大程度的改善(p=0.017)。阿片类药物组在呼吸困难改善的总体印象方面有改善(平均 2.62 [阿片类药物]与-0.65 [非阿片类药物];p=0.0009)。阿片类药物组的 SF-12 生理成分改善更多(p=0.014)。心肺功能变量无变化。
在 3 个月的时间内,给予阿片类药物的耐受性良好且安全。CHF 患者使用阿片类药物缓解呼吸困难的效果可能要在长期用药后才能显现。我们不能从这些数据中得出它们有效的结论,还需要进行一项更长时间的 RCT。