Faculty of Medicine, University of Basel, Basel, Switzerland
Center for Palliative Care Hildegard, Basel, Switzerland.
Heart. 2023 Jun 26;109(14):1064-1071. doi: 10.1136/heartjnl-2022-322074.
For the treatment of breathlessness in heart failure (HF), most textbooks advocate the use of opioids. Yet, meta-analyses are lacking.
A systematic review was performed for randomised controlled trials (RCTs) assessing effects of opioids on breathlessness (primary outcome) in patients with HF. Key secondary outcomes were quality of life (QoL), mortality and adverse effects. Cochrane Central Register of Controlled Trials, MEDLINE and Embase were searched in July 2021. Risk of bias (RoB) and certainty of evidence were assessed by the Cochrane RoB 2 Tool and Grading of Recommendations Assessment, Development and Evaluation criteria, respectively. The random-effects model was used as primary analysis in all meta-analyses.
After removal of duplicates, 1180 records were screened. We identified eight RCTs with 271 randomised patients. Seven RCTs could be included in the meta-analysis for the primary endpoint breathlessness with a standardised mean difference of 0.03 (95% CI -0.21 to 0.28). No study found statistically significant differences between the intervention and placebo. Several key secondary outcomes favoured placebo: risk ratio of 3.13 (95% CI 0.70 to 14.07) for nausea, 4.29 (95% CI 1.15 to 16.01) for vomiting, 4.77 (95% CI 1.98 to 11.53) for constipation and 4.42 (95% CI 0.79 to 24.87) for study withdrawal. All meta-analyses revealed low heterogeneity (I in all these meta-analyses was <8%).
Opioids for treating breathlessness in HF are questionable and may only be the very last option if other options have failed or in case of an emergency.
CRD42021252201.
对于心力衰竭(HF)所致呼吸困难的治疗,大多数教科书都主张使用阿片类药物。然而,目前缺乏荟萃分析。
对评估阿片类药物对 HF 患者呼吸困难(主要结局)影响的随机对照试验(RCT)进行系统评价。关键次要结局为生活质量(QoL)、死亡率和不良反应。2021 年 7 月在 Cochrane 中央对照试验注册库、MEDLINE 和 Embase 进行检索。使用 Cochrane RoB 2 工具评估偏倚风险(RoB),使用推荐评估、制定与评价分级标准评估证据确定性。所有荟萃分析均采用随机效应模型作为主要分析。
剔除重复后,共筛选出 1180 条记录。我们确定了 8 项 RCT,涉及 271 名随机患者。有 7 项 RCT 可纳入主要结局呼吸困难的荟萃分析,标准化均数差为 0.03(95%CI-0.21 至 0.28)。没有研究发现干预组与安慰剂组之间存在统计学差异。一些关键次要结局有利于安慰剂:恶心的风险比为 3.13(95%CI 0.70 至 14.07),呕吐为 4.29(95%CI 1.15 至 16.01),便秘为 4.77(95%CI 1.98 至 11.53),研究退出为 4.42(95%CI 0.79 至 24.87)。所有荟萃分析的异质性均较低(所有这些荟萃分析的 I 均<8%)。
阿片类药物治疗 HF 所致呼吸困难存在争议,只有在其他方法失败或紧急情况下,才可能是最后的选择。
PROSPERO 注册号:CRD42021252201。