首页> 外文期刊>Supportive care in cancer: official journal of the Multinational Association of Supportive Care in Cancer >How successful are we in relieving terminal dyspnea in cancer patients? A real-world multicenter prospective observational study
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How successful are we in relieving terminal dyspnea in cancer patients? A real-world multicenter prospective observational study

机译:我们在癌症患者中缓解终端呼吸困难如何成功? 一个真实的多中心前瞻性观察研究

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Purpose Parenteral morphine is widely used for dyspnea of imminently dying cancer patients, but the outcomes to expect over time remain largely unknown. We examined outcomes after the administration of parenteral morphine infusion over 48 h in cancer patients with a poor performance status. Methods This was a multicenter prospective observational study. Inclusion criteria were metastatic/locally advanced cancer, ECOG performance status = 3-4, a dyspnea intensity >= 2 on a Support Team Assessment Schedule, Japanese version (STAS-J), and receiving specialized palliative care. After initiating parenteral morphine infusion, we measured dyspnea STAS-J as well as Memorial Delirium Assessment Scale (MDAS), item 9, and Communication Capacity Scale (CCS), item 4, every 6 h over 48 h. Results We enrolled 167 patients (median survival = 4 days). The mean age was 70 years, 80 patients (48%) had lung cancer, and 109 (65%) had lung metastases. The mean STAS-J scores decreased from 3.1 (95% confidence interval (CI) = 3.0-3.2) at the baseline to 2.1 (95%CI = 1.9-2.2) at 6 h, and remained 1.6-1.8 over 12-48 h. The proportion of patients with dyspnea relief (STAS-J = 2) and an inability to communicate (CCS item 4 = 3), respectively, over 48 h. Conclusions Overall, terminal dyspnea was relatively well controlled with parenteral morphine, though a significant number of patients continued to suffer from dyspnea. Future efforts are needed to improve outcomes following standardized dyspnea treatment using patient-reported outcomes for imminently dying patients.
机译:目的肠外吗啡广泛用于令人垂死的患有癌症患者的呼吸困难,但随着时间的推移期望的结果在很大程度上是未知的。我们在癌症患者中48小时促进肠外肠外变质输注后检查结果,具有较差的表现状态。方法这是一项多中心的前瞻性观察研究。纳入标准是转移性/局部晚期癌症,ECOG性能状态= 3-4,呼吸困难强度> = 2对支持团队评估计划,日本版(STA-J),以及接受专门的姑息治疗。在启动肠外变质输注后,我们测量了呼吸困难STA-J以及纪念谵妄评估规模(MDAS),第9项和通信容量秤(CCS),项目4,每6 H超过48小时。结果我们注册了167名患者(中位数存活= 4天)。平均年龄为70岁,80名患者(48%)肺癌,109例(65%)肺转移。平均STA-J分数从3.1(95%置信区间(CI)= 3.0-3.2)在6小时的基线下降(95%置信区间(CI)= 3.0-3.2)减少,并且在12-48小时内保持1.6-1.8 。呼吸困难缓解(STA-J = 2)患者的比例分别超过48小时(CCS项4 = 3)。结论总体而言,终末呼吸困难与肠胃外尿机相对良好地控制,尽管大量患者继续患有呼吸困难。需要将来的努力改善使用患者报告的患者的患者报告的患者的标准化呼吸困难治疗后的结果。

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