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首页> 外文期刊>Supportive care in cancer: official journal of the Multinational Association of Supportive Care in Cancer >Prospective, double-blind, randomized trial of equimolar mixture of nitrous oxide/oxygen to prevent pain induced by insertion of venous access ports in cancer patients.
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Prospective, double-blind, randomized trial of equimolar mixture of nitrous oxide/oxygen to prevent pain induced by insertion of venous access ports in cancer patients.

机译:一氧化二氮/氧气等摩尔混合物预防癌症患者因静脉通路插入而引起的疼痛的前瞻性,双盲,随机试验。

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BACKGROUND: To assess the efficacy of equimolar mixture of nitrous oxide/oxygen (EMNO) to prevent pain induced by venous access ports (VAPs) implantation in cancer patients. PATIENTS AND METHODS: In a randomized, double-blind study on an adult population not knowing the effects of EMNO, cancer patients were randomly assigned to breath via a facial mask, EMNO or a placebo mixture comprising 50% oxygen and 50% nitrogen. The primary end-point was the patients' assessment of the severity of pain evaluated using a visual analog scale (VAS, 0 to 100) and the proportion of patients suffering pain in each group. The secondary criteria were side effects, tolerability of EMNO, and the level of satisfaction of both the patients and the medical team. RESULTS: Eighty-three adults (42 in the EMNO group and 41 in the placebo group) were included. VAPs were implanted in the jugular vein in 95% of patients. In the placebo group, 78% of the patients declared that they found VAP implantation painful vs. 34% in the EMNO group (p=0.001). The severity of the pain was reduced by 50% in the EMNO group in comparison with placebo (p=0.0125). Although the median time to perform implantation was strictly identical in both groups (20 min), the estimated duration of surgery seemed longer to patients in the control group. Patient and investigator satisfaction indexes were >90% in both groups. CONCLUSION: EMNO provides an effective solution for the prevention of pain during placement of VAPs.
机译:背景:为了评估等摩尔的一氧化二氮/氧气混合物(EMNO)预防癌症患者因静脉通路(VAP)植入引起的疼痛的功效。患者和方法:在一项针对不知道EMNO影响的成人人群的随机双盲研究中,癌症患者被随机分配通过面罩,EMNO或含50%氧和50%氮的安慰剂混合物进行呼吸。主要终点是使用视觉模拟量表(VAS,0至100)对患者对疼痛严重程度的评估以及每组中疼痛患者的比例。次要标准是副作用,EMNO的耐受性以及患者和医疗团队的满意度。结果:包括八十三名成人(EMNO组为42名,安慰剂组为41名)。 95%的患者将VAP植入颈静脉。在安慰剂组中,有78%的患者宣称他们发现VAP植入感到痛苦,而在EMNO组中,这一比例为34%(p = 0.001)。与安慰剂相比,EMNO组的疼痛严重程度降低了50%(p = 0.0125)。尽管两组的中位植入时间完全相同(20分钟),但对照组的估计手术时间似乎更长。两组患者和研究者的满意度指数均> 90%。结论:EMNO为预防VAP放置期间的疼痛提供了有效的解决方案。

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