Suppr超能文献

吸入式甲氧氟烷用于老年急性创伤疼痛患者的疗效、实用性及安全性:一项随机、对照、多中心、开放标签试验(MEDITA)的亚组分析

Efficacy, Practicality, and Safety of Inhaled Methoxyflurane in Elderly Patients with Acute Trauma Pain: Subgroup Analysis of a Randomized, Controlled, Multicenter, Open-Label Trial (MEDITA).

作者信息

Serra Sossio, Voza Antonio, Ruggiano Germana, Fabbri Andrea, Bonafede Elisabetta, Sblendido Antonella, Soldi Amedeo, Farina Alberto

机构信息

Emergency Department, Maurizio Bufalini Hospital, Cesena, Italy.

Emergency Department, IRCCS Humanitas Research Teaching Hospital, Rozzano, Milan, Italy.

出版信息

J Pain Res. 2020 Jul 16;13:1777-1784. doi: 10.2147/JPR.S255532. eCollection 2020.

Abstract

PURPOSE

Acute trauma pain management in the elderly population is a challenge. Inhaled methoxyflurane represents a promising treatment option; however, data in the elderly population are limited.

PATIENTS AND METHODS

Subgroup, post hoc analysis including 69 patients aged ≥65 years from a randomized, active-controlled, open-label study in the emergency setting. Key inclusion criterion was moderate-to-severe pain (Numerical Rating Scale [NRS] score ≥ 4]) secondary to trauma in a single limb. Patients received inhaled methoxyflurane (3 mL) or standard analgesic treatment (SAT; IV paracetamol 1 g or ketoprofen 100 mg for moderate pain [NRS 4-6] and IV morphine 0.1mg/kg for severe pain [NRS ≥7]). The primary endpoint was the overall change in visual analog scale (VAS) pain intensity from randomization to the next 3, 5, and 10 min. Secondary endpoints included time to onset of pain relief (TOPR), efficacy up to 30 min, judgment of operators and patients, and safety.

RESULTS

Pain reduction over time was similar in both groups. Median TOPR was shorter for methoxyflurane (9 min; 95% CI: 7.8, 10.2 min) than SAT (15 min; 95% CI: 10.2, 19.8 min). In terms of treatment satisfaction, patients and operators rated treatment efficacy and practicality, respectively, as "Excellent" or "Very good" 5.7 times and 3.4 times more frequently than SAT. A similar rate of adverse events (methoxyflurane: 6 events; SAT: 7 events) was recorded, all non-serious. No clinically significant changes in vital signs parameters were observed, and methoxyflurane did not result in cases of bradycardia or hypotension.

CONCLUSION

In elderly patients with trauma pain, inhaled methoxyflurane shows similar pain relief and safety compared to SAT, offering advantages in terms of onset of effect and user's satisfaction. Although this analysis presents some methodological limitations, it provides the first specific evidence of the use of inhaled methoxyflurane in the elderly population.

TRIAL REGISTRATION

EudraCT number: 2017-001565-25; Clinicaltrials.gov identifier NCT03585374.

摘要

目的

老年人群急性创伤疼痛管理是一项挑战。吸入用甲氟烷是一种有前景的治疗选择;然而,老年人群的数据有限。

患者与方法

进行亚组事后分析,纳入来自一项急诊环境下随机、活性对照、开放标签研究的69例年龄≥65岁的患者。关键纳入标准为单肢创伤继发的中重度疼痛(数字评定量表[NRS]评分≥4)。患者接受吸入用甲氟烷(3 mL)或标准镇痛治疗(SAT;中度疼痛[NRS 4 - 6]时静脉注射对乙酰氨基酚1 g或酮洛芬100 mg,重度疼痛[NRS≥7]时静脉注射吗啡0.1mg/kg)。主要终点是从随机分组至接下来3、5和10分钟时视觉模拟量表(VAS)疼痛强度的总体变化。次要终点包括疼痛缓解起效时间(TOPR)、30分钟内的疗效、操作者和患者的评价以及安全性。

结果

两组随时间的疼痛减轻情况相似。甲氟烷组的中位TOPR(9分钟;95%CI:7.8,10.2分钟)短于SAT组(15分钟;95%CI:10.2,19.8分钟)。在治疗满意度方面,患者和操作者将治疗效果和实用性评为“优秀”或“非常好”的频率分别是SAT组 的5.7倍和3.4倍。记录到的不良事件发生率相似(甲氟烷组:6例;SAT组:7例),均不严重。未观察到生命体征参数有临床显著变化,且甲氟烷未导致心动过缓或低血压病例。

结论

在老年创伤疼痛患者中,吸入用甲氟烷与SAT相比显示出相似的疼痛缓解效果和安全性,在起效时间和用户满意度方面具有优势。尽管该分析存在一些方法学局限性,但它提供了吸入用甲氟烷在老年人群中应用的首个具体证据。

试验注册

欧洲临床试验数据库编号:2017 - 001565 - 25;Clinicaltrials.gov标识符NCT03585374。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验