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地塞米松预防 COPD 患者急性高原病的疗效:随机试验。

Efficacy of Dexamethasone in Preventing Acute Mountain Sickness in COPD Patients: Randomized Trial.

机构信息

Department of Respiratory Medicine, University Hospital Zurich, Zurich, Switzerland; Institute of Human Movement Sciences and Sport, Swiss Federal Institute of Technology, Zurich, Switzerland; Kyrgyz-Swiss High Altitude Clinic and Medical Research Center, Tuja-Ashu, Kyrgyz Republic.

Department of Respiratory Medicine, University Hospital Zurich, Zurich, Switzerland; Kyrgyz-Swiss High Altitude Clinic and Medical Research Center, Tuja-Ashu, Kyrgyz Republic.

出版信息

Chest. 2018 Oct;154(4):788-797. doi: 10.1016/j.chest.2018.06.006. Epub 2018 Jul 10.

Abstract

BACKGROUND

Patients with COPD may experience acute mountain sickness (AMS) and other altitude-related adverse health effects (ARAHE) when traveling to high altitudes. This study evaluated whether dexamethasone, a drug used for the prevention of AMS in healthy individuals, would prevent AMS/ARAHE in patients with COPD.

METHODS

This placebo-controlled, double-blind, parallel-design trial included patients with COPD and Global Initiative for Obstructive Lung Disease grade 1 to 2 who were living below 800 m. Patients were randomized to receive dexamethasone (8 mg/d) or placebo starting on the day before ascent and while staying in a high-altitude clinic at 3,100 m for 2 days. The primary outcome assessed during the altitude sojourn was the combined incidence of AMS/ARAHE, defined as an Environmental Symptoms Questionnaire cerebral score evaluating AMS ≥ 0.7 or ARAHE requiring descent or an intervention.

RESULTS

In 60 patients randomized to receive dexamethasone (median [quartiles] age: 57 years [50; 60], FEV 86% predicted [70; 104]; PaO at 760 m: 9.6 kPa [9.2; 10.0]), the incidence of AMS/ARAHE was 22% (13 of 60). In 58 patients randomized to receive placebo (age: 60 y [53; 64]; FEV 94% predicted [76; 103]; PaO: 10.0 kPa [9.1; 10.5]), the incidence of AMS/ARAHE was 24% (14 of 58) (χ statistic vs dexamethasone, P = .749). Dexamethasone mitigated the altitude-induced PaO reduction compared with placebo (mean between-group difference [95% CI], 0.4 kPa [0.0-0.8]; P = .028).

CONCLUSIONS

In lowlanders with mild to moderate COPD, the incidence of AMS/ARAHE at 3,100 m was moderate and not reduced by dexamethasone treatment. Based on these findings, dexamethasone cannot be recommended for the prevention of AMS/ARAHE in patients with COPD undertaking high-altitude travel, although the drug mitigated the altitude-induced hypoxemia.

TRIAL REGISTRY

ClinicalTrials.gov; No.: NCT02450968; URL: www.clinicaltrials.gov.

摘要

背景

患有 COPD 的患者在前往高海拔地区时可能会经历急性高原病(AMS)和其他与海拔相关的不良健康影响(ARAHE)。本研究评估了地塞米松(一种用于预防健康个体 AMS 的药物)是否会预防 COPD 患者的 AMS/ARAHE。

方法

这项安慰剂对照、双盲、平行设计的试验纳入了居住在海拔 800 米以下的 COPD 患者和全球倡议阻塞性肺病分级 1 至 2 级的患者。患者被随机分配接受地塞米松(8mg/d)或安慰剂,在前往海拔 3100 米的高海拔诊所前一天开始服用,并在那里停留两天。在高原逗留期间评估的主要结局是 AMS/ARAHE 的综合发生率,定义为环境症状问卷脑评分评估 AMS≥0.7 或需要下降或干预的 ARAHE。

结果

在随机接受地塞米松(中位数[四分位数]年龄:57 岁[50;60],FEV 86%预测值[70;104];海拔 760 米时的 PaO :9.6kPa [9.2;10.0])的 60 名患者中,AMS/ARAHE 的发生率为 22%(60 名患者中的 13 名)。在随机接受安慰剂(年龄:60y [53;64];FEV 94%预测值[76;103];PaO:10.0kPa [9.1;10.5])的 58 名患者中,AMS/ARAHE 的发生率为 24%(58 名患者中的 14 名)(与地塞米松相比,χ 统计量,P=0.749)。与安慰剂相比,地塞米松减轻了海拔引起的 PaO 降低(组间平均差异[95%CI],0.4kPa[0.0-0.8];P=0.028)。

结论

在患有轻度至中度 COPD 的低海拔人群中,3100 米处的 AMS/ARAHE 发生率适中,用地塞米松治疗并未降低。基于这些发现,不能推荐地塞米松用于预防 COPD 患者在海拔较高地区旅行时发生 AMS/ARAHE,尽管该药物减轻了海拔引起的低氧血症。

试验注册

ClinicalTrials.gov;编号:NCT02450968;网址:www.clinicaltrials.gov。

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