Department of Emergency Medicine, Stanford University School of Medicine, Stanford, California, USA.
Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.
High Alt Med Biol. 2021 Jun;22(2):193-200. doi: 10.1089/ham.2020.0150. Epub 2021 Feb 18.
Small, Elan, Nicholas Juul, David Pomeranz, Patrick Burns, Caleb Phillips, Mary Cheffers, and Grant S. Lipman. Predictive capacity of pulmonary function tests for acute mountain sickness. . 22: 193-200, 2021. Pulmonary function as measured by spirometry has been investigated at altitude with heterogenous results, though data focused on spirometry and acute mountain sickness (AMS) are limited. The objective of this study was to investigate the capacity of pulmonary function tests (PFTs) to predict the development of AMS. This study was a blinded prospective observational study run during a randomized controlled trial comparing acetazolamide, budesonide, and placebo for AMS prevention on White Mountain, CA. Spirometry measurements of forced expiratory volume in one second (FEV), forced vital capacity (FVC), and peak expiratory flow were taken at a baseline altitude of 1,250 m, and the evening of and morning after ascent to 3,810 m. Measurements were assessed for correlation with AMS. One hundred three participants were analyzed with well-matched baseline demographics and AMS incidence of 75 (73%) and severe AMS of 48 (47%). There were no statistically significant associations between changes in mean spirometry values on ascent to high altitude with incidence of AMS or severe AMS. Lake Louise Questionnaire scores were negatively correlated with FVC ( = -0.31) and FEV ( = -0.29) the night of ascent. Baseline PFT had a predictive accuracy of 65%-73% for AMS, with a receiver operating characteristic of 0.51-0.65. Spirometry did not demonstrate statistically significant changes on ascent to high altitude, nor were there significant associations with incidence of AMS or severe AMS. Low-altitude spirometry did not accurately predict development of AMS, and it should not be recommended for risk stratification.
小,埃兰,尼古拉斯·尤尔,大卫·波默兰茨,帕特里克·伯恩斯,凯莱布·菲利普斯,玛丽·谢弗斯,和格兰特·S·利普曼。肺功能测试对急性高山病的预测能力。 22:193-200,2021 年。在高海拔地区,通过肺活量测定法测量的肺功能已经进行了研究,但结果存在差异,尽管专注于肺活量测定法和急性高山病(AMS)的数据有限。本研究的目的是研究肺功能测试(PFT)预测 AMS 发展的能力。 这项研究是在加利福尼亚州白山进行的一项随机对照试验中进行的一项盲前瞻性观察研究,该试验比较了乙酰唑胺、布地奈德和安慰剂对 AMS 的预防作用。在海拔 1250 米的基础海拔和上升到 3810 米的晚上和早上,进行了一秒钟用力呼气量(FEV)、用力肺活量(FVC)和呼气峰值流量的肺活量测定测量。对测量结果与 AMS 的相关性进行了评估。 对 103 名参与者进行了分析,他们的基线人口统计学特征匹配良好,AMS 发病率为 75(73%),严重 AMS 发病率为 48(47%)。在高海拔上升过程中平均肺活量值的变化与 AMS 或严重 AMS 的发病率之间没有统计学上的显著关联。洛矶山问卷评分与 FVC( = -0.31)和 FEV( = -0.29)在上升当晚呈负相关。基线 PFT 对 AMS 的预测准确性为 65%-73%,其接收者操作特征为 0.51-0.65。 肺活量测定法在上升到高海拔时没有显示出统计学上的显著变化,也没有与 AMS 或严重 AMS 的发病率有显著关联。低海拔肺活量测定法不能准确预测 AMS 的发生,因此不建议用于风险分层。