van Patot Martha C Tissot, Leadbetter Guy, Keyes Linda E, Maakestad Kirsten M, Olson Sheryl, Hackett Peter H
Department of Anesthesiology, University of Colorado Denver, Aurora, Colorado 80045, USA.
High Alt Med Biol. 2008 Winter;9(4):289-93. doi: 10.1089/ham.2008.1029.
Previous studies have shown low-dose acetazolamide to be effective in preventing AMS in persons already at high altitude and then moving higher, a relatively low risk situation. We wished to evaluate prophylactic administration of low-dose acetazolamide for reducing the incidence and severity of AMS in a high-risk setting: rapid ascent from 1600 to 4300 m. We performed a double-blind, randomized, placebo-controlled study with human subjects (n=44) exposed to 4300 m for 24 h. Subjects were treated for 3 days prior to ascent to 4300 m and during day 1 at altitude with placebo (n=22) or acetazolamide 250 mg/day (125 mg bid, n=22). AMS diagnosis required both an AMS-C score from the Environmental Symptom Questionnaire-III>or=0.7 and a Lake Louise Symptom (LLS) questionnaire score>or=3 plus headache. Acetazolamide reduced the incidence of AMS compared to placebo-treated subjects (14% vs. 45%, respectively, p=0.02), and the number needed to treat was 3. The AMS-C and LLS scores were lower in acetazolamide-treated subjects, indicating less severe AMS. Low-dose acetazolamide administered prior to ascent and on day 1 at 4300 m effectively reduced the incidence and severity of AMS in a high-risk setting.
先前的研究表明,低剂量乙酰唑胺对预防已身处高海拔地区并继续向更高海拔行进人群的急性高山病有效,这是一种风险相对较低的情况。我们希望评估在高风险环境下预防性给予低剂量乙酰唑胺对降低急性高山病的发病率和严重程度的效果:即从1600米快速上升至4300米。我们对暴露于4300米环境24小时的44名人类受试者进行了一项双盲、随机、安慰剂对照研究。受试者在上升至4300米之前3天以及在海拔4300米处的第1天接受安慰剂(n = 22)或乙酰唑胺250毫克/天(125毫克,每日两次,n = 22)治疗。急性高山病的诊断要求环境症状问卷-III的急性高山病-中枢神经系统(AMS-C)评分≥0.7且路易斯湖症状(LLS)问卷评分≥3并伴有头痛。与接受安慰剂治疗的受试者相比,乙酰唑胺降低了急性高山病的发病率(分别为14%和45%,p = 0.02),治疗所需人数为3。接受乙酰唑胺治疗的受试者的AMS-C和LLS评分较低,表明急性高山病的严重程度较低。在上升前和在4300米处的第1天给予低剂量乙酰唑胺可有效降低高风险环境下急性高山病的发病率和严重程度。