Department of Respiratory Medicine, Terveystalo Hospital, Aninkaistenkatu 13, Turku, Finland.
Am J Respir Crit Care Med. 2010 May 15;181(10):1042-8. doi: 10.1164/rccm.200910-1537OC. Epub 2010 Jan 28.
Gastroesophageal reflux disease (GERD) is common among patients with asthma; however, studies investigating the effect of proton pump inhibitors on asthma outcomes report conflicting results.
To investigate the effect of esomeprazole 40 mg once or twice daily on asthma outcomes in patients with concomitant symptoms of GERD.
This 26-week, randomized, double-blind, placebo-controlled study (NCT00317044) included adult patients (18-70 yr) with moderate-to-severe asthma and symptomatic GERD. The change in morning peak expiratory flow (primary variable), evening peak expiratory flow, FEV(1), asthma symptoms, Asthma Quality of Life Questionnaire, Reflux Disease Questionnaire, and tolerability were assessed.
A total of 961 patients were randomized and 828 completed the study. Relative to baseline, improvement in morning peak expiratory flow was observed for both esomeprazole 40 mg once daily (+3.5 L/min; 95% CI, -3.2 to 10.2) and 40 mg twice daily (+5.5 L/min; 95% CI, -1.2 to 12.2), although no statistically significant between-treatment differences were apparent. At treatment end, both doses of esomeprazole significantly improved FEV(1) versus placebo (+0.09 L and +0.12 L; P = 0.0039 and P < 0.0001, respectively). However, only esomeprazole 40 mg twice daily demonstrated a significant improvement when FEV(1) was calculated over the entire 26-week period (+0.07 L; P = 0.0042). Significant improvements in Asthma Quality of Life Questionnaire total score were demonstrated for both esomeprazole doses compared with placebo (+0.28 and +0.41; P = 0.0006 and P < 0.0001, respectively).
Esomeprazole may improve pulmonary function and asthma-related quality of life. However, the improvements were minor and of small clinical significance.
胃食管反流病(GERD)在哮喘患者中较为常见;然而,研究质子泵抑制剂对哮喘结果的影响的报告结果相互矛盾。
研究每日一次或两次口服埃索美拉唑 40mg 对伴有 GERD 症状的哮喘患者的哮喘结局的影响。
这是一项为期 26 周的随机、双盲、安慰剂对照研究(NCT00317044),纳入了中重度哮喘且伴有 GERD 症状的成年患者(18-70 岁)。主要变量是晨峰值呼气流速(PEF)的变化,还评估了夜间 PEF、FEV1、哮喘症状、哮喘生活质量问卷、反流疾病问卷和耐受性。
共有 961 例患者被随机分组,828 例完成了研究。与基线相比,埃索美拉唑 40mg 每日一次(+3.5L/min;95%CI,-3.2 至 10.2)和每日两次(+5.5L/min;95%CI,-1.2 至 12.2)治疗均观察到晨峰值呼气流速改善,但治疗间差异无统计学意义。治疗结束时,与安慰剂相比,埃索美拉唑两个剂量均显著改善 FEV1(+0.09L 和 +0.12L;P=0.0039 和 P<0.0001)。然而,仅埃索美拉唑 40mg 每日两次治疗时整个 26 周期间 FEV1 改善具有统计学意义(+0.07L;P=0.0042)。与安慰剂相比,埃索美拉唑两个剂量均显著改善哮喘生活质量问卷总分(+0.28 和 +0.41;P=0.0006 和 P<0.0001)。
埃索美拉唑可能改善肺功能和哮喘相关生活质量。然而,改善程度较小,临床意义不大。