Zhongshan Hospital, Fudan University, Shanghai, China.
Central Hospital of Minghang District, Shanghai, China.
Respir Med. 2021 Jun;182:106382. doi: 10.1016/j.rmed.2021.106382. Epub 2021 Mar 30.
The present study compared the effectiveness of asthma control test (ACT)-guided treatment vs. usual care (UC) in patients with asthma from China.
This prospective, phase IV, multicenter, cluster-randomized, open-label 24-week study was conducted in China; patients were randomized to either ACT-guided treatment or UC group. The patients recorded peak expiratory flow, symptoms, and medication in a diary card every day and completed ACT at every clinic visit. For the UC group, patients completed ACT after the physician's treatment decision.
In total, 83.6% patients (n = 443/530; ACT: n = 209, UC: n = 234) completed the study. A significantly higher proportion of patients (adjusted OR [95% CI]: 7.87 (1.29, 48.11; p = 0.027) responded to the treatment and had ACT total score ≥20 or demonstrated an improvement of >3 points in ACT total score in ≥1 post-baseline assessment in the ACT-guided treatment vs. UC group. A higher proportion of patients had an ACT total score ≥20 and an improvement of >3 points in ACT total score at Week 24 in the ACT-guided treatment vs. the UC group (adjusted OR (95% CI):2.28 (1.07, 4.85; p = 0.036). A significant difference (p = 0.005) in change from baseline in ACT total score was observed in ACT-guided treatment vs. UC group at Week 24. The mean annual exacerbation rate was similar in both the groups.
ACT-guided treatment was more effective in achieving ACT total score ≥20 or showing an improvement of >3 points in the ACT total score and well tolerated compared with UC treatment in the 24-week treatment period.
Clinical trials.gov Identifier: NCT02868281, https://clinicaltrials.gov/; GlaxoSmithKline study ID: 201097, https://www.gsk-studyregister.com/.
本研究比较了哮喘控制测试(ACT)指导治疗与常规护理(UC)在中国哮喘患者中的疗效。
这是一项在中国进行的前瞻性、四期、多中心、集群随机、开放性标签、24 周研究;患者被随机分为 ACT 指导治疗组或 UC 组。患者每天在日记卡上记录呼气峰流速、症状和药物使用情况,并在每次就诊时完成 ACT。对于 UC 组,患者在医生治疗决策后完成 ACT。
共有 83.6%的患者(n=443/530;ACT:n=209,UC:n=234)完成了研究。与 UC 组相比,接受 ACT 指导治疗的患者中,有更高比例的患者(调整后的比值比[95%置信区间]:7.87(1.29,48.11;p=0.027)对治疗有反应,且在至少一次基线后评估中 ACT 总分≥20 分或 ACT 总分至少提高 3 分;在 ACT 指导治疗组中,有更高比例的患者在第 24 周时 ACT 总分≥20 分,且 ACT 总分至少提高 3 分(调整后的比值比[95%置信区间]:2.28(1.07,4.85;p=0.036)。与 UC 组相比,ACT 指导治疗组在第 24 周时 ACT 总分从基线的变化差异具有统计学意义(p=0.005)。两组的年平均恶化率相似。
与 UC 治疗相比,在 24 周的治疗期间,ACT 指导治疗在实现 ACT 总分≥20 分或 ACT 总分至少提高 3 分方面更有效,且耐受性良好。
ClinicalTrials.gov 标识符:NCT02868281,https://clinicaltrials.gov/;葛兰素史克研究 ID:201097,https://www.gsk-studyregister.com/。