Department of Pulmonary Medicine, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Department of Medical Microbiology, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Pulm Pharmacol Ther. 2023 Aug;81:102226. doi: 10.1016/j.pupt.2023.102226. Epub 2023 May 23.
Allergic bronchopulmonary aspergillosis (ABPA) is complicated by exacerbations in more than one-third of the subjects. Whether nebulized amphotericin B (NAB) therapy prevents ABPA exacerbations remains unclear.
The primary objective of this systematic review and meta-analysis was to determine the frequency of subjects remaining exacerbation-free, one year after initiating NAB. The key secondary objectives were the time to first exacerbation and the safety of NAB therapy.
We searched the PubMed and Embase databases for studies evaluating ≥5 subjects of ABPA managed with NAB. We report the pooled proportion of ABPA subjects remaining exacerbation free after one year. For the randomized controlled trials (RCTs), we estimate the pooled risk difference (RD) of exacerbation-free status at one year with NAB versus the control arm.
We included five studies for our analysis; three were observational (n = 28) and two RCTs (n = 160). The pooled proportion (95% confidence interval [CI]) of subjects remaining exacerbation free with NAB at one year was 76% (62-88). The pooled RD (95% CI) of an exacerbation-free status at one year was 0.33 (-0.12 to 0.78) and was not significantly different between the NAB and control arms. The time to first exacerbation was longer with NAB than with the standard therapy. No serious adverse events were reported with NAB.
NAB does not improve exacerbation-free status at one year; however, weak evidence suggests it delays ABPA exacerbations. More research using different dosing regimens is required.
三分之一以上的变应性支气管肺曲霉病(ABPA)患者病情会加重。目前尚不清楚雾化两性霉素 B(NAB)治疗是否能预防 ABPA 加重。
本系统评价和荟萃分析的主要目的是确定开始 NAB 治疗一年后,无加重患者的比例。主要次要目标是首次加重的时间和 NAB 治疗的安全性。
我们检索了 PubMed 和 Embase 数据库,以评估接受 NAB 治疗的 ABPA 患者≥5 例的研究。我们报告了一年后无加重的 ABPA 患者的汇总比例。对于随机对照试验(RCT),我们估计了 NAB 组与对照组在一年时无加重状态的汇总风险差(RD)。
我们纳入了五项研究进行分析;其中三项为观察性研究(n=28),两项为 RCT(n=160)。一年时 NAB 治疗无加重的患者汇总比例(95%置信区间[CI])为 76%(62%-88%)。一年时无加重状态的汇总 RD(95%CI)为 0.33(-0.12 至 0.78),NAB 组与对照组之间无显著差异。NAB 组首次加重的时间长于标准治疗组。NAB 未报告严重不良事件。
NAB 不能提高一年时的无加重状态,但有弱证据表明它可延迟 ABPA 加重。需要使用不同的剂量方案进行更多的研究。