Chest Diseases Department, Izmir Katip Celebi University, İzmir, Turkey.
Chest Diseases Department, Ufuk University, Ankara, Turkey.
Eur J Clin Pharmacol. 2024 Jun;80(6):847-853. doi: 10.1007/s00228-024-03637-1. Epub 2024 Feb 23.
Long-acting muscarinic antagonists (LAMA) or beta-2 agonists (LABA) have been recommended for symptom control in group A COPD patients as a first-line bronchodilator treatment in GOLD guidelines. However, there is no mention of priority/superiority between the two treatment options. We aimed to compare the effectiveness of these treatments in this group.
The study cohort was formed of all subjects from six pulmonology clinics with an initial diagnosis of COPD who were new users of a LAMA or LABA from January 2020 to December 2021. Seventy-six group A COPD patients, in whom LABA or LAMA therapy had been started in the last 1 month as a first-line treatment, were included in our study. Participants were evaluated with spirometry, COPD Assessment Test (CAT), mMRC scale, and St. George Respiratory Questionnaire (SGRQ) for three times (baseline, 6-12 months).
There were 76 group A COPD patients with LAMA (67.1%) and LABA (32.9%). The number of patients who improved in CAT score at the end of the first year was significantly higher in patients using LAMA than those using LABA (p = 0.022); the improvement at minimum clinically important difference (MCID) in CAT score of LAMA group at 1 year was also significant (p = 0.044). SGRQ total and impact scores were found to be statistically lower at 1 year compared to baseline in patients using LAMA (p = 0.010 and 0.006, respectively). Significant improvement was detected in CAT and SGRQ scores at the 6 month visit in the LAMA group having emphysema (p = 0.032 and 0.002, respectively).
According to significant improvements in CAT and SGRQ score, LAMA may be preferred over LABA as a bronchodilator agent in group A COPD patients, especially in emphysema-dominant phenotype.
长效抗毒蕈碱药物(LAMA)或β2 受体激动剂(LABA)已被推荐用于 A 组 COPD 患者的症状控制,作为 GOLD 指南中一线支气管扩张剂治疗。然而,两种治疗方案之间并没有提到优先级/优越性。我们旨在比较这两种治疗方法在该组患者中的效果。
研究队列由 2020 年 1 月至 2021 年 12 月期间六家肺病诊所首次诊断为 COPD 的新使用 LAMA 或 LABA 的所有患者组成。我们的研究纳入了 76 名 A 组 COPD 患者,他们在过去 1 个月内开始接受 LABA 或 LAMA 作为一线治疗。通过肺量测定、COPD 评估测试(CAT)、mMRC 量表和圣乔治呼吸问卷(SGRQ)对参与者进行了三次评估(基线、6-12 个月)。
有 76 名 A 组 COPD 患者使用 LAMA(67.1%)和 LABA(32.9%)。在使用 LAMA 的患者中,CAT 评分在第一年结束时改善的患者数量明显多于使用 LABA 的患者(p=0.022);LAMA 组在 CAT 评分的最小临床重要差异(MCID)方面的改善也具有统计学意义(p=0.044)。与基线相比,在使用 LAMA 的患者中,SGRQ 总分和影响评分在第一年均显著降低(p=0.010 和 0.006)。在 LAMA 组的肺气肿患者中,在第 6 个月时 CAT 和 SGRQ 评分均有显著改善(p=0.032 和 0.002)。
根据 CAT 和 SGRQ 评分的显著改善,LAMA 可能优于 LABA,作为 A 组 COPD 患者的支气管扩张剂,特别是在肺气肿为主的表型中。