支气管热成形术治疗伴有严重阻塞性呼吸功能障碍的难治性哮喘的安全性和有效性。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Takahiro Inoue, Sumito Isogai, Naoki Yamamoto, Noriko Hiramatsu, Yoshikazu Niwa, Hideaki Takahashi, Yutaro Kimura, Tomoya Horiguchi, Yasuhiro Goto, Naozumi Hashimoto, Kazuyoshi Imaizumi
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引用次数: 0

摘要

背景:支气管热成形术(BT)是最近开发的一种治疗难治性支气管哮喘的非药物疗法。尽管越来越多的证据表明 BT 对各种表型的重症哮喘有效,但其对肺功能严重受损且不可逆转的患者的安全性和有效性尚不明确:评估 BT 对难治性哮喘患者(包括 1 秒用力呼气容积(FEV1)严重受损的患者)的疗效和安全性:这是一项单中心、回顾性、观察性队列研究:我们回顾性审查了 15 名难治性哮喘患者(哮喘全球倡议 4 级或 5 级)的病历,其中包括气流受限严重受损的患者(支气管扩张剂前 FEV1 预测值%):6 名患者为 G1,9 名患者为 G2。两组患者的临床特征、T2 炎症和同时接受的治疗相同。BT 能明显改善两组患者的哮喘相关症状(使用哮喘控制测试和哮喘生活质量问卷评分)。G1 组的 FEV1 有明显改善,但 G2 组没有。在 BT 治疗后,G2 组有四名患者出现了哮喘加重,需要额外使用全身皮质类固醇(其中两名患者需要长期住院治疗),而 G1 组则没有。在 G1 和 G2 中发现了对 BT 有长期反应的患者(在随访 2 年以上的时间里减少了全身或吸入皮质类固醇用量,但没有新增生物制剂的患者)(分别为 2 人,33.3% 和 4 人,44.4%):结论:对难治性哮喘和重度气流受限患者进行 BT 治疗与对中度气流受限患者进行 BT 治疗同样安全有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Safety and efficacy of bronchial thermoplasty in refractory asthma with severe obstructive respiratory dysfunction.

Background: Bronchial thermoplasty (BT) is a recently developed non-pharmacological therapy for refractory bronchial asthma. Although increasing evidence has suggested that BT is effective for various phenotypes of severe asthma, its safety and efficacy in patients with severe irreversible impaired lung function are unclear.

Objectives: To assess the efficacy and safety of BT in patients with refractory asthma, including patients with a severely impaired forced expiratory volume in 1 second (FEV1).

Design: This was a single-center, retrospective, observational cohort study.

Methods: We retrospectively reviewed the medical records of 15 patients with refractory asthma (Global Initiative for Asthma step 4 or 5), including patients with severely impaired airflow limitation (% predicted pre-bronchodilator FEV1 <60%), who had undergone BT between June 2016 and January 2022. We analyzed the efficacy (change in asthma symptoms, exacerbation rate, pulmonary function, asthma medication, and serum inflammatory chemokine/cytokines before and after BT) and complications in all patients. We compared these data between patients with severe obstructive lung dysfunction [group 1(G1)] and patients with FEV1 ⩾ 60% [group 2 (G2)].

Results: Six patients were in G1 and nine were in G2. Clinical characteristics, T2 inflammation, and concurrent treatment were equivalent in both groups. BT significantly improved asthma-related symptoms (measured using the Asthma Control Test and Asthma Quality of Life Questionnaire scores) in both groups. FEV1 was significantly improved in G1 but not in G2. Four patients in G2, but none in G1, experienced asthma exacerbation requiring additional systemic corticosteroids (including two requiring prolonged hospitalization) after BT. Long-term responders (patients who reduced systemic or inhaled corticosteroid without newly adding biologics in a follow-up > 2 years) of BT were identified in G1 and G2 (n = 2, 33.3% and n = 4, 44.4%, respectively).

Conclusion: BT in patients with refractory asthma and severe airflow limitation is equally safe and efficacious as that in patients with moderate airflow limitation.

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CiteScore
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