Costa Roser, Navarro Annie, Leal Miguel Ángel, Hernández Andrea, Esquinas Cristina, Miravitlles Marc
Pneumology Department, Althaia Xarxa Assistencial Universitària de Manresa, c/ Dr. Joan soler, 1-3, Manresa, 08243, Spain.
Institut de Recerca i Innovació en Ciències de la Vida i de la Salut a la Catalunya Central (IRIS-CC), Vic, Spain.
Sci Rep. 2025 Mar 13;15(1):8773. doi: 10.1038/s41598-025-91763-w.
To evaluate the tolerance and effectiveness of standard doses (StD) and low doses (LoD) of inhaled antibiotics (IA), in patients with chronic obstructive pulmonary disease (COPD) and chronic bronchial infection (CBI) by Pseudomonas aeruginosa (PA). Single-center, observational, retrospective, follow-up study of patients with COPD and CBI by PA treated with IA between 2012 and 2021. One year before and one after the first IA dose were analysed. 87 patients were included (86 men) with a mean FEV1(%) of 46.3%. Intolerance to IA was observed in 54 (62.1%), with a median time of 30 days (IQR: 15, 90). Only a higher FEV1(%) was associated with lower probability of intolerance (hazard ratio: 0.98, 95% confidence interval 0.97 to 0.99; p = 0.021). Seven of 15 (46.6%) patients who did not tolerate StD tolerated LoD. Those unable to tolerate LoD also had worse FEV1(%) (38.4% (SD:18.7%) versus 48.1% (SD: 16.4%); p = 0.018). Treatments lasting 6-12 months improved symptoms and reduced PA isolations (- 2.1; P < 0.001) and exacerbations (-1.7, P < 0.001). In 19 patients LoD treatment reduced exacerbations (-2.1, P = 0.003), days of hospitalization (-7.4, P = 0.036) and PA isolations (-2, P = 0.001) with clinical improvement. Antimicrobial resistance was not observed in any case receiving LoD of IA. More than half of our COPD patients treated with IA for CBI by PA presented respiratory intolerance during the first three months related to greater severity of airway obstruction. Treatment with LoD of IA appears to be an effective and safe alternative for some patients unable to tolerate StD.
为评估标准剂量(StD)和低剂量(LoD)吸入性抗生素(IA)对慢性阻塞性肺疾病(COPD)合并铜绿假单胞菌(PA)所致慢性支气管感染(CBI)患者的耐受性和有效性。对2012年至2021年间接受IA治疗的COPD合并PA所致CBI患者进行单中心、观察性、回顾性随访研究。分析首次IA剂量前一年和后一年的情况。纳入87例患者(86例男性),平均第一秒用力呼气容积(FEV1)为46.3%。54例(62.1%)患者出现IA不耐受,中位时间为30天(四分位间距:15,90)。仅较高的FEV1与较低的不耐受概率相关(风险比:0.98,95%置信区间0.97至0.99;p = 0.021)。15例不耐受StD的患者中有7例(46.6%)耐受LoD。无法耐受LoD的患者FEV1也更差(38.4%(标准差:18.7%)对48.1%(标准差:16.4%);p = 0.018)。持续6 - 12个月的治疗改善了症状,减少了PA分离(-2.1;P < 0.001)和急性加重(-1.7,P < 0.001)。在19例患者中,LoD治疗减少了急性加重(-2.1,P = 0.003)、住院天数(-7.4,P = 0.036)和PA分离(-2,P = 0.001),临床症状改善。接受IA LoD治疗的患者均未观察到耐药情况。我们接受PA所致CBI的IA治疗的COPD患者中,超过一半在最初三个月出现呼吸不耐受,这与气道阻塞更严重有关。对于一些无法耐受StD的患者,IA LoD治疗似乎是一种有效且安全的替代方法。