Effects of long-term tobramycin inhalation solution (TIS) once daily on exacerbation rate in patients with non-cystic fibrosis bronchiectasis

被引:9
作者
Terpstra, Lotte C. C. [1 ]
Altenburg, Josje [2 ]
Bronsveld, Inez [3 ]
de Kruif, Martijn D. D. [4 ]
Berk, Yvonne [5 ]
Snijders, Dominic [6 ]
Rozemeijer, Wouter [7 ]
Heijerman, Harry G. M. [3 ]
Boersma, Wim G. G. [1 ]
机构
[1] Northwest Clin, Dept Pulm Dis, Wilhelminalaan 12, NL-1815 JD Alkmaar, Netherlands
[2] Amsterdam Med Ctr, Dept Pulm Dis, Amsterdam, Netherlands
[3] Univ Utrecht, Dept Pulm Dis, Utrecht, Netherlands
[4] Zuyderland Med Ctr, Dept Pulm Dis, Heerlen, Netherlands
[5] Canisius Wilhelmina Hosp, Dept Pulm Dis, Nijmegen, Netherlands
[6] Spaarne Gasthuis, Dept Pulm Dis, Hoofddorp, Netherlands
[7] Northwest Clin, Dept Med Microbiol, Alkmaar, Netherlands
关键词
Bronchiectasis; Tobramycin inhalation solution; Exacerbations; CHRONIC BRONCHIAL INFECTION; AEROSOLIZED TOBRAMYCIN; INHALED ANTIBIOTICS; ADULT PATIENTS; DOUBLE-BLIND; EFFICACY; SAFETY; PHARMACOKINETICS; VALIDATION; QUESTIONNAIRE;
D O I
10.1186/s12931-022-02243-y
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Use of long-term tobramycin inhalation solution (TIS) has been shown beneficial in cystic fibrosis (CF) and earlier findings also suggest a benefit in non-CF bronchiectasis. We investigated the efficacy and safety of maintenance TIS once daily (OD) in frequent exacerbating bronchiectasis patients chronically infected by different pathogens sensitive for tobramycin. Objective: The primary outcome was the frequency of exacerbations during the 12-month study period. Secondary outcomes were time to first exacerbation, change in lung function and quality of life (QoL), bacterial analysis and safety. Materials/patients: In this multicenter RCT patients aged & GE; 18-year-old were included with confirmed bronchiectasis and & GE; 2 exacerbations in the preceding year. Patients were assigned (1:1) to receive TIS or placebo OD for 1-year.Results58 patients were included of which 52 were analyzed in the mITT analysis. TIS reduced exacerbation frequency with a RR of 0.74 (95% CI 0.49-1.14) (p = 0.15). Within the TIS population a decrease in number of exacerbations was found (2; p = 0.00), which was also seen in the placebo-treated patients (1.5; p = 0.00). In the TIS-treated patients the QoL improved (LRTI-VAS p = 0.02 Leicester Cough p = 0.02) without additional safety concerns. No differences were found for the other secondary outcomes. Conclusion: Long-term TIS OD is a safe treatment modality and showed a non-significant reduced exacerbation frequency of 0.74 as compared to placebo in bronchiectasis patients chronically infected by tobramycin sensitive pathogens. TIS OD may be a potential therapeutic strategy in selected patients with bronchiectasis suffering from a high burden of disease. Trail registration number: The BATTLE study was registered at Clinical trials.gov number: . Date: 13 august 2016.
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页数:11
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