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吸入妥布霉素用于患有支气管扩张症且伴有铜绿假单胞菌慢性支气管感染的非囊性纤维化患者。

Inhaled tobramycin in non-cystic fibrosis patients with bronchiectasis and chronic bronchial infection with Pseudomonas aeruginosa.

作者信息

Drobnic M Estrella, Suñé Pilar, Montoro J Bruno, Ferrer Adelaida, Orriols Ramon

机构信息

Pneumology Service, Department of Medicine, Hospital Vall d'Hebron, Universitat Autonoma de Barcelona, Barcelona, Spain.

出版信息

Ann Pharmacother. 2005 Jan;39(1):39-44. doi: 10.1345/aph.1E099. Epub 2004 Nov 23.

Abstract

BACKGROUND

Non-cystic fibrosis (CF) patients with bronchiectasis usually develop chronic bronchial infection with Pseudomonas aeruginosa (PA) that is related to worsening lung function and increased morbidity and mortality.

OBJECTIVE

To determine whether direct aerosol delivery of tobramycin to the lower airways may control infection and produce only low systemic toxicity.

METHODS

A double-blind, placebo-controlled crossover trial involving 30 patients was conducted to determine the clinical effectiveness and safety of 6-month tobramycin inhalation therapy. Patients received 300 mg of aerosolized tobramycin or placebo twice daily in 2 cycles, each for 6 months, with a one-month washout period. The number of exacerbations, number of hospital admissions, number of hospital admission days, antibiotic use, pulmonary function, quality of life, tobramycin toxicity, density of PA in sputum, emergence of bacterial resistance, and emergence of other opportunistic bacteria were recorded.

RESULTS

The number of admissions and days of admission (mean +/- SD) during the tobramycin period (0.15 +/- 0.37 and 2.05 +/- 5.03) were lower than those during the placebo period (0.75 +/-1.16 and 12.65 +/- 21.8) (p < 0.047). A decrease in PA density in sputum was associated with tobramycin administration in the analysis of the first 6-month cycle (p = 0.038). No significant differences were observed in the number of exacerbations, antibiotic use, pulmonary function, and quality of life. The emergence of bacterial resistance and other bacteria did not differ between the 2 periods of study. Inhaled tobramycin was associated with bronchospasm in 3 patients, but not with detectable ototoxicity or nephrotoxicity.

CONCLUSIONS

Aerosol administration of high-dose tobramycin in non-CF bronchiectatic patients for endobronchial infection with PA appears to be safe and decreases the risk of hospitalization and PA density in sputum. Nevertheless, pulmonary function and quality of life are not improved, and the risk of bronchospasm is appreciable.

摘要

背景

非囊性纤维化(CF)支气管扩张患者通常会发生铜绿假单胞菌(PA)引起的慢性支气管感染,这与肺功能恶化以及发病率和死亡率增加有关。

目的

确定妥布霉素直接雾化吸入下呼吸道是否可控制感染且仅产生低全身毒性。

方法

进行了一项涉及30名患者的双盲、安慰剂对照交叉试验,以确定6个月妥布霉素吸入治疗的临床有效性和安全性。患者在2个疗程中每天两次接受300mg雾化妥布霉素或安慰剂,每个疗程6个月,有1个月的洗脱期。记录急性加重次数、住院次数、住院天数、抗生素使用情况、肺功能、生活质量、妥布霉素毒性、痰液中PA密度、细菌耐药性出现情况以及其他机会性细菌的出现情况。

结果

妥布霉素治疗期间的住院次数和住院天数(均值±标准差)(0.15±0.37和2.05±5.03)低于安慰剂治疗期间(0.75±1.16和12.65±21.8)(p<0.047)。在第一个6个月疗程的分析中,痰液中PA密度的降低与妥布霉素给药有关(p = 0.038)。在急性加重次数、抗生素使用、肺功能和生活质量方面未观察到显著差异。两个研究阶段之间细菌耐药性和其他细菌的出现情况没有差异。吸入妥布霉素与3名患者的支气管痉挛有关,但与可检测到的耳毒性或肾毒性无关。

结论

在非CF支气管扩张患者中,雾化吸入高剂量妥布霉素治疗PA引起的支气管内感染似乎是安全的,并降低了住院风险和痰液中PA密度。然而,肺功能和生活质量并未改善,且支气管痉挛风险较高。

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