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Long-term safety and efficacy of tobramycin in the?management of cystic fibrosis

机译:妥布霉素治疗囊性纤维化的长期安全性和有效性

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摘要

Cystic fibrosis (CF) is a fatal inherited disease caused by mutations in the CF transmembrane conductance regulator ( CFTR ) gene whose mortality is conditioned by a progressive decline in lung function. Bacterial infections play a key role in this decline. Chronic bacterial infection in CF patients varies over time and the presence of Pseudomonas aeruginosa in sputum is a marker of poor prognosis. P. aeruginosa is eradicated from the airways using inhaled antibiotics administered in various formulations and devices. Antipseudomonal antibiotics have extended the survival of CF patients to 40 years. Tobramycin is a bactericidal aminoglycoside antibiotic with demonstrated activity against gram-negative microorganisms. Initially, the drug was administered as an inhaled parenteral solution. Subsequently, a specific tobramycin inhalation solution was developed. PulmoSphere? technology enables dry tobramycin powder to be formulated for inhalation (tobramycin inhalation powder) using a small and portable capsule-based breath-activated device (T-326). Chronic colonization by P. aeruginosa is the main indication for aerosol antibiotic therapy. The American Cystic Fibrosis Foundation, European guidelines, and Spanish consensus guidelines provide different recommendations for eradication.
机译:囊性纤维化(CF)是由CF跨膜电导调节剂(CFTR)基因突变引起的致命遗传性疾病,其死亡率受肺功能逐渐下降的影响。细菌感染在这种下降中起关键作用。 CF患者的慢性细菌感染随时间变化,并且痰中存在铜绿假单胞菌是不良预后的标志。铜绿假单胞菌使用各种制剂和装置吸入的抗生素从呼吸道根除。抗伪疫苗已将CF患者的生存期延长至40年。妥布霉素是一种杀菌的氨基糖苷类抗生素,具有抗革兰氏阴性微生物的活性。最初,该药物以吸入式肠胃外溶液的形式给药。随后,开发了一种特定的妥布霉素吸入溶液。 PulmoSphere?借助这项技术,可以使用小型便携式基于胶囊的呼吸激活装置(T-326)将干燥的妥布霉素粉末制成吸入剂(妥布霉素吸入粉剂)。铜绿假单胞菌的长期定植是气雾剂抗生素治疗的主要指征。美国囊性纤维化基金会,欧洲指南和西班牙共识指南为根除提供了不同的建议。

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