Frequent antibiotic therapy improves survival of cystic fibrosis patients with chronic Pseudomonas aeruginosa infection.

M. Szaff, N. Høiby, E. W. Flensborg
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引用次数: 103

Abstract

During the period 1971-75, 51 cystic fibrosis (CF) patients who contracted chronic P. aeruginosa infection were treated at the Danish CF centre with anti-pseudomonas chemotherapy only when their clinical condition deteriorated considerably. During the period 1976-80, 58 CF patients who contracted chronic P. aeruginosa infection were treated at the Danish CF centre with anti-pseudomonas chemotherapy on a regular basis every 3 months. Each routine 24 day-course of chemotherapy consisted of tobramycin in combination with carbenicillin or other beta-lactam antibiotics with activity against P. aeruginosa. In case of allergy or resistant strains monotherapy with tobramycin was used. The 5-year survival of CF patients from the time of the onset of the chronic P. aeruginosa infection increased from 54% in the first period to 82% in the second period (p less than 0.05), and lung function (peak expiratory flow rate) also improved significantly. It is concluded that intensive "maintenance" chemotherapy against P. aeruginosa improves survival and quality of life of CF patients although permanent eradication of P. aeruginosa is not accomplished.
频繁的抗生素治疗可提高慢性铜绿假单胞菌感染囊性纤维化患者的生存率。
1971- 1975年期间,51名慢性铜绿假单胞菌感染的囊性纤维化(CF)患者在丹麦CF中心接受抗假单胞菌化疗治疗,只有当他们的临床状况明显恶化时。1976- 1980年期间,58名慢性铜绿假单胞菌感染的CF患者在丹麦CF中心接受抗假单胞菌化疗,每3个月定期治疗一次。每个24天的常规化疗疗程由妥布霉素联合卡比西林或其他抗铜绿假单胞菌活性的β -内酰胺类抗生素组成。对于过敏或耐药菌株,采用妥布霉素单药治疗。CF患者自慢性铜绿假单胞菌感染发病时起的5年生存率由第一期的54%提高到第二期的82% (p < 0.05),肺功能(呼气流量峰值)也有明显改善。结论:强化“维持”化疗对铜绿假单胞菌可提高CF患者的生存和生活质量,但不能完全根除铜绿假单胞菌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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