EFFICACY OF AEROSOLIZED TOBRAMYCIN IN PATIENTS WITH CYSTIC-FIBROSIS

被引:358
作者
RAMSEY, BW
DORKIN, HL
EISENBERG, JD
GIBSON, RL
HARWOOD, IR
KRAVITZ, RM
SCHIDLOW, DV
WILMOTT, RW
ASTLEY, SJ
MCBURNIE, MA
WENTZ, K
SMITH, AL
机构
[1] TUFTS UNIV, SCH MED, DEPT PEDIAT, BOSTON, MA 02111 USA
[2] OREGON HLTH SCI UNIV, DEPT PEDIAT, PORTLAND, OR 97201 USA
[3] UNIV CALIF SAN DIEGO, SCH MED, DEPT PEDIAT, SAN DIEGO, CA 92103 USA
[4] TEMPLE UNIV, HLTH SCI CTR, SCH MED, DEPT PEDIAT, PHILADELPHIA, PA 19140 USA
[5] UNIV CINCINNATI, DEPT PEDIAT, CINCINNATI, OH 45221 USA
[6] UNIV WASHINGTON, SCH MED, DEPT PEDIAT, SEATTLE, WA 98195 USA
[7] UNIV WASHINGTON, SCH MED, DEPT BIOSTAT, SEATTLE, WA 98195 USA
[8] UNIV WASHINGTON, SCH MED, DEPT EPIDEMIOL, SEATTLE, WA 98195 USA
[9] UNIV WASHINGTON, SCH COMMUNITY MED, DEPT PEDIAT, SEATTLE, WA 98195 USA
[10] UNIV WASHINGTON, SCH COMMUNITY MED, DEPT BIOSTAT, SEATTLE, WA 98195 USA
[11] UNIV WASHINGTON, SCH COMMUNITY MED, DEPT EPIDEMIOL, SEATTLE, WA 98195 USA
[12] UNIV WASHINGTON, SCH PUBL HLTH, DEPT PEDIAT, SEATTLE, WA 98195 USA
[13] UNIV WASHINGTON, SCH PUBL HLTH, DEPT BIOSTAT, SEATTLE, WA 98195 USA
[14] UNIV WASHINGTON, SCH PUBL HLTH, DEPT EPIDEMIOL, SEATTLE, WA 98195 USA
关键词
D O I
10.1056/NEJM199306173282403
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Direct aerosol delivery of aminoglycosides such as tobramycin to the lower airways of patients with cystic fibrosis may control infection with Pseudomonas aeruginosa and improve pulmonary function, with low systemic toxicity. We conducted a randomized crossover study to evaluate the safety and efficacy of aerosolized tobramycin in patients with cystic fibrosis and P. aeruginosa infections. Methods. Seventy-one patients with stable pulmonary status were recruited from seven U.S. centers for the treatment of cystic fibrosis and randomly assigned to one of two crossover regimens. Group 1 received 600 mg of aerosolized tobramycin for 28 days, followed by half-strength physiologic saline (placebo) for two 28-day periods. Group 2 received placebo for 28 days, followed by tobramycin for two 28-day periods. Pulmonary function, the density of P. aeruginosa in sputum, ototoxicity, nephrotoxicity, and the emergence of tobramycin-resistant P. aeruginosa were monitored. Results. In the first 28-day period, treatment with tobramycin was associated with an increase in the percentage of the value predicted for forced expiratory volume in one second (9.7 percentage points higher than the value for placebo; P<0.001), forced vital capacity (6.2 percentage points higher than the value for placebo; P = 0.014), and forced expiratory flow at the midportion of the vital capacity (13.0 percentage points higher than the value for placebo; P<0.001). A decrease in the density of P. aeruginosa in sputum by a factor of 100 (P<0.001) was found during all periods of tobramycin administration. Neither ototoxicity nor nephrotoxicity was detected. The frequency of the emergence of tobramycin-resistant bacteria was similar during both tobramycin and placebo administration. Conclusions. The short-term aerosol administration of a high dose of tobramycin in patients with clinically stable cystic fibrosis is an efficacious and safe treatment for endobronchial infection with P. aeruginosa.
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收藏
页码:1740 / 1746
页数:7
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