Therapeutic drug monitoring in patients with cystic fibrosis and mycobacterial disease

被引:37
作者
Gilljam, M
Berning, SE
Peloquin, CA
Strandvik, B
Larsson, LO
机构
[1] Univ Gothenburg, Dept Resp Med & Allergol, Gothenburg, Sweden
[2] Univ Gothenburg, Dept Paediat, Gothenburg, Sweden
[3] Univ Gothenburg, Gothenburg Cyst Fibrosis Ctr, Gothenburg, Sweden
[4] Natl Jewish Med & Res Ctr, Denver, CO USA
关键词
cystic fibrosis; mycobacterial disease; therapeutic drug monitoring;
D O I
10.1034/j.1399-3003.1999.14b18.x
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Cystic fibrosis (CF) patients require higher dosages of many antibiotics. The relapse of tuberculosis in one CF patient, and the repeated growth of Mycobacterium avium-intracellulare in another, despite conventional therapy, raised the question of whether the serum levels of the antimycobacterial drugs were adequate. Antimycobacterial drug serum concentrations were assayed in 10 CF patients with pulmonary mycobacterial disease. Serum levels below the proposed target range were seen 2 h after drug intake in the initial four patients treated: for rifampicin in 2/3, ethambutol in 3/4 and for clarithromycin in 2/3 patients, despite standard dosages. Reassays after dose adjustment and assays in sig other patients showed that adequate levels were not achieved 4 h after chlaritromycin in 3/5, ethambutol in 1/5, ciproflaxacin in 1/2 and ofloxacin in 2/2 patients. The patient with relapse of tuberculosis and the patient with continuous growth of M. avium-intracellulare improved and became culture negative after dose adjustment. Low drug serum levels is one reason for therapy failure in cystic fibrosis patients with mycobacterial disease. Therapeutic drug monitoring is recommended.
引用
收藏
页码:347 / 351
页数:5
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