Department of Pediatrics, Children's Hospital Colorado, University of Colorado Anschutz Medical Campus, 13123 E. 16th Ave. B-395 Aurora, CO 80045, United States.
Department of Biostatistics and Informatics, University of Colorado School of Public Health, Aurora, CO 80045, United States.
J Cyst Fibros. 2021 Sep;20(5):772-778. doi: 10.1016/j.jcf.2021.04.011. Epub 2021 May 21.
Treatment failure of Mycobacterium avium complex (MAC) pulmonary disease occurs in about 30% of people with cystic fibrosis (CF) and may be a result of abnormal drug concentrations.
Prospective, cross-over, single-dose PK study of 20 pancreatic insufficient individuals with CF and 10 healthy controls (HC). CF subjects received simultaneous doses of oral azithromycin, ethambutol, and rifampin in the fasting state and with food and pancreatic enzymes, separated by two weeks. HC received fasting doses only. A non-compartmental model was used to estimate PK parameters of drugs and metabolites.
Azithromycin maximum concentration (C ) was higher and rifampin C was lower in fasting CF subjects compared to HC, while other PK measures, including those for ethambutol, were similar. Addition of food and enzymes did not improve the C of the antimycobacterial drugs. Nineteen of 20 CF subjects had one or more abnormal C z-scores in either the fasting or fed state (or both), when compared to HC.
PK profiles of azithromycin and ethambutol were similar between CF and HC, except azithromycin C was slightly higher in people with CF after a single dose. Rifampin PK parameters were altered in persons with CF. Addition of food and enzymes in CF subjects did not improve PK parameters. Standard dosing guidelines should be used as a starting point for people with CF initiating MAC therapy and therapeutic drug monitoring should be routinely performed to prevent the possibility of treatment failure due to abnormal drug concentrations.
ClinicalTrials.gov Identifier: NCT02372383 Prior abstract publication: 1. Martiniano S, Wagner B, Brennan L, Wempe M, Anderson P, Nick J, Sagel S. Pharmacokinetics of oral MAC antibiotics in cystic fibrosis. Am J Resp Crit Care Med A4842-A4842, 2017. 2. Martiniano SL, Wagner BD, Brennan L, Wempe MF, Anderson PL, Nick JA, Sagel SD. Pharmacokinetics of oral MAC antibiotics in cystic fibrosis. J Cyst Fibros 16: S52-53, 2017.
大约 30%的囊性纤维化(CF)患者会出现鸟分枝杆菌复合体(MAC)肺病治疗失败的情况,这可能是由于药物浓度异常所致。
对 20 名胰腺功能不全的 CF 患者和 10 名健康对照者(HC)进行前瞻性、交叉、单次剂量 PK 研究。CF 患者空腹时同时服用口服阿奇霉素、乙胺丁醇和利福平,并在两周后进食和服用胰酶。HC 仅接受空腹剂量。采用非房室模型估算药物和代谢物的 PK 参数。
与 HC 相比,空腹 CF 患者的阿奇霉素最大浓度(C )更高,利福平 C 更低,而其他 PK 指标,包括乙胺丁醇,相似。添加食物和酶并不能改善抗分枝杆菌药物的 C 。与 HC 相比,19/20 的 CF 患者在空腹或进食状态(或两者)下有一种或多种阿奇霉素和利福平的 C z 分数异常。
CF 患者和 HC 之间的阿奇霉素和乙胺丁醇 PK 谱相似,只是 CF 患者单次给药后阿奇霉素 C 略高。CF 患者的利福平 PK 参数发生改变。CF 患者添加食物和酶并不能改善 PK 参数。在开始 MAC 治疗时,应将标准剂量指南作为 CF 患者的起点,并常规进行治疗药物监测,以防止因药物浓度异常导致治疗失败的可能性。
ClinicalTrials.gov 标识符:NCT02372383 先前的摘要出版物:1. Martiniano S, Wagner B, Brennan L, Wempe M, Anderson P, Nick J, Sagel S. 口服 MAC 抗生素在囊性纤维化中的药代动力学。Am J Resp Crit Care Med A4842-A4842,2017. 2. Martiniano SL, Wagner BD, Brennan L, Wempe MF, Anderson PL, Nick JA, Sagel SD. 口服 MAC 抗生素在囊性纤维化中的药代动力学。J Cyst Fibros 16:S52-53,2017.