1 Department of Medicine and.
2 Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, Alberta, Canada.
Ann Am Thorac Soc. 2019 Jul;16(7):853-860. doi: 10.1513/AnnalsATS.201811-773OC.
The potential of azithromycin to alter the antimicrobial and clinical benefits of inhaled tobramycin in patients with cystic fibrosis (CF) has been previously reported. The potential interaction between azithromycin and intravenous antibiotics in the treatment of pulmonary exacerbations is unknown. To determine if chronic azithromycin use as a concomitant therapy is associated with change in lung function after receiving intravenous antibiotic regimens including tobramycin or colistimethate. This was a retrospective cohort study evaluating the association of azithromycin with intravenous tobramycin or colistimethate in adult patients with CF treated for a pulmonary exacerbation. The primary outcome was relative lung function recovery (forced expiratory volume in 1 s [FEV]) after exacerbation treatment. Generalized estimating equations were applied to account for repeated events with independent correlation structures and robust standard errors, incorporating several confounders. A total of 220 exacerbation events occurred in 121 patients in the tobramycin group (47% using azithromycin), and 207 exacerbation events occurred in 86 patients in the colistimethate group (59% using azithromycin). Azithromycin use was associated with less FEV% recovery in patients treated with tobramycin (-3% relative FEV% recovery [95% confidence interval (CI), -7 to 0.2] and -2.64% absolute FEV% change [95% CI, -4.52 to -0.76]). Azithromycin use was associated with greater recovery of FEV% when treated with colistimethate (+3% relative FEV% recovery [95% CI, -0.1 to 7] and 2.00% absolute improvement in FEV% [95% CI, 0.13 to 3.87]). The odds of 90% or 100% recovery to baseline FEV% were lower with azithromycin use in the tobramycin cohort and higher with azithromycin use in the colistimethate cohort but were not statistically significant. Azithromycin use was associated with a more favorable response in adult patients with CF treated with intravenous colistimethate but a less favorable response in those treated with intravenous tobramycin.
阿奇霉素有改变囊性纤维化(CF)患者吸入妥布霉素的抗菌和临床疗效的潜力,这一点先前已有报道。然而,阿奇霉素与静脉用抗生素联合治疗肺部恶化的潜在相互作用尚不清楚。本研究旨在确定慢性阿奇霉素联合治疗是否会影响接受妥布霉素或黏菌素静脉治疗方案后患者的肺功能变化。
这是一项回顾性队列研究,评估了阿奇霉素与 CF 成人患者肺部恶化时接受的静脉用妥布霉素或黏菌素的相关性。主要结局是恶化治疗后相对肺功能恢复(1 秒用力呼气量 [FEV])。采用广义估计方程来解释具有独立相关结构和稳健标准误差的重复事件,并纳入了多个混杂因素。
妥布霉素组共发生 220 例恶化事件(47%的患者使用阿奇霉素),黏菌素组共发生 207 例恶化事件(59%的患者使用阿奇霉素)。与未使用阿奇霉素的患者相比,使用阿奇霉素的患者在接受妥布霉素治疗后的 FEV%恢复较少(相对 FEV%恢复减少 3%[95%置信区间(CI),-7 至 0.2]和绝对 FEV%变化减少 2.64%[95% CI,-4.52 至-0.76])。与未使用阿奇霉素的患者相比,使用阿奇霉素的患者在接受黏菌素治疗后的 FEV%恢复更多(相对 FEV%恢复增加 3%[95% CI,0.1 至 7]和绝对 FEV%改善 2.00%[95% CI,0.13 至 3.87])。在妥布霉素组中,使用阿奇霉素与 90%或 100%恢复到基线 FEV%的几率降低,而在黏菌素组中,使用阿奇霉素与 90%或 100%恢复到基线 FEV%的几率升高,但均无统计学意义。
在接受静脉用黏菌素治疗的 CF 成年患者中,阿奇霉素的使用与更有利的反应相关,但在接受静脉用妥布霉素治疗的患者中,阿奇霉素的使用与反应较差相关。