University of Groningen, University Medical Center Groningen, Department of Pulmonary Diseases and Tuberculosis, Groningen, the Netherlands.
University of Groningen, University Medical Center Groningen, Department of Clinical Pharmacy and Pharmacology, Groningen, the Netherlands.
Antimicrob Agents Chemother. 2022 Feb 15;66(2):e0182921. doi: 10.1128/AAC.01829-21. Epub 2021 Nov 22.
Moxifloxacin is an attractive drug for the treatment of isoniazid-resistant rifampicin-susceptible tuberculosis (TB) or drug-susceptible TB complicated by isoniazid intolerance. However, co-administration with rifampicin decreases moxifloxacin exposure. It remains unclear whether this drug-drug interaction has clinical implications. This retrospective study in a Dutch TB center investigated how rifampicin affected moxifloxacin exposure in patients with isoniazid-resistant or -intolerant TB. Moxifloxacin exposures were measured between 2015 and 2020 in 31 patients with isoniazid-resistant or -intolerant TB receiving rifampicin, and 20 TB patients receiving moxifloxacin without rifampicin. Moxifloxacin exposure, i.e., area under the concentration-time curve (AUC), and attainment of AUC/MIC > 100 were investigated for 400 mg moxifloxacin and 600 mg rifampicin, and increased doses of moxifloxacin (600 mg) or rifampicin (900 mg). Moxifloxacin AUC and peak concentration with a 400 mg dose were decreased when rifampicin was co-administered compared to moxifloxacin alone (ratio of geometric means 0.61 (90% CI (0.53, 0.70) and 0.81 (90% CI (0.70, 0.94), respectively). Among patients receiving rifampicin, 65% attained an AUC/MIC > 100 for moxifloxacin compared to 78% of patients receiving moxifloxacin alone; this difference was not significant. Seven out of eight patients receiving an increased dose of 600 mg moxifloxacin reached the target AUC/MIC > 100. This study showed a clinically significant 39% decrease in moxifloxacin exposure when rifampicin was co-administered. Moxifloxacin dose adjustment may compensate for this drug-drug interaction. Further exploring the impact of higher doses of these drugs in patients with isoniazid resistance or intolerance is paramount.
莫西沙星是治疗异烟肼耐药利福平敏感(TB)或对异烟肼不耐受的药物敏感 TB 的一种有吸引力的药物。然而,与利福平共同给药会降低莫西沙星的暴露。目前尚不清楚这种药物相互作用是否具有临床意义。本研究回顾性分析了荷兰结核病中心的研究结果,以评估利福平对异烟肼耐药或不耐受的 TB 患者莫西沙星暴露的影响。2015 年至 2020 年期间,31 例异烟肼耐药或不耐受的 TB 患者接受利福平联合莫西沙星治疗,20 例接受莫西沙星治疗的 TB 患者未接受利福平治疗。检测了 400mg 莫西沙星和 600mg 利福平,以及增加剂量的莫西沙星(600mg)或利福平(900mg)的莫西沙星暴露量(即浓度-时间曲线下面积(AUC))和 AUC/MIC>100 的达标率。与莫西沙星单药治疗相比,利福平联合莫西沙星治疗时,莫西沙星的 AUC 和峰浓度(400mg 剂量)降低(几何均数比值分别为 0.61(90%CI(0.53,0.70)和 0.81(90%CI(0.70,0.94))。与单独使用莫西沙星的患者(65%)相比,接受利福平治疗的患者中,有 65%的患者达到了莫西沙星的 AUC/MIC>100 的目标,这一差异无统计学意义。8 例接受 600mg 莫西沙星增加剂量的患者中有 7 例达到了目标 AUC/MIC>100。本研究显示,当利福平联合使用时,莫西沙星的暴露量显著降低了 39%。莫西沙星剂量调整可能会补偿这种药物相互作用。进一步研究更高剂量的这些药物在异烟肼耐药或不耐受的患者中的影响至关重要。