Manika K, Chatzika K, Papaioannou M, Kontou P, Boutou A, Zarogoulidis K, Kioumis I
Respiratory Infections Unit, Pulmonary Department, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Intensive Care Unit, G Papanikolaou Hospital, Thessaloniki, Greece.
Int J Tuberc Lung Dis. 2015 Nov;19(11):1383-7. doi: 10.5588/ijtld.14.0935.
Rifampicin (RMP) has been reported to reduce moxifloxacin (MFX) levels, which may interfere with the effectiveness of MFX in treating tuberculosis (TB).
To study the MFX-RMP interaction in patients receiving MFX with or without RMP as part of their anti-tuberculosis treatment regimen.
Patients with pulmonary TB followed up by the Tuberculosis Out-patient Clinic of the Pulmonary Department, Aristotle University of Thessaloniki, Greece, who underwent treatment with MFX during the periods 1 May 2012-30 April 2014 and 1 January-31 March 2015, were included in the study. MFX levels were compared between 12 patients who were receiving RMP (Group 1) and 10 who were not (Group 2).
The participants did not significantly differ in body mass index, days of MFX treatment or MFX dose/kg. Neither the peak concentration (Cmax) nor the 24 h area under the curve (AUC24) differed significantly between the two groups (Group 1, Cmax median 3.9 [range 1.9-4.5] mg/l; AUC24 29.1 [10-47.4] mg·h/l and Group 2, Cmax 4.1 [2-6.4] mg/l; AUC24 36.5 [14.6-54.2] mg·h/l).
Although a decrease in MFX exposure was observed in the RMP-treated group, the effect was lower than previously reported in a real-life setting. The large variability observed in MFX pharmacokinetics in both groups may suggest the need for dose readjustment in some patients, regardless of RMP co-administration.
据报道,利福平(RMP)会降低莫西沙星(MFX)的血药浓度,这可能会影响MFX治疗结核病(TB)的疗效。
研究在接受MFX治疗的患者中,无论是否联合使用RMP作为抗结核治疗方案的一部分,MFX与RMP之间的相互作用。
纳入希腊塞萨洛尼基亚里士多德大学肺科结核病门诊随访的肺结核患者,这些患者在2012年5月1日至2014年4月30日以及2015年1月1日至3月31日期间接受了MFX治疗。比较了12例接受RMP治疗的患者(第1组)和10例未接受RMP治疗的患者(第2组)的MFX血药浓度。
两组患者的体重指数、MFX治疗天数或MFX剂量/千克无显著差异。两组的峰浓度(Cmax)和24小时曲线下面积(AUC24)均无显著差异(第1组,Cmax中位数为3.9[范围1.9 - 4.5]mg/l;AUC24为29.1[10 - 47.4]mg·h/l;第2组,Cmax为4.1[2 - 6.4]mg/l;AUC24为36.5[14.6 - 54.2]mg·h/l)。
虽然在接受RMP治疗的组中观察到MFX暴露量有所下降,但该效应低于先前在实际临床环境中的报道。两组中MFX药代动力学均存在较大变异性,这可能表明无论是否联合使用RMP,部分患者都需要调整剂量。