Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Incheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
PLoS One. 2022 Aug 18;17(8):e0273263. doi: 10.1371/journal.pone.0273263. eCollection 2022.
In 2018, the World Health Organization recommended a 6-month four-drug regimen (rifampicin, ethambutol, pyrazinamide, and levofloxacin) for the treatment of isoniazid-monoresistant tuberculosis. However, the regimen had very low certainty. This cohort study assessed the impact of fluoroquinolone use and initial baseline regimen on treatment effectiveness in isoniazid-monoresistant tuberculosis. This multicenter retrospective cohort study included 318 patients with isoniazid-monoresistant tuberculosis notified between 2011 and 2018 in Korea. Baseline regimens were classified into two groups, namely 6-9-month rifampicin, ethambutol, and pyrazinamide (6-9REZ) and a combination regimen of 2-month rifampicin, ethambutol, pyrazinamide and 7-10-month rifampicin and ethambutol (2REZ/7-10RE). Multivariable logistic regression was performed to assess factors associated with positive treatment outcomes. Of 318 enrolled patients, 234 (73.6%) were treated with the 6-9REZ and 103 (32.4%) with additional fluoroquinolone. In a multivariable logistic regression model comparing the 6-9REZ and 2REZ/7-10RE groups, there was no difference in the odds of positive outcomes (adjusted odds ratio = 1.08, 95% confidence interval = 0.65-1.82). Addition use of fluoroquinolone was not associated with positive treatment outcomes in the whole cohort (adjusted odds ratio = 1.41, 95% confidence interval = 0.87-2.27); however, its additional use was beneficial in the 2REZ/7-10RE subgroup (adjusted odds ratio = 3.58, 95% confidence interval = 1.32-9.75). Both initial baseline regimens, 6-9REZ and 2REZ/7-10RE, were similarly effective. Shortening of the pyrazinamide administration duration with additional fluoroquinolone use could be a safe alternative for patients with potential hepatotoxicity related to pyrazinamide.
2018 年,世界卫生组织建议使用含利福平、乙胺丁醇、吡嗪酰胺和左氧氟沙星的 6 个月四联药物方案治疗异烟肼单耐药结核病。然而,该方案的确定性非常低。本队列研究评估了氟喹诺酮类药物的使用和初始基础方案对异烟肼单耐药结核病治疗效果的影响。这项多中心回顾性队列研究纳入了 2011 年至 2018 年间在韩国确诊的 318 例异烟肼单耐药结核病患者。基础方案分为两组,即 6-9 个月利福平、乙胺丁醇和吡嗪酰胺(6-9REZ)和 2 个月利福平、乙胺丁醇、吡嗪酰胺和 7-10 个月利福平及乙胺丁醇(2REZ/7-10RE)联合方案。采用多变量逻辑回归评估与治疗结果阳性相关的因素。318 名入组患者中,234 例(73.6%)接受 6-9REZ 治疗,103 例(32.4%)接受额外氟喹诺酮类药物治疗。在比较 6-9REZ 和 2REZ/7-10RE 组的多变量逻辑回归模型中,两组治疗结果阳性的比值比无差异(调整比值比=1.08,95%置信区间=0.65-1.82)。氟喹诺酮类药物的附加使用与全队列的治疗结果阳性无关(调整比值比=1.41,95%置信区间=0.87-2.27);然而,其在 2REZ/7-10RE 亚组中是有益的(调整比值比=3.58,95%置信区间=1.32-9.75)。初始基础方案 6-9REZ 和 2REZ/7-10RE 均同样有效。在有吡嗪酰胺相关肝毒性风险的患者中,缩短吡嗪酰胺的给药时间并加用氟喹诺酮类药物可能是一种安全的替代方案。