利福平不耐受患者的特征和治疗结果

R. Mangat, S.K. Brode, H.K. Mah, M.S. Brar, N.F. Sabur
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摘要

背景利福平(RIF)被认为是结核病治疗的主要药物,但其不良反应往往限制了它的使用。方法这项回顾性队列研究检查了在我院接受治疗的结核病患者,并比较了接受 RIF 和不耐受 RIF 的患者。结果共纳入 829 名患者,其中 76 名患者(9%)对 RIF 不耐受。与耐受 RIF 的患者相比,不耐受 RIF 的患者年龄明显偏大(中位年龄:67 岁,IQR 50-78 岁 vs. 48 岁,IQR 31-70 岁;P < 0.0001),更有可能是女性(57% vs. 41%;P = 0.01)和并发糖尿病(37.3% vs. 19%;P < 0.0001)。RIF 不耐受最常见的原因是转氨酶炎(25%)、全血细胞减少(14.5%)、皮疹(17.1%)和胃肠道不耐受(7.8%)。20 名患者随后接受了利福布汀治疗,70% 的患者治疗成功。对 RIF 不耐受的患者的平均治疗时间明显更长(335 天对 270 天;P < 0.001)。结论RIF不耐受在老年患者、女性和并发糖尿病患者中更为常见。不能耐受 RIF 的患者治疗时间较长,但治疗效果无差异。在尝试使用利福布汀时,大多数曾发生过 RIF 相关不良事件的患者都能很好地耐受利福布汀。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characteristics of and treatment outcomes in rifampicin-intolerant patients
BACKGROUNDRifampicin (RIF) is considered the backbone of TB treatment, but adverse effects often limit its use.METHODSThis retrospective cohort study examined patients treated for TB disease at our institution, and compared those who received RIF to those who were intolerant to RIF.RESULTSA total of 829 patients were included. Seventy-six patients (9%) were intolerant to RIF. Patients with RIF intolerance were significantly older (median age: 67 years, IQR 50–78 vs. 48 years, IQR 31–70; P < 0.0001), and were more likely to be female (57% vs. 41%; P = 0.01) and have concurrent diabetes mellitus (37.3% vs. 19%; P < 0.0001) compared to those who tolerated RIF. RIF intolerance was most commonly due to transaminitis (25%), cytopenia (14.5%), rash (17.1%) and gastro-intestinal intolerance (7.8%). Twenty patients were subsequently challenged with rifabutin, and this was successful in 70%. The mean treatment duration was significantly longer in patients who were intolerant to RIF (335 vs. 270 days; P < 0.001). There was no significant difference in treatment outcomes.CONCLUSIONRIF intolerance is more common in older patients, females, and those with concurrent diabetes mellitus. Patients who could not tolerate RIF had a longer duration of therapy, but no difference in treatment outcomes. When attempted, rifabutin was well tolerated in most patients with a previous RIF-related adverse event.
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