Lobato Mark N, Reves Randall R, Jasmer Robert M, Grabau John C, Bock Naomi N, Shang Nong
CDC, 1600 Clifton Rd, Mailstop E-10, Atlanta, GA 30333, USA.
Chest. 2005 Apr;127(4):1296-303. doi: 10.1378/chest.127.4.1296.
Recently, a short-course treatment using 60 daily doses of rifampin and pyrazinamide was recommended for latent tuberculosis (TB) infection (LTBI).
To determine the acceptability, tolerability, and completion of treatment.
Observational cohort study.
Five county jails and TB outreach clinics for homeless populations in three cities.
Study staff enrolled 1,211 patients (844 inmates and 367 homeless persons).
Sites used 60 daily doses of rifampin and pyrazinamide, an approved treatment regimen for LTBI.
Types and frequency of drug-related adverse events and outcomes of treatment.
Prior to treatment, 25 of 1,178 patients (2.1%) had a serum aminotransferase measurement at least 2.5 times the upper limit of normal. Patients who reported excess alcohol use in the past 12 months were more likely than other patients to have an elevated pretreatment serum aminotransferase level (odds ratio, 2.1; 95% confidence interval, 1.1 to 6.1; p = 0.03). Treatment was stopped in 66 of 162 patients (13.4%) who had a drug-related adverse event. Among 715 patients who had serum aminotransferase measured during treatment, 43 patients (6.0%) had an elevation > 5 times the upper limits of normal, including one patient who died of liver failure attributed to treatment. In multivariate analyses, increasing age, an abnormal baseline aspartate aminotransferase level, and unemployment within the past 24 months were independent risk factors for hepatotoxicity. Completion rates were similar in jail inmates (47.5%) and homeless persons (43.6%).
This study detected the first treatment-associated fatality with the rifampin and pyrazinamide regimen, prompting surveillance that detected unacceptable levels of hepatotoxicity and retraction of recommendations for its routine use. Completion rates for LTBI treatment using a short-course regimen exceeds historical rates using isoniazid. Efforts to identify an effective short-course treatment for LTBI should be given a high priority.
最近,推荐使用每日60剂利福平与吡嗪酰胺的短程疗法治疗潜伏性结核感染(LTBI)。
确定该治疗方法的可接受性、耐受性及完成率。
观察性队列研究。
三个城市的五所县级监狱及针对无家可归者的结核病外展诊所。
研究人员招募了1211名患者(844名囚犯和367名无家可归者)。
各研究地点使用每日60剂利福平与吡嗪酰胺,这是一种已获批准的LTBI治疗方案。
药物相关不良事件的类型和频率以及治疗结果。
治疗前,1178名患者中有25名(2.1%)血清转氨酶测量值至少为正常上限的2.5倍。在过去12个月内报告有过量饮酒史的患者比其他患者更有可能出现治疗前血清转氨酶水平升高(比值比为2.1;95%置信区间为1.1至6.1;p = 0.03)。162名出现药物相关不良事件的患者中有66名(13.4%)停止了治疗。在715名治疗期间进行血清转氨酶测量的患者中,43名(6.0%)转氨酶升高超过正常上限的5倍,其中一名患者死于治疗所致的肝功能衰竭。在多变量分析中,年龄增长、基线天门冬氨酸转氨酶水平异常以及过去24个月内失业是肝毒性的独立危险因素。监狱囚犯(47.5%)和无家可归者(43.6%)的完成率相似。
本研究发现了首例与利福平及吡嗪酰胺治疗方案相关的死亡病例,促使进行监测,从而发现了不可接受的肝毒性水平,并撤回了其常规使用的建议。使用短程疗法治疗LTBI的完成率超过了使用异烟肼的历史完成率。应高度优先致力于确定一种有效的LTBI短程治疗方法。