首页> 美国卫生研究院文献>Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America >Flu-like and Other Systemic Drug Reactions Among Persons Receiving Weekly Rifapentine Plus Isoniazid or Daily Isoniazid for Treatment of Latent Tuberculosis Infection in the PREVENT Tuberculosis Study
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Flu-like and Other Systemic Drug Reactions Among Persons Receiving Weekly Rifapentine Plus Isoniazid or Daily Isoniazid for Treatment of Latent Tuberculosis Infection in the PREVENT Tuberculosis Study

机译:在预防性肺结核研究中每周接受利福喷汀加异烟肼或每日异烟肼治疗潜伏性结核感染的人中的类流感反应和其他全身药物反应

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摘要

>Background. Weekly rifapentine plus isoniazid for 3 months (3HP) is as effective as daily isoniazid for 9 months (9H) for latent tuberculosis infection in high-risk persons, but there have been reports of possible flu-like syndrome.>Methods. We identified clinically significant systemic drug reactions (SDR) and evaluated risk factors in patients who did not complete treatment in the PREVENT Tuberculosis study.>Results. Among 7552 persons who received ≥1 dose of study drug, 153 had a SDR: 138/3893 (3.5%) with 3HP vs 15/3659 (0.4%) with 9H (P < .001). In the 3HP arm, 87 (63%) had flu-like syndrome and 23 (17%) had cutaneous reactions; 13/3893 (0.3%) had severe reactions (6 were hypotensive) and 6 reported syncope. Symptoms occurred after a median of 3 doses, and 4 hours after the dose; median time to resolution was 24 hours. There were no deaths. In multivariate logistic regression analysis, factors independently associated with SDR included receipt of 3HP (adjusted odds ratio [aOR] 9.4; 95% confidence interval [CI], 5.5, 16.2), white non-Hispanic race/ethnicity (aOR 3.3; 95% CI, 2.3, 4.7), female sex (aOR 2.0; 95% CI, 1.4, 2.9), age ≥35 years (aOR 2.0; 95% CI, 1.4, 2.9), and lower body mass index (body mass index [BMI]; P = .009). In a separate multivariate analysis among persons who received 3HP, severe SDR were associated with white non-Hispanic race/ethnicity (aOR 5.4; 95% CI, 1.8, 16.3), and receipt of concomitant non-study medications (aOR 5.9; 95% CI, 1.3, 27.1).>Conclusions. SDR were more common with 3HP, and mostly flu-like. Persons of white race, female sex, older age, and lower BMI were at increased risk. Severe reactions were rare and associated with 3HP, concomitant medication, and white race. The underlying mechanism is unclear.>Clinical Trials Registration. .
机译:>背景。对于高危人群,潜伏性肺炎每周加用利福喷汀加异烟肼3个月(3HP)与每日异烟肼9个月(9H)一样有效,但已有报道可能>方法。在PREVENT结核病研究中,我们确定了临床上显着的全身药物反应(SDR),并评估了未完成治疗的患者的危险因素。>结果。 7552接受≥1剂量研究药物的患者,其SDR为:3HP时为138/3893(3.5%),而9H患者为15/3659(0.4%)(P <.001)。在3HP组中,有87(63%)有流感样综合征,有23(17%)有皮肤反应。 13/3893(0.3%)出现严重反应(6例为低血压),有6例报告为晕厥。中位数3剂后和4小时后出现症状。解决问题的中位数时间为24小时。没有死亡。在多因素logistic回归分析中,与SDR独立相关的因素包括3HP的接收(调整后的优势比[aOR] 9.4; 95%置信区间[CI],5.5、16.2),白人非西班牙裔/种族(aOR 3.3; 95% CI,2.3、4.7),女性(aOR 2.0; 95%CI,1.4、2.9),年龄≥35岁(aOR 2.0; 95%CI,1.4、2.9)和较低的体重指数(BMI) ]; P = .009)。在接受3HP的人群中进行的另一项多元分析中,严重的SDR与白人非西班牙裔种族/民族(aOR 5.4; 95%CI,1.8、16.3)以及接受非研究性药物(aOR 5.9; 95%)相关。 CI,1.3,27.1)。>结论。 SDR在3HP中更为常见,且大多是流感样。白人,女性,年龄较大,BMI较低的人患病风险增加。严重的反应很少见,并伴有3HP,伴随用药和白人。潜在的机制尚不清楚。>临床试验注册。

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