Department of Medicine, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Harvard T. H. Chan School of Public Health, Boston, Massachusetts, USA.
Clin Infect Dis. 2023 Sep 18;77(6):892-900. doi: 10.1093/cid/ciad301.
Tuberculosis infection (TBI) and TB disease (TBD) incidence remains poorly described following household contact (HHC) rifampin-/multidrug-resistant TB exposure. We sought to characterize TBI and TBD incidence at 1 year in HHCs and to evaluate TB preventive treatment (TPT) use in high-risk groups.
We previously conducted a cross-sectional study of HHCs with rifampin-/multidrug-resistant TB in 8 high-burden countries and reassessed TBI (interferon-gamma release assay, HHCs aged ≥5 years) and TBD (HHCs all ages) at 1 year. Incidence was estimated across age and risk groups (<5 years; ≥5 years, diagnosed with human immunodeficiency virus [HIV]; ≥5 years, not diagnosed with HIV/unknown, baseline TBI-positive) by logistic or log-binomial regression fitted using generalized estimating equations.
Of 1016 HHCs, 850 (83.7%) from 247 households were assessed (median, 51.4 weeks). Among 242 HHCs, 52 tested interferon-gamma release assay-positive, yielding a 1-year 21.6% (95% confidence interval [CI], 16.7-27.4) TBI cumulative incidence. Sixteen of 742 HHCs developed confirmed (n = 5), probable (n = 3), or possible (n = 8) TBD, yielding a 2.3% (95% CI, 1.4-3.8) 1-year cumulative incidence (1.1%; 95% CI, .5-2.2 for confirmed/probable TBD). TBD relative risk was 11.5-fold (95% CI, 1.7-78.7), 10.4-fold (95% CI, 2.4-45.6), and 2.9-fold (95% CI, .5-17.8) higher in age <5 years, diagnosed with HIV, and baseline TBI high-risk groups, respectively, vs the not high-risk group (P = .0015). By 1 year, 4% (21 of 553) of high-risk HHCs had received TPT.
TBI and TBD incidence continued through 1 year in rifampin-/multidrug-resistant TB HHCs. Low TPT coverage emphasizes the need for evidence-based prevention and scale-up, particularly among high-risk groups.
在与家庭接触(HHC)利福平/耐多药结核暴露后,结核感染(TBI)和结核病(TBD)的发病率仍描述不佳。我们试图描述 HHC 中 1 年时 TBI 和 TBD 的发病率,并评估高危人群中结核预防治疗(TPT)的使用情况。
我们之前在 8 个高负担国家进行了一项利福平/耐多药结核的 HHC 横断面研究,并在 1 年时重新评估了 TBI(干扰素-γ释放试验,HHC 年龄≥5 岁)和 TBD(HHC 所有年龄)。通过广义估计方程拟合的逻辑或对数二项式回归,按年龄和风险组(<5 岁;≥5 岁,诊断为人免疫缺陷病毒 [HIV];≥5 岁,未诊断为 HIV/未知,基线 TBI 阳性)估计发病率。
在 1016 名 HHC 中,有 850 名(来自 247 个家庭)接受了评估(中位数为 51.4 周)。在 242 名 HHC 中,有 52 名干扰素-γ释放试验阳性,导致 1 年累积发病率为 21.6%(95%置信区间 [CI],16.7-27.4)。742 名 HHC 中有 16 名发展为确诊(n=5)、可能(n=3)或可能(n=8)TBD,导致 1 年累积发病率为 2.3%(95%CI,1.4-3.8)(确诊/可能 TBD 为 1.1%;95%CI,.5-2.2)。TBD 的相对风险分别为年龄<5 岁、诊断为 HIV 和基线 TBI 高危组的 11.5 倍(95%CI,1.7-78.7)、10.4 倍(95%CI,2.4-45.6)和 2.9 倍(95%CI,.5-17.8),与非高危组相比(P=.0015)。到 1 年时,4%(21/553)的高危 HHC 接受了 TPT。
在利福平/耐多药结核 HHC 中,TBI 和 TBD 的发病率持续到 1 年。TPT 覆盖率低强调了需要基于证据的预防和扩大规模,特别是在高危人群中。