Romo Matthew L, LaHood Allison, Stagg Helen R, Mitnick Carole D, Trevisi Letizia, Hewison Cathy, Padayachee Shrivani, Flores Edwin Herrera, Oyewusi Lawrence, Khan Palwasha Y, Huerga Helena, Bastard Mathieu, Rich Michael L, Tefera Girum Bayissa, Rashitov Mahmud, Kirakosyan Ohanna, Krisnanda Aga, Toktogonova Atyrkul, Siddiqui Muhammad Rafi, Gómez-Restrepo Camilo, Kotrikadze Tina, Franke Molly F
Department of Global Health and Social Medicine, Harvard Medical School, Boston, Massachusetts, USA.
Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
medRxiv. 2025 Aug 24:2025.08.20.25334077. doi: 10.1101/2025.08.20.25334077.
People who smoke are at increased risk of unfavorable tuberculosis (TB) treatment outcomes compared with those who do not, but the pathways explaining this effect are unclear. We estimated the effect of smoking on a successful end-of-treatment outcome for multidrug-resistant and rifampicin-resistant (MDR/RR) TB and examined if intervening on loss to follow-up mitigates this effect. The endTB Observational Study was a prospective cohort of people with MDR/RR-TB who were treated with longer regimens containing bedaquiline and/or delamanid. We used marginal standardization to examine the effect of smoking (≥1 cigarette daily at enrollment) on treatment success (cured/completed). To simulate intervening on lost to follow-up, we censored participants and applied inverse probability of censoring weights. Among 1786 participants in 12 countries, 539 (30.2%) reported smoking. At the end of treatment, 73.5% of people who smoked and 80.3% of people who did not smoke had treatment success (risk difference in percentage points: -6.8, 95% CI: -11.1, -2.6). After adjusting for baseline confounders including demographics, social history, and comorbidities, the risk difference was similar (-5.2 percentage points) but 95% CIs were less precise (-14.1, 3.2). In a pseudopopulation without loss to follow-up, the risk difference was reduced (-1.9 percentage points; 95% CI: -10.2, 5.1). People who smoked had less frequent MDR/RR-TB treatment success compared with those who did not smoke. A simulated intervention on loss to follow-up reduced this difference, suggesting that pathways related to retention in care were a driver of this effect.
与不吸烟的人相比,吸烟人群出现不良结核病(TB)治疗结果的风险更高,但解释这种影响的途径尚不清楚。我们评估了吸烟对耐多药和利福平耐药(MDR/RR)结核病治疗成功结局的影响,并研究了对失访进行干预是否能减轻这种影响。endTB观察性研究是一项针对MDR/RR-TB患者的前瞻性队列研究,这些患者接受了包含贝达喹啉和/或地拉马尼的更长疗程治疗。我们使用边际标准化来评估吸烟(入组时每天≥1支香烟)对治疗成功(治愈/完成治疗)的影响。为了模拟对失访进行干预,我们对参与者进行截尾并应用截尾权重的逆概率。在12个国家的1786名参与者中,539人(30.2%)报告吸烟。治疗结束时,吸烟人群中有73.5%治疗成功,不吸烟人群中有80.3%治疗成功(百分点风险差异:-6.8,95%CI:-11.1,-2.6)。在调整了包括人口统计学、社会史和合并症在内的基线混杂因素后,风险差异相似(-5.2个百分点),但95%CI的精确性较低(-14.1,3.2)。在无失访的虚拟人群中,风险差异减小(-1.9个百分点;95%CI:-10.2,5.1)。与不吸烟的人相比,吸烟的人MDR/RR-TB治疗成功的频率较低。对失访进行的模拟干预减少了这种差异,表明与坚持治疗相关的途径是这种影响的一个驱动因素。