Felix Bongomin , Martha Namusobya , Ritah Nantale , Daniel S. Ebbs , Charles Batte , Norman van Rhijn , Joseph Baruch Baluku , David W. Denning
{"title":"Mortality hazards after treatment completion of pulmonary tuberculosis in a tertiary hospital in Uganda","authors":"Felix Bongomin , Martha Namusobya , Ritah Nantale , Daniel S. Ebbs , Charles Batte , Norman van Rhijn , Joseph Baruch Baluku , David W. Denning","doi":"10.1016/j.ijregi.2025.100758","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><div>Treated pulmonary tuberculosis (PTB) is associated with long-term complications that contribute to substantial morbidity and mortality. We estimated the incidence and predictors of post-PTB mortality and evaluated whether chronic pulmonary aspergillosis (CPA) independently increases the risk of death.</div></div><div><h3>Methods</h3><div>Between July 1, 2020 and June 30, 2021, we enrolled 162 individuals with treated drug-susceptible PTB who had persistent respiratory symptoms and screened them for CPA using a symptom checklist, chest x-ray, <em>Aspergillus</em> immunoglobulin G-immunoglobulin M point-of-care test, and sputum culture. Between November and December 2024, we followed up all participants via phone calls to determine their vital status. On chest X-ray, PTB was classified as minimal, moderate, and far advanced disease based on involvement of one, two, or more zones, respectively, and coupled to unilateral or bilateral lung disease. Cox proportional hazards regression was used to identify independent predictors of mortality.</div></div><div><h3>Results</h3><div>Thirty-seven (22.8%) participants were lost to follow-up. The median follow-up duration was 3.8 years (interquartile range 3.6-3.9). Of the 125 participants with vital status, their mean age was 33.5 years (±11.7). At baseline, 46 (36.8%) had far advanced PTB, 64 (51.2%) had pulmonary fibrosis, 15 (12.0%) had a history of previous TB, and 34 (27.2%) were living with HIV. Coinfection with PTB and CPA was identified in 31 participants at baseline (24.8%). The median St. George’s respiratory questionnaire score was 50.9 (interquartile range 40.9-63.3), and 32.0% (n = 40) had scores above 60, indicating poor health-related quality of life. Overall mortality was 8.8% (95% confidence interval [CI] 4.4-15.2%), with a mortality rate of 24.3 deaths per 1000 person-years of follow-up. Mortality rates were comparable among participants with and without CPA-PTB coinfection. Independent predictors of mortality included a St. George’s respiratory questionnaire score >60 (adjusted hazard ratio = 2.01; 95% CI 1.49-2.72; <em>P</em> <0.001) and HIV infection (adjusted hazard ratio = 3.04; 95% CI 1.46-6.34; <em>P</em> = 0.029).</div></div><div><h3>Conclusions</h3><div>Post-PTB mortality remains high, with poor health-related quality of life and HIV co-infection emerging as significant independent predictors of death. Integrating long-term follow-up, respiratory rehabilitation, and fungal diagnostics into post-TB care pathways is essential to improve outcomes and reduce preventable mortality.</div></div>","PeriodicalId":73335,"journal":{"name":"IJID regions","volume":"17 ","pages":"Article 100758"},"PeriodicalIF":1.7000,"publicationDate":"2025-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IJID regions","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772707625001936","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives
Treated pulmonary tuberculosis (PTB) is associated with long-term complications that contribute to substantial morbidity and mortality. We estimated the incidence and predictors of post-PTB mortality and evaluated whether chronic pulmonary aspergillosis (CPA) independently increases the risk of death.
Methods
Between July 1, 2020 and June 30, 2021, we enrolled 162 individuals with treated drug-susceptible PTB who had persistent respiratory symptoms and screened them for CPA using a symptom checklist, chest x-ray, Aspergillus immunoglobulin G-immunoglobulin M point-of-care test, and sputum culture. Between November and December 2024, we followed up all participants via phone calls to determine their vital status. On chest X-ray, PTB was classified as minimal, moderate, and far advanced disease based on involvement of one, two, or more zones, respectively, and coupled to unilateral or bilateral lung disease. Cox proportional hazards regression was used to identify independent predictors of mortality.
Results
Thirty-seven (22.8%) participants were lost to follow-up. The median follow-up duration was 3.8 years (interquartile range 3.6-3.9). Of the 125 participants with vital status, their mean age was 33.5 years (±11.7). At baseline, 46 (36.8%) had far advanced PTB, 64 (51.2%) had pulmonary fibrosis, 15 (12.0%) had a history of previous TB, and 34 (27.2%) were living with HIV. Coinfection with PTB and CPA was identified in 31 participants at baseline (24.8%). The median St. George’s respiratory questionnaire score was 50.9 (interquartile range 40.9-63.3), and 32.0% (n = 40) had scores above 60, indicating poor health-related quality of life. Overall mortality was 8.8% (95% confidence interval [CI] 4.4-15.2%), with a mortality rate of 24.3 deaths per 1000 person-years of follow-up. Mortality rates were comparable among participants with and without CPA-PTB coinfection. Independent predictors of mortality included a St. George’s respiratory questionnaire score >60 (adjusted hazard ratio = 2.01; 95% CI 1.49-2.72; P <0.001) and HIV infection (adjusted hazard ratio = 3.04; 95% CI 1.46-6.34; P = 0.029).
Conclusions
Post-PTB mortality remains high, with poor health-related quality of life and HIV co-infection emerging as significant independent predictors of death. Integrating long-term follow-up, respiratory rehabilitation, and fungal diagnostics into post-TB care pathways is essential to improve outcomes and reduce preventable mortality.
目的治疗肺结核(PTB)与长期并发症相关,导致大量发病率和死亡率。我们估计了肺结核后死亡率的发生率和预测因素,并评估了慢性肺曲霉病(CPA)是否独立增加了死亡风险。方法:在2020年7月1日至2021年6月30日期间,我们招募了162名患有持续呼吸道症状的药物敏感肺结核患者,并使用症状检查表、胸部x光片、曲霉免疫球蛋白g-免疫球蛋白M点检测和痰培养筛查CPA。在2024年11月至12月期间,我们通过电话跟踪所有参与者,以确定他们的重要状态。在胸部x线片上,PTB分别根据累及一个、两个或多个区,并合并单侧或双侧肺部疾病,分为轻度、中度和晚期疾病。采用Cox比例风险回归确定死亡率的独立预测因子。结果失访37例(22.8%)。中位随访时间为3.8年(四分位数范围3.6-3.9)。125名健康状况良好的参与者平均年龄为33.5岁(±11.7岁)。基线时,46人(36.8%)患有严重晚期肺结核,64人(51.2%)患有肺纤维化,15人(12.0%)有既往结核病史,34人(27.2%)感染艾滋病毒。在基线时,31名参与者(24.8%)同时感染PTB和CPA。圣乔治呼吸问卷得分中位数为50.9(四分位数范围40.9-63.3),32.0% (n = 40)的得分高于60,表明与健康相关的生活质量较差。总死亡率为8.8%(95%可信区间[CI] 4.4-15.2%),每1000人随访年死亡率为24.3例。有和没有CPA-PTB合并感染的参与者的死亡率是相当的。死亡率的独立预测因子包括圣乔治呼吸系统问卷得分>;60(校正风险比= 2.01;95% CI 1.49-2.72; P <0.001)和HIV感染(校正风险比= 3.04;95% CI 1.46-6.34; P = 0.029)。结论ptb后死亡率仍然很高,健康相关生活质量差和HIV合并感染成为重要的独立死亡预测因素。将长期随访、呼吸康复和真菌诊断纳入结核病后护理途径对于改善结果和降低可预防的死亡率至关重要。