量化巴西结核病治疗过程中的差距:利用国家项目数据进行数学模型研究。

IF 15.8 1区 医学 Q1 Medicine
PLoS Medicine Pub Date : 2024-03-21 eCollection Date: 2024-03-01 DOI:10.1371/journal.pmed.1004361
Sivaram Emani, Kleydson Alves, Layana Costa Alves, Daiane Alves da Silva, Patricia Bartholomay Oliveira, Marcia C Castro, Ted Cohen, Rodrigo de Macedo Couto, Mauro Sanchez, Nicolas A Menzies
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引用次数: 0

摘要

背景:在巴西,许多结核病患者由于诊断延误或漏诊、治疗方案无效或失去随访而得不到适当的治疗。本研究旨在估算巴西结核病治疗过程中的每一个缺口所造成的健康损失和结核病项目成本:我们构建了一个马尔可夫模型,模拟巴西结核病患者的治疗过程和终生健康结果(如死亡、治愈、感染后遗症)。我们按照年龄、人类免疫缺陷病毒(HIV)感染状况、耐药性、居住州和疾病严重程度对模型进行了分层,并为获得假阳性肺结核诊断的非肺结核患者开发了一个平行模型。模型与 2018 年巴西应报疾病信息系统(SINAN)和死亡率信息系统(SIM)的数据(成人和儿童)进行了拟合。利用这些模型,我们评估了当前的项目绩效,并模拟了消除护理级联中特定差距的假设情景,以量化护理级联中的增量健康损失和结核病诊断与治疗成本。通过比较存活率和非致死性残疾与无结核病反事实情景的变化,计算出结核病导致的残疾调整生命年(DALYs)。我们估计,90.0%(95% 不确定区间 [UI]:85.2-93.4)的结核病患者开始接受治疗,10.0%(95% 不确定区间 [UI]:7.6-12.5)的患者死于结核病。在巴西各地,每例肺结核病例造成的可归因于肺结核的残疾调整寿命年数各不相同,从阿克里州的 2.9(95% UI:2.3 至 3.6)个残疾调整寿命年数到南里奥格兰德州的 4.0(95% UI:3.3 至 4.7)个残疾调整寿命年数不等(全国平均为 3.5 [95% UI:2.8 至 4.1])。在整个治疗过程中,延误诊断造成的健康损失最大,其次是结核病后遗症和结核病治疗后的随访损失,如果剔除这些因素,结核病的残疾调整寿命年数将分别减少 71%(95% UI:65 至 76)、41%(95% UI:36 至 49)和 10%(95% UI:7 至 16)。医疗系统的总成本基本未受治疗流程改进的影响,而治疗失败因素的消除则使可归因成本降低了 3.1%(95% UI:1.5 至 5.4)。对假阳性患者的结核病诊断和治疗占项目总成本的 10.2%(95% UI:3.9 至 21.7),但对健康损失的影响微乎其微。为了对项目数据进行分析,我们需要做出一些假设,而且我们无法估计社会因素对治疗结果的影响:在这项研究中,我们注意到诊断延误、疾病后遗症和随访治疗损失是造成巴西结核病负担的主要原因。为改善巴西的结核病负担,应优先考虑减少诊断延误、改善结核病治愈后的医疗保健以及减少治疗后的随访损失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantifying gaps in the tuberculosis care cascade in Brazil: A mathematical model study using national program data.

Background: In Brazil, many individuals with tuberculosis (TB) do not receive appropriate care due to delayed or missed diagnosis, ineffective treatment regimens, or loss-to-follow-up. This study aimed to estimate the health losses and TB program costs attributable to each gap in the care cascade for TB disease in Brazil.

Methods and findings: We constructed a Markov model simulating the TB care cascade and lifetime health outcomes (e.g., death, cure, postinfectious sequelae) for individuals developing TB disease in Brazil. We stratified the model by age, human immunodeficiency virus (HIV) status, drug resistance, state of residence, and disease severity, and developed a parallel model for individuals without TB that receive a false-positive TB diagnosis. Models were fit to data (adult and pediatric) from Brazil's Notifiable Diseases Information System (SINAN) and Mortality Information System (SIM) for 2018. Using these models, we assessed current program performance and simulated hypothetical scenarios that eliminated specific gaps in the care cascade, in order to quantify incremental health losses and TB diagnosis and treatment costs along the care cascade. TB-attributable disability-adjusted life years (DALYs) were calculated by comparing changes in survival and nonfatal disability to a no-TB counterfactual scenario. We estimated that 90.0% (95% uncertainty interval [UI]: 85.2 to 93.4) of individuals with TB disease initiated treatment and 10.0% (95% UI: 7.6 to 12.5) died with TB. The average number of TB-attributable DALYs per incident TB case varied across Brazil, ranging from 2.9 (95% UI: 2.3 to 3.6) DALYs in Acre to 4.0 (95% UI: 3.3 to 4.7) DALYs in Rio Grande do Sul (national average 3.5 [95% UI: 2.8 to 4.1]). Delayed diagnosis contributed the largest health losses along the care cascade, followed by post-TB sequelae and loss to follow up from TB treatment, with TB DALYs reduced by 71% (95% UI: 65 to 76), 41% (95% UI: 36 to 49), and 10% (95% UI: 7 to 16), respectively, when these factors were eliminated. Total health system costs were largely unaffected by improvements in the care cascade, with elimination of treatment failure reducing attributable costs by 3.1% (95% UI: 1.5 to 5.4). TB diagnosis and treatment of false-positive individuals accounted for 10.2% (95% UI: 3.9 to 21.7) of total programmatic costs but contributed minimally to health losses. Several assumptions were required to interpret programmatic data for the analysis, and we were unable to estimate the contribution of social factors to care cascade outcomes.

Conclusions: In this study, we observed that delays to diagnosis, post-disease sequelae and treatment loss to follow-up were primary contributors to the TB burden of disease in Brazil. Reducing delays to diagnosis, improving healthcare after TB cure, and reducing treatment loss to follow-up should be prioritized to improve the burden of TB disease in Brazil.

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来源期刊
PLoS Medicine
PLoS Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
17.60
自引率
0.60%
发文量
227
审稿时长
4-8 weeks
期刊介绍: PLOS Medicine is a prominent platform for discussing and researching global health challenges. The journal covers a wide range of topics, including biomedical, environmental, social, and political factors affecting health. It prioritizes articles that contribute to clinical practice, health policy, or a better understanding of pathophysiology, ultimately aiming to improve health outcomes across different settings. The journal is unwavering in its commitment to uphold the highest ethical standards in medical publishing. This includes actively managing and disclosing any conflicts of interest related to reporting, reviewing, and publishing. PLOS Medicine promotes transparency in the entire review and publication process. The journal also encourages data sharing and encourages the reuse of published work. Additionally, authors retain copyright for their work, and the publication is made accessible through Open Access with no restrictions on availability and dissemination. PLOS Medicine takes measures to avoid conflicts of interest associated with advertising drugs and medical devices or engaging in the exclusive sale of reprints.
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