Torch Consortium FAMPOP Faculty of Medicine and Health Sciences, University of Antwerp, Antwerpen, Belgium.
Department of Computer Science, ADReM Data Lab, University of Antwerp, Antwerpen, Belgium.
PLoS One. 2024 Sep 6;19(9):e0306101. doi: 10.1371/journal.pone.0306101. eCollection 2024.
Rifampicin resistant tuberculosis remains a global health problem with almost half a million new cases annually. In high-income countries patients empirically start a standardized treatment regimen, followed by an individualized regimen guided by drug susceptibility test (DST) results. In most settings, DST information is not available or is limited to isoniazid and fluoroquinolones. Whole genome sequencing could more accurately guide individualized treatment as the full drug resistance profile is obtained with a single test. Whole genome sequencing has not reached its full potential for patient care, in part due to the complexity of translating a resistance profile into the most effective individualized regimen.
We developed a treatment recommender clinical decision support system (CDSS) and an accompanying web application for user-friendly recommendation of the optimal individualized treatment regimen to a clinician.
Following expert stakeholder meetings and literature review, nine drug features and 14 treatment regimen features were identified and quantified. Using machine learning, a model was developed to predict the optimal treatment regimen based on a training set of 3895 treatment regimen-expert feedback pairs. The acceptability of the treatment recommender CDSS was assessed as part of a clinical trial and in a routine care setting. Within the clinical trial setting, all patients received the CDSS recommended treatment. In 8 of 20 cases, the initial recommendation was recomputed because of stock out, clinical contra-indication or toxicity. In routine care setting, physicians rejected the treatment recommendation in 7 out of 15 cases because it deviated from the national TB treatment guidelines. A survey indicated that the treatment recommender CDSS is easy to use and useful in clinical practice but requires digital infrastructure support and training.
Our findings suggest that global implementation of the novel treatment recommender CDSS holds the potential to improve treatment outcomes of patients with RR-TB, especially those with 'difficult-to-treat' forms of RR-TB.
利福平耐药结核病仍然是一个全球性的健康问题,每年有近 50 万例新发病例。在高收入国家,患者根据经验开始标准化治疗方案,然后根据药物敏感性测试 (DST) 结果制定个体化方案。在大多数情况下,DST 信息不可用或仅限于异烟肼和氟喹诺酮类药物。全基因组测序可以更准确地指导个体化治疗,因为可以通过单次测试获得完整的耐药谱。全基因组测序尚未充分发挥其在患者护理中的潜力,部分原因是将耐药谱转化为最有效的个体化治疗方案的复杂性。
我们开发了一种治疗推荐临床决策支持系统 (CDSS) 及其配套的网络应用程序,以便临床医生方便地推荐最佳个体化治疗方案。
在专家利益相关者会议和文献回顾之后,确定并量化了九种药物特征和 14 种治疗方案特征。使用机器学习,我们开发了一种模型,根据 3895 种治疗方案-专家反馈对的训练集来预测最佳治疗方案。该治疗推荐 CDSS 的可接受性作为临床试验和常规护理环境的一部分进行了评估。在临床试验环境中,所有患者均接受了 CDSS 推荐的治疗。在 20 例中有 8 例,由于库存不足、临床禁忌症或毒性,初始推荐被重新计算。在常规护理环境中,由于与国家结核病治疗指南有偏差,医生拒绝了 15 例中的 7 例治疗建议。一项调查表明,该治疗推荐 CDSS 易于使用且在临床实践中有用,但需要数字基础设施支持和培训。
我们的研究结果表明,新型治疗推荐 CDSS 的全球实施有可能改善 RR-TB 患者的治疗结果,特别是那些具有“难治疗”形式的 RR-TB 的患者。