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Evaluation of a medication monitor-based treatment strategy for drug-sensitive tuberculosis patients in China: study protocol for a cluster randomised controlled trial

机译:中国药物敏感结核患者的药物疗效治疗策略评价:集群随机对照试验的研究议定书

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Treatment for drug-sensitive tuberculosis (TB) is taken for at least 6 months and problems with adherence are common. Therefore, there is substantial interest in the possible use of eHealth interventions to support patients to take their treatment. Electronic medication monitors have been shown to improve adherence to TB medication, but the impact on clinical outcomes is unknown. We aim to evaluate the impact of a medication monitor-based treatment strategy for drug-sensitive TB patients on a composite poor outcome measured over 18?months from start of TB treatment. We will conduct an open, pragmatic, cluster randomised superiority trial, with 24 counties/districts in three provinces in China, randomised 1:1 to implement the intervention or standard of care. Adults (aged ≥?18?years) with a new episode of GeneXpert-positive and rifampicin-sensitive pulmonary TB, who plan to be in the study area for the next 18?months, and will receive daily fixed-dose combination tablets for 6 months of treatment are eligible. The intervention is centred around a medication monitor that holds a 1-month supply of medication and has three key functions:?as an audio and visual reminder for patients to take their daily medication; reminds patients of upcoming monthly visit; and records date and time whenever the box is opened. At the monthly follow-up visit, the doctor downloads these data to generate a graphical display of the last month's adherence record for discussion with the patient and potentially to switch the patient to more intensive management. The primary outcome is a composite poor outcome measured over 18?months from start of TB treatment, defined as either of poor outcome at the end of treatment (death, treatment failure, or loss to follow-up) or subsequent recurrence (culture positive for TB at 12 or 18?months or re-starting TB treatment in the follow-up period). An economic evaluation will also be conducted as part of this study. This trial will assess whether a medication monitor-based treatment strategy can improve clinical outcomes for TB patients. Several trials of other eHealth interventions for TB treatment are ongoing and are summarised in this paper. This trial will provide an important part of the emerging evidence base for the potential of eHealth to improve TB treatment outcomes. This trial was registered with Current Controlled Trials (identifier: ISRCTN35812455 ). Registered on May 19, 2016.
机译:对药物敏感结核病(TB)的治疗持续至少6个月,粘附问题是常见的。因此,对可能使用电子健康干预措施来支持患者进行治疗。已显示电子药物监测器可改善粘附到TB药物,但对临床结果的影响是未知的。我们的目标是评估药物敏感的治疗策略对药物敏感TB患者的影响,从TB治疗开始超过18岁以下的数月测量的综合较差的结果。我们将开放,务实,随机的优势试验,三个省在中国的24个县/地区,随机1:1实施干预或护理标准。成人(年龄≥18岁?年)具有新的Genexpert阳性和利福平敏感的肺结核,计划在接下来的18个月内进行研究区域,并将收到每日固定剂组合片剂6几个月的治疗有资格。干预围绕着一种药物监测仪,拥有1个月的药物供应,并有三个关键功能:作为患者的音频和视觉提醒,以获取日常药物;提醒患者即将到来的每月访问;并在打开框时记录日期和时间。在每月后续访问时,医生下载这些数据以生成上个月的遵守记录的图形显示,以便与患者讨论,并可能将患者切换到更密集的管理。主要结果是从结核病治疗开始超过18个月的综合差的结果,定义为治疗结束时的结果(死亡,治疗失败或随访)或随后的复发(培养阳性TB在12或18个月,或在随访期间重新开始结核病治疗)。还将作为本研究的一部分进行的经济评估。该试验将评估一种基于药物监测症的治疗策略是否可以改善TB患者的临床结果。对TB治疗的其他eHealth干预的几项试验正在进行中,并在本文中综述。本次审判将为新兴证据基础提供新出现的证据基础,以改善TB治疗结果。该试验在目前的受控试验中注册(标识符:ISRCTN35812455)。 2016年5月19日注册。

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