Heidelberg University Hospital, German Center of Infection Research, Heidelberg, Germany.
Global Tuberculosis Programme, World Health Organization, 20 Avenue Appia, 1211Geneva, Switzerland.
Bull World Health Organ. 2023 Nov 1;101(11):730-737. doi: 10.2471/BLT.23.290901. Epub 2023 Oct 4.
The World Health Organization has developed target product profiles containing minimum and optimum targets for key characteristics for tests for tuberculosis treatment monitoring and optimization. Tuberculosis treatment optimization refers to initiating or switching to an effective tuberculosis treatment regimen that results in a high likelihood of a good treatment outcome. The target product profiles also cover tests of cure conducted at the end of treatment. The development of the target product profiles was informed by a stakeholder survey, a cost-effectiveness analysis and a patient-care pathway analysis. Additional feedback from stakeholders was obtained by means of a Delphi-like process, a technical consultation and a call for public comment on a draft document. A scientific development group agreed on the final targets in a consensus meeting. For characteristics rated of highest importance, the document lists: (i) high diagnostic accuracy (sensitivity and specificity); (ii) time to result of optimally ≤ 2 hours and no more than 1 day; (iii) required sample type to be minimally invasive, easily obtainable, such as urine, breath, or capillary blood, or a respiratory sample that goes beyond sputum; (iv) ideally the test could be placed at a peripheral-level health facility without a laboratory; and (v) the test should be affordable to low- and middle-income countries, and allow wide and equitable access and scale-up. Use of these target product profiles should facilitate the development of new tuberculosis treatment monitoring and optimization tests that are accurate and accessible for all people being treated for tuberculosis.
世界卫生组织制定了目标产品概况,其中包含了结核病治疗监测和优化用检测的关键特性的最低和最佳目标。结核病治疗优化是指启动或切换到一种有效的结核病治疗方案,从而极有可能获得良好的治疗效果。目标产品概况还涵盖了治疗结束时进行的治愈测试。制定目标产品概况的依据是利益攸关方调查、成本效益分析和患者护理路径分析。通过类似德尔菲的流程、技术咨询和公开征求对草案文件的意见,从利益攸关方那里获得了额外的反馈。一个科学发展小组在一次共识会议上就最终目标达成一致。对于被评为最重要的特性,该文件列出了:(i) 高诊断准确性(敏感性和特异性);(ii) 最佳结果的时间应不超过 2 小时,最长不超过 1 天;(iii) 所需样本类型应为微创、易于获取,例如尿液、呼吸或毛细血管血,或超越痰液的呼吸道样本;(iv) 理想情况下,该检测可在无实验室的基层卫生机构进行;(v) 检测应负担得起中低收入国家,允许广泛和公平地获得和扩大规模。使用这些目标产品概况应有助于开发新的结核病治疗监测和优化检测,这些检测对于所有接受结核病治疗的人来说都是准确和可及的。