rapid diagnostic test

快速诊断试验
  • 文章类型: Journal Article
    背景:精确的公共卫生(PPH)可以通过以时间为目标的监视和干预措施来最大化影响,空间,和流行病学特征。尽管快速诊断测试(RDT)在低资源环境中实现了无处不在的即时测试,他们的影响小于预期,部分原因是缺乏简化数据捕获和分析的功能。
    目的:我们旨在通过定义信息和数据公理以及信息利用指数(IUI)将RDT转变为PPH工具;确定设计功能以最大化IUI;并为模块化RDT功能制定开放指南(OGs),使其与数字健康工具链接以创建RDT-OG系统。
    方法:我们审查了已发表的论文,并与技术领域的专家或RDT用户进行了调查,制造,和部署来定义信息利用的特征和公理。我们开发了一个IUI,从0%到100%,并为33个世界卫生组织资格预审的RDT计算了该指数。开发RDT-OG规格是为了最大限度地提高IUI;通过开发基于OGs的疟疾和COVID-19RDT,在肯尼亚和印度尼西亚使用,评估了可行性和规格。
    结果:调查受访者(n=33)包括16名研究人员,7位技术专家,3家制造商,2名医生或护士,其他5个用户他们最关心RDT的正确使用(30/33,91%),他们的解释(28/33,85%),和可靠性(26/33,79%),并相信基于智能手机的RDT阅读器可以解决一些可靠性问题(28/33,85%),读者对复杂或多重RDT更为重要(33/33,100%)。资格预审的RDT的IUI范围为13%至75%(中位数33%)。相比之下,RDT-OG原型的IUI为91%。通过(1)创建参考RDT-OG原型;(2)在智能手机RDT阅读器上实现其功能和功能,云信息系统,和快速医疗互操作性资源;以及(3)分析RDT-OG与实验室集成的潜在公共卫生影响,监视,和生命统计系统。
    结论:政策制定者和制造商可以定义,采用,并与RDT-OG和数字健康计划协同。RDT-OG方法可以通过适应性干预措施进行实时诊断和流行病学监测,以促进通过PPH控制或消除当前和新出现的疾病。
    BACKGROUND: Precision public health (PPH) can maximize impact by targeting surveillance and interventions by temporal, spatial, and epidemiological characteristics. Although rapid diagnostic tests (RDTs) have enabled ubiquitous point-of-care testing in low-resource settings, their impact has been less than anticipated, owing in part to lack of features to streamline data capture and analysis.
    OBJECTIVE: We aimed to transform the RDT into a tool for PPH by defining information and data axioms and an information utilization index (IUI); identifying design features to maximize the IUI; and producing open guidelines (OGs) for modular RDT features that enable links with digital health tools to create an RDT-OG system.
    METHODS: We reviewed published papers and conducted a survey with experts or users of RDTs in the sectors of technology, manufacturing, and deployment to define features and axioms for information utilization. We developed an IUI, ranging from 0% to 100%, and calculated this index for 33 World Health Organization-prequalified RDTs. RDT-OG specifications were developed to maximize the IUI; the feasibility and specifications were assessed through developing malaria and COVID-19 RDTs based on OGs for use in Kenya and Indonesia.
    RESULTS: The survey respondents (n=33) included 16 researchers, 7 technologists, 3 manufacturers, 2 doctors or nurses, and 5 other users. They were most concerned about the proper use of RDTs (30/33, 91%), their interpretation (28/33, 85%), and reliability (26/33, 79%), and were confident that smartphone-based RDT readers could address some reliability concerns (28/33, 85%), and that readers were more important for complex or multiplex RDTs (33/33, 100%). The IUI of prequalified RDTs ranged from 13% to 75% (median 33%). In contrast, the IUI for an RDT-OG prototype was 91%. The RDT open guideline system that was developed was shown to be feasible by (1) creating a reference RDT-OG prototype; (2) implementing its features and capabilities on a smartphone RDT reader, cloud information system, and Fast Healthcare Interoperability Resources; and (3) analyzing the potential public health impact of RDT-OG integration with laboratory, surveillance, and vital statistics systems.
    CONCLUSIONS: Policy makers and manufacturers can define, adopt, and synergize with RDT-OGs and digital health initiatives. The RDT-OG approach could enable real-time diagnostic and epidemiological monitoring with adaptive interventions to facilitate control or elimination of current and emerging diseases through PPH.
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  • 文章类型: Journal Article
    一直在共同努力,以减少疟疾负担,并使与疟疾有关的死亡率为零。本次调查的目的是评估尼日利亚CrossRiver州公共卫生机构对现行修订后的疟疾控制指南的遵守程度,确定挑战并提出改善治疗结果的方法。
    这是一项混合观察和定性调查,于2022年6月21日至25日在32个公共卫生机构进行。评估了疟疾治疗记录是否遵守国家准则。与36个主要线人和4个有目的地选择的利益攸关方进行了深入访谈,以确定成功和挑战。在记录定性信息的同时,以简单的比例和百分比汇总和呈现定量数据,主题编码的抄本,使用NVivo11软件进行分析和呈现。
    调查显示,矢量控制程序在全州实施不力。对于案例管理,特别是在二级卫生机构中,人们经常对无并发症的疟疾进行推定治疗。超过60%的无并发症疟疾正在使用肠胃外蒿甲醚代替推荐的口服青蒿素联合疗法(ACTs)进行治疗。在约40%的二级医疗机构中,未将青蒿琥酯静脉注射(IV)作为一线药物治疗严重的疟疾。在妊娠期疟疾管理方面取得了重大成功。确定的主要挑战包括:商品缺货,临床人力短缺,对寄生虫学诊断的信任度低。
    调查显示,公共卫生机构中的卫生保健提供者对各类疟疾控制的关键建议的遵守程度低于预期。使用SP进行妊娠的疟疾预防治疗效果更好,也许是因为它包含在ANC包装中。
    UNASSIGNED: There has been a concerted effort to reduce malaria burden and bring malaria related mortality to zero. The objectives of this survey were to assess the level of adherence to the current revised malaria control guidelines in the public health facilities in Cross River State of Nigeria and to identify the challenges as well as suggest ways for improvement in treatment outcomes.
    UNASSIGNED: This was a mixed observational and qualitative survey conducted in 32 public health facilities from 21st to 25th June 2022. Treatment records on malaria were assessed for adherence to the National guidelines. In-depth interviews were conducted with 36 key informants and 4 purposefully selected stakeholders to identify the successes and challenges. Quantitative data were summarized and presented in simple proportions and percentages while qualitative information was recorded, the transcripts thematically coded, analyzed and presented using NVivo 11 software.
    UNASSIGNED: The survey revealed that vector control program was poorly implemented across the state. For case management, presumptive treatment was frequently practiced especially at secondary health facilities for uncomplicated malaria. More than 60% of uncomplicated malaria were being treated with parenteral artemether instead of oral artemisinin combination therapy (ACTs) as recommended. Severe malaria were not treated with Intravenous (IV) Artesunate as first line drug in about 40% of the secondary health facilities. Key successes were noted in malaria management in pregnancy. Major challenges identified include: stock out of commodities, shortage of clinical man power, and low trust in parasitological diagnosis.
    UNASSIGNED: The survey showed that adherence to the key recommendations in various categories of malaria control among health care providers in the public health facilities was below expectation. Malaria preventive treatment in pregnancy with SP fared better perhaps because of its inclusion in ANC packages.
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