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Slide positivity, trends, and risk factors of febrile Plasmodium vivax malaria along the Thailand-Myanmar border, 2018-2023. 2018-2023年泰缅边境发热性间日疟原虫疟疾的阳性、趋势和危险因素
IF 5.5 1区 医学 Pub Date : 2025-08-06 DOI: 10.1186/s40249-025-01350-4
Pyae Linn Aung, Nattawan Rachaphaew, Piyarat Sripoorote, Khaing Zin Zin Htwe, Kritsana Suk-Aum, Jaranit Kaewkungwal, Saranath Lawpoolsri, Liwang Cui, Jetsumon Sattabongkot

Background: Plasmodium vivax is the predominant malaria species in many Southeast Asian countries. Eliminating all human malaria species by 2030 requires greater focus on P. vivax, with targeted measures to address its unique challenges. This study evaluated slide positivity rates, temporal trends, and risk factors associated with febrile P. vivax infections in a malaria-endemic district along the Thailand-Myanmar border.

Methods: This study employed a community-based longitudinal surveillance design over six years (January 2018-December 2023). Data were collected through routine passive case detection at field malaria clinics using extended, standardized case record forms. Malaria diagnosis was conducted via microscopy examination. Descriptive statistics and logistic regression models were used for data analysis.

Results: Among 13,347 febrile malaria-suspected patients, the cumulative slide positivity rate for P. vivax was 11.0%. Although no distinct seasonal peaks were observed, P. vivax cases generally increased in April and again in November and December. Multivariable logistic regression analysis identified several significant risk factors for febrile P. vivax infection, including school-aged children (5-14 years) (aOR: 1.56, 95% CI: 1.24-1.97), working-age adults (15-34 years) (aOR: 1.43, 95% CI: 1.02-2.00), males (aOR: 1.19, 95% CI: 1.06-1.35), Myanmar nationals (aOR: 2.37, 95% CI: 2.01-2.80), and other non-Thai nationals, such as individuals from Laos and Cambodia (aOR: 5.50, 95% CI: 3.36-8.90). A history of malaria (aOR: 1.59, 95% CI: 1.38-1.83), recent travel within two weeks (aOR: 2.38, 95% CI: 1.94-2.92), and engagement in livestock-related occupations (aOR: 2.49, 95% CI: 1.14-5.35) were also associated with higher odds of infection. In contrast, being unemployed (aOR: 0.55, 95% CI: 0.36-0.81), working in occupations such as maid, driver, or teacher (aOR: 0.78, 95% CI: 0.66-0.93), and consistent use of bed nets (aOR: 0.39, 95% CI: 0.30-0.51) significantly reduced infection risk.

Conclusions: This study identified a relatively high slide positivity rate of febrile P. vivax infection in a malaria-endemic district in western Thailand along the Myanmar border. Strengthening malaria surveillance, targeting high-risk populations, ensuring treatment adherence, and promoting early care-seeking behavior are crucial for reducing P. vivax transmission and advancing malaria elimination efforts.

背景:间日疟原虫是东南亚许多国家的主要疟疾种。到2030年消除所有人类疟疾物种需要更加关注间日疟原虫,并采取有针对性的措施来应对其独特的挑战。本研究评估了沿泰国-缅甸边境疟疾流行地区与发热间日疟原虫感染相关的载玻片阳性率、时间趋势和危险因素。方法:本研究采用社区纵向监测设计,为期6年(2018年1月- 2023年12月)。数据是通过在实地疟疾诊所使用扩展的标准化病例记录表进行常规被动病例检测收集的。通过显微镜检查进行疟疾诊断。采用描述性统计和逻辑回归模型进行数据分析。结果:13347例发热疟疑似患者中间日疟原虫累积载玻片阳性率为11.0%。虽然没有观察到明显的季节性高峰,间日疟病例普遍在4月和11月和12月增加。多变量logistic回归分析确定了发热性间日疟原虫感染的几个重要危险因素,包括学龄儿童(5-14岁)(aOR: 1.56, 95% CI: 1.24-1.97)、工作年龄成年人(15-34岁)(aOR: 1.43, 95% CI: 1.02-2.00)、男性(aOR: 1.19, 95% CI: 1.06-1.35)、缅甸国民(aOR: 2.37, 95% CI: 2.01-2.80)和其他非泰国国民,如老挝和柬埔寨人(aOR: 5.50, 95% CI: 3.36-8.90)。疟疾史(aOR: 1.59, 95% CI: 1.38-1.83)、最近两周内的旅行(aOR: 2.38, 95% CI: 1.94-2.92)以及从事与牲畜相关的职业(aOR: 2.49, 95% CI: 1.14-5.35)也与较高的感染几率相关。相比之下,失业(aOR: 0.55, 95% CI: 0.36-0.81)、从事女佣、司机或教师等职业(aOR: 0.78, 95% CI: 0.66-0.93)和持续使用蚊帐(aOR: 0.39, 95% CI: 0.30-0.51)显著降低了感染风险。结论:本研究发现,在泰国西部沿缅甸边境的疟疾流行区,热性间日疟原虫感染的载玻片阳性率相对较高。加强疟疾监测、针对高危人群、确保坚持治疗和促进早期求医行为对于减少间日疟原虫传播和推进消除疟疾工作至关重要。
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引用次数: 0
Enhancing regional disease burden estimates: insights from the comparison of Global Burden of Disease and China's notifiable infectious diseases data with policy implications (2010-2020). 加强区域疾病负担估算:2010-2020年全球疾病负担与中国法定传染病数据比较的启示
IF 5.5 1区 医学 Pub Date : 2025-08-06 DOI: 10.1186/s40249-025-01351-3
Zi-Yu Zhao, Jiao-Jiao Li, Han-Qi Ouyang, Wei-Hao Li, Sheng-Kai Huang, Okugbe Ebiotubo Ohore, Lu Wang, Jürg Utzinger, Guo-Jing Yang

Background: The Global Burden of Disease (GBD) study offers influential Disability-Adjusted Life Years (DALYs) estimates for various diseases. However, discrepancies with national surveillance data raise concerns about accuracy. This study aims to promote the deep integration of the GBD model with localized data and facilitate the development of region-specific models.

Methods: Data for 14 notifiable infectious diseases (NIDs), grouped into intestinal infectious diseases, respiratory infectious diseases, and sexually transmitted and blood-borne infections, were obtained from the Data-center of China Public Health Science. DALYs based on national surveillance data (2010-2020) were calculated using DALY formulas, and discrepancies with GBD estimates were quantified through ratio comparisons. A historical timeline map highlighted key infectious disease control policies and certified disease elimination events in China.

Results: National surveillance data show a decrease in DALYs for 14 NIDs in China, from 6,529,124.62 person-years in 2010 to 6,326,497.18 person-years in 2020. Among them, sexually transmitted and blood-borne infections have the highest burden, with 78% of DALYs attributed to hepatitis B (4,864,028.29 person-years). Respiratory infectious diseases follow, with 99% of DALYs from TB (394,927.70 person-years). Intestinal infectious diseases have the relative lightest burden, with 45% of DALYs from hepatitis E (496.49 person-years). Over 11 years, 9 of the 14 NIDs showed a downward trend. Comparisons reveal that DALYs based on national surveillance data are lower than GBD 2021 estimates.

Conclusions: Considerable differences exist between the GBD estimates and national surveillance data regarding the burden of 14 NIDs in China. Therefore, strengthening national reporting systems and integrating localized data with the GBD model is essential for more accurate disease burden assessments and effective response strategies. Despite significant progress in infectious disease control, China still faces substantial challenges in domestic disease elimination.

背景:全球疾病负担(GBD)研究为各种疾病提供了有影响力的残疾调整生命年(DALYs)估计。然而,与国家监测数据的差异引起了对准确性的担忧。本研究旨在促进GBD模型与本地化数据的深度融合,促进区域模型的发展。方法:从中国公共卫生科学数据中心获取14种法定传染病(NIDs)的数据,分为肠道传染病、呼吸道传染病、性传播和血源性感染。使用DALY公式计算基于国家监测数据(2010-2020年)的DALY,并通过比率比较量化与GBD估计值的差异。历史时间轴地图突出了中国主要传染病控制政策和经认证的疾病消除事件。结果:国家监测数据显示,中国14个NIDs的DALYs从2010年的6,529,124.62人年减少到2020年的6,326,497.18人年。其中,性传播感染和血源性感染负担最重,78%的伤残调整生命年归因于乙型肝炎(4,864,028.29人年)。其次是呼吸道传染病,99%的伤残调整生命年来自结核病(394,927.70人年)。肠道感染性疾病的负担相对较轻,戊型肝炎(496.49人-年)的DALYs占45%。在11年中,14个国家中有9个国家呈现下降趋势。比较表明,基于国家监测数据的伤残调整生命年低于2021年《GBD》估计值。结论:关于中国14个国家传染病负担的GBD估计值与国家监测数据之间存在相当大的差异。因此,加强国家报告系统并将本地化数据与GBD模型相结合,对于更准确地评估疾病负担和制定有效的应对战略至关重要。尽管中国在传染病控制方面取得了重大进展,但在消除国内疾病方面仍面临重大挑战。
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引用次数: 0
From words to action: the development of the Neglected Tropical Disease Inclusion Score Card (NISC). 从语言到行动:被忽视热带病纳入记分卡(NISC)的发展。
IF 5.5 1区 医学 Pub Date : 2025-08-05 DOI: 10.1186/s40249-025-01340-6
Robin van Wijk, Surya J M Baudoin, Bernice Ejiogu, Upasana Regmi, Mathias Duck, Ibrahim Rabiu, Constanze Vettel, Heleen Broekkamp, Roos Geutjes, Ruth M H Peters, Ida J Korfage

Background: The importance of patient participation in designing and delivering services for persons affected by neglected tropical diseases (NTDs) has gained increasing recognition. Responding to this, persons affected by NTDs urged NTD-focused non-governmental organisations (NGOs) to take action. These NGOs are pivotal in addressing healthcare disparities and reaching marginalised communities. To address the insufficient progress on participation, a participatory initiative was launched to develop a tool designed to support NGOs in fostering inclusion and ensuring the meaningful engagement of affected persons in their organisational decision-making processes.

Methods: This research used an iterative, mixed-methods approach involving stakeholder input, semi-structured interviews, and surveys across two phases. Phase 1 included exploratory workshops with persons affected by NTDs and NTD NGO employees which led to the development of a first draft of a self-assessment tool. Phase 2 involved piloting the tool in NTD NGOs. Data were gathered via pre- and post-pilot interviews and surveys. Thematic analysis was used for the qualitative data and descriptive analysis for the quantitative data.

Results: In phase 1, exploratory workshops revealed that meaningful participation involves creating environments where affected persons can openly share priorities and build their capacity. Workshop participants emphasised the need of inclusion at all stages of NGO activities. These insights informed the draft NTD Inclusion Scorecard (NISC), covering six domains. In phase 2, ten pilot sessions were conducted, feedback was gathered from 22 interviewees and 43 survey participants, focusing on the NISC's usability and relevance. While feedback on the NISC was positive, participants highlighted the need for contextualisation, organisational commitment, and adding a communication domain to the NISC.

Conclusions: The NISC is a self-assessment tool for NTD organisations, designed to enhance internal decision-making by fostering awareness of the importance of including the perspectives of persons affected by NTDs. By using the NISC, NGOs can identify gaps in inclusion and participation, improve their decision-making processes and provide services that are relevant and impactful for persons affected by NTDs. This tool provides insights that can guide NGOs in strengthening their role in promoting inclusion and increasing the effectiveness of their programmes.

背景:患者参与为被忽视的热带病(NTDs)患者设计和提供服务的重要性已得到越来越多的认识。对此,受热带病影响的人敦促以热带病为重点的非政府组织采取行动。这些非政府组织在解决保健差距和接触边缘化社区方面发挥着关键作用。为了解决在参与方面进展不足的问题,发起了一项参与性倡议,以开发一种工具,旨在支持非政府组织促进包容并确保受影响者有意义地参与其组织决策过程。方法:本研究采用迭代的混合方法,包括利益相关者输入、半结构化访谈和跨两个阶段的调查。第一阶段包括与受NTDs影响的人和NTDs非政府组织雇员的探索性讲习班,从而制定了自我评估工具的初稿。第二阶段是在新唐病非政府组织中试用该工具。数据通过试点前和试点后的访谈和调查收集。定性数据采用专题分析,定量数据采用描述性分析。结果:在第一阶段,探索性研讨会表明,有意义的参与包括创造环境,使受影响的人可以公开分享优先事项并建立他们的能力。讲习班与会者强调非政府组织活动的所有阶段都需要纳入。这些见解为NTD包含记分卡(NISC)草案提供了信息,涵盖了六个领域。在第二阶段,进行了10次试点会议,收集了22名受访者和43名调查参与者的反馈,重点关注NISC的可用性和相关性。虽然对NISC的反馈是积极的,但参与者强调了对情境化、组织承诺和在NISC中添加通信领域的需求。结论:NISC是NTD组织的自我评估工具,旨在通过培养包括受NTD影响的人的观点的重要性的认识来加强内部决策。通过使用国家信息中心,非政府组织可以确定在包容和参与方面的差距,改进其决策过程,并为受被忽视热带病影响的人提供相关和有影响力的服务。该工具提供了一些见解,可以指导非政府组织加强其在促进包容和提高其计划有效性方面的作用。
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引用次数: 0
Risk factor for gametocyte carriage and gametocytemia in Plasmodium vivax and Plasmodium falciparum. 间日疟原虫和恶性疟原虫配子细胞携带和配子细胞血症的危险因素。
IF 5.5 1区 医学 Pub Date : 2025-08-04 DOI: 10.1186/s40249-025-01352-2
Minxi Li, Yang Bian, Shishao Ruan, Zifang Wu, Di Zhang, Tongyu Ma, Yaming Wu, Xiao Liu, Duo Wang, Jia Lin, Danni Pan, Wenyan Cui, Lin Wang, Haichao Wei, Xuexing Zhang, Qinghui Wang, Weilin Zeng, Zhaoqing Yang, Yaming Cao, Liwang Cui, Daniel M Parker, Yan Zhao

Background: Understanding Plasmodium sexual differentiation is crucial for blocking transmission. This study identified risk factors for gametocyte carriage and gametocytemia in P. vivax and P. falciparum to inform malaria elimination strategies at the China-Myanmar border.

Methods: Gametocytes and asexual parasites were microscopically detected on thick smears collected from 2011 to 2020 in Laiza Township, Kachin State, Myanmar. Mono-/polyclonality were detected by genotyping at Pvmsp3α/β for P. vivax, and Pfmsp1/2 for P. falciparum. Kulldorff's retrospective time scan statistics tested for likely clusters of gametocyte-positive cases over time. Chi-square or Fisher's exact tests compared proportions of gametocyte-positive cases in categorical variables. Generalized linear models assessed risk factors (year, season, demographics, clinical/parasitological features) for gametocyte carriage (logistic regression for a binomial outcome) and gametocytemia (Gaussian regression for continuous outcome), respectively.

Results: During 2011-2020, 8240 patients had P. vivax infections, with 7249 testing positive for gametocytes. Among 510 P. falciparum cases, 56 tested positive for gametocytes. A significant cluster of P. vivax gametocyte carriage occurred from May 2015 to August 2017 (P = 0.001). For P. vivax, dry season, previous malaria history, fever, and parasite density were associated with gametocyte carriage. Gametocyte density increased with asexual parasite density (P < 0.001) but was lower during the rainy season and in those with a history of malaria infection (P < 0.001). Over time, gametocytes carriage proportion increased while density decreased (P < 0.001). For P. falciparum, younger age and previous malaria history were associated with gametocyte carriage, and density was higher in the dry season (P = 0.0115). Polyclonal P. vivax infections had higher gametocyte densities than monoclonal infections (P < 0.0001) and P. falciparum gametocyte density tended to increase with multiplicity of infection.

Conclusions: Younger age, prior malaria infection, travel, and polyclonal infections correlate with higher P. vivax gametocyte prevalence. Gametocyte carriage peakes during the dry season, highlighting the need for seasonal strategies to support malaria elimination. These findings enhance understanding of risk factors for the transmissible stage of the two main human Plasmodium species in the Greater Mekong Subregion border areas.

背景:了解疟原虫的性别分化对阻断传播至关重要。本研究确定间日疟原虫和恶性疟原虫配子细胞携带和配子细胞血症的危险因素,为中缅边境的疟疾消除战略提供信息。方法:对2011 - 2020年在缅甸克钦邦莱扎镇采集的厚涂片进行配子体和无性寄生虫的显微镜检测。间日疟原虫Pvmsp3α/β和恶性疟原虫Pfmsp1/2基因分型检测单/多克隆性。Kulldorff的回顾性时间扫描统计数据测试了随着时间的推移可能出现的配子细胞阳性病例群。卡方检验或Fisher精确检验比较了配子细胞阳性病例在分类变量中的比例。广义线性模型分别评估配子细胞携带(二项结果的逻辑回归)和配子细胞血症(连续结果的高斯回归)的危险因素(年份、季节、人口统计学、临床/寄生虫学特征)。结果:2011-2020年,8240例间日疟原虫感染,其中7249例配子细胞检测阳性。在510例恶性疟原虫病例中,56例配子细胞检测呈阳性。2015年5月至2017年8月间日疟原虫配子体携带显著聚集(P = 0.001)。对于间日疟原虫,干旱季节、既往疟疾史、发热和寄生虫密度与配子体携带有关。结论:年龄较小、既往疟疾感染、旅行和多克隆感染与间日疟原虫配子细胞的高流行率相关。配子体携带在旱季达到高峰,这突出表明需要采取季节性战略来支持消除疟疾。这些发现加强了对大湄公河次区域边境地区两种主要人类疟原虫传播阶段危险因素的认识。
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引用次数: 0
One Health: enabler of effective prevention, control and elimination of emerging and re-emerging infectious diseases. 同一个健康:促进有效预防、控制和消除新出现和再出现的传染病。
IF 5.5 1区 医学 Pub Date : 2025-07-31 DOI: 10.1186/s40249-025-01337-1
Tianyun Li, Xiao-Nong Zhou, Marcel Tanner

Emerging and re-emerging infectious diseases in different soci-ecological settings create unprecedented challenges for global public health and socio-economic development. The One Health concept is based on a systemic, transdisciplinary approach and hence captures the interactions between humans and animals, in a given socio-ecological setting. It could comprehensively address the human-animal-environment interface, the core of zoonotic diseases. Consequently, One Health approach is effective in controlling and eliminating the promoting factors of emerging infectious diseases (EIDs). We explored key principles for the prevention, control and elimination of EIDs through reviewing the transition of public health and global health strategies towards One Health and summarizing some successful experiences in effectively controlling EIDs. Recognizing heterogeneities and strengthening "surveillance-response systems" are the two key principles. It is recommended to promote health equity and conduct cost-effectiveness analysis to address the challenges of heterogeneity. Cross-sectoral collaboration and transdisciplinarity should be strengthened to facilitate the utilizing of systems thinking.

在不同的社会生态环境中新出现和再出现的传染病给全球公共卫生和社会经济发展带来了前所未有的挑战。“同一个健康”概念基于一种系统的、跨学科的方法,因此在特定的社会生态环境中捕捉到了人与动物之间的相互作用。它可以全面解决人-动物-环境界面,人畜共患疾病的核心。因此,“同一个健康”方法在控制和消除新发传染病的促进因素方面是有效的。我们通过回顾公共卫生和全球卫生战略向“同一个健康”的转变,总结有效控制eid的一些成功经验,探讨了预防、控制和消除eid的关键原则。认识到异质性和加强“监测-反应系统”是两个关键原则。建议促进卫生公平并进行成本效益分析,以应对异质性的挑战。应加强跨部门合作和跨学科合作,以促进系统思维的利用。
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引用次数: 0
Test accuracy of loop-mediated isothermal amplification for schistosomiasis in low endemicity areas: a systematic review and meta-analysis. 低流行地区血吸虫病环介导等温扩增的检测准确性:系统回顾和荟萃分析。
IF 5.5 1区 医学 Pub Date : 2025-07-31 DOI: 10.1186/s40249-025-01346-0
Xinjie Zhou, Jiajia Li, Jiayin Qiu, Ting Feng, Chao Lv, Wangping Deng, Robert Bergquist, Jing Xu, Shizhu Li, Zhiqiang Qin

Background: Schistosomiasis, caused by parasitic flatworms of the genus Schistosoma, remains a significant public health challenge in tropical and subtropical regions, affecting over hundreds of millions of people in these areas. Accurate diagnosis is crucial for effective disease control, particularly in low-endemic areas where traditional methods like microscopy are no longer effective. We aimed to evaluate the diagnostic performance of loop-mediated isothermal amplification (LAMP) for Schistosoma infection.

Methods: Adhering to Preferred reporting items for systematic reviews and meta-analyses guidelines, we conducted a comprehensive search on 10 May 2025 across multiple databases including PubMed, Cochrane Library, Latin American and Caribbean Literature on Health Sciences, Embase, China National Knowledge Infrastructure, and Wanfang Data, using keywords such as "schistosom*", "LAMP", and "loop-mediated isothermal amplification". Based on available literature, pooled sensitivity, specificity, positive likelihood ratio (PLR), negative likelihood ratio (NLR) and 95% confidential interval (CI) were calculated using STATA18.0 software. Subgroup analyses and univariable meta-regression were performed to explore the source of heterogeneity. Specifically, subgroup analyses were performed by categorizing into species (S. japonicum, S. mansoni, S. haematobium), sample type (stool, urine, serum, snails), and DNA extraction methods to explore factors influencing test performance.

Results: The study finally included 24 individual studies derived from 14 published articles. The pooled analyses of LAMP data from all included studies resulted in a sensitivity of 0.90 (95% CI: 0.80-0.90), specificity of 0.82 (95% CI: 0.60-0.93), PLR of 4.98 (95% CI: 2.01-12.29), NLR of 0.13 (95% CI: 0.06-0.26) and diagnostic odds ratio of 39 (95% CI: 10-158). The area under the summary receiver operating characteristic curve reached 0.93, indicating excellent diagnostic performance. Subgroup analyses revealed optimal performance for S. japonicum and snail samples with lower heterogeneity (I2 < 50%).

Conclusions: LAMP shows promise as a rapid, sensitive and specific diagnostic tool for schistosomiasis, particularly in resource-limited settings. This technique enables field application, supporting global efforts toward elimination of schistosomiasis by 2030.

背景:由血吸虫属寄生扁虫引起的血吸虫病仍然是热带和亚热带地区的一个重大公共卫生挑战,影响到这些地区数亿人。准确的诊断对于有效的疾病控制至关重要,特别是在显微镜等传统方法不再有效的低流行地区。我们旨在评估环介导等温扩增(LAMP)对血吸虫感染的诊断性能。方法:根据系统评价和荟萃分析指南的首选报告项目,我们于2025年5月10日在PubMed、Cochrane Library、Latin American and Caribbean Literature on Health Sciences、Embase、中国国家知识基础设施和万方数据等多个数据库中进行了全面检索,检索关键词为“血吸虫*”、“LAMP”和“环介导等温扩增”。根据现有文献,采用STATA18.0软件计算合并敏感性、特异性、阳性似然比(PLR)、阴性似然比(NLR)和95%置信区间(CI)。采用亚组分析和单变量元回归来探讨异质性的来源。具体而言,通过分类(日本血吸虫、mansoni血吸虫、haematobium血吸虫)、样品类型(粪便、尿液、血清、钉螺)和DNA提取方法进行亚群分析,探讨影响检测性能的因素。结果:该研究最终纳入了来自14篇已发表文章的24项独立研究。对所有纳入研究的LAMP数据进行汇总分析,结果显示敏感性为0.90 (95% CI: 0.80-0.90),特异性为0.82 (95% CI: 0.60-0.93), PLR为4.98 (95% CI: 2.01-12.29), NLR为0.13 (95% CI: 0.06-0.26),诊断优势比为39 (95% CI: 10-158)。患者工作特征曲线下面积达到0.93,诊断效果良好。亚组分析显示,在日本血吸虫和蜗牛样本中表现最佳,异质性较低(2)。结论:LAMP有望成为血吸虫病的快速、敏感和特异性诊断工具,特别是在资源有限的环境中。该技术可用于实地应用,支持到2030年消除血吸虫病的全球努力。
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引用次数: 0
A spatial clustering-based approach to design monitoring networks of infectious diseases: a case study of hand, foot, and mouth disease. 基于空间聚类的传染病监测网络设计方法:以手足口病为例。
IF 5.5 1区 医学 Pub Date : 2025-07-28 DOI: 10.1186/s40249-025-01331-7
Shuting Li, Yuanhua Liu, Ke Li, Zengliang Wang, Michael P Ward, Wei Tu, Jiayao Xu, Rui Yuan, Lele Zhang, Na Wang, Jidan Zhang, Yu Zhao, Henry S Lynn, Zhaorui Chang, Zhijie Zhang

Background: Effective monitoring of infectious diseases is crucial for safeguarding public health. Compared to comprehensive nationwide surveillance, selecting representative sample cities to constitute the monitoring network for surveillance provides similar effectiveness at a lower cost. We developed Spatial Cluster Stratified Sampling (SCSS) to select sample cities for infectious diseases exhibiting spatial autocorrelation.

Methods: To improve monitoring efficiency for hand, foot, and mouth disease (HFMD), we used SCSS to design a monitoring network, which involved four main steps. First, we used Spatial Kluster Analysis by Tree Edge Removal (SKATER) to stratify the data. Second, we applied the cost-benefit balance to determine the optimal sample size. Third, we performed simple random sampling within each stratum to establish an initial monitoring network. Fourth, we used cyclic optimization to finalize the monitoring network. We evaluated the spatiotemporal representativeness using root mean square error (RMSE), Spearman's rank correlation, global Moran's I, local Getis-Ord G*, and Joinpoint Regression. We also compared the effectiveness of SCSS with K-means, traditional stratified sampling, and simple random sampling using RMSE.

Results: The optimal sample size was determined to be 103. Overall, the predicted values for each city significantly correlated with the true values (r = 0.81, P < 0.001). Both the predicted and true values showed positive spatial autocorrelation (Moran's I > 0, P < 0.05), and the sensitivity, specificity, and accuracy of the predicted local Getis-Ord G* values, evaluated against the true values as the gold standard, were 0.76, 0.91, and 0.87, respectively. The weekly predicted values for each city showed significant correlation with the true values (P < 0.05). The 95% confidence intervals (CI) for the predicted values of joinpoint locations, annual percent change (APC), and average annual percent change (AAPC) encompassed the true values, and the number of joinpoints matched the true values. Among the four methods compared, SCSS exhibited the lowest and most centralized RMSE.

Conclusions: SCSS proved to be more accurate and stable than traditional methods, which overlook spatial information. This method offers a valuable reference for future design of monitoring networks for infectious diseases exhibiting spatial autocorrelation, enabling more efficient and cost-effective surveillance.

背景:有效监测传染病对保障公众健康至关重要。与全国范围的综合监测相比,选择有代表性的样本城市组成监测网络进行监测,以较低的成本提供了相似的效果。采用空间聚类分层抽样(SCSS)方法,选取具有空间自相关性的传染病样本城市。方法:为提高手足口病(手足口病)监测效率,采用SCSS设计监测网络,主要分为四个步骤。首先,我们使用空间聚类分析(Spatial Kluster Analysis by Tree Edge Removal, SKATER)对数据进行分层。其次,运用成本效益平衡法确定最优样本量。第三,在每个地层内进行简单随机抽样,建立初始监测网络。第四,采用循环优化方法确定监测网络。我们使用均方根误差(RMSE)、Spearman等级相关、全局Moran’s I、局部Getis-Ord G*和连接点回归来评估时空代表性。我们还比较了SCSS与K-means、传统分层抽样和使用RMSE的简单随机抽样的有效性。结果:确定最佳样本量为103份。总体而言,各城市的预测值与真实值显著相关(r = 0.81, P = 0, P)。结论:SCSS比忽略空间信息的传统方法更准确、更稳定。该方法为今后设计具有空间自相关性的传染病监测网络提供了有价值的参考,可实现更高效、更经济的监测。
{"title":"A spatial clustering-based approach to design monitoring networks of infectious diseases: a case study of hand, foot, and mouth disease.","authors":"Shuting Li, Yuanhua Liu, Ke Li, Zengliang Wang, Michael P Ward, Wei Tu, Jiayao Xu, Rui Yuan, Lele Zhang, Na Wang, Jidan Zhang, Yu Zhao, Henry S Lynn, Zhaorui Chang, Zhijie Zhang","doi":"10.1186/s40249-025-01331-7","DOIUrl":"10.1186/s40249-025-01331-7","url":null,"abstract":"<p><strong>Background: </strong>Effective monitoring of infectious diseases is crucial for safeguarding public health. Compared to comprehensive nationwide surveillance, selecting representative sample cities to constitute the monitoring network for surveillance provides similar effectiveness at a lower cost. We developed Spatial Cluster Stratified Sampling (SCSS) to select sample cities for infectious diseases exhibiting spatial autocorrelation.</p><p><strong>Methods: </strong>To improve monitoring efficiency for hand, foot, and mouth disease (HFMD), we used SCSS to design a monitoring network, which involved four main steps. First, we used Spatial Kluster Analysis by Tree Edge Removal (SKATER) to stratify the data. Second, we applied the cost-benefit balance to determine the optimal sample size. Third, we performed simple random sampling within each stratum to establish an initial monitoring network. Fourth, we used cyclic optimization to finalize the monitoring network. We evaluated the spatiotemporal representativeness using root mean square error (RMSE), Spearman's rank correlation, global Moran's I, local Getis-Ord G*, and Joinpoint Regression. We also compared the effectiveness of SCSS with K-means, traditional stratified sampling, and simple random sampling using RMSE.</p><p><strong>Results: </strong>The optimal sample size was determined to be 103. Overall, the predicted values for each city significantly correlated with the true values (r = 0.81, P < 0.001). Both the predicted and true values showed positive spatial autocorrelation (Moran's I > 0, P < 0.05), and the sensitivity, specificity, and accuracy of the predicted local Getis-Ord G* values, evaluated against the true values as the gold standard, were 0.76, 0.91, and 0.87, respectively. The weekly predicted values for each city showed significant correlation with the true values (P < 0.05). The 95% confidence intervals (CI) for the predicted values of joinpoint locations, annual percent change (APC), and average annual percent change (AAPC) encompassed the true values, and the number of joinpoints matched the true values. Among the four methods compared, SCSS exhibited the lowest and most centralized RMSE.</p><p><strong>Conclusions: </strong>SCSS proved to be more accurate and stable than traditional methods, which overlook spatial information. This method offers a valuable reference for future design of monitoring networks for infectious diseases exhibiting spatial autocorrelation, enabling more efficient and cost-effective surveillance.</p>","PeriodicalId":48820,"journal":{"name":"Infectious Diseases of Poverty","volume":"14 1","pages":"76"},"PeriodicalIF":5.5,"publicationDate":"2025-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12302676/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144734488","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Are there differences in efficacy and safety between local and imported direct-acting antiviral agents for hepatitis C in China? 在中国,本地和进口的直接作用型丙型肝炎抗病毒药物的疗效和安全性是否存在差异?
IF 5.5 1区 医学 Pub Date : 2025-07-25 DOI: 10.1186/s40249-025-01344-2
Zhitao Wang, Youbing Ran, Yihan Fu, Jing Sun, Yuanli Liu

Background: Despite price advantages, local direct-acting antiviral agents (DAAs) for hepatitis C (hep C) have not been widely used in China compared with the imported ones. There is no evidence on their relative efficacy and safety, nor whether the small market share of local DAAs was attributable to the potential differences.

Methods: This study systematically evaluated the efficacy and safety evidence of 5 local and 6 imported DAAs with valid Chinese registration numbers as of January 25, 2024. Meta-analyses, subgroup analyses and meta-regressions were performed to synthesize evidence and compared the outcomes by using the random-effects empirical Bayes model.

Results: Nineteen randomized controlled trials and 82 single-arm trials (SATs) were included. The results demonstrated no statistically significant difference in 12-week sustained virological response [0.97, (95% confidence interval (CI) 0.95, 0.99) vs 0.96, (95% CI: 0.94, 0.98), P = 0.21], relapse [0.02, (95% CI: 0.01, 0.04) vs 0.02, (95% CI: 0.01, 0.03), P = 0.65], virological breakthrough [0.003, (95% CI: < 0.001, 0.02) vs 0.0000002, (95% CI: < 0.001, 0.0006), P = 0.51] and serious adverse events (SAEs) [0.04, (95% CI: 0.03, 0.06) vs 0.03, (95% CI: 0.02, 0.03), P = 0.12] between local and imported DAAs. By controlling for ethnicities of patients in multiple meta-regression, the local DAAs had a 33.7% higher rate of adverse events (AEs) [0.337, (95% CI: 0.188, 0.486), P < 0.001]. No statistically significant difference was found in the interaction test between local and imported pan-genotypic DAAs regarding the rate of AEs [0.72, (95% CI: 0.64, 0.79) vs 0.73, (95% CI: 0.65, 0.50), P = 0.81].

Conclusions: Current evidence demonstrates no statistically significant differences in efficacy and SAEs between local and imported DAAs. Given that simplified pan-genotypic DAA regimens are now standard care, local pan-genotypic DAAs hold potential to increase hepatitis C virus treatment rates in China. It is critical for local DAA developers to generate more evidence with expanded patient population in terms of age, treatment experience and genotype of hepatitis C virus, conducting head-to-head studies directly comparing the efficacy and safety. Clinical and policy decision-making should be adaptive and evolve as new evidence is generated.

背景:尽管具有价格优势,但国产丙型肝炎直接作用抗病毒药物(DAAs)在中国的应用并不像进口药物那样广泛。没有证据表明它们的相对有效性和安全性,也没有证据表明当地daa的小市场份额是否归因于潜在的差异。方法:本研究系统评价了截至2024年1月25日的5种国产daa和6种进口daa的有效性和安全性证据。采用随机效应实证贝叶斯模型进行meta分析、亚组分析和meta回归分析,综合证据并比较结果。结果:纳入19项随机对照试验和82项单臂试验(SATs)。结果显示,12周持续病毒学应答[0.97,(95%可信区间(CI) 0.95, 0.99) vs 0.96, (95% CI: 0.94, 0.98), P = 0.21],复发率[0.02,(95% CI: 0.01, 0.04) vs 0.02, (95% CI: 0.01, 0.03), P = 0.65],病毒学突破[0.003,(95% CI: P = 0.65)],病毒学突破[0.003],(95% CI:结论:目前证据显示,本地DAAs与进口DAAs在疗效和SAEs方面无统计学差异。鉴于简化的泛基因型DAA方案现在是标准治疗,本地泛基因型DAA有可能提高中国丙型肝炎病毒的治疗率。对于当地的DAA开发人员来说,至关重要的是在年龄、治疗经验和丙型肝炎病毒基因型方面获得更多的证据,进行直接比较疗效和安全性的头对头研究。临床和政策决策应随着新证据的产生而适应和发展。
{"title":"Are there differences in efficacy and safety between local and imported direct-acting antiviral agents for hepatitis C in China?","authors":"Zhitao Wang, Youbing Ran, Yihan Fu, Jing Sun, Yuanli Liu","doi":"10.1186/s40249-025-01344-2","DOIUrl":"10.1186/s40249-025-01344-2","url":null,"abstract":"<p><strong>Background: </strong>Despite price advantages, local direct-acting antiviral agents (DAAs) for hepatitis C (hep C) have not been widely used in China compared with the imported ones. There is no evidence on their relative efficacy and safety, nor whether the small market share of local DAAs was attributable to the potential differences.</p><p><strong>Methods: </strong>This study systematically evaluated the efficacy and safety evidence of 5 local and 6 imported DAAs with valid Chinese registration numbers as of January 25, 2024. Meta-analyses, subgroup analyses and meta-regressions were performed to synthesize evidence and compared the outcomes by using the random-effects empirical Bayes model.</p><p><strong>Results: </strong>Nineteen randomized controlled trials and 82 single-arm trials (SATs) were included. The results demonstrated no statistically significant difference in 12-week sustained virological response [0.97, (95% confidence interval (CI) 0.95, 0.99) vs 0.96, (95% CI: 0.94, 0.98), P = 0.21], relapse [0.02, (95% CI: 0.01, 0.04) vs 0.02, (95% CI: 0.01, 0.03), P = 0.65], virological breakthrough [0.003, (95% CI: < 0.001, 0.02) vs 0.0000002, (95% CI: < 0.001, 0.0006), P = 0.51] and serious adverse events (SAEs) [0.04, (95% CI: 0.03, 0.06) vs 0.03, (95% CI: 0.02, 0.03), P = 0.12] between local and imported DAAs. By controlling for ethnicities of patients in multiple meta-regression, the local DAAs had a 33.7% higher rate of adverse events (AEs) [0.337, (95% CI: 0.188, 0.486), P < 0.001]. No statistically significant difference was found in the interaction test between local and imported pan-genotypic DAAs regarding the rate of AEs [0.72, (95% CI: 0.64, 0.79) vs 0.73, (95% CI: 0.65, 0.50), P = 0.81].</p><p><strong>Conclusions: </strong>Current evidence demonstrates no statistically significant differences in efficacy and SAEs between local and imported DAAs. Given that simplified pan-genotypic DAA regimens are now standard care, local pan-genotypic DAAs hold potential to increase hepatitis C virus treatment rates in China. It is critical for local DAA developers to generate more evidence with expanded patient population in terms of age, treatment experience and genotype of hepatitis C virus, conducting head-to-head studies directly comparing the efficacy and safety. Clinical and policy decision-making should be adaptive and evolve as new evidence is generated.</p>","PeriodicalId":48820,"journal":{"name":"Infectious Diseases of Poverty","volume":"14 1","pages":"75"},"PeriodicalIF":5.5,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12291330/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144709610","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Clinical confirmation of an infection with Echinococcus multilocularis (Mongolian genotype): first case report of human alveolar echinococcosis in Inner Mongolia, China. 多房棘球蚴(蒙古基因型)感染的临床证实:内蒙古首例人肺泡棘球蚴病报告。
IF 5.5 1区 医学 Pub Date : 2025-07-24 DOI: 10.1186/s40249-025-01342-4
Xu Wang, Zhan-Jun Xiao, Chui-Zhao Xue, Wen-Ting Wu, Jiang-Hui Yang, Chun Yan, Ying Wang, Yan Kui, Wen-Bo Luo, Xi Du, Run-Na Zan, Rong-Jian Shang, Sa Li, Rigen Na, Shuai Han, Shi-Zhu Li

Background: Alveolar echinococcosis (AE), caused by the larval stage of Echinococcus multilocularis, poses a substantial global health challenge due to its high mortality profile. This study reports the inaugural human infection of echinococcosis caused by the Mongolian genotype of E. multilocularis in China, also the first reported indigenous AE case in Inner Mongolia.

Case presentation: A 58-year-old female pastoralist from Inner Mongolia, who had no endemic region exposure history but prolonged occupational contact with dogs, presented with severe AE. Clinical examinations revealed a massive hepatic lesion exceeding 10 cm in diameter, accompanied by elevated eosinophils (0.90 × 109/L) and basophils (0.08 × 109/L). Despite undergoing liver transplantation, the patient succumbed postoperatively. Histopathological confirmation and molecular phylogenetics identified the Mongolian genotype of E. multilocularis infection, distinct from the predominant Asian genotype in China. Potential evidence of zoonotic transmission was discovered through genotype-matched E. multilocularis detection in corsac fox (Vulpes corsac) feces from the grasslands along the shores of Hulun Lake (Hulun Buir City, northeastern Inner Mongolia, China).

Conclusions: This report provides the primary evidence of a locally acquired human AE infection in China caused by the Mongolian genotype of Echinococcus multilocularis. The discovery of this case challenges historical classifications of echinococcosis endemic areas. The findings call for revised AE-endemic identification criteria, improved AE diagnostic protocols, and enhanced AE surveillance in the Inner Mongolia region to generate further epidemiological evidence and information on disease progression.

背景:肺泡棘球蚴病(AE)是由多房棘球蚴幼虫期引起的,由于其高死亡率,对全球健康构成了重大挑战。本研究报告了中国首例由蒙古基因型多房棘球绦虫引起的人感染棘球绦虫病,也是内蒙古首例报道的本土棘球绦虫病例。病例表现:内蒙古女牧民,58岁,无疫区暴露史,长期职业接触犬,表现为严重AE。临床检查发现肝脏病变,直径超过10 cm,伴嗜酸性粒细胞升高(0.90 × 109/L),嗜碱性粒细胞升高(0.08 × 109/L)。尽管接受了肝移植,患者还是在术后死亡。组织病理学和分子系统发育证实蒙古多房绦虫感染基因型与中国主要的亚洲基因型不同。通过在内蒙古东北部呼伦贝尔市呼伦贝尔湖滨草原的狐狸粪便中检测到基因型匹配的多房棘球绦虫,发现了人畜共患传播的潜在证据。结论:本报告提供了蒙古基因型多房棘球蚴引起的中国本地获得性人AE感染的初步证据。该病例的发现对棘球蚴病流行地区的历史分类提出了挑战。研究结果呼吁修订AE流行鉴定标准,改进AE诊断方案,并加强内蒙古地区AE监测,以获得进一步的流行病学证据和疾病进展信息。
{"title":"Clinical confirmation of an infection with Echinococcus multilocularis (Mongolian genotype): first case report of human alveolar echinococcosis in Inner Mongolia, China.","authors":"Xu Wang, Zhan-Jun Xiao, Chui-Zhao Xue, Wen-Ting Wu, Jiang-Hui Yang, Chun Yan, Ying Wang, Yan Kui, Wen-Bo Luo, Xi Du, Run-Na Zan, Rong-Jian Shang, Sa Li, Rigen Na, Shuai Han, Shi-Zhu Li","doi":"10.1186/s40249-025-01342-4","DOIUrl":"10.1186/s40249-025-01342-4","url":null,"abstract":"<p><strong>Background: </strong>Alveolar echinococcosis (AE), caused by the larval stage of Echinococcus multilocularis, poses a substantial global health challenge due to its high mortality profile. This study reports the inaugural human infection of echinococcosis caused by the Mongolian genotype of E. multilocularis in China, also the first reported indigenous AE case in Inner Mongolia.</p><p><strong>Case presentation: </strong>A 58-year-old female pastoralist from Inner Mongolia, who had no endemic region exposure history but prolonged occupational contact with dogs, presented with severe AE. Clinical examinations revealed a massive hepatic lesion exceeding 10 cm in diameter, accompanied by elevated eosinophils (0.90 × 10<sup>9</sup>/L) and basophils (0.08 × 10<sup>9</sup>/L). Despite undergoing liver transplantation, the patient succumbed postoperatively. Histopathological confirmation and molecular phylogenetics identified the Mongolian genotype of E. multilocularis infection, distinct from the predominant Asian genotype in China. Potential evidence of zoonotic transmission was discovered through genotype-matched E. multilocularis detection in corsac fox (Vulpes corsac) feces from the grasslands along the shores of Hulun Lake (Hulun Buir City, northeastern Inner Mongolia, China).</p><p><strong>Conclusions: </strong>This report provides the primary evidence of a locally acquired human AE infection in China caused by the Mongolian genotype of Echinococcus multilocularis. The discovery of this case challenges historical classifications of echinococcosis endemic areas. The findings call for revised AE-endemic identification criteria, improved AE diagnostic protocols, and enhanced AE surveillance in the Inner Mongolia region to generate further epidemiological evidence and information on disease progression.</p>","PeriodicalId":48820,"journal":{"name":"Infectious Diseases of Poverty","volume":"14 1","pages":"74"},"PeriodicalIF":5.5,"publicationDate":"2025-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12288280/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144709611","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mass drug administration trials of azithromycin: an analysis to inform future research and guidelines. 阿奇霉素的大规模给药试验:为未来研究和指南提供信息的分析。
IF 8.1 1区 医学 Pub Date : 2025-07-21 DOI: 10.1186/s40249-025-01322-8
Alex C Kong, Anthony D So

Background: In 2020, the World Health Organization published a guideline on the use of mass drug administration (MDA) of the broad-spectrum antibiotic azithromycin to reduce childhood mortality. As MDA-azithromycin to reduce mortality is considered for expansion to more settings and populations, care must be taken to maximize benefits and reduce risks (e.g., antimicrobial resistance or AMR) of this intervention. Completed and ongoing MDA-azithromycin cluster-randomized clinical trials can provide evidence on the extent to which these benefits and risks accrue and identify practices to monitor these effects and address evidence gaps in future trials.

Methods: We examined azithromycin clinical trials registered on ClinicalTrials.gov and the WHO International Clinical Trials Registry Platform from registry inception to December 31, 2023. We included trials for which azithromycin was administered for the prevention or treatment of a disease or condition that was not explicitly diagnosed or necessary for participant inclusion, and for which treatment was randomized by geographic units. We identified evidence, knowledge gaps, and trends and highlights across five domains: (1) targeting of MDA-azithromycin, (2) clinical endpoints, (3) co- and competing interventions, (4) spillover effects, and (5) AMR monitoring.

Results: Of 1589 screened studies, 30 met all inclusion criteria. These trials were conducted in 13 countries, predominantly (26/30) in sub-Saharan Africa. Nearly a third (9/30) of the trials included mortality endpoints, but few (2/9) included cause-specific mortality endpoints. New evidence suggests the benefits of widening the target age group and the persistence of mortality benefits in settings with competing interventions. Published practices to ensure geographic separation of communities in different treatment arms to reduce spillover effects were not customary. We found information on AMR monitoring practices for just over half the trials (16/30). Of these, half (8/16) included both phenotypic and genotypic AMR testing, and more than half collected specimens to assess the nasopharyngeal and gut microbiomes (9/16) and tested for non-macrolide resistance (11/16).

Conclusions: Further long-term MDA-azithromycin studies to determine which additional countries could benefit, interventions to accompany or replace this intervention, and the extent to which AMR spillover occurs may prove valuable as guidelines are revised.

背景:2020年,世界卫生组织发布了一份关于使用广谱抗生素阿奇霉素大规模给药(MDA)以降低儿童死亡率的指南。由于考虑将用于降低死亡率的mda -阿奇霉素推广到更多环境和人群,因此必须注意使这种干预措施的效益最大化并降低风险(例如,抗菌素耐药性或AMR)。完成和正在进行的mda -阿奇霉素集群随机临床试验可以提供证据,证明这些益处和风险的累积程度,并确定监测这些效果的做法,并解决未来试验中证据不足的问题。方法:我们分析了从注册开始到2023年12月31日在ClinicalTrials.gov和WHO国际临床试验注册平台注册的阿奇霉素临床试验。我们纳入了阿奇霉素用于预防或治疗非明确诊断或非参与者纳入所必需的疾病或病症的试验,以及按地理单位随机分配治疗的试验。我们确定了五个领域的证据、知识差距、趋势和重点:(1)靶向mda -阿奇霉素,(2)临床终点,(3)协同和竞争干预措施,(4)溢出效应,(5)AMR监测。结果:在1589项筛选研究中,30项符合所有纳入标准。这些试验在13个国家进行,主要(26/30)在撒哈拉以南非洲。近三分之一(9/30)的试验包括死亡率终点,但很少(2/9)的试验包括病因特异性死亡率终点。新的证据表明,在相互竞争的干预措施环境中,扩大目标年龄组和持续降低死亡率的好处。已公布的确保不同治疗领域的社区在地理上分开以减少溢出效应的做法并非惯例。我们在超过一半的试验(16/30)中发现了有关抗菌素耐药性监测实践的信息。其中,一半(8/16)包括表型和基因型AMR检测,一半以上收集标本评估鼻咽和肠道微生物组(9/16)并检测非大环内酯类药物耐药性(11/16)。结论:随着指南的修订,进一步的长期mda -阿奇霉素研究可能会证明是有价值的,以确定哪些国家可以受益,哪些干预措施可以伴随或取代这种干预措施,以及抗生素耐药性溢出发生的程度。
{"title":"Mass drug administration trials of azithromycin: an analysis to inform future research and guidelines.","authors":"Alex C Kong, Anthony D So","doi":"10.1186/s40249-025-01322-8","DOIUrl":"10.1186/s40249-025-01322-8","url":null,"abstract":"<p><strong>Background: </strong>In 2020, the World Health Organization published a guideline on the use of mass drug administration (MDA) of the broad-spectrum antibiotic azithromycin to reduce childhood mortality. As MDA-azithromycin to reduce mortality is considered for expansion to more settings and populations, care must be taken to maximize benefits and reduce risks (e.g., antimicrobial resistance or AMR) of this intervention. Completed and ongoing MDA-azithromycin cluster-randomized clinical trials can provide evidence on the extent to which these benefits and risks accrue and identify practices to monitor these effects and address evidence gaps in future trials.</p><p><strong>Methods: </strong>We examined azithromycin clinical trials registered on ClinicalTrials.gov and the WHO International Clinical Trials Registry Platform from registry inception to December 31, 2023. We included trials for which azithromycin was administered for the prevention or treatment of a disease or condition that was not explicitly diagnosed or necessary for participant inclusion, and for which treatment was randomized by geographic units. We identified evidence, knowledge gaps, and trends and highlights across five domains: (1) targeting of MDA-azithromycin, (2) clinical endpoints, (3) co- and competing interventions, (4) spillover effects, and (5) AMR monitoring.</p><p><strong>Results: </strong>Of 1589 screened studies, 30 met all inclusion criteria. These trials were conducted in 13 countries, predominantly (26/30) in sub-Saharan Africa. Nearly a third (9/30) of the trials included mortality endpoints, but few (2/9) included cause-specific mortality endpoints. New evidence suggests the benefits of widening the target age group and the persistence of mortality benefits in settings with competing interventions. Published practices to ensure geographic separation of communities in different treatment arms to reduce spillover effects were not customary. We found information on AMR monitoring practices for just over half the trials (16/30). Of these, half (8/16) included both phenotypic and genotypic AMR testing, and more than half collected specimens to assess the nasopharyngeal and gut microbiomes (9/16) and tested for non-macrolide resistance (11/16).</p><p><strong>Conclusions: </strong>Further long-term MDA-azithromycin studies to determine which additional countries could benefit, interventions to accompany or replace this intervention, and the extent to which AMR spillover occurs may prove valuable as guidelines are revised.</p>","PeriodicalId":48820,"journal":{"name":"Infectious Diseases of Poverty","volume":"14 1","pages":"73"},"PeriodicalIF":8.1,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12278655/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144683498","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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Infectious Diseases of Poverty
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