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Hotspot districts of persistent Plasmodium vivax malaria pose a formidable challenge to malaria elimination in India 间日疟原虫持续流行的热点地区对印度消除疟疾构成了巨大挑战
IF 6.2 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-09-18 DOI: 10.1016/j.lansea.2025.100662
Amala Ramasamy , Kannan Thiruvengadam , Anju Viswan K , Rohit Sharma , Shriram Ananganallur Nagarajan , Chander Prakash Yadav , Amit Sharma , Manju Rahi
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引用次数: 0
Epidemiology of Human Metapneumovirus (HMPV) in India: a cross-sectional study 印度人偏肺病毒(HMPV)流行病学:一项横断面研究
IF 6.2 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-09-17 DOI: 10.1016/j.lansea.2025.100667
Rizwan Suliankatchi Abdulkader , Neetu Vijay , Varsha Potdar , Joshua Chadwick , Jitendra Narayan , Sabarinathan Ramasamy , Devika Shanmugasundaram , Selvavinayagam Thirumalaicheri Sivaprakasam , Manoj Murhekar , Nivedita Gupta
<div><h3>Background</h3><div>The Department of Health Research, Ministry of Health and Family Welfare, India, established the Virus Research and Diagnostic Laboratory Network (VRDLN) in 2014 to strengthen viral diagnostic capabilities and provide a system for routine virological surveillance. In 2022, we also initiated the Model for Integrated Influenza Surveillance in Tamil Nadu (MIST) to enhance surveillance of virologic and clinical characteristics of severe acute respiratory infections (SARI) cases in selected sentinel tertiary care hospitals. This study investigates the epidemiology of Human Metapneumovirus (HMPV) in India by analysing data from these distinct but related surveillance systems.</div></div><div><h3>Methods</h3><div>We analysed VRDLN data from 2019 to 2024 to describe HMPV cases based on time, place, and personal characteristics. We presented a comparison of two periods—2019 to 2023 and 2024—to compare historical trends with the current scenario. We also examined detailed clinical and laboratory profiles of HMPV-positive SARI cases collected under the MIST project from 2022 to 2024 (a case series). Hospitals under the VRDLN conducted testing of any physician-referred patient, while MIST exclusively tested SARI patients who met a standardised case definition. While the VRDLN provided an overall picture of the testing and positivity trends, MIST provided details on laboratory parameters, and clinical course and outcomes of positive cases. All laboratories adhered to standardised quality-assured testing protocols and reported data to a centralized database.</div></div><div><h3>Findings</h3><div>Between 2019 and 2023, the VRDLN tested 20,625 patients for HMPV, of whom 1030 (3.2%) were positive. In 2024, 11,155 patients were tested, with 367 (3.3%) confirmed positive. Across both periods, age-stratified analysis indicated that the majority of tests were conducted among children. The highest positivity was observed in those aged 1–2 years, with 4.5% (128/2864) testing positive in 2019–2023 and 4.6% (70/1508) in 2024. Most HMPV-positive cases presented with Acute Respiratory Infection (ARI)/Influenza-like illness (ILI), accounting for 85.4% [566/17,090] of cases in 2019–2023 and 40.3% [148/1697] in 2024, as most testing was carried out among these patients. Fever and cough were the most common symptoms, reported in 70.3% of cases from 2019 to 2023 and 79.6% (292/8398) in 2024, and in 60.5% (401/12,059) and 60.8% (223/5977) of cases, respectively. Under the MIST project, we tested 3599 SARI patients between 2022 and 2023, identifying 28 (0.8%) HMPV-positive cases. Patients experienced a median illness duration of 11 days (interquartile range [IQR]: 7.5–14.5) and stayed in the hospital for a median of 7 days (IQR: 5–9.5). Eight cases required intensive care for a median of 3.5 days (IQR: 2.5–6), while 12 cases needed oxygen support for a median of three days (IQR: 3–5.5). Among the 28 cases, 25 (89.3) showed clinical improvement at disc
印度卫生和家庭福利部卫生研究司于2014年建立了病毒研究和诊断实验室网络(VRDLN),以加强病毒诊断能力并提供常规病毒学监测系统。2022年,我们还启动了泰米尔纳德邦流感综合监测模式(MIST),以加强对选定哨点三级保健医院严重急性呼吸道感染(SARI)病例的病毒学和临床特征的监测。本研究通过分析来自这些不同但相关的监测系统的数据,调查了印度人偏肺病毒(HMPV)的流行病学。方法分析2019 - 2024年VRDLN数据,根据时间、地点和个人特征对HMPV病例进行描述。我们提出了2019年至2023年和2024年两个时期的比较,将历史趋势与当前情景进行比较。我们还检查了2022年至2024年在MIST项目下收集的hmpv阳性SARI病例的详细临床和实验室资料(一个病例系列)。VRDLN下的医院对任何医生转诊的患者进行检测,而MIST只对符合标准化病例定义的严重急性呼吸道感染患者进行检测。VRDLN提供了检测和阳性趋势的总体情况,而MIST提供了实验室参数、阳性病例的临床过程和结果的详细信息。所有实验室都遵守有质量保证的标准化检测方案,并向中央数据库报告数据。在2019年至2023年期间,VRDLN检测了20,625例HMPV患者,其中1030例(3.2%)呈阳性。2024年,11,155例患者接受了检测,其中367例(3.3%)确诊为阳性。在这两个时期,年龄分层分析表明,大多数测试是在儿童中进行的。1-2岁年龄组阳性率最高,2019-2023年阳性率为4.5%(128/2864),2024年阳性率为4.6%(70/1508)。大多数hmpv阳性病例表现为急性呼吸道感染(ARI)/流感样疾病(ILI), 2019-2023年占病例的85.4%[566/17,090],2024年占40.3%[148/1697],因为大多数检测是在这些患者中进行的。发烧和咳嗽是最常见的症状,2019 - 2023年和2024年分别占70.3%和79.6%(292/8398),分别占60.5%(401/ 12059)和60.8%(223/5977)。在MIST项目下,我们在2022年至2023年间检测了3599名SARI患者,确定了28例(0.8%)hmpv阳性病例。患者病程中位数为11天(四分位数差[IQR]: 7.5-14.5),住院时间中位数为7天(IQR: 5-9.5)。8例需要重症监护,中位数为3.5天(IQR: 2.5-6), 12例需要氧气支持,中位数为3天(IQR: 3-5.5)。28例患者出院时临床好转25例(89.3例),1个月随访时健康22例(84.6例)。截至2025年4月,12例患者保持健康,1例出现复发性肺部并发症,6例失去随访。2024年检测的增加和更高的阳性率凸显了印度越来越多的人认识到HMPV是一种重要的呼吸道病原体。然而,我们注意到HMPV的流行病学特征最近没有变化。加强监测网络对于了解这种新出现的病毒性病原体的负担和指导公共卫生政策仍然至关重要。尽管在我们的监测人群中检测到HMPV表明与疾病有潜在关联,但不应将其视为因果关系的明确证据。此外,住院时间应该在潜在的未测量的合并感染和合并症的背景下解释,而不是仅仅归因于HMPV感染。资助:由印度政府卫生和家庭福利部卫生研究司资助。
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引用次数: 0
Incidence patterns of rare cancer in southeast Asian and western Pacific countries (RARECAREnet Asia project): a study using population-based cancer registry data, 2011–2015 东南亚和西太平洋国家罕见癌症发病率模式(RARECAREnet Asia项目):2011-2015年基于人群的癌症登记数据研究
IF 6.2 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-09-12 DOI: 10.1016/j.lansea.2025.100670
Patumrat Sripan , Siti Norbayah Yusof , Donsuk Pongnikorn , Imjai Chitapanarux , Balqis Bahtiar , Nor Saleha Ibrahim Tamin , Karnchana Daoprasert , Narate Waisri , Young-Joo Won , RuRu Chun-Ju Chiang , Annalisa Trama , Hadrien Charvat , Kriengkrai Srithanaviboonchai , Tomohiro Matsuda

Background

In Southeast Asia (SEA), the understanding of most rare cancers is limited, which sometimes leads to delays in diagnosis, treatment, and care. This study aimed to estimate for the first time the incidence of rare cancers in SEA using population-based cancer registry (PBCR) data from the 2011–2015 period.

Methods

This study used data from the nationwide PBCR of Malaysia and two PBCRs in northern Thailand in Chiang Mai and Lampang Cancer registries. The age-standardized incidence rate (ASR) per 100,000 person-year of the rare cancers included in the RARECAREnet list was calculated. All analyses were performed using SEER∗Stat (version 8.3.5). Cancers defined as rare by RARECAREnet in Europe were also rare in Thailand and Malaysia.

Findings

The ASR of some rare cancers in Thailand and Malaysia were greater than that in Japan, Korea, and Taiwan, including some pediatric cancers (pancreatoblastoma and odontogenic malignant tumors) in Malaysia, eye and adnexal cancer, and epithelial tumors of the penis in Thailand. ASR of nasopharyngeal cancer was higher in Thailand and Malaysia than in Japan and Korea but lower compared to Taiwan.

Interpretation

Although most rare cancers were also rare in Thailand and Malaysia, some cancers were not considered rare. However, the incidence of some rare cancers in Thailand and Malaysia were higher than that in Japan, Korea, and Taiwan. To enhance understanding, diagnosis, treatment, and care of rare cancers, reliable epidemiological data needs to be generated under the RARECAREnet Asia project by working with countries in Asia with high-quality PBCRs.

Funding

This study was supported by a UICC Yamagiwa-Yoshida Memorial International Cancer Study Grant (Award/Grant Number: YY/2022-1477) and Government of Japan Ministry of Health Labour and Welfare Grant numbers: 23EA1033, and was partially supported by Chiang Mai University, Thailand.
在东南亚(SEA),对大多数罕见癌症的了解有限,这有时会导致诊断、治疗和护理的延误。本研究旨在利用2011-2015年期间基于人群的癌症登记(PBCR)数据首次估计东南亚地区罕见癌症的发病率。方法:本研究使用了马来西亚全国PBCR和泰国北部清迈和南邦癌症登记处的两个PBCR的数据。计算了RARECAREnet列表中包含的罕见癌症的每10万人年的年龄标准化发病率(ASR)。所有分析均使用SEER * Stat(8.3.5版)进行。在欧洲被RARECAREnet定义为罕见的癌症在泰国和马来西亚也很罕见。发现泰国和马来西亚的一些罕见癌症的ASR高于日本、韩国和台湾,包括马来西亚的一些儿科癌症(胰腺母细胞瘤和牙源性恶性肿瘤),泰国的眼睛和附件癌以及阴茎上皮肿瘤。泰国和马来西亚的鼻咽癌ASR高于日本和韩国,但低于台湾。虽然大多数罕见的癌症在泰国和马来西亚也很罕见,但有些癌症并不被认为是罕见的。然而,泰国和马来西亚的一些罕见癌症的发病率高于日本、韩国和台湾。为了加强对罕见癌症的了解、诊断、治疗和护理,需要通过与拥有高质量pbcr的亚洲国家合作,在RARECAREnet亚洲项目下生成可靠的流行病学数据。本研究由UICC yamagiawa - yoshida纪念国际癌症研究基金(奖励/资助号:YY/2022-1477)和日本厚生劳动省政府资助号:23EA1033支持,泰国清迈大学提供部分支持。
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引用次数: 0
Influenza surveillance and vaccine policy in Thailand—a historical perspective 泰国的流感监测和疫苗政策——历史视角
IF 6.2 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-09-10 DOI: 10.1016/j.lansea.2025.100663
Martha P. Montgomery , Prabda Praphasiri , Darunee Ditsungnoen , Pasakorn Akarasewi , Malinee Chittaganpitch , Pilaipan Puthavathana , Khanchit Limpakarnjanarat , Ponthip Wirachwong , Tawee Chotpitayasunondh , Narumol Sawanpanyalert , Chaninan Sonthichai , William W. Davis , Sonja J. Olsen , Supamit Chunsuttiwat
Prior to 2000, influenza burden in Thailand and other low- and middle-income countries was underappreciated, and influenza vaccination was uncommon. For the last two decades, Thailand Ministry of Public Health (MOPH) and U.S. Centers for Disease Control and Prevention have collaborated to understand influenza burden and the costs and benefits of influenza vaccination in Thailand. Built on a long-standing national disease notification system, Thailand MOPH established robust surveillance platforms for pneumonia and influenza, which provided insights into seasonality, disease incidence, and populations at risk for severe disease. In 2004, human cases of avian influenza brought attention to influenza's pandemic potential. Concern for an influenza pandemic combined with evidence of the cost effectiveness of influenza vaccination accelerated vaccine policy. Surveillance and vaccination policy were leveraged for and strengthened by the 2009 influenza H1N1 and COVID-19 pandemics. This personal view documents Thailand's experience in developing influenza surveillance and influenza vaccination policy.
2000年以前,泰国和其他低收入和中等收入国家的流感负担未得到充分重视,流感疫苗接种也不常见。过去二十年来,泰国公共卫生部和美国疾病控制与预防中心合作,了解泰国的流感负担以及流感疫苗接种的成本和收益。泰国公共卫生部以长期存在的国家疾病通报系统为基础,建立了强有力的肺炎和流感监测平台,提供了有关季节性、疾病发病率和严重疾病风险人群的见解。2004年,禽流感人间病例引起了人们对流感大流行可能性的关注。对流感大流行的关注,加上流感疫苗接种成本效益的证据,加速了疫苗政策。2009年H1N1流感和COVID-19大流行利用并加强了监测和疫苗接种政策。这一个人观点记录了泰国在制定流感监测和流感疫苗接种政策方面的经验。
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引用次数: 0
At a crossroads: HIV response in southeast Asia 十字路口:东南亚的艾滋病毒应对工作
IF 6.2 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-09-01 DOI: 10.1016/j.lansea.2025.100671
The Lancet Regional Health – Southeast Asia
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引用次数: 0
Exploring the association between multi-dimensional poverty and antibiotic resistance: findings from a mixed-methods study in Pakistan 探索多维贫困与抗生素耐药性之间的关系:来自巴基斯坦一项混合方法研究的结果
IF 6.2 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-08-27 DOI: 10.1016/j.lansea.2025.100656
Iltaf Hussain , Muhammad Fawad Rasool , Jamshid Ullah , Muhammad Nafees , Inzemam Khan , Muhtar Kadirhaz , Miaomiao Xu , Chengzhou Tang , Yi Dong , Wei Zhao , Jie Chang , Yu Fang

Background

Poverty is a potential contributor to antibiotic resistance; however, the previous studies have not adequately addressed the role of poverty in shaping antibiotic resistance through social inequalities. Considering this, the current study evaluated the role of multi-dimensional poverty in antibiotic resistance.

Methods

A mixed-method study was conducted in three provinces of Pakistan using multistage sampling to recruit physician-confirmed urinary tract infection (UTI) patients from public laboratories. Antibiotic resistance data were collected from susceptibility reports, while poverty was measured using the multi-dimensional poverty index (MPI). Water, sanitation and hygiene (WASH) practices were assessed through a self-developed, validated questionnaire. Survey-weighted logistic regression analysis examined the association between MPI and antibiotic resistance.

Findings

A total of 698 patients were recruited, with more than half being in some level of deprivation (total = 413, vulnerable: 117, deprived: 76, severely deprived: 220). Multidimensional poverty was independently associated with increased odds of multidrug resistance (MDR). The risk of MDR was significantly increase across the deprivation level in unadjusted analysis (vulnerable; OR: 1.94, 95% CI 1.11–3.39, deprived; OR: 2.05, 95% CI 1.06–3.98, and severely deprived: OR: 1.80, 95% CI 1.04–3.09). After adjusting for antibiotics misuse and poor WASH practices, the association persisted. In the fully adjusted model, the risk of MDR was further increased in the poorer-subgroups, (vulnerable; aORs: 3.03, 95% CI 1.33–6.73, deprived; aOR: 3.01, 95% CI 1.26–7.15, and severely deprived; aOR: 4.28 95% CI 1.74–10.49). The qualitative interviews (n = 34) from patients highlighted that financial barriers drove self-medication with leftover antibiotics and treatment non-adherence. Poor WASH infrastructure was described as a systemic contributor to infection spread. In addition, patients in the poorer subgroups were presented with delayed treatment seeking.

Interpretation

The risk of antibiotic resistance increases with the increasing levels of deprivation; however, we should not assume that higher deprivation directly drives antibiotic resistance. Instead, structural barriers such as limited healthcare access, poor WASH infrastructure, and financial constraints create an environment where self-medication, treatment non-adherence, and infection transmission occur across all poverty levels, not just because of individual choices. These findings emphasize the need for interventions that address healthcare inequities, improve WASH infrastructure, and regulate antibiotic access, combined with behavior-changing interventions.

Funding

This work was funded by the “Young Talent Support Plan” of the Health Science Center, Xi’an Jiao
贫困是抗生素耐药性的一个潜在因素;然而,以前的研究并没有充分解决贫困在通过社会不平等形成抗生素耐药性方面的作用。考虑到这一点,本研究评估了多维贫困在抗生素耐药性中的作用。方法采用混合方法,在巴基斯坦3个省采用多阶段抽样方法,从公共实验室招募医生确诊的尿路感染(UTI)患者。从药敏报告中收集抗生素耐药性数据,而使用多维贫困指数(MPI)衡量贫困。水、环境卫生和个人卫生(WASH)做法通过自行开发的有效问卷进行评估。调查加权logistic回归分析检验了MPI与抗生素耐药性之间的关系。研究结果共招募了698名患者,其中一半以上处于某种程度的剥夺状态(总数= 413,脆弱:117,剥夺:76,严重剥夺:220)。多维贫困与多药耐药(MDR)几率增加独立相关。在未调整的分析中,MDR的风险在剥夺水平上显著增加(脆弱;OR: 1.94, 95% CI 1.11-3.39;剥夺;OR: 2.05, 95% CI 1.06-3.98;严重剥夺:OR: 1.80, 95% CI 1.04-3.09)。在调整了抗生素滥用和不良的WASH做法后,这种关联仍然存在。在完全调整后的模型中,较贫困亚组的耐多药风险进一步增加(易感亚组,aOR: 3.03, 95% CI 1.33-6.73,贫困亚组;aOR: 3.01, 95% CI 1.26-7.15,严重贫困亚组;aOR: 4.28, 95% CI 1.74-10.49)。来自患者的定性访谈(n = 34)强调了经济障碍导致使用剩余抗生素和治疗依从性不强的自我用药。不良的讲卫生基础设施被认为是导致感染传播的一个系统性因素。此外,较贫穷亚组的患者出现了延迟寻求治疗的情况。抗生素耐药性的风险随着剥夺程度的增加而增加;然而,我们不应该假设更高的剥夺直接导致抗生素耐药性。相反,结构性障碍,如有限的医疗服务可及性、落后的讲卫生基础设施和财政限制,创造了一种环境,使自我药疗、不坚持治疗和感染传播发生在所有贫困水平,而不仅仅是由于个人的选择。这些发现强调需要采取干预措施,解决卫生保健不公平问题,改善讲卫生基础设施,规范抗生素获取,并结合改变行为的干预措施。本工作由西安交通大学医学部“青年人才支持计划”和国家自然科学基金(批准号:72274150)资助。
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引用次数: 0
Developing a sustainable patient navigation model for breast cancer care in India: a survivor-led pilot project 在印度为乳腺癌护理开发一个可持续的病人导航模式:一个幸存者主导的试点项目
IF 6.2 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-08-26 DOI: 10.1016/j.lansea.2025.100661
Soumen Das , Tanmoy Kumar Mandal , Anowar Ali Mallick
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引用次数: 0
Leveraging the influenza sentinel surveillance platform for SARS-CoV-2 monitoring in Bangladesh (2020–2024): a prospective sentinel surveillance study 利用流感哨点监测平台在孟加拉国监测SARS-CoV-2(2020-2024):一项前瞻性哨点监测研究
IF 6.2 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-08-21 DOI: 10.1016/j.lansea.2025.100657
Md Ariful Islam , Md Zakiul Hassan , Zubair Akhtar , Saju Bhuiya , Tanzir Ahmed Shuvo , Probir Kumar Ghosh , Asadullah , Md Abdullah Al Jubayer Biswas , Mustafizur Rahman , Mohammad Jubair , Mst Noorjahan Begum , Yeasir Karim , Mohammed Ziaur Rahman , Mohammad Enayet Hossain , Mohammad Niaz Morshed Khan , Tahmina Shirin , Shah Niaz Md Rubaid Anwar , Ahmed Nawsher Alam , Mohammad Ferdous Rahman Sarker , Monalisa , Fahmida Chowdhury

Background

There is limited global evidence on whether influenza sentinel surveillance platforms can be effectively adapted for long-term SARS-CoV-2 monitoring in low-resource contexts. We explored the utility of the hospital-based influenza sentinel surveillance (HBIS) platform for monitoring SARS-CoV-2 in Bangladesh by comparing SARS-CoV-2 detection in HBIS platform with national COVID-19 platform and assessing how its integration into influenza surveillance aligns with national trends.

Methods

From March 2020 to December 2024, we analysed data from patients with severe acute respiratory infection (SARI) and influenza-like illness (ILI) enrolled in HBIS. Socio-demographic and clinical data were recorded, and nasopharyngeal and oropharyngeal swabs were tested for influenza and SARS-CoV-2 using rRT-PCR. Whole-genome sequencing was performed on a subset of SARS-CoV-2–positive samples. Data from national COVID-19 platform were obtained from the Directorate General of Health Services, Bangladesh, and were compared with HBIS platform data using epidemic curves and Pearson correlation analysis.

Findings

Among 25,366 (SARI: 20,226; ILI: 5140) patients, 13.0% (3310) tested positive for influenza, 6.6% (1680) for SARS-CoV-2, and 0.2% (43) were co-infected. SARS-CoV-2 positivity in HBIS (6.8%), including 0.2% co-infections, was lower than the national average (13.1%), but showed a strong correlation with national trends (Pearson r = 0.86, P < 0.001). Sequencing of 234 SARS-CoV-2 strains detected the beta and delta variants in April and May 2021, respectively, and omicron subvariants circulating from 2022 to 2024, aligning with the national COVID-19 platform.

Interpretation

SARS-CoV-2 positivity trends in HBIS platform closely aligned with the national COVID-19 platform, demonstrating its potential as a sustainable platform for COVID-19 monitoring. Our findings underscore the feasibility of influenza sentinel surveillance as an early warning system for future COVID-19 outbreaks or other respiratory viruses of pandemic concern in Bangladesh and similar settings.

Funding

Centers for Disease Control and Prevention (CDC), Atlanta, Georgia, USA (U01GH002259).
关于流感哨点监测平台是否能够有效适应低资源环境下的SARS-CoV-2长期监测,全球证据有限。我们通过比较医院流感哨点监测(HBIS)平台与国家COVID-19平台的SARS-CoV-2检测,并评估其与流感监测的整合如何符合国家趋势,探讨了医院流感哨点监测(HBIS)平台在孟加拉国监测SARS-CoV-2的效用。方法:从2020年3月至2024年12月,我们分析了参加HBIS的严重急性呼吸道感染(SARI)和流感样疾病(ILI)患者的数据。记录社会人口学和临床数据,并使用rRT-PCR对鼻咽和口咽拭子进行流感和SARS-CoV-2检测。对一部分sars - cov -2阳性样本进行了全基因组测序。来自国家COVID-19平台的数据来自孟加拉国卫生服务总局,并使用流行曲线和Pearson相关分析与HBIS平台数据进行比较。结果在25,366例患者(SARI: 20,226例;ILI: 5140例)中,13.0%(3310例)流感检测阳性,6.6%(1680例)SARS-CoV-2检测阳性,0.2%(43例)合并感染。乙肝病毒感染者中SARS-CoV-2阳性(6.8%),包括0.2%的合并感染,低于全国平均水平(13.1%),但与全国趋势有很强的相关性(Pearson r = 0.86, P < 0.001)。对234株SARS-CoV-2株的测序分别于2021年4月和5月检测到β和δ变异,以及2022年至2024年流行的组粒亚变异,与国家COVID-19平台一致。HBIS平台的sars - cov -2阳性趋势与国家COVID-19平台密切相关,显示了其作为COVID-19可持续监测平台的潜力。我们的研究结果强调了流感哨点监测作为孟加拉国和类似环境中未来COVID-19疫情或其他大流行呼吸道病毒的早期预警系统的可行性。美国佐治亚州亚特兰大疾病预防控制中心(CDC)资助(U01GH002259)。
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引用次数: 0
Health system drivers of caesarean deliveries in south Asia: a scoping review 南亚剖腹产的卫生系统驱动因素:范围审查
IF 6.2 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-08-20 DOI: 10.1016/j.lansea.2025.100651
Angel Sudha Veparala , Dorothy Lall , Prashanth N. Srinivas , Kajal Samantaray , Bruno Marchal
Caesarean section (CS) rates are rising across south Asia, often without medical indication, posing significant public health concerns. This Review applied a framework-guided evidence synthesis using a scoping review approach, structured by the Socio-Ecological Model (SEM), to examine health system drivers of CS. Seventy-five studies were included, mainly from India, Bangladesh, and Pakistan. At the individual level, maternal education, socioeconomic status, and birth order influenced CS use. Community-level drivers included family preferences and media exposure. At the provider level, decision-making was shaped by financial incentives, medico-legal concerns, and scheduling convenience. Other system-level drivers, such as private sector dominance, limited regulation, and insurance coverage, were associated with increased CS rates. While most findings aligned with the SEM, some extended beyond its scope. The Review highlights the need for coordinated policy responses across levels, including payment reforms, regulatory oversight, and improved antenatal counselling, to ensure CS use aligns with clinical need rather than socio-economic or institutional pressures.
南亚剖宫产率正在上升,往往没有医学指征,造成重大的公共卫生问题。本综述采用由社会生态模型(SEM)构建的范围审查方法,采用框架指导的证据综合方法来检查CS的卫生系统驱动因素。纳入了75项研究,主要来自印度、孟加拉国和巴基斯坦。在个体层面上,母亲教育程度、社会经济地位和出生顺序影响CS的使用。社区层面的驱动因素包括家庭偏好和媒体曝光。在医疗服务提供者的层面,决策是由财政激励、医疗法律问题和日程安排的便利性决定的。其他系统级驱动因素,如私营部门的主导地位、有限的监管和保险覆盖范围,与CS率的增加有关。虽然大多数发现与扫描电镜一致,但有些发现超出了扫描电镜的范围。《审查报告》强调需要在各级采取协调一致的政策应对措施,包括支付改革、监管监督和改进产前咨询,以确保CS的使用符合临床需求,而不是符合社会经济或体制压力。
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引用次数: 0
Immunogenicity and safety of ‘Comvigen’, a bivalent SARS-CoV-2 vaccine, in comparison to Comirnaty bivalent vaccine in Thailand: a phase 2, non-inferiority randomised trial 与泰国Comvigen二价SARS-CoV-2疫苗相比,Comvigen二价疫苗的免疫原性和安全性:一项2期非劣效性随机试验
IF 6.2 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-08-15 DOI: 10.1016/j.lansea.2025.100650
Watsamon Jantarabenjakul , Rapisa Nantanee , Thanyawee Puthanakit , Sivaporn Gatechompol , Anchalee Avihingsanon , Suda Punrin , Terapong Tantawichien , Sorachai Nitayaphan , Arunee Thitithanyanont , Supranee Buranapraditkun , Anan Jongkaewwattana , Chutitorn Ketloy , Eakachai Prompetchara , Saranath Lawpoolsri , Wassana Wijagkanalan , Mohamad-Gabriel Alameh , Lina Hong , Mijo Samija , Drew Weissman , Kiat Ruxrungtham , Nanthida Wonglertnirant

Background

Strengthening mRNA vaccine development in LMICs is essential for enhancing global pandemic preparedness. This study evaluated the safety and immunogenicity of Comvigen, a bivalent SARS-CoV-2 vaccine, in comparison to the Comirnaty bivalent vaccine (Comirnaty).

Methods

This phase II, randomised, open-label, non-inferiority trial was conducted in Thailand across four centres. Participants (n = 450) were randomly assigned (2:1) to receive either Comvigen (50 μg) or Comirnaty (30 μg), using block randomisation (size = 9). Eligible participants had completed at least 2 doses of any approved COVID-19 vaccine, with the last mRNA-vaccine dose given over 3 months before enrolment. The non-inferiority margin of a geometric mean ratio (GMR) of 0.67. The primary immunogenicity endpoint was pseudovirus neutralisation titres (psVNT-50) against SARS-CoV-2 wild-type and Omicron BA.4/BA.5 at Day 29. Safety outcomes included local and systemic adverse reactions up to six months post-vaccination. Immunogenicity analyses were conducted on the Per-Protocol (PP) population and the modified Intent-to-Treat (mITT) population; safety analyses included all participants. Laboratory personnel were blinded to vaccine assignment (ClinicalTrials.gov: NCT05930730).

Findings

Between October and November 2023, 450 participants were enrolled (median age of 36 years, IQR 30–45). At day 29, the geometric mean titre (GMT) of psVNT-50 against wild-type virus increased from 475.9 to 2062.9 for Comvigen and from 458.8 to 1905.1 for Comirnaty (GMR 1.1, 95% CI: 1.0–1.2), meeting non-inferiority criteria. Against Omicron BA.4/BA.5, GMTs were 3909.8 for Comvigen and 3288.6 for Comirnaty (GMR 1.2, 95% 1.0–1.4). Local and systemic reactions were more frequent with Comvigen (91% vs. 78%, p = 0.0002, 79% vs. 70%, p = 0.028) but were mild or moderate and transient with no difference in fever (6% vs. 5%, p = 0.84).

Interpretation

Comvigen demonstrated non-inferiority immunogenicity to Comirnaty and had a comparable safety profile, supporting mRNA vaccine development for global access and pandemic preparedness.

Funding

Covid-19 Pandemic Emergency Fund granted by Thailand's National Economic and Social Development Council provided major funding. Supplementary funding was provided by National Vaccine Institute (NVI), Thailand; Center of Excellence in Vaccine Research and Development (Chula VRC), Faculty of Medicine, Chulalongkorn University; Chulalongkorn University Second Century Fund (C2F); BioNet-Asia and Public Donation through Covid-19 vaccine development fund of the Faculty of Medicine, Chulalongkorn University and the Thai Red Cross Society, Thailand.
背景:加强中低收入国家mRNA疫苗的开发对于加强全球大流行防范至关重要。本研究评估了Comvigen(一种二价SARS-CoV-2疫苗)与Comirnaty二价疫苗(Comirnaty)的安全性和免疫原性。该II期随机、开放标签、非劣效性试验在泰国的4个中心进行。参与者(n = 450)被随机分配(2:1)接受Comvigen (50 μg)或Comirnaty (30 μg),采用分组随机(size = 9)。符合条件的参与者已完成至少2剂任何批准的COVID-19疫苗,最后一次mrna疫苗剂量在入组前3个多月进行。几何平均比(GMR)的非劣效边际为0.67。主要免疫原性终点是针对SARS-CoV-2野生型和Omicron BA.4/BA的假病毒中和效价(psVNT-50)。第29天。安全性指标包括接种疫苗后6个月的局部和全身不良反应。免疫原性分析对按方案(PP)群体和改良意向治疗(mITT)群体进行;安全性分析包括所有参与者。实验室人员对疫苗分配不知情(ClinicalTrials.gov: NCT05930730)。在2023年10月至11月期间,有450名参与者被纳入研究(中位年龄36岁,IQR 30-45岁)。在第29天,psVNT-50对野生型病毒的几何平均滴度(GMT)从Comvigen的475.9增加到2062.9,comiry的458.8增加到1905.1 (GMR 1.1, 95% CI: 1.0-1.2),符合非劣效性标准。抗欧米克隆BA.4/BA。5、Comvigen的GMTs为3909.8,comirity的GMTs为3288.6 (GMR为1.2,95%为1.0 ~ 1.4)。Comvigen的局部和全身反应更频繁(91%对78%,p = 0.0002, 79%对70%,p = 0.028),但轻度或中度和短暂性反应,发热无差异(6%对5%,p = 0.84)。comvigen显示出对Comirnaty的非劣效性免疫原性,并且具有相当的安全性,支持mRNA疫苗开发用于全球可及性和大流行防范。泰国国家经济和社会发展理事会批准的2019冠状病毒病大流行应急基金提供了主要资金。补充资金由泰国国家疫苗研究所提供;朱拉隆功大学医学院疫苗研究与开发卓越中心;朱拉隆功大学第二世纪基金;亚洲生物网与朱拉隆功大学医学院和泰国红十字会新冠病毒疫苗开发基金的公众捐赠。
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The Lancet regional health. Southeast Asia
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