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The importance of understanding pelvic inflammatory disease as a polymicrobial infection 了解盆腔炎是一种多微生物感染的重要性
IF 13.6 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-10-25 DOI: 10.1016/j.lanepe.2024.101115
Kenyon Chris
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引用次数: 0
Monkeypox clade IIb in France in 2023–2024 2023-2024 年法国将出现猴痘 IIb 支
IF 13.6 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-10-25 DOI: 10.1016/j.lanepe.2024.101114
Mayda Rahi , Sebastien Fouere , Marie Gilbert , Antoine Bachelard , Fabien Taieb , Baptiste Sellem , Florian Herms , Charles Cazanave , Nadia Valin , Gentiane Monsel , Yazdan Yazdanpanah , Jade Ghosn , Nathan Peiffer-Smadja
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引用次数: 0
Effectiveness and cost-effectiveness of online recorded recovery narratives in improving quality of life for people with psychosis experience (NEON Trial): a pragmatic randomised controlled trial 在线记录康复叙事在改善精神病患者生活质量方面的效果和成本效益(NEON 试验):一项实用随机对照试验
IF 13.6 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-10-23 DOI: 10.1016/j.lanepe.2024.101101
Mike Slade , Stefan Rennick-Egglestone , Clare Robinson , Chris Newby , Rachel A. Elliott , Yasmin Ali , Caroline Yeo , Tony Glover , Sean P. Gavan , Luke Paterson , Kristian Pollock , Stefan Priebe , Graham Thornicroft , Jeroen Keppens , Melanie Smuk , Donna Franklin , Rianna Walcott , Julian Harrison , Dan Robotham , Simon Bradstreet , Fiona Ng
<div><h3>Background</h3><div>The Narrative Experiences Online (NEON) Intervention provides self-managed web-based access to mental health recovery narratives (n = 659). We evaluated effectiveness and cost-effectiveness in improving quality of life for adults resident in England with mental health problems and recent psychosis experience.</div></div><div><h3>Methods</h3><div>Prospectively registered pragmatic parallel-group randomised trial controlling for usual care, recruiting from statutory mental health services and through community engagement activities, with a 52-week primary endpoint (ISRCTN11152837). All trial procedures and the NEON Intervention were delivered by an integrated web-application. Randomisation was through an independently generated list (no stratification). Allocation was masked for statistical staff and the Chief Investigator but not participants. Intervention arm participants received immediate NEON Intervention access. Control arm participants received access after completing primary endpoint questionnaires. The primary outcome was quality of life through the Manchester Short Assessment (MANSA). Serious Adverse Events (SAEs) were collected through web-based safety report forms and identified from health service usage data. The primary analysis was by a prospectively described Intention To Treat principle excluding participants who had registered multiple times, with multiple imputation for missing data.</div></div><div><h3>Findings</h3><div>Between 9 March 2020 and 1 March 2021, 739 participants were randomised (intervention:370; control: 369), providing more than 90% power to detect a baseline-adjusted difference of 0.25 in the MANSA score. Mean age was 34.8 years (standard deviation (SD) 12.0), 561 (75.9%) were white British, 443 (59.9%) were female, 609 (82.4%) had accessed specialist care mental health services, and 698 (94.5%) had accessed primary care mental health services. Mean baseline MANSA score was 3.7 for control and intervention arms (SD 0.9 and 1.0). 565 (76.5%) participants provided primary endpoint MANSA data with a mean score of 4.1 (SD 1.0) for both arms. We found no significant difference in Quality of Life between the two arms at the primary endpoint (baseline-adjusted difference 0.07, 95% CI −0.07 to 0.21, p = 0.35). The incremental cost-effectiveness ratio (£110,501 per quality-adjusted life-year (QALY)) exceeded the prospectively defined cost-effectiveness threshold (£30,000 per QALY). 158 (42.8%) control arm and 194 (52.4%) intervention arm participants accessed narratives outside of the NEON Intervention. There were no related serious adverse events (SAEs). 116 unrelated SAEs were reported by control arm participants, and 107 by intervention arm participants.</div></div><div><h3>Interpretation</h3><div>Our findings do not indicate NEON Intervention access for all people with psychosis experience. Future research should consider a) evaluation with current mental health services users; b) optimisa
背景在线叙事经历(NEON)干预提供了基于网络的自我管理心理健康康复叙事(n = 659)。我们评估了NEON干预在改善居住在英格兰、有精神健康问题和近期有精神病经历的成年人生活质量方面的有效性和成本效益。方法前瞻性注册的务实平行组随机试验控制了常规护理,从法定精神健康服务机构和通过社区参与活动招募人员,主要终点为52周(ISRCTN11152837)。所有试验程序和NEON干预措施均由一个综合网络应用程序提供。随机分配通过独立生成的名单进行(不分层)。统计人员和首席研究员对随机分配进行了保密,但未对参与者进行保密。干预组参与者可立即获得NEON干预服务。对照组参与者在完成主要终点调查问卷后接受干预。主要结果是通过曼彻斯特短期评估(MANSA)得出的生活质量。严重不良事件(SAE)通过网络安全报告表收集,并从医疗服务使用数据中识别。研究结果在 2020 年 3 月 9 日至 2021 年 3 月 1 日期间,739 名参与者被随机分配(干预组:370 人;对照组:369 人),超过 90% 的力量可检测到 MANSA 评分中 0.25 的基线调整差异。平均年龄为34.8岁(标准差(SD)12.0),561人(75.9%)为英国白人,443人(59.9%)为女性,609人(82.4%)曾接受过专科精神卫生服务,698人(94.5%)曾接受过初级精神卫生服务。对照组和干预组的基线 MANSA 平均分为 3.7(标度分别为 0.9 和 1.0)。565名(76.5%)参与者提供了主要终点MANSA数据,对照组和干预组的平均得分均为4.1(标准差为1.0)。我们发现,在主要终点时,两组患者的生活质量无明显差异(基线调整后差异为 0.07,95% CI -0.07 至 0.21,p = 0.35)。增量成本效益比(每质量调整生命年 110,501 英镑)超过了预期定义的成本效益阈值(每质量调整生命年 30,000 英镑)。158名(42.8%)对照组参与者和194名(52.4%)干预组参与者获得了NEON干预之外的叙述。没有相关的严重不良事件 (SAE)。对照组参与者报告了 116 起与此无关的 SAE,干预组参与者报告了 107 起。未来的研究应考虑 a) 对当前精神健康服务用户进行评估;b) 优化服务,使用户能够找到促进希望的叙述。
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引用次数: 0
COVID-19 vaccine effectiveness against SARS-CoV-2-confirmed hospitalisation in the eastern part of the WHO European Region (2022-2023): a test-negative case-control study from the EuroSAVE network. 世卫组织欧洲区域东部地区(2022-2023年)COVID-19疫苗对sars - cov -2确诊住院的有效性:来自EuroSAVE网络的检测阴性病例对照研究。
IF 13.6 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-10-22 eCollection Date: 2024-12-01 DOI: 10.1016/j.lanepe.2024.101095
Mark A Katz, Sandra Cohuet, Silvia Bino, Olgha Tarkhan-Mouravi, Besfort Kryeziu, Dinagul Otorbaeva, Kristina Stavridis, Maja Stosic, Jonilda Sulo, Ann Machablishvili, Ariana Kalaveshi, Abdyldaeva Sayragul Zhusupovna, Katerina Kjirkovikj Kolevska, Dragana Plavsa, Iris Hasibra, Khatuna Zakhashvili, Zana Kaçaniku-Deva, Uzakbaeva Aynura Zarylbekovna, Elizabeta Jancheska, Verica Jovanovic, James Humphreys, Jennifer Howard, Kirill Stolyarov, Oksana Artemchuk, Marc-Alain Widdowson, Iris Finci, Angela M C Rose, Richard Pebody

Background: Understanding COVID-19 vaccine effectiveness (VE) in preventing severe disease is critical to inform vaccine policy. We used the test-negative design to estimate VE against SARS-CoV-2-confirmed hospitalisation in adults ≥18 years in the eastern WHO European Region.

Methods: We included patients hospitalised for severe acute respiratory infection (SARI) at sentinel surveillance sites in Albania, Georgia, Kyrgyzstan, North Macedonia, Serbia, and in Kosovo. We collected demographic information, COVID-19 vaccination history, and tested respiratory samples for SARS-CoV-2 by RT-PCR. We calculated VE of any vaccine dose received within 12 months (Annual VE) as [(1 - adjusted Odds Ratio) x 100%] using a one-stage pooled analysis. The reference group included unvaccinated individuals and those who received their last vaccine >12 months before symptom onset.

Findings: During 1 January 1, 2022-November 20, 2023, of 5162 patients, 57.0% (2942) were unvaccinated, 2.5% (129) received only one dose, 26.0% (1340) received only two doses (originally considered a primary series vaccine (PS)), 13.2% (683) received three doses only, and 1.3% (68) received four doses. Most PS vaccines and boosters were BNT162b2 (46.4% (622/1340) and 64.9% (443/683), respectively) and CoronaVac (23.0% (309/1340) and 18.3% (125/683)). No patients received Ad26.COV2.S (Johnson and Johnson) vaccines. Overall, 1009/5162 (19.5%) patients were SARS-CoV-2-positive. VE was 60.1% (95% Confidence Interval (CI) 12.4-81.8) for last vaccine received 14-89 days before symptom onset, 60.0% (95% CI 32.2-76.4) for 90-179 days, 7.0% (95% CI -28.5 to 32.7) for 180-269 days, and -5.4% (95% CI -43.8 to 22.8) for 270-365 days.).

Interpretation: During nearly two years of Omicron circulation in the eastern WHO European Region, COVID-19 vaccination reduced the risk of hospitalisations by more than half for 6 months following vaccination.

Funding: This study was funded by the World Health Organization, Regional Office for Europe through a cooperative agreement with the U.S. Centers for Disease Control and Prevention.

背景:了解COVID-19疫苗在预防严重疾病方面的有效性对制定疫苗政策至关重要。我们采用检测阴性设计来估计世卫组织东欧地区≥18岁成人sars - cov -2确诊住院的VE。方法:我们纳入了阿尔巴尼亚、格鲁吉亚、吉尔吉斯斯坦、北马其顿、塞尔维亚和科索沃哨点监测点因严重急性呼吸道感染(SARI)住院的患者。我们收集了人口统计信息、COVID-19疫苗接种史,并通过RT-PCR检测呼吸道样本中的SARS-CoV-2。我们使用单阶段合并分析计算了12个月内接种任何疫苗剂量的VE(年度VE)为[(1校正优势比)x 100%]。参照组包括未接种疫苗的个体和在症状出现前12个月最后一次接种疫苗的个体。结果:在2022年1月1日至2023年11月20日期间,5162例患者中,57.0%(2942例)未接种疫苗,2.5%(129例)仅接种一剂,26.0%(1340例)仅接种两剂(最初被认为是一级系列疫苗(PS)), 13.2%(683例)仅接种三剂,1.3%(68例)接种四剂。PS疫苗和加强剂以BNT162b2(分别为46.4%(622/1340)和64.9%(443/683))和CoronaVac(23.0%(309/1340)和18.3%(125/683)为主。无患者接受Ad26.COV2治疗。S (Johnson and Johnson)疫苗。总体而言,1009/5162例(19.5%)患者为sars - cov -2阳性。症状出现前14-89天最后一次接种疫苗的VE为60.1%(95%可信区间(CI) 12.4-81.8), 90-179天VE为60.0% (95% CI 32.2-76.4), 180-269天VE为7.0% (95% CI -28.5 - 32.7), 270-365天VE为-5.4% (95% CI -43.8 - 22.8)。解读:在世卫组织东欧区域近两年的欧米克隆循环中,COVID-19疫苗接种将疫苗接种后6个月内的住院风险降低了一半以上。资助:本研究由世界卫生组织欧洲区域办事处通过与美国疾病控制和预防中心的合作协议资助。
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引用次数: 0
Correction to “Impact of liquid sublingual immunotherapy on asthma onset and progression in patients with allergic rhinitis: a nationwide population-based study (EfficAPSI study)” [The Lancet Regional Health – Europe 41 (2024) 100915] 更正 "液体舌下免疫疗法对过敏性鼻炎患者哮喘发病和恶化的影响:一项基于全国人口的研究(EfficAPSI 研究)"[《柳叶刀区域健康-欧洲》41 (2024) 100915]
IF 13.6 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-10-22 DOI: 10.1016/j.lanepe.2024.101120
Pascal Demoly , Mathieu Molimard , Jean-François Bergmann , Bertrand Delaisi , Amandine Gouverneur , Jade Vadel , Cédric Collin , Laurence Girard , Silvia Scurati , Philippe Devillier
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引用次数: 0
Gene therapy for spinal muscular atrophy: timing is key 脊髓性肌萎缩症的基因疗法:时机是关键
IF 13.6 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-10-21 DOI: 10.1016/j.lanepe.2024.101112
Laurent Servais
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引用次数: 0
Is obesity a cause of all cancer types? 肥胖是所有癌症类型的病因吗?
IF 13.6 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-10-21 DOI: 10.1016/j.lanepe.2024.101110
Marc J. Gunter , Amy Berrington de Gonzalez
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引用次数: 0
Sex differences in clinically diagnosed psychiatric disorders over the lifespan: a nationwide register-based study in Sweden. 临床诊断精神疾病的性别差异:瑞典一项基于全国登记的研究。
IF 13.6 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-10-21 eCollection Date: 2024-12-01 DOI: 10.1016/j.lanepe.2024.101105
Yihui Yang, Fang Fang, Filip K Arnberg, Ralf Kuja-Halkola, Brian M D'Onofrio, Henrik Larsson, Isabell Brikell, Zheng Chang, Ole A Andreassen, Paul Lichtenstein, Unnur A Valdimarsdóttir, Donghao Lu

Background: Limited studies exist on sex differences in incidence rates of psychiatric disorders across the lifespan. This study aims to analyze sex differences in the incidence rates of clinically diagnosed psychiatric disorders over the lifespan.

Methods: We conducted a nationwide register-based cohort study, including all individuals who were born in Sweden and lived in Sweden between 2003 and 2019, including 4,818,071 females and 4,837,829 males. We calculated sex- and age-specific standardized incidence rates for any and 10 major types of psychiatric disorders. Multivariable-adjusted incidence rate differences (IRDs) for diagnosed psychiatric disorders between females and males were estimated.

Findings: During a follow-up of 119,420,908 person-years, males showed a higher incidence rate of any diagnosed psychiatric disorder than females at age 5-9 (IRD = -8.93; 95% CI: -9.08 to -8.79; per 1000 person-years), whereas females showed a higher rate than males at age 15-19 (IRD = 9.33; 95% CI: 9.12-9.54) and onwards (except age 60-69). Specifically, among females, excess rates were apparent for depressive, anxiety, eating, stress-related and bipolar disorders at age 10-54, whereas among males, excess rates were pronounced for autism and attention deficit hyperactivity disorders before age 14, drug use disorders at age 15-54, and alcohol use disorders in adulthood. For schizophrenia, the male excess at age 15-49 shifted to female excess at age 60-79. The magnitude of IRDs were greater in recent years and individuals with lower socioeconomic status.

Interpretation: Knowledge about the lifespan and socioeconomic variations in the sex differences in rates of diagnosed psychiatric disorders may inform targeted screening/intervention strategies.

Funding: Vetenskapsrådet, FORTE, Karolinska Institutet Strategic Research Area in Epidemiology and Biostatistics, and Icelandic Research Fund.

背景:关于精神疾病在整个生命周期中发病率的性别差异的研究有限。本研究旨在分析临床诊断的精神疾病在一生中发病率的性别差异。方法:我们进行了一项全国性的基于登记的队列研究,包括2003年至2019年间在瑞典出生并生活在瑞典的所有个体,其中包括4,818,071名女性和4,837,829名男性。我们计算了任何一种和10种主要精神疾病的性别和年龄特异性标准化发病率。对诊断精神障碍的多变量校正发病率差异(IRDs)在女性和男性之间进行估计。结果:在119,420,908人年的随访中,男性在5-9岁时任何诊断出的精神疾病的发病率都高于女性(IRD = -8.93;95% CI: -9.08 ~ -8.79;而15-19岁女性的发病率高于男性(IRD = 9.33;95% CI: 9.12-9.54)及以后(60-69岁除外)。具体来说,在女性中,抑郁、焦虑、饮食、压力相关和双相情感障碍在10-54岁时的过度率是明显的,而在男性中,14岁前的自闭症和注意缺陷多动障碍、15-54岁的药物使用障碍和成年期的酒精使用障碍的过度率是明显的。就精神分裂症而言,男性在15-49岁时的过度行为在60-79岁时转变为女性的过度行为。近年来,社会经济地位较低的个体的IRDs规模更大。解释:关于寿命和社会经济差异在精神疾病诊断率中的性别差异的知识可以为有针对性的筛查/干预策略提供信息。资助:vetenskapsr det、FORTE、卡罗林斯卡学院流行病学和生物统计学战略研究领域以及冰岛研究基金。
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引用次数: 0
Prevalence, predictors, and patterns of patient reported non-motor outcomes six months after stroke: a prospective cohort study 中风六个月后患者报告的非运动结果的发生率、预测因素和模式:一项前瞻性队列研究
IF 13.6 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-10-19 DOI: 10.1016/j.lanepe.2024.101080
Hatice Ozkan , Gareth Ambler , Gargi Banerjee , John J. Mitchell , Carmen Barbato , Simone Browning , Alex P. Leff , Robert J. Simister , David J. Werring

Background

Adverse non-motor outcomes have a major impact on patients and caregivers after stroke, but knowledge of their prevalence, predictors and patterns across multiple health domains remains limited; we therefore aimed to obtain these data in a large observational prospective cohort study.

Methods

We included data from the Stroke Investigation Group in North and Central London (SIGNAL) registry based at the University College London Hospitals (UCLH) Comprehensive Stroke Service which serves a multi-ethnic population of ∼1.6 million people. In adult patients diagnosed with acute stroke due to cerebral ischaemia or intracerebral haemorrhage (ICH) from January 2017 to January 2020 we evaluated non-motor outcomes (anxiety, depression, fatigue, sleep disturbance, social participation, pain, bowel dysfunction, bladder dysfunction, mood problems, communication problems, activities of daily living (ADL), memory and thinking problems) at 6-month follow-up. We evaluated baseline predictors in multivariable logistic regression, and correlations between domains using kappa statistics.

Findings

Follow-up was complete for 3080 of 3338 (92.3%) eligible surviving patients (2534 ischaemic stroke, 547 with ICH; mean age 71.2 years, 1379 (44.8%) female, 1774 (59.3%) white). The most prevalent adverse non-motor outcomes were fatigue 1756 (57%), reduced social participation 1694 (55%), sleep disturbance 1663 (54%), and constipation 1355 (44%). The rates of adverse non-motor outcomes in ⩾ 1, ⩾ 2, ⩾ 3, ⩾ 4, and ⩾ 5 domains were 2310 (75%), 1571 (51%), 1519 (49%), 1232 (40%), and 801 (26%), respectively. Factors associated with adverse non-motor outcomes included stroke due to ICH, stroke severity, previous stroke, or history of cardiovascular disease. We identified moderate correlations between fatigue and sleep disturbance (kappa = 0.72); memory and thinking impairment and reduced ADL (kappa = 0.68); and communication problems and ADL (kappa = 0.70).

Interpretation

Adverse non-motor outcomes are highly prevalent and often multiple at 6-months after stroke: 75% have at least one affected domain; fatigue, sleep disturbance, and reduced social participation each affect over 50% of survivors, and 26% of patients report ≥5 adverse outcomes. Our findings suggest an urgent need to better detect and mitigate these outcomes to improve quality of life after stroke.

Funding

The National Institute for Health and Care Research (NIHR) UCLH Biomedical Research Centre.
背景不良非运动结局对中风后的患者和护理人员有重大影响,但对其发生率、预测因素和多个健康领域的模式的了解仍然有限;因此,我们旨在通过一项大型观察性前瞻性队列研究获得这些数据。方法我们纳入了伦敦大学学院医院(UCLH)综合中风服务机构的伦敦北部和中部中风调查组(SIGNAL)登记数据,该机构服务于 160 万左右的多种族人群。在 2017 年 1 月至 2020 年 1 月期间,我们对因脑缺血或脑内出血(ICH)而被诊断为急性中风的成年患者进行了 6 个月随访,评估了非运动结局(焦虑、抑郁、疲劳、睡眠障碍、社会参与、疼痛、排便功能障碍、膀胱功能障碍、情绪问题、交流问题、日常生活活动(ADL)、记忆和思维问题)。我们在多变量逻辑回归中评估了基线预测因素,并使用 kappa 统计法评估了各领域之间的相关性。研究结果在 3338 例(92.3%)符合条件的存活患者中,有 3080 例(2534 例缺血性中风,547 例 ICH;平均年龄 71.2 岁,1379 例(44.8%)女性,1774 例(59.3%)白人)完成了随访。最常见的非运动不良后果是疲劳 1756 例(57%)、社会参与减少 1694 例(55%)、睡眠障碍 1663 例(54%)和便秘 1355 例(44%)。1 ⩾、2 ⩾、3 ⩾、4 ⩾和 5 ⩾领域的不良非运动结局发生率分别为 2310 (75%)、1571 (51%)、1519 (49%)、1232 (40%) 和 801 (26%)。与不良非运动结局相关的因素包括 ICH 引起的中风、中风严重程度、既往中风或心血管疾病史。我们发现疲劳与睡眠障碍(kappa = 0.72)、记忆和思维障碍与 ADL 减少(kappa = 0.68)、交流问题与 ADL(kappa = 0.70)之间存在中度相关性:75%的患者至少有一个领域受到影响;疲劳、睡眠障碍和社会参与减少各影响超过50%的幸存者,26%的患者报告了≥5种不良后果。我们的研究结果表明,迫切需要更好地检测和减轻这些结果,以改善中风后的生活质量。
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引用次数: 0
Poliovirus circulation in the WHO European region, 2015–2022: a review of data from WHO's three core poliovirus surveillance systems 2015-2022 年世卫组织欧洲地区脊灰病毒流行情况:世卫组织三大核心脊灰病毒监测系统数据回顾
IF 13.6 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-10-19 DOI: 10.1016/j.lanepe.2024.101104
Thea K. Fischer , Caroline K. Johannesen , Kimberley S.M. Benschop , Natasa Berginc , Eugene V. Saxentoff , Shahin Huseynov , José E. Hagan , Heli Harvala

Background

The Global Polio Eradication Initiative (GPEI) has drastically reduced the global incidence of poliomyelitis since its launch in 1988 thanks to effective vaccines and strong global surveillance systems. However, detections of wild-type as well as vaccine-derived poliovirus (VDPV) still occur, also in the WHO European Region. This study aims to describe the poliovirus detection via the acute flaccid paralysis (AFP), clinical enterovirus, and environmental surveillance systems.

Methods

In this study, we review data from annual reports from 2015 to 2022 from the World Health Organization (WHO)'s three core poliovirus surveillance systems in place in the WHO European Region: AFP, clinical enterovirus, and environmental surveillance systems.

Findings

A total of 4324 reported samples were found positive for poliovirus: 477 from AFP surveillance, 394 from clinical surveillance and 3453 from environmental surveillance. Of these, 366 were VDPV, 3952 vaccine strains, and 6 were wild-type poliovirus. 709 were identified as type 1, 399 as type 2, and 1944 type 3, while 1272 samples contained more than one type. Temporal and spatial association of positive environmental samples with positive samples from AFP or clinical enterovirus surveillance was found in only eight countries.

Interpretation

Analysis of poliovirus-positive samples from AFP, clinical enterovirus, and environmental surveillance revealed that type 3 poliovirus was the most prevalent type detected. Most poliovirus-positive samples were identified as vaccine strains. No information on sequences was available.

Funding

This study was funded by WHO Regional Office for Europe and received financial support from the Bill and Melinda Gates Foundation.
背景全球根除脊髓灰质炎行动(GPEI)自 1988 年启动以来,凭借有效的疫苗和强大的全球监测系统,全球脊髓灰质炎发病率大幅下降。然而,野生型脊髓灰质炎病毒和疫苗衍生脊髓灰质炎病毒(VDPV)仍时有发生,在世界卫生组织欧洲地区也是如此。本研究旨在描述通过急性弛缓性麻痹(AFP)、临床肠道病毒和环境监测系统检测脊髓灰质炎病毒的情况。方法在本研究中,我们回顾了世界卫生组织(WHO)在欧洲地区实施的三个核心脊髓灰质炎病毒监测系统从 2015 年到 2022 年的年度报告数据:结果共有 4324 份报告样本发现脊灰病毒呈阳性:共有 4324 份报告样本对脊髓灰质炎病毒呈阳性,其中 477 份来自 AFP 监测系统,394 份来自临床监测系统,3453 份来自环境监测系统。其中 366 例为 VDPV,3952 例为疫苗株,6 例为野生型脊灰病毒。709 个样本被确定为 1 型,399 个样本为 2 型,1944 个样本为 3 型,1272 个样本包含一种以上的类型。对 AFP、临床肠道病毒和环境监测中脊髓灰质炎病毒阳性样本的分析表明,3 型脊髓灰质炎病毒是检测到的最普遍的类型。大多数脊灰病毒阳性样本被鉴定为疫苗株。本研究由世界卫生组织欧洲地区办事处资助,并得到了比尔及梅林达-盖茨基金会的资金支持。
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引用次数: 0
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Lancet Regional Health-Europe
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