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Work ability trajectories and sick leave in individuals with post COVID-19 condition: 3-year follow-up of a population-based cohort COVID-19后个体的工作能力轨迹和病假:基于人群的队列3年随访
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-20 DOI: 10.1016/j.lanepe.2025.101536
Tala Ballouz, Philipp Kerksieck, Sarah R. Haile, Holger Dressel, Oliver Hämmig, Georg F. Bauer, Jan S. Fehr, Milo A. Puhan, Dominik Menges

Background

Data on the longer-term impact of post COVID-19 condition (PCC) on work-related functioning is limited, despite evidence on the persistence of PCC for years after infection. This study aimed to describe changes in work ability and sick leave associated with PCC up to three years post-infection.

Methods

We used data from 667 working-age individuals within a prospective population-based cohort following individuals infected with SARS-CoV-2 between August 2020 and January 2021. PCC was determined at 12 months and work ability was assessed biannually. The impact of SARS-CoV-2 on participants’ physical and mental work performance and COVID-19 related sick leave were assessed at three years.

Findings

Participants with protracted COVID-19 related symptoms at 12 months after infection reported persistently lower work ability scores than those without symptoms, with no evidence of a difference in change over time (−0.12 points per year, 95% CI −0.29 to 0.07). Compared to recovered individuals, work ability scores among those with moderate health impairment improved by +0.72 points per year (95% CI −0.04 to 1.46), while trends were similar among those with mild or severe impairment. A higher proportion of participants with PCC reported worsening in physical and mental performance at work than those without PCC. Among those with PCC, 11.5% (9/78) reported taking COVID-19 related sick leave for one month or more, in contrast to 4.0% (13/327) among those without PCC.

Interpretation

The study highlights the prolonged impact of PCC on work-related functioning and underscores the need for targeted occupational, clinical and social measures for those affected.

Funding

Federal Office of Public Health, Department of Health of the Canton of Zurich, University of Zurich Foundation, Switzerland; Horizon Europe.
背景:关于COVID-19后病情(PCC)对工作功能的长期影响的数据有限,尽管有证据表明PCC在感染后持续数年。本研究旨在描述PCC感染后长达三年的工作能力和病假的变化。方法:我们使用了2020年8月至2021年1月期间感染SARS-CoV-2的前瞻性人群队列中的667名工作年龄个体的数据。12个月时测定PCC,每半年评估一次工作能力。每三年评估新冠肺炎对参与者身心工作表现和新冠肺炎相关病假的影响。在感染后12个月,持续出现COVID-19相关症状的参与者报告的工作能力得分持续低于没有症状的参与者,没有证据表明随时间的变化存在差异(每年- 0.12点,95% CI - 0.29至0.07)。与康复个体相比,中度健康障碍患者的工作能力得分每年提高+0.72分(95% CI为- 0.04至1.46),而轻度或重度健康障碍患者的趋势相似。与没有患前列腺癌的人相比,患前列腺癌的人在工作时身心表现恶化的比例更高。在患有PCC的人中,11.5%(9/78)报告请了一个月或更长时间的与COVID-19相关的病假,而在没有PCC的人中,这一比例为4.0%(13/327)。该研究强调了PCC对工作功能的长期影响,并强调了对受影响者采取有针对性的职业、临床和社会措施的必要性。资助:苏黎世州卫生部联邦公共卫生局,苏黎世大学基金会,瑞士;欧洲地平线。
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引用次数: 0
Risk of new HIV diagnosis by intersecting migration, socioeconomic, and mental health vulnerabilities in the Netherlands: a nationwide analysis of the ATHENA cohort and Statistics Netherlands registry data 荷兰通过交叉移民、社会经济和心理健康脆弱性进行新的艾滋病毒诊断的风险:对雅典娜队列和荷兰统计局登记数据的全国分析
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-20 DOI: 10.1016/j.lanepe.2025.101508
Vita W. Jongen , Anders Boyd , Patrizia Carrieri , Nina Schat , Selwyn H. Lowe , Rosan van Zoest , Marit G.A. van Vonderen , Jolanda Lammers , Mark Verhagen , Ard van Sighem , Marc van der Valk

Background

To further reduce new HIV diagnoses in the Netherlands, individual and structural barriers hindering prevention must be addressed. We aimed to estimate the disproportional burden of new HIV diagnoses and explore how intersecting socio-demographic, socio-economic, and health-related factors jointly influence the risk of a new HIV diagnosis.

Methods

We combined data from the ATHENA cohort, an ongoing nationwide HIV cohort, with registry data from Statistics Netherlands. We selected individuals with a new HIV diagnosis between 1 January 2012 and 31 December 2023 and matched them to individuals from the general population. We assessed determinants of a new HIV diagnosis using a multivariable generalized linear model. We used Multilevel Analysis of Individual Heterogeneity and Discriminatory Accuracy (MAIHDA) to quantify the joint and individual contribution of intersecting variables.

Findings

6055 men and 1020 women were newly diagnosed with HIV. Having a migration background and a low to middle income or income below the poverty line was associated with a higher risk of a new HIV diagnosis for both men (low to middle: adjusted odd ratio (aOR) = 1.24, 95% confidence interval (CI) = 1.17–1.31; below the poverty line: aOR = 1.75, 95% CI = 1.62–1.89) and women (low to middle: aOR = 2.49, 95% CI = 2.05–3.01; below the poverty line: aOR = 4.71, 95% CI = 3.80–5.83). Use of mental health care (aOR = 1.14, 95% CI = 1.01–1.27) or antidepressants (aOR = 1.66, 95% CI = 1.50–1.84) also increased the risk among men; while receiving social welfare (aOR = 1.39, 95% CI = 1.15–1.67) and use of antipsychotic medication (aOR = 1.66, 95% CI = 1.21–2.28) increased the risk among women. Of all intersections identified in MAIHDA, men with a first-generation migration background, income below the poverty line, and who used antidepressants had the highest predicted probability of an HIV diagnosis (0.036%, 95% confidence interval (CI) = 0.025–0.052). Women with a first-generation background, income below the poverty line, who received social welfare, and who used antipsychotic medication had the highest predicted risk (0.019%, 95% CI = 0.011–0.035).

Interpretation

A disproportionally higher burden of a new HIV diagnosis was observed for individuals with a migration background and economic and mental health vulnerabilities. HIV prevention and testing need to be reinforced in these groups.

Funding

Dutch Ministry of Health, Welfare and Sport; TKI Health Holland.
背景:为了进一步减少荷兰的艾滋病毒新诊断,必须解决阻碍预防的个人和结构性障碍。我们的目的是估计新的艾滋病毒诊断的不成比例的负担,并探讨交叉的社会人口、社会经济和健康相关因素如何共同影响新的艾滋病毒诊断的风险。方法:我们将ATHENA队列(一个正在进行的全国性HIV队列)的数据与荷兰统计局的登记数据相结合。我们选择了2012年1月1日至2023年12月31日期间新诊断出艾滋病毒的个体,并将其与一般人群中的个体进行匹配。我们使用多变量广义线性模型评估新HIV诊断的决定因素。我们使用个体异质性和区分精度的多水平分析(MAIHDA)来量化交叉变量的联合和个人贡献。结果发现,6055名男性和1020名女性新诊断为艾滋病毒感染者。具有移民背景和中低收入或低于贫困线的收入与两名男性新诊断艾滋病毒的风险较高相关(低至中:调整奇数比(aOR) = 1.24, 95%置信区间(CI) = 1.17-1.31;低于贫困线:aOR = 1.75, 95% CI = 1.62-1.89)和女性(中低:aOR = 2.49, 95% CI = 2.05-3.01;低于贫困线:aOR = 4.71, 95% CI = 3.80-5.83)。使用精神保健(aOR = 1.14, 95% CI = 1.01-1.27)或抗抑郁药(aOR = 1.66, 95% CI = 1.50-1.84)也增加了男性的风险;接受社会福利(aOR = 1.39, 95% CI = 1.15-1.67)和使用抗精神病药物(aOR = 1.66, 95% CI = 1.21-2.28)增加了女性的风险。在MAIHDA确定的所有交叉点中,第一代移民背景、收入低于贫困线和使用抗抑郁药的男性HIV诊断的预测概率最高(0.036%,95%置信区间(CI) = 0.025-0.052)。第一代家庭背景、收入低于贫困线、接受社会福利和使用抗精神病药物的妇女的预测风险最高(0.019%,95% CI = 0.011-0.035)。对于具有移民背景和经济和心理健康脆弱性的个体,观察到新的艾滋病毒诊断负担不成比例地更高。需要在这些群体中加强艾滋病毒预防和检测。荷兰卫生、福利和体育部;TKI健康荷兰。
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引用次数: 0
European Medicines Agency approvals of new medicines in September and October 2025 欧洲药品管理局将于2025年9月和10月批准新药
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-20 DOI: 10.1016/j.lanepe.2025.101542
Bruno Sepodes , Juan Garcia Burgos , Steffen Thirstrup
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引用次数: 0
Current perspectives on psychedelic treatments in Europe 欧洲迷幻药治疗的当前观点
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-20 DOI: 10.1016/j.lanepe.2025.101537
Santiago Madero , Oscar Soto-Angona , Genis Ona , Jose Sanchez-Moreno , Eduard Vieta
In this viewpoint, we explore the evolving landscape of psychedelic-assisted therapy in Europe, focusing on clinical, regulatory, and therapeutic developments. While access remains limited, recent initiatives in Switzerland, Germany, and the Czech Republic illustrate growing momentum toward regulated use. We examine the debate surrounding psychedelics as pharmacological agents versus psychotherapeutic catalysts and argue for an integrative framework that considers neurobiological mechanisms, subjective experience, and contextual factors. We focus on how their effects, particularly those involving neuroplasticity and critical periods, may interact with psychotherapeutic processes. We highlight the importance of context and psychological support in shaping outcomes and discuss the challenges of implementing scalable care models. Regulatory fragmentation and methodological complexities continue to hinder progress, but publicly funded trials such as EPIsoDE and PsyPal offer promising examples of ethical and effective approaches. In our view, the future of psychedelic therapy lies not in simplifying its complexity, but in embracing it.
在这种观点下,我们探讨了迷幻剂辅助治疗在欧洲的发展前景,重点是临床、监管和治疗的发展。虽然获取途径仍然有限,但瑞士、德国和捷克共和国最近的举措表明,监管使用的势头正在增强。我们研究了围绕致幻剂作为药物制剂与心理治疗催化剂的争论,并提出了一个考虑神经生物学机制、主观经验和环境因素的综合框架。我们关注它们的影响,特别是那些涉及神经可塑性和关键时期的影响,可能与心理治疗过程相互作用。我们强调了环境和心理支持在形成结果中的重要性,并讨论了实施可扩展护理模式的挑战。监管的分散和方法的复杂性继续阻碍着进展,但公共资助的试验,如EPIsoDE和PsyPal,提供了有希望的道德和有效方法的例子。在我们看来,迷幻疗法的未来不在于简化它的复杂性,而在于拥抱它。
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引用次数: 0
Strengthening antimicrobial resistance governance in Europe: a coordinated one health approach 加强欧洲抗微生物药物耐药性治理:协调一致的一种卫生方法
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-18 DOI: 10.1016/j.lanepe.2025.101540
Benjamin Davido , Sofia Ny , Corine van Lingen , Christine Årdal , Laura Alonso Irujo , Sofia Linnros , Lucie Collineau , Nerea Gonzalez Hernandez , Marta Gutierrez Rubio , Giel van de Laar , Lida Politi , Brian Kristensen , Ana Álvarez-Fernández , Yohann Lacotte , Agathe Claude , Marie-Cécile Ploy
Antimicrobial resistance (AMR) causes over 35,000 deaths annually in the EU/EEA and is projected to result in 1.91 million global deaths each year by 2050. The second Joint Action on Antimicrobial Resistance and Healthcare-Associated Infections (EU-JAMRAI-2), uniting 128 partners from 30 countries, represents a coordinated EU/EEA effort to curb AMR through a One Health approach. Although nearly all EU/EEA countries have an AMR National Action Plan, our initial assessment revealed that implementation remains constrained by limited resources, weak intersectoral coordination and fragmented leadership. EU-JAMRAI-2 addresses these challenges by promoting harmonized surveillance, strengthening infection prevention and control, applying behaviorally tailored stewardship interventions, ensuring sustainable access to essential antibiotics, and raising awareness among priority target audiences. By analyzing policy gaps and operational barriers, this paper underscores the need for stronger accountability and political commitment to translate strategies into sustainable action. Strengthening AMR governance through a unified European approach is essential to achieve effective, lasting progress against this silent pandemic.
抗微生物药物耐药性(AMR)每年在欧盟/欧洲经济区造成35 000多人死亡,预计到2050年将导致全球每年191万人死亡。第二次抗微生物药物耐药性和医疗保健相关感染联合行动(EU- jamra2)联合了来自30个国家的128个合作伙伴,代表了欧盟/欧洲经济区通过“同一个健康”方法遏制抗生素耐药性的协调努力。尽管几乎所有欧盟/欧洲经济区国家都有抗微生物药物耐药性国家行动计划,但我们的初步评估显示,实施仍然受到资源有限、部门间协调薄弱和领导分散的制约。eu - jamrai2通过促进协调监测、加强感染预防和控制、采用针对行为的管理干预措施、确保可持续获得基本抗生素以及提高重点目标受众的认识来应对这些挑战。通过分析政策差距和操作障碍,本文强调需要加强问责制和政治承诺,将战略转化为可持续行动。通过统一的欧洲办法加强抗微生物药物耐药性治理,对于在防治这一无声的流行病方面取得有效和持久的进展至关重要。
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引用次数: 0
Cost-effectiveness of pramipexole augmentation for acute phase and maintenance therapy of treatment-resistant depression compared to placebo augmentation: economic evaluation of the PAX-D randomised controlled trial 与安慰剂增强治疗相比,普拉克索增强治疗难治性抑郁症急性期和维持治疗的成本效益:PAX-D随机对照试验的经济评估
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-17 DOI: 10.1016/j.lanepe.2025.101533
Agata Łaszewska , Timea Helter , Ashley Baldwin , Anthony J. Cleare , Philip J. Cowen , Jonathan Evans , Quentin J.M. Huys , Micheal Kurkar , Alexander C. Lewis , Neil Nixon , Abhinav Rastogi , Stuart Watson , John R. Geddes , Michael Browning , Judit Simon

Background

Pramipexole augmentation of antidepressant treatment for treatment-resistant depression (TRD) has been shown to improve symptom burden over 12 weeks but with some adverse effects compared to placebo augmentation. We aimed to evaluate the cost-effectiveness of pramipexole augmentation for TRD.

Methods

We conducted an economic evaluation as part of the PAX-D trial over 12 and 48 weeks. Two costing perspectives, National Health Service and Personal Social Services (NHS + PSS) and societal, were adopted. The primary outcome was quality-adjusted life year (QALY) based on the EQ-5D-5L. Secondary outcomes included year of full capability (YFC) based on the ICECAP-A, and capability-weighted life year (CWLY) based on the OxCAP-MH. Incremental cost-effectiveness ratios (ICERs), cost-effectiveness planes and cost-effectiveness acceptability curves were reported alongside sensitivity analyses. The trial was registered with ISCTRN (ISRCTN84666271) and EudraCT (2019-001023-13) and is complete.

Findings

From the NHS + PSS perspective, mean incremental cost of pramipexole was £60 (95% CI: −£55, £176) over 12 weeks and £811 (95% CI: £110, £1513) over 48 weeks. The difference in QALY gained was 0.012 (95% CI: 0.003, 0.021) over 12 weeks and 0.090 (95% CI: 0.036, 0.144) over 48 weeks, equivalent to 4 (95% CI: 1, 8) and 33 (95% CI: 13, 52) days in perfect health. The ICER was £5069/QALY (95% CI: −£3642, £35,608) over 12 weeks and £9007/QALY (95% CI: £2,219, £27,258) over 48 weeks, representing over 90% probability of cost-effectiveness at £20,000/QALY threshold. From the societal perspective, pramipexole was on average cost saving and more effective over 48 weeks. Alternative analyses provided consistent conclusions.

Interpretation

Pramipexole augmentation for TRD has demonstrated both clinical and cost-effectiveness. Further trials, directly comparing pramipexole to other augmentation strategies, will be useful in determining the position of this repurposed medication in the treatment pathway of depression.

Funding

National Institute for Health and Care Research, Efficacy and Mechanism Evaluation Programme.
研究背景:在治疗难治性抑郁症(TRD)的抗抑郁药物治疗中增加普拉克索已被证明可以改善12周后的症状负担,但与安慰剂增加相比,有一些不良反应。我们的目的是评估增加普拉克索治疗TRD的成本效益。方法作为PAX-D试验的一部分,我们进行了为期12周和48周的经济评估。采用了国民健康服务和个人社会服务(NHS + PSS)和社会两种成本核算视角。主要终点是基于EQ-5D-5L的质量调整生命年(QALY)。次要指标包括基于ICECAP-A的全能力年(YFC)和基于OxCAP-MH的能力加权寿命年(CWLY)。增量成本-效果比(ICERs)、成本-效果平面和成本-效果可接受性曲线与敏感性分析同时报告。该试验已在ISCTRN (ISRCTN84666271)和EudraCT(2019-001023-13)注册,现已完成。从NHS + PSS的角度来看,普拉克索的平均增量成本在12周内为60英镑(95% CI: - 55英镑,176英镑),在48周内为811英镑(95% CI: 110英镑,1513英镑)。在12周内获得的QALY差异为0.012 (95% CI: 0.003, 0.021),在48周内获得的QALY差异为0.090 (95% CI: 0.036, 0.144),相当于完全健康的4 (95% CI: 1, 8)天和33 (95% CI: 13, 52)天。ICER在12周内为5069英镑/QALY (95% CI: - 3642英镑,35,608英镑),在48周内为9007英镑/QALY (95% CI: 2,219英镑,27,258英镑),代表在20,000英镑/QALY阈值下成本效益的概率超过90%。从社会的角度来看,普拉克索在48周内平均节省了成本并更有效。其他分析提供了一致的结论。解释普拉克索对TRD的强化治疗已经证明了临床和成本效益。进一步的试验,直接比较普拉克索与其他增强策略,将有助于确定这种重新定位的药物在抑郁症治疗途径中的地位。资助国家卫生和保健研究所,疗效和机制评估方案。
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引用次数: 0
Announcing the Lancet Migration European Hub and the Lancet Regional Health-Europe Commission on climate change, migration, displacement and health 宣布成立《柳叶刀》欧洲移民中心和《柳叶刀》区域卫生-欧洲委员会,讨论气候变化、移民、流离失所和健康问题
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-17 DOI: 10.1016/j.lanepe.2025.101532
Bernadette N. Kumar , Anand S. Bhopal , Sylvia Garry , Rosemary James , Ozge Karadag , Miriam Orcutt , Shilpa Rao , Shervin Shahnavaz , Santino Severoni , Amirhossein Takian , Pooja Jha , Karl Blanchet
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引用次数: 0
Diagnostic algorithms for tuberculosis in Europe: insights from the European Reference Laboratory Network for Tuberculosis (ERLTB-Net) 欧洲结核病诊断算法:来自欧洲结核病参考实验室网络(ERLTB-Net)的见解
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-15 DOI: 10.1016/j.lanepe.2025.101516
Francesca Saluzzo , Andrea Maurizio Cabibbe , Richard Anthony , Alexandra Aubry , Francis Drobniewski , Yen Holicka , Troels Lillebaek , Rita Macedo , Mikael Mansjö , Viktoria Szél , Ljiljana Žmak , Daniela M. Cirillo , Ramona Groenheit
The reported poor treatment outcomes for extensively drug-resistant tuberculosis (TB) in the European region highlight the urgent need for effective and context-appropriate diagnostic strategies. While the World Health Organisation (WHO) provides model algorithms, these require adaptation to the European Union/European Economic Area (EU/EEA) context, a setting with low TB incidence but high resources. This viewpoint from the European Reference Laboratory Network for TB (ERLTB-Net) proposes a tailored diagnostic algorithm that prioritises the universal use of WHO-recommended molecular rapid diagnostic tests, systematic culture, and whole genome sequencing (WGS). This approach integrates phenotypic drug susceptibility testing strategically and outlines the possible role of targeted next-generation sequencing (tNGS) in the EU/EEA setting. The algorithm also addresses the importance of diagnostic harmonisation, cross-border collaboration, and sustained investment in sequencing capacity. By aligning diagnostic practices with the regional epidemiology and laboratory infrastructure, this stepwise, resource-sensitive approach aims to strengthen TB control, improve treatment outcomes, and guide public health action in the EU/EEA.
据报道,欧洲区域广泛耐药结核病的治疗结果不佳,这突出表明迫切需要制定有效和适合具体情况的诊断战略。虽然世界卫生组织(WHO)提供了模型算法,但这些算法需要适应欧洲联盟/欧洲经济区(EU/EEA)的背景,这是一个结核病发病率低但资源丰富的环境。来自欧洲结核病参考实验室网络(ERLTB-Net)的这一观点提出了一种量身定制的诊断算法,该算法优先考虑普遍使用世卫组织推荐的分子快速诊断检测、系统培养和全基因组测序(WGS)。该方法战略性地整合了表型药敏试验,并概述了靶向下一代测序(tNGS)在欧盟/欧洲经济区环境中的可能作用。该算法还解决了诊断统一、跨境合作和对测序能力持续投资的重要性。通过将诊断实践与区域流行病学和实验室基础设施相结合,这种逐步的、资源敏感的方法旨在加强结核病控制,改善治疗结果,并指导欧盟/欧洲经济区的公共卫生行动。
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引用次数: 0
Outcomes of adults with community-acquired bacterial meningitis in the Netherlands: a prospective nationwide cohort study 荷兰成人社区获得性细菌性脑膜炎的结局:一项前瞻性全国队列研究
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-14 DOI: 10.1016/j.lanepe.2025.101529
Evelien H.G.M. Drost, Eva N. Schepers, Nora Chekrouni, Thijs M. van Soest, Diederik L.H. Koelman, Merijn W. Bijlsma, Matthijs C. Brouwer, Diederik van de Beek

Background

Bacterial meningitis is associated with high rates of unfavourable outcome. We conducted a nationwide prospective study in the Netherlands to evaluate outcome in adults with bacterial meningitis, focusing on pathogen-specific differences, risk factors for unfavourable outcomes, and neurological sequelae.

Methods

Adult patients with community-acquired bacterial meningitis confirmed by lumbar puncture were identified through the database of the Netherlands Reference Laboratory for Bacterial Meningitis and prospectively included. Neurological examinations were performed on admission and discharge by the treating physician, and outcome was assessed using the Glasgow Outcome Scale, with scores of 1–4 classified as unfavourable. Logistic regression was used to evaluate the association between potential predictors and outcome.

Findings

Between January 1, 2006 and January 1, 2024, 2974 patients were included. Streptococcus pneumoniae was the most common pathogen (2029/2974; 68%), followed by Neisseria meningitidis (329/2974; 11%), Listeria monocytogenes (182/2974; 6%), Haemophilus influenzae (119/2974; 4%) and Streptococcus pyogenes (83/2974; 3%). Overall mortality was 17% (516/2974) and remained stable over 18 years (odds ratio per admission year 0·99 [95% CI 0·97–1·01]). Mortality was highest for L. monocytogenes (58/182; 32%), S. pyogenes (16/83; 19%), and S. pneumoniae (365/2029; 18%). Unfavourable outcome occurred in 1161/2974 patients (39%; 95% CI 37–41), and key predictors included advanced age, prolonged symptom duration, systemic or cerebral compromise, low CSF white-cell counts, and absence of adjunctive dexamethasone. Among survivors, neurological sequelae occurred in 1146/2088 patients (55%), including hearing impairment (692/2197; 31%) and cognitive impairment (481/2108; 23%), with highest rates following S. pneumoniae (881/1419; 62%), and S. pyogenes (44/59; 75%).

Interpretation

Mortality and morbidity from bacterial meningitis remain high, especially in L. monocytogenes, S. pyogenes, and S. pneumoniae infections. These findings highlight an urgent need for enhanced vaccination strategies, timely recognition, and improved therapies.

Funding

Netherlands Organization for Health Research and Development (ZonMW).
背景:细菌性脑膜炎与高不良结局率相关。我们在荷兰进行了一项全国范围的前瞻性研究,以评估成人细菌性脑膜炎的预后,重点关注病原体特异性差异、不利预后的危险因素和神经系统后遗症。方法通过荷兰细菌性脑膜炎参考实验室数据库筛选经腰椎穿刺确诊的成年社区获得性细菌性脑膜炎患者,并纳入前瞻性研究。入院和出院时由主治医生进行神经系统检查,并使用格拉斯哥结果量表评估结果,得分为1-4分为不利。使用逻辑回归来评估潜在预测因素与结果之间的关系。在2006年1月1日至2024年1月1日期间,纳入了2974名患者。最常见的病原体是肺炎链球菌(2029/2974;68%),其次是脑膜炎奈瑟菌(329/2974;11%)、单核细胞增生李斯特菌(182/2974;6%)、流感嗜血杆菌(119/2974;4%)和化脓性链球菌(83/2974;3%)。总死亡率为17%(516/2974),在18年内保持稳定(每入院年的优势比0.99 [95% CI 0.97 - 1.01])。死亡率最高的是单核增生乳杆菌(58/182;32%)、化脓性乳杆菌(16/83;19%)和肺炎乳杆菌(365/2029;18%)。1161/2974例患者出现了不良结果(39%;95% CI 37-41),主要预测因素包括高龄、症状持续时间延长、全身或脑损伤、脑脊液白细胞计数低和未使用地塞米松辅助治疗。在幸存者中,1146/2088例患者(55%)出现神经系统后遗症,包括听力障碍(692/2197;31%)和认知障碍(481/2108;23%),发病率最高的是肺炎链球菌(881/1419;62%)和化脓性链球菌(44/59;75%)。细菌性脑膜炎的死亡率和发病率仍然很高,尤其是单核细胞增生乳杆菌、化脓性乳杆菌和肺炎乳杆菌感染。这些发现强调了加强疫苗接种策略、及时认识和改进治疗的迫切需要。荷兰卫生研究与发展组织(卫生研究与发展组织)。
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引用次数: 0
Cancer diagnoses, referrals, and survival in people with a learning disability in the UK: a population-based, matched cohort study 英国学习障碍患者的癌症诊断、转诊和生存率:一项基于人群的匹配队列研究
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-14 DOI: 10.1016/j.lanepe.2025.101519
Oliver John Kennedy , Umesh Chauhan , Louise Gorman , Paul Lorigan , Samuel Merriel , Tjeerd Van Staa , Alison Wright , Darren Mark Ashcroft

Background

People with a learning disability (LD, also known as intellectual disability) face poorer health outcomes, yet the burden of cancer in this population is poorly understood. This study investigated cancer-related outcomes in people with a LD compared to the general population.

Methods

A matched cohort study was conducted using linked primary care, hospital, mortality, and cancer registry data from Clinical Practice Research Datalink (CPRD) Aurum. In total, 180,911 individuals with a LD were matched with 3,405,467 controls. Outcomes included urgent suspected cancer (USC) referrals, cancer diagnoses, treatment within six months, and overall survival (OS) post-diagnosis.

Findings

Individuals with a LD had fewer USC referrals within 28 days of possible cancer symptoms (adjusted risk ratio [aRR] 0.52, 95% confidence interval [CI] 0.49–0.55). LD was associated with several cancers, including sarcoma (adjusted hazard ratio [aHR] 1.98, 1.65–2.39), central nervous system (aHR 3.42, 2.99–3.90), testicular (aHR 2.06, 1.61–2.62), and uterine cancers (aHR 1.69, 1.40–2.05) as well as cancer before age 50 years (aHR 1.74, 1.63–1.86). Absolute incidence was lower in individuals with a LD compared to without (3396 [1.9%] vs 67,506 [2.0%]) due to increased all-cause mortality (aHR 3.19, 3.12–3.27). LD was associated with fewer diagnoses via USC referrals (aRR 0.81, 0.76–0.86), fewer treatments within six months (aRR 0.83, 0.80–0.85) and shorter OS (median 4.4 years, 95% CI 3.9–5.1 vs 9.1 years, 8.8–9.5; aHR 1.73, 1.65–1.83). Melanoma, breast, and prostate cancers were less common but had up to a fourfold increased risk of death after diagnosis in individuals with a LD.

Interpretation

Individuals with a LD have higher cancer risk, more diagnoses outside USC pathways, fewer treatments, and poorer prognosis. Fewer diagnoses of some cancers, alongside worse outcomes, may indicate under-investigation. As premature all-cause mortality improves, cancer burden in this population may rise disproportionately.

Funding

NIHR Greater Manchester Patient Safety Research Collaboration (NIHR204295).
有学习障碍(LD,也称为智力障碍)的人面临着较差的健康结果,但这一人群的癌症负担却知之甚少。这项研究调查了LD患者与一般人群的癌症相关结果。方法采用临床实践研究数据链(CPRD) Aurum的相关初级保健、医院、死亡率和癌症登记数据进行匹配队列研究。总共有180,911名LD患者与3,405,467名对照组相匹配。结果包括紧急疑似癌症(USC)转诊、癌症诊断、6个月内的治疗和诊断后的总生存期(OS)。发现LD患者在可能出现癌症症状的28天内转诊的USC较少(调整风险比[aRR] 0.52, 95%可信区间[CI] 0.49-0.55)。LD与多种癌症相关,包括肉瘤(校正风险比[aHR] 1.98, 1.65-2.39)、中枢神经系统(aHR 3.42, 2.99-3.90)、睾丸癌(aHR 2.06, 1.61-2.62)、子宫癌(aHR 1.69, 1.40-2.05)以及50岁前癌症(aHR 1.74, 1.63-1.86)。由于全因死亡率增加(aHR 3.19, 3.12-3.27), LD患者的绝对发病率低于无LD患者(3396 [1.9%]vs 67,506[2.0%])。LD与通过USC转诊的较少诊断(aRR 0.81, 0.76-0.86),六个月内较少治疗(aRR 0.83, 0.80-0.85)和较短的OS(中位4.4年,95% CI 3.9-5.1 vs 9.1年,8.8-9.5;aHR 1.73, 1.65-1.83)相关。黑色素瘤、乳腺癌和前列腺癌不太常见,但LD患者诊断后死亡风险增加了四倍。解释LD患者患癌症的风险更高,USC途径外的诊断更多,治疗更少,预后更差。一些癌症的诊断率较低,加上预后较差,可能表明尚待调查。随着过早全因死亡率的提高,这一人群的癌症负担可能不成比例地增加。资助nihr大曼彻斯特患者安全研究合作(NIHR204295)。
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引用次数: 0
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Lancet Regional Health-Europe
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