首页 > 最新文献

Lancet Regional Health-Europe最新文献

英文 中文
Frequency and survival of delayed breast cancer diagnosis in women participating at screening mammography in the Netherlands: a population-based study 在荷兰参加乳房x光筛查的妇女中,延迟乳腺癌诊断的频率和生存率:一项基于人群的研究
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-14 DOI: 10.1016/j.lanepe.2025.101526
Lucien E.M. Duijm , Eline L. van der Veer , Hermen C. van Beek , Wikke Setz-Pels , Vivian van Breest Smallenburg , Rob M.G. van Bommel , Clemence L. op de Coul-Froger , Maaike Gielens , Dominique J.P. van Uden , Adri C. Voogd

Background

Although breast cancer screening programmes aim to enable early breast cancer detection, diagnostic delays still occur among participants. Limited information is available on the frequency and survival of women with a delay in breast cancer diagnosis within the screening population. We determined the frequency of various types of delay in breast cancer diagnosis at screening mammography and specified the tumour characteristics, surgical therapy and survival rates of women with these delayed diagnoses, as well as variations in their proportions over time.

Methods

We included 901,133 screening examinations obtained in the southern Netherlands between 1999 and 2019. Screening mammograms of women with interval cancers (ICs) and breast cancers detected at subsequent screening were reviewed to determine whether the cancer had been missed.

Findings

Of the 7129 women with breast cancers, 5419 (76.0%) were diagnosed without delay after recall and 1101 (15.4%) had a true IC (i.e., not detectable at the previous screen). In total, 1601 women experienced a delay in breast cancer diagnosis, comprising the following three study groups: (i) recalled women with a delay in diagnostic work-up (n = 264), (ii) recalled women with screen-detected cancers (SDCs) at subsequent screening and without a delay in diagnostic work-up, that had been missed at the previous screening round (n = 992), and (iii) women with ICs missed at the latest screening round (n = 345). Overall, 26.6% of cancers were associated with a delay (1601/6028), primarily due to SDCs missed at the previous screen (62.0%, 992/1601), followed by missed ICs (21.5%, 345/1601) and misdiagnosis after recall (16.5%, 264/1601). Compared to SDCs missed at the previous screen and misdiagnosis after recall, missed ICs demonstrated the poorest tumour characteristics, highest mastectomy rate (42.6% vs 20.1% and 19.3%, p < 0.0001) and poorest overall survival (5-year rate 86.9% vs 93.8% and 93.8%, p = 0.0017). Temporal trends in tumour characteristics were mainly observed in SDCs missed at the previous screen.

Interpretation

Delayed breast cancer diagnosis at screening mammography or after recall remains a serious point of concern. Most delays are related to SDCs missed at a previous screen, whereas missed ICs show the worst survival.

Funding

This research did not receive any funding.
尽管乳腺癌筛查项目旨在实现早期乳腺癌检测,但在参与者中仍然存在诊断延迟的情况。关于筛查人群中乳腺癌诊断延迟的妇女的频率和生存率的信息有限。我们确定了筛查乳房x光检查中各种类型乳腺癌诊断延迟的频率,并详细说明了这些延迟诊断的女性的肿瘤特征、手术治疗和生存率,以及其比例随时间的变化。方法纳入1999年至2019年在荷兰南部获得的901133例筛查检查。对间隔期癌症(ICs)和随后筛查中发现的乳腺癌妇女的筛查乳房x线照片进行审查,以确定是否遗漏了癌症。结果:在7129例乳腺癌患者中,5419例(76.0%)在召回后立即被诊断出来,1101例(15.4%)有真正的IC(即在之前的筛查中未检测到)。总共有1601名女性经历了乳腺癌诊断的延迟,包括以下三个研究组:(i)在诊断检查中延迟的女性(n = 264), (ii)在随后的筛查中筛查出癌症(sdc)且在诊断检查中没有延迟的女性(n = 992),以及(iii)在最近一轮筛查中遗漏的ic女性(n = 345)。总体而言,26.6%的癌症与延迟相关(1601/6028),主要是由于之前筛查时遗漏的sdc(62.0%, 992/1601),其次是遗漏的ic(21.5%, 345/1601)和回忆后误诊(16.5%,264/1601)。与之前筛查遗漏的scs和回忆后的误诊相比,遗漏的ICs表现出最差的肿瘤特征,最高的乳房切除术率(42.6%对20.1%和19.3%,p < 0.0001)和最差的总生存率(5年生存率86.9%对93.8%和93.8%,p = 0.0017)。肿瘤特征的时间趋势主要观察到之前筛查中遗漏的sdc。解释:乳房x光筛查或召回后延迟的乳腺癌诊断仍然是一个严重的问题。大多数延迟与在前一个屏幕上错过的sdc有关,而错过的ic显示出最差的存活率。这项研究没有得到任何资助。
{"title":"Frequency and survival of delayed breast cancer diagnosis in women participating at screening mammography in the Netherlands: a population-based study","authors":"Lucien E.M. Duijm ,&nbsp;Eline L. van der Veer ,&nbsp;Hermen C. van Beek ,&nbsp;Wikke Setz-Pels ,&nbsp;Vivian van Breest Smallenburg ,&nbsp;Rob M.G. van Bommel ,&nbsp;Clemence L. op de Coul-Froger ,&nbsp;Maaike Gielens ,&nbsp;Dominique J.P. van Uden ,&nbsp;Adri C. Voogd","doi":"10.1016/j.lanepe.2025.101526","DOIUrl":"10.1016/j.lanepe.2025.101526","url":null,"abstract":"<div><h3>Background</h3><div>Although breast cancer screening programmes aim to enable early breast cancer detection, diagnostic delays still occur among participants. Limited information is available on the frequency and survival of women with a delay in breast cancer diagnosis within the screening population. We determined the frequency of various types of delay in breast cancer diagnosis at screening mammography and specified the tumour characteristics, surgical therapy and survival rates of women with these delayed diagnoses, as well as variations in their proportions over time.</div></div><div><h3>Methods</h3><div>We included 901,133 screening examinations obtained in the southern Netherlands between 1999 and 2019. Screening mammograms of women with interval cancers (ICs) and breast cancers detected at subsequent screening were reviewed to determine whether the cancer had been missed.</div></div><div><h3>Findings</h3><div>Of the 7129 women with breast cancers, 5419 (76.0%) were diagnosed without delay after recall and 1101 (15.4%) had a true IC (i.e., not detectable at the previous screen). In total, 1601 women experienced a delay in breast cancer diagnosis, comprising the following three study groups: (i) recalled women with a delay in diagnostic work-up (n = 264), (ii) recalled women with screen-detected cancers (SDCs) at subsequent screening and without a delay in diagnostic work-up, that had been missed at the previous screening round (n = 992), and (iii) women with ICs missed at the latest screening round (n = 345). Overall, 26.6% of cancers were associated with a delay (1601/6028), primarily due to SDCs missed at the previous screen (62.0%, 992/1601), followed by missed ICs (21.5%, 345/1601) and misdiagnosis after recall (16.5%, 264/1601). Compared to SDCs missed at the previous screen and misdiagnosis after recall, missed ICs demonstrated the poorest tumour characteristics, highest mastectomy rate (42.6% vs 20.1% and 19.3%, p &lt; 0.0001) and poorest overall survival (5-year rate 86.9% vs 93.8% and 93.8%, p = 0.0017). Temporal trends in tumour characteristics were mainly observed in SDCs missed at the previous screen.</div></div><div><h3>Interpretation</h3><div>Delayed breast cancer diagnosis at screening mammography or after recall remains a serious point of concern. Most delays are related to SDCs missed at a previous screen, whereas missed ICs show the worst survival.</div></div><div><h3>Funding</h3><div>This research did not receive any funding.</div></div>","PeriodicalId":53223,"journal":{"name":"Lancet Regional Health-Europe","volume":"61 ","pages":"Article 101526"},"PeriodicalIF":13.0,"publicationDate":"2025-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145499918","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A multimodal individualized long-term intervention to prevent functional decline after stroke (LAST-long): a single blinded randomised controlled trial 预防脑卒中后功能衰退的多模式个性化长期干预(LAST-long):一项单盲随机对照试验
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-13 DOI: 10.1016/j.lanepe.2025.101531
Torunn Askim , Sara Rise Langlo , Elin Bergh , Øystein Døhl , Hanne Ellekjær , Anne Hokstad , Håkon Ihle-Hansen , Bent Indredavik , Stian Lydersen , Geske Luzum , Yngve Seljeseth , Toril Skandsen , Ingvild Saltvedt , Bente Thommessen
<div><h3>Background</h3><div>Despite the lack of evidence, the Stroke Action Plan for Europe recommends coordinated support after initial rehabilitation. This trial investigated if a coordinator-led multimodal intervention was superior to standard care in preventing dependency and functional decline after stroke.</div></div><div><h3>Methods</h3><div>In this single blinded randomised controlled multi-centre trial, patients were consecutively screened, included and randomised (1:1) by a web-based randomization system to an intervention or a control group at the out-patient clinics at four Norwegian hospitals three months post-stroke. Blinded assessments were performed at inclusion and at 6-, 12-, and 18-month follow-up. The inclusion criteria were; age ≥18 years, life expectancy ≥12 months (assessed by the physician), modified Rankin Scale (mRS) score <5, vulnerable to functional decline (defined by other measures). The control group received standard care, while the intervention group additionally received monthly follow-up by a community-based stroke coordinator who applied a study specific checklist to identify the patients’ risk profile within multiple domains. Individual goals and action points were defined accordingly. The intervention lasted for 18 months. Mixed models were used to evaluate differences between the groups for the primary endpoint (mRS at 18-month follow-up) and secondary endpoints (activities of daily living, cognitive function, physical function, patient reported outcomes, physical activity, blood pressure, body mass index and blood tests) at 6-, 12-, and 18-month follow-up. The trial was registered at ClinicalTrials.gov identifier: NCT03859063. The trial has been completed.</div></div><div><h3>Findings</h3><div>The LAST-long trial was conducted from April 11, 2019 to August 28, 2024. In total, 301 participants (48% women); mean age 71·3 (SD 12·3) years, National Institute of Health Stroke Scale admission score 3·38 (SD 4·21), and mRS at inclusion 1·6 (SD 0·9), were randomised to the intervention (n = 152) or control (n = 149) group 108.0 (SD 18·5) days post stroke. The number of serious adverse events (deaths, hospitalisation due to cardiovascular events, cerebrovascular events or fall with or without fracture) was 32 (21·1%) in the intervention group and 33 (22·1%) in the control group. At 18 months, the estimated difference between the groups was 0·03 (95% CI: −0·16 to 0·22), p = 0·79 for mRS.</div></div><div><h3>Interpretation</h3><div>The 18-month multimodal intervention was not superior to standard care received by the control group in people with mild stroke. An even longer follow-up period might be needed to investigate the effect of the intervention on hard outcomes like death or recurrent vascular events.</div></div><div><h3>Funding</h3><div>The Research Council of Norway, The Joint Research Committee between St. Olavs Hospital and the Faculty of Medicine and Health Sciences, NTNU (FFU), Foundation Dam.</div></d
尽管缺乏证据,欧洲中风行动计划建议在初始康复后提供协调一致的支持。该试验调查了协调员主导的多模式干预在预防中风后的依赖性和功能下降方面是否优于标准护理。方法在这项单盲随机对照多中心试验中,通过基于网络的随机化系统对患者进行连续筛选,纳入并随机(1:1)分配到卒中后3个月挪威四家医院门诊的干预组或对照组。在纳入和6个月、12个月和18个月随访时进行盲法评估。纳入标准为;年龄≥18岁,预期寿命≥12个月(由医生评估),修改Rankin量表(mRS)评分为5分,易发生功能衰退(由其他指标定义)。对照组接受标准治疗,而干预组每月接受社区卒中协调员的随访,该协调员使用研究特定的检查表来确定患者在多个领域的风险概况。据此确定了个人目标和行动点。干预持续了18个月。使用混合模型来评估6、12和18个月随访时主要终点(18个月随访时的mRS)和次要终点(日常生活活动、认知功能、身体功能、患者报告的结局、身体活动、血压、体重指数和血液检查)组间的差异。该试验在ClinicalTrials.gov注册,识别码:NCT03859063。审判已经结束。LAST-long试验于2019年4月11日至2024年8月28日进行。共有301名参与者(48%为女性);平均年龄73.1岁(SD 12.3),美国国立卫生研究院卒中量表入院评分3.38 (SD 4.21),纳入时的mRS值为1.6 (SD 0.9),随机分为干预组(n = 152)和对照组(n = 149),卒中后108.0 (SD 18.5)天。干预组的严重不良事件(死亡、因心血管事件、脑血管事件住院或跌倒合并或不合并骨折)为32例(21.1%),对照组为33例(22.1%)。在18个月时,两组之间的估计差异为0.03 (95% CI: - 0.16至0.22),mrs . p = 0.79。在轻度中风患者中,18个月的多模式干预并不优于对照组接受的标准治疗。可能需要更长的随访时间来调查干预对死亡或复发性血管事件等硬性结果的影响。资助:挪威研究理事会、挪威科技大学圣奥拉夫斯医院与医学和健康科学学院联合研究委员会、基金会大坝。
{"title":"A multimodal individualized long-term intervention to prevent functional decline after stroke (LAST-long): a single blinded randomised controlled trial","authors":"Torunn Askim ,&nbsp;Sara Rise Langlo ,&nbsp;Elin Bergh ,&nbsp;Øystein Døhl ,&nbsp;Hanne Ellekjær ,&nbsp;Anne Hokstad ,&nbsp;Håkon Ihle-Hansen ,&nbsp;Bent Indredavik ,&nbsp;Stian Lydersen ,&nbsp;Geske Luzum ,&nbsp;Yngve Seljeseth ,&nbsp;Toril Skandsen ,&nbsp;Ingvild Saltvedt ,&nbsp;Bente Thommessen","doi":"10.1016/j.lanepe.2025.101531","DOIUrl":"10.1016/j.lanepe.2025.101531","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Background&lt;/h3&gt;&lt;div&gt;Despite the lack of evidence, the Stroke Action Plan for Europe recommends coordinated support after initial rehabilitation. This trial investigated if a coordinator-led multimodal intervention was superior to standard care in preventing dependency and functional decline after stroke.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Methods&lt;/h3&gt;&lt;div&gt;In this single blinded randomised controlled multi-centre trial, patients were consecutively screened, included and randomised (1:1) by a web-based randomization system to an intervention or a control group at the out-patient clinics at four Norwegian hospitals three months post-stroke. Blinded assessments were performed at inclusion and at 6-, 12-, and 18-month follow-up. The inclusion criteria were; age ≥18 years, life expectancy ≥12 months (assessed by the physician), modified Rankin Scale (mRS) score &lt;5, vulnerable to functional decline (defined by other measures). The control group received standard care, while the intervention group additionally received monthly follow-up by a community-based stroke coordinator who applied a study specific checklist to identify the patients’ risk profile within multiple domains. Individual goals and action points were defined accordingly. The intervention lasted for 18 months. Mixed models were used to evaluate differences between the groups for the primary endpoint (mRS at 18-month follow-up) and secondary endpoints (activities of daily living, cognitive function, physical function, patient reported outcomes, physical activity, blood pressure, body mass index and blood tests) at 6-, 12-, and 18-month follow-up. The trial was registered at ClinicalTrials.gov identifier: NCT03859063. The trial has been completed.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Findings&lt;/h3&gt;&lt;div&gt;The LAST-long trial was conducted from April 11, 2019 to August 28, 2024. In total, 301 participants (48% women); mean age 71·3 (SD 12·3) years, National Institute of Health Stroke Scale admission score 3·38 (SD 4·21), and mRS at inclusion 1·6 (SD 0·9), were randomised to the intervention (n = 152) or control (n = 149) group 108.0 (SD 18·5) days post stroke. The number of serious adverse events (deaths, hospitalisation due to cardiovascular events, cerebrovascular events or fall with or without fracture) was 32 (21·1%) in the intervention group and 33 (22·1%) in the control group. At 18 months, the estimated difference between the groups was 0·03 (95% CI: −0·16 to 0·22), p = 0·79 for mRS.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Interpretation&lt;/h3&gt;&lt;div&gt;The 18-month multimodal intervention was not superior to standard care received by the control group in people with mild stroke. An even longer follow-up period might be needed to investigate the effect of the intervention on hard outcomes like death or recurrent vascular events.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Funding&lt;/h3&gt;&lt;div&gt;The Research Council of Norway, The Joint Research Committee between St. Olavs Hospital and the Faculty of Medicine and Health Sciences, NTNU (FFU), Foundation Dam.&lt;/div&gt;&lt;/d","PeriodicalId":53223,"journal":{"name":"Lancet Regional Health-Europe","volume":"61 ","pages":"Article 101531"},"PeriodicalIF":13.0,"publicationDate":"2025-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145499917","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Ethnic inequalities in all-cause mortality in the UK: the importance of evidence in shaping health policy 英国全因死亡率中的种族不平等:证据在制定卫生政策中的重要性
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-10 DOI: 10.1016/j.lanepe.2025.101530
Peter Goldblatt , Veena Raleigh
{"title":"Ethnic inequalities in all-cause mortality in the UK: the importance of evidence in shaping health policy","authors":"Peter Goldblatt ,&nbsp;Veena Raleigh","doi":"10.1016/j.lanepe.2025.101530","DOIUrl":"10.1016/j.lanepe.2025.101530","url":null,"abstract":"","PeriodicalId":53223,"journal":{"name":"Lancet Regional Health-Europe","volume":"59 ","pages":"Article 101530"},"PeriodicalIF":13.0,"publicationDate":"2025-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145528709","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Ending HIV transmission in Europe 在欧洲终止艾滋病毒传播
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-07 DOI: 10.1016/j.lanepe.2025.101522
Jan A.C. Hontelez , Casper Rokx
{"title":"Ending HIV transmission in Europe","authors":"Jan A.C. Hontelez ,&nbsp;Casper Rokx","doi":"10.1016/j.lanepe.2025.101522","DOIUrl":"10.1016/j.lanepe.2025.101522","url":null,"abstract":"","PeriodicalId":53223,"journal":{"name":"Lancet Regional Health-Europe","volume":"60 ","pages":"Article 101522"},"PeriodicalIF":13.0,"publicationDate":"2025-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145468506","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Management and survival of patients with cancer of unknown primary discussed by a French national multidisciplinary tumour board: a retrospective analysis 法国国家多学科肿瘤委员会讨论了原发不明的癌症患者的管理和生存:回顾性分析
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-07 DOI: 10.1016/j.lanepe.2025.101524
Célia Dupain , Nicolas Jacquin , Aurélien Latouche , Zoé Nevière , Pierre Gestraud , Abderaouf Hamza , Kenza Nedara , Vincent Cockenpot , Janick Selves , Yves Allory , Laëtitia Chanas , Maud Milder , Isabelle Soubeyran , Hélène Blons , Anna Patrikidou , Axel de Bernardi , Julien Masliah-Planchon , Odette Mariani , Etienne Rouleau , Fabienne Escande , Sarah Watson

Background

Recent clinical trials have shown that molecularly-guided treatments can improve survival in patients with cancers of unknown primary (CUP). However, the feasibility and clinical benefit of these treatments for CUP in a real-life setting remain uncertain. In France, a national multidisciplinary tumour board dedicated to patients with CUP (CUP MTB) was created in 2020, with the aims of coordinating pathological and molecular diagnostic analyses and providing a centralised expertise for therapeutic orientation. This study aimed at evaluating the diagnostic and therapeutic impact of the CUP MTB on patients with CUP in a national real-life setting.

Methods

Patient and tumour characteristics, treatments and outcomes are collected prospectively. This study reports the diagnostic and therapeutic impact of all patients discussed in CUP_MTB between July 2020 and December 2023. The diagnostic impact was defined as the identification of a putative tissue of origin, and the initiation of a MTB–oriented treatment. Overall survival was estimated using the Kaplan–Meier method, and hazard ratios were calculated using Cox proportional hazard models.

Findings

A total of 246 CUP patients were referred to CUP_MTB (124 females and 122 men); 187 (76%) underwent pathological and molecular characterizations as recommended by the MTB. Tumour profiling enabled the identification of a putative tissue of origin (TOO) in 130/187 (70%) patients. The most frequent TOO were gastrointestinal (n = 29; 22%), lung (n = 22; 17%), breast (n = 21; 16%), and kidney (n = 19; 15%). 149 (61%) patients received a treatment based on MTB recommendation. 111/149 (74.5%) patients received MTB-oriented treatment, including systemic treatment oriented towards the putative TOO (n = 95, 63.8%), or treatment directed towards a targetable molecular alteration (n = 16, 10.7%). 38 (25.5%) patients for whom no MTB-oriented treatment could be recommended were treated with empiric treatment according to international guidelines. The median overall survival of patients treated with MTB-oriented treatment was 18.6 (IQR = 12.0) months, compared to 11.0 (IQR = 10.5) months in patients with empiric treatment (HR = 0.61, 95% CI 0.38–0.98, p = 0.04).

Interpretation

Integration of clinical, pathological and molecular data within an expert MTB is feasible in a real-life setting, enables access to molecularly guided treatments and improves survival for a large proportion of CUP patients. Our findings highlight the benefits of dedicated MTB and reference centres to improve the management of CUP.

Funding

Institut Curie and the 2025 French Genomic Medicine Initiative.
最近的临床试验表明,分子引导治疗可以提高未知原发癌症(CUP)患者的生存率。然而,在现实生活中,这些治疗CUP的可行性和临床效益仍然不确定。在法国,一个专门针对CUP患者(CUP MTB)的国家多学科肿瘤委员会于2020年成立,目的是协调病理和分子诊断分析,并为治疗方向提供集中的专业知识。本研究旨在评估在国家现实环境中CUP MTB对CUP患者的诊断和治疗影响。方法前瞻性收集患者及肿瘤特征、治疗方法及转归。本研究报告了2020年7月至2023年12月期间在CUP_MTB中讨论的所有患者的诊断和治疗影响。诊断影响被定义为鉴定推定的起源组织,并开始mtb导向的治疗。使用Kaplan-Meier法估计总生存率,使用Cox比例风险模型计算风险比。结果:共有246例CUP患者转诊至CUP_MTB,其中女性124例,男性122例;187例(76%)接受了MTB推荐的病理和分子特征。在130/187例(70%)患者中,肿瘤分析能够识别推定的起源组织(TOO)。最常见的TOO是胃肠道(n = 29; 22%)、肺部(n = 22; 17%)、乳房(n = 21; 16%)和肾脏(n = 19; 15%)。149例(61%)患者接受了基于结核分枝杆菌推荐的治疗。111/149(74.5%)患者接受了mtb导向的治疗,包括针对假定的TOO的全身治疗(n = 95, 63.8%),或针对可靶向分子改变的治疗(n = 16, 10.7%)。38例(25.5%)无法推荐mtb导向治疗的患者根据国际指南接受了经验性治疗。接受mtb导向治疗的患者中位总生存期为18.6 (IQR = 12.0)个月,而经验治疗的患者中位总生存期为11.0 (IQR = 10.5)个月(HR = 0.61, 95% CI 0.38-0.98, p = 0.04)。在专家MTB中整合临床、病理和分子数据在现实生活中是可行的,可以获得分子指导治疗,并提高很大一部分CUP患者的生存率。我们的研究结果强调了专门的MTB和参考中心对改善CUP管理的好处。资助居里研究所和2025年法国基因组医学倡议。
{"title":"Management and survival of patients with cancer of unknown primary discussed by a French national multidisciplinary tumour board: a retrospective analysis","authors":"Célia Dupain ,&nbsp;Nicolas Jacquin ,&nbsp;Aurélien Latouche ,&nbsp;Zoé Nevière ,&nbsp;Pierre Gestraud ,&nbsp;Abderaouf Hamza ,&nbsp;Kenza Nedara ,&nbsp;Vincent Cockenpot ,&nbsp;Janick Selves ,&nbsp;Yves Allory ,&nbsp;Laëtitia Chanas ,&nbsp;Maud Milder ,&nbsp;Isabelle Soubeyran ,&nbsp;Hélène Blons ,&nbsp;Anna Patrikidou ,&nbsp;Axel de Bernardi ,&nbsp;Julien Masliah-Planchon ,&nbsp;Odette Mariani ,&nbsp;Etienne Rouleau ,&nbsp;Fabienne Escande ,&nbsp;Sarah Watson","doi":"10.1016/j.lanepe.2025.101524","DOIUrl":"10.1016/j.lanepe.2025.101524","url":null,"abstract":"<div><h3>Background</h3><div>Recent clinical trials have shown that molecularly-guided treatments can improve survival in patients with cancers of unknown primary (CUP). However, the feasibility and clinical benefit of these treatments for CUP in a real-life setting remain uncertain. In France, a national multidisciplinary tumour board dedicated to patients with CUP (CUP MTB) was created in 2020, with the aims of coordinating pathological and molecular diagnostic analyses and providing a centralised expertise for therapeutic orientation. This study aimed at evaluating the diagnostic and therapeutic impact of the CUP MTB on patients with CUP in a national real-life setting.</div></div><div><h3>Methods</h3><div>Patient and tumour characteristics, treatments and outcomes are collected prospectively. This study reports the diagnostic and therapeutic impact of all patients discussed in CUP_MTB between July 2020 and December 2023. The diagnostic impact was defined as the identification of a putative tissue of origin, and the initiation of a MTB–oriented treatment. Overall survival was estimated using the Kaplan–Meier method, and hazard ratios were calculated using Cox proportional hazard models.</div></div><div><h3>Findings</h3><div>A total of 246 CUP patients were referred to CUP_MTB (124 females and 122 men); 187 (76%) underwent pathological and molecular characterizations as recommended by the MTB. Tumour profiling enabled the identification of a putative tissue of origin (TOO) in 130/187 (70%) patients. The most frequent TOO were gastrointestinal (n = 29; 22%), lung (n = 22; 17%), breast (n = 21; 16%), and kidney (n = 19; 15%). 149 (61%) patients received a treatment based on MTB recommendation. 111/149 (74.5%) patients received MTB-oriented treatment, including systemic treatment oriented towards the putative TOO (n = 95, 63.8%), or treatment directed towards a targetable molecular alteration (n = 16, 10.7%). 38 (25.5%) patients for whom no MTB-oriented treatment could be recommended were treated with empiric treatment according to international guidelines. The median overall survival of patients treated with MTB-oriented treatment was 18.6 (IQR = 12.0) months, compared to 11.0 (IQR = 10.5) months in patients with empiric treatment (HR = 0.61, 95% CI 0.38–0.98, p = 0.04).</div></div><div><h3>Interpretation</h3><div>Integration of clinical, pathological and molecular data within an expert MTB is feasible in a real-life setting, enables access to molecularly guided treatments and improves survival for a large proportion of CUP patients. Our findings highlight the benefits of dedicated MTB and reference centres to improve the management of CUP.</div></div><div><h3>Funding</h3><div><span>Institut Curie</span> and the 2025 <span>French Genomic Medicine Initiative</span>.</div></div>","PeriodicalId":53223,"journal":{"name":"Lancet Regional Health-Europe","volume":"60 ","pages":"Article 101524"},"PeriodicalIF":13.0,"publicationDate":"2025-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145468474","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The estimated impact of mandatory front-of-pack nutrition labelling policies on adult obesity prevalence and obesity-related mortality in England: a modelling study 强制性包装正面营养标签政策对英国成人肥胖患病率和肥胖相关死亡率的估计影响:一项模型研究
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-04 DOI: 10.1016/j.lanepe.2025.101506
Rebecca Evans , Martin O'Flaherty , I Gusti Ngurah Edi Putra , Chris Kypridemos , Eric Robinson , Zoé Colombet

Background

Since 2013, front-of-pack traffic light labels have been implemented voluntarily on packaged food in the UK. The UK Government is now considering alternative labelling approaches which may be more effective, such as Chile's mandatory nutrient warning labels. The present study aimed to estimate the impact of mandatorily implementing (i) traffic light labels and (ii) nutrient warning labels on population-level obesity prevalence and mortality in England.

Methods

A microsimulation model was built to simulate the effects of implementing mandatory front-of-pack nutrition labels (nutrient warning and traffic light) on assumed changes in daily energy intake from packaged food (due to consumer behaviour change and reformulation), and subsequent population-level obesity prevalence and mortality due to changes in BMI. We modelled the population of England, aged 30–89 years, over 20 years (2024–2043) using a synthetic population stratified by age, sex and Index of Multiple Deprivation. The model simulates individuals' life courses and counterfactuals under different policy scenarios, allowing detailed assessment of policies on exposures, disease risk, and mortality.

Findings

Compared to the baseline scenario (current voluntary implementation of traffic light labelling), mandatory implementation of traffic light labelling was estimated to reduce obesity prevalence by 2.34 percentage points (95% UI 0.67–4.31) and prevent or postpone 57,000 (95% UI 13,000–160,000) obesity-related deaths. Mandatory implementation of nutrient warning labelling was estimated to have a larger impact; a 4.44 percentage point (95% UI 0.08–10.76) reduction in obesity prevalence and 110,000 (95% UI 2000–420,000) fewer obesity-related deaths.

Interpretation

This work offers the first modelled estimation of the impact of introducing mandatory front-of-pack nutrition labels on obesity prevalence in the adult population in England. Findings suggest that mandatory implementation of nutrient warning labels would reduce prevalence of obesity and related deaths, compared to current voluntary or mandatory implementation of traffic light labelling, and should therefore be considered by the UK Government.

Funding

European Research Council.
自2013年以来,英国在包装食品上自愿实施了包装前红绿灯标签。英国政府现在正在考虑可能更有效的替代标签方法,例如智利的强制性营养警告标签。本研究旨在估计强制实施(i)交通灯标签和(ii)营养警告标签对英格兰人口水平肥胖患病率和死亡率的影响。方法建立微观模拟模型,模拟实施强制性包装前营养标签(营养警告和红绿灯)对包装食品每日能量摄入(由于消费者行为改变和重新配方)的假设变化的影响,以及随后由于BMI变化导致的人群水平肥胖患病率和死亡率。我们使用按年龄、性别和多重剥夺指数(Index of Multiple Deprivation)分层的合成人口,对20多年(2024-2043)年龄在30-89岁之间的英格兰人口进行了建模。该模型模拟了不同政策情景下个人的生命历程和反事实,允许对暴露、疾病风险和死亡率的政策进行详细评估。研究结果与基线情景(目前自愿实施交通灯标识)相比,强制性实施交通灯标识估计可将肥胖患病率降低2.34个百分点(95% UI 0.67-4.31),并预防或推迟57,000例(95% UI 13,000-160,000)与肥胖相关的死亡。强制性实施营养警告标签估计会产生更大的影响;肥胖患病率降低4.44个百分点(95% UI为0.08-10.76),与肥胖相关的死亡人数减少11万人(95% UI为2000 - 42万人)。这项工作提供了第一个模型估计引入强制性包装前营养标签对英国成年人肥胖患病率的影响。研究结果表明,与目前自愿或强制实施交通灯标签相比,强制实施营养警告标签将减少肥胖患病率和相关死亡,因此英国政府应予以考虑。资助欧洲研究委员会。
{"title":"The estimated impact of mandatory front-of-pack nutrition labelling policies on adult obesity prevalence and obesity-related mortality in England: a modelling study","authors":"Rebecca Evans ,&nbsp;Martin O'Flaherty ,&nbsp;I Gusti Ngurah Edi Putra ,&nbsp;Chris Kypridemos ,&nbsp;Eric Robinson ,&nbsp;Zoé Colombet","doi":"10.1016/j.lanepe.2025.101506","DOIUrl":"10.1016/j.lanepe.2025.101506","url":null,"abstract":"<div><h3>Background</h3><div>Since 2013, front-of-pack traffic light labels have been implemented voluntarily on packaged food in the UK. The UK Government is now considering alternative labelling approaches which may be more effective, such as Chile's mandatory nutrient warning labels. The present study aimed to estimate the impact of mandatorily implementing (i) traffic light labels and (ii) nutrient warning labels on population-level obesity prevalence and mortality in England.</div></div><div><h3>Methods</h3><div>A microsimulation model was built to simulate the effects of implementing mandatory front-of-pack nutrition labels (nutrient warning and traffic light) on assumed changes in daily energy intake from packaged food (due to consumer behaviour change and reformulation), and subsequent population-level obesity prevalence and mortality due to changes in BMI. We modelled the population of England, aged 30–89 years, over 20 years (2024–2043) using a synthetic population stratified by age, sex and Index of Multiple Deprivation. The model simulates individuals' life courses and counterfactuals under different policy scenarios, allowing detailed assessment of policies on exposures, disease risk, and mortality.</div></div><div><h3>Findings</h3><div>Compared to the baseline scenario (current voluntary implementation of traffic light labelling), mandatory implementation of traffic light labelling was estimated to reduce obesity prevalence by 2.34 percentage points (95% UI 0.67–4.31) and prevent or postpone 57,000 (95% UI 13,000–160,000) obesity-related deaths. Mandatory implementation of nutrient warning labelling was estimated to have a larger impact; a 4.44 percentage point (95% UI 0.08–10.76) reduction in obesity prevalence and 110,000 (95% UI 2000–420,000) fewer obesity-related deaths.</div></div><div><h3>Interpretation</h3><div>This work offers the first modelled estimation of the impact of introducing mandatory front-of-pack nutrition labels on obesity prevalence in the adult population in England. Findings suggest that mandatory implementation of nutrient warning labels would reduce prevalence of obesity and related deaths, compared to current voluntary or mandatory implementation of traffic light labelling, and should therefore be considered by the UK Government.</div></div><div><h3>Funding</h3><div>European Research Council.</div></div>","PeriodicalId":53223,"journal":{"name":"Lancet Regional Health-Europe","volume":"60 ","pages":"Article 101506"},"PeriodicalIF":13.0,"publicationDate":"2025-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145790205","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Suicide after involuntary psychiatric care: a nationwide cohort study in Sweden 非自愿精神治疗后自杀:瑞典的一项全国性队列研究
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-04 DOI: 10.1016/j.lanepe.2025.101504
Leoni Grossmann , Fred Johansson , Seena Fazel , Ralf Kuja-Halkola , Björn Bråstad , David Mataix-Cols , Lorena Fernández de la Cruz , Bo Runeson , Paul Lichtenstein , Zheng Chang , Henrik Larsson , Isabell Brikell , Brian D'Onofrio , Ronnie Pingel , Christian Rück , John Wallert

Background

Little is known about the risk of suicide in individuals treated against their will in involuntary psychiatric care (IPC). This population-based study provides a first comprehensive description of suicide among individuals who experienced IPC.

Methods

We studied all individuals discharged from IPC in Sweden from 2010 through 2020. Clinical and sociodemographic characteristics are reported followed by suicide risk for the complete IPC population and stratified by sex, age, IPC history, and diagnostic category. Crude and adjusted relative risks compared to all individuals discharged from psychiatric in- and outpatient care and the general population were estimated using Poisson regression. Suicide methods, seasonal trends, and geographical variance are also reported.

Findings

We identified 72 275 patients treated in IPC with a total of 134 514 inpatient care episodes (mean age = 44·8 years, 37 462 [51·8%] males). Of these, 2104 (2·9%) died by suicide over a median follow-up time of 4·4 years (IQR: 1⋅8–7⋅5). Suicide decedents were younger, more often male, single, diagnosed with personality and substance use disorders, and had a history of self-harm and IPC, compared to those who did not die by suicide. The absolute risk (crude incidence rate (IR) per 100 000 person-years) for all IPC patients was highest closest to discharge (IR1month = 2941 [2538, 3408]) and decreased thereafter (IR5years = 738 [705, 773]). Suicide risk in IPC patients was elevated relative to psychiatric inpatients (crude IR ratio (IRR)5years = 1·57 [1·48, 1·65]), psychiatric outpatients (IRR5years = 3·77 [3·58, 3·97]), and the general population (IRR5years = 55·52 [52·65, 58·54]).

Interpretation

We found substantial risk differences in distinct subgroups of IPC patients and an excess suicide risk among IPC patients compared to other clinical populations. These findings warrant further investigation as they could inform clinicians and policy makers regarding potential risk stratification, monitoring, and care. Preventing suicides after IPC should be a priority.

Funding

VR, ALF Medicine, CIMED, FORTE, and Söderström König Foundation.
背景:在非自愿精神科护理(IPC)中,人们对违背个人意愿接受治疗的个体的自杀风险知之甚少。这项以人群为基础的研究首次全面描述了IPC患者的自杀情况。方法研究2010 - 2020年瑞典所有从IPC出院的个体。报告全部IPC人群的临床和社会人口学特征,然后是自杀风险,并按性别、年龄、IPC病史和诊断类别进行分层。使用泊松回归估计所有从精神科住院和门诊出院的个体与一般人群的粗风险和调整后的相对风险。自杀方式、季节趋势和地域差异也有报道。结果:我们确定了72 275例IPC患者,共134 514次住院治疗(平均年龄= 44.8岁,男性37 462例(51.8%))。其中,2104人(2.9%)在平均4年的随访时间内自杀死亡(IQR: 1⋅8-7⋅5)。与非自杀者相比,自杀者更年轻,多为男性,单身,被诊断患有人格和物质使用障碍,有自残史和IPC。所有IPC患者的绝对风险(每10万人年的粗发病率(IR))在最接近出院时最高(ir1个月= 2941[2538,3408]),此后降低(ir5年= 738[705,773])。IPC患者的自杀风险相对于精神科住院患者(IRR粗比值(IRR)5年= 1.57[1.48,1.65])、精神科门诊患者(IRR = 3.77[3.58, 3.97])和一般人群(IRR = 55·52[52.65,58·54])均有升高。我们发现IPC患者的不同亚组存在显著的风险差异,与其他临床人群相比,IPC患者的自杀风险较高。这些发现值得进一步调查,因为它们可以为临床医生和政策制定者提供有关潜在风险分层、监测和护理的信息。预防IPC后的自杀应该是优先考虑的。FundingVR, ALF Medicine, CIMED, FORTE和Söderström König Foundation。
{"title":"Suicide after involuntary psychiatric care: a nationwide cohort study in Sweden","authors":"Leoni Grossmann ,&nbsp;Fred Johansson ,&nbsp;Seena Fazel ,&nbsp;Ralf Kuja-Halkola ,&nbsp;Björn Bråstad ,&nbsp;David Mataix-Cols ,&nbsp;Lorena Fernández de la Cruz ,&nbsp;Bo Runeson ,&nbsp;Paul Lichtenstein ,&nbsp;Zheng Chang ,&nbsp;Henrik Larsson ,&nbsp;Isabell Brikell ,&nbsp;Brian D'Onofrio ,&nbsp;Ronnie Pingel ,&nbsp;Christian Rück ,&nbsp;John Wallert","doi":"10.1016/j.lanepe.2025.101504","DOIUrl":"10.1016/j.lanepe.2025.101504","url":null,"abstract":"<div><h3>Background</h3><div>Little is known about the risk of suicide in individuals treated against their will in involuntary psychiatric care (IPC). This population-based study provides a first comprehensive description of suicide among individuals who experienced IPC.</div></div><div><h3>Methods</h3><div>We studied all individuals discharged from IPC in Sweden from 2010 through 2020. Clinical and sociodemographic characteristics are reported followed by suicide risk for the complete IPC population and stratified by sex, age, IPC history, and diagnostic category. Crude and adjusted relative risks compared to all individuals discharged from psychiatric in- and outpatient care and the general population were estimated using Poisson regression. Suicide methods, seasonal trends, and geographical variance are also reported.</div></div><div><h3>Findings</h3><div>We identified 72 275 patients treated in IPC with a total of 134 514 inpatient care episodes (mean age = 44·8 years, 37 462 [51·8%] males). Of these, 2104 (2·9%) died by suicide over a median follow-up time of 4·4 years (IQR: 1⋅8–7⋅5). Suicide decedents were younger, more often male, single, diagnosed with personality and substance use disorders, and had a history of self-harm and IPC, compared to those who did not die by suicide. The absolute risk (crude incidence rate (IR) per 100 000 person-years) for all IPC patients was highest closest to discharge (IR<sub>1month</sub> = 2941 [2538, 3408]) and decreased thereafter (IR<sub>5years</sub> = 738 [705, 773]). Suicide risk in IPC patients was elevated relative to psychiatric inpatients (crude IR ratio (IRR)<sub>5years</sub> = 1·57 [1·48, 1·65]), psychiatric outpatients (IRR<sub>5years</sub> = 3·77 [3·58, 3·97]), and the general population (IRR<sub>5years</sub> = 55·52 [52·65, 58·54]).</div></div><div><h3>Interpretation</h3><div>We found substantial risk differences in distinct subgroups of IPC patients and an excess suicide risk among IPC patients compared to other clinical populations. These findings warrant further investigation as they could inform clinicians and policy makers regarding potential risk stratification, monitoring, and care. Preventing suicides after IPC should be a priority.</div></div><div><h3>Funding</h3><div><span>VR</span>, <span>ALF</span> Medicine, <span>CIMED</span>, <span>FORTE,</span> and <span>Söderström König Foundation</span>.</div></div>","PeriodicalId":53223,"journal":{"name":"Lancet Regional Health-Europe","volume":"60 ","pages":"Article 101504"},"PeriodicalIF":13.0,"publicationDate":"2025-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145468505","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Percutaneous and surgical management of aortic stenosis in the SWEDEHEART registry (2013–2023): a nationwide observational study SWEDEHEART登记(2013-2023):一项全国性的观察性研究:经皮和手术治疗主动脉瓣狭窄
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-03 DOI: 10.1016/j.lanepe.2025.101520
Johannes Tödt , Sasha Koul , Troels Yndigegn , Oskar Angerås , Henrik Bjursten , Shahab Nozohoor , Örjan Friberg , Jenny Backes , Stefan James , Björn Redfors , Patrik Gilje , Ashkan Labaf , Henrik Hagström , Andreas Rück , Matthias Götberg , Moman Aladdin Mohammad

Background

Management of severe aortic stenosis (AS) has evolved over the past decade, driven by the widespread adoption of transcatheter aortic valve implantation (TAVI). This study aims to assess trends in procedural volumes, patient characteristics, and outcomes for patients undergoing TAVI or surgical aortic valve replacement (SAVR) in Sweden.

Methods

This was a descriptive, non-comparative, nationwide cohort study using the SWEDEHEART registry. We included 21,383 patients who underwent TAVI or SAVR between 2013 and 2023 (11,366 TAVI and 10,017 SAVR). Trends in patient characteristics, preoperative risk, complications and mortality were examined.

Findings

TAVI procedures increased from 307 (26.1%, n = 307/1174) in 2013 to 1851 (71.2%, n = 1851/2601) in 2023, while SAVR volumes declined from ∼1000 annually before 2018 to roughly 750 procedures annually. Median age of TAVI patients were 81 (IQR 77, 85) years and 71 (IQR 65, 76) years for SAVR patients. The median EuroSCORE II for TAVI decreased from 5.6 (IQR 3.3, 10.2) to 2.7 (IQR 1.7, 4.6) (p = 0.002), and STS-PROM from 3.3 (IQR 1.9, 4.1) to 1.6 (IQR 1.1, 2.8) (p = 0.0021). Among SAVR patients, EuroSCORE II decreased from 1.5 (IQR 1.0, 2.3) to 1.3 (IQR 0.9, 2.1) (p = 0.022) and STS-PROM from 1.8 (IQR 1.2, 3.0) to 1.6 (IQR 1.1, 2.6) (p = 0.0082). Any in-hospital complications declined significantly for TAVI (29.2%, n = 210/719 to 13.2%, n = 244/1851), while SAVR complication rates increased slightly (18.4%, n = 354/1921 to 18.7%, n = 140/750). In-hospital mortality for TAVI declined from 3.6% (n = 26/719) to 1.0% (n = 18/1851), and 1-year mortality from 11.1% to 6.9% (p = 0.019). SAVR in-hospital all-cause death decreased from 1.6% to 0.4% (n = 3/750) and 5.0% to 2.2% for 1-year mortality (p = 0.013).

Interpretation

TAVI has become the predominant treatment strategy for AS in Sweden expanding access within the treated cohort. Despite this, current 2023 SAVR results demonstrate similar in-hospital complication rates compared to TAVI (18.7% vs 13.2%), but lower in-hospital (0.4% vs 1.0%) and 1-year mortality rates (2.2% vs 6.9%).

Funding

This study was supported by ALF and national research funding bodies.
在过去的十年中,由于经导管主动脉瓣植入术(TAVI)的广泛采用,严重主动脉瓣狭窄(AS)的治疗已经发生了变化。本研究旨在评估瑞典接受TAVI或外科主动脉瓣置换术(SAVR)患者的手术量、患者特征和结果的趋势。方法:这是一项描述性、非比较性、全国性队列研究,使用SWEDEHEART登记。我们纳入了2013年至2023年间接受TAVI或SAVR的21,383例患者(11,366例TAVI和10,017例SAVR)。检查了患者特征、术前风险、并发症和死亡率的趋势。研究发现,stavi程序从2013年的307例(26.1%,n = 307/1174)增加到2023年的1851例(71.2%,n = 1851/2601),而SAVR数量从2018年之前的每年约1000例下降到每年约750例。TAVI患者的中位年龄为81 (IQR 77, 85)岁,SAVR患者的中位年龄为71 (IQR 65, 76)岁。TAVI的中位EuroSCORE II从5.6 (IQR 3.3, 10.2)降至2.7 (IQR 1.7, 4.6) (p = 0.002), STS-PROM从3.3 (IQR 1.9, 4.1)降至1.6 (IQR 1.1, 2.8) (p = 0.0021)。在SAVR患者中,EuroSCORE II从1.5 (IQR 1.0, 2.3)降至1.3 (IQR 0.9, 2.1) (p = 0.022), STS-PROM从1.8 (IQR 1.2, 3.0)降至1.6 (IQR 1.1, 2.6) (p = 0.0082)。TAVI患者院内并发症发生率明显下降(29.2%,n = 210/719 ~ 13.2%, n = 244/1851),而SAVR并发症发生率略有上升(18.4%,n = 354/1921 ~ 18.7%, n = 140/750)。TAVI的住院死亡率从3.6% (n = 26/719)降至1.0% (n = 18/1851), 1年死亡率从11.1%降至6.9% (p = 0.019)。院内全因死亡率SAVR从1.6%降至0.4% (n = 3/750), 1年死亡率从5.0%降至2.2% (p = 0.013)。在瑞典,tavi已成为AS的主要治疗策略,扩大了治疗队列的可及性。尽管如此,目前2023年的SAVR结果显示,与TAVI相比,住院并发症发生率相似(18.7%对13.2%),但住院(0.4%对1.0%)和1年死亡率(2.2%对6.9%)较低。本研究得到了ALF和国家研究资助机构的支持。
{"title":"Percutaneous and surgical management of aortic stenosis in the SWEDEHEART registry (2013–2023): a nationwide observational study","authors":"Johannes Tödt ,&nbsp;Sasha Koul ,&nbsp;Troels Yndigegn ,&nbsp;Oskar Angerås ,&nbsp;Henrik Bjursten ,&nbsp;Shahab Nozohoor ,&nbsp;Örjan Friberg ,&nbsp;Jenny Backes ,&nbsp;Stefan James ,&nbsp;Björn Redfors ,&nbsp;Patrik Gilje ,&nbsp;Ashkan Labaf ,&nbsp;Henrik Hagström ,&nbsp;Andreas Rück ,&nbsp;Matthias Götberg ,&nbsp;Moman Aladdin Mohammad","doi":"10.1016/j.lanepe.2025.101520","DOIUrl":"10.1016/j.lanepe.2025.101520","url":null,"abstract":"<div><h3>Background</h3><div>Management of severe aortic stenosis (AS) has evolved over the past decade, driven by the widespread adoption of transcatheter aortic valve implantation (TAVI). This study aims to assess trends in procedural volumes, patient characteristics, and outcomes for patients undergoing TAVI or surgical aortic valve replacement (SAVR) in Sweden.</div></div><div><h3>Methods</h3><div>This was a descriptive, non-comparative, nationwide cohort study using the SWEDEHEART registry. We included 21,383 patients who underwent TAVI or SAVR between 2013 and 2023 (11,366 TAVI and 10,017 SAVR). Trends in patient characteristics, preoperative risk, complications and mortality were examined.</div></div><div><h3>Findings</h3><div>TAVI procedures increased from 307 (26.1%, n = 307/1174) in 2013 to 1851 (71.2%, n = 1851/2601) in 2023, while SAVR volumes declined from ∼1000 annually before 2018 to roughly 750 procedures annually. Median age of TAVI patients were 81 (IQR 77, 85) years and 71 (IQR 65, 76) years for SAVR patients. The median EuroSCORE II for TAVI decreased from 5.6 (IQR 3.3, 10.2) to 2.7 (IQR 1.7, 4.6) (p = 0.002), and STS-PROM from 3.3 (IQR 1.9, 4.1) to 1.6 (IQR 1.1, 2.8) (p = 0.0021). Among SAVR patients, EuroSCORE II decreased from 1.5 (IQR 1.0, 2.3) to 1.3 (IQR 0.9, 2.1) (p = 0.022) and STS-PROM from 1.8 (IQR 1.2, 3.0) to 1.6 (IQR 1.1, 2.6) (p = 0.0082). Any in-hospital complications declined significantly for TAVI (29.2%, n = 210/719 to 13.2%, n = 244/1851), while SAVR complication rates increased slightly (18.4%, n = 354/1921 to 18.7%, n = 140/750). In-hospital mortality for TAVI declined from 3.6% (n = 26/719) to 1.0% (n = 18/1851), and 1-year mortality from 11.1% to 6.9% (p = 0.019). SAVR in-hospital all-cause death decreased from 1.6% to 0.4% (n = 3/750) and 5.0% to 2.2% for 1-year mortality (p = 0.013).</div></div><div><h3>Interpretation</h3><div>TAVI has become the predominant treatment strategy for AS in Sweden expanding access within the treated cohort. Despite this, current 2023 SAVR results demonstrate similar in-hospital complication rates compared to TAVI (18.7% vs 13.2%), but lower in-hospital (0.4% vs 1.0%) and 1-year mortality rates (2.2% vs 6.9%).</div></div><div><h3>Funding</h3><div>This study was supported by <span>ALF</span> and national research funding bodies.</div></div>","PeriodicalId":53223,"journal":{"name":"Lancet Regional Health-Europe","volume":"60 ","pages":"Article 101520"},"PeriodicalIF":13.0,"publicationDate":"2025-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145468473","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Brand-specific influenza vaccine effectiveness in three Nordic countries during the 2024–2025 season: a target trial emulation study based on registry data 2024-2025年三个北欧国家品牌特异性流感疫苗有效性:基于注册数据的目标试验模拟研究
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-03 DOI: 10.1016/j.lanepe.2025.101518
Kristyna Faksova , Emilia Myrup Thiesson , Nicklas Pihlström , Ulrike Baum , Tor Biering-Sørensen , Eero Poukka , Tuija Leino , Rickard Ljung , Anders Hviid

Background

Seasonal influenza causes substantial morbidity and mortality in older adults. While vaccination is recommended in Nordic countries for individuals aged ≥65 years, brand-specific effectiveness estimates are scarce but essential for regulatory decision-making. We evaluated brand-specific effectiveness of seasonal influenza vaccines against laboratory-confirmed influenza-related outcomes in Denmark, Finland, and one Swedish region during the 2024/2025 season.

Methods

We conducted a nationwide cohort study using target trial emulation and linked health registries. Individuals aged ≥65 years were matched 1:1, comparing seasonal influenza vaccine recipients to non-recipients. Cumulative incidences of laboratory-confirmed influenza A and B, influenza-related hospitalisation, and death were assessed at 18 weeks post-immunisation. Vaccine effectiveness (VE) was calculated as 1 minus the risk ratio.

Findings

A total of 1,164,686 matched pairs were included (mean age 75.4 years, standard deviation 7.3). Overall VE against influenza-related hospitalisation was 46.8% (95% CI 40.8–52.9), with risk differences of −21.3 (−28.9 to −13.8) and −99.3 (−119.6 to −79.1) in Finland and Denmark, respectively, per 100,000 vaccinated individuals. Brand-specific VE was 63.4% (38.1–88.7) for Efluelda Tetra (split virion-high dose), 48.2% (40.8–55.6) for Fluad Tetra (subunit standard-dose adjuvanted), 43.6% (23.7–63.6) for Vaxigrip Tetra (split virion standard-dose), and 30.6% (−7.8 to 69.1) for Influvac Tetra (subunit standard-dose). VE waned by −6.5 percentage points (−10.5 to −2.5) every 3 weeks.

Interpretation

Seasonal influenza vaccines moderately reduced the risk of severe outcomes in older adults. Efluelda Tetra and Fluad Tetra appeared to offer favourable protection in their respective target groups, supporting their use in the 2025/2026 season. Annual monitoring using Nordic registries is crucial for informing evidence-based vaccination strategies and regulatory decisions.

Funding

European Medicines Agency.
背景:季节性流感在老年人中引起大量发病率和死亡率。虽然北欧国家建议65岁以上的个体接种疫苗,但品牌特定的有效性估计很少,但对监管决策至关重要。在丹麦、芬兰和瑞典的一个地区,我们评估了季节性流感疫苗在2024/2025年流感季对实验室确认的流感相关结果的品牌特异性有效性。方法我们采用目标试验模拟和相关健康登记进行了一项全国性队列研究。年龄≥65岁的个体1:1匹配,比较季节性流感疫苗接种者和未接种者。在免疫接种后18周评估实验室确诊的甲型和乙型流感、流感相关住院和死亡的累积发病率。疫苗有效性(VE)计算为1减去风险比。结果:共纳入1164686对配对对象(平均年龄75.4岁,标准差7.3)。流感相关住院的总体VE为46.8% (95% CI 40.8-52.9),在芬兰和丹麦,每10万名接种疫苗者的风险差异分别为- 21.3(- 28.9至- 13.8)和- 99.3(- 119.6至- 79.1)。依fluelda Tetra(高病毒粒子分裂剂量)的品牌特异性VE为63.4% (38.1-88.7),Fluad Tetra(亚单位标准剂量佐剂)的品牌特异性VE为48.2% (40.8-55.6),Vaxigrip Tetra(病毒粒子分裂标准剂量)的品牌特异性VE为43.6% (23.7-63.6),Influvac Tetra(亚单位标准剂量)的品牌特异性VE为30.6%(- 7.8 - 69.1)。VE每3周下降- 6.5个百分点(- 10.5 ~ - 2.5)。季节性流感疫苗可适度降低老年人发生严重后果的风险。Efluelda Tetra和Fluad Tetra似乎在各自的目标人群中提供了有利的保护,支持其在2025/2026赛季的使用。利用北欧登记进行年度监测对于为基于证据的疫苗接种战略和监管决策提供信息至关重要。资助欧洲药品管理局。
{"title":"Brand-specific influenza vaccine effectiveness in three Nordic countries during the 2024–2025 season: a target trial emulation study based on registry data","authors":"Kristyna Faksova ,&nbsp;Emilia Myrup Thiesson ,&nbsp;Nicklas Pihlström ,&nbsp;Ulrike Baum ,&nbsp;Tor Biering-Sørensen ,&nbsp;Eero Poukka ,&nbsp;Tuija Leino ,&nbsp;Rickard Ljung ,&nbsp;Anders Hviid","doi":"10.1016/j.lanepe.2025.101518","DOIUrl":"10.1016/j.lanepe.2025.101518","url":null,"abstract":"<div><h3>Background</h3><div>Seasonal influenza causes substantial morbidity and mortality in older adults. While vaccination is recommended in Nordic countries for individuals aged ≥65 years, brand-specific effectiveness estimates are scarce but essential for regulatory decision-making. We evaluated brand-specific effectiveness of seasonal influenza vaccines against laboratory-confirmed influenza-related outcomes in Denmark, Finland, and one Swedish region during the 2024/2025 season.</div></div><div><h3>Methods</h3><div>We conducted a nationwide cohort study using target trial emulation and linked health registries. Individuals aged ≥65 years were matched 1:1, comparing seasonal influenza vaccine recipients to non-recipients. Cumulative incidences of laboratory-confirmed influenza A and B, influenza-related hospitalisation, and death were assessed at 18 weeks post-immunisation. Vaccine effectiveness (VE) was calculated as 1 minus the risk ratio.</div></div><div><h3>Findings</h3><div>A total of 1,164,686 matched pairs were included (mean age 75.4 years, standard deviation 7.3). Overall VE against influenza-related hospitalisation was 46.8% (95% CI 40.8–52.9), with risk differences of −21.3 (−28.9 to −13.8) and −99.3 (−119.6 to −79.1) in Finland and Denmark, respectively, per 100,000 vaccinated individuals. Brand-specific VE was 63.4% (38.1–88.7) for Efluelda Tetra (split virion-high dose), 48.2% (40.8–55.6) for Fluad Tetra (subunit standard-dose adjuvanted), 43.6% (23.7–63.6) for Vaxigrip Tetra (split virion standard-dose), and 30.6% (−7.8 to 69.1) for Influvac Tetra (subunit standard-dose). VE waned by −6.5 percentage points (−10.5 to −2.5) every 3 weeks.</div></div><div><h3>Interpretation</h3><div>Seasonal influenza vaccines moderately reduced the risk of severe outcomes in older adults. Efluelda Tetra and Fluad Tetra appeared to offer favourable protection in their respective target groups, supporting their use in the 2025/2026 season. Annual monitoring using Nordic registries is crucial for informing evidence-based vaccination strategies and regulatory decisions.</div></div><div><h3>Funding</h3><div><span>European Medicines Agency</span>.</div></div>","PeriodicalId":53223,"journal":{"name":"Lancet Regional Health-Europe","volume":"60 ","pages":"Article 101518"},"PeriodicalIF":13.0,"publicationDate":"2025-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145468471","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Examination of self-harm clustering in adolescent peer networks: a nationwide registry cohort study in Finland 青少年同伴网络中自我伤害聚类的检验:芬兰一项全国性登记队列研究
IF 13 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-11-02 DOI: 10.1016/j.lanepe.2025.101517
Jussi Alho , Roger T. Webb , Mai Gutvilig , Ripsa Niemi , Kaisla Komulainen , Kimmo Suokas , Petri Böckerman , Marko Elovainio , Nav Kapur , Christian Hakulinen

Background

Clusters of self-harming behaviour among adolescents have been observed, yet population-based epidemiological evidence is lacking. This study aims to address this lack by examining the clustering of self-harming behaviour within adolescent peer networks at the population level.

Methods

We used nationwide registry data on Finnish people born between January 1, 1985, and December 31, 2000, to examine whether having same-grade schoolmates who had self-harmed was associated with greater subsequent self-harm risk. Cohort members were followed up until first recorded self-harm episode, emigration, death, or December 31, 2020, whichever came first. Hazard ratios (HRs) were estimated using mixed-effects Cox proportional hazards models adjusted for a comprehensive set of individual-, parental-, school-, and area-level covariates.

Findings

The cohort comprised 913,149 Finnish residents. Having same-grade schoolmates who had self-harmed between school-starting age and finishing ninth grade was associated with a higher, albeit small in magnitude, HR of subsequent self-harm over a median of 11.6 years of follow-up (HR 1.05, [95% CI 1.01–1.09]). HR was not consistently higher over follow-up time but was highest in the beginning of follow-up when the cohort members were around age 16 (1.45 [1.25–1.69]). Limiting exposure to schoolmates’ self-harm episodes to 1 year consistently showed the highest risk around age 16, regardless of whether the exposure occurred in ninth grade (1.49 [1.21–1.82]) or eighth grade (1.36 [1.07–1.74]), with follow-up commencing after the respective grade.

Interpretation

While we cannot rule out residual confounding, our findings suggest that self-harm may socially transmit within adolescent peer networks. The observed highest risk around age 16 suggests that external stressors associated with transitioning to new life stages at this age may moderate the impact of peer self-harm exposure. Prevention and intervention measures that consider possible peer influences on adolescents’ self-harming behaviour may help reduce the public health burden of self-harm.

Funding

European Research Council and Research Council of Finland.
背景:在青少年中已观察到群集的自残行为,但缺乏基于人群的流行病学证据。本研究旨在通过在人口水平上检查青少年同伴网络中自残行为的聚类来解决这一不足。方法:我们使用了1985年1月1日至2000年12月31日之间出生的芬兰人的全国登记数据,以检验有自残行为的同年级同学是否与后来自残的风险更大有关。对队列成员进行随访,直到首次记录自残事件、移民、死亡或2020年12月31日,以先到者为准。使用混合效应Cox比例风险模型对综合的个体、父母、学校和地区协变量进行调整,估计风险比(hr)。该队列包括913149名芬兰居民。同年级同学在入学年龄到九年级结束期间有过自残行为,在随访的中位数11.6年期间,自残风险比较高(尽管幅度较小)(风险比1.05,[95% CI 1.01-1.09])。HR在随访期间并不一致较高,但在随访开始时,队列成员年龄在16岁左右时最高(1.45[1.25-1.69])。将接触同学自残事件限制在1年内,无论接触发生在九年级(1.49[1.21-1.82])还是八年级(1.36[1.07-1.74]),均在16岁左右显示出最高的风险,随访开始于相应年级之后。解释:虽然我们不能排除残留的混杂因素,但我们的研究结果表明,自残可能在青少年同伴网络中传播。观察到的16岁左右的最高风险表明,与这个年龄过渡到新生活阶段相关的外部压力源可能会缓和同伴自残暴露的影响。考虑到同伴对青少年自残行为可能产生的影响的预防和干预措施可能有助于减轻自残造成的公共卫生负担。资助欧洲研究理事会和芬兰研究理事会。
{"title":"Examination of self-harm clustering in adolescent peer networks: a nationwide registry cohort study in Finland","authors":"Jussi Alho ,&nbsp;Roger T. Webb ,&nbsp;Mai Gutvilig ,&nbsp;Ripsa Niemi ,&nbsp;Kaisla Komulainen ,&nbsp;Kimmo Suokas ,&nbsp;Petri Böckerman ,&nbsp;Marko Elovainio ,&nbsp;Nav Kapur ,&nbsp;Christian Hakulinen","doi":"10.1016/j.lanepe.2025.101517","DOIUrl":"10.1016/j.lanepe.2025.101517","url":null,"abstract":"<div><h3>Background</h3><div>Clusters of self-harming behaviour among adolescents have been observed, yet population-based epidemiological evidence is lacking. This study aims to address this lack by examining the clustering of self-harming behaviour within adolescent peer networks at the population level.</div></div><div><h3>Methods</h3><div>We used nationwide registry data on Finnish people born between January 1, 1985, and December 31, 2000, to examine whether having same-grade schoolmates who had self-harmed was associated with greater subsequent self-harm risk. Cohort members were followed up until first recorded self-harm episode, emigration, death, or December 31, 2020, whichever came first. Hazard ratios (HRs) were estimated using mixed-effects Cox proportional hazards models adjusted for a comprehensive set of individual-, parental-, school-, and area-level covariates.</div></div><div><h3>Findings</h3><div>The cohort comprised 913,149 Finnish residents. Having same-grade schoolmates who had self-harmed between school-starting age and finishing ninth grade was associated with a higher, albeit small in magnitude, HR of subsequent self-harm over a median of 11.6 years of follow-up (HR 1.05, [95% CI 1.01–1.09]). HR was not consistently higher over follow-up time but was highest in the beginning of follow-up when the cohort members were around age 16 (1.45 [1.25–1.69]). Limiting exposure to schoolmates’ self-harm episodes to 1 year consistently showed the highest risk around age 16, regardless of whether the exposure occurred in ninth grade (1.49 [1.21–1.82]) or eighth grade (1.36 [1.07–1.74]), with follow-up commencing after the respective grade.</div></div><div><h3>Interpretation</h3><div>While we cannot rule out residual confounding, our findings suggest that self-harm may socially transmit within adolescent peer networks. The observed highest risk around age 16 suggests that external stressors associated with transitioning to new life stages at this age may moderate the impact of peer self-harm exposure. Prevention and intervention measures that consider possible peer influences on adolescents’ self-harming behaviour may help reduce the public health burden of self-harm.</div></div><div><h3>Funding</h3><div><span>European Research Council</span> and <span>Research Council of Finland</span>.</div></div>","PeriodicalId":53223,"journal":{"name":"Lancet Regional Health-Europe","volume":"60 ","pages":"Article 101517"},"PeriodicalIF":13.0,"publicationDate":"2025-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145468472","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Lancet Regional Health-Europe
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1