首页 > 最新文献

Swiss medical weekly最新文献

英文 中文
Supplementum 295: Abstracts of the 48th IHF World Hospital Congress (Geneva, November 10-13, 2025). 附录295:第48届IHF世界医院大会(2025年11月10日至13日,日内瓦)摘要。
IF 1.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-27 DOI: 10.57187/5258
International Hospital Federation
{"title":"Supplementum 295: Abstracts of the 48th IHF World Hospital Congress (Geneva, November 10-13, 2025).","authors":"International Hospital Federation","doi":"10.57187/5258","DOIUrl":"https://doi.org/10.57187/5258","url":null,"abstract":"","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"156 ","pages":""},"PeriodicalIF":1.9,"publicationDate":"2026-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146107407","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effectiveness of community mental health nursing on psychiatric hospitalisations in Switzerland: a mirror-image analysis. 瑞士精神病院社区精神卫生护理的有效性:镜像分析。
IF 1.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-12-23 DOI: 10.57187/s.4692
Anna Hegedüs, Dirk Richter

  BACKGROUND: Community mental health nursing has gained importance in Switzerland as part of a broader shift towards community-based psychiatric care. While community mental health nursing services are increasingly implemented, empirical evidence on their effectiveness in reducing psychiatric hospitalisations remains limited. This study aims to evaluate the effect of community mental health nursing on psychiatric hospitalisations and to identify risk factors for hospitalisation during community mental health nursing care.

Methods: We conducted a naturalistic observational study using data from two linked national databases: the HomeCareData register and the Medical Statistics of Hospitals. The study included adults who were admitted to community mental health nursing services between January 2020 and December 2022 and whose data was documented in HomeCareData. With mirror-image methods, we compared psychiatric hospitalisation rates in equally long pre-index and post-index periods, defined by each individual's duration of community mental health nursing care, with each participant serving as their own control. The start of community mental health nursing care was defined as the index date. For a sensitivity analysis, individuals hospitalised within 60 days before the start of community mental health nursing were excluded to address potential regression to the mean effects. Uni- and multivariable logistic regression were used to identify risk factors of hospitalisation during community mental health nursing care.

Results: The study sample comprised 5252 individuals with a mean age of 52 years; 66% were female. The primary mirror-image analysis revealed a significant reduction in psychiatric hospitalisations following the start of community mental health nursing (unadjusted Incidence Rate Ratio: 0.60; 95% confidence interval: 0.55-0.65). No significant effect was observed in the sensitivity analysis (unadjusted Incidence Rate Ratio: 0.97; 95% confidence interval: 0.87-1.09). Multivariable logistic regression identified previous psychiatric hospitalisations and compulsory admissions as significant risk factors of hospitalisation during community mental health nursing care. Sociodemographic and diagnostic variables showed no significant associations.

Conclusions: This is the first study to show a reduction in psychiatric hospitalisations after participation in community mental health nursing services in Switzerland. However, this effect was not confirmed in the sensitivity analysis which may suggest a regression to the mean effect. The study demonstrates the feasibility of using linked routine data to evaluate real-world mental health interventions and underscores the need for broader data coverage and improved documentation to strengthen future research.

背景:社区精神卫生护理在瑞士越来越重要,它是向社区精神护理更广泛转变的一部分。虽然越来越多地实施社区精神卫生护理服务,但其在减少精神病住院治疗方面的有效性的经验证据仍然有限。本研究旨在评估社区心理健康护理对精神科住院的影响,并探讨社区心理健康护理对精神科住院的影响因素。方法:我们进行了一项自然观察性研究,使用了来自两个相互关联的国家数据库的数据:HomeCareData注册和医院医学统计。该研究包括在2020年1月至2022年12月期间接受社区心理健康护理服务的成年人,他们的数据记录在HomeCareData中。通过镜像方法,我们比较了指数前和指数后同样长的精神病住院率,指数前和指数后由每个人的社区精神卫生护理时间定义,每个参与者作为自己的对照。以社区精神卫生护理开始时间为指标日期。为了进行敏感性分析,在社区精神卫生护理开始前60天内住院的个体被排除在外,以解决可能回归到平均效应的问题。采用单变量和多变量logistic回归分析社区精神卫生护理期间住院的危险因素。结果:研究样本包括5252人,平均年龄52岁;66%是女性。初步镜像分析显示,社区精神卫生护理开始后,精神病住院人数显著减少(未经调整的发病率比:0.60;95%可信区间:0.55-0.65)。敏感性分析未观察到显著影响(未调整的发病率比:0.97;95%可信区间:0.87-1.09)。多变量logistic回归分析发现以往精神科住院和强制入院是社区精神卫生护理期间住院的重要危险因素。社会人口学和诊断变量显示无显著相关性。结论:这是第一项研究表明,在瑞士参加社区精神卫生护理服务后,精神病住院率降低。然而,这种效应在敏感性分析中没有得到证实,这可能表明回归到平均效应。该研究证明了使用相关常规数据来评估现实世界心理健康干预措施的可行性,并强调需要更广泛的数据覆盖和改进文件,以加强未来的研究。
{"title":"Effectiveness of community mental health nursing on psychiatric hospitalisations in Switzerland: a mirror-image analysis.","authors":"Anna Hegedüs, Dirk Richter","doi":"10.57187/s.4692","DOIUrl":"10.57187/s.4692","url":null,"abstract":"<p><p>  BACKGROUND: Community mental health nursing has gained importance in Switzerland as part of a broader shift towards community-based psychiatric care. While community mental health nursing services are increasingly implemented, empirical evidence on their effectiveness in reducing psychiatric hospitalisations remains limited. This study aims to evaluate the effect of community mental health nursing on psychiatric hospitalisations and to identify risk factors for hospitalisation during community mental health nursing care.</p><p><strong>Methods: </strong>We conducted a naturalistic observational study using data from two linked national databases: the HomeCareData register and the Medical Statistics of Hospitals. The study included adults who were admitted to community mental health nursing services between January 2020 and December 2022 and whose data was documented in HomeCareData. With mirror-image methods, we compared psychiatric hospitalisation rates in equally long pre-index and post-index periods, defined by each individual's duration of community mental health nursing care, with each participant serving as their own control. The start of community mental health nursing care was defined as the index date. For a sensitivity analysis, individuals hospitalised within 60 days before the start of community mental health nursing were excluded to address potential regression to the mean effects. Uni- and multivariable logistic regression were used to identify risk factors of hospitalisation during community mental health nursing care.</p><p><strong>Results: </strong>The study sample comprised 5252 individuals with a mean age of 52 years; 66% were female. The primary mirror-image analysis revealed a significant reduction in psychiatric hospitalisations following the start of community mental health nursing (unadjusted Incidence Rate Ratio: 0.60; 95% confidence interval: 0.55-0.65). No significant effect was observed in the sensitivity analysis (unadjusted Incidence Rate Ratio: 0.97; 95% confidence interval: 0.87-1.09). Multivariable logistic regression identified previous psychiatric hospitalisations and compulsory admissions as significant risk factors of hospitalisation during community mental health nursing care. Sociodemographic and diagnostic variables showed no significant associations.</p><p><strong>Conclusions: </strong>This is the first study to show a reduction in psychiatric hospitalisations after participation in community mental health nursing services in Switzerland. However, this effect was not confirmed in the sensitivity analysis which may suggest a regression to the mean effect. The study demonstrates the feasibility of using linked routine data to evaluate real-world mental health interventions and underscores the need for broader data coverage and improved documentation to strengthen future research.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"4692"},"PeriodicalIF":1.9,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145865580","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Molecular epidemiology of respiratory syncytial virus in Switzerland 2019-2024 from nucleic acid testing and whole-genome sequencing. 基于核酸检测和全基因组测序的2019-2024年瑞士呼吸道合胞病毒分子流行病学研究
IF 1.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-12-23 DOI: 10.57187/s.4600
Alexander Kuznetsov, Rainer Gosert, Ulrich Heininger, Nina Khanna, Sarah Tschudin-Sutter, Richard A Neher, Karoline Leuzinger

Background and aims: Respiratory syncytial virus (RSV) infection is one of the leading causes of hospitalisation in infants, the elderly and immunocompromised patients, with significant morbidity and mortality rates. Despite its global impact, epidemiological surveillance of RSV in Switzerland has historically been limited compared to the USA and European countries. A significant surge in RSV activity and hospitalisations after the COVID-19 pandemic, along with the introduction of new monoclonal antibodies and RSV vaccines, has led to an increased interest in the molecular epidemiology of RSV. To ensure continued efficacy of the new preventive options, monitoring of the genetic diversity of circulating RSV strains, their evolutionary dynamics and the potential emergence of resistance mutations is of central importance. The present study aimed to characterise the genetic diversity and seasonal trends of RSV dynamics in Switzerland from 2019 to 2024, mainly over the last two post-pandemic winter seasons (2022/23 and 2023/24).

Methods: A total of 48,897 respiratory clinical specimens from 30,782 patients with respiratory tract infections were tested for RSV at a tertiary care centre in Northwestern Switzerland between July 2019 and June 2024. RSV activity over these seasons was investigated. Amplicon-based whole-genome sequencing was performed on 182 selected samples, with 125 high-quality consensus genomes and phylogenies reconstructed. Lineage distribution and seasonal subtype prevalence were compared to European data.

Results: RSV activity was absent during the 2020/21 pandemic season, but surged with an off-season peak in summer 2021. RSV B predominated during the 2022/23 season, while a shift to RSV A occurred in the 2023/24 winter season, which is in line with neighbouring European countries. Lineage subtype distribution showed high concordance with circulating European strains. RSV A exhibited greater diversity (mean pairwise Hamming distance 0.015, SD 0.006) than RSV B (mean 0.006, 0.003), with all current strains falling within G protein duplication clades A.D.1, 2, 3 and 5 for RSV A, and B.D.E.1 and B.D.4.1.1 for RSV B.

Conclusion: By contributing 125 newly assembled RSV genome sequences, we have significantly increased the number of publicly available whole-genome sequences from Switzerland. Our study provides a genomic surveillance of RSV in Switzerland, analysing seasonal patterns, alternating subtype dominance, and consistency with broader European trends. A comprehensive understanding of the molecular epidemiology of RSV enables healthcare providers and public health authorities to monitor the effectiveness of current vaccines and monoclonal antibodies, associate lineages and serotypes with disease severity, implement timely interventions and detect emerging variants, ultimately reducing the burden of RSV-related illnesses.

背景和目的:呼吸道合胞病毒(RSV)感染是婴儿、老年人和免疫功能低下患者住院的主要原因之一,具有很高的发病率和死亡率。尽管其具有全球影响,但与美国和欧洲国家相比,瑞士对RSV的流行病学监测历来有限。在2019冠状病毒病大流行之后,随着新的单克隆抗体和RSV疫苗的引入,RSV活性和住院人数大幅增加,导致人们对RSV分子流行病学的兴趣增加。为确保新的预防措施持续有效,监测流行RSV毒株的遗传多样性、它们的进化动态和耐药性突变的潜在出现至关重要。本研究旨在描述2019年至2024年瑞士RSV动态的遗传多样性和季节性趋势,主要是在大流行后的最后两个冬季(2022/23和2023/24)。方法:2019年7月至2024年6月,在瑞士西北部的一家三级医疗中心,对来自30,782例呼吸道感染患者的48,897份呼吸道临床标本进行了RSV检测。对这些季节的RSV活性进行了调查。对182个样本进行了基于扩增子的全基因组测序,重建了125个高质量的一致性基因组和系统发育。谱系分布和季节性亚型流行率与欧洲数据进行了比较。结果:在2020/21大流行季节,RSV活动不存在,但在2021年夏季出现淡季高峰。RSV B型在2022/23季节占主导地位,而RSV a型在2023/24冬季季节发生转变,这与邻近的欧洲国家一致。谱系亚型分布与欧洲流行株高度一致。RSV A比RSV B表现出更大的多样性(平均两两汉明距离为0.015,标准差为0.006,0.003),所有现有菌株都属于RSV A的G蛋白重复分支A.D.1, 2,3和5,以及RSV B的B.D.E.1和B.D.4.1.1。结论:通过贡献125个新组装的RSV基因组序列,我们显著增加了来自瑞士的公开全基因组序列的数量。我们的研究提供了瑞士RSV的基因组监测,分析了季节模式、交替亚型优势以及与更广泛的欧洲趋势的一致性。对RSV分子流行病学的全面了解使卫生保健提供者和公共卫生当局能够监测当前疫苗和单克隆抗体的有效性,将谱系和血清型与疾病严重程度联系起来,及时实施干预措施并发现新出现的变异,最终减轻RSV相关疾病的负担。
{"title":"Molecular epidemiology of respiratory syncytial virus in Switzerland 2019-2024 from nucleic acid testing and whole-genome sequencing.","authors":"Alexander Kuznetsov, Rainer Gosert, Ulrich Heininger, Nina Khanna, Sarah Tschudin-Sutter, Richard A Neher, Karoline Leuzinger","doi":"10.57187/s.4600","DOIUrl":"https://doi.org/10.57187/s.4600","url":null,"abstract":"<p><strong>Background and aims: </strong>Respiratory syncytial virus (RSV) infection is one of the leading causes of hospitalisation in infants, the elderly and immunocompromised patients, with significant morbidity and mortality rates. Despite its global impact, epidemiological surveillance of RSV in Switzerland has historically been limited compared to the USA and European countries. A significant surge in RSV activity and hospitalisations after the COVID-19 pandemic, along with the introduction of new monoclonal antibodies and RSV vaccines, has led to an increased interest in the molecular epidemiology of RSV. To ensure continued efficacy of the new preventive options, monitoring of the genetic diversity of circulating RSV strains, their evolutionary dynamics and the potential emergence of resistance mutations is of central importance. The present study aimed to characterise the genetic diversity and seasonal trends of RSV dynamics in Switzerland from 2019 to 2024, mainly over the last two post-pandemic winter seasons (2022/23 and 2023/24).</p><p><strong>Methods: </strong>A total of 48,897 respiratory clinical specimens from 30,782 patients with respiratory tract infections were tested for RSV at a tertiary care centre in Northwestern Switzerland between July 2019 and June 2024. RSV activity over these seasons was investigated. Amplicon-based whole-genome sequencing was performed on 182 selected samples, with 125 high-quality consensus genomes and phylogenies reconstructed. Lineage distribution and seasonal subtype prevalence were compared to European data.</p><p><strong>Results: </strong>RSV activity was absent during the 2020/21 pandemic season, but surged with an off-season peak in summer 2021. RSV B predominated during the 2022/23 season, while a shift to RSV A occurred in the 2023/24 winter season, which is in line with neighbouring European countries. Lineage subtype distribution showed high concordance with circulating European strains. RSV A exhibited greater diversity (mean pairwise Hamming distance 0.015, SD 0.006) than RSV B (mean 0.006, 0.003), with all current strains falling within G protein duplication clades A.D.1, 2, 3 and 5 for RSV A, and B.D.E.1 and B.D.4.1.1 for RSV B.</p><p><strong>Conclusion: </strong>By contributing 125 newly assembled RSV genome sequences, we have significantly increased the number of publicly available whole-genome sequences from Switzerland. Our study provides a genomic surveillance of RSV in Switzerland, analysing seasonal patterns, alternating subtype dominance, and consistency with broader European trends. A comprehensive understanding of the molecular epidemiology of RSV enables healthcare providers and public health authorities to monitor the effectiveness of current vaccines and monoclonal antibodies, associate lineages and serotypes with disease severity, implement timely interventions and detect emerging variants, ultimately reducing the burden of RSV-related illnesses.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"4600"},"PeriodicalIF":1.9,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145865660","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Survival and quality of life after liver transplantation in patients with or without pre-transplant alcohol abstinence: a retrospective cohort study. 肝移植前戒酒或不戒酒患者的生存和生活质量:一项回顾性队列研究
IF 1.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-12-23 DOI: 10.57187/s.4381
Felix A Fries, Sena Blümel, Beat Müllhaupt, Andre Richter, On Behalf Of The Swiss Transplant Cohort Study

  INTRODUCTION: Most European transplant centres require patients to abstain from alcohol consumption for at least 6 months to be listed for liver transplantation, even though delayed transplantation is associated with increased mortality. This study examined the effects of a shorter duration of alcohol abstinence before placement on the waiting list for liver transplantation on post-transplant survival and quality of life. This article contributes to the ongoing debate on whether patients with less than 6 months of alcohol abstinence should be categorically excluded from transplantation.

Methods:  This retrospective cohort study analysed patients at the University Hospital Zurich who underwent liver transplantation for any indication between 2011 and 2019. Patients younger than 18 years and those with acute liver failure were excluded. The follow-up period was 3 years. The outcomes were post-transplant survival and quality of life in patients with less than (group 1) or more than (group 2) 6 months of abstinence before being listed for liver transplantation. Survival was compared using log-rank tests, and quality of life (scored from 0 to 100) was compared using multivariate ANOVA with repeated measures.

Results:  Of the 206 included patients, 50 (24%) had abstained from alcohol for less than 6 months before being listed for liver transplantation (group 1). The cohort had a median (IQR) age at transplantation of 59 (53-64) years, and 155 (75%) were men. Three-year survival was similar in patients with less than or more than 6 months of alcohol abstinence before listing (76% [95% CI, 62%; 86%] vs 78% [95% CI, 70%; 83%]). No significant differences in quality-of-life scores were observed between groups (F(2,244) = 0.814, p = 0.435), and no significant changes in quality of life over time were found within each group (F(1,133) = 0.346, p = 0.557). The median (IQR) quality of life score at 36 months after transplantation was 80 (56-92) in patients with less than 6 months of abstinence before listing versus 78 (63-90) in those with more than 6 months of abstinence.

Conclusion:  Post-transplant survival and quality of life did not differ between patients with less than 6 months and those with more than 6 months of alcohol abstinence before being listed for liver transplantation. These findings suggest that the strict 6-month abstinence requirement for inclusion on the waiting list should be reconsidered to prevent patients from being denied access to life-saving transplantation solely because of a shorter abstinence duration.

大多数欧洲移植中心要求患者戒酒至少6个月才能列入肝移植名单,即使延迟移植与死亡率增加有关。本研究考察了在肝移植等待名单前较短的戒酒时间对移植后生存和生活质量的影响。这篇文章有助于讨论是否应该将戒酒少于6个月的患者排除在移植手术之外。方法:这项回顾性队列研究分析了2011年至2019年期间在苏黎世大学医院因任何适应症接受肝移植的患者。年龄小于18岁的患者和急性肝衰竭患者被排除在外。随访期为3年。结果是肝移植前禁欲时间少于(第一组)或多于(第二组)6个月的患者的移植后生存和生活质量。生存率采用log-rank检验进行比较,生活质量(评分从0到100)采用重复测量的多变量方差分析进行比较。结果:纳入的206例患者中,50例(24%)在列入肝移植名单前戒酒少于6个月(1组)。该队列移植时的中位(IQR)年龄为59岁(53-64)岁,其中155名(75%)为男性。清单前戒酒少于或超过6个月的患者的3年生存率相似(76% [95% CI, 62%; 86%] vs 78% [95% CI, 70%; 83%])。各组患者的生活质量评分无显著差异(F(2244) = 0.814, p = 0.435),各组患者的生活质量随时间变化无显著差异(F(1133) = 0.346, p = 0.557)。移植后36个月的生活质量中位数(IQR)评分为:戒毒前少于6个月的患者为80分(56-92分),而戒毒超过6个月的患者为78分(63-90分)。结论:肝移植前戒酒少于6个月的患者与戒酒超过6个月的患者的移植后生存和生活质量无显著差异。这些发现表明,应该重新考虑列入等待名单的严格的6个月禁欲要求,以防止患者仅仅因为较短的禁欲时间而被拒绝获得挽救生命的移植。
{"title":"Survival and quality of life after liver transplantation in patients with or without pre-transplant alcohol abstinence: a retrospective cohort study.","authors":"Felix A Fries, Sena Blümel, Beat Müllhaupt, Andre Richter, On Behalf Of The Swiss Transplant Cohort Study","doi":"10.57187/s.4381","DOIUrl":"10.57187/s.4381","url":null,"abstract":"<p><p>  INTRODUCTION: Most European transplant centres require patients to abstain from alcohol consumption for at least 6 months to be listed for liver transplantation, even though delayed transplantation is associated with increased mortality. This study examined the effects of a shorter duration of alcohol abstinence before placement on the waiting list for liver transplantation on post-transplant survival and quality of life. This article contributes to the ongoing debate on whether patients with less than 6 months of alcohol abstinence should be categorically excluded from transplantation.</p><p><strong>Methods: </strong> This retrospective cohort study analysed patients at the University Hospital Zurich who underwent liver transplantation for any indication between 2011 and 2019. Patients younger than 18 years and those with acute liver failure were excluded. The follow-up period was 3 years. The outcomes were post-transplant survival and quality of life in patients with less than (group 1) or more than (group 2) 6 months of abstinence before being listed for liver transplantation. Survival was compared using log-rank tests, and quality of life (scored from 0 to 100) was compared using multivariate ANOVA with repeated measures.</p><p><strong>Results: </strong> Of the 206 included patients, 50 (24%) had abstained from alcohol for less than 6 months before being listed for liver transplantation (group 1). The cohort had a median (IQR) age at transplantation of 59 (53-64) years, and 155 (75%) were men. Three-year survival was similar in patients with less than or more than 6 months of alcohol abstinence before listing (76% [95% CI, 62%; 86%] vs 78% [95% CI, 70%; 83%]). No significant differences in quality-of-life scores were observed between groups (F(2,244) = 0.814, p = 0.435), and no significant changes in quality of life over time were found within each group (F(1,133) = 0.346, p = 0.557). The median (IQR) quality of life score at 36 months after transplantation was 80 (56-92) in patients with less than 6 months of abstinence before listing versus 78 (63-90) in those with more than 6 months of abstinence.</p><p><strong>Conclusion: </strong> Post-transplant survival and quality of life did not differ between patients with less than 6 months and those with more than 6 months of alcohol abstinence before being listed for liver transplantation. These findings suggest that the strict 6-month abstinence requirement for inclusion on the waiting list should be reconsidered to prevent patients from being denied access to life-saving transplantation solely because of a shorter abstinence duration.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"4381"},"PeriodicalIF":1.9,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145865654","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Passive RSV immunisation using nirsevimab in neonatal care: a structured multidisciplinary approach and immunisation data from a Swiss tertiary centre. 新生儿护理中使用nirseimab的被动RSV免疫:来自瑞士三级中心的结构化多学科方法和免疫数据。
IF 1.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-12-23 DOI: 10.57187/s.4689
Katalin Kalya, Jehudith Fontijn, Flurina Famos, Dirk Bassler, Nicole Ochsenbein-Kölble, Ladina Vonzun

Background: Respiratory syncytial virus (RSV) infection is a major cause of severe lower respiratory tract infections in newborns and young infants, especially during the winter season from October to March. In Switzerland, RSV infection represents a leading cause of hospital admissions among newborns. Since October 2024, a long-acting monoclonal antibody, nirsevimab (Beyfortus®), has been available in Switzerland for standard care in newborns.

Objectives: This paper presents a multidisciplinary, standardised protocol for the administration of nirsevimab, as well as immunisation data from the first season of application in 2024/25 at a tertiary centre in Switzerland.

Methods: A protocol for implementing the RSV immunisation strategy was developed at University Hospital Zurich by a multidisciplinary team of obstetricians, neonatologists, nurses, from in- and outpatient services. The focus was on prenatal counselling during outpatient consultations as well as inpatient procedures on maternity and neonatology wards. The goal was to provide expectant parents with consistent information by different healthcare professionals. Neonatal immunisation data from the first season in 2024/25 (25 October to 31 March ) were retrieved from patient charts (Yes/No) in a retrospective, quality control, observational cohort study. All newborns discharged from the maternity ward or the neonatology unit of our centre were included in the analysis.

Results: The protocol included early and multidisciplinary parental education, offering consistent oral and written information, as well as opportunities to discuss their questions regarding the new immunisation, ensured informed consent and enabled timely administration of nirsevimab by healthcare professionals in the obstetrics and neonatology units. Over the 2024/25 season, 78% of the newborns were immunised before leaving hospital care: 78% (588/758) of newborns discharged home from the maternity ward were immunised and 82% (125/153) of those discharged home from the neonatology unit were immunised.   CONCLUSION: The implementation of passive RSV immunisation was overall successful with an immunisation rate of around 80% for the first season in 2024/25.

背景:呼吸道合胞病毒(RSV)感染是新生儿和婴幼儿严重下呼吸道感染的主要原因,特别是在10月至3月的冬季。在瑞士,呼吸道合胞病毒感染是新生儿住院的主要原因。自2024年10月以来,一种长效单克隆抗体nirsevimab (Beyfortus®)已在瑞士用于新生儿的标准护理。目的:本文提出了一种多学科、标准化的nirsevimab给药方案,以及瑞士某三级中心在2024/25年度第一个应用季节的免疫数据。方法:在苏黎世大学医院,一个由产科医生、新生儿专家、门诊护士组成的多学科团队制定了RSV免疫策略实施方案。重点是门诊咨询期间的产前咨询以及产科和新生儿病房的住院程序。目的是为准父母提供不同医疗保健专业人员提供的一致信息。在一项回顾性、质量控制、观察性队列研究中,从患者图表(是/否)中检索了2014 /25年度(10月25日至3月31日)第一季的新生儿免疫数据。所有从产科病房或本中心新生儿科出院的新生儿都被纳入分析。结果:该方案包括早期和多学科的父母教育,提供一致的口头和书面信息,以及讨论他们关于新免疫接种的问题的机会,确保知情同意,并使产科和新生儿单位的卫生保健专业人员能够及时给药尼瑟维单抗。在2014 /25年度,78%的新生儿在出院前接种了疫苗:78%(588/758)从产科出院的新生儿接种了疫苗,82%(125/153)从新生儿病房出院的新生儿接种了疫苗。结论:被动RSV免疫的实施总体上是成功的,在2024/25年度的第一个季节免疫接种率约为80%。
{"title":"Passive RSV immunisation using nirsevimab in neonatal care: a structured multidisciplinary approach and immunisation data from a Swiss tertiary centre.","authors":"Katalin Kalya, Jehudith Fontijn, Flurina Famos, Dirk Bassler, Nicole Ochsenbein-Kölble, Ladina Vonzun","doi":"10.57187/s.4689","DOIUrl":"10.57187/s.4689","url":null,"abstract":"<p><strong>Background: </strong>Respiratory syncytial virus (RSV) infection is a major cause of severe lower respiratory tract infections in newborns and young infants, especially during the winter season from October to March. In Switzerland, RSV infection represents a leading cause of hospital admissions among newborns. Since October 2024, a long-acting monoclonal antibody, nirsevimab (Beyfortus®), has been available in Switzerland for standard care in newborns.</p><p><strong>Objectives: </strong>This paper presents a multidisciplinary, standardised protocol for the administration of nirsevimab, as well as immunisation data from the first season of application in 2024/25 at a tertiary centre in Switzerland.</p><p><strong>Methods: </strong>A protocol for implementing the RSV immunisation strategy was developed at University Hospital Zurich by a multidisciplinary team of obstetricians, neonatologists, nurses, from in- and outpatient services. The focus was on prenatal counselling during outpatient consultations as well as inpatient procedures on maternity and neonatology wards. The goal was to provide expectant parents with consistent information by different healthcare professionals. Neonatal immunisation data from the first season in 2024/25 (25 October to 31 March ) were retrieved from patient charts (Yes/No) in a retrospective, quality control, observational cohort study. All newborns discharged from the maternity ward or the neonatology unit of our centre were included in the analysis.</p><p><strong>Results: </strong>The protocol included early and multidisciplinary parental education, offering consistent oral and written information, as well as opportunities to discuss their questions regarding the new immunisation, ensured informed consent and enabled timely administration of nirsevimab by healthcare professionals in the obstetrics and neonatology units. Over the 2024/25 season, 78% of the newborns were immunised before leaving hospital care: 78% (588/758) of newborns discharged home from the maternity ward were immunised and 82% (125/153) of those discharged home from the neonatology unit were immunised.   CONCLUSION: The implementation of passive RSV immunisation was overall successful with an immunisation rate of around 80% for the first season in 2024/25.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"4689"},"PeriodicalIF":1.9,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145865584","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Limitation of therapeutic efforts in internal medicine: a retrospective analysis of evolution and determinants (2013-2023) in a Swiss university hospital. 在内科的治疗努力的局限性:在瑞士大学医院的演变和决定因素的回顾性分析(2013-2023)。
IF 1.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-12-23 DOI: 10.57187/s.4477
Malik Benmachiche, Claudio Sartori, Peter Vollenweider, Pedro Marques-Vidal
<p><strong>Background/aims: </strong>In-hospital goals of care documentation is crucial for determining the adequate level of care in case of life-threatening emergencies. They might include limitation of therapeutic efforts, such as Do Not Resuscitate, Do Not Admit to intensive care unit (ICU) and Do Not Admit to intermediate care unit (IMCU) orders, or a "comfort care only" instruction. An ethical recommendation has recently been published to guide Do Not Resuscitate decisions, and several studies have shown a poor prognosis of frail multimorbid patients in case of critical illness. However, little is known on the use of limitation of therapeutic efforts other than Do Not Resuscitate in a hospital internal medicine population. We evaluated the evolution and determinants of the limitations of therapeutic efforts Do Not Resuscitate, Do Not Admit to ICU and Do Not Admit to IMCU between January 2013 and July 2023.</p><p><strong>Materials and methods: </strong>We conducted a retrospective observational study in a Swiss university hospital internal medicine service. Overall, 51,569 hospital stays (28,273 patients) were included. We assessed the yearly prevalence of the different limitations of therapeutic efforts and searched for the determinants of each limitation of therapeutic effort through multivariable analysis with adjustments for year of hospitalisation, age, sex, religion, co-diagnoses, hospital length of stay, ICU or IMCU admission.</p><p><strong>Results: </strong>The prevalence of Do Not Resuscitate, Do Not Admit to ICU and Do Not Admit to IMCU increased between 2013 and 2023 from 47.5%, 4.5% and 0.8%, respectively, to 58%, 31.4% and 14.6%. In multivariable analysis, the main factor associated with limitation of therapeutic efforts overall was older age, with odds ratios and 95% confidence intervals of 406 (329-501) (Do Not Resuscitate), 8.98 (7.93-10.2) (Do Not Admit to ICU) and 7.52 (6.25-9.05) (Do Not Admit to IMCU) for the >85 relative to the 56-65 year subgroup. The comorbidities most associated with limitation of therapeutic efforts were metastatic cancer and dementia: 7.59 (6.54-8.82) and 5.49 (4.74-6.37), respectively, for Do Not Resuscitate; 2.19 (1.96-2.45) and 1.72 (1.59-1.87) for Do Not Admit to ICU; and 2.13 (1.81-2.50) and 2.10 (1.89-2.34) for Do Not Admit to IMCU. Male sex was associated with lower limitation of therapeutic efforts: 0.66 (0.61-0.72) for Do Not Resuscitate, 0.83 (0.79-0.88) for Do Not Admit to ICU and 0.84 (0.77-0.92) for Do Not Admit to IMCU.</p><p><strong>Conclusion: </strong>The prevalence of limitation of therapeutic efforts in hospitalised medicine patients of our hospital increased during the past decade, with a remarkably large increase in limitation of admission to ICU (7-fold increase) and IMCU (18-fold increase). The main determinants of limitation of therapeutic efforts are older age, metastatic cancer and dementia. Reasons for the lower prevalence of limitation of therapeutic efforts in males shou
背景/目的:在危及生命的紧急情况下,医院内护理记录的目标对于确定适当的护理水平至关重要。它们可能包括治疗努力的限制,如不要复苏,不要进入重症监护病房(ICU)和不要进入中级监护病房(IMCU)命令,或“仅提供舒适护理”指令。最近发表了一项伦理建议,以指导不复苏的决定,几项研究表明,在危重疾病的情况下,虚弱的多病患者预后不良。然而,在医院内科人群中,除了不复苏之外,对限制治疗努力的使用知之甚少。我们评估了2013年1月至2023年7月期间“不复苏”、“不住院ICU”和“不住院IMCU”治疗措施局限性的演变和决定因素。材料和方法:我们在瑞士大学医院内科进行了一项回顾性观察研究。总共包括51,569次住院(28,273例患者)。我们评估了不同治疗努力局限性的年度患病率,并通过多变量分析(包括住院年份、年龄、性别、宗教、合并诊断、住院时间、ICU或IMCU入院)寻找每种治疗努力局限性的决定因素。结果:2013 - 2023年,不复苏、不入院ICU和不入院IMCU的患病率分别从47.5%、4.5%和0.8%上升至58%、31.4%和14.6%。在多变量分析中,与总体治疗效果限制相关的主要因素是年龄较大,相对于56-65岁亚组,bbb85患者的优势比和95%置信区间分别为406(329-501)(不复苏)、8.98(7.93-10.2)(不入院ICU)和7.52(6.25-9.05)(不入院IMCU)。与治疗努力限制最相关的合并症是转移性癌症和痴呆:不复苏分别为7.59(6.54-8.82)和5.49 (4.74-6.37);未入住ICU的分别为2.19(1.96 ~ 2.45)和1.72 (1.59 ~ 1.87);不允许进入IMCU的分数分别为2.13(1.81-2.50)和2.10(1.89-2.34)。男性与治疗努力下限相关:不复苏0.66(0.61-0.72),不收治ICU 0.83(0.79-0.88),不收治IMCU 0.84(0.77-0.92)。结论:近十年来,我院住院内科患者治疗努力受限的发生率有所上升,其中ICU和IMCU的住院限制明显增加(分别增加7倍和18倍)。限制治疗努力的主要决定因素是年龄较大,转移性癌症和痴呆。应探讨男性患病率较低和治疗努力受限的原因。
{"title":"Limitation of therapeutic efforts in internal medicine: a retrospective analysis of evolution and determinants (2013-2023) in a Swiss university hospital.","authors":"Malik Benmachiche, Claudio Sartori, Peter Vollenweider, Pedro Marques-Vidal","doi":"10.57187/s.4477","DOIUrl":"10.57187/s.4477","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background/aims: &lt;/strong&gt;In-hospital goals of care documentation is crucial for determining the adequate level of care in case of life-threatening emergencies. They might include limitation of therapeutic efforts, such as Do Not Resuscitate, Do Not Admit to intensive care unit (ICU) and Do Not Admit to intermediate care unit (IMCU) orders, or a \"comfort care only\" instruction. An ethical recommendation has recently been published to guide Do Not Resuscitate decisions, and several studies have shown a poor prognosis of frail multimorbid patients in case of critical illness. However, little is known on the use of limitation of therapeutic efforts other than Do Not Resuscitate in a hospital internal medicine population. We evaluated the evolution and determinants of the limitations of therapeutic efforts Do Not Resuscitate, Do Not Admit to ICU and Do Not Admit to IMCU between January 2013 and July 2023.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Materials and methods: &lt;/strong&gt;We conducted a retrospective observational study in a Swiss university hospital internal medicine service. Overall, 51,569 hospital stays (28,273 patients) were included. We assessed the yearly prevalence of the different limitations of therapeutic efforts and searched for the determinants of each limitation of therapeutic effort through multivariable analysis with adjustments for year of hospitalisation, age, sex, religion, co-diagnoses, hospital length of stay, ICU or IMCU admission.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;The prevalence of Do Not Resuscitate, Do Not Admit to ICU and Do Not Admit to IMCU increased between 2013 and 2023 from 47.5%, 4.5% and 0.8%, respectively, to 58%, 31.4% and 14.6%. In multivariable analysis, the main factor associated with limitation of therapeutic efforts overall was older age, with odds ratios and 95% confidence intervals of 406 (329-501) (Do Not Resuscitate), 8.98 (7.93-10.2) (Do Not Admit to ICU) and 7.52 (6.25-9.05) (Do Not Admit to IMCU) for the &gt;85 relative to the 56-65 year subgroup. The comorbidities most associated with limitation of therapeutic efforts were metastatic cancer and dementia: 7.59 (6.54-8.82) and 5.49 (4.74-6.37), respectively, for Do Not Resuscitate; 2.19 (1.96-2.45) and 1.72 (1.59-1.87) for Do Not Admit to ICU; and 2.13 (1.81-2.50) and 2.10 (1.89-2.34) for Do Not Admit to IMCU. Male sex was associated with lower limitation of therapeutic efforts: 0.66 (0.61-0.72) for Do Not Resuscitate, 0.83 (0.79-0.88) for Do Not Admit to ICU and 0.84 (0.77-0.92) for Do Not Admit to IMCU.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;The prevalence of limitation of therapeutic efforts in hospitalised medicine patients of our hospital increased during the past decade, with a remarkably large increase in limitation of admission to ICU (7-fold increase) and IMCU (18-fold increase). The main determinants of limitation of therapeutic efforts are older age, metastatic cancer and dementia. Reasons for the lower prevalence of limitation of therapeutic efforts in males shou","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"4477"},"PeriodicalIF":1.9,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145865609","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Monitoring of antimicrobial stewardship implementation in Swiss hospitals: results from a national survey. 瑞士医院抗菌药物管理实施的监测:一项全国性调查的结果。
IF 1.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-12-23 DOI: 10.57187/s.4860
Marcus Eder, Vinciane Vouets, Alexandra U Scherrer, Simon Gottwalt, Philipp Jent, Laurence Senn, On Behalf Of The StAR-Consortium

  AIM: Antimicrobial stewardship (AMS) is essential to containing antimicrobial resistance. Under the Swiss Strategy on Antibiotic Resistance (StAR), a nationwide survey was conducted to assess antimicrobial stewardship implementation in acute care hospitals and inform future national stewardship strategies.

Methods: A total of 136 acute care hospitals in Switzerland were invited to complete a questionnaire adapted from a validated Dutch tool and modified for the Swiss context. The questionnaire gathered information on whether a formal antimicrobial stewardship programme was present (primary outcome), institutional characteristics, as well as key antimicrobial stewardship activities (secondary outcomes) such as guideline implementation, education, raising awareness, prescription restrictions, and audits. Descriptive statistics and analyses compared the implementation of antimicrobial stewardship activities by the presence of a formal antimicrobial stewardship programme.

Results: Sixty-nine hospitals completed the survey (response rate: 51%); these hospitals represent 67% of all patient discharges in Switzerland in 2023. Although 86% reported engaging in at least one antimicrobial stewardship activity, only 47% had a formal antimicrobial stewardship programme (primary outcome). Most institutions reported providing infectious diseases specialist consult services (93%), clinical pharmacy support (84%), and microbiology advice (78%). Treatment guidelines (90%) and monitoring antimicrobial use (85%) were widely implemented. However, critical stewardship measures such as prescription audits with feedback were underutilised (20%), and few hospitals (18%) had allocated dedicated staff resources for antimicrobial stewardship. Hospitals with formal antimicrobial stewardship programmes reported key activities such as guideline use, prescriber education, antimicrobial restrictions, and audits more frequently.

Conclusion: This nationwide survey demonstrates encouraging progress in antimicrobial stewardship implementation since 2017, with most hospitals reporting stewardship activities and half having established a formal antimicrobial stewardship programme. However, critical gaps remain, highlighting the need for strengthened coordination and national support for hospitals to establish formal antimicrobial stewardship programmes to ensure the implementation and a sustainable impact of key antimicrobial stewardship activities.

目的:抗菌素管理(AMS)对控制抗菌素耐药性至关重要。根据瑞士抗生素耐药性战略(StAR),开展了一项全国性调查,以评估急症护理医院抗菌素管理的实施情况,并为未来的国家管理战略提供信息。方法:瑞士共136家急症护理医院被邀请完成一份调查问卷,该问卷改编自经过验证的荷兰工具,并根据瑞士的情况进行了修改。问卷收集了关于是否存在正式的抗菌素管理规划(主要结果)、机构特征以及关键的抗菌素管理活动(次要结果),如指南实施、教育、提高认识、处方限制和审计等信息。描述性统计和分析比较了抗菌素管理活动的实施与正式抗菌素管理规划的存在。结果:69家医院完成调查,回复率为51%;到2023年,这些医院占瑞士所有出院病人的67%。尽管86%的人报告参与了至少一项抗菌素管理活动,但只有47%的人有正式的抗菌素管理规划(主要结果)。大多数机构报告提供传染病专家咨询服务(93%)、临床药学支持(84%)和微生物学咨询(78%)。治疗指南(90%)和监测抗菌素使用(85%)得到了广泛实施。然而,关键的管理措施,如带反馈的处方审计未得到充分利用(20%),少数医院(18%)为抗菌素管理分配了专门的人力资源。拥有正式抗菌素管理规划的医院报告了一些关键活动,如指南的使用、处方医生教育、抗菌素限制和更频繁的审计。结论:这项全国性调查显示,自2017年以来,抗菌素管理实施取得了令人鼓舞的进展,大多数医院报告了管理活动,一半医院建立了正式的抗菌素管理规划。然而,仍然存在重大差距,突出表明需要加强协调和国家对医院的支持,以建立正式的抗微生物药物管理规划,以确保关键的抗微生物药物管理活动得到实施并产生可持续影响。
{"title":"Monitoring of antimicrobial stewardship implementation in Swiss hospitals: results from a national survey.","authors":"Marcus Eder, Vinciane Vouets, Alexandra U Scherrer, Simon Gottwalt, Philipp Jent, Laurence Senn, On Behalf Of The StAR-Consortium","doi":"10.57187/s.4860","DOIUrl":"https://doi.org/10.57187/s.4860","url":null,"abstract":"<p><p>  AIM: Antimicrobial stewardship (AMS) is essential to containing antimicrobial resistance. Under the Swiss Strategy on Antibiotic Resistance (StAR), a nationwide survey was conducted to assess antimicrobial stewardship implementation in acute care hospitals and inform future national stewardship strategies.</p><p><strong>Methods: </strong>A total of 136 acute care hospitals in Switzerland were invited to complete a questionnaire adapted from a validated Dutch tool and modified for the Swiss context. The questionnaire gathered information on whether a formal antimicrobial stewardship programme was present (primary outcome), institutional characteristics, as well as key antimicrobial stewardship activities (secondary outcomes) such as guideline implementation, education, raising awareness, prescription restrictions, and audits. Descriptive statistics and analyses compared the implementation of antimicrobial stewardship activities by the presence of a formal antimicrobial stewardship programme.</p><p><strong>Results: </strong>Sixty-nine hospitals completed the survey (response rate: 51%); these hospitals represent 67% of all patient discharges in Switzerland in 2023. Although 86% reported engaging in at least one antimicrobial stewardship activity, only 47% had a formal antimicrobial stewardship programme (primary outcome). Most institutions reported providing infectious diseases specialist consult services (93%), clinical pharmacy support (84%), and microbiology advice (78%). Treatment guidelines (90%) and monitoring antimicrobial use (85%) were widely implemented. However, critical stewardship measures such as prescription audits with feedback were underutilised (20%), and few hospitals (18%) had allocated dedicated staff resources for antimicrobial stewardship. Hospitals with formal antimicrobial stewardship programmes reported key activities such as guideline use, prescriber education, antimicrobial restrictions, and audits more frequently.</p><p><strong>Conclusion: </strong>This nationwide survey demonstrates encouraging progress in antimicrobial stewardship implementation since 2017, with most hospitals reporting stewardship activities and half having established a formal antimicrobial stewardship programme. However, critical gaps remain, highlighting the need for strengthened coordination and national support for hospitals to establish formal antimicrobial stewardship programmes to ensure the implementation and a sustainable impact of key antimicrobial stewardship activities.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"4860"},"PeriodicalIF":1.9,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145865631","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The digital stethoscope: Why Switzerland's Electronic Health Record requires citizen testing. 数字听诊器:为什么瑞士的电子健康记录需要公民检测。
IF 1.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-12-22 DOI: 10.57187/s.5160
Barbara C Biedermann, Peter Grolimund, Bruno Wildhaber, Ernst Hafen

  Switzerland's Electronic Patient Record (EPR) system faces a critical adoption crisis: less than 2% of the population has opened an account despite years of investment. To understand this failure from the citizen's perspective, we launched the first "expedition" in which 120 volunteers ("salutonauts") systematically tested Switzerland's current digital health infrastructure by opening EPRs, requesting their health data and documenting their experiences. This represents the first real-world, citizen-led assessment of Switzerland's health data infrastructure. Our findings reveal three fundamental insights. First, citizens appreciate the concept of personally controlled health records governed by a trustworthy national framework. Second, the current EPR implementation is both impractical and economically untenable under existing conditions: opening an EPR nationwide would cost CHF 400 million (calculated from required man-hours alone), while uploading historic documents would cost CHF 1 billion, and obtaining insurance claims data would cost over CHF 5 billion in lost productivity. Third, the recently announced draft of the new Electronic Health Dossier Law (E-GD) comes at a critical moment, since evidence-based redesign of the EPR system is essential. 95% of participants valued comprehensive medical checkups producing structured data, demonstrating citizens' appetite for high-quality digital health records when they provide tangible benefits. Our expedition methodology, which is agile, citizen-centred and involves real-world testing, offers a replicable model for evaluating digital health initiatives before massive implementation costs are incurred. With the E-GD revision underway, Switzerland has a unique opportunity to develop an EPR system that serves patients and physicians above all. Successful implementation requires EPR opening at birth by default (with the ability to opt-out), the AI-powered automation of data collection and uploading, seamless healthcare professional interfaces, and using the EPR as the billing data gateway. The alternative - i.e. continuing the current approach - virtually guarantees failure based on economic factors alone.

瑞士的电子病历(EPR)系统面临着严重的采用危机:尽管多年的投资,但只有不到2%的人口开设了账户。为了从公民的角度理解这一失败,我们发起了第一次“探险”,其中120名志愿者(“致敬者”)通过开放epr,要求他们提供健康数据并记录他们的经验,系统地测试了瑞士目前的数字卫生基础设施。这是对瑞士卫生数据基础设施进行的首次真实的、公民主导的评估。我们的发现揭示了三个基本见解。首先,公民欣赏由可信赖的国家框架管理的个人控制的健康记录的概念。其次,在现有条件下,目前的EPR实施既不现实,也不经济:在全国范围内开设EPR将花费4亿瑞士法郎(仅按所需工时计算),而上传历史文件将花费10亿瑞士法郎,获取保险索赔数据将花费超过50亿瑞士法郎的生产力损失。第三,最近公布的新电子卫生档案法(E-GD)草案正值关键时刻,因为基于证据的电子卫生档案系统重新设计至关重要。95%的参与者重视产生结构化数据的全面医疗检查,这表明公民在提供切实利益时对高质量数字健康记录的兴趣。我们的考察方法灵活,以公民为中心,涉及现实世界的测试,为在产生大量实施成本之前评估数字健康举措提供了一个可复制的模型。随着E-GD修订的进行,瑞士有一个独特的机会来开发一个为患者和医生服务的EPR系统。成功实施EPR需要在出生时默认打开EPR(可以选择退出)、人工智能驱动的数据收集和上传自动化、无缝的医疗保健专业界面,以及使用EPR作为计费数据网关。另一种选择- -即继续目前的做法- -仅从经济因素来看,几乎肯定会失败。
{"title":"The digital stethoscope: Why Switzerland's Electronic Health Record requires citizen testing.","authors":"Barbara C Biedermann, Peter Grolimund, Bruno Wildhaber, Ernst Hafen","doi":"10.57187/s.5160","DOIUrl":"https://doi.org/10.57187/s.5160","url":null,"abstract":"<p><p>  Switzerland's Electronic Patient Record (EPR) system faces a critical adoption crisis: less than 2% of the population has opened an account despite years of investment. To understand this failure from the citizen's perspective, we launched the first \"expedition\" in which 120 volunteers (\"salutonauts\") systematically tested Switzerland's current digital health infrastructure by opening EPRs, requesting their health data and documenting their experiences. This represents the first real-world, citizen-led assessment of Switzerland's health data infrastructure. Our findings reveal three fundamental insights. First, citizens appreciate the concept of personally controlled health records governed by a trustworthy national framework. Second, the current EPR implementation is both impractical and economically untenable under existing conditions: opening an EPR nationwide would cost CHF 400 million (calculated from required man-hours alone), while uploading historic documents would cost CHF 1 billion, and obtaining insurance claims data would cost over CHF 5 billion in lost productivity. Third, the recently announced draft of the new Electronic Health Dossier Law (E-GD) comes at a critical moment, since evidence-based redesign of the EPR system is essential. 95% of participants valued comprehensive medical checkups producing structured data, demonstrating citizens' appetite for high-quality digital health records when they provide tangible benefits. Our expedition methodology, which is agile, citizen-centred and involves real-world testing, offers a replicable model for evaluating digital health initiatives before massive implementation costs are incurred. With the E-GD revision underway, Switzerland has a unique opportunity to develop an EPR system that serves patients and physicians above all. Successful implementation requires EPR opening at birth by default (with the ability to opt-out), the AI-powered automation of data collection and uploading, seamless healthcare professional interfaces, and using the EPR as the billing data gateway. The alternative - i.e. continuing the current approach - virtually guarantees failure based on economic factors alone.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"5160"},"PeriodicalIF":1.9,"publicationDate":"2025-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145865591","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The role of advance directives in preventing compulsory placement and coercive measures in Switzerland: a need to review present practice. 事先指示在瑞士防止强制安置和强制措施方面的作用:有必要审查目前的做法。
IF 1.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-12-19 DOI: 10.57187/s.4616
Nikola Biller-Andorno, Sophie Gloeckler

In Switzerland, where individual self-determination and self-responsibility are strong values, coercive measures are still very present in the care of individuals with mental health conditions. In 2022, over 18,000 cases of compulsory care placements were recorded - one of the highest rates in Europe [1]. The Swiss Academy of Medical Sciences (SAMS) is reviewing its guidelines on coercion to better support practice. The present viewpoint aims to contribute to such efforts by focusing on the role of advance directives in preventing unwanted compulsory placement and coercive measures. Advance directives support individuals to document treatment preferences in anticipation of future incapacity. There is, though, differentiation between psychiatric and non-psychiatric cases: while treatment refusals for somatic conditions are typically considered binding, the preferences expressed in psychiatric advance directives can be overridden following compulsory placement. This creates a double standard that undermines self-determination for individuals with mental health conditions. The present article advocates for uniform legal standards that would grant psychiatric advance directives equal binding force. It explores the validity of common arguments against doing so, suggesting that objections often rely on inconsistent or ethically flawed reasoning. The piece lays out arguments in support of modifying policy on psychiatric advance directives, suggesting that comparably binding directives might enhance patient autonomy, reduce the harm of coercive interventions, promote goal-concordant care, strengthen oversight, and address discriminatory policy. As the Swiss Academy of Medical Sciences revisits guidelines on coercive practices, it is a good moment to consider the potential value of binding psychiatric advance directives as tools to uphold patient autonomy and contribute to broader efforts to reduce the harm of coercive practices.

在瑞士,个人自决和自我责任是非常重要的价值观,但在照顾有精神健康问题的个人方面,仍然非常存在强制措施。2022年,记录在案的强制性护理安置案例超过1.8万例,是欧洲最高的比率之一。瑞士医学科学院(SAMS)正在审查其关于强迫的指导方针,以更好地支持实践。目前的观点旨在通过集中讨论预先指示在防止不必要的强制安置和强制措施方面的作用来促进这种努力。预先指示支持个人记录治疗偏好,以预测未来的丧失能力。然而,精神病学和非精神病学病例之间是有区别的:虽然对躯体疾病的治疗拒绝通常被认为是有约束力的,但精神病学预先指示中表达的偏好可以在强制安置后被推翻。这造成了双重标准,破坏了精神健康状况患者的自决权。本文提倡统一的法律标准,赋予精神病学预先指示同等的约束力。它探讨了反对这样做的常见论点的有效性,表明反对意见往往依赖于不一致或道德上有缺陷的推理。这篇文章列出了支持修改精神科预先指示政策的论据,表明具有同等约束力的指示可能会增强患者的自主权,减少强制性干预的危害,促进目标一致的护理,加强监督,并解决歧视性政策。随着瑞士医学科学院(Swiss Academy of Medical Sciences)重新审视强制性做法的指导方针,这是一个很好的时机,可以考虑将具有约束力的精神病学预先指示作为维护患者自主权的工具的潜在价值,并为减少强制性做法的危害做出更广泛的贡献。
{"title":"The role of advance directives in preventing compulsory placement and coercive measures in Switzerland: a need to review present practice.","authors":"Nikola Biller-Andorno, Sophie Gloeckler","doi":"10.57187/s.4616","DOIUrl":"https://doi.org/10.57187/s.4616","url":null,"abstract":"<p><p>In Switzerland, where individual self-determination and self-responsibility are strong values, coercive measures are still very present in the care of individuals with mental health conditions. In 2022, over 18,000 cases of compulsory care placements were recorded - one of the highest rates in Europe [1]. The Swiss Academy of Medical Sciences (SAMS) is reviewing its guidelines on coercion to better support practice. The present viewpoint aims to contribute to such efforts by focusing on the role of advance directives in preventing unwanted compulsory placement and coercive measures. Advance directives support individuals to document treatment preferences in anticipation of future incapacity. There is, though, differentiation between psychiatric and non-psychiatric cases: while treatment refusals for somatic conditions are typically considered binding, the preferences expressed in psychiatric advance directives can be overridden following compulsory placement. This creates a double standard that undermines self-determination for individuals with mental health conditions. The present article advocates for uniform legal standards that would grant psychiatric advance directives equal binding force. It explores the validity of common arguments against doing so, suggesting that objections often rely on inconsistent or ethically flawed reasoning. The piece lays out arguments in support of modifying policy on psychiatric advance directives, suggesting that comparably binding directives might enhance patient autonomy, reduce the harm of coercive interventions, promote goal-concordant care, strengthen oversight, and address discriminatory policy. As the Swiss Academy of Medical Sciences revisits guidelines on coercive practices, it is a good moment to consider the potential value of binding psychiatric advance directives as tools to uphold patient autonomy and contribute to broader efforts to reduce the harm of coercive practices.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"4616"},"PeriodicalIF":1.9,"publicationDate":"2025-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145865646","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Impact of the COVID-19 pandemic on routine childhood immunisation coverage and timeliness in Switzerland: a retrospective analysis using data from the Swiss National Vaccination Coverage Survey, 2019-2023. 2019冠状病毒病大流行对瑞士常规儿童免疫接种覆盖率和及时性的影响:使用2019-2023年瑞士全国疫苗接种覆盖率调查数据的回顾性分析
IF 1.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-12-17 DOI: 10.57187/s.4525
Vasiliki Baroutsou, Monica N Wymann, Jan S Fehr, Phung Lang

Background: The coronavirus disease 2019 (COVID-19) pandemic has disrupted healthcare systems worldwide, leading to concerns about reduced access to routine childhood immunisations. However, comprehensive data on how the pandemic specifically impacted paediatric vaccination coverage in Switzerland remain limited across the country. The present study provides an analysis of the timeliness and coverage of routine childhood immunisations in Switzerland before and during the COVID-19 pandemic, offering insights into potential fluctuations in coverage.

Aims: To assess the impact of the COVID-19 pandemic on routine childhood immunisation in Switzerland by comparing vaccination coverage and timeliness for children under 35 months of age before and during the pandemic. Additionally, the study seeks to identify factors associated with the likelihood of children receiving vaccinations, considering demographic and geographic variables.

Methods: We used 2019-2023 data from the Swiss National Vaccination Coverage Survey (SNVCS), a cross-sectional survey that collected immunisation information of children under 35 months of age from a nationally representative sample of households. Children who were eligible for a vaccine from March 2020 to March 2021 were considered as the COVID-affected group and those eligible for a vaccine before this date were included in the pre-COVID-19 cohort. Coverage of the following vaccine doses was considered: diphtheria at one, two and three doses (Di1, Di2, Di3); pneumococcus at one, two and three doses (PCV1, PCV2, PCV3); and measles first and second dose (MCV1, MCV2). Vaccine timeliness was defined as receiving a dose on time with a tolerance period of 30 days. We used logistic regression models to identify and understand the factors that might influence vaccination rates.

Results: For the diphtheria vaccines (Di1, Di2, Di3), while coverage remained high, there was a slight decrease observed in timely vaccination rates for some doses, with reductions of around 1% to 3% compared to pre-COVID-19 levels. The impact on PCV1, PCV2 and PCV3 showed similar trends, with slight reductions in coverage during the pandemic, but these differences were not statistically significant. For measles-containing vaccines (MCV1 and MCV2), coverage during the pandemic was higher compared to pre-COVID-19 rates. Geographic and demographic factors, such as an urban setting, nationality and linguistic region, significantly influence childhood vaccination rates in Switzerland.

Conclusion: While minor declines in vaccine timeliness were observed (diphtheria vaccine, pneumococcal conjugate vaccine), the overall likelihood of vaccination was not significantly affected by the COVID-19 pandemic. However, changes in vaccination recommendations introduced in 2019 may have influenced these trends.

背景:2019年冠状病毒病(COVID-19)大流行扰乱了全球卫生保健系统,导致人们对常规儿童免疫接种机会减少的担忧。然而,关于大流行如何具体影响瑞士儿科疫苗接种覆盖率的综合数据在全国范围内仍然有限。本研究分析了瑞士在COVID-19大流行之前和期间常规儿童免疫接种的及时性和覆盖率,为覆盖率的潜在波动提供了见解。目的:通过比较大流行之前和期间35个月以下儿童的疫苗接种覆盖率和及时性,评估COVID-19大流行对瑞士常规儿童免疫接种的影响。此外,考虑到人口和地理变量,该研究试图确定与儿童接种疫苗可能性相关的因素。方法:我们使用了瑞士国家疫苗接种覆盖率调查(SNVCS)的2019-2023年数据,这是一项横断面调查,从全国代表性的家庭样本中收集了35个月以下儿童的免疫接种信息。在2020年3月至2021年3月期间有资格接种疫苗的儿童被视为受covid -19影响的组,在此日期之前有资格接种疫苗的儿童被纳入covid -19前队列。考虑了以下疫苗剂量的覆盖范围:白喉一剂、二剂和三剂(Di1、Di2、Di3);肺炎球菌一剂、二剂和三剂(PCV1、PCV2、PCV3);麻疹第一剂和第二剂(MCV1、MCV2)。疫苗及时性定义为按时接种疫苗,耐受期为30天。我们使用逻辑回归模型来识别和理解可能影响疫苗接种率的因素。结果:对于白喉疫苗(Di1、Di2、Di3),尽管覆盖率仍然很高,但一些剂量的及时疫苗接种率略有下降,与covid -19前的水平相比下降了约1%至3%。对PCV1、PCV2和PCV3的影响表现出类似的趋势,在大流行期间覆盖率略有下降,但这些差异在统计上并不显著。对于含麻疹疫苗(MCV1和MCV2),大流行期间的覆盖率高于covid -19前的覆盖率。地理和人口因素,如城市环境、国籍和语言区域,对瑞士的儿童疫苗接种率有重大影响。结论:虽然疫苗及时性略有下降(白喉疫苗、肺炎球菌结合疫苗),但总体接种可能性未受COVID-19大流行的显著影响。然而,2019年疫苗接种建议的变化可能影响了这些趋势。
{"title":"Impact of the COVID-19 pandemic on routine childhood immunisation coverage and timeliness in Switzerland: a retrospective analysis using data from the Swiss National Vaccination Coverage Survey, 2019-2023.","authors":"Vasiliki Baroutsou, Monica N Wymann, Jan S Fehr, Phung Lang","doi":"10.57187/s.4525","DOIUrl":"https://doi.org/10.57187/s.4525","url":null,"abstract":"<p><strong>Background: </strong>The coronavirus disease 2019 (COVID-19) pandemic has disrupted healthcare systems worldwide, leading to concerns about reduced access to routine childhood immunisations. However, comprehensive data on how the pandemic specifically impacted paediatric vaccination coverage in Switzerland remain limited across the country. The present study provides an analysis of the timeliness and coverage of routine childhood immunisations in Switzerland before and during the COVID-19 pandemic, offering insights into potential fluctuations in coverage.</p><p><strong>Aims: </strong>To assess the impact of the COVID-19 pandemic on routine childhood immunisation in Switzerland by comparing vaccination coverage and timeliness for children under 35 months of age before and during the pandemic. Additionally, the study seeks to identify factors associated with the likelihood of children receiving vaccinations, considering demographic and geographic variables.</p><p><strong>Methods: </strong>We used 2019-2023 data from the Swiss National Vaccination Coverage Survey (SNVCS), a cross-sectional survey that collected immunisation information of children under 35 months of age from a nationally representative sample of households. Children who were eligible for a vaccine from March 2020 to March 2021 were considered as the COVID-affected group and those eligible for a vaccine before this date were included in the pre-COVID-19 cohort. Coverage of the following vaccine doses was considered: diphtheria at one, two and three doses (Di1, Di2, Di3); pneumococcus at one, two and three doses (PCV1, PCV2, PCV3); and measles first and second dose (MCV1, MCV2). Vaccine timeliness was defined as receiving a dose on time with a tolerance period of 30 days. We used logistic regression models to identify and understand the factors that might influence vaccination rates.</p><p><strong>Results: </strong>For the diphtheria vaccines (Di1, Di2, Di3), while coverage remained high, there was a slight decrease observed in timely vaccination rates for some doses, with reductions of around 1% to 3% compared to pre-COVID-19 levels. The impact on PCV1, PCV2 and PCV3 showed similar trends, with slight reductions in coverage during the pandemic, but these differences were not statistically significant. For measles-containing vaccines (MCV1 and MCV2), coverage during the pandemic was higher compared to pre-COVID-19 rates. Geographic and demographic factors, such as an urban setting, nationality and linguistic region, significantly influence childhood vaccination rates in Switzerland.</p><p><strong>Conclusion: </strong>While minor declines in vaccine timeliness were observed (diphtheria vaccine, pneumococcal conjugate vaccine), the overall likelihood of vaccination was not significantly affected by the COVID-19 pandemic. However, changes in vaccination recommendations introduced in 2019 may have influenced these trends.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"155 ","pages":"4525"},"PeriodicalIF":1.9,"publicationDate":"2025-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145865636","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","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
Swiss medical weekly
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