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Costs and acceptability of simplified monitoring in HIV-suppressed patients switching to dual therapy: the SIMPL'HIV open-label, factorial randomised controlled trial. 对转为双重疗法的艾滋病病毒抑制患者进行简化监测的成本和可接受性:SIMPL'HIV 开放标签、因子随机对照试验。
IF 2.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-04-15 DOI: 10.57187/s.3762
Annalisa Marinosci, Delphine Sculier, Gilles Wandeler, Sabine Yerly, Marcel Stoeckle, Enos Bernasconi, Dominique L Braun, Pietro Vernazza, Matthias Cavassini, Marta Buzzi, Karin J Metzner, Laurent Decosterd, Huldrych F Günthard, Patrick Schmid, Andreas Limacher, Mattia Branca, Alexandra Calmy
<p><strong>Background: </strong>Clinical and laboratory monitoring of patients on antiretroviral therapy is an integral part of HIV care and determines whether treatment needs enhanced adherence or modification of the drug regimen. However, different monitoring and treatment strategies carry different costs and health consequences.</p><p><strong>Materials and methods: </strong>The SIMPL'HIV study was a randomised trial that assessed the non-inferiority of dual maintenance therapy. The co-primary outcome was a comparison of costs over 48 weeks of dual therapy with standard antiretroviral therapy and the costs associated with a simplified HIV care approach (patient-centred monitoring [PCM]) versus standard, tri-monthly routine monitoring. Costs included outpatient medical consultations (HIV/non-HIV consultations), non-medical consultations, antiretroviral therapy, laboratory tests and hospitalisation costs. PCM participants had restricted immunological and blood safety monitoring at weeks 0 and 48, and they were offered the choice to complete their remaining study visits via a telephone call, have medications delivered to a specified address, and to have blood tests performed at a location of their choice. We analysed the costs of both strategies using invoices for medical consultations issued by the hospital where the patient was followed, as well as those obtained from health insurance companies. Secondary outcomes included differences between monitoring arms for renal function, lipids and glucose values, and weight over 48 weeks. Patient satisfaction with treatment and monitoring was also assessed using visual analogue scales.</p><p><strong>Results: </strong>Of 93 participants randomised to dolutegravir plus emtricitabine and 94 individuals to combination antiretroviral therapy (median nadir CD4 count, 246 cells/mm3; median age, 48 years; female, 17%),patient-centred monitoring generated no substantial reductions or increases in total costs (US$ -421 per year [95% CI -2292 to 1451]; p = 0.658). However, dual therapy was significantly less expensive (US$ -2620.4 [95% CI -2864.3 to -2331.4]) compared to standard triple-drug antiretroviral therapy costs. Approximately 50% of participants selected one monitoring option, one-third chose two, and a few opted for three. The preferred option was telephone calls, followed by drug delivery. The number of additional visits outside the study schedule did not differ by type of monitoring. Patient satisfaction related to treatment and monitoring was high at baseline, with no significant increase at week 48.</p><p><strong>Conclusions: </strong>Patient-centred monitoring did not reduce costs compared to standard monitoring in individuals switching to dual therapy or those continuing combined antiretroviral therapy. In this representative sample of patients with suppressed HIV, antiretroviral therapy was the primary factor driving costs, which may be reduced by using generic drugs to mitigate the high cost of li
背景:对接受抗逆转录病毒治疗的患者进行临床和实验室监测是 HIV 护理不可或缺的一部分,可确定是否需要加强治疗的依从性或修改药物方案。然而,不同的监测和治疗策略会产生不同的成本和健康后果:SIMPL'HIV研究是一项随机试验,旨在评估双重维持疗法的非劣效性。共同主要结果是比较双重疗法与标准抗逆转录病毒疗法 48 周的成本,以及简化 HIV 护理方法(以患者为中心的监测 [PCM])与标准的三个月一次常规监测的相关成本。费用包括门诊医疗咨询(HIV/非 HIV 咨询)、非医疗咨询、抗逆转录病毒疗法、实验室检测和住院费用。PCM 参与者在第 0 周和第 48 周接受了有限制的免疫和血液安全监测,他们可以选择通过电话完成剩余的研究访问、将药物送到指定地址,以及在自己选择的地点进行血液化验。我们使用随访医院开具的医疗咨询发票以及从医疗保险公司获得的发票分析了两种策略的成本。次要结果包括 48 周内各监测组在肾功能、血脂和血糖值以及体重方面的差异。此外,还使用视觉模拟量表评估了患者对治疗和监测的满意度:在随机接受多罗替拉韦加恩曲他滨治疗的 93 名患者和接受联合抗逆转录病毒治疗的 94 名患者中(CD4 细胞计数中位数为 246 cells/mm3;年龄中位数为 48 岁;女性占 17%),以患者为中心的监测并未显著降低或增加总成本(每年 -421 美元 [95% CI -2292 至 1451];P = 0.658)。然而,与标准的三药抗逆转录病毒疗法费用相比,双重疗法的费用要低得多(-2620.4 美元 [95% CI -2864.3 至 -2331.4])。约 50%的参与者选择了一种监测方案,三分之一选择了两种,少数选择了三种。首选方案是打电话,其次是送药。研究计划外的额外就诊次数不因监测类型而异。患者对治疗和监测的满意度在基线时很高,在第 48 周时没有显著提高:结论:与标准监测相比,以患者为中心的监测并未降低转为双重疗法或继续接受联合抗逆转录病毒疗法的患者的成本。在这个具有代表性的艾滋病病毒感染者样本中,抗逆转录病毒疗法是导致成本增加的主要因素,而通过使用非专利药物来降低终身艾滋病治疗的高昂成本,可能会降低成本:试验注册:ClinicalTrials.gov NCT03160105。
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引用次数: 0
Feasibility and cost-effectiveness of genetic counselling for all patients with newly diagnosed ovarian cancer: a single-centre retrospective study. 为所有新诊断卵巢癌患者提供遗传咨询的可行性和成本效益:一项单中心回顾性研究。
IF 2.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-04-15 DOI: 10.57187/s.3386
Saskia Schlootz, Flurina A M Saner, Manuela Rabaglio, Sara Imboden, Julian Wampfler

Background and aims of the study: Due to its importance for treatment and potential prevention in family members, germline testing for BRCA1/2 in patients with newly diagnosed ovarian cancer is decisive and considered a standard of care. Maintenance therapy with poly(ADP-ribose) polymerase (PARP) inhibitors substantially improves progression-free survival in patients with BRCA mutations and homologous recombination-deficient tumours by inducing synthetic lethality. In Switzerland, they are licensed only for these patients. Therefore, it is crucial to test patients early while they are receiving adjuvant chemotherapy. This study aimed to determine whether genetic counselling followed by homologous recombination deficiency testing is feasible for initialising maintenance therapy within eight weeks and cost-effective in daily practice in Switzerland compared to somatic tumour analysis of all patients at diagnosis.

Methods: This single-centre retrospective study included 44 patients with newly diagnosed high-grade serous ovarian cancer of a Federation of Gynaecology and Obstetrics (FIGO) stage of IIIA-IVB diagnosed between 12/2020 and 12/2022. It collected the outcomes of genetic counselling, germline testing, and somatic Geneva test for homologous recombination deficiency. Delays in initiating maintenance therapy, total testing costs per patient, and progression-free survival were examined to assess feasibility and cost-effectiveness in clinical practice.

Results: Thirty-seven of 44 patients (84%) with newly diagnosed ovarian cancer received counselling, of which 34 (77%) were tested for germline BRCA and other homologous recombination repair gene mutations. Five (15%) BRCA and three (9%) other homologous recombination deficiency mutations were identified. Eleven of the remaining 26 patients (42%) had tumours with somatic homologous recombination deficiency. The mean time to the initiation of maintenance therapy of 5.2 weeks was not longer than in studies for market authorisation (SOLO1, PAOLA, and PRIMA). The mean testing costs per patient were 3880 Swiss Franks (CHF), compared to 5624 CHF if all patients were tested at diagnosis with the myChoice CDx test (p <0.0001).

Conclusion: Using genetic counselling to consent patients with newly diagnosed ovarian cancer for germline testing fulfils the international gold standard. Subsequent somatic homologous recombination deficiency analysis complements testing and identifies more patients who will benefit from PARP inhibitor maintenance therapy. Contrary to previous health cost model studies, the procedure does not increase testing costs in the Swiss population and does not delay maintenance therapy. Therefore, all patients should be offered a primary germline analysis. The challenge for the future will be to ensure sufficient resources for prompt genetic counselling and germline testing.

研究背景和目的:对新诊断的卵巢癌患者进行 BRCA1/2 基因检测对治疗和潜在的预防具有重要意义,因此被认为是治疗的标准。多聚(ADP-核糖)聚合酶(PARP)抑制剂通过诱导合成致死率,大大改善了 BRCA 基因突变和同源重组缺陷肿瘤患者的无进展生存期。在瑞士,PARP 抑制剂仅被许可用于这些患者。因此,在患者接受辅助化疗期间对其进行早期检测至关重要。本研究旨在确定,与诊断时对所有患者进行体细胞肿瘤分析相比,在瑞士,遗传咨询后进行同源重组缺陷检测是否可在八周内启动维持治疗,以及在日常实践中是否具有成本效益:这项单中心回顾性研究纳入了 44 名新确诊的高级别浆液性卵巢癌患者,这些患者在 2020 年 12 月至 2022 年 12 月期间被诊断为妇产科联盟(FIGO)分期 IIIA-IVB 级。该研究收集了遗传咨询、种系检测和同源重组缺陷体细胞日内瓦检测的结果。对开始维持治疗的延迟、每位患者的总检测成本和无进展生存期进行了研究,以评估临床实践中的可行性和成本效益:44 名新确诊卵巢癌患者中有 37 人(84%)接受了咨询,其中 34 人(77%)接受了种系 BRCA 和其他同源重组修复基因突变检测。发现了 5 例(15%)BRCA 基因突变和 3 例(9%)其他同源重组缺陷基因突变。其余26名患者中有11人(42%)的肿瘤存在体细胞同源重组缺陷。开始维持治疗的平均时间为 5.2 周,并不长于市场授权研究(SOLO1、PAOLA 和 PRIMA)。每位患者的平均检测费用为 3880 瑞士法郎(CHF),而如果所有患者都在诊断时接受 myChoice CDx 检测,则平均检测费用为 5624 瑞士法郎(P利用遗传咨询同意新诊断卵巢癌患者进行种系检测符合国际黄金标准。随后进行的体细胞同源重组缺陷分析是对检测的补充,可识别出更多可从 PARP 抑制剂维持治疗中获益的患者。与之前的健康成本模型研究相反,该程序不会增加瑞士人群的检测成本,也不会延迟维持治疗。因此,所有患者都应接受初级种系分析。未来的挑战将是确保有足够的资源进行及时的遗传咨询和种系检测。
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引用次数: 0
SARS-CoV-2 immunity and reasons for non-vaccination among healthcare workers from eastern and northern Switzerland: results from a nested multicentre cross-sectional study. 瑞士东部和北部医护人员的 SARS-CoV-2 免疫力和不接种疫苗的原因:一项巢状多中心横断面研究的结果。
IF 2.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-04-13 DOI: 10.57187/s.3734
Selina Albrecht, Fabian Grässli, Alexia Cusini, Angela Brucher, Stephan Goppel, Elsbeth Betschon, J Carsten Möller, Manuela Ortner, Markus Ruetti, Reto Stocker, Danielle Vuichard-Gysin, Ulrike Besold, Lorenz Risch, Matthias Von Kietzell, Matthias Schlegel, Pietro Vernazza, Stefan P Kuster, Christian R Kahlert, Philipp Kohler

Aims of the study: We aimed to assess the extent of SARS-CoV-2 humoral immunity elicited by previous infections and/or vaccination among healthcare workers, and to identify reasons why healthcare workers decided against vaccination.

Methods: This nested cross-sectional study included volunteer healthcare workers from 14 healthcare institutions in German-speaking Switzerland. In January 2021, SARS-CoV-2 vaccines were available for healthcare workers. In May and June 2022, participants answered electronic questionnaires regarding baseline characteristics including SARS-CoV-2 vaccination status (with one or more vaccine doses defined as vaccinated) and previous SARS-CoV-2 infections. Unvaccinated participants indicated their reasons for non-vaccination. Participants underwent testing for SARS-CoV-2 anti-spike (anti-S) and anti-nucleocapsid (anti-N) antibodies. Antibody prevalence was described across age groups. In addition, we performed multivariable logistic regression to identify baseline characteristics independently associated with non-vaccination and described reasons for non-vaccination.

Results: Among 22,438 eligible employees, 3,436 (15%) participated; the median age was 43.7 years (range 16-73), 2,794 (81.3%) were female, and 1,407 (47.7%) identified as nurses; 3,414 (99.4%) underwent serology testing, among whom 3,383 (99.0%) had detectable anti-S (3,357, 98.3%) antibodies, anti-N (2,396, 70.1%) antibodies, or both (2,370, 69.4%). A total of 296 (8.6%) healthcare workers were unvaccinated, whereas 3,140 (91.4%) were vaccinated. In multivariable analysis, age (adjusted OR [aOR] 1.02 per year, 95% CI 1.01-1.03), being a physician (aOR 3.22, 95% CI 1.75-5.92) or administrator (aOR 1.88, 95% CI 1.27-2.80), and having higher education (aOR 2.23, 95% CI 1.09-4.57) were positively associated with vaccine uptake, whereas working in non-acute care (aOR 0.58, 95% CI 0.34-0.97), active smoking (aOR 0.68, 95% CI 0.51-0.91), and taking prophylactic home remedies against SARS-CoV-2 (aOR 0.42, 95% CI 0.31-0.56) were negatively associated. Important reasons for non-vaccination were a belief that the vaccine might not have long-lasting immunity (267/291, 92.1%) and a preference for gaining naturally acquired instead of vaccine-induced immunity (241/289, 83.4%).

Conclusions: Almost all healthcare workers in our cohort had specific antibodies against SARS-CoV-2 from natural infection and/or from vaccination. Young healthcare workers and those working in non-acute settings were less likely to be vaccinated, whereas physicians and administrative staff showed higher vaccination uptake. Presumed ineffectiveness of the vaccine is an important reason for non-vaccination.

研究目的我们的目的是评估医护人员因既往感染和/或接种疫苗而产生的 SARS-CoV-2 体液免疫的程度,并找出医护人员决定不接种疫苗的原因:这项嵌套横断面研究包括来自瑞士德语区 14 家医疗机构的志愿医护人员。2021 年 1 月,医护人员可接种 SARS-CoV-2 疫苗。2022 年 5 月和 6 月,参与者回答了有关基线特征的电子问卷,包括 SARS-CoV-2 疫苗接种情况(接种一剂或一剂以上疫苗定义为已接种)和既往 SARS-CoV-2 感染情况。未接种者说明了未接种的原因。参与者接受了 SARS-CoV-2 抗尖峰抗体(anti-S)和抗核头壳抗体(anti-N)检测。我们对各年龄组的抗体流行率进行了描述。此外,我们还进行了多变量逻辑回归,以确定与未接种疫苗独立相关的基线特征,并描述了未接种疫苗的原因:在 22,438 名符合条件的员工中,3,436 人(15%)参与其中;年龄中位数为 43.7 岁(16-73 岁不等),2,794 人(81.3%)为女性,1,407 人(47.7%)为护士;3,414 人(99.3,414人(99.4%)接受了血清学检测,其中3,383人(99.0%)检测到抗S抗体(3,357人,98.3%)、抗N抗体(2,396人,70.1%)或两者(2,370人,69.4%)。共有 296 名医护人员(8.6%)未接种疫苗,而 3140 名医护人员(91.4%)接种了疫苗。在多变量分析中,年龄(调整 OR [aOR] 每年 1.02,95% CI 1.01-1.03)、医生(aOR 3.22,95% CI 1.75-5.92)或行政人员(aOR 1.88,95% CI 1.27-2.80)以及受过高等教育(aOR 2.23,95% CI 1.09-4.57)与疫苗接种率呈正相关。57)与疫苗接种率呈正相关,而在非急症护理机构工作(aOR 0.58,95% CI 0.34-0.97)、主动吸烟(aOR 0.68,95% CI 0.51-0.91)和在家中服用预防 SARS-CoV-2 的药物(aOR 0.42,95% CI 0.31-0.56)则呈负相关。不接种疫苗的重要原因是认为疫苗可能不会产生持久的免疫力(267/291,92.1%),以及希望获得自然获得的免疫力而不是疫苗诱导的免疫力(241/289,83.4%):结论:在我们的队列中,几乎所有医护人员都有通过自然感染和/或接种疫苗获得的针对 SARS-CoV-2 的特异性抗体。年轻医护人员和在非急诊环境中工作的医护人员接种疫苗的可能性较低,而医生和行政人员的接种率较高。认为疫苗无效是不接种疫苗的一个重要原因。
{"title":"SARS-CoV-2 immunity and reasons for non-vaccination among healthcare workers from eastern and northern Switzerland: results from a nested multicentre cross-sectional study.","authors":"Selina Albrecht, Fabian Grässli, Alexia Cusini, Angela Brucher, Stephan Goppel, Elsbeth Betschon, J Carsten Möller, Manuela Ortner, Markus Ruetti, Reto Stocker, Danielle Vuichard-Gysin, Ulrike Besold, Lorenz Risch, Matthias Von Kietzell, Matthias Schlegel, Pietro Vernazza, Stefan P Kuster, Christian R Kahlert, Philipp Kohler","doi":"10.57187/s.3734","DOIUrl":"10.57187/s.3734","url":null,"abstract":"<p><strong>Aims of the study: </strong>We aimed to assess the extent of SARS-CoV-2 humoral immunity elicited by previous infections and/or vaccination among healthcare workers, and to identify reasons why healthcare workers decided against vaccination.</p><p><strong>Methods: </strong>This nested cross-sectional study included volunteer healthcare workers from 14 healthcare institutions in German-speaking Switzerland. In January 2021, SARS-CoV-2 vaccines were available for healthcare workers. In May and June 2022, participants answered electronic questionnaires regarding baseline characteristics including SARS-CoV-2 vaccination status (with one or more vaccine doses defined as vaccinated) and previous SARS-CoV-2 infections. Unvaccinated participants indicated their reasons for non-vaccination. Participants underwent testing for SARS-CoV-2 anti-spike (anti-S) and anti-nucleocapsid (anti-N) antibodies. Antibody prevalence was described across age groups. In addition, we performed multivariable logistic regression to identify baseline characteristics independently associated with non-vaccination and described reasons for non-vaccination.</p><p><strong>Results: </strong>Among 22,438 eligible employees, 3,436 (15%) participated; the median age was 43.7 years (range 16-73), 2,794 (81.3%) were female, and 1,407 (47.7%) identified as nurses; 3,414 (99.4%) underwent serology testing, among whom 3,383 (99.0%) had detectable anti-S (3,357, 98.3%) antibodies, anti-N (2,396, 70.1%) antibodies, or both (2,370, 69.4%). A total of 296 (8.6%) healthcare workers were unvaccinated, whereas 3,140 (91.4%) were vaccinated. In multivariable analysis, age (adjusted OR [aOR] 1.02 per year, 95% CI 1.01-1.03), being a physician (aOR 3.22, 95% CI 1.75-5.92) or administrator (aOR 1.88, 95% CI 1.27-2.80), and having higher education (aOR 2.23, 95% CI 1.09-4.57) were positively associated with vaccine uptake, whereas working in non-acute care (aOR 0.58, 95% CI 0.34-0.97), active smoking (aOR 0.68, 95% CI 0.51-0.91), and taking prophylactic home remedies against SARS-CoV-2 (aOR 0.42, 95% CI 0.31-0.56) were negatively associated. Important reasons for non-vaccination were a belief that the vaccine might not have long-lasting immunity (267/291, 92.1%) and a preference for gaining naturally acquired instead of vaccine-induced immunity (241/289, 83.4%).</p><p><strong>Conclusions: </strong>Almost all healthcare workers in our cohort had specific antibodies against SARS-CoV-2 from natural infection and/or from vaccination. Young healthcare workers and those working in non-acute settings were less likely to be vaccinated, whereas physicians and administrative staff showed higher vaccination uptake. Presumed ineffectiveness of the vaccine is an important reason for non-vaccination.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"154 ","pages":"3734"},"PeriodicalIF":2.9,"publicationDate":"2024-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140857850","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
Core stories of physicians on a Swiss internal medicine ward during the first COVID-19 wave: a qualitative exploration. 瑞士内科病房医生在 COVID-19 第一波期间的核心故事:定性探索。
IF 2.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-03-29 DOI: 10.57187/s.3760
Vanessa Kraege, Amaelle Gavin, Julieta Norambuena, Friedrich Stiefel, Marie Méan, Céline Bourquin

Introduction: The first COVID-19 wave (2020), W1, will remain extraordinary due to its novelty and the uncertainty on how to handle the pandemic. To understand what physicians went through, we collected narratives of frontline physicians working in a Swiss university hospital during W1.

Methods: Physicians in the Division of Internal Medicine of Lausanne University Hospital (CHUV) were invited to send anonymous narratives to an online platform, between 28 April and 30 June 2020. The analysed material consisted of 13 written texts and one audio record. They were examined by means of a narrative analysis based on a holistic content approach, attempting to identify narrative highlights, referred to as foci, in the texts.

Results: Five main foci were identified: danger and threats, acquisition of knowledge and practices, adaptation to a changing context, commitment to the profession, and sense of belonging to the medical staff. In physicians' narratives, danger designated a variety of rather negative feelings and emotions, whereas threats were experienced as being dangerous for others, but also for oneself. The acquisition of knowledge and practices focus referred to the different types of acquisition that took place during W1. The narratives that focused on adaptation reflected how physicians coped with W1 and private or professional upheavals. COVID-19 W1 contributed to revealing a natural commitment (or not) of physicians towards the profession and patients, accompanied by the concern of offering the best possible care to all. Lastly, sense of belonging referred to the team and its reconfiguration during W1.

Conclusions: Our study deepens the understanding of how physicians experienced the pandemic both in their professional and personal settings. It offers insights into how they prepared and reacted to a pandemic. The foci reflect topics that are inherent to a physician's profession, whatever the context. During a pandemic, these foundational elements are particularly challenged. Strikingly, these topics are not studied in medical school, thus raising the general question of how students are prepared for the medical profession.

导言:COVID-19 的第一波(2020 年),即 W1,由于其新颖性和如何应对大流行的不确定性,仍将是非同寻常的。为了了解医生的经历,我们收集了 W1 期间在瑞士一所大学医院工作的一线医生的叙述:方法:我们邀请洛桑大学医院(CHUV)内科的医生在 2020 年 4 月 28 日至 6 月 30 日期间向在线平台发送匿名叙述。分析材料包括 13 篇书面文字和 1 份录音。我们采用基于整体内容法的叙事分析方法对这些文本进行了研究,试图找出文本中的叙事重点(称为焦点):结果:确定了五个主要焦点:危险和威胁、知识和实践的获得、适应不断变化的环境、对职业的承诺以及对医务人员的归属感。在医生的叙述中,"危险 "指的是各种相当负面的感觉和情绪,而 "威胁 "则指对他人和对自己的危险。获取知识和实践的重点指的是 W1 期间发生的不同类型的获取。以适应为重点的叙述反映了医生如何应对 W1 和私人或职业动荡。COVID-19 W1有助于揭示医生对职业和病人的自然承诺(或不承诺),以及为所有人提供尽可能好的护理的关切。最后,归属感指的是 W1 期间的团队及其重组:我们的研究加深了对医生在职业和个人环境中如何经历大流行病的理解。我们的研究加深了对医生在职业和个人环境中如何经历大流行病的了解,并为他们如何准备和应对大流行病提供了见解。无论在什么情况下,研究的重点都反映了医生职业所固有的主题。在大流行病期间,这些基本要素尤其面临挑战。令人震惊的是,医学院并没有学习这些内容,这就提出了一个普遍的问题,即学生们是如何为从事医疗职业做好准备的。
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引用次数: 0
Impact of shift work and other work-related factors on anti-SARS-CoV-2 spike-protein serum concentrations in healthcare workers after primary mRNA vaccination - a retrospective cohort study. 轮班工作和其他工作相关因素对医护人员接种初级 mRNA 疫苗后抗 SARS-CoV-2 棘蛋白血清浓度的影响--一项回顾性队列研究。
IF 2.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-03-27 DOI: 10.57187/s.3708
Gianluca Mauro Menghini, Robert Thurnheer, Christian R Kahlert, Philipp Kohler, Fabian Grässli, Reto Stocker, Manuel Battegay, Danielle Vuichard-Gysin

Background: Knowing whether shift work negatively affects the immune system's response to COVID-19 vaccinations could be valuable for planning future vaccination campaigns for healthcare workers. We aimed to determine the impact of working late or night shifts on serum anti-SARS-CoV-2 spike protein immunoglobulin G (anti-S) antibody levels after primary SARS-CoV-2-mRNA vaccination.

Methods: To obtain detailed information on shift work, we sent a separate online questionnaire to 1475 eligible healthcare workers who participated in a prospective longitudinal study conducted in 15 healthcare institutions in Switzerland. We asked all vaccinated healthcare workers with available anti-S antibody levels after vaccination to complete a brief online survey on their working schedules within one week before and after primary mRNA vaccination. We used multivariate regression to evaluate the association between work shifts around primary vaccination and anti-S antibody levels. We adjusted for confounders already known to influence vaccine efficacy (e.g. age, sex, immunosuppression, and obesity) and for variables significant at the 0.05 alpha level in the univariate analyses.

Results: The survey response rate was 43% (n = 638). Ninety-eight responders were excluded due to unknown vaccination dates, different vaccines, or administration of the second dose shortly (within 14 days) after or before serologic follow-up. Of the 540 healthcare workers included in our analysis, 175 (32.4%) had worked at least one late or night shift within seven days before and/or after primary vaccination. In the univariate analyses, working late or night shifts was associated with a nonsignificant -15.1% decrease in serum anti-S antibody levels (p = 0.090). In the multivariate analysis, prior infection (197.2% increase; p <0.001) and immunisation with the mRNA-1273 vaccine (63.7% increase compared to the BNT162b2 vaccine; p <0.001) were the strongest independent factors associated with increased anti-S antibody levels. However, the impact of shift work remained statistically nonsignificant (-13.5%, p = 0.108).

Conclusion: Working late or night shifts shortly before or after mRNA vaccination against COVID-19 does not appear to significantly impact serum anti-S antibody levels. This result merits consideration since it supports flexible vaccination appointments for healthcare workers, including those working late or night shifts.

背景:了解轮班工作是否会对免疫系统对 COVID-19 疫苗接种的反应产生负面影响,对于规划未来的医护人员疫苗接种活动很有价值。我们的目的是确定晚班或夜班对接种 SARS-CoV-2-mRNA 疫苗后血清中抗 SARS-CoV-2 尖峰蛋白免疫球蛋白 G(抗 S)抗体水平的影响:为了获得有关轮班工作的详细信息,我们向 1475 名符合条件的医护人员发送了一份单独的在线问卷,这些医护人员参加了在瑞士 15 家医疗机构开展的一项前瞻性纵向研究。我们要求所有接种疫苗后有抗 S 抗体水平的医护人员完成一份简短的在线调查,了解他们在接种初级 mRNA 疫苗前后一周内的工作时间安排。我们使用多元回归法评估了初次接种疫苗前后的工作班次与抗 S 抗体水平之间的关系。我们对已知会影响疫苗疗效的混杂因素(如年龄、性别、免疫抑制和肥胖)以及在单变量分析中显著性达到 0.05 alpha 水平的变量进行了调整:调查回复率为 43%(n = 638)。由于接种日期不详、接种了不同的疫苗或在血清学随访后不久(14 天内)或之前接种了第二剂疫苗,98 名回复者被排除在外。在纳入分析的 540 名医护人员中,有 175 人(32.4%)在初次接种疫苗之前和/或之后的七天内至少上过一次晚班或夜班。在单变量分析中,上晚班或夜班与血清抗 S 抗体水平下降-15.1%无显著相关性(p = 0.090)。在多变量分析中,既往感染(增加 197.2%;p = 0.090)与血清抗 S 抗体水平的下降无关(p = 0.090):接种 COVID-19 mRNA 疫苗前后上晚班或夜班似乎不会对血清抗 S 抗体水平产生显著影响。这一结果值得考虑,因为它支持医护人员(包括上晚班或夜班的医护人员)灵活预约疫苗接种时间。
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引用次数: 0
Association between the number of symptomatic mpox cases and the detection of mpox virus DNA in wastewater in Switzerland: an observational surveillance study. 瑞士无症状水痘病例数量与废水中检测到的水痘病毒 DNA 之间的关系:一项观察性监测研究。
IF 2.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-03-07 DOI: 10.57187/s.3706
Claudia Bagutti, Monica Alt Hug, Philippe Heim, Evelyn Ilg Hampe, Philipp Hübner, Timothy R Julian, Katrin N Koch, Kerstin Grosheintz, Melanie Kraus, Carla Schaubhut, Rahel Tarnutzer, Eva Würfel, Simon Fuchs, Sarah Tschudin-Sutter

Aim of the study: The COVID-19 pandemic has drawn attention to the benefit of wastewater-based epidemiology, particularly when case numbers are underreported. Underreporting may be an issue with mpox, where biological reasons and stigma may prevent patients from getting tested. Therefore, we aimed to assess the validity of wastewater surveillance for monitoring mpox virus DNA in wastewater of a Central European city and its association with official case numbers.

Methods: Wastewater samples were collected between 1 July and 28 August 2022 in the catchment area of Basel, Switzerland, and the number of mpox virus genome copies they contained was determined by real-time quantitative PCR. Logistic regression analyses were used to determine the odds of detectability of mpox virus DNA in wastewater, categorised as detectable or undetectable. Mann-Whitney U tests were used to determine associations between samples that tested positive for the mpox virus and officially reported cases and patients' recorded symptomatic phases.

Results: Mpox virus DNA was detected in 15 of 39 wastewater samples. The number of positive wastewater samples was associated with the number of symptomatic cases (odds ratio [OR] = 2.18, 95% confidence interval (CI) = 1.38-3.43, p = 0.001). The number of symptomatic cases differed significantly between days with positive versus negative wastewater results (median = 11 and 8, respectively, p = 0.0024).

Conclusion: Mpox virus DNA was detectable in wastewater, even when officially reported case numbers were low (0-3 newly reported mpox cases corresponding to 6-12 symptomatic patients). Detectability in wastewater was significantly associated with the number of symptomatic patients within the catchment area. These findings illustrate the value of wastewater-based surveillance systems when assessing the prevalence of emerging and circulating infectious diseases.

研究目的:COVID-19 大流行使人们注意到基于废水的流行病学的益处,尤其是在病例数被低报的情况下。低报可能是水痘的一个问题,因为生理原因和耻辱感可能会阻碍患者接受检测。因此,我们旨在评估废水监测对监测中欧某城市废水中天花病毒 DNA 的有效性及其与官方病例数的关联:方法:我们于 2022 年 7 月 1 日至 8 月 28 日期间在瑞士巴塞尔集水区采集了废水样本,并通过实时定量 PCR 测定了其中所含的 mpox 病毒基因组拷贝数。采用逻辑回归分析确定废水中检测到 mpox 病毒 DNA 的几率,分为可检测到和不可检测到两种情况。曼-惠特尼 U 检验用于确定水痘病毒检测呈阳性的样本与官方报告的病例和患者记录的症状阶段之间的关联:结果:39 份废水样本中有 15 份检测到麻风腮病毒 DNA。阳性废水样本的数量与有症状病例的数量相关(几率比 [OR] = 2.18,95% 置信区间 (CI) = 1.38-3.43,p = 0.001)。有症状病例的数量在废水结果为阳性和阴性的天数之间存在显著差异(中位数分别为 11 天和 8 天,p = 0.0024):结论:即使官方报告的病例数很少(0-3 个新报告的麻风病例对应 6-12 个有症状的病人),废水中也能检测到麻风病毒 DNA。废水中的可检测性与集水区内有症状患者的数量有显著关联。这些发现说明了基于废水的监测系统在评估新发和流行性传染病流行情况时的价值。
{"title":"Association between the number of symptomatic mpox cases and the detection of mpox virus DNA in wastewater in Switzerland: an observational surveillance study.","authors":"Claudia Bagutti, Monica Alt Hug, Philippe Heim, Evelyn Ilg Hampe, Philipp Hübner, Timothy R Julian, Katrin N Koch, Kerstin Grosheintz, Melanie Kraus, Carla Schaubhut, Rahel Tarnutzer, Eva Würfel, Simon Fuchs, Sarah Tschudin-Sutter","doi":"10.57187/s.3706","DOIUrl":"https://doi.org/10.57187/s.3706","url":null,"abstract":"<p><strong>Aim of the study: </strong>The COVID-19 pandemic has drawn attention to the benefit of wastewater-based epidemiology, particularly when case numbers are underreported. Underreporting may be an issue with mpox, where biological reasons and stigma may prevent patients from getting tested. Therefore, we aimed to assess the validity of wastewater surveillance for monitoring mpox virus DNA in wastewater of a Central European city and its association with official case numbers.</p><p><strong>Methods: </strong>Wastewater samples were collected between 1 July and 28 August 2022 in the catchment area of Basel, Switzerland, and the number of mpox virus genome copies they contained was determined by real-time quantitative PCR. Logistic regression analyses were used to determine the odds of detectability of mpox virus DNA in wastewater, categorised as detectable or undetectable. Mann-Whitney U tests were used to determine associations between samples that tested positive for the mpox virus and officially reported cases and patients' recorded symptomatic phases.</p><p><strong>Results: </strong>Mpox virus DNA was detected in 15 of 39 wastewater samples. The number of positive wastewater samples was associated with the number of symptomatic cases (odds ratio [OR] = 2.18, 95% confidence interval (CI) = 1.38-3.43, p = 0.001). The number of symptomatic cases differed significantly between days with positive versus negative wastewater results (median = 11 and 8, respectively, p = 0.0024).</p><p><strong>Conclusion: </strong>Mpox virus DNA was detectable in wastewater, even when officially reported case numbers were low (0-3 newly reported mpox cases corresponding to 6-12 symptomatic patients). Detectability in wastewater was significantly associated with the number of symptomatic patients within the catchment area. These findings illustrate the value of wastewater-based surveillance systems when assessing the prevalence of emerging and circulating infectious diseases.</p>","PeriodicalId":22111,"journal":{"name":"Swiss medical weekly","volume":"154 ","pages":"3706"},"PeriodicalIF":2.9,"publicationDate":"2024-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140868570","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
Pembrolizumab-associated anti-MDA5 dermatomyositis in a patient with lung cancer: a first case report. 肺癌患者中与 Pembrolizumab 相关的抗 MDA5 皮肌炎:首例病例报告。
IF 2.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-03-04 DOI: 10.57187/s.3513
Antonino Marcello Pilia, Lorenzo Salvati, Alessia Guidolin, Francesca Mazzoni, Lorenzo Antonuzzo, Paola Parronchi, Francesco Liotta

We report the first case of anti-melanoma differentiation-associated gene 5 (MDA5)-positive dermatomyositis as a systemic immune-related adverse event in a 64-year-old man receiving pembrolizumab to treat advanced lung cancer. The patient experienced hypothyroidism, myalgia, skin involvement, dyspnoea and diarrhoea. Laboratory tests revealed raised inflammatory markers, hypercreatinekinasemia and anti-MDA5 autoantibodies. Electroneuromyography and pathognomonic signs on physical examination confirmed the diagnosis of pauci-myopathic dermatomyositis. Pembrolizumab was discontinued and immunosuppressive therapy led to rapid and progressive improvement, with complete remission of dermatomyositis. This case report widens the spectrum of systemic immune-related adverse events associated with pembrolizumab.

我们报告了首例抗黑色素瘤分化相关基因5(MDA5)阳性皮肌炎的全身免疫相关不良事件,患者是一名64岁的男性,正在接受pembrolizumab治疗晚期肺癌。患者出现甲状腺功能减退、肌痛、皮肤受累、呼吸困难和腹泻。实验室检查显示炎症指标升高、高肌酸血症和抗MDA5自身抗体。体格检查中的电肌电图和病理征象证实了该病的诊断,即贫肌病性皮肌炎。患者停用了 Pembrolizumab,接受免疫抑制治疗后病情得到了快速、渐进的改善,皮肌炎完全缓解。本病例报告扩大了与 Pembrolizumab 相关的全身免疫相关不良事件的范围。
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引用次数: 0
Palliative sedation - revised recommendations. 姑息镇静--修订建议。
IF 2.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-02-15 DOI: 10.57187/s.3590
Michel Beauverd, Marta Mazzoli, Josiane Pralong, Martyna Tomczyk, Steffen Eychmüller, Jan Gaertner

Palliative sedation is defined as the monitored use of medications intended to induce a state of decreased or absent awareness (unconsciousness) to relieve the burden of otherwise intractable suffering in a manner ethically acceptable to the patient, their family, and healthcare providers. In Switzerland, the prevalence of continuous deep sedation until death increased from 4.7% in 2001 to 17.5% of all deceased in 2013, depending on the research method used and on regional variations. Yet, these numbers may be overestimated due to a lack of understanding of the term "continuous deep sedation" by for example respondents of the questionnaire-based study. Inadequately trained and inexperienced healthcare professionals may incorrectly or inappropriately perform palliative sedation due to uncertainties regarding its definitions and practice. Therefore, the expert members of the Bigorio group and the authors of this manuscript believe that national recommendations should be published and made available to healthcare professionals to provide practical, terminological, and ethical guidance. The Bigorio group is the working group of the Swiss Palliative Care Society whose task is to publish clinical recommendations at a national level in Switzerland. These recommendations aim to provide guidance on the most critical questions and issues related to palliative sedation. The Swiss Society of Palliative Care (palliative.ch) mandated a writing board comprising four clinical experts (three physicians and one ethicist) and two national academic experts to revise the 2005 Bigorio guidelines. A first draft was created based on a narrative literature review, which was internally reviewed by five academic institutions (Lausanne, Geneva, Bern, Zürich, and Basel) and the heads of all working groups of the Swiss Society of Palliative Care before finalising the guidelines. The following themes are discussed regarding palliative sedation: (a) definitions and clinical aspects, (b) the decision-making process, (c) communication with patients and families, (d) patient monitoring, (e) pharmacological approaches, and (f) ethical and controversial issues. Palliative sedation must be practised with clinical and ethical accuracy and competence to avoid harm and ethically questionable use. Specialist palliative care teams should be consulted before initiating palliative sedation to avoid overlooking other potential treatment options for the patient's symptoms and suffering.

姑息镇静被定义为在监控下使用药物,以诱导意识减退或缺失(无意识)的状态,从而以患者、家属和医疗服务提供者在道德上可接受的方式减轻原本难以承受的痛苦。在瑞士,持续深度镇静直至死亡的比例从2001年的4.7%上升到2013年的17.5%,这取决于所使用的研究方法和地区差异。然而,由于问卷调查的受访者等对 "持续深度镇静 "一词缺乏了解,这些数字可能被高估了。培训不足和缺乏经验的医护人员可能会因姑息镇静的定义和实践的不确定性而错误或不适当地实施姑息镇静。因此,比戈里奥小组的专家成员和本手稿的作者认为,应该发布国家建议,并提供给医护专业人员,以提供实用、术语和伦理方面的指导。比戈里奥小组是瑞士姑息关怀协会(Swiss Palliative Care Society)的一个工作小组,其任务是在瑞士全国范围内发布临床建议。这些建议旨在为姑息镇静相关的最关键问题提供指导。瑞士姑息关怀协会(palliative.ch)授权一个由四位临床专家(三位医生和一位伦理学家)和两位国内学术专家组成的写作委员会对2005年比戈里奥指南进行修订。在文献综述的基础上撰写了初稿,并由五家学术机构(洛桑、日内瓦、伯尔尼、苏黎世和巴塞尔)和瑞士姑息关怀协会所有工作组的负责人进行了内部审查,最终确定了该指南。该指南讨论了姑息镇静的以下主题:(a) 定义和临床方面,(b) 决策过程,(c) 与患者和家属的沟通,(d) 患者监测,(e) 药物治疗方法,(f) 伦理和争议问题。姑息镇静必须以临床和伦理的准确性和能力来实施,以避免伤害和伦理问题。在启动姑息镇静治疗前,应咨询姑息关怀专家团队,以避免忽略其他可能解决病人症状和痛苦的治疗方案。
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引用次数: 0
Who was at risk of trauma-related injuries during the COVID-19 pandemic? A retrospective study from a level 1 trauma centre in Switzerland. 在 COVID-19 大流行期间,谁有可能受到与创伤相关的伤害?一项来自瑞士一级创伤中心的回顾性研究。
IF 2.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-01-20 DOI: 10.57187/s.3539
Till Flury, Joël Gerber, Helen Anwander, Martin Müller, Dominik A Jakob, Aristomenis Exadaktylos, Karsten Klingberg

Introduction: During the first wave of the COVID-19 pandemic, increasingly strict restrictions were imposed on the activities of the Swiss population, with a peak from 21 March to 27 April 2020. Changes in trauma patterns during the pandemic and the lockdown have been described in various studies around the world, and highlight some particularly exposed groups of people. The objective of this study was to assess changes in trauma-related presentations to the emergency department (ED) during the first wave of the COVID-19 pandemic, as compared to the same period in the previous year, with a particular focus on vulnerable populations.

Materials and methods: All trauma-related admissions to our ED in the first half of 2019 and 2020 were included. Patient demographics, trauma mechanism, affected body region, injury severity and discharge type were extracted from our hospital information system. Trauma subpopulations, such as interpersonal violence, self-inflicted trauma, geriatric trauma and sports-related trauma were analysed.

Results: A total of 5839 ED presentations were included in our study, of which 39.9% were female. Median age was 40 years (interquartile range: 27-60). In comparison to 2019, there was a 15.5% decrease in trauma-related ED presentations in the first half of 2020. This decrease was particularly marked in the 2-month March/April period, with a drop of 36.8%. In 2020, there was a reduction in injuries caused by falls of less than 3 metres or by mechanical force. There was a marked decrease in sports-related trauma and an increase in injuries related to pedal cycles. Geriatric trauma, self-harm and assault-related injuries remained stable.

Conclusion: This study described changes in trauma patterns and highlighted populations at risk of trauma during the pandemic in Switzerland in the context of previous international studies.These results may contribute to resource management in a future pandemic.

导言:在 COVID-19 大流行的第一波期间,瑞士民众的活动受到越来越严格的限制,高峰期为 2020 年 3 月 21 日至 4 月 27 日。世界各地的多项研究都描述了大流行和封锁期间创伤模式的变化,并强调了一些特别易受感染的人群。本研究的目的是评估在 COVID-19 大流行的第一波期间,急诊科(ED)收治的创伤相关病例与上一年同期相比的变化情况,尤其关注弱势群体:纳入了我院急诊科在 2019 年和 2020 年上半年收治的所有与创伤相关的患者。我们从医院信息系统中提取了患者的人口统计数据、创伤机制、受影响的身体部位、受伤严重程度和出院类型。对人际暴力、自伤创伤、老年创伤和运动相关创伤等创伤亚群进行了分析:研究共纳入了 5839 例急诊室就诊病例,其中 39.9% 为女性。年龄中位数为 40 岁(四分位数间距:27-60)。与 2019 年相比,2020 年上半年与创伤相关的急诊就诊人数减少了 15.5%。这一下降在 3 月/4 月这两个月尤为明显,下降了 36.8%。2020 年,由 3 米以下高处坠落或机械外力造成的伤害有所减少。与运动有关的创伤明显减少,而与脚踏车有关的伤害则有所增加。老年创伤、自我伤害和攻击相关的伤害保持稳定:这项研究描述了创伤模式的变化,并结合以往的国际研究强调了瑞士大流行期间的创伤高危人群。
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引用次数: 0
Long-term course of neutralising antibodies against SARS-CoV-2 in vaccinated and unvaccinated staff and residents in a Swiss nursing home: a cohort study 2021–2022 瑞士一家疗养院中已接种和未接种疫苗的工作人员和住客体内针对 SARS-CoV-2 的中和抗体的长期变化过程:一项队列研究 2021-2022 年
IF 2.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-12-22 DOI: 10.57187/s.3502
Lisa Perrig, I. Abela, Nicolas Banholzer, Annette Audigé, Selina Epp, C. Mugglin, Kathrin Zürcher, Matthias Egger, Alexandra Trkola, Lukas Fenner
BACKGROUND: Given their high-risk resident population, nursing homes were critical institutions in the COVID-19 pandemic, calling for continued monitoring and vaccine administration to healthcare workers and residents. Here, we studied long-term severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) immunity in vaccinated and unvaccinated healthcare workers and residents of a nursing home in Switzerland between February 2021 and June 2022. METHODS: Our study comprised 45 participants, of which 39 were healthcare workers and six were residents. All participants were offered a maximum of three mRNA vaccine doses (Pfizer/BioNTech, BNT162b2) in December 2020, January 2021, and November/December 2021. Thirty-five participants received three vaccinations, seven either one or two, and three remained unvaccinated. We collected four blood samples: one in March 2021 and three during follow-ups in November 2021, February 2022, and June 2022. We performed a multifactorial serological SARS-CoV-2 assay (ABCORA) for immunoglobulin G, A, and M responses to spike (receptor-binding domain, S1, and S2) and nucleocapsid (N) proteins. Furthermore, we assessed predicted neutralisation activity based on signal over cutoff in ABCORA. We collected epidemiological data from participants via a standardised questionnaire. RESULTS: Thirty-two (71%) of the 45 participants showed hybrid immunity from combined vaccination and previous infection; 10 (22%) had only vaccine-induced immunity; and three (7%) had only post-infection immunity. Participants with hybrid immunity showed the highest predicted neutralisation activity at the end of the study period (median Sum S1 = 273), and unvaccinated participants showed the lowest (median Sum S1 = 41). Amongst participants who reported a SARS-CoV-2 infection, median Sum S1 levels increased with the number of vaccinations (p = 0.077). The healthcare worker group showed a significant time-dependent decrease in median Sum S1 after base immunisation (93% decrease, p = 0.0005) and the booster dose (26% decrease, p = 0.010). Predicted neutralisation activity was lower amongst residents (adjusted ratio of means [AM] = 0.7, 95% confidence interval [CI] = 0.3–1.0) and amongst smokers (AM = 0.5, 95% CI 0.3–0.8). Activity increased with the number of vaccinations (booster: AM = 3.6, 95% CI 1.5–8.8; no booster: AM = 2.3, 95% CI 0.9–2.5). Positive SARS-CoV-2 infection status tended to confer higher predicted neutralisation levels (AM = 1.5, 95% CI 0.9–2.5). CONCLUSIONS: Our study of the long-term serological course of SARS-CoV-2 in a nursing home showed that the first SARS-CoV-2 booster vaccine was essential for maintaining antiviral antibody levels. Hybrid immunity sustained SARS-CoV-2 immunity at the highest level. In critical settings such as nursing homes, monitoring the SARS-CoV-2 immune status may guide booster vaccinations.
背景:在 COVID-19 大流行中,疗养院因其高风险居民群体而成为关键机构,因此需要对医护人员和居民进行持续监测和疫苗接种。在此,我们研究了 2021 年 2 月至 2022 年 6 月期间瑞士一家疗养院中已接种和未接种疫苗的医护人员和居民对严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)的长期免疫力。方法:我们的研究由 45 名参与者组成,其中 39 人为医护人员,6 人为居民。所有参与者在 2020 年 12 月、2021 年 1 月和 2021 年 11 月/12 月最多可接种三次 mRNA 疫苗(辉瑞/BioNTech,BNT162b2)。35 名参与者接种了三次疫苗,7 名参与者接种了一次或两次疫苗,3 名参与者未接种疫苗。我们采集了四份血样:一份在 2021 年 3 月,三份在 2021 年 11 月、2022 年 2 月和 2022 年 6 月的随访期间。我们进行了多因素血清学 SARS-CoV-2 检测(ABCORA),以检测免疫球蛋白 G、A 和 M 对尖峰蛋白(受体结合域、S1 和 S2)和核壳蛋白(N)的反应。此外,我们还根据 ABCORA 中超过截止值的信号评估了预测的中和活性。我们通过标准化问卷收集了参与者的流行病学数据。结果:45名参与者中有32人(71%)表现出接种疫苗和既往感染的混合免疫力;10人(22%)只有疫苗诱导的免疫力;3人(7%)只有感染后免疫力。在研究结束时,具有混合免疫力的参与者的预测中和活性最高(中位数 S1 = 273),而未接种疫苗的参与者的预测中和活性最低(中位数 S1 = 41)。在报告感染过 SARS-CoV-2 的参与者中,Sum S1 的中位数随接种疫苗次数的增加而增加(p = 0.077)。医护人员组在基础免疫接种(下降 93%,p = 0.0005)和加强免疫接种(下降 26%,p = 0.010)后,Sum S1 中位数出现了显著的随时间变化的下降。居民(调整后均值比 [AM] = 0.7,95% 置信区间 [CI] = 0.3-1.0)和吸烟者(AM = 0.5,95% 置信区间 [CI] 0.3-0.8)的预测中和活性较低。随着疫苗接种次数的增加,活动性也随之增加(加强型:AM = 3.6,95% CI 1.5-8.8;无加强型:AM = 2.3,95% CI 0.9-2.5)。SARS-CoV-2感染阳性往往会带来更高的预测中和水平(AM = 1.5,95% CI 0.9-2.5)。结论:我们对疗养院中 SARS-CoV-2 的长期血清学过程进行的研究表明,第一次接种 SARS-CoV-2 加强型疫苗对维持抗病毒抗体水平至关重要。混合免疫将 SARS-CoV-2 的免疫力维持在最高水平。在疗养院等关键环境中,监测 SARS-CoV-2 免疫状态可为加强免疫提供指导。
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Swiss medical weekly
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