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Burden of disease of respiratory syncytial virus in older adults and adults considered at high risk of severe infection. 老年人和被认为有严重感染高风险的成年人呼吸道合胞体病毒疾病负担
Pub Date : 2025-01-02 eCollection Date: 2025-01-01 DOI: 10.14745/ccdr.v51i01a04
Elissa M Abrams, Pamela Doyon-Plourde, Phaedra Davis, Liza Lee, Abbas Rahal, Nicholas Brousseau, Winnie Siu, April Killikelly

Background: Availability of new vaccines for adults has increased interest in understanding Canada's respiratory syncytial virus (RSV) burden in older adults and adults considered at high risk of severe infection.

Objective: To characterize the burden of RSV disease in Canada by joint analysis of the published literature and hospitalization data from a healthcare administrative database.

Methods: Electronic databases of published literature were searched to identify studies and systematic reviews reporting data on outpatient visits, hospitalizations, intensive care unit (ICU) admissions and deaths associated with RSV infection in adults. For the hospitalization data analysis, hospital discharge records were extracted from the Canadian Institute of Health Information Discharge Abstract Database for all patients admitted to an acute care facility for RSV infection defined by ICD-10 codes from 2010 to 2020 and 2021 to 2023.

Results: Overall, 26 studies, including seven systematic reviews, were identified and summarized. Evidence suggests that medically attended RSV respiratory tract infections (RTI) are frequently causing 4.7%-7.8% of symptomatic RTI in adults 60 years of age and older. Incidence of RSV RTI increases with age and presence of underlying medical conditions. This trend was consistently observed across all RSV clinical outcomes of interest. Patients who reside in long-term care or other chronic care facilities have a higher likelihood of severe clinical outcomes compared to patients with other living situations upon hospital admission. Approximately 10% of older adults hospitalized with RSV infection require ICU admission. Although data are limited, the case fatality ratio (CFR) among those admitted to hospital varies between 5% and 10%. Some evidence suggests that RSV burden may be close to the influenza burden in older adults. In general, the results from the Canadian hospitalization data support the rapid review findings. Rates of hospitalization, ICU admission and death associated with RSV all increased with age, with 16% of hospitalizations resulting in ICU admission and with an in-hospital CFR of 9%.

Conclusion: In adults, the burden of severe RSV outcomes in general increases with age and presence of comorbidities.

背景:成人新疫苗的可用性增加了人们对了解加拿大老年人和被认为有严重感染高风险的成年人呼吸道合胞病毒(RSV)负担的兴趣。目的:通过联合分析已发表的文献和来自卫生保健管理数据库的住院数据,了解加拿大RSV疾病的负担特征。方法:检索已发表文献的电子数据库,以确定报告与成人RSV感染相关的门诊就诊、住院、重症监护病房(ICU)入院和死亡数据的研究和系统综述。对于住院数据分析,从加拿大卫生信息研究所出院摘要数据库中提取2010年至2020年和2021年至2023年根据ICD-10代码定义的RSV感染入住急性护理机构的所有患者的出院记录。结果:总共确定并总结了26项研究,包括7项系统综述。有证据表明,在60岁及以上的成年人中,接受医学治疗的RSV呼吸道感染(RTI)经常导致4.7%-7.8%的症状性RTI。RSV RTI的发病率随着年龄和潜在疾病的存在而增加。这一趋势在所有RSV临床结果中一致观察到。与其他生活环境的患者相比,住在长期护理机构或其他慢性护理机构的患者在入院时出现严重临床结果的可能性更高。大约10%的因呼吸道合胞病毒感染住院的老年人需要住进ICU。虽然数据有限,但住院患者的病死率(CFR)在5%至10%之间。一些证据表明,呼吸道合胞病毒负担可能接近老年人的流感负担。总的来说,加拿大住院数据的结果支持快速审查结果。与RSV相关的住院率、ICU住院率和死亡率均随着年龄的增长而增加,16%的住院导致ICU住院,住院CFR为9%。结论:在成人中,严重RSV结果的负担通常随着年龄和合并症的存在而增加。
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引用次数: 0
Surveillance of laboratory exposures to human pathogens and toxins, Canada, 2023. 人类病原体和毒素的实验室暴露监测,加拿大,2023年。
Pub Date : 2025-01-02 eCollection Date: 2025-01-01 DOI: 10.14745/ccdr.v51i01a03
Abdulwadud Nafees, Audrey Gauthier, Antoinette N Davis, Emily F Tran, Christine Abalos, Christa M Girincuti, Samuel Bonti-Ankomah

Background: The Public Health Agency of Canada oversees the Human Pathogens and Toxins Act and Human Pathogens and Toxins Regulations, and monitors human pathogen and toxin incidents in licensed facilities to minimize exposure impact at the individual and population level.

Objective: To provide an overview of confirmed laboratory exposure incidents in Canada in 2023.

Methods: Confirmed exposure incident reports in 2023 were analyzed using R 4.2.2, Microsoft Excel and SAS.

Results: In 2023, 207 incident reports were received, including 63 confirmed exposure incidents that affected 85 individuals. The academic sector accounted for 50.8% (n=32) of the reported confirmed exposure incidents. Microbiology (n=33; 52.4%) was the predominant activity being performed, with the most common occurrence types being sharps-related (n=22; 27.2%) and procedure-related (n=16; 19.8%). Human interaction (n=36; 57.1%) and standard operating procedures (n=24; 38.1%) were the most frequent root causes cited, with corrective actions often directly addressing these causes. Most of the 85 affected individuals were technicians/technologists (n=55; 64.7%) and had a median of 11 years of laboratory experience. Sixty-seven human pathogens and toxins (HPTs) were implicated in the confirmed exposure incidents, with bacteria (n=36; 53.7%) being the most common biological agent type. The median time between the incident and the reporting date was six days.

Conclusion: The number of confirmed exposure incidents increased in 2023 compared to 2022. Microbiology was most often the activity being performed at the time of exposure, and occurrence-types, root causes and HPTs implicated in 2023 mirrored those cited in 2022.

背景:加拿大公共卫生署负责监督《人类病原体和毒素法》和《人类病原体和毒素条例》,并监测许可设施中的人类病原体和毒素事件,以尽量减少个人和人群一级的接触影响。目的:提供2023年加拿大实验室暴露事件的概况。方法:采用r4.2.2软件、Microsoft Excel软件和SAS软件对2023年确诊的暴露事件报告进行分析。结果:2023年,共收到207起事件报告,其中63起确诊暴露事件,影响85人。在报告确认的暴露事件中,学术部门占50.8% (n=32)。微生物学(n = 33;52.4%)为主要活动,最常见的发生类型为尖锐相关(n=22;27.2%)和手术相关(n=16;19.8%)。人际互动(n=36;57.1%)和标准操作程序(n=24;38.1%)是最常见的根本原因,纠正措施通常直接解决这些原因。85名受影响的个人中,大多数是技术人员/技术人员(n=55;64.7%),平均有11年的实验室经验。67种人类病原体和毒素(HPTs)与确认的暴露事件有关,其中细菌(n=36;53.7%)是最常见的生物制剂类型。从事件发生到报告日期的中间时间是6天。结论:与2022年相比,2023年确诊暴露事件数量有所增加。微生物学是暴露时最常见的活动,2023年涉及的发生类型、根本原因和HPTs与2022年引用的相同。
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引用次数: 0
Summary of the National Advisory Committee on Immunization (NACI) Statement-Updated guidance on Imvamune in the context of a routine immunization program. 国家免疫咨询委员会(NACI)声明摘要-在常规免疫规划背景下更新的免疫指南。
Pub Date : 2025-01-02 eCollection Date: 2025-01-01 DOI: 10.14745/ccdr.v51i01a01
Nicole Forbes, Josh Montroy, Marina I Salvadori, Kristin Klein

Background: Mpox is a viral illness related to smallpox. It can cause flu-like symptoms and a rash, and in severe cases, can lead to hospitalization or death. The Imvamune® vaccine offers protection against mpox. Consistent with global trends, mpox cases in Canada have been reported primarily among men who have sex with men (MSM), with sexual contact as the predominantly reported mode of transmission. While the incidence of mpox in Canada has significantly declined since the fall of 2022, mpox remains an important public health concern with the potential for future resurgence.

Methods: The National Advisory Committee on Immunization (NACI) reviewed available evidence on the clinical benefits and risks of Imvamune. This evidence included studies assessing the vaccine effectiveness estimates from real-world evidence, as well as pre- and post-market licensure safety data. NACI has also considered additional factors including ethics, equity, feasibility and acceptability. Guidance on the use of Imvamune in the context of international travel was developed in collaboration with the Canadian Committee to Advise on Tropical Medicine and Travel (CATMAT).

Results: NACI concluded that available evidence supported the vaccine's effectiveness and safety in preventing mpox infection.

Conclusion: Building on previous interim guidance from NACI recommending the use of Imvamune for pre-exposure vaccination in the context of ongoing mpox outbreaks, NACI now recommends that Imvamune be used in the context of a focused routine immunization program. Individuals at high risk of mpox, including MSM who meet high-risk criteria such as having more than one sexual partner, should receive two doses of Imvamune administered by subcutaneous injection at least 28 days apart.

背景:Mpox是一种与天花相关的病毒性疾病。它会引起类似流感的症状和皮疹,在严重的情况下,可能导致住院或死亡。Imvamune®疫苗提供预防m痘的保护。与全球趋势一致,加拿大报告的麻疹病例主要发生在男男性行为者(MSM)中,性接触是报告的主要传播方式。虽然自2022年秋季以来,加拿大的m痘发病率已显著下降,但m痘仍然是一个重要的公共卫生问题,未来可能再次出现。方法:国家免疫咨询委员会(National Advisory Committee on Immunization, NACI)审查了现有的关于免疫接种的临床获益和风险的证据。这些证据包括根据真实证据评估疫苗有效性估计的研究,以及上市前和上市后许可安全性数据。NACI还考虑了其他因素,包括道德、公平、可行性和可接受性。关于在国际旅行中使用Imvamune的指南是与加拿大热带医学和旅行咨询委员会(CATMAT)合作制定的。结果:NACI得出结论,现有证据支持疫苗在预防m痘感染方面的有效性和安全性。结论:在国家免疫联盟先前建议在持续的m痘暴发背景下使用Imvamune进行暴露前疫苗接种的临时指导的基础上,国家免疫联盟现在建议在重点常规免疫规划的背景下使用Imvamune。m痘高危人群,包括符合高危标准(如有不止一个性伴侣)的男男性行为者,应至少间隔28天皮下注射两剂免疫疫苗。
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引用次数: 0
Is there sufficient evidence to inform personal protective equipment choices for healthcare workers caring for patients with viral hemorrhagic fevers? 是否有足够的证据提示照顾病毒性出血热患者的卫生保健工作者选择个人防护装备?
Pub Date : 2025-01-02 eCollection Date: 2025-01-01 DOI: 10.14745/ccdr.v51i01a02
Amanda Graham, Steven Ettles, Maureen McGrath, Toju Ogunremi, Jennifer Selkirk, Natalie Bruce

Background: Ugandan health authorities declared an outbreak of Ebola disease (EBOD), caused by the Sudan virus, in September 2022. A rapid review was conducted to update the Public Health Agency of Canada's guidelines for infection prevention and control measures for EBOD in healthcare settings to prepare for potential introduction of cases.

Objective: Summarize the available evidence on personal protective equipment (PPE) use by healthcare workers (HCWs) to prevent exposure to and transmission of viral hemorrhagic fevers (VHFs), including Ebola virus.

Methods: Electronic databases were searched to identify peer-reviewed evidence published from July 2014-October 2022. Peer-reviewed primary studies and literature reviews, in English or French, reporting on PPE for VHFs and filoviruses in the healthcare context were eligible for inclusion. Literature review processes were conducted by two reviewers using DistillerSR® systematic review software and the Public Health Agency of Canada's Infection Prevention and Control Critical Appraisal Toolkit. An environmental scan of grey literature was also conducted to inform the rapid review.

Results: The database search yielded 417 citations and 29 studies were considered eligible for critical appraisal. In total, 20 studies were included in the narrative synthesis of evidence. The evidence base was limited regarding comparative effectiveness of types of PPE for preventing exposure to and transmission of VHFs to HCWs. Four studies reported on exposure to and transmission of a VHF. Sixteen studies provided data on other relevant topics, such as simulated contamination and lab-based tests of PPE integrity.

Conclusion: There is limited evidence with which to draw conclusions on the comparative effectiveness of PPE to prevent exposure to and transmission of VHFs to HCWs. Additional research is required to determine the optimal PPE to protect HCWs from exposure to and transmission of VHFs.

背景:乌干达卫生当局于2022年9月宣布发生由苏丹病毒引起的埃博拉疫情。进行了一次快速审查,以更新加拿大公共卫生署关于卫生保健环境中EBOD感染预防和控制措施的指南,为可能出现的病例做好准备。目的:总结卫生保健工作者(HCWs)使用个人防护装备(PPE)预防包括埃博拉病毒在内的病毒性出血热(vhf)暴露和传播的现有证据。方法:检索电子数据库,检索2014年7月至2022年10月发表的同行评议证据。报告卫生保健环境中vhf和丝状病毒防护措施的英文或法文同行评议的初步研究和文献综述符合纳入条件。文献综述过程由两名审稿人使用DistillerSR®系统评价软件和加拿大公共卫生署感染预防和控制关键评价工具包进行。还对灰色文献进行了环境扫描,以便为快速审查提供信息。结果:数据库检索产生了417条引用,29项研究被认为有资格进行关键评价。总共有20项研究被纳入证据的叙述性综合。关于不同类型的个人防护用品在防止接触甚高频和将甚高频传播给卫生工作者方面的相对有效性,证据基础有限。四项研究报告了甚高频的接触和传播。16项研究提供了其他相关主题的数据,例如模拟污染和基于实验室的个人防护装备完整性测试。结论:关于个人防护装备在防止接触甚高频病毒并将其传播给卫生工作者方面的相对有效性,目前尚无证据可据此得出结论。需要进一步研究以确定保护卫生工作者免受甚高频接触和传播的最佳个人防护装备。
{"title":"Is there sufficient evidence to inform personal protective equipment choices for healthcare workers caring for patients with viral hemorrhagic fevers?","authors":"Amanda Graham, Steven Ettles, Maureen McGrath, Toju Ogunremi, Jennifer Selkirk, Natalie Bruce","doi":"10.14745/ccdr.v51i01a02","DOIUrl":"https://doi.org/10.14745/ccdr.v51i01a02","url":null,"abstract":"<p><strong>Background: </strong>Ugandan health authorities declared an outbreak of Ebola disease (EBOD), caused by the Sudan virus, in September 2022. A rapid review was conducted to update the Public Health Agency of Canada's guidelines for infection prevention and control measures for EBOD in healthcare settings to prepare for potential introduction of cases.</p><p><strong>Objective: </strong>Summarize the available evidence on personal protective equipment (PPE) use by healthcare workers (HCWs) to prevent exposure to and transmission of viral hemorrhagic fevers (VHFs), including Ebola virus.</p><p><strong>Methods: </strong>Electronic databases were searched to identify peer-reviewed evidence published from July 2014-October 2022. Peer-reviewed primary studies and literature reviews, in English or French, reporting on PPE for VHFs and filoviruses in the healthcare context were eligible for inclusion. Literature review processes were conducted by two reviewers using DistillerSR® systematic review software and the Public Health Agency of Canada's Infection Prevention and Control Critical Appraisal Toolkit. An environmental scan of grey literature was also conducted to inform the rapid review.</p><p><strong>Results: </strong>The database search yielded 417 citations and 29 studies were considered eligible for critical appraisal. In total, 20 studies were included in the narrative synthesis of evidence. The evidence base was limited regarding comparative effectiveness of types of PPE for preventing exposure to and transmission of VHFs to HCWs. Four studies reported on exposure to and transmission of a VHF. Sixteen studies provided data on other relevant topics, such as simulated contamination and lab-based tests of PPE integrity.</p><p><strong>Conclusion: </strong>There is limited evidence with which to draw conclusions on the comparative effectiveness of PPE to prevent exposure to and transmission of VHFs to HCWs. Additional research is required to determine the optimal PPE to protect HCWs from exposure to and transmission of VHFs.</p>","PeriodicalId":94304,"journal":{"name":"Canada communicable disease report = Releve des maladies transmissibles au Canada","volume":"51 1","pages":"7-15"},"PeriodicalIF":0.0,"publicationDate":"2025-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11706576/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142960949","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The prevalence of HIV pre-exposure prophylaxis (HIV-PrEP) use and HIV-PrEP-to-need ratio in nine Canadian provinces, 2018-2021. 2018-2021年加拿大9省艾滋病毒暴露前预防(HIV- prep)使用率和HIV- prep需求比
Pub Date : 2025-01-02 eCollection Date: 2025-01-01 DOI: 10.14745/ccdr.v51i01a05
Nashira Popovic, Qiuying Yang, Laurence Campeau, Janelle Elliott, Anson Williams, Viviane D Lima, Paul Sereda, Joseph Cox

Background: Measuring trends in HIV pre-exposure prophylaxis (HIV-PrEP) uptake is important to inform planning for prevention programs and policies. The HIV-PrEP-to-need ratio (PnR) is a construct used by public health organizations to explore disparities in the provision of HIV-PrEP across geographic areas and demographic categories (e.g., age, sex).

Methods: This is a retrospective database review study using administrative pharmacy data, containing limited demographic information, from nine Canadian provinces. Annual estimates of persons taking HIV-PrEP and PnR were generated using data from the company IQVIA and the BC Centre for Excellence on HIV/AIDS. Data on new HIV diagnoses were obtained from the National HIV Surveillance System. The PnR was defined as the number of HIV-PrEP users divided by the number of new HIV diagnoses annually and is interpreted as the number of HIV-negative people using HIV-PrEP each year for every person newly diagnosed with HIV.

Results: In 2021, an estimated 23,644 individuals were prescribed HIV-PrEP, corresponding to an HIV-PrEP prevalence of 66.9 per 100,000 persons. This represents a 1.8-fold increase since 2018. The overall PnR was 16.8, meaning that for every person newly diagnosed with HIV, 17 HIV-negative individuals were taking HIV-PrEP. There were disparities between provinces (PnR range: 1.5/100,000-37.7/100,000) and between males and females (PnR 22.6 and 1.2, respectively). Females, individuals aged 0-19 years, and those in Manitoba, Saskatchewan and Prince Edward Island, had lower levels of HIV-PrEP use relative to epidemic need.

Conclusion: In Canada, the use of HIV-PrEP increased from 2018 to 2021 and uptake varied by age, sex and province. HIV-PrEP-to-need ratio is a useful measure to assess uptake of HIV-PrEP as a prevention strategy and could be used to explore disparities in provision across provinces and available demographic categories. However, PnR could be improved with more information on key populations and other attributes, such as race/ethnicity, socioeconomic status and residence of city/rural area.

背景:测量艾滋病毒暴露前预防(HIV- prep)使用趋势对制定预防方案和政策具有重要意义。艾滋病毒预防与需求比率(PnR)是公共卫生组织用来探索不同地理区域和人口类别(如年龄、性别)提供艾滋病毒预防方面的差异的一种结构。方法:这是一项回顾性数据库回顾研究,使用来自加拿大九个省的行政药房数据,包含有限的人口统计信息。利用IQVIA公司和不列颠哥伦比亚省艾滋病毒/艾滋病卓越中心的数据,对服用艾滋病毒prep和PnR的人进行了年度估计。新的艾滋病毒诊断数据来自国家艾滋病毒监测系统。PnR被定义为HIV- prep使用者的数量除以每年新诊断的HIV病毒的数量,并被解释为每年使用HIV- prep的HIV阴性患者的数量与每一个新诊断的HIV病毒感染者的数量。结果:2021年,估计有23,644人接受了HIV-PrEP处方,相当于每10万人中有66.9人感染HIV-PrEP。这是自2018年以来的1.8倍。总体PnR为16.8,这意味着每有一个新诊断为艾滋病毒的人,就有17个艾滋病毒阴性的人正在接受艾滋病毒预防。省际间(PnR为1.5/10万~ 37.7/10万)和男女间(PnR分别为22.6和1.2)存在差异。年龄在0-19岁之间的女性,以及马尼托巴省、萨斯喀彻温省和爱德华王子岛的女性,与流行病的需要相比,使用HIV-PrEP的水平较低。结论:在加拿大,从2018年到2021年,HIV-PrEP的使用有所增加,且使用情况因年龄、性别和省份而异。HIV-PrEP与需求的比率是评估将HIV-PrEP作为一项预防战略的采用情况的有用措施,可用于探索各省和现有人口类别之间提供的差异。然而,PnR可以通过更多关于关键人口和其他属性的信息来改进,例如种族/民族、社会经济地位和城市/农村地区的居住地。
{"title":"The prevalence of HIV pre-exposure prophylaxis (HIV-PrEP) use and HIV-PrEP-to-need ratio in nine Canadian provinces, 2018-2021.","authors":"Nashira Popovic, Qiuying Yang, Laurence Campeau, Janelle Elliott, Anson Williams, Viviane D Lima, Paul Sereda, Joseph Cox","doi":"10.14745/ccdr.v51i01a05","DOIUrl":"https://doi.org/10.14745/ccdr.v51i01a05","url":null,"abstract":"<p><strong>Background: </strong>Measuring trends in HIV pre-exposure prophylaxis (HIV-PrEP) uptake is important to inform planning for prevention programs and policies. The HIV-PrEP-to-need ratio (PnR) is a construct used by public health organizations to explore disparities in the provision of HIV-PrEP across geographic areas and demographic categories (e.g., age, sex).</p><p><strong>Methods: </strong>This is a retrospective database review study using administrative pharmacy data, containing limited demographic information, from nine Canadian provinces. Annual estimates of persons taking HIV-PrEP and PnR were generated using data from the company IQVIA and the BC Centre for Excellence on HIV/AIDS. Data on new HIV diagnoses were obtained from the National HIV Surveillance System. The PnR was defined as the number of HIV-PrEP users divided by the number of new HIV diagnoses annually and is interpreted as the number of HIV-negative people using HIV-PrEP each year for every person newly diagnosed with HIV.</p><p><strong>Results: </strong>In 2021, an estimated 23,644 individuals were prescribed HIV-PrEP, corresponding to an HIV-PrEP prevalence of 66.9 per 100,000 persons. This represents a 1.8-fold increase since 2018. The overall PnR was 16.8, meaning that for every person newly diagnosed with HIV, 17 HIV-negative individuals were taking HIV-PrEP. There were disparities between provinces (PnR range: 1.5/100,000-37.7/100,000) and between males and females (PnR 22.6 and 1.2, respectively). Females, individuals aged 0-19 years, and those in Manitoba, Saskatchewan and Prince Edward Island, had lower levels of HIV-PrEP use relative to epidemic need.</p><p><strong>Conclusion: </strong>In Canada, the use of HIV-PrEP increased from 2018 to 2021 and uptake varied by age, sex and province. HIV-PrEP-to-need ratio is a useful measure to assess uptake of HIV-PrEP as a prevention strategy and could be used to explore disparities in provision across provinces and available demographic categories. However, PnR could be improved with more information on key populations and other attributes, such as race/ethnicity, socioeconomic status and residence of city/rural area.</p>","PeriodicalId":94304,"journal":{"name":"Canada communicable disease report = Releve des maladies transmissibles au Canada","volume":"51 1","pages":"35-42"},"PeriodicalIF":0.0,"publicationDate":"2025-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11709143/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142961003","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Using behavioural science to improve antibiotic stewardship in Canadian long-term care homes: Protocol for a multi-center cluster randomized quality improvement study. 使用行为科学改善加拿大长期护理院的抗生素管理:一项多中心集群随机质量改进研究的协议。
Pub Date : 2025-01-02 eCollection Date: 2025-01-01 DOI: 10.14745/ccdr.v51i01a06
Tyler Good, Jorida Cila, Rhiannon Mosher, Klajdi Puka, Shaghig Reynolds, Barbara Catt, Aboubakar Mounchili, Denise Gravel-Tropper, Patrick Quail, Allison McGeer, Andrea Moser, Madeleine Ashcroft, Peter Daley, Katrina Piggott, Jerome Leis, Mark Morrissey

Background: Antimicrobial resistance (AMR) is associated with significant human and financial costs, particularly among vulnerable populations like older adults living in long-term care homes (LTCHs). Urinary tract infection (UTI) is the leading indication for antibiotic use in this population, with some estimates suggesting that up to 70% of these prescriptions may be avoidable.

Objective: The purpose of this study is to develop and test novel behavioural science-informed antimicrobial stewardship (AMS) quality improvement strategies in Canadian LTCHs, which aim to decrease unnecessary testing and treatment for residents who lack the minimum clinical signs and symptoms of UTI.

Intervention: The quality improvement strategy is a two-pronged approach that includes 1) targeted education for essential care providers (family and friends of LTCH residents) about UTI and benefits of AMS, which strives to outline a positive role for this group in UTI management, and 2) monthly feedback to LTCH staff on their facility's urine culture ordering rates.

Outcomes: The protocol was piloted in a single LTCH; a process evaluation of the pilot implementation served to refine the research protocol, which is being implemented in eight LTCHs across Canada using an eight-month stepped wedge randomized cluster design.

Conclusion: This protocol represents a behavioural science-informed intervention to improve AMS across LTCHs. If successful, this model of care could be scalable across Canadian LTCHs, offering an inclusive approach that aims to empower clinicians, non-regulated healthcare staff, residents and their family and friends to improve health outcomes as antibiotic stewards.

背景:抗菌素耐药性(AMR)与巨大的人力和财务成本相关,特别是在弱势人群中,如生活在长期护理之家(LTCHs)的老年人中。尿路感染(UTI)是这一人群使用抗生素的主要指征,一些估计表明,多达70%的此类处方是可以避免的。目的:本研究的目的是在加拿大LTCHs中开发和测试新的基于行为科学的抗菌药物管理(AMS)质量改进策略,旨在减少对缺乏尿路感染最低临床体征和症状的居民不必要的检测和治疗。干预:质量改进策略是一个双管齐下的方法,包括1)对基本护理提供者(LTCH居民的家人和朋友)进行针对性的教育,了解尿路感染和AMS的好处,努力概述该群体在尿路感染管理中的积极作用;2)每月向LTCH工作人员反馈其设施的尿液培养定诊率。结果:该方案在单个LTCH中试点;试点实施的过程评估有助于完善研究方案,该方案正在加拿大的八个ltch中实施,采用八个月的阶梯楔形随机聚类设计。结论:该方案代表了一种行为科学知情的干预措施,以改善ltch的AMS。如果成功,这种护理模式可以在加拿大的LTCHs中推广,提供一种包容性的方法,旨在使临床医生、不受监管的医疗保健人员、居民及其家人和朋友能够作为抗生素管理员改善健康结果。
{"title":"Using behavioural science to improve antibiotic stewardship in Canadian long-term care homes: Protocol for a multi-center cluster randomized quality improvement study.","authors":"Tyler Good, Jorida Cila, Rhiannon Mosher, Klajdi Puka, Shaghig Reynolds, Barbara Catt, Aboubakar Mounchili, Denise Gravel-Tropper, Patrick Quail, Allison McGeer, Andrea Moser, Madeleine Ashcroft, Peter Daley, Katrina Piggott, Jerome Leis, Mark Morrissey","doi":"10.14745/ccdr.v51i01a06","DOIUrl":"https://doi.org/10.14745/ccdr.v51i01a06","url":null,"abstract":"<p><strong>Background: </strong>Antimicrobial resistance (AMR) is associated with significant human and financial costs, particularly among vulnerable populations like older adults living in long-term care homes (LTCHs). Urinary tract infection (UTI) is the leading indication for antibiotic use in this population, with some estimates suggesting that up to 70% of these prescriptions may be avoidable.</p><p><strong>Objective: </strong>The purpose of this study is to develop and test novel behavioural science-informed antimicrobial stewardship (AMS) quality improvement strategies in Canadian LTCHs, which aim to decrease unnecessary testing and treatment for residents who lack the minimum clinical signs and symptoms of UTI.</p><p><strong>Intervention: </strong>The quality improvement strategy is a two-pronged approach that includes 1) targeted education for essential care providers (family and friends of LTCH residents) about UTI and benefits of AMS, which strives to outline a positive role for this group in UTI management, and 2) monthly feedback to LTCH staff on their facility's urine culture ordering rates.</p><p><strong>Outcomes: </strong>The protocol was piloted in a single LTCH; a process evaluation of the pilot implementation served to refine the research protocol, which is being implemented in eight LTCHs across Canada using an eight-month stepped wedge randomized cluster design.</p><p><strong>Conclusion: </strong>This protocol represents a behavioural science-informed intervention to improve AMS across LTCHs. If successful, this model of care could be scalable across Canadian LTCHs, offering an inclusive approach that aims to empower clinicians, non-regulated healthcare staff, residents and their family and friends to improve health outcomes as antibiotic stewards.</p>","PeriodicalId":94304,"journal":{"name":"Canada communicable disease report = Releve des maladies transmissibles au Canada","volume":"51 1","pages":"43-53"},"PeriodicalIF":0.0,"publicationDate":"2025-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11709424/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142961006","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Popularity of HIV self-tests may say more about the state of our primary care system than about the device itself. 艾滋病毒自检的普及可能更多地说明了我们初级保健系统的状况,而不是设备本身。
Pub Date : 2024-12-05 eCollection Date: 2024-12-01 DOI: 10.14745/ccdr.v50i12da04
Alexandra Musten, Patrick O'Byrne

Background: In Canada, HIV transmission continues to disproportionately affect the same communities of gay men, bisexual men and men who have sex with men (gbMSM); members of African, Caribbean or Black communities (ACB); people who use injection drugs; Indigenous people; and women who belong to the aforementioned groups. While primary care is an ideal location for HIV testing for members of these groups, many people do not have access to such healthcare services. In response, we launched GetaKit to distribute HIV self-tests.

Methods: In light of reduced access to healthcare services as a result of the pandemic and in anticipation of Health Canada's approval of an HIV self-test, a clinician-scientist research team at the University of Ottawa developed GetaKit: an online platform to provide access to sexual health services. When GetaKit first launched in Ottawa in July 2020 with funding from the Ontario Ministry of Health, its objectives were to ensure that access to the newly approved device remained 1) clinically appropriate, 2) accessible and 3) linked to care.

Results: Over the course of the study, there were a stable number of individuals who reported having never been tested for HIV before. These individuals tended to be younger and more likely to be members of racialized minority groups; similar characteristics to those who also face the most barriers to primary care access.

Conclusion: With new reports indicating that nearly six million Canadians are without a primary care provider, it was proposed that the popularity of the HIV self-test may tell more about this lack of access than about the utility of the device itself. While projects like GetaKit should be part of the broader strategy to overcome historic testing barriers, such as geographic distance and inconvenient clinic hours, it is important that this occurs in an environment where a strong primary care health system can support treatment, follow-up and specialist referrals, as required.

背景:在加拿大,艾滋病毒传播继续不成比例地影响同一社区的男同性恋、双性恋和男男性行为者(gbMSM);非洲、加勒比或黑人社区成员;使用注射毒品的人;原住民;以及属于上述群体的女性。虽然初级保健是这些群体成员进行艾滋病毒检测的理想场所,但许多人无法获得此类卫生保健服务。作为回应,我们启动了GetaKit,分发艾滋病毒自检。方法:鉴于大流行导致获得保健服务的机会减少,并预期加拿大卫生部将批准艾滋病毒自我检测,渥太华大学的一个临床科学家研究小组开发了GetaKit:一个提供性健康服务的在线平台。2020年7月,在安大略省卫生部的资助下,GetaKit首次在渥太华推出时,其目标是确保获得新批准的设备保持1)临床适宜,2)可获得,3)与护理相关。结果:在研究过程中,有稳定数量的人报告说他们以前从未接受过艾滋病毒检测。这些人往往更年轻,更有可能是种族化的少数群体的成员;与那些在获得初级保健方面也面临最大障碍的人具有相似的特征。结论:新的报告表明,近600万加拿大人没有初级保健提供者,有人提出,艾滋病毒自检的普及可能更多地说明了这种缺乏途径,而不是设备本身的效用。虽然GetaKit等项目应成为更广泛战略的一部分,以克服地理距离和门诊时间不方便等历史检测障碍,但重要的是,这是在一个强大的初级保健卫生系统能够根据需要支持治疗、随访和专家转诊的环境中进行的。
{"title":"Popularity of HIV self-tests may say more about the state of our primary care system than about the device itself.","authors":"Alexandra Musten, Patrick O'Byrne","doi":"10.14745/ccdr.v50i12da04","DOIUrl":"10.14745/ccdr.v50i12da04","url":null,"abstract":"<p><strong>Background: </strong>In Canada, HIV transmission continues to disproportionately affect the same communities of gay men, bisexual men and men who have sex with men (gbMSM); members of African, Caribbean or Black communities (ACB); people who use injection drugs; Indigenous people; and women who belong to the aforementioned groups. While primary care is an ideal location for HIV testing for members of these groups, many people do not have access to such healthcare services. In response, we launched GetaKit to distribute HIV self-tests.</p><p><strong>Methods: </strong>In light of reduced access to healthcare services as a result of the pandemic and in anticipation of Health Canada's approval of an HIV self-test, a clinician-scientist research team at the University of Ottawa developed GetaKit: an online platform to provide access to sexual health services. When GetaKit first launched in Ottawa in July 2020 with funding from the Ontario Ministry of Health, its objectives were to ensure that access to the newly approved device remained 1) clinically appropriate, 2) accessible and 3) linked to care.</p><p><strong>Results: </strong>Over the course of the study, there were a stable number of individuals who reported having never been tested for HIV before. These individuals tended to be younger and more likely to be members of racialized minority groups; similar characteristics to those who also face the most barriers to primary care access.</p><p><strong>Conclusion: </strong>With new reports indicating that nearly six million Canadians are without a primary care provider, it was proposed that the popularity of the HIV self-test may tell more about this lack of access than about the utility of the device itself. While projects like GetaKit should be part of the broader strategy to overcome historic testing barriers, such as geographic distance and inconvenient clinic hours, it is important that this occurs in an environment where a strong primary care health system can support treatment, follow-up and specialist referrals, as required.</p>","PeriodicalId":94304,"journal":{"name":"Canada communicable disease report = Releve des maladies transmissibles au Canada","volume":"50 12","pages":"436-446"},"PeriodicalIF":0.0,"publicationDate":"2024-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11629877/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142815448","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mycobacterium tuberculosis pseudo-outbreak due to laboratory cross-contamination: A molecular epidemiology outbreak investigation. 实验室交叉污染引起的结核分枝杆菌伪暴发:一次分子流行病学暴发调查。
Pub Date : 2024-12-05 eCollection Date: 2024-12-01 DOI: 10.14745/ccdr.v50i12da03
Nayla Léveillé, Floriane Point, Josée Houde, Michael Hall, Hafid Souhaline, Marie-Andrée Leblanc, Pierre-Marie Akochy, Simon Grandjean Lapierre

Background: Mycobacterial culture is routinely performed to diagnose tuberculosis (TB) in Canada. Globally, meta-analyses suggest that up to 2% of positive cultures are falsely positive for Mycobacterium tuberculosis due to laboratory cross-contamination. Five patients from distinct clinical institutions in Montréal were diagnosed with culture-positive TB as their clinical samples were processed in a centralized mycobacteria laboratory. Cross-contamination was suspected due to culture positivity in an organ donor with low TB pre-test probability. We describe a TB pseudo-outbreak due to laboratory cross-contamination and assess the role of conventional typing (i.e., mycobacterial interspersed repetitive unit variable number of tandem repeats [MIRU-VNTR]) and whole-genome sequencing (WGS) in supporting the investigation.

Methods: Patients' epidemiological risk factors and clinical presentations were reviewed. The trajectories of pre- and per-analytic samples were retraced to identify potential cross-contamination events. Tuberculosis isolates were characterized by MIRU-VNTR and WGS using Oxford Nanopore Technology (ONT). The bioinformatic pipeline tbpore (v0.7.1) cluster was used for phylogenetic analyses.

Results: Two patients had previous exposure to endemic settings and clinical symptoms compatible with TB. Culture media inoculation overlapped in time for four patients, including one with suspected pulmonary cavitary disease and an organ donor whose organs had been transplanted in three different receivers. The MIRU-VNTR and WGS typing confirmed isolates from those four patients to be identical.

Conclusion: Clinical, laboratory and molecular typing data, including results from ONT sequencing, were considered sufficiently robust to confirm laboratory cross-contamination and TB therapy was discontinued including in all organ transplant recipients.

背景:在加拿大,分枝杆菌培养是诊断结核病的常规方法。在全球范围内,荟萃分析表明,由于实验室交叉污染,高达2%的阳性培养物为结核分枝杆菌假阳性。在集中的分枝杆菌实验室处理临床样本时,来自montracimal不同临床机构的5名患者被诊断为培养阳性结核。由于一名器官供体培养阳性,且结核病检测前概率低,因此怀疑存在交叉污染。我们描述了一起由实验室交叉污染引起的结核病伪暴发,并评估了传统分型(即分枝杆菌穿插重复单位可变数目串联重复序列[MIRU-VNTR])和全基因组测序(WGS)在支持调查中的作用。方法:回顾性分析患者的流行病学危险因素及临床表现。分析前和分析后样品的轨迹被追溯,以确定潜在的交叉污染事件。采用牛津纳米孔技术(ONT)对结核分离株进行MIRU-VNTR和WGS鉴定。采用生物信息学管道tbpore (v0.7.1)聚类进行系统发育分析。结果:两名患者曾接触过地方性环境,临床症状与结核病相符。四名患者的培养基接种时间重叠,包括一名疑似肺腔疾病患者和一名器官捐赠者,他的器官被移植给了三个不同的接受者。MIRU-VNTR和WGS分型证实这4例患者的分离株是相同的。结论:临床、实验室和分子分型数据,包括ONT测序结果,被认为足够可靠,可以确认实验室交叉污染,并停止结核病治疗,包括所有器官移植受者。
{"title":"<i>Mycobacterium tuberculosis</i> pseudo-outbreak due to laboratory cross-contamination: A molecular epidemiology outbreak investigation.","authors":"Nayla Léveillé, Floriane Point, Josée Houde, Michael Hall, Hafid Souhaline, Marie-Andrée Leblanc, Pierre-Marie Akochy, Simon Grandjean Lapierre","doi":"10.14745/ccdr.v50i12da03","DOIUrl":"10.14745/ccdr.v50i12da03","url":null,"abstract":"<p><strong>Background: </strong>Mycobacterial culture is routinely performed to diagnose tuberculosis (TB) in Canada. Globally, meta-analyses suggest that up to 2% of positive cultures are falsely positive for <i>Mycobacterium tuberculosis</i> due to laboratory cross-contamination. Five patients from distinct clinical institutions in Montréal were diagnosed with culture-positive TB as their clinical samples were processed in a centralized mycobacteria laboratory. Cross-contamination was suspected due to culture positivity in an organ donor with low TB pre-test probability. We describe a TB pseudo-outbreak due to laboratory cross-contamination and assess the role of conventional typing (i.e., mycobacterial interspersed repetitive unit variable number of tandem repeats [MIRU-VNTR]) and whole-genome sequencing (WGS) in supporting the investigation.</p><p><strong>Methods: </strong>Patients' epidemiological risk factors and clinical presentations were reviewed. The trajectories of pre- and per-analytic samples were retraced to identify potential cross-contamination events. Tuberculosis isolates were characterized by MIRU-VNTR and WGS using Oxford Nanopore Technology (ONT). The bioinformatic pipeline tbpore (v0.7.1) cluster was used for phylogenetic analyses.</p><p><strong>Results: </strong>Two patients had previous exposure to endemic settings and clinical symptoms compatible with TB. Culture media inoculation overlapped in time for four patients, including one with suspected pulmonary cavitary disease and an organ donor whose organs had been transplanted in three different receivers. The MIRU-VNTR and WGS typing confirmed isolates from those four patients to be identical.</p><p><strong>Conclusion: </strong>Clinical, laboratory and molecular typing data, including results from ONT sequencing, were considered sufficiently robust to confirm laboratory cross-contamination and TB therapy was discontinued including in all organ transplant recipients.</p>","PeriodicalId":94304,"journal":{"name":"Canada communicable disease report = Releve des maladies transmissibles au Canada","volume":"50 12","pages":"430-435"},"PeriodicalIF":0.0,"publicationDate":"2024-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11629878/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142815446","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Summary of the National Advisory Committee on Immunization (NACI) Statement: Updated guidance on human papillomavirus (HPV) vaccines. 国家免疫咨询委员会(NACI)声明摘要:关于人乳头瘤病毒(HPV)疫苗的最新指南。
Pub Date : 2024-12-05 eCollection Date: 2024-12-01 DOI: 10.14745/ccdr.v50i12da01
Nicole Forbes, Josh Montroy, Marina I Salvadori, Vinita Dubey

Background: Without vaccination, approximately 75% of people in Canada will acquire a human papillomavirus (HPV) infection in their lifetime. HPV vaccine coverage rates continue to fall short of the national goal of 90% coverage for two or more doses by 17 years of age. Recent evidence and World Health Organization (WHO) guidance now support a 1- or 2-dose schedule for younger age groups, which can simplify vaccination efforts and improve coverage rates compared to a multi-dose immunization program.

Methods: The National Advisory Committee on Immunization (NACI) reviewed available evidence on the clinical benefits and risks of a 1-dose HPV vaccine schedule, as well as additional factors, including ethics, equity, feasibility and acceptability. The evidence and programmatic considerations were organized using a process informed by the Grading of Recommendations Assessment, Development and Evaluations (GRADE) framework and all of the information was used to facilitate NACI guidance development.

Results: A 1-dose schedule is highly effective against HPV infection based on available evidence in younger female populations, with current follow-up of up to 11 years following vaccination. Infectious disease modelling shows that a 1-dose strategy in males and females in Canada is expected to have similar health outcomes over the short and long term compared to two doses.

Conclusion: NACI updated recommendations for individuals 9 to 20 years of age to receive one dose of 9vHPV (Gardasil-9, Merck) vaccine. For individuals 21 years of age and older, a 2-dose schedule should be administered. Individuals considered immunocompromised and individuals infected with HIV should receive a 3-dose series. NACI also issued a discretionary recommendation for HPV vaccination for individuals 27 years and older, and updated guidance to allow HPV vaccine during pregnancy.

背景:如果不接种疫苗,加拿大大约75%的人一生中会感染人乳头瘤病毒(HPV)。人乳头瘤病毒疫苗接种率继续低于国家目标,即到17岁时接种两剂或两剂以上疫苗的接种率达到90%。最近的证据和世界卫生组织(世卫组织)指南现在支持针对较年轻年龄组的1剂或2剂计划,与多剂免疫规划相比,这可以简化疫苗接种工作并提高覆盖率。方法:国家免疫咨询委员会(NACI)审查了1剂HPV疫苗接种计划的临床获益和风险的现有证据,以及其他因素,包括伦理、公平性、可行性和可接受性。证据和方案考虑是通过建议分级评估、发展和评估(GRADE)框架来组织的,所有信息都用于促进NACI指南的制定。结果:根据现有证据,接种1剂疫苗对年轻女性人群的HPV感染非常有效,目前接种后随访时间长达11年。传染病模型表明,与两次剂量相比,加拿大男性和女性的一次剂量战略预计在短期和长期内产生类似的健康结果。结论:NACI更新了9至20岁个体接种一剂9vHPV (Gardasil-9,默克)疫苗的建议。对于21岁及以上的个体,应按2次剂量服用。被认为免疫功能低下和感染艾滋病毒的个体应接受3剂系列疫苗。NACI还发布了针对27岁及以上个体接种HPV疫苗的酌情建议,并更新了允许在怀孕期间接种HPV疫苗的指南。
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引用次数: 0
Popularity of HIV self-tests may say more about the state of our primary care system than about the device itself. 艾滋病毒自检的普及可能更多地说明了我们初级保健系统的状况,而不是设备本身。
Pub Date : 2024-12-05 eCollection Date: 2024-12-01 DOI: 10.14745/ccdr.v50i12da02
Alexandra Musten, Patrick O'Byrne

Background: In Canada, HIV transmission continues to disproportionately affect the same communities of gay men, bisexual men and men who have sex with men (gbMSM); members of African, Caribbean or Black communities (ACB); people who use injection drugs; Indigenous people; and women who belong to the aforementioned groups. While primary care is an ideal location for HIV testing for members of these groups, many people do not have access to such healthcare services. In response, we launched GetaKit to distribute HIV self-tests.

Methods: In light of reduced access to healthcare services as a result of the pandemic and in anticipation of Health Canada's approval of an HIV self-test, a clinician-scientist research team at the University of Ottawa developed GetaKit: an online platform to provide access to sexual health services. When GetaKit first launched in Ottawa in July 2020 with funding from the Ontario Ministry of Health, its objectives were to ensure that access to the newly approved device remained 1) clinically appropriate, 2) accessible and 3) linked to care.

Results: Over the course of the study, there were a stable number of individuals who reported having never been tested for HIV before. These individuals tended to be younger and more likely to be members of racialized minority groups; similar characteristics to those who also face the most barriers to primary care access.

Conclusion: With new reports indicating that nearly six million Canadians are without a primary care provider, it was proposed that the popularity of the HIV self-test may tell more about this lack of access than about the utility of the device itself. While projects like GetaKit should be part of the broader strategy to overcome historic testing barriers, such as geographic distance and inconvenient clinic hours, it is important that this occurs in an environment where a strong primary care health system can support treatment, follow-up and specialist referrals, as required.

背景:在加拿大,艾滋病毒传播继续不成比例地影响同一社区的男同性恋、双性恋和男男性行为者(gbMSM);非洲、加勒比或黑人社区成员;使用注射毒品的人;原住民;以及属于上述群体的女性。虽然初级保健是这些群体成员进行艾滋病毒检测的理想场所,但许多人无法获得此类卫生保健服务。作为回应,我们启动了GetaKit,分发艾滋病毒自检。方法:鉴于大流行导致获得保健服务的机会减少,并预期加拿大卫生部将批准艾滋病毒自我检测,渥太华大学的一个临床科学家研究小组开发了GetaKit:一个提供性健康服务的在线平台。2020年7月,在安大略省卫生部的资助下,GetaKit首次在渥太华推出时,其目标是确保获得新批准的设备保持1)临床适宜,2)可获得,3)与护理相关。结果:在研究过程中,有稳定数量的人报告说他们以前从未接受过艾滋病毒检测。这些人往往更年轻,更有可能是种族化的少数群体的成员;与那些在获得初级保健方面也面临最大障碍的人具有相似的特征。结论:新的报告表明,近600万加拿大人没有初级保健提供者,有人提出,艾滋病毒自检的普及可能更多地说明了这种缺乏途径,而不是设备本身的效用。虽然GetaKit等项目应成为更广泛战略的一部分,以克服地理距离和门诊时间不方便等历史检测障碍,但重要的是,这是在一个强大的初级保健卫生系统能够根据需要支持治疗、随访和专家转诊的环境中进行的。
{"title":"Popularity of HIV self-tests may say more about the state of our primary care system than about the device itself.","authors":"Alexandra Musten, Patrick O'Byrne","doi":"10.14745/ccdr.v50i12da02","DOIUrl":"10.14745/ccdr.v50i12da02","url":null,"abstract":"<p><strong>Background: </strong>In Canada, HIV transmission continues to disproportionately affect the same communities of gay men, bisexual men and men who have sex with men (gbMSM); members of African, Caribbean or Black communities (ACB); people who use injection drugs; Indigenous people; and women who belong to the aforementioned groups. While primary care is an ideal location for HIV testing for members of these groups, many people do not have access to such healthcare services. In response, we launched GetaKit to distribute HIV self-tests.</p><p><strong>Methods: </strong>In light of reduced access to healthcare services as a result of the pandemic and in anticipation of Health Canada's approval of an HIV self-test, a clinician-scientist research team at the University of Ottawa developed GetaKit: an online platform to provide access to sexual health services. When GetaKit first launched in Ottawa in July 2020 with funding from the Ontario Ministry of Health, its objectives were to ensure that access to the newly approved device remained 1) clinically appropriate, 2) accessible and 3) linked to care.</p><p><strong>Results: </strong>Over the course of the study, there were a stable number of individuals who reported having never been tested for HIV before. These individuals tended to be younger and more likely to be members of racialized minority groups; similar characteristics to those who also face the most barriers to primary care access.</p><p><strong>Conclusion: </strong>With new reports indicating that nearly six million Canadians are without a primary care provider, it was proposed that the popularity of the HIV self-test may tell more about this lack of access than about the utility of the device itself. While projects like GetaKit should be part of the broader strategy to overcome historic testing barriers, such as geographic distance and inconvenient clinic hours, it is important that this occurs in an environment where a strong primary care health system can support treatment, follow-up and specialist referrals, as required.</p>","PeriodicalId":94304,"journal":{"name":"Canada communicable disease report = Releve des maladies transmissibles au Canada","volume":"50 12","pages":"426-429"},"PeriodicalIF":0.0,"publicationDate":"2024-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11629879/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142815447","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Canada communicable disease report = Releve des maladies transmissibles au Canada
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