首页 > 最新文献

Canada communicable disease report = Releve des maladies transmissibles au Canada最新文献

英文 中文
Differences in sensationalism in international news media reporting of COVID-19: An exploratory analysis using the Global Public Health Intelligence Network (GPHIN) system.
Pub Date : 2025-02-12 eCollection Date: 2025-02-01 DOI: 10.14745/ccdr.v51i23a05
Joanna Przepiorkowski, Tenzin Norzin, Abdelhamid Zaghlool, Florence Tanguay, Dorcas Taylor, Victor Gallant, Linlu Zhao

Background: The Global Public Health Intelligence Network (GPHIN) is an event-based surveillance platform that collects thousands of pieces of open-source information, including international news media, across multiple languages on a daily basis. Analysts have observed that news media reporting in some languages tended to use more sensational wording to describe major health events. There has been minimal research exploring potential differences in sensationalism in international news media reporting to confirm these observations.

Objective: This exploratory study assessed the differences in the level of sensationalism in early international news media reporting of COVID-19 through a mixed-methods analysis.

Methods: Relevant news media articles received in GPHIN seven days following the Public Health Emergency of International Concern declaration of COVID-19 by the World Health Organization were extracted for screening and analysis. An adapted tool was used to measure the sensationalism of pandemic-related health news. Deductive thematic analysis was conducted to examine themes of sensationalism. Differences in prevalence of sensationalism in news media reporting by language and country/territory of publication were assessed. Sentiment analysis assessed the sentiment and emotional tone of the news media articles.

Results: Of 951 news articles that met the eligibility criteria, 155 contained sensationalism. There were significant differences between languages (French, Russian and Spanish) and various domains of sensationalism. This study also found a more negative emotional tone in news media articles with sensationalism.

Conclusion: This exploratory study showed that language has the potential to impact the perception of health events using more sensationalized language.

{"title":"Differences in sensationalism in international news media reporting of COVID-19: An exploratory analysis using the Global Public Health Intelligence Network (GPHIN) system.","authors":"Joanna Przepiorkowski, Tenzin Norzin, Abdelhamid Zaghlool, Florence Tanguay, Dorcas Taylor, Victor Gallant, Linlu Zhao","doi":"10.14745/ccdr.v51i23a05","DOIUrl":"10.14745/ccdr.v51i23a05","url":null,"abstract":"<p><strong>Background: </strong>The Global Public Health Intelligence Network (GPHIN) is an event-based surveillance platform that collects thousands of pieces of open-source information, including international news media, across multiple languages on a daily basis. Analysts have observed that news media reporting in some languages tended to use more sensational wording to describe major health events. There has been minimal research exploring potential differences in sensationalism in international news media reporting to confirm these observations.</p><p><strong>Objective: </strong>This exploratory study assessed the differences in the level of sensationalism in early international news media reporting of COVID-19 through a mixed-methods analysis.</p><p><strong>Methods: </strong>Relevant news media articles received in GPHIN seven days following the Public Health Emergency of International Concern declaration of COVID-19 by the World Health Organization were extracted for screening and analysis. An adapted tool was used to measure the sensationalism of pandemic-related health news. Deductive thematic analysis was conducted to examine themes of sensationalism. Differences in prevalence of sensationalism in news media reporting by language and country/territory of publication were assessed. Sentiment analysis assessed the sentiment and emotional tone of the news media articles.</p><p><strong>Results: </strong>Of 951 news articles that met the eligibility criteria, 155 contained sensationalism. There were significant differences between languages (French, Russian and Spanish) and various domains of sensationalism. This study also found a more negative emotional tone in news media articles with sensationalism.</p><p><strong>Conclusion: </strong>This exploratory study showed that language has the potential to impact the perception of health events using more sensationalized language.</p>","PeriodicalId":94304,"journal":{"name":"Canada communicable disease report = Releve des maladies transmissibles au Canada","volume":"51 2-3","pages":"102-111"},"PeriodicalIF":0.0,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11845173/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143485123","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
Cost effectiveness of a 21-valent pneumococcal conjugate vaccine in adults: A systematic review of economic evaluations.
Pub Date : 2025-02-12 eCollection Date: 2025-02-01 DOI: 10.14745/ccdr.v51i23a03
Alison E Simmons, Raphael Ximenes, Gebremedhin B Gebretekle, Marina I Salvadori, Eva Wong, Ashleigh R Tuite

Background: In July 2024, Health Canada authorized a 21-valent pneumococcal conjugate vaccine (Pneu-C-21) for use in adults.

Objective: To conduct a systematic review of the cost-effectiveness of Pneu-C-21 for preventing pneumococcal disease in adults.

Methods: We conducted a systematic search of the literature and National Immunization Technical Advisory Groups' websites on July 3, 2024. We included economic evaluations that assessed Pneu-C-21 as a vaccination strategy among adults aged 18 years and older. Costs were adjusted to 2023 Canadian dollars.

Results: We identified 10 studies in our search, five of which were summarized in our review. No economic evaluations were conducted in Canada. All economic evaluations used static cohort models and incorporated indirect effects from paediatric pneumococcal conjugate vaccination in primary or sensitivity analyses. Although incremental cost-effectiveness ratios were heterogeneous across included economic evaluations, overall, they qualitatively identified the same vaccination strategies as optimal within the given age and risk groups. Pneu-C-21 is likely to be cost-effective in adults aged 65 years and older and adults under the age of 65 years with specific high risk conditions.

Conclusion: Pneu-C-21 is likely to be cost-effective in adults within specific age and risk groups. The applicability of the included economic evaluations to adults living in Canada is limited because the serotype-specific incidence of pneumococcal disease and the impact of indirect effects from pediatric vaccination varies by region and over time.

{"title":"Cost effectiveness of a 21-valent pneumococcal conjugate vaccine in adults: A systematic review of economic evaluations.","authors":"Alison E Simmons, Raphael Ximenes, Gebremedhin B Gebretekle, Marina I Salvadori, Eva Wong, Ashleigh R Tuite","doi":"10.14745/ccdr.v51i23a03","DOIUrl":"10.14745/ccdr.v51i23a03","url":null,"abstract":"<p><strong>Background: </strong>In July 2024, Health Canada authorized a 21-valent pneumococcal conjugate vaccine (Pneu-C-21) for use in adults.</p><p><strong>Objective: </strong>To conduct a systematic review of the cost-effectiveness of Pneu-C-21 for preventing pneumococcal disease in adults.</p><p><strong>Methods: </strong>We conducted a systematic search of the literature and National Immunization Technical Advisory Groups' websites on July 3, 2024. We included economic evaluations that assessed Pneu-C-21 as a vaccination strategy among adults aged 18 years and older. Costs were adjusted to 2023 Canadian dollars.</p><p><strong>Results: </strong>We identified 10 studies in our search, five of which were summarized in our review. No economic evaluations were conducted in Canada. All economic evaluations used static cohort models and incorporated indirect effects from paediatric pneumococcal conjugate vaccination in primary or sensitivity analyses. Although incremental cost-effectiveness ratios were heterogeneous across included economic evaluations, overall, they qualitatively identified the same vaccination strategies as optimal within the given age and risk groups. Pneu-C-21 is likely to be cost-effective in adults aged 65 years and older and adults under the age of 65 years with specific high risk conditions.</p><p><strong>Conclusion: </strong>Pneu-C-21 is likely to be cost-effective in adults within specific age and risk groups. The applicability of the included economic evaluations to adults living in Canada is limited because the serotype-specific incidence of pneumococcal disease and the impact of indirect effects from pediatric vaccination varies by region and over time.</p>","PeriodicalId":94304,"journal":{"name":"Canada communicable disease report = Releve des maladies transmissibles au Canada","volume":"51 2-3","pages":"84-91"},"PeriodicalIF":0.0,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11839088/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143470153","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
Comparison of 13-, 15- and 20-valent pneumococcal conjugate vaccines in the paediatric Canadian population: A cost-utility analysis. 加拿大儿童接种 13 价、15 价和 20 价肺炎球菌结合疫苗的比较:成本效用分析。
Pub Date : 2025-02-12 eCollection Date: 2025-02-01 DOI: 10.14745/ccdr.v51i23a02
Alison E Simmons, Gebremedhin B Gebretekle, Robert Pless, Aleksandra Wierzbowski, Matthew Tunis, Ashleigh R Tuite

Background: Two pneumococcal conjugate vaccines, covering 15 and 20 Streptococcus pneumoniae serotypes (Pneu-C-15 and Pneu-C-20, respectively), were recently approved for use in the Canadian paediatric population.

Objective: To assess the cost-effectiveness of Pneu-C-15 and Pneu-C-20 in unvaccinated infants initiating routine pneumococcal vaccination, compared to the currently used 13-valent conjugate vaccine (Pneu-C-13).

Methods: A static cohort model was used to estimate sequential incremental cost-effectiveness ratios (ICERs in 2022 Canadian dollars per quality-adjusted life year [QALY]) of Pneu-C-13, Pneu-C-15 and Pneu-C-20 in the paediatric population starting their primary series. Costs and outcomes were calculated over a 10-year time horizon at the program level and a lifetime time horizon at the individual level and discounted at a rate of 1.5% per year. We explored the impact of uncertainties in model parameters and assumptions in scenario and sensitivity analyses.

Results: Routine use of Pneu-C-20 and, to a lesser extent, Pneu-C-15 is projected to reduce pneumococcal disease burden, compared to Pneu-C-13. Based on product cost assumptions, sequential ICERs for Pneu-C-15 and Pneu-C-20 were $58,800 and $135,200 per QALY gained from the health system perspective and $18,272 and $93,416 per QALY gained from the societal perspective, excluding indirect effects. A reduction in serotype-attributable disease due to indirect vaccine effects of 5% or greater resulted in ICERs below $30,000 per QALY gained for Pneu-C-15 and Pneu-C-20, with the optimal strategy determined by the magnitude and time to reach a reduction in pneumococcal disease.

Conclusion: Both Pneu-C-15 and Pneu-C-20 are expected to increase QALYs in Canadian children compared to Pneu-C-13 and may be cost-effective interventions.

{"title":"Comparison of 13-, 15- and 20-valent pneumococcal conjugate vaccines in the paediatric Canadian population: A cost-utility analysis.","authors":"Alison E Simmons, Gebremedhin B Gebretekle, Robert Pless, Aleksandra Wierzbowski, Matthew Tunis, Ashleigh R Tuite","doi":"10.14745/ccdr.v51i23a02","DOIUrl":"10.14745/ccdr.v51i23a02","url":null,"abstract":"<p><strong>Background: </strong>Two pneumococcal conjugate vaccines, covering 15 and 20 <i>Streptococcus pneumoniae</i> serotypes (Pneu-C-15 and Pneu-C-20, respectively), were recently approved for use in the Canadian paediatric population.</p><p><strong>Objective: </strong>To assess the cost-effectiveness of Pneu-C-15 and Pneu-C-20 in unvaccinated infants initiating routine pneumococcal vaccination, compared to the currently used 13-valent conjugate vaccine (Pneu-C-13).</p><p><strong>Methods: </strong>A static cohort model was used to estimate sequential incremental cost-effectiveness ratios (ICERs in 2022 Canadian dollars per quality-adjusted life year [QALY]) of Pneu-C-13, Pneu-C-15 and Pneu-C-20 in the paediatric population starting their primary series. Costs and outcomes were calculated over a 10-year time horizon at the program level and a lifetime time horizon at the individual level and discounted at a rate of 1.5% per year. We explored the impact of uncertainties in model parameters and assumptions in scenario and sensitivity analyses.</p><p><strong>Results: </strong>Routine use of Pneu-C-20 and, to a lesser extent, Pneu-C-15 is projected to reduce pneumococcal disease burden, compared to Pneu-C-13. Based on product cost assumptions, sequential ICERs for Pneu-C-15 and Pneu-C-20 were $58,800 and $135,200 per QALY gained from the health system perspective and $18,272 and $93,416 per QALY gained from the societal perspective, excluding indirect effects. A reduction in serotype-attributable disease due to indirect vaccine effects of 5% or greater resulted in ICERs below $30,000 per QALY gained for Pneu-C-15 and Pneu-C-20, with the optimal strategy determined by the magnitude and time to reach a reduction in pneumococcal disease.</p><p><strong>Conclusion: </strong>Both Pneu-C-15 and Pneu-C-20 are expected to increase QALYs in Canadian children compared to Pneu-C-13 and may be cost-effective interventions.</p>","PeriodicalId":94304,"journal":{"name":"Canada communicable disease report = Releve des maladies transmissibles au Canada","volume":"51 2-3","pages":"68-83"},"PeriodicalIF":0.0,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11842121/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143470220","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 mpox outbreak in Canada, April 28-December 31, 2022.
Pub Date : 2025-02-12 eCollection Date: 2025-02-01 DOI: 10.14745/ccdr.v51i23a04
Meera Bhulabhai, Jeyasakthi Venugopal, Mireille Plamondon, Geneviève Bergeron, Geneviève Cadieux, Jesse Kancir, Mayank Singal, Katherine Twohig, Austin Zygmunt, Erin Schillberg, Rukshanda Ahmad, Julia Paul

Background: Mpox is an infectious disease caused by the monkeypox virus (MPXV), closely related to the virus that causes smallpox. In May 2022, cases of mpox were reported in previously non-endemic countries including Canada.

Objective: To summarize the epidemiology of the mpox outbreak in Canada, as well as key public health response activities, between April and December 2022.

Methods: The Public Health Agency of Canada (PHAC) worked closely with local, provincial and territorial public health authorities to develop national case investigation and reporting tools, including national case definitions for confirmed and probable mpox cases. Based on de-identified case data submitted to PHAC, patterns and trends were examined, including the distribution of cases by sociodemographic, clinical and transmission factors.

Results: Overall, 1,474 mpox cases (1,396 confirmed, 78 probable) were reported to PHAC. All reported cases were associated with MPXV clade IIb. Mpox disproportionately affected gay, bisexual and other men who have sex with men (80.0%) and those between 20-49 years of age (86.0%). Available data suggests that the most likely mode of disease acquisition was through sexual contact, with limited evidence on other possible modes of transmission. Some cases were hospitalized (3.0%); however, there were no mpox-related deaths in Canada.

Conclusion: Rapid coordination and surveillance activities supported the timely implementation of tailored interventions, including the procurement and distribution of vaccines. These actions, coupled with vaccination uptake and behavioural changes, contributed to reducing transmission and health impacts of mpox on the Canadian population.

{"title":"Summary of the mpox outbreak in Canada, April 28-December 31, 2022.","authors":"Meera Bhulabhai, Jeyasakthi Venugopal, Mireille Plamondon, Geneviève Bergeron, Geneviève Cadieux, Jesse Kancir, Mayank Singal, Katherine Twohig, Austin Zygmunt, Erin Schillberg, Rukshanda Ahmad, Julia Paul","doi":"10.14745/ccdr.v51i23a04","DOIUrl":"10.14745/ccdr.v51i23a04","url":null,"abstract":"<p><strong>Background: </strong>Mpox is an infectious disease caused by the monkeypox virus (MPXV), closely related to the virus that causes smallpox. In May 2022, cases of mpox were reported in previously non-endemic countries including Canada.</p><p><strong>Objective: </strong>To summarize the epidemiology of the mpox outbreak in Canada, as well as key public health response activities, between April and December 2022.</p><p><strong>Methods: </strong>The Public Health Agency of Canada (PHAC) worked closely with local, provincial and territorial public health authorities to develop national case investigation and reporting tools, including national case definitions for confirmed and probable mpox cases. Based on de-identified case data submitted to PHAC, patterns and trends were examined, including the distribution of cases by sociodemographic, clinical and transmission factors.</p><p><strong>Results: </strong>Overall, 1,474 mpox cases (1,396 confirmed, 78 probable) were reported to PHAC. All reported cases were associated with MPXV clade IIb. Mpox disproportionately affected gay, bisexual and other men who have sex with men (80.0%) and those between 20-49 years of age (86.0%). Available data suggests that the most likely mode of disease acquisition was through sexual contact, with limited evidence on other possible modes of transmission. Some cases were hospitalized (3.0%); however, there were no mpox-related deaths in Canada.</p><p><strong>Conclusion: </strong>Rapid coordination and surveillance activities supported the timely implementation of tailored interventions, including the procurement and distribution of vaccines. These actions, coupled with vaccination uptake and behavioural changes, contributed to reducing transmission and health impacts of mpox on the Canadian population.</p>","PeriodicalId":94304,"journal":{"name":"Canada communicable disease report = Releve des maladies transmissibles au Canada","volume":"51 2-3","pages":"93-101"},"PeriodicalIF":0.0,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11838821/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143470155","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
Cost-effectiveness of respiratory syncytial virus vaccination strategies for older Canadian adults: A multi-model comparison.
Pub Date : 2025-02-12 eCollection Date: 2025-02-01 DOI: 10.14745/ccdr.v51i23a01
Monica Rudd, Alison E Simmons, Gebremedhin B Gebretekle, Ashleigh R Tuite

Background: Two respiratory syncytial virus (RSV) vaccines are currently approved for use in adults aged 60 years and older in Canada.

Objective: To conduct a multi-model comparison to explore the impact of alternate model structural and methodological assumptions on the estimated cost-effectiveness of RSV adult vaccination programs.

Methods: We compared three static cost-utility models developed by the Public Health Agency of Canada, GSK and Pfizer using a common set of input parameters. Each model evaluated sequential incremental cost-effectiveness ratios in 2023 Canadian dollars per quality-adjusted life year (QALY) for a set of policy alternatives, with vaccine eligibility determined by combinations of age and chronic medical condition (CMC) status. Results were calculated for each vaccine separately for scenarios assuming two or three years of vaccine protection using the health system perspective and a 1.5% annual discount rate.

Results: The three cost-utility models were broadly concordant across the scenarios modeled. In all scenarios, focusing on vaccination of people with CMCs was preferred over broader age-based policies. Respiratory syncytial virus vaccination for people with CMCs over the age of 70 years was most commonly identified as the optimal policy when using a cost-effectiveness threshold of $50,000/QALY. When only considering policies based on age criteria, vaccinating people over 80 years was cost-effective at this threshold.

Conclusion: A multi-model comparison of Canadian cost-utility models shows that RSV vaccination programs for RSV are likely cost-effective for some groups of older adults in Canada. These findings were consistent across models, despite differences in model structure.

{"title":"Cost-effectiveness of respiratory syncytial virus vaccination strategies for older Canadian adults: A multi-model comparison.","authors":"Monica Rudd, Alison E Simmons, Gebremedhin B Gebretekle, Ashleigh R Tuite","doi":"10.14745/ccdr.v51i23a01","DOIUrl":"10.14745/ccdr.v51i23a01","url":null,"abstract":"<p><strong>Background: </strong>Two respiratory syncytial virus (RSV) vaccines are currently approved for use in adults aged 60 years and older in Canada.</p><p><strong>Objective: </strong>To conduct a multi-model comparison to explore the impact of alternate model structural and methodological assumptions on the estimated cost-effectiveness of RSV adult vaccination programs.</p><p><strong>Methods: </strong>We compared three static cost-utility models developed by the Public Health Agency of Canada, GSK and Pfizer using a common set of input parameters. Each model evaluated sequential incremental cost-effectiveness ratios in 2023 Canadian dollars per quality-adjusted life year (QALY) for a set of policy alternatives, with vaccine eligibility determined by combinations of age and chronic medical condition (CMC) status. Results were calculated for each vaccine separately for scenarios assuming two or three years of vaccine protection using the health system perspective and a 1.5% annual discount rate.</p><p><strong>Results: </strong>The three cost-utility models were broadly concordant across the scenarios modeled. In all scenarios, focusing on vaccination of people with CMCs was preferred over broader age-based policies. Respiratory syncytial virus vaccination for people with CMCs over the age of 70 years was most commonly identified as the optimal policy when using a cost-effectiveness threshold of $50,000/QALY. When only considering policies based on age criteria, vaccinating people over 80 years was cost-effective at this threshold.</p><p><strong>Conclusion: </strong>A multi-model comparison of Canadian cost-utility models shows that RSV vaccination programs for RSV are likely cost-effective for some groups of older adults in Canada. These findings were consistent across models, despite differences in model structure.</p>","PeriodicalId":94304,"journal":{"name":"Canada communicable disease report = Releve des maladies transmissibles au Canada","volume":"51 2-3","pages":"54-67"},"PeriodicalIF":0.0,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11845172/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143484866","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
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。
{"title":"Burden of disease of respiratory syncytial virus in older adults and adults considered at high risk of severe infection.","authors":"Elissa M Abrams, Pamela Doyon-Plourde, Phaedra Davis, Liza Lee, Abbas Rahal, Nicholas Brousseau, Winnie Siu, April Killikelly","doi":"10.14745/ccdr.v51i01a04","DOIUrl":"https://doi.org/10.14745/ccdr.v51i01a04","url":null,"abstract":"<p><strong>Background: </strong>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.</p><p><strong>Objective: </strong>To characterize the burden of RSV disease in Canada by joint analysis of the published literature and hospitalization data from a healthcare administrative database.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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%.</p><p><strong>Conclusion: </strong>In adults, the burden of severe RSV outcomes in general increases with age and presence of comorbidities.</p>","PeriodicalId":94304,"journal":{"name":"Canada communicable disease report = Releve des maladies transmissibles au Canada","volume":"51 1","pages":"26-34"},"PeriodicalIF":0.0,"publicationDate":"2025-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11709116/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142960943","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
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。
{"title":"Surveillance of laboratory exposures to human pathogens and toxins, Canada, 2023.","authors":"Abdulwadud Nafees, Audrey Gauthier, Antoinette N Davis, Emily F Tran, Christine Abalos, Christa M Girincuti, Samuel Bonti-Ankomah","doi":"10.14745/ccdr.v51i01a03","DOIUrl":"10.14745/ccdr.v51i01a03","url":null,"abstract":"<p><strong>Background: </strong>The Public Health Agency of Canada oversees the <i>Human Pathogens and Toxins Act</i> and <i>Human Pathogens and Toxins Regulations</i>, and monitors human pathogen and toxin incidents in licensed facilities to minimize exposure impact at the individual and population level.</p><p><strong>Objective: </strong>To provide an overview of confirmed laboratory exposure incidents in Canada in 2023.</p><p><strong>Methods: </strong>Confirmed exposure incident reports in 2023 were analyzed using R 4.2.2, Microsoft Excel and SAS.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":94304,"journal":{"name":"Canada communicable disease report = Releve des maladies transmissibles au Canada","volume":"51 1","pages":"16-25"},"PeriodicalIF":0.0,"publicationDate":"2025-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11717171/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142961000","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 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。
{"title":"Summary of the National Advisory Committee on Immunization (NACI) Statement-Updated guidance on Imvamune in the context of a routine immunization program.","authors":"Nicole Forbes, Josh Montroy, Marina I Salvadori, Kristin Klein","doi":"10.14745/ccdr.v51i01a01","DOIUrl":"https://doi.org/10.14745/ccdr.v51i01a01","url":null,"abstract":"<p><strong>Background: </strong>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.</p><p><strong>Methods: </strong>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).</p><p><strong>Results: </strong>NACI concluded that available evidence supported the vaccine's effectiveness and safety in preventing mpox infection.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":94304,"journal":{"name":"Canada communicable disease report = Releve des maladies transmissibles au Canada","volume":"51 1","pages":"1-6"},"PeriodicalIF":0.0,"publicationDate":"2025-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11708810/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142960996","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
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
期刊
Canada communicable disease report = Releve des maladies transmissibles au Canada
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:481959085
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