Pub Date : 2025-04-04eCollection Date: 2025-06-01DOI: 10.3138/jammi-2024-0027
Muhammad Morshed, Maud Vallée, Hong Yuan Zhou, Maan Hasso, Derek Stein, Vanessa Tran, Ayushi Regmi, Ameeta E Singh, Kristy Hayden, Sapan Jindal, Todd F Hatchette
Syphilis, caused by the bacterium Treponema pallidum, is a centuries-old sexually transmitted disease that continues to be a significant global health concern. Despite the efficacy of penicillin the disease has seen a resurgence worldwide, including in Canada. In 2022, Canada reported 13,953 cases of infectious syphilis, representing a 109% increase since 2018, and 117 cases of congenital syphilis, a staggering 599% increase. Historically, gay and bisexual men who have sex with men have been predominantly affected; however, recent years have seen a significant rise in female cases, contributing to the increase in congenital syphilis. Syphilis diagnosis is complex, requiring specialized expertise. The Canadian Public Health Laboratory Network last updated its laboratory diagnosis guidelines in 2015. Given the advancements in diagnostic techniques and the pressing need for updated guidance, this document provides an overview of the syphilis-causing pathogen T. pallidum, its transmission, pathogenesis, and clinical manifestations. It also reviews the epidemiology of syphilis, highlighting recent trends in Canada, and discusses current and emerging serological laboratory diagnostic techniques. This updated guidance aims to equip health care professionals with the latest knowledge and recommended testing algorithms to accurately diagnose and manage syphilis, ultimately helping to address the rising rates of this disease and improve public health outcomes in Canada.
{"title":"Canadian Public Health Laboratory Network National Syphilis In-Laboratory Serological Testing Recommendations.","authors":"Muhammad Morshed, Maud Vallée, Hong Yuan Zhou, Maan Hasso, Derek Stein, Vanessa Tran, Ayushi Regmi, Ameeta E Singh, Kristy Hayden, Sapan Jindal, Todd F Hatchette","doi":"10.3138/jammi-2024-0027","DOIUrl":"10.3138/jammi-2024-0027","url":null,"abstract":"<p><p>Syphilis, caused by the bacterium <i>Treponema pallidum</i>, is a centuries-old sexually transmitted disease that continues to be a significant global health concern. Despite the efficacy of penicillin the disease has seen a resurgence worldwide, including in Canada. In 2022, Canada reported 13,953 cases of infectious syphilis, representing a 109% increase since 2018, and 117 cases of congenital syphilis, a staggering 599% increase. Historically, gay and bisexual men who have sex with men have been predominantly affected; however, recent years have seen a significant rise in female cases, contributing to the increase in congenital syphilis. Syphilis diagnosis is complex, requiring specialized expertise. The Canadian Public Health Laboratory Network last updated its laboratory diagnosis guidelines in 2015. Given the advancements in diagnostic techniques and the pressing need for updated guidance, this document provides an overview of the syphilis-causing pathogen <i>T. pallidum</i>, its transmission, pathogenesis, and clinical manifestations. It also reviews the epidemiology of syphilis, highlighting recent trends in Canada, and discusses current and emerging serological laboratory diagnostic techniques. This updated guidance aims to equip health care professionals with the latest knowledge and recommended testing algorithms to accurately diagnose and manage syphilis, ultimately helping to address the rising rates of this disease and improve public health outcomes in Canada.</p>","PeriodicalId":36782,"journal":{"name":"JAMMI","volume":"10 2","pages":"112-126"},"PeriodicalIF":0.0,"publicationDate":"2025-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12253939/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144650811","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}
Pub Date : 2025-03-26eCollection Date: 2025-03-01DOI: 10.3138/jammi-2025-0203
Joan L Robinson, Jesse Papenburg
{"title":"An Update on Prevention of Paediatric Respiratory Syncytial Virus Hospitalizations in Canada.","authors":"Joan L Robinson, Jesse Papenburg","doi":"10.3138/jammi-2025-0203","DOIUrl":"10.3138/jammi-2025-0203","url":null,"abstract":"","PeriodicalId":36782,"journal":{"name":"JAMMI","volume":"10 1","pages":"2-5"},"PeriodicalIF":0.0,"publicationDate":"2025-03-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12258633/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144650850","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}
Pub Date : 2025-03-26eCollection Date: 2025-03-01DOI: 10.3138/jammi-10-1-ed
Gerald A Evans
{"title":"10 Years of <i>JAMMI</i>: The Tin Anniversary.","authors":"Gerald A Evans","doi":"10.3138/jammi-10-1-ed","DOIUrl":"https://doi.org/10.3138/jammi-10-1-ed","url":null,"abstract":"","PeriodicalId":36782,"journal":{"name":"JAMMI","volume":"10 1","pages":"1"},"PeriodicalIF":0.0,"publicationDate":"2025-03-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12269312/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144660663","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}
Pub Date : 2025-03-26eCollection Date: 2025-03-01DOI: 10.3138/jammi-2024-0006
Madison Robertson, Emilie Norris-Roozmon, Rylan Egan
Background: Lyme disease (LD) is a multisystemic disease without a current approved human vaccine. Increasing infection rates have created pressure to improve the diagnosis and treatment of LD in Canada. This study aims to inform LD care through the exploration of health care practitioner (HCP) perspectives, experiences, beliefs, and knowledge of LD diagnosis and treatment.
Methods: Canadian HCPs took part in bilingual (English and French) semi-structured interviews to explore their experiences and perspectives related to LD diagnosis and treatment. Major themes within and between participants were identified using inductive thematic analysis and axial coding.
Results: A total of 43 HCPs working in LD-related fields participated in this study. Four major themes were identified; HCPs have: 1) Similar perspectives regarding antibiotic use, regional influences, and physician referral; 2) diverse perspectives on the use of serology testing and barriers for LD diagnosis and treatment between endemic and nonendemic regions; 3) challenges and disagreement toward diagnosing and treating chronic LD; and 4) trust in one (among several) LD guidelines, yet consult a variety of secondary sources for additional LD knowledge.
Discussion: The findings reveal a pressing need for greater consistency among HCPs regarding the diagnosis and treatment of LD in Canada. Variation can be attributed to diverse beliefs, perspectives, and approaches within LD practitioners generally, but is particularly evident when addressing, acknowledging, and defining chronic LD.
背景:莱姆病(LD)是一种多系统疾病,目前尚无批准的人用疫苗。在加拿大,不断增加的感染率给改善LD的诊断和治疗带来了压力。本研究旨在探讨卫生保健从业人员(health care practitioner, HCP)对LD诊治的观点、经验、信念和知识,为LD护理提供信息。方法:加拿大HCPs参与双语(英语和法语)半结构化访谈,探讨他们与LD诊断和治疗相关的经验和观点。主要主题内部和参与者之间确定使用归纳主题分析和轴向编码。结果:共有43名在ld相关领域工作的医护人员参与了本研究。确定了四个主要主题;HCPs有:1)关于抗生素使用、地区影响和医生转诊的相似观点;2)流行地区和非流行地区对血清学检测的使用和LD诊断和治疗障碍的不同看法;3)慢性LD诊断与治疗的挑战与分歧;4)相信一个(或几个)LD指导方针,但要获得额外的LD知识,请参考各种次要来源。讨论:研究结果表明,迫切需要在加拿大HCPs之间对LD的诊断和治疗进行更大的一致性。变异通常可以归因于LD从业者的不同信仰、观点和方法,但在处理、承认和定义慢性LD时尤其明显。
{"title":"Understanding the Perspectives, Experiences, Beliefs, and Knowledge of Health Care Practitioners on the Diagnosis and Treatment of Lyme Disease in Canada.","authors":"Madison Robertson, Emilie Norris-Roozmon, Rylan Egan","doi":"10.3138/jammi-2024-0006","DOIUrl":"10.3138/jammi-2024-0006","url":null,"abstract":"<p><strong>Background: </strong>Lyme disease (LD) is a multisystemic disease without a current approved human vaccine. Increasing infection rates have created pressure to improve the diagnosis and treatment of LD in Canada. This study aims to inform LD care through the exploration of health care practitioner (HCP) perspectives, experiences, beliefs, and knowledge of LD diagnosis and treatment.</p><p><strong>Methods: </strong>Canadian HCPs took part in bilingual (English and French) semi-structured interviews to explore their experiences and perspectives related to LD diagnosis and treatment. Major themes within and between participants were identified using inductive thematic analysis and axial coding.</p><p><strong>Results: </strong>A total of 43 HCPs working in LD-related fields participated in this study. Four major themes were identified; HCPs have: 1) Similar perspectives regarding antibiotic use, regional influences, and physician referral; 2) diverse perspectives on the use of serology testing and barriers for LD diagnosis and treatment between endemic and nonendemic regions; 3) challenges and disagreement toward diagnosing and treating chronic LD; and 4) trust in one (among several) LD guidelines, yet consult a variety of secondary sources for additional LD knowledge.</p><p><strong>Discussion: </strong>The findings reveal a pressing need for greater consistency among HCPs regarding the diagnosis and treatment of LD in Canada. Variation can be attributed to diverse beliefs, perspectives, and approaches within LD practitioners generally, but is particularly evident when addressing, acknowledging, and defining chronic LD.</p>","PeriodicalId":36782,"journal":{"name":"JAMMI","volume":"10 1","pages":"53-72"},"PeriodicalIF":0.0,"publicationDate":"2025-03-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12258639/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144650857","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}
Pub Date : 2025-02-26eCollection Date: 2025-06-01DOI: 10.3138/jammi-2024-0025
Jollee St Fung, Victoria J Cook, James Johnston, William J Connors
Background: Updated global tuberculosis (TB) guidelines recommend the novel oral 6-month bedaquiline, pretomanid, linezolid, and moxifloxacin (BPaLM) regimen for multidrug-resistant TB (MDR-TB) based on superior efficacy and reduced toxicity demonstrated in clinical trials. These trials were dominated by isolated pulmonary TB; thus, data for BPaLM effectiveness for extrapulmonary tuberculosis (EPTB) remains limited.
Methods: We describe the safe and effective use of BPaLM in a patient for the treatment of MDR-TB involving an extrapulmonary site.
Results: Bedaquiline and pretomanid were obtained through the Health Canada Special Access Program and from the manufacturers 3 weeks later. The patient with gastrointestinal and subclinical pulmonary TB tolerated the 6 months of BPaLM well with no treatment interruptions. There was sustained microbiological and clinical response at 6 months after treatment completion.
Conclusion: Shorter duration, improved effectiveness, and reduced toxicity suggests that BPaLM should be considered when determining the ideal treatment regimen for MDR-TB. A more streamlined process for the procurement of bedaquiline and pretomanid will help minimize treatment initiation delay and overall isolation period. Further research is also needed to clarify longer-term outcomes and optimal dosing of BPaLM for EPTB, especially in more severe forms of disease or with malabsorption concerns.
{"title":"Bedaquiline, Pretomanid, Linezolid, and Moxifloxacin Treatment for Multi-Drug Resistant Extrapulmonary Tuberculosis in Canada: A Report.","authors":"Jollee St Fung, Victoria J Cook, James Johnston, William J Connors","doi":"10.3138/jammi-2024-0025","DOIUrl":"10.3138/jammi-2024-0025","url":null,"abstract":"<p><strong>Background: </strong>Updated global tuberculosis (TB) guidelines recommend the novel oral 6-month bedaquiline, pretomanid, linezolid, and moxifloxacin (BPaLM) regimen for multidrug-resistant TB (MDR-TB) based on superior efficacy and reduced toxicity demonstrated in clinical trials. These trials were dominated by isolated pulmonary TB; thus, data for BPaLM effectiveness for extrapulmonary tuberculosis (EPTB) remains limited.</p><p><strong>Methods: </strong>We describe the safe and effective use of BPaLM in a patient for the treatment of MDR-TB involving an extrapulmonary site.</p><p><strong>Results: </strong>Bedaquiline and pretomanid were obtained through the Health Canada Special Access Program and from the manufacturers 3 weeks later. The patient with gastrointestinal and subclinical pulmonary TB tolerated the 6 months of BPaLM well with no treatment interruptions. There was sustained microbiological and clinical response at 6 months after treatment completion.</p><p><strong>Conclusion: </strong>Shorter duration, improved effectiveness, and reduced toxicity suggests that BPaLM should be considered when determining the ideal treatment regimen for MDR-TB. A more streamlined process for the procurement of bedaquiline and pretomanid will help minimize treatment initiation delay and overall isolation period. Further research is also needed to clarify longer-term outcomes and optimal dosing of BPaLM for EPTB, especially in more severe forms of disease or with malabsorption concerns.</p>","PeriodicalId":36782,"journal":{"name":"JAMMI","volume":"10 2","pages":"203-208"},"PeriodicalIF":0.0,"publicationDate":"2025-02-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12253933/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144650810","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}
Pub Date : 2025-02-10eCollection Date: 2025-03-01DOI: 10.3138/jammi-2023-0041
Sydney London, Gerry McDonald, Kobe Roberts, Cheryl Foo, Natalie Bridger, Joanna Joyce, Peter Daley
Introduction: Prospective audit and feedback (PAF) are an antimicrobial stewardship intervention that reduces use of broad-spectrum antimicrobials among in-patients. The objective of this study was to assess the impact of adherence to PAF recommendations on the duration of broad-spectrum antimicrobials and patient outcomes.
Methods: This retrospective cohort study included adult in-patients at two tertiary care hospitals in St. John's, Newfoundland and Labrador Canada. PAF included all prescriptions for piperacillin/tazobactam, meropenem, ertapenem, and imipenem, reviewed by an infectious disease specialist on day 3 of therapy, with recommendations provided in the electronic medical record. The primary outcome was duration of treatment following PAF. Secondary outcomes were time to all-cause mortality, time to readmission, length of stay, and time to Clostridiodes difficile infection. Adherence categories were compared.
Results: Of the recommendations, 394 out of 786 (50.1%) were completely followed, 18.3% were partially followed, and 31.6% were not followed. There were no significant differences in adherence category based on patient age (p = 0.48) or sex (p = 0.93). Adherence category was associated with a graded reduction in mean duration of target antimicrobial treatment following PAF (p < 0.001), and length of stay after PAF (p < 0.05). Adherence category was not associated with mortality (log-rank = 0.58), readmission rate (log-rank p = 0.33), C. difficile DNA (log-rank p = 0.24) or C. difficile toxin (log-rank p = 0.084).
Conclusions: Adherence to PAF reduces antimicrobial use and length of stay without creating harms, such as readmission. This shows that PAF can be beneficial, and future research should be tailored to increasing adherence to PAF recommendations.
前瞻性审核和反馈(PAF)是一种抗菌药物管理干预措施,可减少住院患者使用广谱抗菌药物。本研究的目的是评估遵守PAF建议对广谱抗菌剂持续时间和患者预后的影响。方法:本回顾性队列研究包括加拿大纽芬兰省圣约翰市和拉布拉多省两家三级医院的成年住院患者。PAF包括所有哌拉西林/他唑巴坦、美罗培南、厄他培南和亚胺培南的处方,由传染病专家在治疗的第3天审查,并在电子病历中提供建议。主要终点是PAF后的治疗时间。次要结局为全因死亡率时间、再入院时间、住院时间和艰难梭菌感染时间。比较依从性类别。结果:786例患者中,394例(50.1%)完全遵医嘱,18.3%部分遵医嘱,31.6%未遵医嘱。基于患者年龄(p = 0.48)或性别(p = 0.93)的依从性类别无显著差异。依从性类别与PAF后目标抗菌药物治疗的平均持续时间的分级减少(p < 0.001)和PAF后的住院时间(p < 0.05)相关。依从性类别与死亡率(log-rank = 0.58)、再入院率(log-rank p = 0.33)、艰难梭菌DNA (log-rank p = 0.24)或艰难梭菌毒素(log-rank p = 0.084)无关。结论:坚持PAF可减少抗菌药物的使用和住院时间,而不会造成诸如再入院等危害。这表明PAF可能是有益的,未来的研究应该针对增加对PAF建议的依从性进行调整。
{"title":"Impact of Adherence With In-Patient Prospective Audit and Feedback Recommendations on Patient and Economic Outcomes.","authors":"Sydney London, Gerry McDonald, Kobe Roberts, Cheryl Foo, Natalie Bridger, Joanna Joyce, Peter Daley","doi":"10.3138/jammi-2023-0041","DOIUrl":"10.3138/jammi-2023-0041","url":null,"abstract":"<p><strong>Introduction: </strong>Prospective audit and feedback (PAF) are an antimicrobial stewardship intervention that reduces use of broad-spectrum antimicrobials among in-patients. The objective of this study was to assess the impact of adherence to PAF recommendations on the duration of broad-spectrum antimicrobials and patient outcomes.</p><p><strong>Methods: </strong>This retrospective cohort study included adult in-patients at two tertiary care hospitals in St. John's, Newfoundland and Labrador Canada. PAF included all prescriptions for piperacillin/tazobactam, meropenem, ertapenem, and imipenem, reviewed by an infectious disease specialist on day 3 of therapy, with recommendations provided in the electronic medical record. The primary outcome was duration of treatment following PAF. Secondary outcomes were time to all-cause mortality, time to readmission, length of stay, and time to <i>Clostridiodes difficile</i> infection. Adherence categories were compared.</p><p><strong>Results: </strong>Of the recommendations, 394 out of 786 (50.1%) were completely followed, 18.3% were partially followed, and 31.6% were not followed. There were no significant differences in adherence category based on patient age (<i>p</i> = 0.48) or sex (<i>p</i> = 0.93). Adherence category was associated with a graded reduction in mean duration of target antimicrobial treatment following PAF (<i>p</i> < 0.001), and length of stay after PAF (<i>p</i> < 0.05). Adherence category was not associated with mortality (log-rank = 0.58), readmission rate (log-rank <i>p</i> = 0.33), <i>C. difficile</i> DNA (log-rank <i>p</i> = 0.24) or <i>C. difficile</i> toxin (log-rank <i>p</i> = 0.084).</p><p><strong>Conclusions: </strong>Adherence to PAF reduces antimicrobial use and length of stay without creating harms, such as readmission. This shows that PAF can be beneficial, and future research should be tailored to increasing adherence to PAF recommendations.</p>","PeriodicalId":36782,"journal":{"name":"JAMMI","volume":"10 1","pages":"32-39"},"PeriodicalIF":0.0,"publicationDate":"2025-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12258645/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144650853","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}
Pub Date : 2025-01-31eCollection Date: 2025-03-01DOI: 10.3138/jammi-2024-0031
Élodie Gemme, Philippe Lagacé-Wiens, Yoav Keynan, Terry Wuerz, James McEachern, John M Embil
Background: Tularemia is a zoonotic disease of the Northern Hemisphere caused by Francisella tularensis. Given its diverse animal reservoir and wide range of transmission modes, a thorough history of potential exposure is paramount. In the right context, fever combined with skin eruption and lymphadenopathy should raise the possibility of tularemia. Additionally, health care providers should be mindful that F. tularensis is a risk group 3 pathogen and a category A bioterrorism agent and presents a risk for laboratory personnel due to its aerosolization potential, low infectious dose, and fatality rate ranging from 2% to 60%.
Method: Retrospective single chart review.
Results: We describe a 65-year-old man with tularemia working as a bear-hunting guide whose management was delayed despite a fairly typical presentation due to lack of awareness regarding this disease. This case also demonstrates the need for safer referral practices and improved communications with the laboratory to ensure personnel are taking the appropriate measures while handling patient samples to avoid potentially serious consequences.
Conclusion: The diagnosis was confirmed from a neck mass biopsy and the patient made a complete recovery with appropriate antibiotic treatment.
{"title":"Neck Mass: Tularemia Misdiagnosed as a Possible Malignancy.","authors":"Élodie Gemme, Philippe Lagacé-Wiens, Yoav Keynan, Terry Wuerz, James McEachern, John M Embil","doi":"10.3138/jammi-2024-0031","DOIUrl":"10.3138/jammi-2024-0031","url":null,"abstract":"<p><strong>Background: </strong>Tularemia is a zoonotic disease of the Northern Hemisphere caused by <i>Francisella tularensis</i>. Given its diverse animal reservoir and wide range of transmission modes, a thorough history of potential exposure is paramount. In the right context, fever combined with skin eruption and lymphadenopathy should raise the possibility of tularemia. Additionally, health care providers should be mindful that <i>F. tularensis</i> is a risk group 3 pathogen and a category A bioterrorism agent and presents a risk for laboratory personnel due to its aerosolization potential, low infectious dose, and fatality rate ranging from 2% to 60%.</p><p><strong>Method: </strong>Retrospective single chart review.</p><p><strong>Results: </strong>We describe a 65-year-old man with tularemia working as a bear-hunting guide whose management was delayed despite a fairly typical presentation due to lack of awareness regarding this disease. This case also demonstrates the need for safer referral practices and improved communications with the laboratory to ensure personnel are taking the appropriate measures while handling patient samples to avoid potentially serious consequences.</p><p><strong>Conclusion: </strong>The diagnosis was confirmed from a neck mass biopsy and the patient made a complete recovery with appropriate antibiotic treatment.</p>","PeriodicalId":36782,"journal":{"name":"JAMMI","volume":"10 1","pages":"84-89"},"PeriodicalIF":0.0,"publicationDate":"2025-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12258629/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144650856","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}
Pub Date : 2025-01-30eCollection Date: 2025-03-01DOI: 10.3138/jammi-2024-0015
Wayne Leung, Janhavi Bhalla, Lili Ataie, Sameer Elsayed, Lise Bondy, Megan Devlin, Sarah Shalhoub, Huma Saeed, Mahshid Mohammadi, Michael Silverman, Reza Rahimi Shahmirzadi
Introduction: Treatment of acute bacterial skin and skin structure infections (ABSSSIs) with intravenous (IV) antibiotics is difficult in marginalized populations, such as people who inject drugs, due to issues such as unstable housing or mental health conditions. These factors often require extended hospital admissions for IV antibiotics. Dalbavancin, a novel lipoglycopeptide antibiotic effective against gram-positive bacteria, lasts over 14 days and may be suitable for patients who struggle with traditional IV antibiotic administration.
Methods: This was a case series in which we reviewed 19 patients referred to our cellulitis clinic in London, Ontario, Canada, between February 1 and July 30, 2023, who received a single dose of IV dalbavancin for ABSSSIs as out-patients. Those who were enrolled had severe infections requiring IV antibiotics, with psychosocial factors pre-cluding out-patient IV therapy, or were at high risk of non-adherence to oral antibiotics.
Results: The median age of patients was 43 (range 36-56 years); they were mostly male (74%), unemployed (89%), and with unstable housing (58%). Positive outcomes were observed in 13 out of 19 (68%) patients; 3 out of 19 had indeterminate outcomes (could not be reached for follow-up but were not admitted to any institution within our catchment area) and 3 out of 19 had negative outcomes (needed further antibiotics following dalbavancin).
Conclusion: Our experience shows that a single IV dose of dalbavancin is effective in treating ABSSSIs in patients with complex psychosocial factors, as positive outcomes were observed in most patients. Dalbavancin eliminates the need for indwelling IV access and may reduce hospital admissions for patients for whom traditional antibiotic regimens may be challenging.
{"title":"Use of Dalbavancin in Treatment of Acute Bacterial Skin and Skin Structure Infections: Case Series from a Canadian Perspective.","authors":"Wayne Leung, Janhavi Bhalla, Lili Ataie, Sameer Elsayed, Lise Bondy, Megan Devlin, Sarah Shalhoub, Huma Saeed, Mahshid Mohammadi, Michael Silverman, Reza Rahimi Shahmirzadi","doi":"10.3138/jammi-2024-0015","DOIUrl":"10.3138/jammi-2024-0015","url":null,"abstract":"<p><strong>Introduction: </strong>Treatment of acute bacterial skin and skin structure infections (ABSSSIs) with intravenous (IV) antibiotics is difficult in marginalized populations, such as people who inject drugs, due to issues such as unstable housing or mental health conditions. These factors often require extended hospital admissions for IV antibiotics. Dalbavancin, a novel lipoglycopeptide antibiotic effective against gram-positive bacteria, lasts over 14 days and may be suitable for patients who struggle with traditional IV antibiotic administration.</p><p><strong>Methods: </strong>This was a case series in which we reviewed 19 patients referred to our cellulitis clinic in London, Ontario, Canada, between February 1 and July 30, 2023, who received a single dose of IV dalbavancin for ABSSSIs as out-patients. Those who were enrolled had severe infections requiring IV antibiotics, with psychosocial factors pre-cluding out-patient IV therapy, or were at high risk of non-adherence to oral antibiotics.</p><p><strong>Results: </strong>The median age of patients was 43 (range 36-56 years); they were mostly male (74%), unemployed (89%), and with unstable housing (58%). Positive outcomes were observed in 13 out of 19 (68%) patients; 3 out of 19 had indeterminate outcomes (could not be reached for follow-up but were not admitted to any institution within our catchment area) and 3 out of 19 had negative outcomes (needed further antibiotics following dalbavancin).</p><p><strong>Conclusion: </strong>Our experience shows that a single IV dose of dalbavancin is effective in treating ABSSSIs in patients with complex psychosocial factors, as positive outcomes were observed in most patients. Dalbavancin eliminates the need for indwelling IV access and may reduce hospital admissions for patients for whom traditional antibiotic regimens may be challenging.</p>","PeriodicalId":36782,"journal":{"name":"JAMMI","volume":"10 1","pages":"40-52"},"PeriodicalIF":0.0,"publicationDate":"2025-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12258635/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144650858","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}
Pub Date : 2025-01-30eCollection Date: 2025-03-01DOI: 10.3138/jammi-2024-0018
Agatha Jassem, Tess MacIntyre, Yin Chang, Frankie Tsang, Janet Fung, Mel Krajden, Jennifer Grant, Linda Hoang
Background: Global reports suggest heightened Mycoplasma pneumoniae (Mp) activity during the fall of 2023. However, it is unclear how testing strategy changes and preventative measures implemented during the COVID-19 pandemic influenced these conclusions. The objective of this study was to summarize the effects of implementing a new respiratory testing method (Luminex NxTAG Respiratory Pathogen Panel [RPP]) on the rate of detection of three types of atypical bacteria (AB) (Mp, Legionella pneumophila [Lp], and Chlamydophila pneumoniae [Cp]) in British Columbia (BC), as well as to summarize case detections throughout the province during and after the COVID-19 pandemic to determine if there were emerging concerns regarding Mp infections in BC as seen in other jurisdictions.
Methods: We analyzed 2013-2023 laboratory testing data from the provincial lab in BC, divided into periods before syndromic testing, after syndromic testing was implemented (via xTAG RPP), during the COVID-19 pandemic, and after the pandemic.
Results: Following introduction of the Luminex NxTAG RPP, detection of Mp and Cp cases increased 11-fold and 4-fold, respectively, while Lp detection was not significantly affected. Relatively few cases of Mp were recorded during the COVID-19 pandemic, although following relaxation of COVID-19 pandemic mitigation measures, Mp resurgent activity was observed that remained within expected levels.
Conclusions: Detection of AB in BC increased following implementation of the Luminex NxTAG RPP, decreased during the COVID-19 pandemic, and returned to seasonal circulation after the pandemic.
{"title":"Detection of Atypical Bacteria, Including <i>Mycoplasma Pneumoniae</i>, British Columbia, Canada, 2013-2023.","authors":"Agatha Jassem, Tess MacIntyre, Yin Chang, Frankie Tsang, Janet Fung, Mel Krajden, Jennifer Grant, Linda Hoang","doi":"10.3138/jammi-2024-0018","DOIUrl":"10.3138/jammi-2024-0018","url":null,"abstract":"<p><strong>Background: </strong>Global reports suggest heightened <i>Mycoplasma pneumoniae</i> (Mp) activity during the fall of 2023. However, it is unclear how testing strategy changes and preventative measures implemented during the COVID-19 pandemic influenced these conclusions. The objective of this study was to summarize the effects of implementing a new respiratory testing method (Luminex NxTAG Respiratory Pathogen Panel [RPP]) on the rate of detection of three types of atypical bacteria (AB) (Mp, <i>Legionella pneumophila</i> [Lp], and <i>Chlamydophila pneumoniae</i> [Cp]) in British Columbia (BC), as well as to summarize case detections throughout the province during and after the COVID-19 pandemic to determine if there were emerging concerns regarding Mp infections in BC as seen in other jurisdictions.</p><p><strong>Methods: </strong>We analyzed 2013-2023 laboratory testing data from the provincial lab in BC, divided into periods before syndromic testing, after syndromic testing was implemented (via xTAG RPP), during the COVID-19 pandemic, and after the pandemic.</p><p><strong>Results: </strong>Following introduction of the Luminex NxTAG RPP, detection of Mp and Cp cases increased 11-fold and 4-fold, respectively, while Lp detection was not significantly affected. Relatively few cases of Mp were recorded during the COVID-19 pandemic, although following relaxation of COVID-19 pandemic mitigation measures, Mp resurgent activity was observed that remained within expected levels.</p><p><strong>Conclusions: </strong>Detection of AB in BC increased following implementation of the Luminex NxTAG RPP, decreased during the COVID-19 pandemic, and returned to seasonal circulation after the pandemic.</p>","PeriodicalId":36782,"journal":{"name":"JAMMI","volume":"10 1","pages":"73-77"},"PeriodicalIF":0.0,"publicationDate":"2025-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12258644/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144650851","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}
Pub Date : 2025-01-28eCollection Date: 2025-03-01DOI: 10.3138/jammi-2023-0038
Anish Krishnan, Irina Rajakumar, Joanne Salmon
Background: Vancomycin resistant Enterococcus faecium (VRE) bacteremia and infective endocarditis (IE) are difficult to treat and associated with high mortality.
Methods: We describe a case of a 78-year-old male with VRE prosthetic valve endocarditis treated with combined daptomycin/ampicillin. We review published literature on the treatment of VRE IE and summarize other published case reports of daptomycin combination therapy.
Results: Prompt clearance of bacteremia was achieved. Cardiac valve replacement surgery was pursued but was followed by post-operative complications and ultimately the patient did not survive.
Conclusion: There is limited published literature on the treatment of VRE IE and an optimal antibiotic regimen has not been established. This case adds to the growing body of literature demonstrating the use of daptomycin and beta-lactam combination therapy for VRE bacteremia and endocarditis. Combination therapy may be an appropriate choice for select cases; however, reports of treatment failure warrant caution.
{"title":"Vancomycin-Resistant <i>Enterococcus Faecium</i> Prosthetic Valve Endocarditis Treated with Daptomycin and Ampicillin Combination.","authors":"Anish Krishnan, Irina Rajakumar, Joanne Salmon","doi":"10.3138/jammi-2023-0038","DOIUrl":"10.3138/jammi-2023-0038","url":null,"abstract":"<p><strong>Background: </strong>Vancomycin resistant <i>Enterococcus faecium</i> (VRE) bacteremia and infective endocarditis (IE) are difficult to treat and associated with high mortality.</p><p><strong>Methods: </strong>We describe a case of a 78-year-old male with VRE prosthetic valve endocarditis treated with combined daptomycin/ampicillin. We review published literature on the treatment of VRE IE and summarize other published case reports of daptomycin combination therapy.</p><p><strong>Results: </strong>Prompt clearance of bacteremia was achieved. Cardiac valve replacement surgery was pursued but was followed by post-operative complications and ultimately the patient did not survive.</p><p><strong>Conclusion: </strong>There is limited published literature on the treatment of VRE IE and an optimal antibiotic regimen has not been established. This case adds to the growing body of literature demonstrating the use of daptomycin and beta-lactam combination therapy for VRE bacteremia and endocarditis. Combination therapy may be an appropriate choice for select cases; however, reports of treatment failure warrant caution.</p>","PeriodicalId":36782,"journal":{"name":"JAMMI","volume":"10 1","pages":"90-96"},"PeriodicalIF":0.0,"publicationDate":"2025-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12263162/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144650859","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}