Pub Date : 2025-08-08Print Date: 2025-07-01DOI: 10.1503/cjs.014425
Chad G Ball, Edward J Harvey, Andrew W Kirkpatrick
{"title":"L’introduction des dispositifs médicaux modernes entraîne-t-elle un problème de sécurité?","authors":"Chad G Ball, Edward J Harvey, Andrew W Kirkpatrick","doi":"10.1503/cjs.014425","DOIUrl":"10.1503/cjs.014425","url":null,"abstract":"","PeriodicalId":9573,"journal":{"name":"Canadian Journal of Surgery","volume":"68 4","pages":"E335-E336"},"PeriodicalIF":2.2,"publicationDate":"2025-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12342830/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144803607","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-08Print Date: 2025-07-01DOI: 10.1503/cjs.000825
Samuel Lamarre Skulsky, Eisar Al-Sukhni, Roselyne Villiard, Ting Li, Mo Yu Li, Jerry T Dang
The incidence of early-onset colorectal cancer (CRC), defined as CRC occurring in individuals younger than 50 years, is increasing globally. Emerging evidence suggests that the incidence and prevalence of CRC in individuals aged 45-49 years approach those in individuals aged 50-59 years. To address this concerning trend, many health care systems and clinical specialist societies are advocating for lowering the age of initiation for CRC screening in individuals at average risk to 45 years. The present review, provided by the Canadian Association of General Surgeons Clinical Practice Committee, gives an overview of the current CRC screening guidelines in Canada, the rationale for earlier screening, and the challenges and impact of lowering the screening age to 45 years to health care systems in Canada.
{"title":"Canadian considerations on updating the age of initiation for colorectal cancer screening in individuals at average risk.","authors":"Samuel Lamarre Skulsky, Eisar Al-Sukhni, Roselyne Villiard, Ting Li, Mo Yu Li, Jerry T Dang","doi":"10.1503/cjs.000825","DOIUrl":"10.1503/cjs.000825","url":null,"abstract":"<p><p>The incidence of early-onset colorectal cancer (CRC), defined as CRC occurring in individuals younger than 50 years, is increasing globally. Emerging evidence suggests that the incidence and prevalence of CRC in individuals aged 45-49 years approach those in individuals aged 50-59 years. To address this concerning trend, many health care systems and clinical specialist societies are advocating for lowering the age of initiation for CRC screening in individuals at average risk to 45 years. The present review, provided by the Canadian Association of General Surgeons Clinical Practice Committee, gives an overview of the current CRC screening guidelines in Canada, the rationale for earlier screening, and the challenges and impact of lowering the screening age to 45 years to health care systems in Canada.</p>","PeriodicalId":9573,"journal":{"name":"Canadian Journal of Surgery","volume":"68 4","pages":"E313-E324"},"PeriodicalIF":2.2,"publicationDate":"2025-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12342832/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144803605","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-08Print Date: 2025-07-01DOI: 10.1503/cjs.013825
Chad G Ball, Edward J Harvey, Andrew W Kirkpatrick
{"title":"Do we have a safety issue with the introduction of modern medical devices?","authors":"Chad G Ball, Edward J Harvey, Andrew W Kirkpatrick","doi":"10.1503/cjs.013825","DOIUrl":"10.1503/cjs.013825","url":null,"abstract":"","PeriodicalId":9573,"journal":{"name":"Canadian Journal of Surgery","volume":"68 4","pages":"E333-E334"},"PeriodicalIF":2.2,"publicationDate":"2025-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12342831/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144803606","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-08Print Date: 2025-07-01DOI: 10.1503/cjs.012824
Marguerite Mainprize, Anton Svendrovski, Christoph Paasch, Ayse Yilbas, Joel Katz
Background: Sex differences in chronic postsurgical pain have been reported, with the main findings indicating that females experience a greater incidence and severity of pain than males; however, it remains unclear to what these sex differences are attributable. We sought to compare pain and related psychological factors between a matched sample of male and female patients 3 months and 1 year after Shouldice repair.
Methods: Male and female participants who underwent Shouldice repair were manually matched 1:1 and compared on 10 variables: age, body mass index, smoking status, preoperative depression and anxiety scores, living status (alone or with others), American Society of Anesthesiologists physical status health classification, preoperative chronic pain, preoperative hernia pain, preoperative pain catastrophizing scores, and nerve handling during surgery. Data on pain were collected from questionnaires administered 3 months and 1 year postoperatively, and data on participant clinical characteristics were collected from operative notes and patient charts.
Results: There were 28 matched male-female pairs at 3 months and 21 at 1 year. The average age preoperatively was 56.18 ± 12.48 years. At 3 months postoperative, 18 females and 6 males had pain (p = 0.001), with females reporting more frequent (p = 0.004) and longer durations (p = 0.005) of pain. The 3-month postoperative Brief Pain Inventory Numeric Rating Scale scores (0-10) showed that in terms of pain severity, females had higher "worst pain" (1.61 ± 1.85 v. 0.32 ± 0.77, p = 0.002), "average pain" (0.86 ± 1.08 v. 0.14 ± 0.45, p = 0.002), and "pain now" (0.43 ± 1.20 v. 0 ± 0, p = 0.010) scores than males. Significant differences were not found in the incidence, severity, frequency, or duration of pain between females and males at 1 year.
Conclusion: After matching on important confounders, sex differences were found in pain frequency, duration, incidence, and severity at 3 months after Shouldice repair. However, by 1 year after surgery the differences were no longer significant.
背景:已经报道了慢性术后疼痛的性别差异,主要发现表明女性经历的疼痛发生率和严重程度高于男性;然而,这些性别差异的原因尚不清楚。我们试图比较肩部修复术后3个月和1年的男性和女性患者的疼痛和相关心理因素。方法:对行肩关节修复术的男性和女性患者进行1:1的手工匹配,比较10个变量:年龄、体重指数、吸烟状况、术前抑郁和焦虑评分、生活状况(单独或与他人)、美国麻醉医师协会身体状况健康分类、术前慢性疼痛、术前疝痛、术前疼痛灾难化评分、术中神经处理。疼痛数据从术后3个月和1年的问卷调查中收集,参与者的临床特征数据从手术记录和患者图表中收集。结果:3月龄时雌雄配对28对,1岁时雌雄配对21对。术前平均年龄56.18±12.48岁。术后3个月,18名女性和6名男性出现疼痛(p = 0.001),女性报告的疼痛频率更高(p = 0.004),持续时间更长(p = 0.005)。术后3个月的简短疼痛量表评分(0-10)显示,在疼痛严重程度方面,女性的“最严重疼痛”(1.61±1.85 vs . 0.32±0.77,p = 0.002)、“平均疼痛”(0.86±1.08 vs . 0.14±0.45,p = 0.002)和“现在疼痛”(0.43±1.20 vs .0±0,p = 0.010)得分高于男性。在1年内,女性和男性在疼痛的发生率、严重程度、频率或持续时间方面没有发现显著差异。结论:在对重要混杂因素进行匹配后,在肩胛修复术后3个月的疼痛频率、持续时间、发生率和严重程度上存在性别差异。然而,手术后1年,差异不再显著。试验注册:Clinicaltrials.gov # NCT03986060。
{"title":"Matching males and females undergoing Shouldice repair using a prospective, longitudinal design.","authors":"Marguerite Mainprize, Anton Svendrovski, Christoph Paasch, Ayse Yilbas, Joel Katz","doi":"10.1503/cjs.012824","DOIUrl":"10.1503/cjs.012824","url":null,"abstract":"<p><strong>Background: </strong>Sex differences in chronic postsurgical pain have been reported, with the main findings indicating that females experience a greater incidence and severity of pain than males; however, it remains unclear to what these sex differences are attributable. We sought to compare pain and related psychological factors between a matched sample of male and female patients 3 months and 1 year after Shouldice repair.</p><p><strong>Methods: </strong>Male and female participants who underwent Shouldice repair were manually matched 1:1 and compared on 10 variables: age, body mass index, smoking status, preoperative depression and anxiety scores, living status (alone or with others), American Society of Anesthesiologists physical status health classification, preoperative chronic pain, preoperative hernia pain, preoperative pain catastrophizing scores, and nerve handling during surgery. Data on pain were collected from questionnaires administered 3 months and 1 year postoperatively, and data on participant clinical characteristics were collected from operative notes and patient charts.</p><p><strong>Results: </strong>There were 28 matched male-female pairs at 3 months and 21 at 1 year. The average age preoperatively was 56.18 ± 12.48 years. At 3 months postoperative, 18 females and 6 males had pain (<i>p</i> = 0.001), with females reporting more frequent (<i>p</i> = 0.004) and longer durations (<i>p</i> = 0.005) of pain. The 3-month postoperative Brief Pain Inventory Numeric Rating Scale scores (0-10) showed that in terms of pain severity, females had higher \"worst pain\" (1.61 ± 1.85 v. 0.32 ± 0.77, <i>p</i> = 0.002), \"average pain\" (0.86 ± 1.08 v. 0.14 ± 0.45, <i>p</i> = 0.002), and \"pain now\" (0.43 ± 1.20 v. 0 ± 0, <i>p</i> = 0.010) scores than males. Significant differences were not found in the incidence, severity, frequency, or duration of pain between females and males at 1 year.</p><p><strong>Conclusion: </strong>After matching on important confounders, sex differences were found in pain frequency, duration, incidence, and severity at 3 months after Shouldice repair. However, by 1 year after surgery the differences were no longer significant.</p><p><strong>Trial registration: </strong>Clinicaltrials.gov # NCT03986060.</p>","PeriodicalId":9573,"journal":{"name":"Canadian Journal of Surgery","volume":"68 4","pages":"E325-E332"},"PeriodicalIF":2.2,"publicationDate":"2025-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12342833/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144803608","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-15Print Date: 2025-07-01DOI: 10.1503/cjs.012024
Daniel Josué Guerra Ordaz, Peter Tai, Antoine Lalonde, Magdalena Cordoba, Éolie Delisle, Sophie Nguyen, Rocío Branes, Maryam Mozafarinia, Carlos Cordoba
Background: Bibliometric analysis is a research tool for evaluating and analyzing scholarly output and impact within a specific domain. This study aimed to assess the quantity and quality of plastic surgery research conducted by Canadian-affiliated authors from 1999 to 2023.
Methods: We conducted a comprehensive bibliometric analysis using the Web of Science Core Collection to retrieve data from 60 leading plastic surgery journals, focusing on original articles and reviews published between 1999 and 2023. The InCites Benchmarking & Analytics platform evaluated the publications' quantity and quality. Quality assessment employed 2 key metrics:: category-normalized citation impact (CNCI) and the percentage of publications in the top quartile of journals (%Q1) based on impact factors. We used VOSviewer to map collaborative relationships among universities over various periods.
Results: Canada ranked as the 11th leading contributor globally, with 4446 publications. Nationally, the University of Toronto accounted for more than 30% of Canadian contributions. In terms of quality, Canada led with a CNCI of 1.09 and 21% of publications in the %Q1. Within Canada, McMaster University had the highest CNCI at 1.33, while Dalhousie University ranked highest in %Q1 at 32.3%. Our VOSviewer map of institutional collaborations revealed increased cooperation between Canadian universities and international institutions over the last 25 years.
Conclusion: Over the last 25 years, the trajectory of Canadian plastic surgery literature has been characterized by continuous expansion while maintaining high quality. Efforts should be made to continue to increase the quality and quantity of Canadian research while sustaining international collaborations.
背景:文献计量分析是一种评估和分析特定领域学术产出和影响的研究工具。本研究旨在评估1999年至2023年加拿大附属作者进行的整形手术研究的数量和质量。方法:我们使用Web of Science Core Collection进行了全面的文献计量分析,检索了60份领先的整形外科期刊的数据,重点是1999年至2023年间发表的原创文章和评论。InCites Benchmarking & Analytics平台对出版物的数量和质量进行了评估。质量评估采用了两个关键指标:类别标准化引用影响(CNCI)和基于影响因子的期刊前四分之一的出版物百分比(%Q1)。我们使用VOSviewer来绘制不同时期大学之间的合作关系。结果:加拿大在全球排名第11位,发表了4446篇论文。在全国范围内,多伦多大学占加拿大捐款的30%以上。在质量方面,加拿大以1.09的CNCI领先,占第一季度出版物的21%。在加拿大,麦克马斯特大学的CNCI最高,为1.33,而达尔豪斯大学的%Q1排名最高,为32.3%。我们的VOSviewer机构合作地图显示,在过去的25年里,加拿大大学和国际机构之间的合作有所增加。结论:在过去的25年里,加拿大整形外科文献的发展轨迹是在保持高质量的同时不断扩大。应努力继续提高加拿大研究的质量和数量,同时保持国际合作。
{"title":"A 25-year retrospective of Canadian plastic surgery research and its influence: a bibliometric study.","authors":"Daniel Josué Guerra Ordaz, Peter Tai, Antoine Lalonde, Magdalena Cordoba, Éolie Delisle, Sophie Nguyen, Rocío Branes, Maryam Mozafarinia, Carlos Cordoba","doi":"10.1503/cjs.012024","DOIUrl":"10.1503/cjs.012024","url":null,"abstract":"<p><strong>Background: </strong>Bibliometric analysis is a research tool for evaluating and analyzing scholarly output and impact within a specific domain. This study aimed to assess the quantity and quality of plastic surgery research conducted by Canadian-affiliated authors from 1999 to 2023.</p><p><strong>Methods: </strong>We conducted a comprehensive bibliometric analysis using the Web of Science Core Collection to retrieve data from 60 leading plastic surgery journals, focusing on original articles and reviews published between 1999 and 2023. The InCites Benchmarking & Analytics platform evaluated the publications' quantity and quality. Quality assessment employed 2 key metrics:: category-normalized citation impact (CNCI) and the percentage of publications in the top quartile of journals (%Q1) based on impact factors. We used VOSviewer to map collaborative relationships among universities over various periods.</p><p><strong>Results: </strong>Canada ranked as the 11th leading contributor globally, with 4446 publications. Nationally, the University of Toronto accounted for more than 30% of Canadian contributions. In terms of quality, Canada led with a CNCI of 1.09 and 21% of publications in the %Q1. Within Canada, McMaster University had the highest CNCI at 1.33, while Dalhousie University ranked highest in %Q1 at 32.3%. Our VOSviewer map of institutional collaborations revealed increased cooperation between Canadian universities and international institutions over the last 25 years.</p><p><strong>Conclusion: </strong>Over the last 25 years, the trajectory of Canadian plastic surgery literature has been characterized by continuous expansion while maintaining high quality. Efforts should be made to continue to increase the quality and quantity of Canadian research while sustaining international collaborations.</p>","PeriodicalId":9573,"journal":{"name":"Canadian Journal of Surgery","volume":"68 4","pages":"E296-E304"},"PeriodicalIF":2.2,"publicationDate":"2025-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12279391/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144641888","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-15Print Date: 2025-07-01DOI: 10.1503/cjs.010224
Luc Dubois, J Andrew McClure, Philip M Jones, Marko Mrkobrada, Suzanne Flier, Blayne Welk, Kelly Vogt
Background: Use of poton pump inhibitors (PPIs) is associated with increased risk of Clostridioides difficile-associated colitis, pneumonia, and acute kidney injury. Their effect on postoperative complications is unknown. The objective of this study was to investigate the association between PPIs and the risk of C. difficile-associated colitis, pneumonia, and acute kidney injury following elective surgery.
Methods: In this population-based, matched cohort study, we identified patients who had filled a PPI prescription within 90 days before major elective surgery (2010-2019). Study outcomes included C. difficile-associated colitis, pneumonia, acute kidney injury, gastrointestinal bleeding, and death within 90 days of surgery. We matched patients 1-to-1 on the basis of age, sex, procedure, date of surgery, and a propensity score predicting PPI exposure. We used logistic regression to evaluate between-group differences.
Results: Of 313 163 patients, 89 047 (28.4%) used PPIs; of those, 79 681 were successfully matched to patients who did not use PPIs. The risk of the composite outcome (acute kidney injury, pneumonia, C. difficile-associated colitis, and death) among the patients who used PPIs was slightly higher than among the patients who did not use PPIs (10.6% v. 10.2 4%), and was driven primarily by a higher rate of pneumonia among those who used PPIs (4.0% v. 3.7%). There was a lower rate of gastrointestinal bleeding among the patients who used PPIs (1.6% v. 1.8%). The risk of pneumonia was most pronounced in the subgroup undergoing hip and knee replacement (odds ratio 1.21, 95% confidence interval 1.08-1.36; p = 0.001). There were no significant differences between groups with regard to rates of C. difficile-associated colitis or acute kidney injury.
Conclusion: We found that preoperative PPI use was associated with higher rates of pneumonia, particularly among patients undergoing hip and knee replacement surgery, and lower rates of gastrointestinal bleeding. Patients taking a PPI before surgery should be targeted for therapies aimed at reducing pneumonia risk, such as aggressive chest physiotherapy, following their operation.
背景:使用质子泵抑制剂(PPIs)与艰难梭状芽胞杆菌相关性结肠炎、肺炎和急性肾损伤的风险增加有关。它们对术后并发症的影响尚不清楚。本研究的目的是调查PPIs与择期手术后艰难梭菌相关结肠炎、肺炎和急性肾损伤风险之间的关系。方法:在这项基于人群的匹配队列研究中,我们确定了在重大择期手术(2010-2019)前90天内服用PPI处方的患者。研究结果包括难辨梭菌相关结肠炎、肺炎、急性肾损伤、胃肠道出血和手术90天内死亡。我们根据年龄、性别、手术、手术日期和预测PPI暴露的倾向评分对患者进行1对1的匹配。我们使用逻辑回归来评估组间差异。结果:313163例患者中,89047例(28.4%)使用PPIs;其中,79681名患者成功与未使用PPIs的患者匹配。使用PPIs的患者发生复合结局(急性肾损伤、肺炎、艰难梭菌相关结肠炎和死亡)的风险略高于未使用PPIs的患者(10.6% vs 10.4%),主要原因是使用PPIs的患者肺炎发生率较高(4.0% vs 3.7%)。使用ppi的患者胃肠道出血发生率较低(1.6% vs . 1.8%)。肺炎的风险在行髋关节和膝关节置换术的亚组中最为明显(优势比1.21,95%可信区间1.08-1.36;P = 0.001)。在艰难梭菌相关结肠炎或急性肾损伤发生率方面,两组间无显著差异。结论:我们发现术前使用PPI与较高的肺炎发生率相关,特别是在接受髋关节和膝关节置换手术的患者中,以及较低的胃肠道出血发生率。术前服用PPI的患者应在手术后接受旨在降低肺炎风险的治疗,如积极的胸部物理治疗。
{"title":"Association between preoperative proton pump inhibitor use and postoperative infectious and renal complications following major elective surgery.","authors":"Luc Dubois, J Andrew McClure, Philip M Jones, Marko Mrkobrada, Suzanne Flier, Blayne Welk, Kelly Vogt","doi":"10.1503/cjs.010224","DOIUrl":"10.1503/cjs.010224","url":null,"abstract":"<p><strong>Background: </strong>Use of poton pump inhibitors (PPIs) is associated with increased risk of <i>Clostridioides difficile</i>-associated colitis, pneumonia, and acute kidney injury. Their effect on postoperative complications is unknown. The objective of this study was to investigate the association between PPIs and the risk of <i>C. difficile</i>-associated colitis, pneumonia, and acute kidney injury following elective surgery.</p><p><strong>Methods: </strong>In this population-based, matched cohort study, we identified patients who had filled a PPI prescription within 90 days before major elective surgery (2010-2019). Study outcomes included <i>C. difficile</i>-associated colitis, pneumonia, acute kidney injury, gastrointestinal bleeding, and death within 90 days of surgery. We matched patients 1-to-1 on the basis of age, sex, procedure, date of surgery, and a propensity score predicting PPI exposure. We used logistic regression to evaluate between-group differences.</p><p><strong>Results: </strong>Of 313 163 patients, 89 047 (28.4%) used PPIs; of those, 79 681 were successfully matched to patients who did not use PPIs. The risk of the composite outcome (acute kidney injury, pneumonia, <i>C. difficile</i>-associated colitis, and death) among the patients who used PPIs was slightly higher than among the patients who did not use PPIs (10.6% v. 10.2 4%), and was driven primarily by a higher rate of pneumonia among those who used PPIs (4.0% v. 3.7%). There was a lower rate of gastrointestinal bleeding among the patients who used PPIs (1.6% v. 1.8%). The risk of pneumonia was most pronounced in the subgroup undergoing hip and knee replacement (odds ratio 1.21, 95% confidence interval 1.08-1.36; <i>p</i> = 0.001). There were no significant differences between groups with regard to rates of <i>C. difficile</i>-associated colitis or acute kidney injury.</p><p><strong>Conclusion: </strong>We found that preoperative PPI use was associated with higher rates of pneumonia, particularly among patients undergoing hip and knee replacement surgery, and lower rates of gastrointestinal bleeding. Patients taking a PPI before surgery should be targeted for therapies aimed at reducing pneumonia risk, such as aggressive chest physiotherapy, following their operation.</p>","PeriodicalId":9573,"journal":{"name":"Canadian Journal of Surgery","volume":"68 4","pages":"E305-E312"},"PeriodicalIF":2.2,"publicationDate":"2025-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12279390/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144641889","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-15Print Date: 2025-07-01DOI: 10.1503/cjs.007124
Jovana Momic, Laura Allen, Kelly Vogt, Daniele Wiseman, Bradley Moffat
Background: Traditionally, pulmonary thrombi following trauma were believed to occur secondary to embolization from deep vein thrombosis (DVT). However, computed tomography (CT) during initial trauma resuscitation has identified pulmonary thrombi, which raises the possibility of primary pulmonary thrombosis as a distinct clinical entity. This study identifies cases of pulmonary thrombosis identified immediately after trauma and describes associated injury patterns and treatments.
Methods: We conducted a retrospective review of the trauma and radiology registries at a Canadian level-1 trauma centre from January 2010 to April 2021. A chart review identified patients with pulmonary thrombi on initial CT. We extracted and analyzed patient demographic characteristics, mechanism of injury, summary of injuries, treatments, and outcomes.
Results: A total of 24 patients (15 male, 9 female; mean age 54, standard deviation [SD] 18.6, yr) met the inclusion criteria. All patients experienced blunt trauma (mean Injury Severity Score 23.5, SD 9.5). Rib fractures (n = 11, 46%), pneumohemothorax (n = 7, 29%), and spinal fractures (n = 8, 33%) were common. Four patients had a concomitant DVT, and 10 patients did not undergo assessment for DVT; 10 patients were identified as having primary pulmonary thrombosis. Treatment was started in 18 patients (75%): 9 patients were treated with dalteparin, 2 with dalteparin and inferior vena cava (IVC) filter, 6 with IVC filter in isolation, and 1 with IVC filter and intravenous heparin. Five patients (21%) died from their injuries.
Conclusion: Early pulmonary thrombosis was associated with chest injuries, often without DVT. These findings challenge the traditionally held view of DVT embolization as the cause of pulmonary thrombosis immediately following trauma and suggest that primary pulmonary thrombosis is a distinct clinical entity.
{"title":"Traumatic primary pulmonary thrombosis: injury and treatment patterns of a distinct clinical entity.","authors":"Jovana Momic, Laura Allen, Kelly Vogt, Daniele Wiseman, Bradley Moffat","doi":"10.1503/cjs.007124","DOIUrl":"10.1503/cjs.007124","url":null,"abstract":"<p><strong>Background: </strong>Traditionally, pulmonary thrombi following trauma were believed to occur secondary to embolization from deep vein thrombosis (DVT). However, computed tomography (CT) during initial trauma resuscitation has identified pulmonary thrombi, which raises the possibility of primary pulmonary thrombosis as a distinct clinical entity. This study identifies cases of pulmonary thrombosis identified immediately after trauma and describes associated injury patterns and treatments.</p><p><strong>Methods: </strong>We conducted a retrospective review of the trauma and radiology registries at a Canadian level-1 trauma centre from January 2010 to April 2021. A chart review identified patients with pulmonary thrombi on initial CT. We extracted and analyzed patient demographic characteristics, mechanism of injury, summary of injuries, treatments, and outcomes.</p><p><strong>Results: </strong>A total of 24 patients (15 male, 9 female; mean age 54, standard deviation [SD] 18.6, yr) met the inclusion criteria. All patients experienced blunt trauma (mean Injury Severity Score 23.5, SD 9.5). Rib fractures (<i>n</i> = 11, 46%), pneumohemothorax (<i>n</i> = 7, 29%), and spinal fractures (<i>n</i> = 8, 33%) were common. Four patients had a concomitant DVT, and 10 patients did not undergo assessment for DVT; 10 patients were identified as having primary pulmonary thrombosis. Treatment was started in 18 patients (75%): 9 patients were treated with dalteparin, 2 with dalteparin and inferior vena cava (IVC) filter, 6 with IVC filter in isolation, and 1 with IVC filter and intravenous heparin. Five patients (21%) died from their injuries.</p><p><strong>Conclusion: </strong>Early pulmonary thrombosis was associated with chest injuries, often without DVT. These findings challenge the traditionally held view of DVT embolization as the cause of pulmonary thrombosis immediately following trauma and suggest that primary pulmonary thrombosis is a distinct clinical entity.</p>","PeriodicalId":9573,"journal":{"name":"Canadian Journal of Surgery","volume":"68 4","pages":"E289-E295"},"PeriodicalIF":2.2,"publicationDate":"2025-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12279389/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144641890","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-10Print Date: 2025-07-01DOI: 10.1503/cjs.012923
Krista Hardy, Caleb Leung, Jonathan Seto, Simon Tewes, Wenjing He, Ashley Vergis
Background: Laparoscopic Roux-en-Y gastric bypass (LRYGB) is a common bariatric procedure, but patients often experience extended inpatient stays. Given that Enhanced Recovery After Surgery (ERAS) protocols aim to expedite recovery and discharge, we sought to evaluate the impact of introducing an overnight short-stay unit with ERAS protocols, along with transfer protocols for patients requiring prolonged care.
Methods: We retrospectively reviewed prospectively collected data on LRYGBs performed between November 2017 and December 2020. Postoperative evaluations were conducted 16-21 hours after surgery. Patients were educated about potential complications and required to stay within 1 hour of a tertiary centre for 7 days. We analyzed descriptive outcomes including length of stay (LOS), 30-day emergency department (ED) presentations, and 7-day and 30-day readmissions.
Results: Among the 439 patients, the postoperative day 1 discharge rate was 94.8%, and the day 2 discharge rate was 1.8%. A small proportion of patients (2.7%) required transfer for anticipated prolonged LOS, primarily for delayed intra-abdominal hemorrhage requiring reoperation (66.7%) and as a precautionary measure for technically challenging procedures (16.7%). Two brief admissions to the intensive care unit occurred, with no deaths. Overall, 45 (10.3%) patients presented to the ED within 30 days, 12 (2.7%) patients were readmitted within 7 days, and 18 (4.1%) patients were readmitted within 30 days. Gastrointestinal intolerance was the most common reason for readmission.
Conclusion: An ERAS protocol for LRYGB enabled safe next-day discharge for 94.8% of patients. Rates of ED presentation and readmission aligned with existing literature, supporting the feasibility of next-day discharge for appropriately selected patients. These findings contribute to the evidence base for optimizing postoperative care and enhancing patient outcomes in bariatric surgery.
{"title":"Enhanced Recovery After Surgery and next-day discharge after laparoscopic Roux-en-Y gastric bypass.","authors":"Krista Hardy, Caleb Leung, Jonathan Seto, Simon Tewes, Wenjing He, Ashley Vergis","doi":"10.1503/cjs.012923","DOIUrl":"10.1503/cjs.012923","url":null,"abstract":"<p><strong>Background: </strong>Laparoscopic Roux-en-Y gastric bypass (LRYGB) is a common bariatric procedure, but patients often experience extended inpatient stays. Given that Enhanced Recovery After Surgery (ERAS) protocols aim to expedite recovery and discharge, we sought to evaluate the impact of introducing an overnight short-stay unit with ERAS protocols, along with transfer protocols for patients requiring prolonged care.</p><p><strong>Methods: </strong>We retrospectively reviewed prospectively collected data on LRYGBs performed between November 2017 and December 2020. Postoperative evaluations were conducted 16-21 hours after surgery. Patients were educated about potential complications and required to stay within 1 hour of a tertiary centre for 7 days. We analyzed descriptive outcomes including length of stay (LOS), 30-day emergency department (ED) presentations, and 7-day and 30-day readmissions.</p><p><strong>Results: </strong>Among the 439 patients, the postoperative day 1 discharge rate was 94.8%, and the day 2 discharge rate was 1.8%. A small proportion of patients (2.7%) required transfer for anticipated prolonged LOS, primarily for delayed intra-abdominal hemorrhage requiring reoperation (66.7%) and as a precautionary measure for technically challenging procedures (16.7%). Two brief admissions to the intensive care unit occurred, with no deaths. Overall, 45 (10.3%) patients presented to the ED within 30 days, 12 (2.7%) patients were readmitted within 7 days, and 18 (4.1%) patients were readmitted within 30 days. Gastrointestinal intolerance was the most common reason for readmission.</p><p><strong>Conclusion: </strong>An ERAS protocol for LRYGB enabled safe next-day discharge for 94.8% of patients. Rates of ED presentation and readmission aligned with existing literature, supporting the feasibility of next-day discharge for appropriately selected patients. These findings contribute to the evidence base for optimizing postoperative care and enhancing patient outcomes in bariatric surgery.</p>","PeriodicalId":9573,"journal":{"name":"Canadian Journal of Surgery","volume":"68 4","pages":"E274-E280"},"PeriodicalIF":2.2,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12263330/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144607458","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-10Print Date: 2025-07-01DOI: 10.1503/cjs.012724
Hilalion San Ahn, Alexie Leclerc, Jennifer Shamess, Jordi Pardo, Catherine Dube, Alaa Rostom, Natalia Calo, Kednapa Thavorn, Daniel I McIsaac, David Smith, Husein Moloo
Background: Most guidelines recommend use of sterile water in single-use plastic bottles for irrigation in colonoscopy, a recommendation extrapolated from case reports of infection linked to endoscopic retrograde cholangiopancreatography. Our objective was to identify evidence exploring the impact of tap versus sterile water in colonoscopy on patient, health care resource, and environmental outcomes.
Methods: We performed a scoping review and included any study examining the effects of irrigation source during colonoscopy. A health information specialist searched Embase, MEDLINE, CINAHL, and Web of Science from inception to March 2024 using Peer Review of Electronic Search Strategies standards. Two reviewers performed screening and data extraction using a standardized form. We conducted a quantitative analysis of patient outcomes.
Results: Of 335 identified articles, we included 3. All were prospective studies published between 1996 and 2002. Overall, 137 colonoscopies and 38 flexible sigmoidoscopies were reported. Two studies compared sterile versus tap water, with 7 of 118 (6%) and 35 of 327 (11%) positive water cultures, respectively. There were no clinical adverse events. One study compared tap water at warm versus room temperature and measured patient pain scores (2/10 and 4/10, respectively). Infectious complications were not reported.
Conclusion: There is limited evidence to support either tap or sterile water in irrigation for colonoscopy, but potable tap water may be a safe choice and is environmentally and economically more beneficial than sterile water. In the context of the climate crisis and increasing economic health care burden, tap water in reusable bottles should be strongly considered for irrigation in colonoscopy. Registration: Open Science Framework Registry, https://osf.io/8dgck.
背景:大多数指南建议在结肠镜检查中使用一次性塑料瓶中的无菌水进行冲洗,这一建议是从内镜逆行胆管造影术相关感染的病例报告中推断出来的。我们的目的是寻找证据,探讨结肠镜检查中自来水与无菌水对患者、医疗资源和环境结果的影响。方法:我们进行了一项范围综述,并纳入了所有在结肠镜检查中检查灌源效果的研究。一名健康信息专家使用电子搜索策略标准的同行评审对Embase、MEDLINE、CINAHL和Web of Science进行了从成立到2024年3月的搜索。两名审稿人使用标准化表格进行筛选和数据提取。我们对患者结果进行了定量分析。结果:在鉴定的335篇文章中,我们纳入了3篇。所有研究都是在1996年至2002年间发表的前瞻性研究。总共报道了137例结肠镜检查和38例乙状结肠镜检查。两项研究将无菌水与自来水进行了比较,118人中有7人(6%)培养阳性,327人中有35人(11%)培养阳性。无临床不良事件。一项研究比较了温水和室温下的自来水,并测量了患者的疼痛评分(分别为2/10和4/10)。感染并发症未见报道。结论:支持自来水或无菌水用于结肠镜冲洗的证据有限,但饮用自来水可能是一种安全的选择,并且在环境和经济上比无菌水更有益。在气候危机和经济卫生保健负担增加的背景下,应强烈考虑在结肠镜检查中使用可重复使用的瓶装自来水进行灌溉。注册:Open Science Framework Registry, https://osf.io/8dgck。
{"title":"Testing the precautionary principle: a scoping review comparing potable tap and sterile water for irrigation in colonoscopy.","authors":"Hilalion San Ahn, Alexie Leclerc, Jennifer Shamess, Jordi Pardo, Catherine Dube, Alaa Rostom, Natalia Calo, Kednapa Thavorn, Daniel I McIsaac, David Smith, Husein Moloo","doi":"10.1503/cjs.012724","DOIUrl":"10.1503/cjs.012724","url":null,"abstract":"<p><strong>Background: </strong>Most guidelines recommend use of sterile water in single-use plastic bottles for irrigation in colonoscopy, a recommendation extrapolated from case reports of infection linked to endoscopic retrograde cholangiopancreatography. Our objective was to identify evidence exploring the impact of tap versus sterile water in colonoscopy on patient, health care resource, and environmental outcomes.</p><p><strong>Methods: </strong>We performed a scoping review and included any study examining the effects of irrigation source during colonoscopy. A health information specialist searched Embase, MEDLINE, CINAHL, and Web of Science from inception to March 2024 using Peer Review of Electronic Search Strategies standards. Two reviewers performed screening and data extraction using a standardized form. We conducted a quantitative analysis of patient outcomes.</p><p><strong>Results: </strong>Of 335 identified articles, we included 3. All were prospective studies published between 1996 and 2002. Overall, 137 colonoscopies and 38 flexible sigmoidoscopies were reported. Two studies compared sterile versus tap water, with 7 of 118 (6%) and 35 of 327 (11%) positive water cultures, respectively. There were no clinical adverse events. One study compared tap water at warm versus room temperature and measured patient pain scores (2/10 and 4/10, respectively). Infectious complications were not reported.</p><p><strong>Conclusion: </strong>There is limited evidence to support either tap or sterile water in irrigation for colonoscopy, but potable tap water may be a safe choice and is environmentally and economically more beneficial than sterile water. In the context of the climate crisis and increasing economic health care burden, tap water in reusable bottles should be strongly considered for irrigation in colonoscopy. <b>Registration:</b> Open Science Framework Registry, https://osf.io/8dgck.</p>","PeriodicalId":9573,"journal":{"name":"Canadian Journal of Surgery","volume":"68 4","pages":"E281-E288"},"PeriodicalIF":2.2,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12263332/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144607459","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-06-18Print Date: 2025-05-01DOI: 10.1503/cjs.015723
Stuti M Tanya, Anne Xuan-Lan Nguyen, Maxine Joly-Chevrier, Daiana Roxana Pur, Sanjay Sharma, Fiona Costello, Femida Kherani, Vincent Quoc-Huy Trinh, Isabelle Hardy, Leonardo Lando
Background: Disparate gender representation among Canadian academic surgeons is documented; however, the association of academic rank with research productivity across all surgical specialties is not well understood. Our objective was to assess differences in gender representation by academic rank and research productivity metrics for surgical specialties in Canadian academic centres.
Methods: This retrospective, cross-sectional, comparative study used online public databases in 2021. Data sources included the Canadian Resident Matching Service program descriptions, College of Physicians and Surgeons databases, the Scopus platform, and professional websites. Gender distribution by academic rank, research productivity metrics, institution, and surgical specialty were tested for a 0.5 proportion rate. We used a generalized logistic regression model adjusting for confounders to assess gender association with ordinally ranked academic rank. We defined significance by p < 0.05 with reported 95% confidence intervals.
Results: We assessed 10 surgical specialties across 17 Canadian academic institutions. Women surgeons were underrepresented in 16 out of 17 centres (p < 0.001), comprising the majority in only obstetrics-gynecology (p < 0.001). Women were also less represented as assistant (37%), associate (27%), and full professors (18%) (p < 0.001), with lower mean h-index (6.4, p < 0.001), years active in research (11.5, p < 0.001), number of publications (18, p < 0.001), and m-quotient (0.42, p < 0.001). Multivariate analysis showed that men were more likely to be represented in senior professorship regardless of research productivity, institution, and specialty determinants (odds ratio 1.30-1.33, p = 0.001-0.024).
Conclusion: Women surgeons were underrepresented across all academic ranks, were less likely to achieve senior professorship, and had lower research productivity metrics.
{"title":"Gender representation in professorship and research productivity across all surgical specialties in Canadian academic institutions.","authors":"Stuti M Tanya, Anne Xuan-Lan Nguyen, Maxine Joly-Chevrier, Daiana Roxana Pur, Sanjay Sharma, Fiona Costello, Femida Kherani, Vincent Quoc-Huy Trinh, Isabelle Hardy, Leonardo Lando","doi":"10.1503/cjs.015723","DOIUrl":"10.1503/cjs.015723","url":null,"abstract":"<p><strong>Background: </strong>Disparate gender representation among Canadian academic surgeons is documented; however, the association of academic rank with research productivity across all surgical specialties is not well understood. Our objective was to assess differences in gender representation by academic rank and research productivity metrics for surgical specialties in Canadian academic centres.</p><p><strong>Methods: </strong>This retrospective, cross-sectional, comparative study used online public databases in 2021. Data sources included the Canadian Resident Matching Service program descriptions, College of Physicians and Surgeons databases, the Scopus platform, and professional websites. Gender distribution by academic rank, research productivity metrics, institution, and surgical specialty were tested for a 0.5 proportion rate. We used a generalized logistic regression model adjusting for confounders to assess gender association with ordinally ranked academic rank. We defined significance by <i>p</i> < 0.05 with reported 95% confidence intervals.</p><p><strong>Results: </strong>We assessed 10 surgical specialties across 17 Canadian academic institutions. Women surgeons were underrepresented in 16 out of 17 centres (<i>p</i> < 0.001), comprising the majority in only obstetrics-gynecology (<i>p</i> < 0.001). Women were also less represented as assistant (37%), associate (27%), and full professors (18%) (<i>p</i> < 0.001), with lower mean <i>h</i>-index (6.4, <i>p</i> < 0.001), years active in research (11.5, <i>p</i> < 0.001), number of publications (18, <i>p</i> < 0.001), and <i>m</i>-quotient (0.42, <i>p</i> < 0.001). Multivariate analysis showed that men were more likely to be represented in senior professorship regardless of research productivity, institution, and specialty determinants (odds ratio 1.30-1.33, <i>p</i> = 0.001-0.024).</p><p><strong>Conclusion: </strong>Women surgeons were underrepresented across all academic ranks, were less likely to achieve senior professorship, and had lower research productivity metrics.</p>","PeriodicalId":9573,"journal":{"name":"Canadian Journal of Surgery","volume":"68 3","pages":"E253-E264"},"PeriodicalIF":2.2,"publicationDate":"2025-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12180920/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144324590","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}