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}
Pub Date : 2025-06-18Print Date: 2025-05-01DOI: 10.1503/cjs.009924
Brodie Nolan, Morgan Schellenberg, Chad G Ball, Kelly N Vogt, Jordan Nantais
SummaryAlthough blood transfusion as a clinical practice dates back several centuries, the optimal approach remains controversial. In the last decade there has been renewed interest in whole blood transfusion over component therapy for trauma patients. A recent multicentre prospective study assessed the impact of whole blood resuscitation on survival among injured patients in hemorrhagic shock presenting to trauma centres in the United States. We have undertaken an Evidence Based Review in Surgery of that study to appraise how its authors tackled an important clinical question with increasing relevance in modern trauma practice: What is the role of whole blood in trauma resuscitation?
{"title":"Evidence Based Reviews in Surgery: a critical appraisal of whole blood resuscitation in injured patients.","authors":"Brodie Nolan, Morgan Schellenberg, Chad G Ball, Kelly N Vogt, Jordan Nantais","doi":"10.1503/cjs.009924","DOIUrl":"10.1503/cjs.009924","url":null,"abstract":"<p><p><b>Summary</b>Although blood transfusion as a clinical practice dates back several centuries, the optimal approach remains controversial. In the last decade there has been renewed interest in whole blood transfusion over component therapy for trauma patients. A recent multicentre prospective study assessed the impact of whole blood resuscitation on survival among injured patients in hemorrhagic shock presenting to trauma centres in the United States. We have undertaken an Evidence Based Review in Surgery of that study to appraise how its authors tackled an important clinical question with increasing relevance in modern trauma practice: What is the role of whole blood in trauma resuscitation?</p>","PeriodicalId":9573,"journal":{"name":"Canadian Journal of Surgery","volume":"68 3","pages":"E271-E273"},"PeriodicalIF":2.2,"publicationDate":"2025-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12180917/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144324589","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.012424
Marko Simunovic, Christine Fahim, Vanja Grubac, David R Urbach, Greg Pond, Erin Kennedy, Nancy N Baxter
Background: Given that diagnostic, neoadjuvant treatment, and surgical approaches to rectal cancer have changed markedly in the last 25 years, knowledge translation (KT) may be useful to optimize rectal cancer surgery and improve patient outcomes. We sought to evaluate the impact of surgeon-directed KT to improve the quality of rectal cancer surgery on local tumour recurrence in Ontario.
Methods: Ontario's 14 health regions were previously categorized into 2 high-intensity and 12 low-intensity KT regions, based on KT methods (e.g., theory, audit, feedback), applied from 2006 to 2012 to improve the quality of rectal cancer surgery. In the high-intensity regions, efforts encouraged preoperative magnetic resonance imaging, appropriate radiation, and optimal surgical technique. We abstracted hospital chart data from across Ontario for a random sample of cases from 2010 to 2012 based on the respective population of a region and the relative hospital case volume within their region. The main study outcome was local tumour recurrence.
Results: In the high-intensity and low-intensity KT regions, we reviewed data from 523 (48.6%) and 557 (51.4%) patients, respectively. Descriptive variables (e.g., age, sex, tumour stage) were similar between groups. In the high- and low-intensity regions, the proportion of patients with a permanent stoma was 31.4% and 26.4% (p = 0.08), the proportion with positive radial margins was 8.0% and 6.1% (p = 0.2), and the proportion with local tumour recurrence was 6.3% and 5.2% (p = 0.2), respectively. The adjusted risk of time to local recurrence was similar in the high- and low-intensity KT regions (hazard ratio 0.72, 95% confidence interval 0.50-1.05).
Conclusion: The use of resource-intense methods was not associated with improved patient outcomes, including local tumour recurrence. New approaches are needed to optimize the population-level quality of rectal cancer surgery.
{"title":"High- versus low-intensity knowledge translation interventions for surgeons and rates of local tumour recurrence after rectal cancer surgery: an Ontario study.","authors":"Marko Simunovic, Christine Fahim, Vanja Grubac, David R Urbach, Greg Pond, Erin Kennedy, Nancy N Baxter","doi":"10.1503/cjs.012424","DOIUrl":"10.1503/cjs.012424","url":null,"abstract":"<p><strong>Background: </strong>Given that diagnostic, neoadjuvant treatment, and surgical approaches to rectal cancer have changed markedly in the last 25 years, knowledge translation (KT) may be useful to optimize rectal cancer surgery and improve patient outcomes. We sought to evaluate the impact of surgeon-directed KT to improve the quality of rectal cancer surgery on local tumour recurrence in Ontario.</p><p><strong>Methods: </strong>Ontario's 14 health regions were previously categorized into 2 high-intensity and 12 low-intensity KT regions, based on KT methods (e.g., theory, audit, feedback), applied from 2006 to 2012 to improve the quality of rectal cancer surgery. In the high-intensity regions, efforts encouraged preoperative magnetic resonance imaging, appropriate radiation, and optimal surgical technique. We abstracted hospital chart data from across Ontario for a random sample of cases from 2010 to 2012 based on the respective population of a region and the relative hospital case volume within their region. The main study outcome was local tumour recurrence.</p><p><strong>Results: </strong>In the high-intensity and low-intensity KT regions, we reviewed data from 523 (48.6%) and 557 (51.4%) patients, respectively. Descriptive variables (e.g., age, sex, tumour stage) were similar between groups. In the high- and low-intensity regions, the proportion of patients with a permanent stoma was 31.4% and 26.4% (<i>p</i> = 0.08), the proportion with positive radial margins was 8.0% and 6.1% (<i>p</i> = 0.2), and the proportion with local tumour recurrence was 6.3% and 5.2% (<i>p</i> = 0.2), respectively. The adjusted risk of time to local recurrence was similar in the high- and low-intensity KT regions (hazard ratio 0.72, 95% confidence interval 0.50-1.05).</p><p><strong>Conclusion: </strong>The use of resource-intense methods was not associated with improved patient outcomes, including local tumour recurrence. New approaches are needed to optimize the population-level quality of rectal cancer surgery.</p>","PeriodicalId":9573,"journal":{"name":"Canadian Journal of Surgery","volume":"68 3","pages":"E245-E252"},"PeriodicalIF":2.2,"publicationDate":"2025-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12180919/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144324591","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.000325
Riley Hemstock, Sheila McRae, Ian Laxdal, Thomas Mutter, Kevin Friesen, Heather J Prior, Jason Old, Gregory Stranges, Devin Lemmex, James Dubberley, Jonathan Marsh, Robert Longstaffe, Peter MacDonald, Jarret Woodmass
Background: Outpatient overprescribing of opioids in the postoperative period contributes to the opioid epidemic. Given that patient education and evidence-informed prescription protocols have reduced postoperative opioid use in small, randomized trials, we sought to evaluate the effectiveness of a multimodal opioid reduction protocol, implemented institution-wide at an outpatient Canadian orthopedic surgery centre.
Methods: In this pre-post intervention study, we used deidentified health administrative data from a provincial data repository to identify all opioid-naive patients who underwent outpatient shoulder or knee surgery at a single institution between 2013 and 2022. An opioid restriction protocol was implemented in 2019, including an educational pamphlet, perioperative verbal education, and a standardized postoperative analgesic prescription. Outcomes analyzed included dispensed morphine milligram equivalents (MME) per patient within 180 days of surgery and chronic opioid use, defined as opioids dispensed 180-270 days after surgery. Prescriptions dispensed from any provider were included.
Results: We included 8244 patients preintervention and 2205 patients postintervention in the analyses. The average MME dispensed per patient decreased by 18% (57.8 MME, 95% confidence interval 45.0-70.6). The proportion of patients who filled opioid prescriptions beyond 180 days after surgery decreased from 4.8% to 2.6% (p < 0.001). These findings remained consistent after adjustment for age, sex, socioeconomic status, mental health, and medical comorbidity in multivariable regression analyses.
Conclusion: The volume of opioids dispensed and the number of chronic opioid users were significantly reduced among patients who underwent outpatient orthopedic surgery after the institution-wide implementation of a multimodal postoperative opioid reduction protocol.
{"title":"Changes in opioid distribution and chronic opioid users following outpatient orthopedic surgery: a pre-post intervention study.","authors":"Riley Hemstock, Sheila McRae, Ian Laxdal, Thomas Mutter, Kevin Friesen, Heather J Prior, Jason Old, Gregory Stranges, Devin Lemmex, James Dubberley, Jonathan Marsh, Robert Longstaffe, Peter MacDonald, Jarret Woodmass","doi":"10.1503/cjs.000325","DOIUrl":"10.1503/cjs.000325","url":null,"abstract":"<p><strong>Background: </strong>Outpatient overprescribing of opioids in the postoperative period contributes to the opioid epidemic. Given that patient education and evidence-informed prescription protocols have reduced postoperative opioid use in small, randomized trials, we sought to evaluate the effectiveness of a multimodal opioid reduction protocol, implemented institution-wide at an outpatient Canadian orthopedic surgery centre.</p><p><strong>Methods: </strong>In this pre-post intervention study, we used deidentified health administrative data from a provincial data repository to identify all opioid-naive patients who underwent outpatient shoulder or knee surgery at a single institution between 2013 and 2022. An opioid restriction protocol was implemented in 2019, including an educational pamphlet, perioperative verbal education, and a standardized postoperative analgesic prescription. Outcomes analyzed included dispensed morphine milligram equivalents (MME) per patient within 180 days of surgery and chronic opioid use, defined as opioids dispensed 180-270 days after surgery. Prescriptions dispensed from any provider were included.</p><p><strong>Results: </strong>We included 8244 patients preintervention and 2205 patients postintervention in the analyses. The average MME dispensed per patient decreased by 18% (57.8 MME, 95% confidence interval 45.0-70.6). The proportion of patients who filled opioid prescriptions beyond 180 days after surgery decreased from 4.8% to 2.6% (<i>p</i> < 0.001). These findings remained consistent after adjustment for age, sex, socioeconomic status, mental health, and medical comorbidity in multivariable regression analyses.</p><p><strong>Conclusion: </strong>The volume of opioids dispensed and the number of chronic opioid users were significantly reduced among patients who underwent outpatient orthopedic surgery after the institution-wide implementation of a multimodal postoperative opioid reduction protocol.</p>","PeriodicalId":9573,"journal":{"name":"Canadian Journal of Surgery","volume":"68 3","pages":"E265-E270"},"PeriodicalIF":2.2,"publicationDate":"2025-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12180918/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144324588","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 : 2025-06-10Print Date: 2025-05-01DOI: 10.1503/cjs.003423
Jude Kornelsen, Gal Av-Gay, Anshu Parajulee, Nancy Humber, Sean Ebert, Tom Skinner, Kathrin Stoll
Background: Many rural communities have lost local access to procedural care, and although rural surgical services have endured in some regions, questions regarding quality and safety of care have persisted. Using retrospective observational data, we sought to compare adverse outcomes of the most common surgical procedures performed at rural facilities in British Columbia and outcomes by provider specialty. Our objective was to show whether the efficacy of surgical care at rural facilities is comparable to that of larger referral facilities and whether family physicians with enhanced surgical skills (FPESS) have outcomes comparable to those of specialists at referral facilities for low-morbidity patients.
Methods: We included patients who had a colonoscopy, hernia repair, appendectomy, or cesarean delivery at 1 of 7 rural hospitals in BC that participated in the Rural Surgical and Obstetrics Networks of BC and corresponding referral facilities between 2016 and 2021. To control for differences in the acuity of patients between facility types, we risk stratified data by patient comorbidity level, in addition to adjusting for other demographic differences using multivariable Firth logistic regression analysis. We also compared the outcomes of FPESS with those of regional specialists for low-acuity patients in a similar manner. We calculated adjusted odds ratios (ORs), used tests of noninferiority to obtain p values for the adjusted ORs, and calculated E-values to estimate the extent to which our findings could be due to other unmeasured confounding.
Results: Most surgical procedures at rural hospitals were performed by FPESS (n = 4403, 34.9%) and visiting general surgeons (n = 7317, 57.9%). We found that the quality of care at rural facilities was at least equivalent to the quality at referral facilities in rural BC for colonoscopy, hernia repair, and appendectomy, and that FPESS had outcomes at least equivalent to those of specialists for low-acuity patients.
Conclusion: Our findings provide evidence in favour of the efficacy of rural procedural care at BC facilities, and although these results are not inherently generalizable to other populations, we believe they illustrate the potential for high-quality rural care for low-acuity procedures in similar settings. These findings are an important step toward documenting rural-specific outcomes and creating attendant benchmarks for rural practice.
{"title":"Rural surgical and obstetric facility-level outcomes for index procedures: a retrospective cohort study (2016-2021).","authors":"Jude Kornelsen, Gal Av-Gay, Anshu Parajulee, Nancy Humber, Sean Ebert, Tom Skinner, Kathrin Stoll","doi":"10.1503/cjs.003423","DOIUrl":"10.1503/cjs.003423","url":null,"abstract":"<p><strong>Background: </strong>Many rural communities have lost local access to procedural care, and although rural surgical services have endured in some regions, questions regarding quality and safety of care have persisted. Using retrospective observational data, we sought to compare adverse outcomes of the most common surgical procedures performed at rural facilities in British Columbia and outcomes by provider specialty. Our objective was to show whether the efficacy of surgical care at rural facilities is comparable to that of larger referral facilities and whether family physicians with enhanced surgical skills (FPESS) have outcomes comparable to those of specialists at referral facilities for low-morbidity patients.</p><p><strong>Methods: </strong>We included patients who had a colonoscopy, hernia repair, appendectomy, or cesarean delivery at 1 of 7 rural hospitals in BC that participated in the Rural Surgical and Obstetrics Networks of BC and corresponding referral facilities between 2016 and 2021. To control for differences in the acuity of patients between facility types, we risk stratified data by patient comorbidity level, in addition to adjusting for other demographic differences using multivariable Firth logistic regression analysis. We also compared the outcomes of FPESS with those of regional specialists for low-acuity patients in a similar manner. We calculated adjusted odds ratios (ORs), used tests of noninferiority to obtain <i>p</i> values for the adjusted ORs, and calculated E-values to estimate the extent to which our findings could be due to other unmeasured confounding.</p><p><strong>Results: </strong>Most surgical procedures at rural hospitals were performed by FPESS (<i>n</i> = 4403, 34.9%) and visiting general surgeons (<i>n</i> = 7317, 57.9%). We found that the quality of care at rural facilities was at least equivalent to the quality at referral facilities in rural BC for colonoscopy, hernia repair, and appendectomy, and that FPESS had outcomes at least equivalent to those of specialists for low-acuity patients.</p><p><strong>Conclusion: </strong>Our findings provide evidence in favour of the efficacy of rural procedural care at BC facilities, and although these results are not inherently generalizable to other populations, we believe they illustrate the potential for high-quality rural care for low-acuity procedures in similar settings. These findings are an important step toward documenting rural-specific outcomes and creating attendant benchmarks for rural practice.</p>","PeriodicalId":9573,"journal":{"name":"Canadian Journal of Surgery","volume":"68 3","pages":"E221-E234"},"PeriodicalIF":2.2,"publicationDate":"2025-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12169910/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144265314","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 : 2025-06-10Print Date: 2025-05-01DOI: 10.1503/cjs.003824
Jeremie Thibault, Walid Naciri, Dominique M Rouleau, Julien Chapleau
Background: Although fluoroscopy is used routinely, surgeons and orthopedic residents are inadequately educated about the dangers associated with radiation exposure and protective measures in the operating room. We sought to report the average radiation exposure during common orthopedic trauma procedures for different team members and to determine if the fluoroscopy emitting report is correlated with the radiation measured in the room.
Methods: We conducted a prospective observational study over 3 months in a level 1 trauma centre. We collected radiation levels from dosimeters in different standardized locations at 1 m, 2 m, and 3 m from the C-arm machine, labelled as dosimeters A, B, and C, corresponding to the locations of the surgeon, anesthesiologist, and nurse, respectively). We classified mean exposure (and standard deviations [SDs] according to the body part exposed and the dose delivered.
Results: We included recordings from 100 patients who underwent surgery for fractures, of which 50 involved a distal extremity, 31 involved a proximal extremity and 19 involved the pelvic area. Dosimeter A (surgeon) recorded a significantly higher amount of radiation at a mean of 20.35 (SD 54.25) μSv than the other 2 dosimeters (B [anesthesiologist]: 0.87 [SD 1.55] μSv; C [nurse]: 0.49 [SD 0.92] μSv), regardless of the fracture location. Higher radiation levels were recorded for fixation of centrally located fractures, followed by lower-extremity fractures and upper-extremity fractures. Half-dose and quarter-dose fluoroscopy emitted statistically lower radiation than standard-dose fluoroscopy. The radiation report from the fluoroscopy machine was highly correlated with the measured radiation (ρ = 0.93; r2 = 0.909, p < 0.001).
Conclusion: Radiation exposure is much higher closer to the fluoroscopy machine and decreases following an inverse-square law from the radiation source, becoming negligible at 2 m from the source. Using the low-dose radiation mode can significantly decrease radiation exposure.
{"title":"Intraoperative radiation exposure in a level 1 trauma centre orthopedic operating room.","authors":"Jeremie Thibault, Walid Naciri, Dominique M Rouleau, Julien Chapleau","doi":"10.1503/cjs.003824","DOIUrl":"10.1503/cjs.003824","url":null,"abstract":"<p><strong>Background: </strong>Although fluoroscopy is used routinely, surgeons and orthopedic residents are inadequately educated about the dangers associated with radiation exposure and protective measures in the operating room. We sought to report the average radiation exposure during common orthopedic trauma procedures for different team members and to determine if the fluoroscopy emitting report is correlated with the radiation measured in the room.</p><p><strong>Methods: </strong>We conducted a prospective observational study over 3 months in a level 1 trauma centre. We collected radiation levels from dosimeters in different standardized locations at 1 m, 2 m, and 3 m from the C-arm machine, labelled as dosimeters A, B, and C, corresponding to the locations of the surgeon, anesthesiologist, and nurse, respectively). We classified mean exposure (and standard deviations [SDs] according to the body part exposed and the dose delivered.</p><p><strong>Results: </strong>We included recordings from 100 patients who underwent surgery for fractures, of which 50 involved a distal extremity, 31 involved a proximal extremity and 19 involved the pelvic area. Dosimeter A (surgeon) recorded a significantly higher amount of radiation at a mean of 20.35 (SD 54.25) μSv than the other 2 dosimeters (B [anesthesiologist]: 0.87 [SD 1.55] μSv; C [nurse]: 0.49 [SD 0.92] μSv), regardless of the fracture location. Higher radiation levels were recorded for fixation of centrally located fractures, followed by lower-extremity fractures and upper-extremity fractures. Half-dose and quarter-dose fluoroscopy emitted statistically lower radiation than standard-dose fluoroscopy. The radiation report from the fluoroscopy machine was highly correlated with the measured radiation (ρ = 0.93; <i>r</i> <sup>2</sup> = 0.909, <i>p</i> < 0.001).</p><p><strong>Conclusion: </strong>Radiation exposure is much higher closer to the fluoroscopy machine and decreases following an inverse-square law from the radiation source, becoming negligible at 2 m from the source. Using the low-dose radiation mode can significantly decrease radiation exposure.</p>","PeriodicalId":9573,"journal":{"name":"Canadian Journal of Surgery","volume":"68 3","pages":"E235-E241"},"PeriodicalIF":2.2,"publicationDate":"2025-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12169909/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144265313","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}