Pub Date : 2025-10-01Epub Date: 2025-05-26DOI: 10.1177/15533506251344055
Muhammed Said Dalkılıç, Abdullah Şişik, Mehmet Gençtürk, Merih Yılmaz, Hasan Erdem, Chetan Parmar
BackgroundLaparoscopic sleeve gastrectomy (LSG) is the most widely performed bariatric procedure. While advancements like staple line reinforcement (SLR) have reduced hemorrhagic complications, bleeding risks persist. Tranexamic acid (TXA), an antifibrinolytic agent, has shown promise in mitigating bleeding risks in various surgical disciplines, but its efficacy in LSG with SLR remains unexplored. This study aims to evaluate the effect of intraoperative TXA administration on postoperative bleeding outcomes in patients undergoing LSG with oversewing and omentopexy.MethodsThis prospective observational cohort study included 233 patients undergoing LSG with oversewing and omentopexy. Patients were divided into 2 groups: 1 received 1 g of TXA intraoperatively, while the other did not. Hemoglobin differences at 24 and 48 hours postoperatively were the primary outcomes. Secondary outcomes included blood transfusion necessity, re-intervention rates, and 30-day surgical complications.ResultsThere was no statistically significant difference in hemoglobin changes at 24 hours (TXA group: 0.8 ± 0.7 g/dL, 95% CI: 0.67-0.93; control group: 0.9 ± 0.9 g/dL, 95% CI: 0.74-1.06; P = 0.125) or at 48 hours (TXA group: 1.4 ± 1.5 g/dL, 95% CI: 1.12-1.68; control group: 1.5 ± 1.4 g/dL, 95% CI: 1.25-1.75; P = 0.167) between the groups. No patients required transfusions or re-interventions. Five patients in the control group exhibited hemorrhagic drainage exceeding 150 mL, while none in the TXA group experienced similar complications. Length of hospital stay and operative time were similar between the groups (P = 0.124 and 0.746, respectively).ConclusionsTranexamic acid may not significantly impact major bleeding complications following LSG with oversewing and omentopexy but appears to reduce minor hemorrhagic events.
{"title":"The Effect of Prophylactic Intraoperative Tranexamic Acid Use on Bleeding After Laparoscopic Sleeve Gastrectomy With Omentopexy: A Prospective Cohort Study.","authors":"Muhammed Said Dalkılıç, Abdullah Şişik, Mehmet Gençtürk, Merih Yılmaz, Hasan Erdem, Chetan Parmar","doi":"10.1177/15533506251344055","DOIUrl":"10.1177/15533506251344055","url":null,"abstract":"<p><p>BackgroundLaparoscopic sleeve gastrectomy (LSG) is the most widely performed bariatric procedure. While advancements like staple line reinforcement (SLR) have reduced hemorrhagic complications, bleeding risks persist. Tranexamic acid (TXA), an antifibrinolytic agent, has shown promise in mitigating bleeding risks in various surgical disciplines, but its efficacy in LSG with SLR remains unexplored. This study aims to evaluate the effect of intraoperative TXA administration on postoperative bleeding outcomes in patients undergoing LSG with oversewing and omentopexy.MethodsThis prospective observational cohort study included 233 patients undergoing LSG with oversewing and omentopexy. Patients were divided into 2 groups: 1 received 1 g of TXA intraoperatively, while the other did not. Hemoglobin differences at 24 and 48 hours postoperatively were the primary outcomes. Secondary outcomes included blood transfusion necessity, re-intervention rates, and 30-day surgical complications.ResultsThere was no statistically significant difference in hemoglobin changes at 24 hours (TXA group: 0.8 ± 0.7 g/dL, 95% CI: 0.67-0.93; control group: 0.9 ± 0.9 g/dL, 95% CI: 0.74-1.06; <i>P</i> = 0.125) or at 48 hours (TXA group: 1.4 ± 1.5 g/dL, 95% CI: 1.12-1.68; control group: 1.5 ± 1.4 g/dL, 95% CI: 1.25-1.75; <i>P</i> = 0.167) between the groups. No patients required transfusions or re-interventions. Five patients in the control group exhibited hemorrhagic drainage exceeding 150 mL, while none in the TXA group experienced similar complications. Length of hospital stay and operative time were similar between the groups (<i>P</i> = 0.124 and 0.746, respectively).ConclusionsTranexamic acid may not significantly impact major bleeding complications following LSG with oversewing and omentopexy but appears to reduce minor hemorrhagic events.</p>","PeriodicalId":22095,"journal":{"name":"Surgical Innovation","volume":" ","pages":"409-416"},"PeriodicalIF":1.6,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144151351","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-01DOI: 10.1177/15533506251383671
Sara Saffari, Esther Ochoa, Daniel Colchado, Amy Liao, Justin M Sacks, Mohamed A Zayed, Xiaowei Li
Arteriovenous fistulas (AVFs) are the gold standard for vascular access to facilitate hemodialysis, yet traditional surgical techniques are technically demanding, time-intensive, and costly. Additionally, limited suitable AVF sites, due to patient anatomy, vessel quality, and prior access exhaustion, necessitate exploration of novel options. This cadaveric proof-of-concept study introduces the anterior interosseous artery-cephalic vein as a novel AVF site and evaluates the feasibility of a 3D-printed sutureless anastomotic device, the Vaso-Stent, compared to conventional handsewn techniques. Fresh-frozen cadaveric upper limbs were procured to test the surgical feasibility of the proposed AVF model. Surgical exposure of the interosseous artery and adjacent cephalic vein were uncomplicated. A 3D-printed Vaso-Stent was manufactured and facilitated efficient anastomosis in under 1 min, compared with the 4.5 min required for a standard handsewn technique. The device demonstrated ease of placement, robust structural integrity, and resistance to tensile forces. These findings highlight that the Vaso-Stent can provide a simple alternative for AVF creation that reduces operative time and highlight the anterior interosseous artery-cephalic vein configuration as a new and unique hemodialysis access opportunity.
{"title":"Cadaveric Feasibility of A 3D-Printed Vaso-Stent for Sutureless Anterior Interosseous Artery-Cephalic Vein Anastomosis: A Novel Approach to Arteriovenous Access Creation.","authors":"Sara Saffari, Esther Ochoa, Daniel Colchado, Amy Liao, Justin M Sacks, Mohamed A Zayed, Xiaowei Li","doi":"10.1177/15533506251383671","DOIUrl":"https://doi.org/10.1177/15533506251383671","url":null,"abstract":"<p><p>Arteriovenous fistulas (AVFs) are the gold standard for vascular access to facilitate hemodialysis, yet traditional surgical techniques are technically demanding, time-intensive, and costly. Additionally, limited suitable AVF sites, due to patient anatomy, vessel quality, and prior access exhaustion, necessitate exploration of novel options. This cadaveric proof-of-concept study introduces the anterior interosseous artery-cephalic vein as a novel AVF site and evaluates the feasibility of a 3D-printed sutureless anastomotic device, the Vaso-Stent, compared to conventional handsewn techniques. Fresh-frozen cadaveric upper limbs were procured to test the surgical feasibility of the proposed AVF model. Surgical exposure of the interosseous artery and adjacent cephalic vein were uncomplicated. A 3D-printed Vaso-Stent was manufactured and facilitated efficient anastomosis in under 1 min, compared with the 4.5 min required for a standard handsewn technique. The device demonstrated ease of placement, robust structural integrity, and resistance to tensile forces. These findings highlight that the Vaso-Stent can provide a simple alternative for AVF creation that reduces operative time and highlight the anterior interosseous artery-cephalic vein configuration as a new and unique hemodialysis access opportunity.</p>","PeriodicalId":22095,"journal":{"name":"Surgical Innovation","volume":" ","pages":"15533506251383671"},"PeriodicalIF":1.6,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145201372","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-01Epub Date: 2025-05-28DOI: 10.1177/15533506251345275
Usamah Ahmed, Jacob Rosenberg, Jason Joe Baker
BackgroundMesh reinforcement is recommended for ventral hernia repair and can include various materials in different combinations. This study analyzed the mesh materials used and their temporal trends in ventral hernia repair in Denmark over the past 17 years.MethodsThis study utilized prospectively collected data from the Danish Ventral Hernia Database, maintained from its inception in 2007 to 2023. The data were cleaned and organized by mesh material. All ventral hernia repairs with mesh were included.ResultsA total of 47,716 operations were included, utilizing many different mesh materials. Polypropylene meshes were used in 62% of the repairs, polyester in 26%, and fully absorbable meshes in 0.7%. Per- and polyfluoroalkyl substances (PFAS)-based meshes were most commonly used from 2007 to 2011 but then experienced a marked decline, followed by a slight increase in 2023. While the use of other absorbable components in semi-absorbable meshes followed a rise-and-fall pattern during the study period, only polylactic acid (PLA) showed a steady increase from 2013 onward.ConclusionA wide range of mesh materials and composites have been utilized for ventral hernia repair from 2007 to 2023. Polypropylene-based meshes were most commonly used, followed by polyester. The use of various absorbable composite materials varied considerably over time. The diversity of mesh materials and substantial temporal variations highlight gaps in evidence-based clinical practice and the need for improved regulations. These findings emphasize the importance of developing standardized guidelines for mesh selection in ventral hernia repair.
{"title":"Trends in Mesh Materials for Ventral Hernia Repair: A 17-Year Nationwide Registry-Based Study.","authors":"Usamah Ahmed, Jacob Rosenberg, Jason Joe Baker","doi":"10.1177/15533506251345275","DOIUrl":"10.1177/15533506251345275","url":null,"abstract":"<p><p>BackgroundMesh reinforcement is recommended for ventral hernia repair and can include various materials in different combinations. This study analyzed the mesh materials used and their temporal trends in ventral hernia repair in Denmark over the past 17 years.MethodsThis study utilized prospectively collected data from the Danish Ventral Hernia Database, maintained from its inception in 2007 to 2023. The data were cleaned and organized by mesh material. All ventral hernia repairs with mesh were included.ResultsA total of 47,716 operations were included, utilizing many different mesh materials. Polypropylene meshes were used in 62% of the repairs, polyester in 26%, and fully absorbable meshes in 0.7%. Per- and polyfluoroalkyl substances (PFAS)-based meshes were most commonly used from 2007 to 2011 but then experienced a marked decline, followed by a slight increase in 2023. While the use of other absorbable components in semi-absorbable meshes followed a rise-and-fall pattern during the study period, only polylactic acid (PLA) showed a steady increase from 2013 onward.ConclusionA wide range of mesh materials and composites have been utilized for ventral hernia repair from 2007 to 2023. Polypropylene-based meshes were most commonly used, followed by polyester. The use of various absorbable composite materials varied considerably over time. The diversity of mesh materials and substantial temporal variations highlight gaps in evidence-based clinical practice and the need for improved regulations. These findings emphasize the importance of developing standardized guidelines for mesh selection in ventral hernia repair.</p>","PeriodicalId":22095,"journal":{"name":"Surgical Innovation","volume":" ","pages":"417-427"},"PeriodicalIF":1.6,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144174068","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-01Epub Date: 2025-07-09DOI: 10.1177/15533506251360166
Jacob Chisholm, Benjamin Littlejohns
Background/NeedLaparoscopic surgeons waste time with instrument exchange. This is due to the poor design of existing instrument holders or quivers.Device DescriptionWe developed an instrument holder for laparoscopic instruments, energy devices and suction irrigators which correct the design deficiencies of existing quivers.Preliminary ResultsFollowing the use of 3D printed prototyping a design was finalised and patented. Initial samples met all design objectives on mock patient testing.Current StatusMedsafe registration was achieved in New Zealand in September 2023. In December 2024 a Conformity Assessment Certificate was issued by the Therapeutic Goods Administration (TGA) along with an application for inclusion in the Australian Register of Therapeutic Goods (ARTG). The Surgirack™ can now be supplied in Australia and New Zealand.
{"title":"Surgirack™: Laparoscopic Instrument Holder to Facilitate Instrument Exchange.","authors":"Jacob Chisholm, Benjamin Littlejohns","doi":"10.1177/15533506251360166","DOIUrl":"10.1177/15533506251360166","url":null,"abstract":"<p><p>Background/NeedLaparoscopic surgeons waste time with instrument exchange. This is due to the poor design of existing instrument holders or quivers.Device DescriptionWe developed an instrument holder for laparoscopic instruments, energy devices and suction irrigators which correct the design deficiencies of existing quivers.Preliminary ResultsFollowing the use of 3D printed prototyping a design was finalised and patented. Initial samples met all design objectives on mock patient testing.Current StatusMedsafe registration was achieved in New Zealand in September 2023. In December 2024 a Conformity Assessment Certificate was issued by the Therapeutic Goods Administration (TGA) along with an application for inclusion in the Australian Register of Therapeutic Goods (ARTG). The Surgirack™ can now be supplied in Australia and New Zealand.</p>","PeriodicalId":22095,"journal":{"name":"Surgical Innovation","volume":" ","pages":"465-468"},"PeriodicalIF":1.6,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144592422","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
BackgroundLaparoscopic transabdominal preperitoneal (TAPP) hernioplasty, a minimally invasive procedure, reduces postoperative pain and recovery time but faces challenges like the "ping-pong effect" (alternating focus between operative field and monitors) and a 1%-2% error rate due to anatomical misidentification, risking complications like vascular injuries.ObjectiveTo develop and validate HernIA, an AI-based system for real-time segmentation of anatomical structures in TAPP, targeting an Intersection over Union (IoU) ≥85% and error reduction ≥50% compared to manual identification.MethodsHernIA employs YOLOv11m-seg, trained on 21 443 annotated laparoscopic images from 45 TAPP procedures at Clinica Colón and Hospital de Campaña Escuela Hogar. Annotation by expert laparoscopists achieved high inter-rater reliability (Cohen's kappa = 0.87). Validation used 5-fold cross-validation and a 10 800-frame dataset.ResultsHernIA achieved an IoU of 89.4% (±2.1%), Jaccard Index of 81.2%, mAP@50 of 92.3%, and F1 score of 0.94 (confidence threshold ∼0.45). It reduced identification errors by 62% in a simulated TAPP environment (10 800 frames, 24 FPS, 42 ms latency). Clinical validation was limited to one case of bilateral hernia repair.ConclusionHernIA enhances surgical precision and training in TAPP, with potential to reduce complications. Multi-center trials are needed to confirm generalizability.
腹腔镜经腹腹膜前疝成形术(TAPP)是一种微创手术,减少了术后疼痛和恢复时间,但面临着“乒乓效应”(手术视野和监护仪交替聚焦)和1%-2%的解剖学错误识别错误率等挑战,有血管损伤等并发症的风险。目的开发并验证HernIA,一种基于人工智能的TAPP解剖结构实时分割系统,与人工识别相比,IoU≥85%,错误率≥50%。方法shernia使用YOLOv11m-seg,对临床Colón和Campaña Escuela Hogar医院45例TAPP手术的21443张带注释的腹腔镜图像进行训练。腹腔镜专家的注释具有较高的评分间可靠性(Cohen’s kappa = 0.87)。验证使用5次交叉验证和10个800帧的数据集。结果shernia的IoU为89.4%(±2.1%),Jaccard指数为81.2%,mAP@50为92.3%,F1评分为0.94(置信阈值~ 0.45)。它在模拟TAPP环境(10800帧,24 FPS, 42毫秒延迟)中减少了62%的识别错误。临床验证仅限于一例双侧疝修补术。结论疝术提高了TAPP的手术精度和训练水平,具有减少并发症的潜力。需要多中心试验来证实其普遍性。
{"title":"HernIA: Real-Time Anatomical Structure Segmentation in Video Laparoscopic Inguinal Hernioplasties With AI.","authors":"Franco J Marcelo, Pablo Zalazar, Florisel Papasidero, Ciro Hernandez, Jorge Ruiz Todone","doi":"10.1177/15533506251352101","DOIUrl":"10.1177/15533506251352101","url":null,"abstract":"<p><p>BackgroundLaparoscopic transabdominal preperitoneal (TAPP) hernioplasty, a minimally invasive procedure, reduces postoperative pain and recovery time but faces challenges like the \"ping-pong effect\" (alternating focus between operative field and monitors) and a 1%-2% error rate due to anatomical misidentification, risking complications like vascular injuries.ObjectiveTo develop and validate HernIA, an AI-based system for real-time segmentation of anatomical structures in TAPP, targeting an Intersection over Union (IoU) ≥85% and error reduction ≥50% compared to manual identification.MethodsHernIA employs YOLOv11m-seg, trained on 21 443 annotated laparoscopic images from 45 TAPP procedures at Clinica Colón and Hospital de Campaña Escuela Hogar. Annotation by expert laparoscopists achieved high inter-rater reliability (Cohen's kappa = 0.87). Validation used 5-fold cross-validation and a 10 800-frame dataset.ResultsHernIA achieved an IoU of 89.4% (±2.1%), Jaccard Index of 81.2%, mAP@50 of 92.3%, and F1 score of 0.94 (confidence threshold ∼0.45). It reduced identification errors by 62% in a simulated TAPP environment (10 800 frames, 24 FPS, 42 ms latency). Clinical validation was limited to one case of bilateral hernia repair.ConclusionHernIA enhances surgical precision and training in TAPP, with potential to reduce complications. Multi-center trials are needed to confirm generalizability.</p>","PeriodicalId":22095,"journal":{"name":"Surgical Innovation","volume":" ","pages":"442-449"},"PeriodicalIF":1.6,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144317884","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-01Epub Date: 2025-05-05DOI: 10.1177/15533506251336824
Sem F Hardon, Tim Horeman, Sophie J M Reijers, Linda J Schoonmade, Freek Daams, Donald L van der Peet
BackgroundTechnological innovations have significantly enhanced the objective assessment of technical skills in minimally invasive surgery, offering substantial potential for proficiency-based training. However, the integration of these innovative tools into surgical education curricula remains limited. This study aims to evaluate the adoption and implementation of data-driven assessment tools within laparoscopic simulation training.MethodsA systematic search of PubMed and Embase was conducted following PRISMA guidelines, identifying studies that employed objective assessments of technical skills in surgical training curricula. Eligible studies utilized data-driven assessment methods as part of structured training programs for surgical residents. A descriptive analysis was performed on the included studies.ResultsFrom 2814 identified articles, 718 were eligible for full-text screening, and 35 studies met the inclusion criteria. These studies described the implementation of 14 different data-driven tools in laparoscopic skills training. Most tools focused on assessing instrument handling, measuring parameters such as motion speed, path length, and accuracy. Only three studies evaluated tissue handling skills using metrics like knot quality, tissue handling forces, and anastomotic integrity.ConclusionsThe adoption of data-driven tools in laparoscopic simulation training is progressing slowly and exhibits considerable variability. Most technologies emphasize instrument handling, while tools for assessing tissue manipulation and force application are limited. To improve training outcomes, a combination of motion- and force-based assessment tools should be considered, enabling a more comprehensive evaluation of technical skills in minimally invasive surgery.
{"title":"The Implementation of Data-Driven Assessment into Laparoscopic Skills Training: A Systematic Review.","authors":"Sem F Hardon, Tim Horeman, Sophie J M Reijers, Linda J Schoonmade, Freek Daams, Donald L van der Peet","doi":"10.1177/15533506251336824","DOIUrl":"10.1177/15533506251336824","url":null,"abstract":"<p><p>BackgroundTechnological innovations have significantly enhanced the objective assessment of technical skills in minimally invasive surgery, offering substantial potential for proficiency-based training. However, the integration of these innovative tools into surgical education curricula remains limited. This study aims to evaluate the adoption and implementation of data-driven assessment tools within laparoscopic simulation training.MethodsA systematic search of PubMed and Embase was conducted following PRISMA guidelines, identifying studies that employed objective assessments of technical skills in surgical training curricula. Eligible studies utilized data-driven assessment methods as part of structured training programs for surgical residents. A descriptive analysis was performed on the included studies.ResultsFrom 2814 identified articles, 718 were eligible for full-text screening, and 35 studies met the inclusion criteria. These studies described the implementation of 14 different data-driven tools in laparoscopic skills training. Most tools focused on assessing instrument handling, measuring parameters such as motion speed, path length, and accuracy. Only three studies evaluated tissue handling skills using metrics like knot quality, tissue handling forces, and anastomotic integrity.ConclusionsThe adoption of data-driven tools in laparoscopic simulation training is progressing slowly and exhibits considerable variability. Most technologies emphasize instrument handling, while tools for assessing tissue manipulation and force application are limited. To improve training outcomes, a combination of motion- and force-based assessment tools should be considered, enabling a more comprehensive evaluation of technical skills in minimally invasive surgery.</p>","PeriodicalId":22095,"journal":{"name":"Surgical Innovation","volume":" ","pages":"450-464"},"PeriodicalIF":1.6,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12402525/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143998372","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 : 2025-10-01Epub Date: 2025-06-10DOI: 10.1177/15533506251351461
Marco Antonio Altamirano-Cruz
{"title":"Comments on \"Minimally Invasive Treatment of Pelvic Fractures With Titanium Elastic Nailing: An Innovative Technology\".","authors":"Marco Antonio Altamirano-Cruz","doi":"10.1177/15533506251351461","DOIUrl":"10.1177/15533506251351461","url":null,"abstract":"","PeriodicalId":22095,"journal":{"name":"Surgical Innovation","volume":" ","pages":"478"},"PeriodicalIF":1.6,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144267255","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-01Epub Date: 2025-05-19DOI: 10.1177/15533506251339929
Lasse W P Van 't Hof, Isabelle T S Koster, Richard M Van den Elzen, Mark-Bram Bouman, Matthijs Botman, Caroline Driessen
BackgroundIndocyanine-Green Fluorescence Angiography (ICG-FA) is widely used in reconstructive surgery, providing real-time visualization of flap perfusion. Accurate assessment of perfusion is especially critical in lower extremity reconstructions, where complications like necrosis and venous congestion can lead to poor outcomes, including amputation. Although ICG-FA is commonly available, its interpretation remains subjective and heavily reliant on the surgeon's experience. These challenges underline the importance of integrating objective, data-driven assessment tools into surgical practice.MethodsAs part of a larger, ongoing prospective study, three illustrative cases of lower extremity reconstructions using perforator-based fasciocutaneous flaps were selected. Intraoperative ICG-FA was performed using a surgical microscope with integrated fluorescence imaging. Fluorescence-time-curves (FTCs) were generated using specialized software, and associated quantitative perfusion parameters were compared across three cases: two patients with perfusion-related complications and one patient without complications.ResultsIntraoperative clinical assessment appeared satisfactory in all cases, and no changes in surgical management were made based on the subjective interpretation of ICG-FA. In contrast, quantitative analysis of ICG-FA revealed abnormal perfusion patterns in the two flaps that developed complications, identifying perfusion deficits not evident through conventional assessment.ConclusionThese findings suggest that FTCs derived from ICG-FA data can predict perfusion-related complications. Integrating quantitative ICG-FA analysis into clinical practice may yield a significant advancement in reconstructive surgery, especially in lower extremity reconstructions.Clinical trial nameICG Indocyanine Green in Reconstructive Surgery (ICG-R).ClinicalTrials.gov IDNCT06129669 (https://clinicaltrials.gov/study/NCT06129669?cond=NCT06129669&rank=1).
{"title":"Quantitative Perfusion Assessment Using Indocyanine Green in Lower Extremity Perforator Flaps.","authors":"Lasse W P Van 't Hof, Isabelle T S Koster, Richard M Van den Elzen, Mark-Bram Bouman, Matthijs Botman, Caroline Driessen","doi":"10.1177/15533506251339929","DOIUrl":"10.1177/15533506251339929","url":null,"abstract":"<p><p>BackgroundIndocyanine-Green Fluorescence Angiography (ICG-FA) is widely used in reconstructive surgery, providing real-time visualization of flap perfusion. Accurate assessment of perfusion is especially critical in lower extremity reconstructions, where complications like necrosis and venous congestion can lead to poor outcomes, including amputation. Although ICG-FA is commonly available, its interpretation remains subjective and heavily reliant on the surgeon's experience. These challenges underline the importance of integrating objective, data-driven assessment tools into surgical practice.MethodsAs part of a larger, ongoing prospective study, three illustrative cases of lower extremity reconstructions using perforator-based fasciocutaneous flaps were selected. Intraoperative ICG-FA was performed using a surgical microscope with integrated fluorescence imaging. Fluorescence-time-curves (FTCs) were generated using specialized software, and associated quantitative perfusion parameters were compared across three cases: two patients with perfusion-related complications and one patient without complications.ResultsIntraoperative clinical assessment appeared satisfactory in all cases, and no changes in surgical management were made based on the subjective interpretation of ICG-FA. In contrast, quantitative analysis of ICG-FA revealed abnormal perfusion patterns in the two flaps that developed complications, identifying perfusion deficits not evident through conventional assessment.ConclusionThese findings suggest that FTCs derived from ICG-FA data can predict perfusion-related complications. Integrating quantitative ICG-FA analysis into clinical practice may yield a significant advancement in reconstructive surgery, especially in lower extremity reconstructions.Clinical trial nameICG Indocyanine Green in Reconstructive Surgery (ICG-R).ClinicalTrials.gov IDNCT06129669 (https://clinicaltrials.gov/study/NCT06129669?cond=NCT06129669&rank=1).</p>","PeriodicalId":22095,"journal":{"name":"Surgical Innovation","volume":" ","pages":"435-441"},"PeriodicalIF":1.6,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12402519/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144094932","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 : 2025-10-01Epub Date: 2025-06-17DOI: 10.1177/15533506251348535
Huadong Du, Yingmo Shen, Huiqi Yang, Yilin Zhu
ObjectiveThe aim of this study was to explore the safety and efficacy of retroperitoneal laparoscopic repair of primary lumbar hernia using Self-Gripping mesh.MethodsThis retrospective study included 11 patients with primary lumbar hernias who underwent retroperitoneal laparoscopic repair with Self-Gripping mesh from May 2020 to October 2023 in our hospital. Observation indicators were intraoperative measured diameter of hernia ring defect, operation time, length of hospital stay, postoperative follow-up, complications, postoperative visual analogue scale (VAS) score, chronic pain.ResultsThe operations were completed successfully in 11 cases. The mean diameter of hernia ring was 2.57 ± 0.49 cm (ranged from 2.0 to 3.0 cm), the mean operation time was 53.31 ± 19.33 min (ranged from 35 to 90 min), the intraoperative blood loss was 3.01 ± 1.43 mL (ranged from 2 to 10 mL), and the mean postoperative hospital stay was 2.43 ± 1.41 days (ranged from 1 to 4 days). The mean postoperative VAS scores at 24 h were 1.10 ± 0.32 (ranged from 1 to 2). All cases were followed up for 21.05 ± 16.73 months (ranged from 3 to 42 months) without seroma, hematoma, incision or mesh infection, recurrence and obvious chronic pain.ConclusionRetroperitoneal laparoscopic repair of primary lumbar hernia using Self-Gripping mesh is safe and feasible. Its efficacy in the short term is favorable.
目的探讨后腹腔镜下应用自夹持补片修复原发性腰疝的安全性和有效性。方法回顾性分析2020年5月至2023年10月在我院行腹膜后腹腔镜下自夹持补片修复术的11例原发性腰疝患者。观察指标为术中测量疝环缺损直径、手术时间、住院时间、术后随访、并发症、术后视觉模拟评分(VAS)、慢性疼痛。结果11例手术均顺利完成。平均疝环直径2.57±0.49 cm (2.0 ~ 3.0 cm),平均手术时间53.31±19.33 min (35 ~ 90 min),术中出血量3.01±1.43 mL (2 ~ 10 mL),平均住院时间2.43±1.41 d (1 ~ 4 d)。术后24 h VAS评分平均为1.10±0.32分(1 ~ 2分)。所有病例随访21.05±16.73个月(3 ~ 42个月),无血肿、血肿、切口或补片感染、复发及明显慢性疼痛。结论经腹膜后腹腔镜下应用自夹持补片修复原发性腰疝是安全可行的。短期内效果良好。
{"title":"Retroperitoneal Laparoscopic Repair of Primary Lumbar Hernia Using Self-Gripping Mesh.","authors":"Huadong Du, Yingmo Shen, Huiqi Yang, Yilin Zhu","doi":"10.1177/15533506251348535","DOIUrl":"10.1177/15533506251348535","url":null,"abstract":"<p><p>ObjectiveThe aim of this study was to explore the safety and efficacy of retroperitoneal laparoscopic repair of primary lumbar hernia using Self-Gripping mesh.MethodsThis retrospective study included 11 patients with primary lumbar hernias who underwent retroperitoneal laparoscopic repair with Self-Gripping mesh from May 2020 to October 2023 in our hospital. Observation indicators were intraoperative measured diameter of hernia ring defect, operation time, length of hospital stay, postoperative follow-up, complications, postoperative visual analogue scale (VAS) score, chronic pain.ResultsThe operations were completed successfully in 11 cases. The mean diameter of hernia ring was 2.57 ± 0.49 cm (ranged from 2.0 to 3.0 cm), the mean operation time was 53.31 ± 19.33 min (ranged from 35 to 90 min), the intraoperative blood loss was 3.01 ± 1.43 mL (ranged from 2 to 10 mL), and the mean postoperative hospital stay was 2.43 ± 1.41 days (ranged from 1 to 4 days). The mean postoperative VAS scores at 24 h were 1.10 ± 0.32 (ranged from 1 to 2). All cases were followed up for 21.05 ± 16.73 months (ranged from 3 to 42 months) without seroma, hematoma, incision or mesh infection, recurrence and obvious chronic pain.ConclusionRetroperitoneal laparoscopic repair of primary lumbar hernia using Self-Gripping mesh is safe and feasible. Its efficacy in the short term is favorable.</p>","PeriodicalId":22095,"journal":{"name":"Surgical Innovation","volume":" ","pages":"428-434"},"PeriodicalIF":1.6,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144310443","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-01Epub Date: 2025-07-24DOI: 10.1177/15533506251362370
Tina Bharani, Divyansh Agarwal
BackgroundThe early 20th century saw pioneering work by Frank and Lillian Gilbreth, regarded as the founders of surgical ergonomics, which brought scientific management in surgery and operating rooms. Through time and motion studies, their research helped improve the operative workflow and surgical efficiency.MethodsTo document the historical work of Gilbreths in surgical ergonomics, we conducted primary archival research at the Purdue University Archives and Special Collections (West Lafayette, IN), and integrated a collection of secondary sources across various formats and modalities.Results and ConclusionWe describes the early works of Gilbreths in surgical ergonomics and highlight how their motion research in the operating room evolved to incorporate ergonomics and decrease operative fatigue. The Gilbreths were proponents of promoting the adoption of management practices for operating rooms and standardization in hospital design, equipment, and patient records to improve efficiency in health care delivery. Through analysis of their published and unpublished work, we describe how their ideas are still in widespread use today to eliminate unnecessary motions and foster ergonomics in the operating room and in the field of surgery in general.
20世纪初,被视为外科人体工程学创始人的弗兰克和莉莲·吉尔布雷斯(Frank and Lillian Gilbreth)的开创性工作为外科和手术室带来了科学管理。通过时间和运动研究,他们的研究有助于改善手术流程和手术效率。方法为了记录Gilbreths在外科人体工程学方面的历史工作,我们在普渡大学档案和特别收藏(West Lafayette, in)进行了初步档案研究,并整合了各种格式和模式的二手资料。结果与结论我们描述了Gilbreths在手术人体工程学方面的早期工作,并强调了他们在手术室的运动研究是如何发展到结合人体工程学和减少手术疲劳的。Gilbreths夫妇是推动手术室管理实践和医院设计、设备和患者记录标准化的支持者,以提高医疗保健服务的效率。通过分析他们发表的和未发表的作品,我们描述了他们的想法如何在今天仍然被广泛使用,以消除不必要的动作,促进手术室和外科领域的人体工程学。
{"title":"The Gilbreth Contribution to Operating Room Management and Surgical Ergonomics.","authors":"Tina Bharani, Divyansh Agarwal","doi":"10.1177/15533506251362370","DOIUrl":"10.1177/15533506251362370","url":null,"abstract":"<p><p>BackgroundThe early 20th century saw pioneering work by Frank and Lillian Gilbreth, regarded as the founders of surgical ergonomics, which brought scientific management in surgery and operating rooms. Through time and motion studies, their research helped improve the operative workflow and surgical efficiency.MethodsTo document the historical work of Gilbreths in surgical ergonomics, we conducted primary archival research at the Purdue University Archives and Special Collections (West Lafayette, IN), and integrated a collection of secondary sources across various formats and modalities.Results and ConclusionWe describes the early works of Gilbreths in surgical ergonomics and highlight how their motion research in the operating room evolved to incorporate ergonomics and decrease operative fatigue. The Gilbreths were proponents of promoting the adoption of management practices for operating rooms and standardization in hospital design, equipment, and patient records to improve efficiency in health care delivery. Through analysis of their published and unpublished work, we describe how their ideas are still in widespread use today to eliminate unnecessary motions and foster ergonomics in the operating room and in the field of surgery in general.</p>","PeriodicalId":22095,"journal":{"name":"Surgical Innovation","volume":" ","pages":"469-477"},"PeriodicalIF":1.6,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144699570","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}