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Immunotherapy in the surgical patient: Perioperative considerations. 手术患者的免疫治疗:围手术期注意事项。
IF 9.6 1区 医学 Q1 SURGERY Pub Date : 2026-07-21 DOI: 10.1093/bjs/znag096
Nicola McShane,Ciaran M Hurley,Roisin T Dolan
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引用次数: 0
Explaining increased locoregional failure following TNT in RAPIDO. 解释RAPIDO中TNT后局部失败增加的原因。
IF 9.6 1区 医学 Q1 SURGERY Pub Date : 2026-07-15 DOI: 10.1093/bjs/znag095
P J Nilsson,I Prata,M D Tanaka,A M Couwenberg,B van Etten,G A P Hospers,B Glimelius,C J H van de Velde
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引用次数: 0
Short-term economic impact of early leaks following metabolic bariatric surgery. 代谢性减肥手术后早期泄漏的短期经济影响。
IF 9.6 1区 医学 Q1 SURGERY Pub Date : 2026-07-11 DOI: 10.1093/bjs/znag072
José M Balibrea,Javier Osorio,Joaquín Resa,María Álvarez,Mireya Robles-Plaza,Julen Monje,Miguel Ángel Casado,Laura Salinas-Ortega
BACKGROUNDDespite its low incidence, leaks result in high morbidity and represent the second cause of death after metabolic bariatric surgery (MBS). The economic impact of diagnosing and managing early leaks after MBS was assessed within the Spanish Health System.METHODA cost analysis model was developed to estimate the resource consumption of patients with early leaks after laparoscopic sleeve gastrectomy (LSG) and laparoscopic Roux-en-Y gastric bypass (LRYGB). Through a comprehensive literature review, an epidemiological framework was established to estimate the incidence of early leaks. Patients were classified into fourteen scenarios based on the type of MBS performed, initial management of the early leak (conservative, endoscopic and/or surgical), and the need for a secondary treatment. Resource consumption over a one-year time horizon was collected based on clinical practice, and unit costs in year 2025 were obtained from national databases. All parameters were validated by a panel of experts, and sensitivity analyses were conducted to assess the robustness of the results.RESULTSTotal costs of early leaks reached €4,199,549, including €3,469,303 after LSG (82 events/year) and €730,246 after LRYGB (18 events/year). The cost per patient with an early leak after LSG ranged from €13,358 to €94,532, with a weighted average cost of €42,285 and after LRYGB from €13,110 to €94,284, with a weighted average cost of €40,971. Hospital stays and health procedures represented the highest cost. The sensitivity analysis results ranged between €1,189,220- €7,209,878.CONCLUSIONSEarly leak after MBS markedly increased health resource utilization, mainly due to an increase in hospitalizations, with cost increase associated with the complexity of the event.
背景:尽管发生率低,但泄漏导致高发病率,是继代谢减肥手术(MBS)之后的第二大死亡原因。在西班牙卫生系统内评估了MBS后诊断和管理早期泄漏的经济影响。方法建立成本分析模型,评估腹腔镜袖式胃切除术(LSG)和腹腔镜Roux-en-Y胃旁路术(LRYGB)术后早期泄漏患者的资源消耗。通过全面的文献回顾,建立了一个流行病学框架来估计早期泄漏的发生率。根据MBS的类型、早期泄漏的初始处理(保守、内窥镜和/或手术)以及是否需要二次治疗,将患者分为14种情况。根据临床实践收集一年时间范围内的资源消耗,从国家数据库获取2025年的单位成本。所有参数均由专家小组验证,并进行敏感性分析以评估结果的稳健性。结果早期泄漏的总成本为4,199,549欧元,其中LSG后为3,469,303欧元(82事件/年),LRYGB后为730,246欧元(18事件/年)。LSG术后早期泄漏患者的人均成本为13,358欧元至94,532欧元,加权平均成本为42,285欧元;LRYGB术后患者的人均成本为13,110欧元至94,284欧元,加权平均成本为40,971欧元。住院和医疗费用最高。敏感度分析结果介于1189220欧元至7209878欧元之间。结论MBS后早期泄漏显著提高了卫生资源利用率,主要是由于住院次数的增加,费用的增加与事件的复杂性有关。
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引用次数: 0
Patient-Reported Outcomes in Masculinizing Gender-Affirming Chest Surgery: Validation of the GENDER-Q Chest Scales. 男性化性别确认胸部手术患者报告的结果:性别- q胸部量表的验证。
IF 9.6 1区 医学 Q1 SURGERY Pub Date : 2026-07-08 DOI: 10.1093/bjs/znag089
Caleb Haley,Shane D Morrison,Manraj N Kaur,Charlene Rae,Megan Lane,Danny A Young-Afat,Tim C van de Grift,Nicola R Dean,Kathleen A Armstrong,Devin Coon,Zac A Cannell,Christian X Lava,Sylvie D Cornacchi,Alexis Laungani,Margriet G Mullender,Jens Ahm Sørensen,Lotte Poulsen,Jack G Graesser,Thomas Satterwhite,Allison C Hu,Gerhard S Mundinger,Hilliard T Brydges,Jessica J Hsu,Blair R Peters,Jens U Berli,Christodoulos Kaoutzanis,Nargis Kalia,Rachel Bluebond-Langner,Oren Ganor,Alireza Hamidian Jahromi,Bashar A Hassan,Fan Liang,John H Pang,Edward C Ray,Gabriel A Del Corral,Kenneth L Fan,Lily R Mundy,Andrea L Pusic,Anne F Klassen
INTRODUCTIONMasculinizing gender-affirming chest surgery is the most frequently accessed gender-affirming procedure. The GENDER-Q Chest scales were developed to better assess patient-reported outcomes in masculinizing gender-affirming chest surgery, yet previous psychometric assessment of these scales is limited. The objective of this study was to assess the construct validity of the GENDER-Q Chest scales (Chest, Nipples & Areolas, and Scars).METHODSAn international, cross-sectional study was performed to develop the GENDER-Q between February 2022 and March 2024. Individuals were included in this analysis if they had sought or received masculinizing gender-affirming chest surgery and completed the GENDER-Q Chest scale. Construct validity was assessed for each scale by testing a priori hypotheses. According to Consensus-based Standards for the Selection of Health Measurement Instruments guidelines, greater than 75% acceptance of hypotheses indicates sufficient evidence of construct validity.RESULTSA total of 2,846 participants completed the GENDER-Q Chest scale. For the GENDER-Q Chest, Nipples & Areolas, and Scars scales, 95% (21/22), 79% (15/19), and 100% (12/12) of hypotheses were accepted for each scale, respectively. Patients who underwent surgery and do not currently need revisions reported the highest satisfaction, while patients who had not yet undergone surgery reported the lowest satisfaction.CONCLUSIONThe GENDER-Q Chest scales evidenced construct validity to measure appearance of chest, nipples, and scars for individuals seeking or undergoing masculinizing gender-affirming chest surgery. The GENDER-Q Chest scales provide a robust, validated approach for assessing outcomes in this context and are well-suited for generating high-quality evidence on patient-reported outcomes.
男性化的性别确认胸部手术是最常见的性别确认手术。GENDER-Q胸部量表是为了更好地评估患者报告的男性化性别肯定胸部手术的结果而开发的,然而以前对这些量表的心理测量评估是有限的。本研究的目的是评估GENDER-Q胸部量表(胸部、乳头和乳晕、疤痕)的结构效度。方法在2022年2月至2024年3月期间进行了一项国际横断面研究,以开发GENDER-Q。如果个人曾寻求或接受过男性化的性别确认胸部手术,并完成了GENDER-Q胸部量表,则将其纳入本分析。通过检验先验假设来评估每个量表的结构效度。根据基于共识的健康测量工具选择标准指南,假设接受度大于75%表明有足够的证据表明结构效度。结果共有2,846名参与者完成了性别- q胸部量表。对于GENDER-Q胸部、乳头和乳晕和疤痕量表,每个量表的假设接受率分别为95%(21/22)、79%(15/19)和100%(12/12)。接受手术且目前不需要翻修的患者满意度最高,而尚未接受手术的患者满意度最低。结论GENDER-Q胸围量表对寻求或正在进行男性化性别肯定胸围手术的个体测量胸部、乳头和疤痕的外观具有结构效度。GENDER-Q胸部量表提供了一种稳健、有效的方法来评估这种情况下的结果,非常适合为患者报告的结果生成高质量的证据。
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引用次数: 0
Making the OR work: a socio-material study of ergonomics in the operating room. 使手术室工作:手术室人体工程学的社会-物质研究。
IF 9.6 1区 医学 Q1 SURGERY Pub Date : 2026-07-06 DOI: 10.1093/bjs/znag083
Alexis Mah,Csilla Kalocsai,Fahad Alam,Allia Karim,Jeremie Larouche,M Susan Hallbeck,Tara Cohen,Anna Ding,Jessica Armah,Julie Hallet,
INTRODUCTIONPoor operating room (OR) ergonomics pose risk of injury to OR staff, worsening patient outcomes and threatening workforce wellness and sustainability. How OR staff navigate ergonomic barriers in the interdisciplinary team environment was examined in this qualitative study.METHODSSemi-structured, open-ended interviews of surgeons, anaesthesiologists and OR nurses were conducted at single institution using a socio-material approach with interview-to-the-double. Transcripts were coded by two independent researchers. Themes in the data were outlined using the System Engineering Initiative for Patient Safety (SEIPS) framework.RESULTSFive major themes were identified. First, physical environment issues creating cognitive and physical frictions, such as tripping hazards and improper room layouts. Second, influence of social positionality, with hierarchy by role and experience and social dynamics leading to differential capacity to adjust. Third, team collaboration, with lack of interdisciplinary work and communication and high staff turnover. Fourth, burden of self-initiated work arounds, outlining conflict between system/organizational issues but individual solutions. Fifth, institutional support, with lack of leadership engagement. Participants suggested solutions including accommodations to foster a collaborative approach to managing discomfort in the OR, and new team communication tools.CONCLUSIONSErgonomic barriers were described within the work system of the SEIPS framework. Social positionality and differential levels of agency, as well as lack of team collaboration and misperceptions of others' roles, were central to ergonomic challenges. Conflicts between problems lying with the system/organization, but solution being left to individuals, were also central to challenges to optimal OR ergonomics.
糟糕的手术室(OR)人体工程学对手术室员工造成伤害的风险,使患者的预后恶化,并威胁到员工的健康和可持续性。在这个定性研究中,我们考察了手术室员工如何在跨学科团队环境中克服人体工程学障碍。方法采用社会材料访谈法对单个机构的外科医生、麻醉师和手术室护士进行半结构化、开放式访谈。转录本由两名独立研究人员编码。数据中的主题使用患者安全系统工程倡议(SEIPS)框架进行概述。结果确定了五个主要主题。首先,物理环境问题产生认知和物理摩擦,如绊倒危险和不适当的房间布局。第二,社会地位的影响,角色和经验的等级和社会动态导致不同的调整能力。第三,团队协作,缺乏跨学科的工作和沟通,人员流动率高。第四,自我启动工作的负担,概述系统/组织问题与个人解决方案之间的冲突。第五,缺乏领导参与的机构支持。与会者提出了解决方案,包括促进协作方法来管理手术室的不适,以及新的团队沟通工具。结论在SEIPS框架的工作体系中,存在一定的基因障碍。社会地位和不同级别的代理,以及缺乏团队合作和对他人角色的误解,是人体工程学挑战的核心。问题之间的冲突存在于系统/组织中,但解决方案留给个人,这也是优化或人体工程学挑战的核心。
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引用次数: 0
A randomized, noninferiority clinical trial of Single-Shot Intrathecal Morphine versus Continuous Wound Infiltration for postoperative pain control after open pancreatoduodenectomy. 一项随机、非劣效性临床试验:单针鞘内吗啡与持续伤口浸润用于胰十二指肠切除术后疼痛控制。
IF 9.6 1区 医学 Q1 SURGERY Pub Date : 2026-07-06 DOI: 10.1093/bjs/znag088
Soohyuk Yoon,Taeyup Kim,Ho-Jin Lee,Nanhee Park,Hye-Sol Jung,Young Jae Cho,Wooil Kwon,Joon Seong Park,Chul-Woo Jung,Jin-Young Jang
BACKGROUNDIntrathecal morphine (ITM) and continuous wound infiltration (CWI) are two alternatives to thoracic epidural analgesia in major abdominal surgery, but direct comparative studies are lacking. We evaluated whether ITM is noninferior to CWI after open pancreatoduodenectomy.METHODSAn open-label, randomised, noninferiority clinical trial conducted at a tertiary hospital. Adult patients undergoing elective open pancreatoduodenectomy were randomised 1:1 to receive either a single-shot ITM (0.2 mg) or bilateral preperitoneal CWI. Both groups received standardised multimodal and intravenous patient-controlled analgesia (IV-PCA). The primary outcome was the mean coughing pain score, averaged across 24, 48, and 72 h postoperatively, analysed for noninferiority using the 95% confidence interval (noninferiority margin: 1.0). Secondary outcomes included the mean resting pain score, pain score at each time point (2, 24, 48, and 72 h), IV-PCA fentanyl consumption, EuroQol 5-Dimension 5-Level utility score, and postoperative complications.RESULTSIn the per-protocol population (n = 92), ITM was noninferior to CWI for the primary outcome (ITM: 5.7 ± 1.7 vs. CWI: 6.1 ± 1.5; mean difference -0.5, 95% confidence interval -1.1 to 0.2). ITM was also noninferior to CWI regarding the mean resting pain score. ITM provided significantly lower pain scores at 2 h postoperatively, both at rest and on coughing, with a sustained reduction on coughing at 24 h and reduced fentanyl consumption. Otherwise comparable, ITM increased respiratory depression and pruritus within 24 h.CONCLUSIONITM provides noninferior overall and superior early analgesia to CWI after open pancreatoduodenectomy, although careful monitoring for early side effects is warranted.TRIAL REGISTRATIONClinicalTrials.gov Identifier (No. NCT06761989, https://clinicaltrials.gov/study/NCT06761989) registered on 30 December 2024.
背景鞘内吗啡(ITM)和连续伤口浸润(CWI)是腹部大手术中胸段硬膜外镇痛的两种替代方法,但缺乏直接的比较研究。我们评估了开放式胰十二指肠切除术后ITM是否优于CWI。方法在某三级医院进行开放标签、随机、非劣效性临床试验。接受择期开放式胰十二指肠切除术的成年患者按1:1随机分组,接受单次ITM (0.2 mg)或双侧腹膜前CWI。两组均采用标准化多模式和静脉自控镇痛(IV-PCA)。主要结局是术后24、48和72小时的平均咳嗽疼痛评分,使用95%可信区间(非劣效性界限:1.0)进行非劣效性分析。次要结局包括平均静息疼痛评分、每个时间点(2、24、48和72 h)的疼痛评分、IV-PCA芬太尼用量、EuroQol 5维5级效用评分和术后并发症。结果在按方案人群(n = 92)中,ITM的主要结局不逊于CWI (ITM: 5.7±1.7 vs. CWI: 6.1±1.5;平均差值为-0.5,95%置信区间为-1.1至0.2)。在平均静息疼痛评分方面,ITM也不逊于CWI。ITM在术后2小时的疼痛评分显著降低,无论是休息时还是咳嗽时,24小时咳嗽持续减少,芬太尼用量减少。相比之下,ITM在24小时内增加了呼吸抑制和瘙痒。结论ITM对开放式胰十二指肠切除术后CWI提供了良好的早期镇痛效果,但需要仔细监测早期副作用。临床试验注册号:clinicaltrials .govNCT06761989, https://clinicaltrials.gov/study/NCT06761989)于2024年12月30日注册。
{"title":"A randomized, noninferiority clinical trial of Single-Shot Intrathecal Morphine versus Continuous Wound Infiltration for postoperative pain control after open pancreatoduodenectomy.","authors":"Soohyuk Yoon,Taeyup Kim,Ho-Jin Lee,Nanhee Park,Hye-Sol Jung,Young Jae Cho,Wooil Kwon,Joon Seong Park,Chul-Woo Jung,Jin-Young Jang","doi":"10.1093/bjs/znag088","DOIUrl":"https://doi.org/10.1093/bjs/znag088","url":null,"abstract":"BACKGROUNDIntrathecal morphine (ITM) and continuous wound infiltration (CWI) are two alternatives to thoracic epidural analgesia in major abdominal surgery, but direct comparative studies are lacking. We evaluated whether ITM is noninferior to CWI after open pancreatoduodenectomy.METHODSAn open-label, randomised, noninferiority clinical trial conducted at a tertiary hospital. Adult patients undergoing elective open pancreatoduodenectomy were randomised 1:1 to receive either a single-shot ITM (0.2 mg) or bilateral preperitoneal CWI. Both groups received standardised multimodal and intravenous patient-controlled analgesia (IV-PCA). The primary outcome was the mean coughing pain score, averaged across 24, 48, and 72 h postoperatively, analysed for noninferiority using the 95% confidence interval (noninferiority margin: 1.0). Secondary outcomes included the mean resting pain score, pain score at each time point (2, 24, 48, and 72 h), IV-PCA fentanyl consumption, EuroQol 5-Dimension 5-Level utility score, and postoperative complications.RESULTSIn the per-protocol population (n = 92), ITM was noninferior to CWI for the primary outcome (ITM: 5.7 ± 1.7 vs. CWI: 6.1 ± 1.5; mean difference -0.5, 95% confidence interval -1.1 to 0.2). ITM was also noninferior to CWI regarding the mean resting pain score. ITM provided significantly lower pain scores at 2 h postoperatively, both at rest and on coughing, with a sustained reduction on coughing at 24 h and reduced fentanyl consumption. Otherwise comparable, ITM increased respiratory depression and pruritus within 24 h.CONCLUSIONITM provides noninferior overall and superior early analgesia to CWI after open pancreatoduodenectomy, although careful monitoring for early side effects is warranted.TRIAL REGISTRATIONClinicalTrials.gov Identifier (No. NCT06761989, https://clinicaltrials.gov/study/NCT06761989) registered on 30 December 2024.","PeriodicalId":136,"journal":{"name":"British Journal of Surgery","volume":"36 1","pages":""},"PeriodicalIF":9.6,"publicationDate":"2026-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148388604","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Gut Microbiome in Surgical Oncology: Mechanisms, Perioperative Outcomes, and Therapeutic Opportunities. 外科肿瘤学中的肠道微生物组:机制、围手术期结果和治疗机会。
IF 9.6 1区 医学 Q1 SURGERY Pub Date : 2026-06-29 DOI: 10.1093/bjs/znag082
Jerry Dang,Yung Lee,Mélissa V Wills,J Mark Brown,Karen Madsen,Valentin Mocanu
INTRODUCTIONThe gut microbiome is a fundamental determinant of gastrointestinal physiology. It is essential in maintaining host homeostasis while also implicated in cancer pathogenesis and alteration in physiological response to surgical stress. This narrative review evaluates the microbiome's mechanistic role in surgical oncology, assessing it as a biomarker for risk stratification and an emerging therapeutic target.METHODThe current literature was synthesized to examine microbial impacts on tumourigenesis and perioperative surgical outcomes across the lower and upper gastrointestinal tracts (including the gut-lung axis), the hepatopancreatobiliary system, and extra-abdominal malignancies (breast cancer and melanoma).RESULTSDysbiotic microbial signatures, termed the oncobiome, actively drive tumour progression and immune evasion. Perioperative interventions induce acute microbial shifts linked to serious complications such as anastomotic leaks and pneumonia. Clinically, targeted modulation yields significant benefits as demonstrated by: perioperative synbiotics reducing infectious complications by 45% in colorectal surgery and 64% in major liver surgery. Furthermore, preoperative oral care reduces post-esophagectomy pneumonia by up to 50%, while Helicobacter pylori eradication halves metachronous gastric cancer risk. However, a detrimental "antibiotic paradox" exists in melanoma, where pre-treatment antibiotic exposure severely impairs immune checkpoint inhibitor efficacy. Conversely, faecal microbiota transplantation can reverse this immunotherapy resistance, achieving up to 80% response rates in trials.CONCLUSIONThe microbiome is a critical, modifiable determinant of both short-term surgical recovery and long-term oncologic survival. Future surgical oncology practice will need to integrate precision surgical microbiome-mediated biotherapeutics to optimise outcomes in multidisciplinary cancer care.
肠道微生物群是胃肠道生理的基本决定因素。它在维持宿主体内平衡中是必不可少的,同时也涉及癌症的发病机制和对手术应激的生理反应的改变。这篇叙述性综述评估了微生物组在外科肿瘤学中的机制作用,评估了它作为风险分层的生物标志物和新兴的治疗靶点。方法综合目前的文献,研究微生物对上下胃肠道(包括肠-肺轴)、肝胆胰系统和腹外恶性肿瘤(乳腺癌和黑色素瘤)的肿瘤发生和围手术期手术结果的影响。结果:被称为肿瘤组的非生态微生物特征,积极地驱动肿瘤进展和免疫逃避。围手术期干预引起急性微生物转移,与吻合口渗漏和肺炎等严重并发症有关。临床上,靶向调节产生了显著的益处,如:围手术期合生剂可使结直肠手术的感染并发症减少45%,大肝脏手术的感染并发症减少64%。此外,术前口腔护理可将食管切除术后肺炎降低50%,而幽门螺杆菌根除可使异时性胃癌风险减半。然而,在黑色素瘤中存在有害的“抗生素悖论”,治疗前抗生素暴露严重损害免疫检查点抑制剂的疗效。相反,粪便微生物群移植可以逆转这种免疫治疗耐药性,在试验中达到80%的应答率。结论微生物组是短期手术恢复和长期肿瘤生存的关键、可改变的决定因素。未来的外科肿瘤学实践将需要整合精确的外科微生物组介导的生物疗法,以优化多学科癌症治疗的结果。
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引用次数: 0
Trimester-Specific Safety of Laparoscopic versus Open Abdominal Surgery During Pregnancy: A Systematic Review and Meta-analysis. 妊娠期间腹腔镜与开放式腹部手术的妊娠特异性安全性:一项系统综述和荟萃分析。
IF 9.6 1区 医学 Q1 SURGERY Pub Date : 2026-06-29 DOI: 10.1093/bjs/znag084
Siran Wan,Wei Lin,Xue Zhang,Saidi Hu,Chenchen Luo,Shunhong Zhang,Elaine Dos Ramos Amado Dos Ramos,Lucilia Fernandes de Almeida,Lin-Yong Zhao
BACKGROUNDCurrent guidelines endorse laparoscopy for non-obstetric abdominal surgery during pregnancy regardless of trimester, but recent data suggest trimester-specific fetal risks. This study compared maternal and fetal safety of laparoscopic versus open surgery, focusing on trimester-specific and pathology-stratified outcomes.METHODSA systematic review and meta-analysis followed PRISMA 2020 (CRD420261295995). PubMed, Embase and Cochrane Library were searched for comparative studies (randomised controlled trials and cohort studies) of laparoscopic versus open surgery for acute appendicitis, gallstone disease and adnexal masses. Random-effects meta-analysis synthesised data on fetal loss, preterm delivery, maternal complications and hospital stay.RESULTSTwenty-two studies comprising 28,160 pregnant women (15,786 laparoscopic, 12,374 open) were included. Laparoscopy was associated with a higher risk of fetal loss than open surgery (Odds ratio (OR) 2.02; 95% CI 1.40-2.92; P < 0.001). A first-trimester subgroup analysis showed a persistent trend towards higher fetal loss with laparoscopy (OR 1.35; 95% CI 0.84-2.19). Laparoscopy reduced preterm delivery (OR 0.56; 95% CI 0.34-0.94; P = 0.020) and maternal complications (OR 0.45; 95% CI 0.30-0.68; P < 0.001). Trimester-specific analysis revealed a significantly elevated risk of composite adverse fetal outcomes for laparoscopy during the second trimester (OR 2.35; 95% CI 1.15-4.77; P = 0.020) and a similar trend in the third trimester.CONCLUSIONLaparoscopy confers maternal benefits and reduces preterm delivery but is associated with higher fetal loss and elevated composite adverse outcomes in the second trimester.
背景:目前的指南支持在妊娠期间进行腹腔镜非产科腹部手术,无论妊娠期如何,但最近的数据表明妊娠期特有的胎儿风险。本研究比较了腹腔镜手术与开放手术的母婴安全性,重点关注妊娠特异性和病理分层结果。方法采用PRISMA 2020 (CRD420261295995)进行系统评价和meta分析。检索PubMed、Embase和Cochrane图书馆的比较研究(随机对照试验和队列研究),比较腹腔镜手术与开放手术治疗急性阑尾炎、胆结石疾病和附件肿块的疗效。随机效应荟萃分析综合了胎儿丢失、早产、产妇并发症和住院时间的数据。结果纳入22项研究,共28160例孕妇,其中腹腔镜15786例,开放12374例。腹腔镜手术与开放手术相比,胎儿丢失的风险更高(优势比(OR) 2.02;95% ci 1.40-2.92;P < 0.001)。早期妊娠亚组分析显示,腹腔镜手术导致胎儿丢失的持续趋势较高(OR 1.35; 95% CI 0.84-2.19)。腹腔镜检查减少了早产(OR 0.56; 95% CI 0.34-0.94; P = 0.020)和产妇并发症(OR 0.45; 95% CI 0.30-0.68; P < 0.001)。妊娠期特异性分析显示,在妊娠中期腹腔镜检查复合不良胎儿结局的风险显著升高(OR 2.35; 95% CI 1.15-4.77; P = 0.020),在妊娠晚期也有类似的趋势。结论腹腔镜手术对产妇有利,可减少早产,但与妊娠中期胎儿丢失和复合不良结局升高相关。
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引用次数: 0
Patient-led, home-based follow-up for colorectal cancer: the DISTANCE multicentre stepped-wedge cluster-randomised trial. 以患者为主导,以家庭为基础的结直肠癌随访:DISTANCE多中心楔形步聚随机试验
IF 9.6 1区 医学 Q1 SURGERY Pub Date : 2026-06-26 DOI: 10.1093/bjs/znag081
M H Elise van Driel,Hidde Swartjes,Jobbe M G Lemmens,Seyed M Qaderi,Steven Teerenstra,Jose A E Custers,Marloes A G Elferink,Bob J van Wely,Johanne G Bloemen,Wilhelmina M U van Grevenstein,Peter van Duijvendijk,Emiel G G Verdaasdonk,Marnix A J de Roos,Veerle M H Coupé,Geraldine R Vink,Cornelis Verhoef,Dirk J Grünhagen,Johannes H W de Wilt
INTRODUCTIONColorectal cancer (CRC) incidence is rising, consequentially traditional follow-up care models are increasingly unsustainable. Patient-led, home-based follow-up (PHFU) may offer a promising alternative to reduce hospital visits while maintaining patient well-being.METHODSThe DISTANCE trial is a stepped-wedge cluster randomised trial conducted in six hospitals in the Netherlands. A total of 354 stage I-III CRC survivors, disease-free at 12 months post-surgery, assigned to either PHFU or standard follow-up. The primary endpoint was the number of hospital contacts. Secondary endpoints included quality of life (QoL, EORTC QLQ-C30), cancer-related worry (CWS), and psychological distress (HADS).RESULTSIn the intention-to-treat (ITT) analysis, no significant difference in hospital contacts was observed. In the as-treated (AT) analysis, PHFU reduced hospital contacts by 38% compared to standard follow-up (RR 0.62, 95% CI 0.51-0.75, p < 0.001). There was substantial crossover, with 117 patients assigned to PHFU receiving standard follow-up and 10 patients assigned to standard follow-up receiving PHFU. No significant differences were found in QoL or psychological distress between the two groups.CONCLUSIONThe DISTANCE trial suggests that PHFU is a feasible and effective alternative to standard hospital-based follow-up for CRC survivors.TOC Summary.
结直肠癌(CRC)的发病率正在上升,因此传统的随访治疗模式越来越难以为继。以患者为主导、以家庭为基础的随访(PHFU)可能提供一种有希望的替代方案,以减少住院次数,同时保持患者的健康。方法DISTANCE试验是一项在荷兰6家医院进行的楔形聚类随机试验。共有354例I-III期结直肠癌幸存者,术后12个月无疾病,分配到PHFU或标准随访。主要终点是医院接触者的数量。次要终点包括生活质量(QoL, EORTC QLQ-C30)、癌症相关担忧(CWS)和心理困扰(HADS)。结果在意向治疗(ITT)分析中,医院接触者无显著差异。在治疗后(AT)分析中,与标准随访相比,PHFU减少了38%的医院接触(RR 0.62, 95% CI 0.51-0.75, p < 0.001)。有大量交叉,117例患者被分配到PHFU接受标准随访,10例患者被分配到标准随访接受PHFU。两组患者的生活质量和心理困扰均无显著差异。结论:DISTANCE试验表明,对于结直肠癌幸存者来说,PHFU是一种可行且有效的替代标准医院随访的方法。TOC总结。
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引用次数: 0
Surgical Outcomes from Nationwide Implementation of the International Best-Practice for Locally Advanced Pancreatic Cancer (PREOPANC-4) study. 局部晚期胰腺癌国际最佳实践(preopac -4)研究在全国实施的手术结果
IF 9.6 1区 医学 Q1 SURGERY Pub Date : 2026-06-22 DOI: 10.1093/bjs/znag075
Thomas F Stoop,Leonard W F Seelen,Freek R van 't Land,Jacobien C M Scheepens,Mahsoem Ali,Anna C van der Hout,B Marion van der Kolk,Bert A Bonsing,Daan J Lips,Eric R Manusama,François E J A Willemsen,Freek Daams,Geert Kazemier,Gijs A Patijn,Ignace H de Hingh,Jan H Wijsman,Jennifer Schreinemakers,Joris I Erdmann,J Sven D Mieog,Joost M Klaase,Judith A C Rietjens,Koop Bosscha,Lysanne P M Beuk,Maarten W Nijkamp,Marcel den Dulk,Marnix P M Kop,Mike S L Liem,Misha Luyer,Martijn W J Stommel,Olivier R Busch,Sebastiaan Festen,Stefan Bouwense,Tom M Karsten,Tom W van Ravens,Ulff P Neumann,Vincent E de Meijer,Vincent B Nieuwenhuijs,Werner A Draaisma,Wouter Derksen,Thomas L Bollen,Bas Groot Koerkamp,Casper H J van Eijck,I Quintus Molenaar,Christopher L Wolfgang,Marco Del Chiaro,Matthew H G Katz,Thilo Hackert,Johanna W Wilmink,Hjalmar C van Santvoort,Roeland F de Wilde,Marc G Besselink,
BACKGROUNDIn expert centers, surgical resection rates of locally advanced pancreatic cancer (LAPC) following induction chemotherapy have increased beyond 20% with subsequent 25% five-year overall survival (OS). In the Netherlands, however, the historical low 8% LAPC resection rate compared with 23% in international expert centers reflects relative reluctance. Thereby, opportunities to achieve long-term survival in appropriately selected patients may be missed. This study evaluated whether nationwide implementation of international multidisciplinary best-practice for LAPC management is feasible while maintaining surgical safety benchmarks (in-hospital/30-day major morbidity <50% and mortality ≤5%).METHODSA multidisciplinary protocol was designed in collaboration with four international experts and prospectively implemented nationwide within the Dutch Pancreatic Cancer Group (DPCG) (2022-2024). This observational cohort included consecutive patients diagnosed with LAPC, defined by DPCG criteria. Eligible patients had radiologically non-progressive disease after at least four months of multi-agent chemotherapy. All patients who underwent resection were included in this safety analysis. A predefined sub-group analysis included patients with National Comprehensive Cancer Network (NCCN) LAPC. Primary outcomes included in-hospital/30-day major morbidity (i.e., Clavien-Dindo grade ≥IIIa) and mortality. The expected number of resections was 53.RESULTSOverall, 180 patients with LAPC underwent surgical exploration, of whom 155 (86%) underwent resection in 11 centers. Most (74%) resections were performed in the three LAPC surgical centers. Extended resections were performed in 77% of patients, including portomesenteric venous (60%), multivisceral (23%), and arterial (21%) resections. In-hospital/30-day major morbidity rate was 44% and mortality rate was 0.6%, both within pre-established safety benchmarks. Benchmarks were also reached for patients with NCCN LAPC (49% major morbidity, 2% mortality).CONCLUSIONNationwide implementation of the international best-practice for LAPC was feasible with nearly three times more resections performed than expected, while morbidity and mortality remained well within predefined safety benchmarks.
背景:在专家中心,局部晚期胰腺癌(LAPC)诱导化疗后的手术切除率已超过20%,随后的5年总生存率(OS)为25%。然而,在荷兰,与国际专家中心的23%相比,历史最低的8%的LAPC切除率反映了相对的不情愿。因此,在适当选择的患者中实现长期生存的机会可能会被错过。本研究评估了在全国范围内实施国际多学科LAPC管理最佳实践是否可行,同时保持手术安全基准(住院/30天主要发病率<50%,死亡率≤5%)。方法与四位国际专家合作设计了一项多学科方案,并在荷兰胰腺癌小组(DPCG)(2022-2024)全国范围内实施。该观察性队列包括经DPCG标准诊断为LAPC的连续患者。符合条件的患者在至少4个月的多药化疗后,放射学上没有进展。所有接受手术切除的患者都被纳入这项安全性分析。预先定义的亚组分析包括国家综合癌症网络(NCCN) LAPC患者。主要结局包括住院/30天主要发病率(即Clavien-Dindo分级≥IIIa)和死亡率。预期手术数量为53例。结果总共有180例LAPC患者接受了手术探查,其中155例(86%)在11个中心接受了手术切除。大多数(74%)手术在三家LAPC手术中心进行。77%的患者进行了扩展切除,包括门肠静脉(60%)、多脏器(23%)和动脉(21%)切除。住院/30天主要发病率为44%,死亡率为0.6%,均在预先确定的安全基准范围内。NCCN型LAPC患者也达到了基准(主要发病率49%,死亡率2%)。结论:在全国范围内实施LAPC的国际最佳实践是可行的,手术数量是预期的近三倍,而发病率和死亡率保持在预定的安全基准之内。
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British Journal of Surgery
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