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Carbohydrate Antigen 19-9, Carcinoembryonic Antigen, and Carbohydrate Antigen 72-4 in Gastric Cancer: Is the Old Band Still Playing? 碳水化合物抗原19-9、癌胚抗原和碳水化合物抗原72-4在胃癌中的作用:老乐队还在演奏吗?
IF 1.6 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2018-09-01 Epub Date: 2018-04-24 DOI: 10.1159/000488240
Andrey Iskrenov Kotzev, Peter Vassilev Draganov

Background: Gastric cancer (GC) is characterized by aggressive behavior and a high mortality rate. The diagnosis of GC is challenging because the GC is often diagnosed in an advanced stage. The use of tumor markers is a putative way to improve the detection and treatment in patients with GC.

Summary: In this article, we review the significance of serum carbohydrate antigen (CA) 19-9, carcinoembryonic antigen (CEA), and CA 72-4 in GC. The results from different studies regarding the diagnostic and prognostic role of CA 19-9, CEA, and CA 72-4 in GC are encouraging, but inadequate sensitivity and specificity obstruct their use as standardized and unconditionally reliable markers in GC. New prospective clinical trials are mandatory for clarifying their value in GC.

Key message: CA 19-9, CEA, and CA 72-4 should not be used for screening and early diagnosis in GC, whereas they are beneficial in the detection of late GC. CA 19-9, CEA, and CA 72-4 could be used as prognostic and monitoring tools in GC, and their combined measurement in shorter periods of time is the best method to increase sensitivity and specificity.

Practical implications: Serum CA 19-9, CEA, and CA 72-4 are useful diagnostic and prognostic tumor markers in GC.

背景:胃癌具有侵袭性行为和高死亡率的特点。胃癌的诊断具有挑战性,因为胃癌通常在晚期诊断。肿瘤标志物的使用被认为是提高胃癌患者的检测和治疗的一种方法。摘要:本文综述了血清碳水化合物抗原(CA) 19-9、癌胚抗原(CEA)和CA 72-4在胃癌中的意义。关于CA 19-9、CEA和CA 72-4在胃癌中的诊断和预后作用的不同研究结果令人鼓舞,但灵敏度和特异性不足阻碍了它们作为胃癌标准化和无条件可靠的标志物的使用。新的前瞻性临床试验必须明确其在GC中的价值。关键信息:CA 19-9、CEA和CA 72-4不应用于胃癌的筛查和早期诊断,而它们对晚期胃癌的检测是有益的。CA 19-9、CEA和CA 72-4可作为GC的预后和监测工具,在较短时间内联合检测是提高敏感性和特异性的最佳方法。实际意义:血清ca19 -9、CEA和ca72 -4是胃癌有用的诊断和预后肿瘤标志物。
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引用次数: 28
Intraplatelet Vascular Endothelial Growth Factor and Platelet-Derived Growth Factor: New Biomarkers in Carcinoembryonic Antigen-Negative Colorectal Cancer? 血小板内血管内皮生长因子和血小板衍生生长因子:癌胚抗原阴性结直肠癌的新生物标志物?
IF 1.6 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2018-09-01 Epub Date: 2018-02-16 DOI: 10.1159/000486894
Charbel Chater, Anne Bauters, Claire Beugnet, Lena M'Ba, Moshe Rogosnitzky, Philippe Zerbib

Background/aim: Colorectal cancer (CRC) is associated with high incidence and mortality rates. Carcinoembryonic antigen (CEA), a prognostic biomarker for recurrent CRC following curative resection, suffers from low sensitivity, especially in early-stage screening. Intraplatelet angiogenesis regulators (IPAR), such as vascular endothelial growth factor (VEGF) and platelet-derived growth factor (PDGF), have been identified as important regulators of tumor growth in CRC. The aim of this study was to confirm the higher preoperative level of IPAR (VEGF and PDGF) in CRC patients compared to controls and to measure IPAR in CEA-negative CRC patients.

Methods: The data and blood of 30 CRC patients and 30 presumably healthy controls were prospectively analyzed and compared.

Results: We confirmed elevated preoperative intraplatelet VEGF and PDGF levels in CRC patients compared to controls. Importantly, IPAR were significantly elevated even in CEA-negative CRC patients.

Conclusion: Elevated preoperative intraplatelet VEGF and PDGF levels in CRC patients suggest new possibilities for postoperative monitoring in CRC patients, especially when CEA is negative.

背景/目的:结直肠癌(CRC)具有高发病率和高死亡率。癌胚抗原(CEA)是治疗性切除后复发性结直肠癌的预后生物标志物,其敏感性较低,尤其是在早期筛查中。血小板内血管生成调节剂(IPAR),如血管内皮生长因子(VEGF)和血小板衍生生长因子(PDGF),已被确定为结直肠癌肿瘤生长的重要调节剂。本研究的目的是确认CRC患者术前IPAR (VEGF和PDGF)水平高于对照组,并测量cea阴性CRC患者的IPAR。方法:对30例结直肠癌患者和30例推定健康对照者的资料和血液进行前瞻性分析和比较。结果:我们证实,与对照组相比,CRC患者术前血小板内VEGF和PDGF水平升高。重要的是,即使在cea阴性的CRC患者中,IPAR也显著升高。结论:结直肠癌患者术前血小板内VEGF和PDGF水平升高,为结直肠癌患者术后监测提供了新的可能性,特别是当CEA阴性时。
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引用次数: 8
Network Meta-Analysis of Adjuvant Chemotherapy following Resection of Colorectal Liver Metastases. 结直肠肝转移瘤切除术后辅助化疗的网络meta分析。
IF 1.6 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2018-09-01 Epub Date: 2018-07-25 DOI: 10.1159/000490763
Paschalis Gavriilidis, Aurelio Tobias, Robert P Sutcliffe, Daniel Azoulay, Keith J Roberts

Objective: Six principal adjuvant chemotherapy treatments (ACTs) are currently available for patients with resected colorectal liver metastases. This meta-analysis was designed to determine the optimal ACT, as evaluated by 2-year disease-free survival (DFS) and 5-year overall survival (OS) rates as well as by hepatic recurrences and adverse events (AEs).

Methods: A systematic literature search of the PubMed, EMBASE, Medline, Cochrane Library, and Google Scholar databases was performed. The probability of the optimal therapeutic scheme and the mean ranking were estimated for each treatment using network meta-analysis.

Results: Systemic chemotherapy (SCT) had the best 2-year DFS rate (hazard ratio [HR] = 0.78, 95% confidence interval [CI] = 0.48-1.27, 95% prediction interval [PI] = 0.17-3.56, surface under the cumulative ranking area [SUCRA] = 73) and the lowest AE rate (estimated SUCRA = 65 and predicted SUCRA = 62). Hepatic arterial infusion (HAI) plus SCT had the best 5-year OS rate (HR = 0.81, 95% CI = 0.64-1.01, 95% PI = 0.50-1.29) and the lowest hepatic recurrence rate (odds ratio = 2.87, 95% CI = 1.56-5.30, 95% PI = 0.61-13.62).

Conclusion: Both SCT and HAI plus SCT showed superior efficacy and safety. Clinical trials in homogeneous populations with strict selection criteria are needed to compare these two ACTs.

目的:目前有6种主要的辅助化疗(act)可用于结直肠肝转移切除患者。该荟萃分析旨在确定最佳ACT,通过2年无病生存(DFS)和5年总生存(OS)率以及肝脏复发和不良事件(ae)进行评估。方法:系统检索PubMed、EMBASE、Medline、Cochrane Library和Google Scholar数据库的文献。使用网络荟萃分析估计每种治疗方案的最佳治疗方案的概率和平均排名。结果:全身化疗(SCT)的2年DFS率最高(风险比[HR] = 0.78, 95%可信区间[CI] = 0.48 ~ 1.27, 95%预测区间[PI] = 0.17 ~ 3.56,累积排序区下表面[SUCRA] = 73), AE率最低(估计SUCRA = 65,预测SUCRA = 62)。肝动脉输注(HAI) + SCT具有最佳的5年OS (HR = 0.81, 95% CI = 0.64-1.01, 95% PI = 0.50-1.29)和最低的肝脏复发率(优势比= 2.87,95% CI = 1.56-5.30, 95% PI = 0.61-13.62)。结论:SCT与HAI + SCT均具有较好的疗效和安全性。需要在具有严格选择标准的同质人群中进行临床试验来比较这两种ACTs。
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引用次数: 2
Survival of Hepatocellular Carcinoma Patients Treated with Sorafenib beyond Progression. 索拉非尼治疗肝细胞癌患者进展后的生存率。
IF 1.6 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2018-09-01 Epub Date: 2018-04-11 DOI: 10.1159/000487635
Leonidas Apostolidis, Jan Pfeiffenberger, Daniel Gotthardt, Boris Radeleff, Arianeb Mehrabi, Peter Schemmer, Dirk Jäger, Peter Schirmacher, Wolfgang Stremmel, Henning Schulze-Bergkamen, Christoph Springfeld, Karl Heinz Weiss

Background/aim: Sorafenib leads to improved survival in advanced hepatocellular carcinoma (HCC) patients. Continuation of sorafenib beyond progression has been a possible treatment strategy when further approved therapeutic agents are lacking.

Methods: We performed a retrospective analysis of all HCC patients at our institution with documented disease progression under treatment with sorafenib. Overall survival (OS) from start of sorafenib treatment was compared between patients who received sorafenib for > 3 weeks beyond progression (group 1) and those who discontinued sorafenib ≤3 weeks after progression (group 2). Group 1 was further subdivided into those patients who received sorafenib for > 3 months (group 1a) and those who received it for ≤3 months (group 1b).

Results: A total of 71 patients were analyzed. Median OS for all patients was 15.4 months. OS in group 1 (15.6 months) and 2 (13.0 months) was similar (p = 0.90). Patients in group 1a showed significantly prolonged median OS (19.7 months) compared to that of patients in group 1b (13.6 months, p = 0.004), and they showed a trend towards prolonged OS compared to group 2 (p = 0.126). For patients with a poor prognosis according to their Child-Pugh stage, performance status, alpha-fetoprotein, and response to prior sorafenib treatment, OS was significantly prolonged in group 1 versus group 2 (12.1 vs. 6.4 months, p = 0.019).

Conclusion: In HCC patients, continuing sorafenib beyond progression for > 3 months is associated with improved survival compared to discontinuing sorafenib within 3 months. Furthermore, patients with a poor prognosis who continue sorafenib beyond progression in general show significantly prolonged survival.

背景/目的:索拉非尼可提高晚期肝细胞癌(HCC)患者的生存率。当缺乏进一步批准的治疗药物时,继续使用索拉非尼是一种可能的治疗策略。方法:我们对我院所有在索拉非尼治疗下有疾病进展记录的HCC患者进行了回顾性分析。从索拉非尼治疗开始的总生存期(OS)比较进展后接受索拉非尼治疗> 3周的患者(1组)和进展后≤3周停用索拉非尼的患者(2组)。1组进一步细分为接受索拉非尼治疗> 3个月的患者(1a组)和接受索拉非尼治疗≤3个月的患者(1b组)。结果:共分析71例患者。所有患者的中位OS为15.4个月。第1组(15.6个月)和第2组(13.0个月)的OS相似(p = 0.90)。与1b组(13.6个月,p = 0.004)相比,1a组患者的中位生存期明显延长(19.7个月);与2组相比,1a组患者的中位生存期有延长的趋势(p = 0.126)。根据Child-Pugh分期、运动状态、甲胎蛋白和对先前索拉非尼治疗的反应,预后较差的患者,1组OS明显延长(12.1个月vs 6.4个月,p = 0.019)。结论:在HCC患者中,与在3个月内停用索拉非尼相比,继续使用索拉非尼超过进展期3个月与生存率提高相关。此外,预后不良的患者在进展后继续使用索拉非尼,一般会显着延长生存期。
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引用次数: 9
Beyond the Beyond: A Case of an Extraordinary Response to Multiple Lines of Therapy in a de novo Metastatic HER2-Negative Gastric Cancer Patient. 超越超越:一个新发转移性her2阴性胃癌患者对多种治疗的非凡反应的案例。
IF 1.6 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2018-09-01 Epub Date: 2018-07-27 DOI: 10.1159/000488983
Cinzia Baldessari, Fabio Gelsomino, Andrea Spallanzani, Giuseppe Pugliese, Luca Reggiani Bonetti, Stefania Bettelli, Stefano Cascinu

Background: Gastric cancer is the fourth cause of cancer-related death in Europe and the prognosis of these patients remains dismal. It has been demonstrated that chemotherapy improved survival compared with best supportive care and recently, subsequent lines of therapy, also with new drugs, obtained positive results.

Summary: We present the case of a patient diagnosed with a de novo metastatic gastric cancer who experienced an extraordinary long response to multiple lines of chemotherapy (FOLFOX6, paclitaxel plus ramucirumab, FOLFIRI, rechallenge with FOLFOX6).

Key message: Gastric cancer therapy should be considered as the result of a strategy based on the patient's condition, and tolerance and response to various therapies. The emerging evidence of the role of subsequent lines of therapy, along with the recognition of the pivotal role of nutritional support and the availability of new drugs, should help clinicians in the management of patients with gastric cancer.

Practical implications: We propose a practical therapeutic algorithm in order to help clinicians who deal with patients with gastric cancer.

背景:胃癌是欧洲癌症相关死亡的第四大原因,这些患者的预后仍然令人沮丧。已经证明,与最佳支持治疗相比,化疗提高了生存率,最近,后续的治疗,也包括新药,取得了积极的结果。摘要:我们报告了一例被诊断为新发转移性胃癌的患者,他对多线化疗(FOLFOX6,紫杉醇加ramucirumab, FOLFIRI, FOLFOX6再挑战)有非常长的反应。关键信息:胃癌治疗应根据患者的病情、对各种治疗的耐受性和反应来考虑策略的结果。随着对营养支持的关键作用的认识和新药物的可用性,后续治疗线的作用的新证据应该有助于临床医生对胃癌患者的管理。实际意义:我们提出了一个实用的治疗算法,以帮助临床医生谁处理胃癌患者。
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引用次数: 4
No Evidence for an Association between JC Polyomavirus Infection and Gastroduodenal Diseases. 没有证据表明JC多瘤病毒感染与胃十二指肠疾病有关。
IF 1.6 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2018-09-01 Epub Date: 2018-07-11 DOI: 10.1159/000489928
Azadeh Yazdani Cherati, Yousef Yahyapour, Mohammad Ranaee, Mehdi Rajabnia, Javad Shokri Shirvani, Mahmoud Hajiahmadi, Farzin Sadeghi

Background: Helicobacter pylori (HP) infection is one of the hypothesized infectious etiologies of gastric cancer (GC) and other gastroduodenal diseases. It was suggested that other infectious agents, including oncogenic viruses, may increase the risk of gastroduodenal diseases. A number of reports regarding JC polyomavirus (JCPyV) have shown that JCPyV could be implicated in colorectal cancer and gastrointestinal carcinogenesis.

Objective: The current investigation aimed to investigate whether JCPyV could have any association with the pathogenesis of gastroduodenal diseases either alone or together with HP.

Methods: A total of 237 fresh or formalin-fixed and paraffin-embedded gastroduodenal samples were examined by quantitative real-time polymerase chain reaction targeting the JCPyV large tumor antigen (LTag) oncogene, and viral load was determined as viral copy number/cell.

Results: In total, 2 out of 237 samples (0.8%) were positive for JCPyV LTag DNA. One positive sample derived from diffuse-type gastric adenocarcinoma (6.8 × 10-3 copies/cell) and other JCPyV-positive sample obtained from a patient with gastritis (2.5 × 10-3 copies/cell) were recorded. Both JCPyV-positive samples were negative for HP infection.

Conclusion: This study suggests no association between JCPyV infection and GC or other gastroduodenal diseases. The very low frequency of JCPyV LTag sequences in GC is an important aspect that weakens the hypothesis of the pathogenic role of JCPyV in gastric tumor induction.

背景:幽门螺杆菌(Helicobacter pylori, HP)感染是胃癌(GC)和其他胃十二指肠疾病的假设感染病因之一。提示其他感染因子,包括致癌病毒,可能增加胃十二指肠疾病的风险。许多关于JC多瘤病毒(JCPyV)的报道表明,JCPyV可能与结直肠癌和胃肠道癌变有关。目的:本研究旨在探讨JCPyV是否单独或与HP一起与胃十二指肠疾病的发病机制有关。方法:采用实时荧光定量聚合酶链反应检测新鲜、福尔马林固定和石蜡包埋胃十二指肠标本237份,检测jjcpyv大肿瘤抗原(LTag)致癌基因,以病毒拷贝数/细胞为单位测定病毒载量。结果:237份样本中有2份(0.8%)jjcpyv LTag DNA阳性。我们记录了一份来自弥漫性胃腺癌的阳性样本(6.8 × 10-3拷贝/细胞)和另一份来自胃炎患者的jcpyv阳性样本(2.5 × 10-3拷贝/细胞)。两份jcpyv阳性样本均为HP感染阴性。结论:本研究提示JCPyV感染与GC或其他胃十二指肠疾病无相关性。JCPyV LTag序列在胃癌中的极低频率是削弱JCPyV在胃肿瘤诱导中的致病作用假设的一个重要方面。
{"title":"No Evidence for an Association between JC Polyomavirus Infection and Gastroduodenal Diseases.","authors":"Azadeh Yazdani Cherati,&nbsp;Yousef Yahyapour,&nbsp;Mohammad Ranaee,&nbsp;Mehdi Rajabnia,&nbsp;Javad Shokri Shirvani,&nbsp;Mahmoud Hajiahmadi,&nbsp;Farzin Sadeghi","doi":"10.1159/000489928","DOIUrl":"https://doi.org/10.1159/000489928","url":null,"abstract":"<p><strong>Background: </strong><i>Helicobacter pylori</i> (HP) infection is one of the hypothesized infectious etiologies of gastric cancer (GC) and other gastroduodenal diseases. It was suggested that other infectious agents, including oncogenic viruses, may increase the risk of gastroduodenal diseases. A number of reports regarding JC polyomavirus (JCPyV) have shown that JCPyV could be implicated in colorectal cancer and gastrointestinal carcinogenesis.</p><p><strong>Objective: </strong>The current investigation aimed to investigate whether JCPyV could have any association with the pathogenesis of gastroduodenal diseases either alone or together with HP.</p><p><strong>Methods: </strong>A total of 237 fresh or formalin-fixed and paraffin-embedded gastroduodenal samples were examined by quantitative real-time polymerase chain reaction targeting the JCPyV large tumor antigen (LTag) oncogene, and viral load was determined as viral copy number/cell.</p><p><strong>Results: </strong>In total, 2 out of 237 samples (0.8%) were positive for JCPyV LTag DNA. One positive sample derived from diffuse-type gastric adenocarcinoma (6.8 × 10<sup>-3</sup> copies/cell) and other JCPyV-positive sample obtained from a patient with gastritis (2.5 × 10<sup>-3</sup> copies/cell) were recorded. Both JCPyV-positive samples were negative for HP infection.</p><p><strong>Conclusion: </strong>This study suggests no association between JCPyV infection and GC or other gastroduodenal diseases. The very low frequency of JCPyV LTag sequences in GC is an important aspect that weakens the hypothesis of the pathogenic role of JCPyV in gastric tumor induction.</p>","PeriodicalId":45017,"journal":{"name":"Gastrointestinal Tumors","volume":"5 1-2","pages":"47-53"},"PeriodicalIF":1.6,"publicationDate":"2018-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000489928","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36805670","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Front & Back Matter 正面和背面
IF 1.6 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2018-09-01 DOI: 10.1159/000493441
J. Szepietowski, E. Weisshaar, V. Blanchette, L. Brandão, V. Breakey, S. Revel-Vilk, Q. Nguyen, E. Rodrigues, M. Farah, W. Mieler, D. Do, O. Michielin, G. Coukos, Jing-yuan Fang, P. Malfertheiner, M. Büchler
submission deadline: 6 April 2018 Early registration deadline: 25 June 2018 www.ilca2018.org THE INTERNATIONAL LIVER CANCER ASSOCIATION ANNOUNCES ITS 12 TH ANNUAL CONFERENCE
提前注册截止日期:2018年6月25日www.ilca2018.org国际肝癌协会宣布其第12届年会
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引用次数: 0
Finally, a Minimally Invasive Option for Intrahepatic Inferior Vena Cava Invasion by Hepatocellular Carcinoma. 最后,一种治疗肝细胞癌肝内下腔静脉侵犯的微创选择。
IF 1.6 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2018-09-01 Epub Date: 2018-08-17 DOI: 10.1159/000491694
Erik Soule, Jerry Matteo

Background: Major vessel invasion is a late manifestation of hepatocellular carcinoma, which may directly result in mortality if left untreated. Surgical resection may be an option for select patients; however, surgery may be contraindicated. Contraindications include multifocal disease, poor liver reserve, inability to tolerate surgery, and patient preference. Cryoablation is a minimally invasive therapy utilized for treating hepatic neoplasms by subjecting them to extreme cold temperatures. The "thermal sink" effect describes cryoablation near flowing blood such as that found in high volumes within major vascular structures. Thermodynamics dictates that proximity to the flowing intravascular compartment will decrease ice formation, and therefore, tumor destruction.

Methods: This report describes a novel palliative technique to induce temporary cessation of the blood flow in the intrahepatic inferior vena cava (IVC), thus enabling the operator to perform cryoablation targeting invasive cancer within.

Results: Adequate ablation using this technique allowed a patient with IVC invasion 9 months of survival.

Conclusion: Quality of life during this time was maximized, as recovery time from this procedure is minimal.

背景:大血管侵犯是肝细胞癌的晚期表现,如果不及时治疗,可能直接导致死亡。手术切除可能是选择的患者;然而,手术可能是禁忌。禁忌症包括多灶性疾病、肝脏储备不良、不能耐受手术和患者偏好。冷冻消融是一种微创疗法,用于治疗肝脏肿瘤,使其处于极冷的温度下。“热沉”效应描述了在流动血液附近的冷冻消融,例如在主要血管结构中发现的高容量血液。热力学表明,靠近流动的血管内腔室会减少冰的形成,从而减少肿瘤的破坏。方法:本报告描述了一种新的姑息治疗技术,可以诱导肝内下腔静脉(IVC)的血液流动暂时停止,从而使操作员能够针对肝内的浸润性癌症进行冷冻消融。结果:使用该技术进行充分的消融可使下腔静脉侵入患者存活9个月。结论:这段时间的生活质量得到了最大限度的提高,因为该手术的恢复时间最短。
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引用次数: 8
Contents Volume 4, 2017 目录2017年第4卷
IF 1.6 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2018-02-01 DOI: 10.1159/000487415
P. Malfertheiner, Jing-yuan Fang, P. Malfertheiner, M. Büchler, Y. Kodera, Yingbin Liu, K. Mönkemüller, G. Nakayama, G. Rogler, M. Scharl, Jianqiu Sheng, Masao Tanaka, J. Lanschot, Ming-Rong Wang, B. Wiedenmann, Kaichun Wu, Jie Xu, P. Zhou
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引用次数: 0
Impact of Three-Dimensional Surgical Simulation on Pancreatic Surgery. 三维手术模拟对胰腺手术的影响。
IF 1.6 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2018-02-01 Epub Date: 2017-12-07 DOI: 10.1159/000484894
Ryoichi Miyamoto, Yukio Oshiro, Ken Nakayama, Nobuhiro Ohkohchi

Background/aims: Anatomical variations are frequently encountered during hepato-biliary-pancreatic surgeries, requiring surgeons to have a precise understanding of the surgical anatomy in order to perform a safe surgery. We evaluated the impact of novel three-dimensional (3D) surgical simulation on pancreatic surgeries to enhance surgical residents' understanding.

Methodology: Between January 2013 and May 2014, 61 preoperative 3D surgical simulations were performed. The consistency (0-10, with 10 representing 100% consistency) among the 15 surgical residents' anatomical drawings from multidetector computed tomography images and the simulated 3D images by SYNAPSE VINCENT® was assessed. We divided the surgical residents into two groups - first- to fifth-year postgraduate doctors (group A) and sixth- to tenth-year postgraduate doctors (group B) - and compared the self-assessment scores between these two groups.

Results: In terms of the self-assessment scores, a statistically significant difference was observed between the two groups (p < 0.001).

Conclusions: In this study, 3D surgical simulation was useful for preoperative assessments prior to pancreatic surgery, especially in younger postgraduate surgeons.

背景/目的:肝胆胰手术中经常遇到解剖变异,这要求外科医生对手术解剖有准确的了解,以便进行安全的手术。我们评估了新型三维(3D)手术模拟对胰腺手术的影响,以提高外科住院医师的理解。方法:2013年1月至2014年5月,进行61例术前3D手术模拟。评估了15名外科住院医师多探测器计算机断层扫描图像和SYNAPSE VINCENT®模拟3D图像的解剖图之间的一致性(0-10,10代表100%一致性)。我们将外科住院医师分为两组——一至五年级研究生医生组(A组)和六至十年级研究生医生组(B组)——并比较两组之间的自我评估分数。结果:两组患者自评得分比较,差异有统计学意义(p < 0.001)。结论:在本研究中,三维手术模拟对胰腺手术前的术前评估是有用的,特别是对年轻的研究生外科医生。
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引用次数: 15
期刊
Gastrointestinal Tumors
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