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Long-Term Endoscopic Follow-Up of Patients with Chronic Radiation Proctopathy after Brachytherapy for Prostate Cancer. 前列腺癌近距离放射治疗后慢性放射直病变患者的长期内镜随访。
Pub Date : 2016-01-01 Epub Date: 2016-06-09 DOI: 10.1155/2016/1414090
Masahiro Ohtani, Hiroyuki Suto, Takuto Nosaka, Yasushi Saito, Yoshihiko Ozaki, Ryoko Hayama, Tatsushi Naito, Kazuto Takahashi, Kazuya Ofuji, Hidetaka Matsuda, Katsushi Hiramatsu, Tomoyuki Nemoto, Hiroki Shioura, Hirohiko Kimura, Yoshitaka Aoki, Osamu Yokoyama, Yasunari Nakamoto

Background. Chronic radiation proctopathy (CRP) is late toxicity and associated with morbidity. Aim. To investigate the predictors of prognosis in patients with CRP after brachytherapy (BT). Methods. One hundred four patients with prostate cancer were treated with BT or BT followed by external-beam radiotherapy (BT + EBRT). We retrospectively investigated the 5-year incidence of rectal bleeding and endoscopic findings of CRP using the Vienna Rectoscopy Score (VRS). Twenty patients with VRS ≥ 1 were divided into the improved VRS group without treatment, unchanged VRS group, and treated group. The parameters associated with alteration of VRS were analyzed. Results. The incidence of rectal bleeding was 24%. The risk of rectal bleeding was higher in patients treated with BT + EBRT compared to those treated with BT (p < 0.0001). The incidence of superficial microulceration was higher in the improved VRS group than in the unchanged VRS group (p < 0.05). The incidence of multiple confluent telangiectasia or superficial ulcers > 1 cm(2) was higher in the treated group than in both the improved and unchanged VRS groups (p < 0.05). Conclusions. Patients treated with BT + EBRT have a high risk of CRP. Endoscopic findings were useful for prognostic prediction of CRP.

背景。慢性放射性直病变(CRP)是一种晚期毒性疾病,并伴有发病率。的目标。探讨近距离放射治疗(BT)后CRP患者预后的预测因素。方法。本文对104例前列腺癌患者进行BT或BT + EBRT外束放疗。我们使用维也纳直肠镜检查评分(VRS)回顾性调查了5年直肠出血的发生率和CRP的内镜检查结果。将20例VRS≥1的患者分为未经治疗的VRS改善组、VRS不变组和治疗组。分析了与VRS变化相关的参数。结果。直肠出血发生率为24%。与接受BT治疗的患者相比,接受BT + EBRT治疗的患者直肠出血的风险更高(p < 0.0001)。改良VRS组浅表微瘘发生率高于未改变VRS组(p < 0.05)。治疗组多发合流性毛细血管扩张或> 1 cm(2)的浅表溃疡发生率高于改善组和未改变组(p < 0.05)。结论。接受BT + EBRT治疗的患者发生CRP的风险较高。内镜检查结果对CRP的预后预测是有用的。
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引用次数: 1
Efficacy of the Ovesco Clip for Closure of Endoscope Related Perforations. Ovesco夹封闭内窥镜相关穿孔的疗效观察。
Pub Date : 2016-01-01 Epub Date: 2016-05-16 DOI: 10.1155/2016/9371878
Phonthep Angsuwatcharakon, Piyapan Prueksapanich, Pradermchai Kongkam, Thawee Rattanachu-Ek, Jaksin Sottisuporn, Rungsun Rerknimitr

Aim. To study the efficacy and other treatment outcomes of Ovesco clip closure of iatrogenic perforation. Methods. Retrospective study from 3 tertiary-care hospitals in Thailand. Patients with iatrogenic perforation who underwent immediate endoscopic closure by Ovesco clip were included. Patients' demographic data, perforation size, number of Ovesco clips used, fasting day, length of hospital stay, success rates, and complication rate were recorded. Technical success was defined as closure achievement during endoscopic procedure and clinical success was defined as the patient can be discharged without the need of additional surgical or radiological intervention. Results. There were 6 iatrogenic perforations in 2 male and 4 female patients. The median age was 59 years (range 39-78 years). The locations of perforation were 5 duodenal walls and 1 rectosigmoid junction. The median perforation size was 13 mm (range 10-40 mm). The technical success was 100% and the clinical success was 83.3%. The success rates per locations were 100% in colon and 80% in duodenum, respectively. The median fasting time was 5 days (range 1-10 days) and the median length of hospital stay was 10 days (range 2-22 days). There was no mortality in any. Conclusion. Ovesco clip seems to be an effective and safe tool for a closure of iatrogenic perforation.

的目标。探讨Ovesco夹封堵医源性穿孔的疗效及其他治疗效果。方法。来自泰国3家三级医院的回顾性研究。医源性穿孔患者接受立即内窥镜封闭Ovesco夹。记录患者的人口统计数据、穿孔大小、使用Ovesco夹的次数、禁食天数、住院时间、成功率和并发症发生率。技术成功被定义为在内镜手术过程中完成闭合,临床成功被定义为患者无需额外的手术或放射干预即可出院。结果。医源性穿孔6例,男2例,女4例。中位年龄为59岁(39-78岁)。穿孔部位为5个十二指肠壁和1个直肠乙状结肠交界处。中位穿孔尺寸为13 mm(范围10-40 mm)。技术成功率100%,临床成功率83.3%。结肠和十二指肠各部位的成功率分别为100%和80%。中位禁食时间为5天(范围1-10天),中位住院时间为10天(范围2-22天)。没有死亡率。结论。Ovesco夹似乎是一种有效和安全的工具,用于关闭医源性穿孔。
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引用次数: 18
Analysis of Non-Small Bowel Lesions Detected by Capsule Endoscopy in Patients with Potential Small Bowel Bleeding. 潜在小肠出血患者胶囊内镜检查非小肠病变的分析。
Pub Date : 2016-01-01 Epub Date: 2016-03-22 DOI: 10.1155/2016/9063293
Fatma Ebru Akin, Oyku Tayfur Yurekli, Aylin Demirezer Bolat, Mustafa Tahtacı, Huseyin Koseoglu, Eyup Selvi, Naciye Semnur Buyukasik, Osman Ersoy

Gastrointestinal (GI) bleeding cases in whom source cannot be identified after conventional upper and lower GI endoscopy are defined as potential small bowel bleeding. We aimed to search for lesions in the reach of conventional endoscopy in patients to whom video capsule endoscopy (VCE) had been applied for potential small bowel bleeding. 114 patients who had VCE evaluation for potential small bowel bleeding between January 2009 and August 2015 were retrospectively evaluated. Mean age of the patients was 55 ± 17 years. Female/male ratio is 39/75. In 58 patients (50.9%) bleeding lesion could be determined. Among these 58 patients 8 patients' lesions were in the reach of conventional endoscopes. Overall these 8 patients comprised 7% of patients in whom VCE was performed for potential small bowel bleeding. Among these 8 patients 5 had colonic lesions (4 angiodysplasia, 1 ulcerated polypoid cecal lesion), 2 had gastric lesions (1 GAVE, 1 anastomotic bleeding), and 1 patient had a bleeding lesion in the duodenal bulbus. Although capsule endoscopy is usually performed for potential small bowel bleeding gastroenterologists should always keep in mind that these patients may be suffering from bleeding from non-small bowel segments and should carefully review images captured from non-small bowel areas.

经常规上消化道和下消化道内镜检查无法确定来源的胃肠道出血病例被定义为潜在的小肠出血。我们的目的是寻找在传统内镜检查范围内的病变,这些患者已应用视频胶囊内镜检查潜在的小肠出血。回顾性分析了2009年1月至2015年8月间114例因潜在小肠出血而进行VCE评估的患者。患者平均年龄55±17岁。男女比例是39/75。58例(50.9%)患者可确定出血性病变。在58例患者中,8例病变在常规内窥镜可及范围内。总体而言,这8例患者占因潜在小肠出血而行VCE患者的7%。8例患者中,结肠病变5例(血管发育不全4例,盲肠息肉样溃疡1例),胃病变2例(腹腔出血1例,吻合口出血1例),十二指肠球部出血1例。虽然胶囊内窥镜检查通常用于潜在的小肠出血,但胃肠病学家应始终牢记,这些患者可能患有非小肠部分的出血,因此应仔细检查从非小肠区域拍摄的图像。
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引用次数: 5
Spiral Enteroscopy Utilizing Capsule Location Index for Achieving High Diagnostic and Therapeutic Yield 利用胶囊定位指数的螺旋肠镜检查达到高诊断和治疗率
Pub Date : 2015-11-19 DOI: 10.1155/2015/793516
R. Mandaliya, Jason Korenblit, B. O'hare, A. Shnitser, Ramalinga Kedika, R. Matro, D. Halegoua-De Marzio, A. Infantolino, M. Conn
Background and Aim. Spiral enteroscopy (SE) is a new small bowel endoscopic technique. Our aim is to review the diagnostic and therapeutic yield, safety of SE, and the predictive role of prior capsule endoscopy (CE) at an academic center. Methods. A retrospective review of patients undergoing SE after prior CE between 2008 and 2013 was performed. Capsule location index (CLI) was defined as the fraction of total small bowel transit time when the lesion was seen on CE. Results. A total of 174 SEs were performed: antegrade (147) and retrograde (27). Abnormalities on SE were detected in 65% patients. The procedure was safe in patients with surgically altered bowel anatomy (n = 12). The diagnostic yield of antegrade SE decreased with increasing CLI range. The diagnostic yield of retrograde SE decreased on decreasing CLI range. A CLI cutoff of 0.6 was derived that determined the initial route of SE. Vascular ectasias seen on CE were detected in 83% cases on SE; p < 0.01. Conclusions. SE is safe with a high diagnostic and therapeutic yield. CLI is predictive of the success of SE and determines the best route of SE. The type of small bowel pathology targeted by SE may affect its utility and yield.
背景和目的。螺旋肠镜是一种新型的小肠内镜技术。我们的目的是在一个学术中心回顾SE的诊断和治疗率、安全性以及先前胶囊内窥镜检查(CE)的预测作用。方法。对2008年至2013年间既往CE后接受SE治疗的患者进行回顾性研究。胶囊定位指数(CLI)被定义为在CE上看到病变时,总小肠通过时间的分数。结果。共行174例se:顺行147例,逆行27例。65%的患者检测到SE异常。手术对肠道解剖改变的患者是安全的(n = 12)。顺行性SE的诊断率随着CLI范围的增大而降低。逆行性SE的诊断率随着CLI范围的减小而降低。得到的CLI截断值为0.6,确定了SE的初始路由。CE检查发现血管扩张的病例占83%;P < 0.01。结论。SE是安全的,具有较高的诊断和治疗率。CLI可以预测SE的成功,并确定SE的最佳路由。小肠病理类型可能影响其效用和产量。
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引用次数: 7
Laparoscopic treatment of 1522 adnexal masses: an 8-year experience. 腹腔镜治疗附件肿物1522例:8年经验。
Pub Date : 2015-01-01 Epub Date: 2015-02-11 DOI: 10.1155/2015/979162
I Grammatikakis, P Trompoukis, S Zervoudis, C Mavrelos, P Economides, V Tziortzioti, N Evangelinakis, D Kassanos

Objective. To reevaluate the long-term effectiveness and safety of laparoscopy in benign ovarian pathology. Materials and Methods. 1522 women with benign adnexal cysts, laparoscopically treated in the 3rd Department of Ob/Gyn, General University hospital "Attikon" and "Lito" Maternity Hospital between July 1998 and December 2006, were included. Results. The diagnosis in 1222 (80,6%) cases was endometriosis of the ovary, 60 (4%) hydrosalpinx, 51 (3,3%) serous cystadenomas, 44 (2,9%) dermoid ovarian cyst, 38 (2,5%) borderline tumors, 35 (2,3%) unruptured follicles, and 33 (2,2%) paraovarian cysts. In 174 cases (11,5%) laparoscopy was converted to laparotomy due to technical difficulties or suspicion of cancer. In particular, laparotomy was performed in 119 (8%) women due to severe adhesions and 18 (1,2%) women due to bleeding that could not be controlled safely by laparoscopy. In 36 (2,4%) women frozen section during operation revealed malignancy and laparoscopy was converted to laparotomy. A few operative complications were recorded like post-op fever, small hematomas at the trocar entries. Conclusions. Laparoscopic surgery seems to offer significant advantages such as reduced hospital stay, less adverse effects, better quality of life, and superior vision especially on surgical treatment of cases like endometriosis.

目标。目的:重新评价腹腔镜治疗卵巢良性病变的远期疗效和安全性。材料与方法:选取1998年7月至2006年12月在阿提康综合大学医院和利托妇产医院妇产科第三科腹腔镜治疗的1522例良性附件囊肿患者。结果。1222例(806%)诊断为卵巢子宫内膜异位症,60例(4%)输卵管积水,51例(3.3%)浆液性囊腺瘤,44例(2.9%)卵巢皮样囊肿,38例(2.5%)交界性肿瘤,35例(2.3%)未破裂卵泡,33例(2.2%)卵巢旁囊肿。174例(11.5%)由于技术困难或怀疑癌症而转为开腹手术。其中119例(8%)因严重粘连而行剖腹手术,18例(1.2%)因出血不能通过腹腔镜安全控制而行剖腹手术。36例(2.4%)妇女术中冰冻切片发现恶性肿瘤,腹腔镜转为开腹手术。少数手术并发症如术后发热,套管针入口小血肿。结论。腹腔镜手术似乎具有显著的优势,如缩短住院时间,减少不良反应,提高生活质量,以及优越的视力,特别是在子宫内膜异位症的手术治疗中。
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引用次数: 15
Treatment of Internal Hemorrhoids by Endoscopic Sclerotherapy with Aluminum Potassium Sulfate and Tannic Acid. 硫酸铝钾联合单宁酸治疗内痔的内镜硬化疗法。
Pub Date : 2015-01-01 Epub Date: 2015-07-12 DOI: 10.1155/2015/517690
Yuichi Tomiki, Seigo Ono, Jun Aoki, Rina Takahashi, Shun Ishiyama, Kiichi Sugimoto, Yukihiro Yaginuma, Yutaka Kojima, Michitoshi Goto, Atsushi Okuzawa, Kazuhiro Sakamoto

Objective. A new sclerosing agent for hemorrhoids, aluminum potassium sulfate and tannic acid (ALTA), is attracting attention as a curative treatment for internal hemorrhoids without resection. The outcome and safety of ALTA sclerotherapy using an endoscope were investigated in the present study. Materials and Methods. Subjects comprised 83 internal hemorrhoid patients (61 males and 22 females). An endoscope was inserted and retroflexed in the rectum, and a 1st-step injection was applied to the upper parts of the hemorrhoids. The retroflexed scope was returned to the normal position, and 2nd-4th-step injections were applied to the middle and lower parts of the hemorrhoids under direct vision. The effects of endoscopic ALTA sclerotherapy were determined by evaluating the condition of the hemorrhoids using an anoscope and interviewing the patient 28 days after the treatment. Results. A cure, improvement, and failure were observed in 54 (65.1%), 27 (32.5%), and 2 (2.4%) patients, respectively, treated with ALTA. Complications developed in 4 patients (mild fever in 3 and hematuria in 1). Recurrence occurred in 9.6%. Conclusions. The results of the present study suggest that endoscopic ALTA has the potential to become a useful and minimally invasive approach for ALTA sclerotherapy.

目标。一种新型痔疮硬化剂硫酸铝钾单宁酸(ALTA)作为一种不切除内痔的根治性治疗方法正受到人们的关注。本研究探讨了内窥镜下ALTA硬化治疗的疗效和安全性。材料与方法。研究对象为83例内痔患者(男61例,女22例)。在直肠内插入内窥镜并后旋,第一步注射到痔疮上部。将后屈镜恢复到正常位置,在直视下对痔中下部进行第2 -4步注射。内镜下ALTA硬化治疗的效果是通过使用肛门镜评估痔疮状况并在治疗后28天对患者进行访谈来确定的。结果。在接受ALTA治疗的患者中,分别有54例(65.1%)、27例(32.5%)和2例(2.4%)患者治愈、改善和失败。4例出现并发症(3例轻度发热,1例血尿),9.6%出现复发。结论。本研究结果表明,内镜下ALTA有可能成为一种有用的微创ALTA硬化治疗方法。
{"title":"Treatment of Internal Hemorrhoids by Endoscopic Sclerotherapy with Aluminum Potassium Sulfate and Tannic Acid.","authors":"Yuichi Tomiki,&nbsp;Seigo Ono,&nbsp;Jun Aoki,&nbsp;Rina Takahashi,&nbsp;Shun Ishiyama,&nbsp;Kiichi Sugimoto,&nbsp;Yukihiro Yaginuma,&nbsp;Yutaka Kojima,&nbsp;Michitoshi Goto,&nbsp;Atsushi Okuzawa,&nbsp;Kazuhiro Sakamoto","doi":"10.1155/2015/517690","DOIUrl":"https://doi.org/10.1155/2015/517690","url":null,"abstract":"<p><p>Objective. A new sclerosing agent for hemorrhoids, aluminum potassium sulfate and tannic acid (ALTA), is attracting attention as a curative treatment for internal hemorrhoids without resection. The outcome and safety of ALTA sclerotherapy using an endoscope were investigated in the present study. Materials and Methods. Subjects comprised 83 internal hemorrhoid patients (61 males and 22 females). An endoscope was inserted and retroflexed in the rectum, and a 1st-step injection was applied to the upper parts of the hemorrhoids. The retroflexed scope was returned to the normal position, and 2nd-4th-step injections were applied to the middle and lower parts of the hemorrhoids under direct vision. The effects of endoscopic ALTA sclerotherapy were determined by evaluating the condition of the hemorrhoids using an anoscope and interviewing the patient 28 days after the treatment. Results. A cure, improvement, and failure were observed in 54 (65.1%), 27 (32.5%), and 2 (2.4%) patients, respectively, treated with ALTA. Complications developed in 4 patients (mild fever in 3 and hematuria in 1). Recurrence occurred in 9.6%. Conclusions. The results of the present study suggest that endoscopic ALTA has the potential to become a useful and minimally invasive approach for ALTA sclerotherapy. </p>","PeriodicalId":11288,"journal":{"name":"Diagnostic and Therapeutic Endoscopy","volume":"2015 ","pages":"517690"},"PeriodicalIF":0.0,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2015/517690","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33900378","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: 21
Comparison of Capsule Endoscopy Findings to Subsequent Double Balloon Enteroscopy: A Dual Center Experience. 胶囊内窥镜检查结果与随后的双球囊肠镜检查结果的比较:双中心经验。
Pub Date : 2015-01-01 Epub Date: 2015-09-01 DOI: 10.1155/2015/438757
Amandeep S Kalra, Andrew J Walker, Mark E Benson, Anurag Soni, Nalini M Guda, Mehak Misha, Deepak V Gopal

Background. There has been a growing use of both capsule endoscopy (CE) and double balloon enteroscopy (DBE) to diagnose and treat patients with obscure gastrointestinal blood loss and suspected small bowel pathology. Aim. To compare and correlate sequential CE and DBE findings in a large series of patients at two tertiary level hospitals in Wisconsin. Methods. An IRB approved retrospective study of patients who underwent sequential CE and DBE, at two separate tertiary care academic centers from May 2007 to December 2011, was performed. Results. 116 patients were included in the study. The mean age ± SD was 66.6 ± 13.2 years. There were 56% males and 43.9% females. Measure of agreement between prior capsule and DBE findings was performed using kappa statistics, which gave kappa value of 0.396 with P < 0.001. Also contingency coefficient was calculated and was found to be 0.732 (P < 0.001). Conclusions. Our study showed good overall agreement between DBE and CE. Findings of angioectasia had maximum agreement of 69%.

背景。胶囊内窥镜(CE)和双气囊肠镜(DBE)越来越多地用于诊断和治疗胃肠道出血不明和疑似小肠病理的患者。的目标。比较和关联威斯康星州两家三级医院大量患者的连续CE和DBE结果。方法。2007年5月至2011年12月,在两个独立的三级医疗学术中心进行了一项经IRB批准的回顾性研究,患者接受了连续CE和DBE。结果:116例患者纳入研究。平均年龄±SD为66.6±13.2岁。男性占56%,女性占43.9%。使用kappa统计量测量先前胶囊与DBE结果之间的一致性,kappa值为0.396,P < 0.001。权变系数为0.732 (P < 0.001)。结论。我们的研究显示DBE和CE之间的总体一致性很好。血管扩张的结果最大一致性为69%。
{"title":"Comparison of Capsule Endoscopy Findings to Subsequent Double Balloon Enteroscopy: A Dual Center Experience.","authors":"Amandeep S Kalra,&nbsp;Andrew J Walker,&nbsp;Mark E Benson,&nbsp;Anurag Soni,&nbsp;Nalini M Guda,&nbsp;Mehak Misha,&nbsp;Deepak V Gopal","doi":"10.1155/2015/438757","DOIUrl":"https://doi.org/10.1155/2015/438757","url":null,"abstract":"<p><p>Background. There has been a growing use of both capsule endoscopy (CE) and double balloon enteroscopy (DBE) to diagnose and treat patients with obscure gastrointestinal blood loss and suspected small bowel pathology. Aim. To compare and correlate sequential CE and DBE findings in a large series of patients at two tertiary level hospitals in Wisconsin. Methods. An IRB approved retrospective study of patients who underwent sequential CE and DBE, at two separate tertiary care academic centers from May 2007 to December 2011, was performed. Results. 116 patients were included in the study. The mean age ± SD was 66.6 ± 13.2 years. There were 56% males and 43.9% females. Measure of agreement between prior capsule and DBE findings was performed using kappa statistics, which gave kappa value of 0.396 with P < 0.001. Also contingency coefficient was calculated and was found to be 0.732 (P < 0.001). Conclusions. Our study showed good overall agreement between DBE and CE. Findings of angioectasia had maximum agreement of 69%. </p>","PeriodicalId":11288,"journal":{"name":"Diagnostic and Therapeutic Endoscopy","volume":"2015 ","pages":"438757"},"PeriodicalIF":0.0,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2015/438757","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34116148","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: 11
High Definition Colonoscopy Combined with i-SCAN Imaging Technology Is Superior in the Detection of Adenomas and Advanced Lesions Compared to High Definition Colonoscopy Alone. 高清结肠镜检查与 i-SCAN 成像技术相结合在腺瘤和晚期病变的检测方面优于单独使用高清结肠镜检查。
Pub Date : 2015-01-01 Epub Date: 2015-06-18 DOI: 10.1155/2015/167406
Erik A Bowman, Patrick R Pfau, Arnab Mitra, Mark Reichelderfer, Deepak V Gopal, Benjamin S Hall, Mark E Benson

Background. Improved detection of adenomatous polyps using i-SCAN has mixed results in small studies. Utility of i-SCAN as a primary surveillance modality for colorectal cancer screening during colonoscopy is uncertain. Aim. Comparing high definition white light endoscopy (HDWLE) to i-SCAN in their ability to detect adenomas during colonoscopy. Methods. Prospective cohort study of 1936 average risk patients who had a screening colonoscopy at an ambulatory procedure center. Patients underwent colonoscopy with high definition white light endoscopy withdrawal versus i-SCAN withdrawal during endoscopic screening exam. Primary outcome measurement was adenoma detection rate for i-SCAN versus high definition white light endoscopy. Secondary measurements included polyp size, pathology, and morphology. Results. 1007 patients underwent colonoscopy with i-SCAN and 929 with HDWLE. 618 adenomas were detected in the i-SCAN group compared to 402 in the HDWLE group (p < 0.01). More advanced adenomas (≥10 mm) were found by i-SCAN, 79 versus 47 (p = 0.021) and based upon histology alone 37 versus 18 (p = 0.028). Conclusions. i-SCAN detected significantly more adenomas and advanced adenomas compared to high definition white light endoscopy.

背景。在一些小型研究中,使用 i-SCAN 提高腺瘤息肉检测率的结果好坏参半。i-SCAN 作为结肠镜检查期间结直肠癌筛查的主要监测方式,其效用尚不确定。目的是比较高清白光内窥镜(HDWLE)和 i-SCAN 在结肠镜检查期间检测腺瘤的能力。方法:前瞻性队列研究对 1936 名在门诊手术中心接受结肠镜筛查的平均风险患者进行前瞻性队列研究。患者在接受结肠镜检查时,在内镜筛查检查过程中使用高清白光内镜抽取法和 i-SCAN 抽取法。主要结果是i-SCAN与高清白光内镜的腺瘤检出率。次要指标包括息肉大小、病理和形态。结果1007 名患者接受了 i-SCAN 结肠镜检查,929 名患者接受了高清白光内镜检查。i-SCAN 组检测出 618 个腺瘤,而 HDWLE 组检测出 402 个(P < 0.01)。i-SCAN 发现的晚期腺瘤(≥10 毫米)更多,分别为 79 个和 47 个(p = 0.021),而仅根据组织学发现的腺瘤则分别为 37 个和 18 个(p = 0.028)。结论:与高清白光内窥镜检查相比,i-SCAN 发现的腺瘤和晚期腺瘤明显更多。
{"title":"High Definition Colonoscopy Combined with i-SCAN Imaging Technology Is Superior in the Detection of Adenomas and Advanced Lesions Compared to High Definition Colonoscopy Alone.","authors":"Erik A Bowman, Patrick R Pfau, Arnab Mitra, Mark Reichelderfer, Deepak V Gopal, Benjamin S Hall, Mark E Benson","doi":"10.1155/2015/167406","DOIUrl":"10.1155/2015/167406","url":null,"abstract":"<p><p>Background. Improved detection of adenomatous polyps using i-SCAN has mixed results in small studies. Utility of i-SCAN as a primary surveillance modality for colorectal cancer screening during colonoscopy is uncertain. Aim. Comparing high definition white light endoscopy (HDWLE) to i-SCAN in their ability to detect adenomas during colonoscopy. Methods. Prospective cohort study of 1936 average risk patients who had a screening colonoscopy at an ambulatory procedure center. Patients underwent colonoscopy with high definition white light endoscopy withdrawal versus i-SCAN withdrawal during endoscopic screening exam. Primary outcome measurement was adenoma detection rate for i-SCAN versus high definition white light endoscopy. Secondary measurements included polyp size, pathology, and morphology. Results. 1007 patients underwent colonoscopy with i-SCAN and 929 with HDWLE. 618 adenomas were detected in the i-SCAN group compared to 402 in the HDWLE group (p < 0.01). More advanced adenomas (≥10 mm) were found by i-SCAN, 79 versus 47 (p = 0.021) and based upon histology alone 37 versus 18 (p = 0.028). Conclusions. i-SCAN detected significantly more adenomas and advanced adenomas compared to high definition white light endoscopy. </p>","PeriodicalId":11288,"journal":{"name":"Diagnostic and Therapeutic Endoscopy","volume":"2015 ","pages":"167406"},"PeriodicalIF":0.0,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488533/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33898666","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: 0
Opioid use is not associated with incomplete wireless capsule endoscopy for inpatient or outpatient procedures. 阿片类药物的使用与住院或门诊手术不完全无线胶囊内窥镜检查无关。
Pub Date : 2014-01-01 Epub Date: 2014-08-19 DOI: 10.1155/2014/651259
Bryan Kleinman, Peter P Stanich, Kavita Betkerur, Kyle Porter, Marty M Meyer

Objective. Wireless capsule endoscopy (WCE) is commonly used to directly visualize the small bowel. Opioids have variably been linked with incomplete studies and prolonged transit times in heterogeneous cohorts. We aimed to investigate the effect of opioid use on WCE for inpatient and outpatient cohorts. Methods. We performed a retrospective review of patients receiving WCE at our institution from April 2010 to March 2013. Demographic data, medical history, and WCE details were collected. Transit times were compared by log-rank analysis. Multivariable logistic regression and Cox proportional hazard models were utilized. Results. We performed 314 outpatient and 280 inpatient WCE that met study criteria. In the outpatient cohort, gastric transit time (GTT) was not significantly different between opioid and nonopioid users. Completion rates were similar as well (88% and 87%, P = 0.91). In the inpatient cohort, GTT was significantly longer in patients receiving opioids than in patients not receiving opioids (44 versus 23 min, P = 0.04), but completion rates were similar (71% versus 75%, P = 0.31). Conclusion. Opioid use within 24 hours of WCE did not significantly affect completion rates for inpatients or outpatients. GTT was prolonged in inpatients receiving opioids but not in outpatients.

目标。无线胶囊内窥镜(WCE)通常用于直接观察小肠。阿片类药物与异质性队列中不完整的研究和延长的转运时间有不同的联系。我们的目的是调查阿片类药物使用对住院和门诊患者WCE的影响。方法。我们对2010年4月至2013年3月在我院接受WCE治疗的患者进行了回顾性研究。收集了人口统计数据、病史和WCE详细信息。通过对数秩分析比较运输时间。采用多变量logistic回归和Cox比例风险模型。结果。我们进行了314例符合研究标准的门诊WCE和280例住院WCE。在门诊队列中,胃转运时间(GTT)在阿片类药物和非阿片类药物使用者之间没有显著差异。完成率相似(88%和87%,P = 0.91)。在住院患者队列中,接受阿片类药物治疗的患者GTT明显长于未接受阿片类药物治疗的患者(44分钟对23分钟,P = 0.04),但完成率相似(71%对75%,P = 0.31)。结论。在WCE的24小时内使用阿片类药物对住院和门诊患者的完成率没有显著影响。接受阿片类药物治疗的住院患者GTT延长,而门诊患者没有延长。
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引用次数: 3
Interobserver agreement for single operator choledochoscopy imaging: can we do better? 单一手术者胆道镜成像的观察者间一致性:我们能做得更好吗?
Pub Date : 2014-01-01 Epub Date: 2014-10-08 DOI: 10.1155/2014/730731
Amrita Sethi, Theodore Doukides, Divyesh V Sejpal, Douglas K Pleskow, Adam Slivka, Douglas G Adler, Raj J Shah, Steven A Edmundowicz, Takao Itoi, Bret T Petersen, Frank G Gress, Monica Gaidhane, Michel Kahaleh

Background. The SpyGlass Direct Visualization System (Boston Scientific, Natick, MA) is routinely used during single operator choledochoscopy (SOC) to identify biliary lesions or strictures with a diagnostic accuracy up to 88%. The objective of this study was to determine the interobserver agreement (IOA) of modified scoring criteria for diagnosing biliary lesions/strictures. Methods. 27 SPY SOC video clips were reviewed and scored by 9 interventional endoscopists based on published criteria that included the presence and severity of surface structure, vasculature visualization, lesions, and findings. Results. Overall IOA was "slight" for all variables. The K statistics are as follows: surface (K = 0.12, SE = 0.02); vessels (K = 0.14, SE = 0.02); lesions (K = 0.11, SE = 0.02); findings (K = 0.08, SE = 0.03); and final diagnosis (K = 0.08, SE = 0.02). The IOA for "findings" and "final diagnosis" was also only "slight." The final diagnosis was malignant (11), benign (11), and indeterminate (5). Conclusion. IOA using the modified criteria of SOC images was slight to almost poor. The average accuracy was less than 50%. These findings reaffirm that imaging criteria for benign and malignant biliary pathology need to be formally established and validated.

背景。SpyGlass直接可视化系统(Boston Scientific, Natick, MA)通常用于单操作员胆道镜检查(SOC),以识别胆道病变或狭窄,诊断准确率高达88%。本研究的目的是确定用于诊断胆道病变/狭窄的改进评分标准的观察者间一致性(IOA)。方法:9名介入内窥镜医师根据公开的标准对27个SPY SOC视频片段进行了回顾和评分,包括表面结构的存在和严重程度、脉管系统的可视化、病变和发现。结果。所有变量的总体IOA都是“轻微的”。K统计量如下:表面(K = 0.12, SE = 0.02);血管(K = 0.14, SE = 0.02);病变(K = 0.11, SE = 0.02);结果(K = 0.08, SE = 0.03);和最终诊断(K = 0.08, SE = 0.02)。“发现”和“最终诊断”的IOA也只有“轻微”。最终诊断为恶性(11例),良性(11例),不确定(5例)。使用改进的SOC图像标准的IOA轻微到几乎很差。平均准确率低于50%。这些发现重申了胆道良性和恶性病理的影像学标准需要正式建立和验证。
{"title":"Interobserver agreement for single operator choledochoscopy imaging: can we do better?","authors":"Amrita Sethi,&nbsp;Theodore Doukides,&nbsp;Divyesh V Sejpal,&nbsp;Douglas K Pleskow,&nbsp;Adam Slivka,&nbsp;Douglas G Adler,&nbsp;Raj J Shah,&nbsp;Steven A Edmundowicz,&nbsp;Takao Itoi,&nbsp;Bret T Petersen,&nbsp;Frank G Gress,&nbsp;Monica Gaidhane,&nbsp;Michel Kahaleh","doi":"10.1155/2014/730731","DOIUrl":"https://doi.org/10.1155/2014/730731","url":null,"abstract":"<p><p>Background. The SpyGlass Direct Visualization System (Boston Scientific, Natick, MA) is routinely used during single operator choledochoscopy (SOC) to identify biliary lesions or strictures with a diagnostic accuracy up to 88%. The objective of this study was to determine the interobserver agreement (IOA) of modified scoring criteria for diagnosing biliary lesions/strictures. Methods. 27 SPY SOC video clips were reviewed and scored by 9 interventional endoscopists based on published criteria that included the presence and severity of surface structure, vasculature visualization, lesions, and findings. Results. Overall IOA was \"slight\" for all variables. The K statistics are as follows: surface (K = 0.12, SE = 0.02); vessels (K = 0.14, SE = 0.02); lesions (K = 0.11, SE = 0.02); findings (K = 0.08, SE = 0.03); and final diagnosis (K = 0.08, SE = 0.02). The IOA for \"findings\" and \"final diagnosis\" was also only \"slight.\" The final diagnosis was malignant (11), benign (11), and indeterminate (5). Conclusion. IOA using the modified criteria of SOC images was slight to almost poor. The average accuracy was less than 50%. These findings reaffirm that imaging criteria for benign and malignant biliary pathology need to be formally established and validated. </p>","PeriodicalId":11288,"journal":{"name":"Diagnostic and Therapeutic Endoscopy","volume":"2014 ","pages":"730731"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2014/730731","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32816946","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: 30
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Diagnostic and Therapeutic Endoscopy
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