首页> 外文期刊>Endoscopy: Journal for Clinical Use Biopsy and Technique >Prospective multicenter performance evaluation of the second-generation colon capsule compared with colonoscopy.
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Prospective multicenter performance evaluation of the second-generation colon capsule compared with colonoscopy.

机译:与结肠镜检查相比,对第二代结肠囊进行了多中心前瞻性评估。

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BACKGROUND AND STUDY AIMS: A second-generation capsule endoscopy system, using the PillCam Colon 2, was developed to increase sensitivity for colorectal polyp detection compared with the first-generation system. The performance of this new system is reported. PATIENTS AND METHODS: In a five-center feasibility study, second-generation capsule endoscopy was prospectively compared with conventional colonoscopy as gold standard for the detection of colorectal polyps and other colonic disease, in a cohort of patients scheduled for colonoscopy and having known or suspected colonic disease. Colonoscopy was independently performed within 10 hours after capsule ingestion. Capsule-positive but colonoscopy-negative cases were counted as false-positive. RESULTS: 104 patients (mean age 49.8 years) were enrolled; data from 98 were analyzed. Patient rate for polyps of any size was 44 %, 53 % of these patients having adenomas. No adverse events related to either procedure were reported. The capsule sensitivity for the detection of patients with polyps >or= 6 mm was 89 % (95 % confidence interval [CI] 70 - 97) and for those with polyps >or= 10 mm it was 88 % (95 %CI 56 - 98), with specificities of 76 % (95 %CI 72 - 78) and 89 % (95 %CI 86 - 90), respectively. Both polyps missed by colonoscopy and mismatch in polyp size by study definition lowered specificity. Overall colon cleanliness for capsule endoscopy was adequate in 78 % of patients (95 %CI 68 - 86). CONCLUSIONS: The new second-generation colon capsule endoscopy is a safe and effective method for visualizing the colon and detecting colonic lesions. Sensitivity and specificity for detecting colorectal polyps appear to be very good, suggesting a potential for improved accuracy compared with the first-generation system. Further prospective and comparative studies are needed.
机译:背景和研究目的:与第一代系统相比,开发了使用PillCam Colon 2的第二代胶囊内窥镜系统,以提高对结肠直肠息肉检测的敏感性。报告了此新系统的性能。患者和方法:在一个五中心可行性研究中,在预定进行结肠镜检查且已知或疑似患者的队列中,将第二代胶囊内镜检查与常规结肠镜检查作为检测结肠直肠息肉和其他结肠疾病的金标准进行了前瞻性比较。结肠疾病。胶囊摄取后10小时内独立进行结肠镜检查。胶囊阳性但结肠镜检查阴性的病例被视为假阳性。结果:104例患者(平均年龄49.8岁)入组。分析来自98的数据。任何大小的息肉的患者比率为44%,其中53%的患者患有腺瘤。没有报告与这两种手术相关的不良事件。检出息肉≥6 mm的患者的胶囊敏感度为89%(95%置信区间[CI] 70-97),检出息肉> or = 10 mm的患者的胶囊敏感度为88%(95%CI 56- 98),特异性分别为76%(95%CI 72-78)和89%(95%CI 86-90)。结肠镜检查遗漏的息肉和研究定义的息肉大小不匹配都会降低特异性。胶囊内窥镜检查的总体结肠清洁度在78%的患者中是足够的(95%CI 68-86)。结论:新型第二代结肠囊内窥镜检查是一种可视化结肠和检测结肠病变的安全有效的方法。检测大肠息肉的敏感性和特异性似乎非常好,这表明与第一代系统相比,其准确性可能有所提高。需要进一步的前瞻性和比较研究。

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