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Colonoscopy-related complications in a nationwide immunochemical fecal occult blood test-based colorectal cancer screening program

机译:基于全国免疫化学粪便潜血试验的结肠直肠癌筛查计划中的结肠镜检查相关并发症

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Background: The Danish national screening program for colorectal cancer (CRC) consists of an immunochemical fecal occult blood test (iFOBT) followed by colonoscopy. The Danish Colorectal Cancer Screening Database (DCCSD) records data on the incidence of hospital-registered complications after colonoscopy. However, the validity of these data is unknown, and the incidence of complications is potentially underreported. Objective: To evaluate the validity of the colonoscopy complications registered in the DCCSD by using medical records as the reference. Further, to evaluate the incidence of complications leading to hospital contact. Methods: Among 14,671 individuals with a positive iFOBT result and a colonoscopy procedure performed from March 3, 2014 to December 31, 2014, we selected 295 individuals for medical record review. We calculated sensitivity as the proportion of true complications registered in the DCCSD out of all complications found in the medical records, and the positive predictive value (PPV) as the number of true complications in the DCCSD out of all DCCSD-registered complications. On the basis of the medical record data, we calculated the incidence proportion of hospital-registered complications overall and by subtype. Results: In total, we reviewed 286 records and found 102 individuals with at least one complication. The sensitivity of the DCCSD for any complication was 29.4% (95% CI: 20.8–39.3) and the PPV was 88.2% (95% CI: 72.6–96.7). On the basis of the medical record data, the incidence proportion of any complication after colonoscopy was 0.70% (95% CI: 0.57–0.84) and that of perforation or lesion was 0.10% (95% CI: 0.06–0.17); bleeding, 0.41% (95% CI: 0.31–0.53); post-polypectomy syndrome, 0.16% (95% CI: 0.10–0.24); and other medical complications, 0.04 (95% CI: 0.02–0.09). Conclusion: The DCCSD has low sensitivity for complications, and improvements in data registration are warranted. The incidence proportion of any hospital-treated post-colonoscopy complication was 0.70% in 2014, which was the first year of the Danish national CRC screening program. This is within the range of complications reported by other studies.
机译:背景:丹麦国家大肠癌筛查计划(CRC)包括免疫化学粪便潜血试验(iFOBT),然后进行结肠镜检查。丹麦结肠直肠癌筛查数据库(DCCSD)记录了结肠镜检查后医院登记的并发症发生率的数据。但是,这些数据的有效性是未知的,并发症的发生率可能被低估。目的:以医疗记录为参考,评估DCCSD中登记的结肠镜检查并发症的有效性。此外,评估导致医院接触的并发症的发生率。方法:从2014年3月3日至2014年12月31日,在iFOBT结果为阳性并进行结肠镜检查的14,671名患者中,我们选择了295名患者进行病历审查。我们将敏感度计算为在病历中发现的所有并发症中DCCSD中记录的真正并发症的比例,将阳性预测值(PPV)作为所有DCCSD中记录的并发症中DCCSD中真正并发症的数量。根据病历数据,我们按整体和亚型计算了医院登记并发症的发生比例。结果:总共,我们审查了286记录,发现102例患者中至少有一种并发症。 DCCSD对任何并发症的敏感性为29.4%(95%CI:20.8–39.3),PPV为88.2%(95%CI:72.6–96.7)。根据病历数据,结肠镜检查后任何并发症的发生比例为0.70%(95%CI:0.57–0.84),穿孔或病变的发生率为0.10%(95%CI:0.06-0.17);出血,0.41%(95%CI:0.31-0.53);息肉切除术后综合征,0.16%(95%CI:0.10–0.24);和其他医疗并发症,0.04(95%CI:0.02–0.09)。结论:DCCSD对并发症的敏感性较低,因此有必要改善数据注册。 2014年,这是丹麦国家CRC筛查计划的第一年,任何医院治疗的结肠镜检查后并发症的发生率均为0.70%。这在其他研究报告的并发症范围内。

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