Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania.
Division of Gastroenterology and Hepatology, Stanford University School of Medicine, Stanford, California.
Gastroenterology. 2018 Feb;154(3):540-555.e8. doi: 10.1053/j.gastro.2017.10.006. Epub 2017 Oct 12.
The full spectrum of serious non-gastrointestinal post-colonoscopy complications has not been well characterized. We analyzed rates of and factors associated with adverse post-colonoscopy gastrointestinal (GI) and non-gastrointestinal events (cardiovascular, pulmonary, or infectious) attributable to screening or surveillance colonoscopy (S-colo) and non-screening or non-surveillance colonoscopy (NS-colo).
We performed a population-based study of colonoscopy complications using databases from California hospital-owned and nonhospital-owned ambulatory facilities, emergency departments, and hospitals from January 1, 2005 through December 31, 2011. We identified patients who underwent S-colo (1.58 million), NS-colo (1.22 million), or low-risk comparator procedures (joint injection, aspiration, lithotripsy; arthroscopy, carpal tunnel; or cataract; 2.02 million) in California's Ambulatory Services Databases. We identified patients who developed adverse events within 30 days, and factors associated with these events, through patient-level linkage to California's Emergency Department and Inpatient Databases.
After S-colo, the numbers of lower GI bleeding, perforation, myocardial infarction, and ischemic stroke per 10,000-persons were 5.3 (95% confidence interval [CI], 4.8-5.9), 2.9 (95% CI, 2.5-3.3), 2.5 (95% CI, 2.1-2.9), and 4.7 (95% CI, 4.1-5.2) without biopsy or intervention; with biopsy or intervention, numbers per 10,000-persons were 36.4 (95% CI, 35.1-37.6), 6.3 (95% CI, 5.8-6.8), 4.2 (95% CI, 3.8-4.7), and 9.1 (95% CI, 8.5-9.7). Rates of dysrhythmia were higher. After NS-colo, event rates were substantially higher. Most serious complications led to hospitalization, and most GI complications occurred within 14 days of colonoscopy. Ranges of adjusted odds ratios for serious GI complications, myocardial infarction, ischemic stroke, and serious pulmonary events after S-colo vs comparator procedures were 2.18 (95% CI, 2.02-2.36) to 5.13 (95% CI, 4.81-5.47), 0.67 (95% CI, 0.56-0.81) to 0.99 (95% CI, 0.83-1.19), 0.66 (95% CI, 0.59-0.75) to 1.13 (95% CI, 0.99-1.29), and 0.64 (95% CI, 0.61-0.68) to 1.05 (95% CI, 0.98-1.11). Biopsy or intervention, comorbidity, black race, low income, public insurance, and NS-colo were associated with post-colonoscopy adverse events.
In a population-based study in California, we found that following S-colo, rates of serious GI adverse events were low but clinically relevant, and that rates of myocardial infarction, stroke, and serious pulmonary events were no higher than after low-risk comparator procedures. Rates of myocardial infarction are similar to, but rates of stroke are higher than, those reported for the general population.
尚未充分描述严重非胃肠道结肠镜检查后并发症的全貌。我们分析了归因于筛查或监测结肠镜检查(S-colo)和非筛查或非监测结肠镜检查(NS-colo)的不良胃肠道(GI)和非胃肠道事件(心血管、肺部或感染)的发生率和相关因素。
我们使用加利福尼亚州医院所有和非医院所有门诊设施、急诊部和医院的数据库,从 2005 年 1 月 1 日至 2011 年 12 月 31 日,开展了结肠镜检查并发症的基于人群的研究。我们在加利福尼亚州门诊服务数据库中确定了接受 S-colo(158 万例)、NS-colo(122 万例)或低风险对照程序(关节注射、抽吸、碎石术;关节镜检查、腕管松解术;或白内障)的患者。我们通过患者与加利福尼亚州急诊部和住院部数据库的患者水平链接,确定了在 30 天内发生不良事件的患者,并确定了这些事件的相关因素。
在 S-colo 后,每 10000 人发生下胃肠道出血、穿孔、心肌梗死和缺血性中风的数量分别为 5.3(95%置信区间[CI],4.8-5.9)、2.9(95% CI,2.5-3.3)、2.5(95% CI,2.1-2.9)和 4.7(95% CI,4.1-5.2),无活检或干预;活检或干预后,每 10000 人发生的数量分别为 36.4(95% CI,35.1-37.6)、6.3(95% CI,5.8-6.8)、4.2(95% CI,3.8-4.7)和 9.1(95% CI,8.5-9.7)。心律失常的发生率更高。在 NS-colo 后,事件发生率明显更高。大多数严重并发症导致住院治疗,大多数胃肠道并发症发生在结肠镜检查后 14 天内。S-colo 与对照程序相比,严重 GI 并发症、心肌梗死、缺血性中风和严重肺部事件的调整后比值比范围为 2.18(95% CI,2.02-2.36)至 5.13(95% CI,4.81-5.47)、0.67(95% CI,0.56-0.81)至 0.99(95% CI,0.83-1.19)、0.66(95% CI,0.59-0.75)至 1.13(95% CI,0.99-1.29)和 0.64(95% CI,0.61-0.68)至 1.05(95% CI,0.98-1.11)。活检或干预、合并症、黑种人、低收入、公共保险和 NS-colo 与结肠镜检查后不良事件相关。
在加利福尼亚州的一项基于人群的研究中,我们发现,在接受 S-colo 后,严重胃肠道不良事件的发生率虽然较低,但具有临床意义,并且心肌梗死、中风和严重肺部事件的发生率与低风险对照程序相比并不更高。心肌梗死的发生率与一般人群相似,但中风的发生率高于一般人群。