Complications of colonoscopy surveillance of patients with Lynch syndrome - 33 years of follow up.

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY Familial Cancer Pub Date : 2024-08-05 DOI:10.1007/s10689-024-00416-w
Alexander Frank, Sophie Walton Bernstedt, Nigin Jamizadeh, Anna Forsberg, Charlotte Hedin, Johannes Blom, Ann-Sofie Backman
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Abstract

Background and study aims: Lynch syndrome (LS) is a hereditary autosomal dominant condition, with an increased lifetime risk of developing malignancies including colorectal cancer (CRC). Current guidelines differ in recommended colonoscopy-surveillance intervals from 1 to 2 years. Although colonoscopy is considered a safe procedure, there are risks of severe adverse events (SAEs), such as perforation and bleeding, as well as adverse events (AEs), such as abdominal discomfort and post-colonoscopy gastrointestinal infections. Colonoscopy-related bleeding and perforation rates have been reported 0.17% and 0.11%, respectively. However, there are insufficient data regarding complications of colonoscopy-surveillance for LS patients. This study aims to investigate the risk of AEs among LS patients during colonoscopy in the Stockholm region.

Patients and methods: This retrospective cohort study includes 351 LS patients undergoing endoscopic surveillance at the Karolinska University Hospital, August 1989 - April 2021. Data from endoscopic surveillance colonoscopies were extracted from patients' medical records.

Results: Of 1873 endoscopies in 351 LS patients, 12 complications (AEs) were documented within 30 days (0.64%) and with a total of 3 bleedings (SAEs, 0.16%). No perforations were identified.

Conclusion: Colonoscopy surveillance for LS patients shows a comparatively low risk of AEs per-examination. Colonoscopy complications per-patient, including both SAEs and AEs, show a significantly higher risk. Colonoscopy complications only including SAEs, show a comparatively low risk. Understanding the lifetime risk of surveillance-related colonoscopy complications is important when designing targeted surveillance programmes.

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林奇综合征患者结肠镜检查监测并发症 - 33 年的随访。
背景和研究目的:林奇综合征(LS)是一种遗传性常染色体显性遗传病,终生罹患包括结肠直肠癌(CRC)在内的恶性肿瘤的风险增加。目前的指南建议结肠镜检查-监测的间隔时间从 1 年到 2 年不等。虽然结肠镜检查被认为是一种安全的检查方法,但也存在穿孔和出血等严重不良事件(SAE)以及腹部不适和结肠镜检查后胃肠道感染等不良事件(AE)的风险。据报道,结肠镜检查相关出血率和穿孔率分别为 0.17% 和 0.11%。然而,有关LS患者结肠镜监测并发症的数据并不充分。本研究旨在调查斯德哥尔摩地区 LS 患者在结肠镜检查期间发生 AEs 的风险:这项回顾性队列研究包括 1989 年 8 月至 2021 年 4 月期间在卡罗林斯卡大学医院接受内镜监测的 351 名 LS 患者。从患者的医疗记录中提取了内镜监测结肠镜检查的数据:在 351 名 LS 患者的 1873 次内镜检查中,有 12 例并发症(AE)在 30 天内发生(0.64%),共有 3 例出血(SAE,0.16%)。未发现穿孔:结论:对 LS 患者进行结肠镜检查监测显示,每次检查发生 AE 的风险相对较低。结肠镜检查并发症(包括 SAE 和 AE)发生在每位患者身上的风险明显较高。仅包括 SAE 的结肠镜检查并发症显示出相对较低的风险。在设计有针对性的监控计划时,了解与监控相关的结肠镜检查并发症的终生风险非常重要。
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来源期刊
Familial Cancer
Familial Cancer 医学-遗传学
CiteScore
4.10
自引率
4.50%
发文量
36
审稿时长
6-12 weeks
期刊介绍: In recent years clinical cancer genetics has become increasingly important. Several events, in particular the developments in DNA-based technology, have contributed to this evolution. Clinical cancer genetics has now matured to a medical discipline which is truly multidisciplinary in which clinical and molecular geneticists work together with clinical and medical oncologists as well as with psycho-social workers. Due to the multidisciplinary nature of clinical cancer genetics most papers are currently being published in a wide variety of journals on epidemiology, oncology and genetics. Familial Cancer provides a forum bringing these topics together focusing on the interests and needs of the clinician. The journal mainly concentrates on clinical cancer genetics. Most major areas in the field shall be included, such as epidemiology of familial cancer, molecular analysis and diagnosis, clinical expression, treatment and prevention, counselling and the health economics of familial cancer.
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