Digestive Disease Center, Institute for Digestive Research, Department of Internal Medicine, Soonchunhyang University College of Medicine, Seoul, South Korea.
J Dig Dis. 2018 May;19(5):279-287. doi: 10.1111/1751-2980.12600. Epub 2018 Jun 6.
Limited evidence is available on rebleeding due to nonsteroidal anti-inflammatory drugs (NSAIDs)-induced enteropathy. Previous studies have primarily analyzed endoscopic findings. Therefore, there is a need to evaluate their clinical implications for patients. This study aimed to evaluate the rebleeding rate and its related risk factors in patients with NSAIDs-induced enteropathy.
Of 402 patients with obscure gastrointestinal bleeding who were evaluated with capsule endoscopy, 49 were diagnosed with NSAIDs-induced enteropathy. The clinical characteristics of the patients were retrospectively analyzed. The Charlson comorbidity index was used to stratify the comorbidities. For patients who used additional drugs that influenced their tendency to bleeding, the odds ratio was calculated and used for a quantitative comparison.
The rebleeding rate in patients with NSAIDs-induced enteropathy was 20.4%, within a mean duration of 23.4 months. Age ≥65 years (hazard ratio [HR] 8.628, 95% confidence interval [CI] 1.152-64.625), no additional use of mucoprotective agents (HR 11.712, 95% CI 1.278-76.098) and the continuation of NSAIDs after the first bleeding episode (HR 9.861, 95% CI 1.395-98.344) were independently related to rebleeding due to NSAIDs-induced enteropathy. The underlying comorbidities, drug-related rebleeding risk scores and therapeutic use of proton pump inhibitors were not significantly different (P = 0.209, 0.212 and 0.720, respectively).
Approximately one-fifth of patients with NSAIDs-induced enteropathy showed rebleeding within 2 years. A careful long-term follow-up should be offered to elderly patients with NSAIDs-induced enteropathy who need continuous NSAID treatment without the additional use of mucoprotective medications.
非甾体抗炎药(NSAIDs)诱导性肠病导致再出血的证据有限。先前的研究主要分析了内镜检查结果。因此,需要评估其对患者的临床意义。本研究旨在评估 NSAIDs 诱导性肠病患者的再出血率及其相关危险因素。
在接受胶囊内镜检查的 402 例不明原因胃肠道出血患者中,49 例被诊断为 NSAIDs 诱导性肠病。回顾性分析患者的临床特征。采用 Charlson 合并症指数对合并症进行分层。对于使用其他影响出血倾向的药物的患者,计算比值比并进行定量比较。
在 NSAIDs 诱导性肠病患者中,再出血率为 20.4%,平均随访时间为 23.4 个月。年龄≥65 岁(风险比[HR]8.628,95%置信区间[CI]1.152-64.625)、不额外使用黏膜保护剂(HR 11.712,95%CI 1.278-76.098)和首次出血后继续使用 NSAIDs(HR 9.861,95%CI 1.395-98.344)与 NSAIDs 诱导性肠病再出血独立相关。潜在合并症、药物相关再出血风险评分和质子泵抑制剂的治疗使用无显著差异(P=0.209、0.212 和 0.720)。
大约五分之一的 NSAIDs 诱导性肠病患者在 2 年内出现再出血。对于需要持续 NSAID 治疗且不额外使用黏膜保护剂的 NSAIDs 诱导性肠病老年患者,应提供仔细的长期随访。