The Impact of Cannabis Use on Clinical Outcomes in Inflammatory Bowel Disease: A Population-based Longitudinal Cohort Study

被引:6
|
作者
Glickman, Danny [1 ]
Dalessio, Shannon [2 ]
Raup-Konsavage, Wesley M. [3 ]
Vrana, Kent E. [3 ]
Coates, Matthew D. [3 ]
机构
[1] Penn State Coll Med, Hershey, PA USA
[2] Penn State Coll Med, Div Gastroenterol & Hepatol, Dept Med, Hershey, PA USA
[3] Penn State Coll Med, Dept Pharmacol, Hershey, PA USA
基金
美国国家卫生研究院;
关键词
inflammatory bowel disease; ulcerative colitis; Crohn's disease; cannabis; CROHNS;
D O I
10.1093/ibd/izad151
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Cannabis use is common in inflammatory bowel disease (IBD). Recent studies demonstrated that use of cannabis may relieve symptoms; however, it is still unclear how safe cannabis and its derivatives are for IBD patients. We performed this study to evaluate the impact of cannabis use on several key clinical outcomes in IBD. Methods: We performed a retrospective study using the TriNetX Diamond Network. Cannabis use and noncannabis use subcohorts were identified for 3 patient groups: (1) IBD, (2) Crohn's disease (CD), and (3) ulcerative colitis (UC). Baseline differences between subcohorts for each group were controlled by propensity score matching. In each group, we compared relative incidence of emergency department (ED) visits, hospitalization, corticosteroid use, opioid use, IBD-related surgery, and death between cannabis users and noncannabis users. Results: Inflammatory bowel disease cannabis users demonstrated an increased risk for corticosteroid use (risk ratios [R],1.095; 95% CI, 1.021-1.174; P =.011), ED visits (RR, 2.143; 95% CI, 2.034-2.257; P <.001), hospitalizations (RR, 1.925; 95% CI, 1.783-2.079; P <.001) and opioid use (RR, 1.35; 95% CI, 1.14-1.6); P <.001), but not an increased risk of IBD-related surgery or death. The CD and UC groups exhibited similar outcomes, except only CD demonstrated an increased risk for corticosteroid and opioid use. Conclusions: Cannabis use in IBD patients is associated with several poor clinical outcomes, including increased risk of corticosteroid and opioid use, ED visits and hospitalization, though not IBD-related surgery or death. It is not clear what drives these risks or whether they are directly related to IBD-associated disease activity or other factors. Further prospective studies are warranted to more carefully investigate these relationships.
引用
收藏
页码:1055 / 1061
页数:7
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