TY - JOUR
T1 - Risk for Post-Colonoscopy Irritable Bowel Syndrome in Patients With and Without Antibiotic Exposure
T2 - A Retrospective Cohort Study
AU - Vajravelu, Ravy K.
AU - Shapiro, Jordan M.
AU - Ni, Josephine
AU - Thanawala, Shivani U.
AU - Lewis, James D.
AU - El-Serag, Hashem B.
N1 - Funding Information:
Conflicts of interest This author discloses the following: Dr Lewis has served as a consultant to AbbVie, Arena Pharmaceuticals, Bristol-Myers Squibb, Bridge Biotherapeutics, Celgene, Gilead, Janssen, Johnson & Johnson Consumer Inc, Lilly, Merck, Nestle Health Science, Pfizer, Samsung Bioepis, Takeda, and UCB and has received research funding from Nestle Health Science, Janssen, and Takeda. The remaining authors disclose no conflicts.
Funding Information:
Funding Hashem B. El-Serag is supported by NIH/NIDDK—P30-DK056338. Josephine Ni is supported by NIH/NIDDK—K08-DK123316, Burroughs Wellcome Fund Career Awards for Medical Scientists. Shivani U. Thanawala is supported by NIH/NIDDK—T32-DK007740. Ravy K. Vajravelu is supported by NIH/NIDDK—K08-DK119475. This research was funded by the National Institutes of Health in the United States (NIH/NIDDK—K08-DK119475 to RKV). The funders of this study had no role in the study design, data collection, data analysis, data interpretation, or presentation of the results.
Publisher Copyright:
© 2022 AGA Institute
PY - 2022/6
Y1 - 2022/6
N2 - Background & Aims: Laboratory studies have demonstrated that antibiotic use in conjunction with bowel purgatives causes alterations to the gut microbiota. Because gut microbiota changes may be a trigger for the development of irritable bowel syndrome (IBS), we sought to assess whether individuals who undergo bowel cleansing for colonoscopy and have concurrent antibiotic exposure develop IBS at higher rates than individuals who undergo colonoscopy without antibiotic exposure. Methods: We used data from Optum's de-identified Clinformatics Data Mart Database in the United States to study a cohort of 50- to 55-year-olds who underwent screening colonoscopy. Individuals exposed to antibiotics within 14 days of colonoscopy were propensity-score matched to individuals who were not exposed to antibiotics around colonoscopy. The primary outcome was a new IBS diagnosis, and the composite outcome was a new claim for IBS, IBS medications, or IBS symptoms. The association of antibiotic exposure and the outcomes was calculated using Cox proportional hazards regression. Results: There were 408,714 individuals who met criteria for the screening colonoscopy cohort. Of these, 24,617 (6.0%) were exposed to antibiotics around the time of colonoscopy, and they were propensity-score matched to 24,617 individuals not exposed to antibiotics. There was no statistically significant association between antibiotic use and IBS (hazard ratio, 1.11; 95% confidence interval, 0.89–1.39), but there was a weak association between antibiotic use and the composite outcome (hazard ratio, 1.12; 95% confidence interval, 1.02–1.24; number needed to harm, 94). Conclusions: Individuals concurrently exposed to antibiotics and bowel purgative had slightly higher rates of surrogate IBS outcomes compared with matched controls who did not receive antibiotics concurrently with bowel purgative.
AB - Background & Aims: Laboratory studies have demonstrated that antibiotic use in conjunction with bowel purgatives causes alterations to the gut microbiota. Because gut microbiota changes may be a trigger for the development of irritable bowel syndrome (IBS), we sought to assess whether individuals who undergo bowel cleansing for colonoscopy and have concurrent antibiotic exposure develop IBS at higher rates than individuals who undergo colonoscopy without antibiotic exposure. Methods: We used data from Optum's de-identified Clinformatics Data Mart Database in the United States to study a cohort of 50- to 55-year-olds who underwent screening colonoscopy. Individuals exposed to antibiotics within 14 days of colonoscopy were propensity-score matched to individuals who were not exposed to antibiotics around colonoscopy. The primary outcome was a new IBS diagnosis, and the composite outcome was a new claim for IBS, IBS medications, or IBS symptoms. The association of antibiotic exposure and the outcomes was calculated using Cox proportional hazards regression. Results: There were 408,714 individuals who met criteria for the screening colonoscopy cohort. Of these, 24,617 (6.0%) were exposed to antibiotics around the time of colonoscopy, and they were propensity-score matched to 24,617 individuals not exposed to antibiotics. There was no statistically significant association between antibiotic use and IBS (hazard ratio, 1.11; 95% confidence interval, 0.89–1.39), but there was a weak association between antibiotic use and the composite outcome (hazard ratio, 1.12; 95% confidence interval, 1.02–1.24; number needed to harm, 94). Conclusions: Individuals concurrently exposed to antibiotics and bowel purgative had slightly higher rates of surrogate IBS outcomes compared with matched controls who did not receive antibiotics concurrently with bowel purgative.
KW - Antibiotics
KW - Colonoscopy
KW - Health Services Research
KW - Irritable Bowel Syndrome
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UR - http://www.scopus.com/inward/citedby.url?scp=85120004605&partnerID=8YFLogxK
U2 - 10.1016/j.cgh.2021.08.049
DO - 10.1016/j.cgh.2021.08.049
M3 - Article
C2 - 34481956
AN - SCOPUS:85120004605
SN - 1542-3565
VL - 20
SP - e1305-e1322
JO - Clinical Gastroenterology and Hepatology
JF - Clinical Gastroenterology and Hepatology
IS - 6
ER -