TY - JOUR
T1 - Opioid Analgesics Do Not Improve Abdominal Pain or Quality of Life in Crohn’s Disease
AU - Coates, M. D.
AU - Seth, N.
AU - Clarke, K.
AU - Abdul-Baki, H.
AU - Mahoney, N.
AU - Walter, V.
AU - Regueiro, M. D.
AU - Ramos-Rivers, C.
AU - Koutroubakis, I. E.
AU - Bielefeldt, K.
AU - Binion, D. G.
N1 - Publisher Copyright:
© 2019, Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2020/8/1
Y1 - 2020/8/1
N2 - Background: Abdominal pain and opioid analgesic use are common in Crohn’s disease (CD). Aims: We sought to identify factors associated with abdominal pain in CD and evaluate the impact of opioid analgesics on pain and quality-of-life scores in this setting. Methods: We performed a longitudinal cohort study using a prospective, consented IBD natural history registry from a single academic center between 2009 and 2013. Consecutive CD patients were followed for at least 1 year after an index visit. Data were abstracted regarding pain experience (from validated surveys), inflammatory activity (using endoscopic/histologic findings), laboratory studies, coexistent psychiatric disorders, medical therapy, opioid analgesic, and tobacco use. Results: Of 542 CD patients (56.6% women), 232 (42.8%) described abdominal pain. Individuals with pain were more likely to undergo surgery and were more frequently prescribed analgesics and/or antidepressants/anxiolytics. Elevated ESR (OR 1.79; 95%CI 1.11–2.87), coexistent anxiety/depression (OR 1.87; 95%CI 1.13–3.09), smoking (OR 2.08; 95%CI 1.27–3.40), and opioid use (OR 2.46; 95%CI 1.33–4.57) were independently associated with abdominal pain. Eighty patients (14.8%) were prescribed opioids, while 31 began taking them at or after the index visit. Patients started on opioids demonstrated no improvement in abdominal pain or quality-of-life scores on follow-up compared to patients not taking opioids. Conclusions: Abdominal pain is common in CD and is associated with significant opioid analgesic utilization and increased incidence of anxiety/depression, smoking, and elevated inflammatory markers. Importantly, opioid use in CD was not associated with improvement in pain or quality-of-life scores. These findings reinforce the limitations of currently available analgesics in IBD and support exploration of alternative therapies.
AB - Background: Abdominal pain and opioid analgesic use are common in Crohn’s disease (CD). Aims: We sought to identify factors associated with abdominal pain in CD and evaluate the impact of opioid analgesics on pain and quality-of-life scores in this setting. Methods: We performed a longitudinal cohort study using a prospective, consented IBD natural history registry from a single academic center between 2009 and 2013. Consecutive CD patients were followed for at least 1 year after an index visit. Data were abstracted regarding pain experience (from validated surveys), inflammatory activity (using endoscopic/histologic findings), laboratory studies, coexistent psychiatric disorders, medical therapy, opioid analgesic, and tobacco use. Results: Of 542 CD patients (56.6% women), 232 (42.8%) described abdominal pain. Individuals with pain were more likely to undergo surgery and were more frequently prescribed analgesics and/or antidepressants/anxiolytics. Elevated ESR (OR 1.79; 95%CI 1.11–2.87), coexistent anxiety/depression (OR 1.87; 95%CI 1.13–3.09), smoking (OR 2.08; 95%CI 1.27–3.40), and opioid use (OR 2.46; 95%CI 1.33–4.57) were independently associated with abdominal pain. Eighty patients (14.8%) were prescribed opioids, while 31 began taking them at or after the index visit. Patients started on opioids demonstrated no improvement in abdominal pain or quality-of-life scores on follow-up compared to patients not taking opioids. Conclusions: Abdominal pain is common in CD and is associated with significant opioid analgesic utilization and increased incidence of anxiety/depression, smoking, and elevated inflammatory markers. Importantly, opioid use in CD was not associated with improvement in pain or quality-of-life scores. These findings reinforce the limitations of currently available analgesics in IBD and support exploration of alternative therapies.
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U2 - 10.1007/s10620-019-05968-x
DO - 10.1007/s10620-019-05968-x
M3 - Article
C2 - 31758431
AN - SCOPUS:85075315687
SN - 0163-2116
VL - 65
SP - 2379
EP - 2387
JO - Digestive Diseases and Sciences
JF - Digestive Diseases and Sciences
IS - 8
ER -