2022
DOI: 10.1007/s10620-022-07379-x
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Safety and Efficacy of Eluxadoline in Patients with Irritable Bowel Syndrome-Diarrhea With or Without Bile Acid Diarrhea: Open-Label Study

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Cited by 4 publications
(3 citation statements)
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“…The efficacy of eluxadoline in patients with BAD was studied in a single-center, open-label study of 24 patients with IBS-D, 12 of whom had BAD. In this study, it was shown that eluxadoline improved stool consistency and decreased abdominal pain in patients with IBS-D regardless of BAD status [41].…”
Section: Eluxadolinementioning
confidence: 61%
“…The efficacy of eluxadoline in patients with BAD was studied in a single-center, open-label study of 24 patients with IBS-D, 12 of whom had BAD. In this study, it was shown that eluxadoline improved stool consistency and decreased abdominal pain in patients with IBS-D regardless of BAD status [41].…”
Section: Eluxadolinementioning
confidence: 61%
“…Indeed, a posthoc analysis of the above-mentioned trials and a subsequent study confirmed its safety and efficacy up to 52 weeks of treatment in patients with IBS-D not responding to loperamide, 89,90 while a recent study reported its efficacy also on patients with IBS-D with concurrent bile acid diarrhea. 91 Finally, an updated metaanalysis of 42 trials performed a head-to-head comparison of eluxadoline with antispasmodics and concluded that eluxadoline was at least as effective as antispasmodics, but due to the higher amount of adverse events reported, antispasmodics still represent the first choice for the treatment of IBS-D. 92…”
Section: Eluxadolinementioning
confidence: 99%
“…In this issue of Digestive Diseases and Sciences, Vijayvargiya et al [7] from the Mayo Clinic performed a rigorous, open-label cohort study on patients meeting Rome IV criteria for IBS-D who received eluxadoline at its FDAapproved dose of 100 mg twice daily for 4 weeks (including an appropriate 2-week run-in period). The purpose of the study was to distinguish pathophysiologic entities such as BAD from all-encompassing symptom-based classifications such as IBS-D. All patients underwent baseline diagnostics for bile acid diarrhea using fasting serum 7α-hydroxy-4cholesten-3-one (7α-C4) levels, a biomarker of hepatic bile acid synthesis; this test has been previously validated to have a sensitivity of 90% and specificity of 79% to detect bile acid malabsorption [8].…”
mentioning
confidence: 99%