Article

Loperamide's Role in Conjunction With Fecal Microbiota Transplantation to Treat Recurrent C difficile

FMT was highly successful for the treatment of recurrent C difficile, and the cure rate was similar between groups who did and did not receive loperamide prior to the procedure.

Vipul Nayi, MD

Vipul Nayi, MD

The evidence supporting fecal microbiota transplantation (FMT) as a treatment option for recurrent Clostridioides difficile infection (rCDI) is increasing, and the procedure is now widely considered a highly effective therapy.

Some studies have posited that administering loperamide prior to FMT could boost its efficacy in staving off rCDI because it could extend the amount of time donor stool is in contact with the recipient’s colon before expulsion.

Other research, however, has suggested that loperamide could be associated with megacolon.

In research presented as a poster at the American College of Gastroenterology’s Annual Scientific Meeting (ACG 2019) in San Antonio, Texas, investigators with Montefiore Medical Center sought to evaluate whether loperamide administered prior to FMT for rCDI treatment improves resolution rates.

The retrospective observational cohort study comprised patients between the ages of 18 and 75 years who underwent FMT for the treatment of rCDI between 2014 and 2017 at Montefiore Medical Center in Bronx, New York. rCDI was defined as > 3 bouts of CDI with recurrence of symptoms within 8 weeks of antibiotic therapy. Patients with severe or complicated CDI, inflammatory bowel disease, irritable bowel syndrome, motility disorder, or who were immunocompromised or did not complete the follow-up telephone survey were excluded.

Investigators gathered data on loperamide use prior to FMT and resolution of diarrhea based on chart reviews and telephone surveys with participants. The research team defined cure of rCDI as resolution of diarrhea at 8 weeks of FMT, and used bivariate analyses to compare rCDI cure rates and adverse events between those who took loperamide prior to FMT and those who did not.

A total of 15 patients met inclusion criteria (mean age 53±20 years, 80% female [n=12], average of 2.5±0.7 different courses of antibiotics before FMT). All but 1 of the patients (93%) achieved diarrhea resolution at 8 weeks post FMT procedure, and 6 out of 15 patients (40%) took loperamide prior to the FMT procedure, all of whom experienced cure of rCDI compared with 8 of 9 patients who did not take loperamide (100% vs 89%, respectively; p >0.99).

FMT-related adverse events were reported by patients in the group that did not receive loperamide, including subjective fever (n=2, 13.3%), lactose intolerance (n=1; 0.7%), celiac disease (n=1, 0.7%) and rectal bleeding (n=1, 0.7%).

“In our cohort, FMT was highly successful for the treatment of rCDI,” investigators concluded. “rCDI cure was similar between groups who did and did not receive loperamide, which may be attributable to the overall high rCDI cure rates reported. In our small study, loperamide did not result in increased FMT-related adverse events. A future trial randomizing patients with rCDI to loperamide vs placebo might provide additional insight.”

The poster, “The Role of Loperamide in Conjunction With Fecal Microbiota Transplantation (FMT) for Recurrent Clostridioides difficile Infection (rCDI),” was presented Sunday, October 27, 2019, at the American College of Gastroenterology Annual Scientific Meeting (ACG 2019) in San Antonio, Texas.

Related Videos
| Image Credit: X
Ahmad Masri, MD, MS | Credit: Oregon Health and Science University
Ahmad Masri, MD, MS | Credit: Oregon Health and Science University
Stephen Nicholls, MBBS, PhD | Credit: Monash University
Marianna Fontana, MD, PhD: Nex-Z Shows Promise in ATTR-CM Phase 1 Trial | Image Credit: Radcliffe Cardiology
Zerlasiran Achieves Durable Lp(a) Reductions at 60 Weeks, with Stephen J. Nicholls, MD, PhD | Image Credit: Monash University
Gaith Noaiseh, MD: Nipocalimab Improves Disease Measures, Reduces Autoantibodies in Sjogren’s
A. Sidney Barritt, MD | Credit: UNC School of Medicine
Muthiah Vaduganathan, MD, MPH | Credit: Brigham and Women's Hospital
© 2024 MJH Life Sciences

All rights reserved.