TY - JOUR
T1 - Outcomes with Fidaxomicin Therapy in Clostridium difficile Infection
AU - Spiceland, Clayton M.
AU - Khanna, Sahil
AU - Pardi, Darrell S.
N1 - Funding Information:
Received for publication July 10, 2016; accepted November 2, 2016. From the *Department of Internal Medicine; and wDivision of Gas-troenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, MN. Supported by Merck Pharmaceuticals. Presented at Digestive Diseases Week 2016 in San Diego and was awarded a Poster of Distinction. D.S.P. has served as a consultant for Merck Pharmaceuticals with honorarium being paid to Mayo Clinic. S.K. serves as a consultant for Rebiotix Inc. with honorarium being paid to Mayo Clinic. C.M.S. has nothing to disclose. Address correspondence to: Sahil Khanna, MBBS, Division of Gas-troenterology and Hepatology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905 (e-mail: khanna.sahil@mayo.edu). Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. DOI: 10.1097/MCG.0000000000000769
Publisher Copyright:
© 2016 Wolters Kluwer Health, Inc. All rights reserved.
PY - 2018
Y1 - 2018
N2 - Background and Goals: Fidaxomicin is a new antibiotic used to treat Clostridium difficile infection (CDI). Given limited clinical experience with fidaxomicin, we assessed outcomes in a diverse cohort of patients with CDI treated with fidaxomicin. Study: All CDI cases treated with fidaxomicin at 3 referral centers over a 4-year period were included. Response was defined as resolution of diarrhea and recurrence was defined by recurrence of CDI within 8 weeks of the end of treatment. Results: Overall, 81 patients (median age 55.9 y; 53% female; 26% with inflammatory bowel disease) were included. Response occurred in 90%. Responders had fewer prior CDI episodes [median 1 (range, 0 to 8)] than nonresponders [median 2.5 (range, 1 to 8)], P=0.01. Response after a first CDI episode was 100%, 96% after 1 prior episode, and 82% after 2 or more, P=0.02. Recurrence occurred in 19%. Patients without recurrence had fewer prior episodes of CDI [median 1 (range, 0 to 6)] than patients who recurred [median 2 (range, 1 to 8)], P=0.005. Recurrence after a first episode was 0%, 23% after 1 prior episode, and 29% after 2 or more, P=0.005. All patients with inflammatory bowel disease responded either with improvement of symptoms or a negative C. difficile test; 19% recurred. Conclusions: All patients with a first CDI episode treated with fidaxomicin responded with no recurrences. Patients with prior CDI episodes were less likely to respond (especially with more than 1 prior episode) and more likely to recur, suggesting a greater clinical benefit of fidaxomicin earlier in the course of CDI.
AB - Background and Goals: Fidaxomicin is a new antibiotic used to treat Clostridium difficile infection (CDI). Given limited clinical experience with fidaxomicin, we assessed outcomes in a diverse cohort of patients with CDI treated with fidaxomicin. Study: All CDI cases treated with fidaxomicin at 3 referral centers over a 4-year period were included. Response was defined as resolution of diarrhea and recurrence was defined by recurrence of CDI within 8 weeks of the end of treatment. Results: Overall, 81 patients (median age 55.9 y; 53% female; 26% with inflammatory bowel disease) were included. Response occurred in 90%. Responders had fewer prior CDI episodes [median 1 (range, 0 to 8)] than nonresponders [median 2.5 (range, 1 to 8)], P=0.01. Response after a first CDI episode was 100%, 96% after 1 prior episode, and 82% after 2 or more, P=0.02. Recurrence occurred in 19%. Patients without recurrence had fewer prior episodes of CDI [median 1 (range, 0 to 6)] than patients who recurred [median 2 (range, 1 to 8)], P=0.005. Recurrence after a first episode was 0%, 23% after 1 prior episode, and 29% after 2 or more, P=0.005. All patients with inflammatory bowel disease responded either with improvement of symptoms or a negative C. difficile test; 19% recurred. Conclusions: All patients with a first CDI episode treated with fidaxomicin responded with no recurrences. Patients with prior CDI episodes were less likely to respond (especially with more than 1 prior episode) and more likely to recur, suggesting a greater clinical benefit of fidaxomicin earlier in the course of CDI.
KW - Clostridium difficile infection
KW - colitis
KW - fidaxomicin
KW - outcomes
KW - recurrence
UR - http://www.scopus.com/inward/record.url?scp=85007275314&partnerID=8YFLogxK
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U2 - 10.1097/MCG.0000000000000769
DO - 10.1097/MCG.0000000000000769
M3 - Article
C2 - 28009682
AN - SCOPUS:85007275314
SN - 0192-0790
VL - 52
SP - 151
EP - 154
JO - Journal of Clinical Gastroenterology
JF - Journal of Clinical Gastroenterology
IS - 2
ER -