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An Antimicrobial Stewardship Program's Real‐World Experience with Fidaxomicin for Treatment of Clostridium difficile Infection: A Case Series
Author(s) -
Vargo Craig A.,
Bauer Karri A.,
Mangino Julie E.,
Johnston Jessica E.W.,
Goff Debra A.
Publication year - 2014
Publication title -
pharmacotherapy: the journal of human pharmacology and drug therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.227
H-Index - 109
eISSN - 1875-9114
pISSN - 0277-0008
DOI - 10.1002/phar.1451
Subject(s) - fidaxomicin , medicine , clostridium difficile , diarrhea , antimicrobial stewardship , clinical trial , retrospective cohort study , surgery , antibiotic resistance , vancomycin , biology , bacteria , microbiology and biotechnology , genetics , staphylococcus aureus , antibiotics
Study Objective To evaluate real‐world clinical and economic outcomes in patients with Clostridium difficile infection ( CDI ) treated with fidaxomicin. Design Retrospective case series. Setting Academic medical center. Patients A total of 61 patients with CDI who were treated with fidaxomicin monotherapy or combination therapy from September 2011 to December 2012. Measurements and Main Results Data on demographics, infection characteristics, and clinical and economic outcomes were evaluated. Clinical cure was defined as resolution of diarrhea (less than or equal to three unformed stools for at least 2 consecutive days) maintained for the duration of therapy with no further requirement for CDI therapy and was achieved in 44 (72.1%) patients. Clinical cure was significantly higher for patients receiving fidaxomicin monotherapy compared with fidaxomicin combination therapy (25/29 [86.2%] patients vs 19/32 [59.4%] patients, p=0.04). Clinical cure was similar in patients with a first or prior CDI episode (65.5% vs 78.1%, p=0.27) and in patients with severe versus nonsevere disease (68.4% vs 73.8%, p=0.66). Recurrence occurred in 6 (13.6%) of the 44 patients who achieved clinical cure. Mortality attributable to CDI was 11.5%, and 30‐day readmission rate was 4.9%. Median cost accrued during CDI was $19,483/patient. Conclusion Our real‐world experience with fidaxomicin significantly differs from the findings of phase III clinical trials. Fidaxomicin is also associated with substantial costs. Multicenter studies are needed to determine the optimal role of fidaxomicin in the treatment of CDI .