The use of fidaxomicin for Clostridioides difficile infection (CDI) has increased significantly since 2021 but it remains underutilized, researchers reported today in Clinical Infectious Diseases.
Using the PINC AI Healthcare database, researchers from Washington University School of Medicine and Merck examined records on adults who received CDI treatment before and after 2021, when updated guidelines from the Infectious Diseases Society of America (IDSA) recommended fidaxomicin as the only first-line agent for CDI, with vancomycin as an alternative option. Prior to 2021 vancomycin and metronidazole had been the recommended first-line agents for CDI, which is the most common healthcare-associated infection in adults and affects an estimated 460,000 US patients each year. Evidence on how CDI treatment patterns have changed since the 2021 guidelines has been limited.
Fidaxomicin use more than doubles
A total of 45,049 patients from 779 US hospitals were included in the study, with 29,520 in the pre-period (January 2020 to June 2021) and 15,529 in the post-period (October 2021 to September 2022). From the pre-period to the post-period, fidaxomicin use increased from 5.9% to 13.7%, while vancomycin used declined from 87.9% to 82.9% and metronidazole from 21.6% to 17.2%. Among census regions, increases in fidaxomicin use were smallest in the northeast, and greatest in the south.
In a secondary analysis that compared clinical and cost outcomes among patients treated exclusively with fidaxomicin versus vancomycin, fidaxomicin was associated with lower CDI recurrence (6.1% vs 10.2%) and higher sustained clinical response (91.7% vs 87.9%), while 90-day post-discharge costs were similar. The study authors note that these findings are consistent with prior research.
"While fidaxomicin use for CDI increased (and more than doubled) since the publication of the updated IDSA guidelines, it remained low relative to vancomycin and metronidazole use," the study authors wrote. "These novel findings imply that a substantial number of patients could have received the benefits of fidaxomicin if more hospitals had followed the ISDA 2021 guidelines."