» Articles » PMID: 39355263

A Retrospective Assessment of Guideline Adherence and Treatment Outcomes From Infection Following the IDSA 2021 Clinical Guideline Update: Infection

Overview
Date 2024 Oct 2
PMID 39355263
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The 2021 update to the Infectious Diseases Society of America infection (CDI) guidelines recommended fidaxomicin as the preferred treatment over vancomycin for patients with initial and recurrent CDI. Few studies have examined how treatment patterns and clinical outcomes of hospitalized CDI patients changed after the postguideline update or contemporary real-world outcomes of fidaxomicin vs vancomycin.

Methods: This retrospective, observational study used the PINC AI Healthcare Database on adult patients who received CDI treatment between 1/2020 and 6/2021 (pre period) and between 10/2021 and 9/2022 (post period). We examined treatment patterns of fidaxomicin, vancomycin, and metronidazole, as well as clinical and health care resource use outcomes of patients treated exclusively with fidaxomicin vs vancomycin, using nearest-neighbor propensity matching and hierarchical regression methods. As a sensitivity analysis, we repeated the fidaxomicin vs vancomycin comparisons among patients with recurrent and nonrecurrent index infections.

Results: A total of 45 049 patients with CDI from 779 US hospitals met initial inclusion criteria. Comparing the pre vs post periods, the proportion of patients treated with fidaxomicin increased from 5.9% to 13.7% ( < .001), vancomycin use decreased from 87.9% to 82.9% ( < .001), and metronidazole use decreased from 21.6% to 17.2% ( < .001). When comparing fidaxomicin vs vancomycin in the post period, fidaxomicin was associated with lower CDI recurrence (6.1% vs 10.2%; < .001) and higher sustained clinical response (91.7% vs 87.8%; < .001). Ninety-day postdischarge costs were not significantly different between groups. A sensitivity analyses showed similar findings.

Conclusions: Since the 2021 guideline update, fidaxomicin use has increased significantly but could be further utilized given its association with better clinical outcomes and no increase in postdischarge costs.

References
1.
Nathwani D, Cornely O, Van Engen A, Odufowora-Sita O, Retsa P, O Odeyemi I . Cost-effectiveness analysis of fidaxomicin versus vancomycin in Clostridium difficile infection. J Antimicrob Chemother. 2014; 69(11):2901-12. PMC: 4195473. DOI: 10.1093/jac/dku257. View

2.
Cornely O, Crook D, Esposito R, Poirier A, Somero M, Weiss K . Fidaxomicin versus vancomycin for infection with Clostridium difficile in Europe, Canada, and the USA: a double-blind, non-inferiority, randomised controlled trial. Lancet Infect Dis. 2012; 12(4):281-9. DOI: 10.1016/S1473-3099(11)70374-7. View

3.
Dubberke E, Olsen M . Burden of Clostridium difficile on the healthcare system. Clin Infect Dis. 2012; 55 Suppl 2:S88-92. PMC: 3388018. DOI: 10.1093/cid/cis335. View

4.
Louie T, Cannon K, Byrne B, Emery J, Ward L, Eyben M . Fidaxomicin preserves the intestinal microbiome during and after treatment of Clostridium difficile infection (CDI) and reduces both toxin reexpression and recurrence of CDI. Clin Infect Dis. 2012; 55 Suppl 2:S132-42. PMC: 3388020. DOI: 10.1093/cid/cis338. View

5.
Al Momani L, Abughanimeh O, Boonpheng B, Gabriel J, Young M . Fidaxomicin vs Vancomycin for the Treatment of a First Episode of Clostridium Difficile Infection: A Meta-analysis and Systematic Review. Cureus. 2018; 10(6):e2778. PMC: 6089486. DOI: 10.7759/cureus.2778. View