4.7 Article

Cost-effectiveness of bezlotoxumab and fidaxomicin for initial Clostridioides difficile infection

Journal

CLINICAL MICROBIOLOGY AND INFECTION
Volume 27, Issue 10, Pages 1448-1454

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.cmi.2021.04.004

Keywords

Bacterial resistance; Bezlotoxumab; Clostridioidesdifficileinfection; Cost-effectiveness analysis; Extended-pulsed fidaxomicin; Fidaxomicin; Incremental cost-effectiveness ratio

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The study evaluated the cost-effectiveness of fidaxomicin and bezlotoxumab in treating initial CDI compared to standard therapy with oral vancomycin. Extended-pulsed fidaxomicin was found to be the most cost-effective treatment, while standard fidaxomicin was more effective than vancomycin and the bezlotoxumab-containing regimen required higher costs.
Objectives: Treatment of Clostridioides difficile infection (CDI) has undergone significant change in recent years with the introduction of fidaxomicin and bezlotoxumab. This study evaluated the cost-effectiveness of fidaxomicin and bezlotoxumab for initial CDI compared with standard therapy with oral vancomycin. Methods: A Markov model with eight health states was built based on transition probabilities, costs and health utilities derived from literature to evaluate the cost-effectiveness of standard fidaxomicin, bezlotoxumab plus vancomycin, and extended-pulsed fidaxomicin versus standard oral vancomycin over a lifetime horizon from the US societal perspective. Results: For overall CDI treatment, oral vancomycin had a cost of $39 178 and was associated with a gain of 11.64 quality-adjusted life-years (QALYs). Extended-pulsed fidaxomicin had a higher QALY gain of 11.65 at a lower cost of $37 613, and therefore was dominant over vancomycin. Standard fidaxomicin had a QALY gain of 11.94 versus vancomycin at an incremental cost of $495 per QALY. Bezlotoxumab plus vancomycin led to a QALY gain of 11.77 at an incremental cost of $17 746 per QALY. At the willingness-to-pay (WTP) threshold of $150 000 per QALY, extended-pulsed fidaxomicin, bezlotoxumab plus vanco-mycin and standard fidaxomicin were more cost-effective compared with vancomycin alone, yielding incremental net monetary benefits of $3248, $17 011 and $44 308, respectively. One-way sensitivity analysis suggested that the probabilities of sustained cure from the initial episode were the most sen-sitive inputs, and results were overall not particularly sensitive to any drug costs. Conclusions: Based on a WTP threshold of $150 000, standard fidaxomicin was estimated to be the most cost-effective treatment. Standard-of-care vancomycin was dominated by extended-pulsed fidaxomicin for treating an episode of CDI and preventing further recurrence, and the addition of bezlotoxumab to vancomycin was dominated by standard fidaxomicin. Jiahe Chen, Clin Microbiol Infect 2021;27:1448 (c) 2021 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.

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