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Finding value in novel antibiotics: How can infectious diseases adopt incremental cost-effectiveness to improve new antibiotic utilization?
Van Helden, Sean R; Schulz, Lucas T; Wimmer, Megan; Cancelliere, Victoria L; Rose, Warren E.
Affiliation
  • Van Helden SR; Pharmacy Practice and Translational Research Division, University of Wisconsin-Madison School of Pharmacy, United States.
  • Schulz LT; Pharmacy Practice and Translational Research Division, University of Wisconsin-Madison School of Pharmacy, United States; Department of Pharmacy, UW Health, United States. Electronic address: schulz1@wisc.edu.
  • Wimmer M; Pharmacy Practice and Translational Research Division, University of Wisconsin-Madison School of Pharmacy, United States.
  • Cancelliere VL; Pharmacy Practice and Translational Research Division, University of Wisconsin-Madison School of Pharmacy, United States.
  • Rose WE; Pharmacy Practice and Translational Research Division, University of Wisconsin-Madison School of Pharmacy, United States; Department of Pharmacy, UW Health, United States.
Diagn Microbiol Infect Dis ; 109(2): 116245, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38522368
ABSTRACT
Research and development of innovative antimicrobials is paramount to addressing the antimicrobial resistance threat. Although antimicrobial discovery and development has increased, difficulties have emerged in the pharmaceutical industry after market approval. In this minireview, we summarize clinical trial data on recently approved antibiotics, calculate incremental cost-effectiveness ratio (ICER) values, and explore ways to adapt ICER calculations to the limitations of antimicrobial clinical trial design. We provide a systematic review and analysis of randomized, controlled studies of antibiotics approved from 2014 - 2022 and extracted the relevant clinical data. Adapted-ICER (aICER) calculations were conducted using the primary condition-specific outcome that was reported in each study (percent mortality or percent cure rate). The literature search identified 18 studies for the 8 total antibiotics which met inclusion criteria and contained data required for aICER calculation. aICER values ranged from -$17,374 to $4,966 per percent mortality and -$43,931 to $2,529 per percent cure rate. With regards to mortality, ceftolozane/tazobactam and imipenem/cilastatin/relebactam proved cost efficacious, with aICER values of $4,965 per percent mortality and $1,955 per percent mortality respectively. Finding value in novel antibiotic agents is imperative to further justifying their development, and aICER values are the most common method of determining value in healthcare. The current outcomes of clinical trials are difficult to translate to aICER, which most effectively use Quality-Adjusted Life Years (QALY) as the quality standard in other fields such as oncology. Future antimicrobial trials should consider introducing methods of assessing measures of health gain such as QALY to better translate the value of novel antimicrobials in healthcare.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cost-Benefit Analysis / Anti-Bacterial Agents Limits: Humans Language: En Journal: Diagn Microbiol Infect Dis Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cost-Benefit Analysis / Anti-Bacterial Agents Limits: Humans Language: En Journal: Diagn Microbiol Infect Dis Year: 2024 Document type: Article Affiliation country: Country of publication: