Real-World Budget Impact of Fidaxomicin versus Vancomycin or Metronidazole for In-Hospital Treatment of Clostridioides difficile Infection

被引:7
作者
Whitney, Laura [1 ,4 ]
Nesnas, John [1 ,5 ]
Planche, Timothy [2 ,3 ]
机构
[1] St Georges Univ Hosp NHS Fdn Trust, London SW17 0QT, England
[2] St Georges Univ Hosp NHS Fdn Trust, Infect Care Grp, London SW17 0QT, England
[3] St Georges Univ London, Inst Infect & Immun, London SW17 0RE, England
[4] NHS England, London, England
[5] Pfizer Ltd, Surrey, England
来源
ANTIBIOTICS-BASEL | 2023年 / 12卷 / 01期
关键词
Clostridioides difficile; fidaxomicin; healthcare resource utilization; real-world outcomes; recurrence; COST-EFFECTIVENESS ANALYSIS; OPT-80; EPIDEMIOLOGY; MICROBIOTA;
D O I
10.3390/antibiotics12010106
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Fidaxomicin, a macrocyclic antibiotic, selectively kills Clostridioides difficile and reduces C. difficile infection (CDI) recurrence compared with vancomycin, but some studies and guidelines report fidaxomicin as being less cost-effective. The aim of this study was to compare the cost-effectiveness and budget impact of fidaxomicin versus vancomycin or metronidazole for treating CDI in a real-world UK setting. Data were retrospectively collected from medical records of 86 patients with CDI treated with vancomycin or metronidazole at a single UK hospital between April 2011 and March 2012, and prospectively from 62 patients with CDI treated with fidaxomicin between August 2012 and July 2013. CDI cases were matched by age, financial year, and healthcare resource use to control cases. CDI recurrence rates were lower with fidaxomicin (6.5%) than vancomycin/metronidazole (19.8%). An estimated 12 additional recurrent CDIs were prevented with fidaxomicin treatment. Patients with CDI had significantly higher healthcare costs than those without CDI, with a mean excess spend of GBP 10,748 and GBP 17,451 per patient in the fidaxomicin (p = 0.015) and vancomycin/metronidazole cohorts (p < 0.001), respectively. A second CDI was associated with mean excess costs of GBP 8373 and GBP 20,249 per patient in the fidaxomicin and vancomycin/metronidazole cohorts, respectively. Despite higher fidaxomicin drug costs, overall cost savings were estimated at GBP 140,292 (GBP 2125 per CDI). In this real-world study, first-line CDI treatment with fidaxomicin reduced healthcare costs versus vancomycin/metronidazole, consistent with previous studies.
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页数:11
相关论文
共 32 条
[1]   Comparative efficacy of treatments for Clostridium difficile infection: a systematic review and network meta-analysis [J].
Beinortas, Tumas ;
Burr, Nicholas E. ;
Wilcox, Mark H. ;
Subramanian, Venkataraman .
LANCET INFECTIOUS DISEASES, 2018, 18 (09) :1035-1044
[2]   Fidaxomicin versus vancomycin for infection with Clostridium difficile in Europe, Canada, and the USA: a double-blind, non-inferiority, randomised controlled trial [J].
Cornely, Oliver A. ;
Crook, Derrick W. ;
Esposito, Roberto ;
Poirier, Andre ;
Somero, Michael S. ;
Weiss, Karl ;
Sears, Pamela ;
Gorbach, Sherwood .
LANCET INFECTIOUS DISEASES, 2012, 12 (04) :281-289
[3]   Effects of control interventions on Clostridium difficile infection in England: an observational study [J].
Dingle, Kate E. ;
Didelot, Xavier ;
Quan, T. Phuong ;
Eyre, David W. ;
Stoesser, Nicole ;
Golubchik, Tanya ;
Harding, Rosalind M. ;
Wilson, Daniel J. ;
Griffiths, David ;
Vaughan, Alison ;
Finney, John M. ;
Wyllie, David H. ;
Oakley, Sarah J. ;
Fawley, Warren N. ;
Freeman, Jane ;
Morris, Kirsti ;
Martin, Jessica ;
Howard, Philip ;
Gorbach, Sherwood ;
Goldstein, Ellie J. C. ;
Citron, Diane M. ;
Hopkins, Susan ;
Hope, Russell ;
Johnson, Alan P. ;
Wilcox, Mark H. ;
Peto, Timothy E. A. ;
Walker, A. Sarah ;
Crook, Derrick W. .
LANCET INFECTIOUS DISEASES, 2017, 17 (04) :411-421
[4]   Colonization Resistance of the Gut Microbiota against Clostridium difficile [J].
Elena Perez-Cobas, Ana ;
Moya, Andres ;
Jose Gosalbes, Maria ;
Latorre, Amparo .
ANTIBIOTICS-BASEL, 2015, 4 (03) :337-357
[5]   Healthcare resource utilization and direct medical costs associated with index and recurrent Clostridioides difficile infection: a real-world data analysis [J].
Feuerstadt, Paul ;
Stong, Laura ;
Dahdal, David N. ;
Sacks, Naomi ;
Lang, Kathleen ;
Nelson, Winnie W. .
JOURNAL OF MEDICAL ECONOMICS, 2020, 23 (06) :603-609
[6]  
Johnson AP, 2007, CURR OPIN INVEST DR, V8, P168
[7]   RECURRENCES OF CLOSTRIDIUM-DIFFICILE DIARRHEA NOT CAUSED BY THE ORIGINAL INFECTING ORGANISM [J].
JOHNSON, S ;
ADELMANN, A ;
CLABOTS, CR ;
PETERSON, LR ;
GERDING, DN .
JOURNAL OF INFECTIOUS DISEASES, 1989, 159 (02) :340-343
[8]   Clinical Practice Guideline by the Infectious Diseases Society of America (IDSA) and Society for Healthcare Epidemiology of America (SHEA): 2021 Focused Update Guidelines on Management of Clostridioides difficile Infection in Adults [J].
Johnson, Stuart ;
Lavergne, Valery ;
Skinner, Andrew M. ;
Gonzales-Luna, Anne J. ;
Garey, Kevin W. ;
Kelly, Ciaran P. ;
Wilcox, Mark H. .
CLINICAL INFECTIOUS DISEASES, 2021, 73 (05) :E1029-E1044
[9]   Excess length of hospital stay, mortality and cost attributable to Clostridioides (Clostridium) difficile infection and recurrence: a nationwide analysis in Japan [J].
Kimura, T. ;
Stanhope, S. ;
Sugitani, T. .
EPIDEMIOLOGY & INFECTION, 2020, 148
[10]   Healthcare burden of recurrent Clostridioides difficile infection in Japan: A retrospective database study [J].
Kunishima, Hiroyuki ;
Ito, Kaoru ;
Laurent, Thomas ;
Abe, Machiko .
JOURNAL OF INFECTION AND CHEMOTHERAPY, 2018, 24 (11) :892-901