Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Mar;29(2):79-83.
doi: 10.1136/ejhpharm-2021-002951.

Effects of cascade reporting of susceptibility profiles for Enterobacterales on broad-spectrum antibiotics use and resistance

Affiliations

Effects of cascade reporting of susceptibility profiles for Enterobacterales on broad-spectrum antibiotics use and resistance

Laura Heireman et al. Eur J Hosp Pharm. 2022 Mar.

Abstract

Objective: To reduce the inappropriate use of broad-spectrum antibiotics in a 1000+ bed acute tertiary care hospital by the introduction of cascade antimicrobial susceptibility reporting for Enterobacterales.

Methods: Over a 1-year period, we selectively suppressed reporting of susceptibility to the broad-spectrum antibiotics piperacillin-tazobactam (TZP) and meropenem (MEM) for Enterobacterales strains susceptible to amoxicillin-clavulanic acid (AMC) and negative for extended-spectrum β-lactamase (ESBL). We measured the effects on hospital-wide antibiotic consumption (defined daily doses/1000 admissions) and resistance of Escherichia coli and Klebsiella pneumoniae on two levels. First, we compared resistance and antibiotic use for the antibiotics impacted by the intervention (AMC, TZP and MEM) with control antibiotics that were consistently reported (fluoroquinolones, trimethoprim-sulfamethoxazole and third-generation cephalosporins). Second, we compared the resistance for TZP and MEM with a control pathogen (Pseudomonas aeruginosa) and studied the impact on rate of Clostridioides difficile-associated diarrhoea in our hospital.

Results: We observed an overall increased use of AMC relative to overall antibiotic consumption (20.0%, p<0.0001) together with a decreased use of TZP (-11.9%, p=0.049) and unchanged use of MEM (p=0.68) relative to overall antibiotic consumption. As for resistance, the number of ESBL-positive K. pneumoniae strains diminished by 5.9% (p<0.0001). When focusing on intensive care units, the carbapenemase-producing Enterobacterales (CPE) rate also decreased by 4.5% (p=0.0091). For E. coli, no significant difference in ESBL (p=0.33) and CPE (p=0.48) rates were observed. No significant difference in the rate of C. difficile infections was observed (p=0.40).

Conclusions: Restricted susceptibility reporting of TZP and MEM was associated with a significant increased use of AMC and decreased use of TZP relative to overall antibiotic consumption and significant reduction in ESBL- and CPE-positive K. pneumoniae strains.

Keywords: clinical laboratory techniques; clinical medicine; hospital; laboratories; microbiological techniques; microbiology.

PubMed Disclaimer

Conflict of interest statement

Competing interests: JDW: grant from the Flanders Research Foundation during the conduct of the study (Senior Clinical Investigator Grant); consulted for Accelerate, Bayer Healthcare, Cubist, Grifols, MSD and Pfizer (honoraria were paid to his institution).

Figures

Figure 1
Figure 1
Proportion of consumption (defined daily doses/1000 admisssions) of each antibiotic relative to overall antibiotic use before and after the introduction of selective antimicrobial susceptibility reporting. *Denotes a statistically significant difference. AMC, amoxicillin-clavulanic acid; CRO, ceftriaxone; CTX, cefotaxime; FQ, fluoroquinolones; MEM, meropenem; SXT, trimethoprim-sulfamethoxazole; TZP, piperacillin-tazobactam.
Figure 2
Figure 2
Proportion of antibiotic resistance of Escherichia coli, Klebsiella pneumoniae and Pseudomonas aeruginosa before and after the introduction of selective antimicrobial susceptibility reporting. *Denotes a statistically significant difference. AMC, amoxicillin-clavulanic acid; CAZ, ceftazidime; CPE, carpabenemase-producing Enterobacterales; CRO, ceftriaxone; ESBL, extended-spectrum β-lactamases; FQ, fluoroquinolones; MEM, meropenem; SXT trimethoprim-sulfamethoxazole; TZP, piperacillin-tazobactam.

Similar articles

Cited by

References

    1. Kaye KS, Pogue JM. Infections caused by resistant gram-negative bacteria: epidemiology and management. Pharmacotherapy 2015;35:949–62. 10.1002/phar.1636 - DOI - PubMed
    1. Nordmann P, Poirel L. Epidemiology and diagnostics of carbapenem resistance in gram-negative bacteria. Clin Infect Dis 2019;69:S521–8. 10.1093/cid/ciz824 - DOI - PMC - PubMed
    1. Magiorakos AP, Burns K, Rodríguez Baño J, et al. . Infection prevention and control measures and tools for the prevention of entry of carbapenem-resistant Enterobacteriaceae into healthcare settings: guidance from the European Centre for Disease Prevention and Control. Antimicrob Resist Infect Control 2017;6:113. 10.1186/s13756-017-0259-z - DOI - PMC - PubMed
    1. Stainton SM, Thabit AK, Kuti JL, et al. . Prevalence, patient characteristics and outcomes of a novel piperacillin/tazobactam-resistant, pan-β-lactam-susceptible phenotype in Enterobacteriaceae: implications for selective reporting. Clin Microbiol Infect 2017;23:581–2. 10.1016/j.cmi.2017.02.012 - DOI - PubMed
    1. Brolund A, Lagerqvist N, Byfors S. Worsening epidemiological situation of carbapenemase-producing Enterobacterales in Europe, assessment by national experts from 37 countries, July 2018. Euro Surveill 2019:17–24. - PMC - PubMed

MeSH terms

Substances