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Evaluation of intravenous amoxicillin-clavulanate use in two Canadian hospitals

Published online by Cambridge University Press:  14 February 2024

Maggie Wong
Affiliation:
Department of Pharmacy, Royal Columbian Hospital, New Westminster, BC, Canada
Sangita Malhotra
Affiliation:
Division of Infectious Diseases, Department of Medicine, University of British Columbia, Vancouver, BC, Canada Division of Infectious Diseases, Department of Medicine, Fraser Health Authority, New Westminster, BC, Canada
Kevin Afra*
Affiliation:
Division of Infectious Diseases, Department of Medicine, University of British Columbia, Vancouver, BC, Canada Division of Infectious Diseases, Department of Medicine, Fraser Health Authority, Surrey, BC, Canada
*
Corresponding author: Kevin Afra; Email: [email protected]

Abstract

We describe our experience with intravenous amoxicillin-clavulanate, which is new to the Canadian market. The majority of patients were successfully de-escalated from piperacillin-tazobactam or a carbapenem for respiratory infections or skin and soft tissue infections. Intravenous amoxicillin-clavulanate provides a good alternative in an era of rising Pseudomonas aeruginosa resistance.

Type
Concise Communication
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2024. Published by Cambridge University Press on behalf of The Society for Healthcare Epidemiology of America

Intravenous (IV) amoxicillin-clavulanate has been used in Europe for years with success. Reference Gaillat, Bru and Sedallian1,Reference Fernandez-Sabe, Carratala and Dorca2 This product has been available in Canada since 2020, and on our hospital formulary since 2022. Historically, ceftriaxone is used empirically for inpatients with community-acquired infections, while those with hospital-acquired infections would receive piperacillin-tazobactam.

The prevalence of multidrug resistance Pseudomonas aeruginosa is increasing and varies from 15% to 30 worldwide. Reference Horcajada, Montero and Oliver3 In our health authority, the prevalence of Pseudomonas aeruginosa for hospital-acquired pneumonia is 15%. Multiple studies showed that exposures to piperacillin-tazobactam and carbapenems were associated with increased risk of multidrug resistant P. aeruginosa. Reference Raman, Avendano, Chan, Merchant and Puzniak4,Reference Harris, Perencevich, Roghmann, Morris, Kaye and Johnson5 Amoxicillin-clavulanate does not have activity against P. aeruginosa and is narrower in spectrum than piperacillin-tazobactam 6 ; therefore, its use in selected cases may decrease antibiotic resistance.

The objectives of our study are: (1) describe the prescribing pattern of IV amoxicillin-clavulanate since being added to hospital formulary; (2) evaluate whether IV amoxicillin-clavulanate is used appropriately; (3) identify where IV amoxicillin-clavulanate is used to de-escalate from other broad-spectrum antibiotics.

Methods

This retrospective case series took place at a 447-bed tertiary hospital and a 178-bed community hospital in British Columbia, Canada from October 2022 to April 2023. An antimicrobial stewardship (AMS) pharmacist and infectious diseases (ID)/AMS physician presented to hospitalists, surgeons, and other medical staff at both sites when IV amoxicillin-clavulanate was added to the formulary. Both hospitals had pre-existing AMS prospective audit and feedback, recommendations for de-escalation to IV amoxicillin-clavulanate were incorporated into daily practice following formulary addition.

All admitted adult patients on IV amoxicillin-clavulanate were included. We used AMS software (Lumed, Sherbrooke, Canada) to identify patients who received IV amoxicillin-clavulanate, and collected demographic and clinical data via the electronic medical record. Primary outcomes included appropriateness of indication and duration of IV amoxicillin-clavulanate and clinical success. Appropriate indications for IV amoxicillin-clavulanate were based on provincial guidelines (Supplemental Table 1). Transition to oral therapy was assessed as part of appropriateness of indication on day 3 of IV amoxicillin-clavulanate. Appropriate duration of therapy was based on locally approved guidelines. Clinical success was defined as not requiring re-escalation to piperacillin-tazobactam or a carbapenem during hospitalization within 30 days of IV amoxicillin-clavulanate. Secondary outcomes included readmission rate, reason(s) for readmission, and mortality rate within 30 days of stopping IV amoxicillin-clavulanate. Patients who received less than 24 hours of IV amoxicillin-clavulanate were excluded from evaluation of clinical success and secondary outcomes. Only the first episode of IV amoxicillin-clavulanate use was evaluated for primary and secondary outcomes. An AMS pharmacist reviewed all cases, with verification by an ID/AMS physician for cases with ambiguous outcomes. Descriptive statistics were used for analysis. A letter of exemption from the institutional research ethics board was obtained.

Results

One hundred and thirteen charts were identified. Two patients were excluded as they did not receive IV amoxicillin-clavulanate per the medication administration record. Patient characteristics, indications, type of prescriber, duration, and reasons for choosing IV amoxicillin-clavulanate are summarized in Table 1. Respiratory tract (complex parapneumonic effusions and empyema), and skin or soft tissue infections (diabetic foot infections and post-operative infections) were the most common indications. IV amoxicillin-clavulanate was used for de-escalation from piperacillin-tazobactam or a carbapenem in 59% of cases.

Table 1. Summary of patient demographics and prescribing pattern of intravenous (IV) amoxicillin-clavulanate

a Does not add up to 111, as patient can have > 1 infection

Primary and secondary outcomes are summarized in Table 2. IV amoxicillin-clavulanate was prescribed appropriately in 95% of cases, of which 12% were based on AMS recommendations. IV amoxicillin-clavulanate was the only option in one-third of the cases (eg culture grew Enterococcus species), whereas ceftriaxone with or without metronidazole could have been used in the remaining cases. The main reason for choosing IV amoxicillin-clavulanate in those cases was to facilitate subsequent direct oral transition. ID physicians and hospitalists were the main prescribers. Reasons why transition to oral amoxicillin-clavulanate was not feasible are shown in Table 2.

Table 2. Summary of primary and secondary outcomes

a Does not add up to 55, as patient can have > 1 reason

Clinical success was reviewed in 97 patients, 13 patients received less than 1 day of therapy and were excluded. One patient was lost to follow-up. Clinical success was achieved in 72% of patients, and IV amoxicillin-clavulanate was well tolerated. Clinical deterioration while on treatment was the main reason for re-escalation to other broad-spectrum antibiotics.

Discussion

There is a scarcity of literature to describe the use of IV amoxicillin-clavulanate in Canada. A pilot study in Alberta evaluated IV amoxicillin-clavulanate as an alternative to piperacillin-tazobactam for general surgery patients. However, the uptake by surgeons was low, which the authors attributed to the unfamiliarity of this new product. Reference Drost, Rajakumar and Rennert-May7 In contrast, we educated a broad range of prescribers (eg, hospitalists, respirologists, general surgeons) when IV amoxicillin-clavulanate was added to formulary, plus ongoing education via prospective audit and feedback.

IV amoxicillin-clavulanate was used for de-escalation from piperacillin-tazobactam in 59% of patients. One can argue that ceftriaxone with or without metronidazole may also be used, but IV amoxicillin-clavulanate was the only choice in one-third of these patients due to culture susceptibility, drug allergy, etc. A number of these patients were also thought to have failed ceftriaxone prior to escalation to piperacillin-tazobactam.

Amoxicillin-clavulanate may have some preferable characteristics compared to ceftriaxone. Third-generation cephalosporins are more strongly associated with healthcare-associated Clostridioides difficile infection than beta-lactam-β-lactamase inhibitor combinations. Reference Slimings and Riley8 Cephalosporins also have a stronger association than beta-lactam-β-lactamase inhibitor combinations with acquiring colonization with extended-spectrum β-lactamase-producing Gram-negative bacilli. Reference Tacconelli, Górska and De Angelis9

Another advantage of IV amoxicillin-clavulanate is that it allows for direct oral transition. The median duration of IV amoxicillin-clavulanate was 5 days. Most patients requiring prolonged therapy (> 7 days) were reviewed by specialists (e.g., ID physicians, respirologists). A number of patients had empyema or complex parapneumonic effusions; these findings were similar to a study by Artoisenet et al. Reference Artoisenet, Ausselet, Delaere and Spinewine10 ID specialists prescribed IV amoxicillin-clavulanate in 40% of cases. Their patients typically had complex skin and soft tissue infections, diabetic foot infections, or bone and joint infections; once deemed not to have risk factors for P. aeruginosa or other resistant organisms, they were de-escalated to IV amoxicillin-clavulanate.

Clinical success was achieved in 72% of our patients. The reasons for broadening therapy were multifactorial including inadequate source control, patient risk factors, and prolonged hospitalization leading to growth of multidrug resistant organisms. Fifteen percent of patients were readmitted within 30 days of IV amoxicillin-clavulanate use; the majority were for reasons unrelated to the original infection. Mortality rate was 18%, mainly from cancer-related complications.

One strength of this study is inclusion of both a tertiary hospital and a smaller community hospital to compare their prescribing patterns of IV amoxicillin-clavulanate. We noted that all the inappropriate duration happened at the community hospital; this is possibly due to fewer ID physician and AMS pharmacist present at that site. A limitation is missing information for some patients due to the retrospective nature of this study. We did not evaluate the total days of piperacillin-tazobactam potentially saved by switching to IV amoxicillin-clavulanate. Since the cost of both IV antibiotics is similar, we do not expect substantial drug cost savings with the switch.

In an era of rising antibiotic resistance, IV amoxicillin-clavulanate provides a good alternative for patients who do not require piperacillin-tazobactam. Our study describes those who would benefit from this regimen: empirically for patients with community-acquired respiratory infections (eg empyema), complicated skin and soft tissue infections (eg diabetic foot infections), or when polymicrobial coverage is needed (eg intra-abdominal infections).

Supplementary material

The supplementary material for this article can be found at https://doi.org/10.1017/ash.2024.18

Financial support

None reported.

Competing interests

All authors report no conflicts of interest relevant to this article.

Author contribution

MW – Conceptualization of study protocol, data collection and analysis, and writing of the original manuscript.

SM – Review and edit the manuscript.

KA – Conceptualization of study protocol, review, and edit the manuscript.

References

Gaillat, J, Bru, JP, Sedallian, A. Penicillin G/Ofloxacin versus Erythromycin/Amoxicillin-Clavulanate in the treatment of severe community-acquired pneumonia. Eur J Clin Microbiol Infect Dis 1994;13:639644.CrossRefGoogle ScholarPubMed
Fernandez-Sabe, N, Carratala, J, Dorca, J, et al. Efficacy and safety of sequential amoxicillin-clavulanate in the treatment of anaerobic lung infections. Eur J Clin Microbiol Infect Dis 2003;22:185187.CrossRefGoogle ScholarPubMed
Horcajada, JP, Montero, M, Oliver, A, et al. Epidemiology and treatment of multidrug-resistant and extensively drug-resistant pseudomonas aeruginosa infections. Clin Microbiol Rev 2019;32:e0003119 CrossRefGoogle ScholarPubMed
Raman, G, Avendano, E, Chan, J., Merchant, S, Puzniak, L. Risk factors for hospitalized patients with resistant or multidrug-resistant pseudomonas aeruginosa infections: a systematic review and meta-analysis. Antimicrobial Resistance and Infection Control 2018;7:79.CrossRefGoogle ScholarPubMed
Harris, AD, Perencevich, E, Roghmann, M, Morris, G, Kaye, KS, Johnson, JA. Risk factors for piperacillin-tazobactam-resistant pseudomonas aeruginosa among hospitalized patients. Antimicrobial agents and chemotherapy 2002;46:854858 CrossRefGoogle ScholarPubMed
BC Provincial Antimicrobial Clinical Expert (PACE) Committee. Summary guideline on IV amoxicillin-clavulanate. http://www.bccdc.ca/Documents/IV%20Amoxicillin-Clavulanate%20Summary.pdf. Published 2022. Accessed August 10, 2023.Google Scholar
Drost, SA, Rajakumar, I, Rennert-May, E. Pilot study evaluating intravenous amoxicillin-clavulanate as an alternative to piperacillin-tazobactam for general surgery patients. Antimicrobial Stewardship and Healthcare Epidemiology 2023;3:e43.CrossRefGoogle ScholarPubMed
Slimings, C, Riley, TV. Antibiotics and healthcare facility-associated Clostridioides difficile infection: systematic review and meta-analysis 2020 update. J Antimicrob Chemother 2021;76:16761688.CrossRefGoogle ScholarPubMed
Tacconelli, E, Górska, A, De Angelis, G, et al. Estimating the association between antibiotic exposure and colonization with extended-spectrum β-lactamase-producing Gram-negative bacteria using machine learning methods: a multicentre, prospective cohort study. Clin Microbiol Infect 2020;26:8794.CrossRefGoogle ScholarPubMed
Artoisenet, C, Ausselet, N, Delaere, B, Spinewine, A. Evaluation of the appropriateness of intravenous Amoxicillin/Clavulanate prescription in a teaching hospital. Acta Clinica Belgica 2013;68:8186.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. Summary of patient demographics and prescribing pattern of intravenous (IV) amoxicillin-clavulanate

Figure 1

Table 2. Summary of primary and secondary outcomes

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