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Trends in hospital antibiotic utilization during the coronavirus disease 2019 (COVID-19) pandemic: A multicenter interrupted time-series analysis

Published online by Cambridge University Press:  28 July 2022

Marion Elligsen
Affiliation:
Department of Pharmacy, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada Sunnybrook Research Institute, Toronto, Ontario, Canada
Michael Wan
Affiliation:
Department of Pharmacy, St Joseph’s Health Centre, Unity Health Toronto, Toronto, Ontario, Canada
Philip W. Lam
Affiliation:
Division of Infectious Diseases, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada Division of Infectious Diseases, Department of Medicine, University of Toronto, Toronto, Ontario, Canada
Jennifer Lo
Affiliation:
Department of Pharmacy, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada
Linda R. Taggart
Affiliation:
Division of Infectious Diseases, Department of Medicine, University of Toronto, Toronto, Ontario, Canada Division of Infectious Diseases, Department of Medicine, St Michael’s Hospital, Unity Health Toronto, Toronto, Ontario, Canada
April J. Chan
Affiliation:
Department of Pharmacy, St Joseph’s Health Centre, Unity Health Toronto, Toronto, Ontario, Canada
Mark Downing
Affiliation:
Division of Infectious Diseases, St Joseph’s Health Centre, Unity Health Toronto, Toronto, Ontario, Canada
Kevin Gough
Affiliation:
Division of Infectious Diseases, Department of Medicine, University of Toronto, Toronto, Ontario, Canada Division of Infectious Diseases, Department of Medicine, St Michael’s Hospital, Unity Health Toronto, Toronto, Ontario, Canada
Jenny Seah
Affiliation:
Department of Pharmacy, St Joseph’s Health Centre, Unity Health Toronto, Toronto, Ontario, Canada
Elizabeth Leung*
Affiliation:
Department of Pharmacy, St Michael’s Hospital, Unity Health Toronto, Toronto, Ontario, Canada Li Ka Shing Knowledge Institute, Toronto, Ontario, Canada Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Ontario, Canada
*
Author for correspondence: Beth Leung, PharmD, MSCI, BCPS AQ-ID, St Michael’s Hospital—Unity Health Toronto, 30 Bond Street, Toronto, ONM5B 1W8. E-mail: [email protected]

Abstract

Objective:

To describe the evolution of respiratory antibiotic prescribing during the coronavirus disease 2019 (COVID-19) pandemic across 3 large hospitals that maintained antimicrobial stewardship services throughout the pandemic.

Design:

Retrospective interrupted time-series analysis.

Setting:

A multicenter study was conducted including medical and intensive care units (ICUs) from 3 hospitals within a Canadian epicenter for COVID-19.

Methods:

Interrupted time-series analysis was used to analyze rates of respiratory antibiotic utilization measured in days of therapy per 1,000 patient days (DOT/1,000 PD) in medical units and ICUs. Each of the first 3 waves of the pandemic were compared to the baseline.

Results:

Within the medical units, use of respiratory antibiotics increased during the first wave of the pandemic (rate ratio [RR], 1.76; 95% CI, 1.38–2.25) but returned to the baseline in waves 2 and 3 despite more COVID-19 admissions. In ICU, the use of respiratory antibiotics increased in wave 1 (RR, 1.30; 95% CI, 1.16–1.46) and wave 2 of the pandemic (RR, 1.21; 95% CI, 1.11–1.33) and returned to the baseline in the third wave, which had the most COVID-19 admissions.

Conclusions:

After an initial surge in respiratory antibiotic prescribing, we observed the normalization of prescribing trends at 3 large hospitals throughout the COVID-19 pandemic. This trend may have been due to the timely generation of new research and guidelines developed with frontline clinicians, allowing for the active application of new research to clinical practice.

Type
Original Article
Creative Commons
Creative Common License - CCCreative Common License - BYCreative Common License - NCCreative Common License - SA
This is an Open Access article, distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike licence (http://creativecommons.org/licenses/by-nc-sa/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the same Creative Commons licence is used to distribute the re-used or adapted article and the original article is properly cited. The written permission of Cambridge University Press must be obtained prior to any commercial use.
Copyright
© The Author(s), 2022. Published by Cambridge University Press on behalf of The Society for Healthcare Epidemiology of America

The first case of coronavirus disease 2019 (COVID-19) in Canada was identified on January 23, 2020, in Toronto, Canada. Reference Marchand-Senécal, Kozak and Mubareka1 From that point forward, COVID-19 cases waxed and waned throughout the city, which is Canada’s largest city by population and one of the country’s epicenters during the COVID-19 pandemic. In Toronto, there have been 5 pandemic waves to date. 2 Since 2013, Antimicrobial Stewardship has been a required organizational practice for Canadian healthcare organizations accredited by Accreditation Canada. 3 Antimicrobial stewardship programs (ASPs) aim to optimize antimicrobial use to ultimately improve patient outcomes, decrease adverse drug events, and reduce or stabilize levels of antibiotic resistance. Reference Peragine, Walker, Simor, Walker, Kiss and Leis4,Reference Dellit, Owens and McGowan5 However, at the outset of the pandemic, many ASPs worldwide temporarily halted or reduced their functions, due to many factors including staff redeployment. Reference Ashiru-Oredope, Kerr and Hughes6Reference Ng, Tan and Heng8 At the beginning of the pandemic, increased antibiotic prescribing may have been caused by evolving COVID-19 diagnostic criteria and the unclear risk of concomitant bacterial pneumonia with a novel viral pathogen.

Our ASPs faced many challenges throughout the pandemic (eg, increasing admissions of patients with COVID-19 and strain on staff resources), but we continued with efforts to minimize unnecessary antibiotic use in conjunction with regional guidelines and emerging literature. Notably, a landmark systematic living review (first published by Langford et al Reference Langford, So and Raybardhan9 in July 2020) identified a 3.5% rate of coinfection with bacterial pathogens at the time of presentation to the hospital. Regional COVID-19 therapeutic guidelines were developed and updated in real time by local stakeholder groups. Over time, these evolved into a provincial advisory body, and included guidance on the appropriateness of antibiotics for bacterial coinfection. Reference Langford, So and Raybardhan9,10 These resources empowered ASPs to limit the use of antibiotics in patients admitted with COVID-19 using a variety of established stewardship strategies including audit and feedback, educational interventions, and development of local guidelines and order sets.

Data describing the effect of the COVID-19 pandemic on antimicrobial consumption trends are limited, but concern is increasing that the pandemic has exacerbated and accelerated the development of antimicrobial resistance worldwide. Reference Getahun, Smith, Trivedi, Paulin and Balkhy11 Most of the published data on antimicrobial use during the pandemic describes outpatient trends. Reference King, Lovegrove and Shehab12Reference Kitano, Brown and Daneman15 Although some published data are available from the inpatient setting (generally demonstrating increased rates of antimicrobial prescribing during the first wave of the COVID-19 pandemic), most of these studies have only described early pandemic prescribing, and antibiotic use metrics were not always standardized to patient volumes or compared to baseline prescribing patterns. Reference Stevens, Jensen, Kooda, Mara, O’Horo and Shah16Reference Henig, Kehat and Meijer19 Published data on the impact of the pandemic on ASPs, and how changes in ASPs may have affected antimicrobial consumption trends, are also limited. One study, which demonstrated a decrease in antimicrobial prescribing in COVID-19 units compared to historical controls, hypothesized that the ASP was responsible for the decreased rates of antimicrobial use. However, the intensity of their COVID-19–specific multidisciplinary ASP infrastructure may not be generalizable to many institutions, due to the human resources required to sustain such an intervention over a prolonged period. Reference Henig, Kehat and Meijer19 In addition, different factors are likely to influence antimicrobial use in inpatient and outpatient settings (eg, in the outpatient setting, initial decreased visits were associated with decreased antimicrobial prescribing), and it is important to understand the effects of the pandemic on antimicrobial prescribing across the spectrum of care. The objective of this study was to describe the evolution of prescribing of antibiotics commonly used for community-onset respiratory infections during the COVID-19 pandemic across 3 large hospitals that maintained ASP services throughout the pandemic, despite significant strain on healthcare resources.

Methods

Study setting, design, and participants

This multicenter, retrospective study of antibiotics commonly used for community-onset respiratory infections was conducted within medical floors and intensive care units (ICUs), at St Michael’s Hospital (463 beds, tertiary-care, academic hospital), St Joseph’s Health Centre (372 beds, community teaching hospital) and Sunnybrook Health Sciences Centre (690 beds, tertiary-care academic hospital) located in Toronto, Ontario, Canada between March 2019 and June 2021. The medical floors and ICUs included in this study cared for patients admitted with COVID-19.

Antimicrobial stewardship programs

All 3 institutions had an active ASP during the entire study period, along with an intensive audit-and-feedback program that remained active throughout the pandemic. During the pandemic, our ASPs altered how services were provided locally (eg, staff redeployment and implementing teleconferenced clinical services to support physical distancing), resulting in variations and slight modifications of each study site’s ASP activities. Details of each respective hospital’s ASP services before and during the pandemic are outlined in Appendix 1. Overall, there were no major changes to clinical ASP services; examples of core ASP activities that were continued across all sites during the pandemic included prospective audit and feedback, educational interventions, and development of local guidelines and order sets.

Development of evidence and guidelines to guide use of antibiotics in COVID-19

Regional COVID-19 therapeutic guidelines were released in March 2020, which included guidance on the appropriateness of antibiotics for bacterial coinfection at time of presentation to hospital. 20 Recommendations were stratified based on severity of illness. In patients with mild-to-moderate disease, these guidelines recommended against the use of antibiotics “outside approved clinical trials or where other indications would justify its use.” In critically ill patients, initial guidelines recommended antibiotics for all patients admitted with COVID-19; this guidance was updated on April 3, 2020, and antibiotics were recommended “if bacterial coinfection was suspected.” Prior to the third wave of COVID-19, on February 25, 2021, the guidelines were updated further with an explicit recommendation to discourage the use of antibiotics upon hospital admission for critically ill patients; advising that “bacterial coinfection is uncommon in COVID-19 pneumonia at presentation. Do not add empiric antibiotics for bacterial pneumonia unless bacterial infection is strongly suspected.” 10 These changes to the guideline were based on the landmark systematic review observing low bacterial coinfection rates by Langford et al Reference Langford, So and Raybardhan9 (in conjunction with the Toronto Antimicrobial Resistance Research Network).

Outcomes

The primary outcome of this study was the combined monthly rates of respiratory antibiotic use measured in days of therapy per 1,000 patient days (DOT/1,000 PD) in medical wards and medical-surgical ICUs across all 3 institutions for each pandemic wave. For this study, we defined “respiratory antibiotics” as antibiotics commonly used for respiratory infections: amoxicillin-clavulanic acid, azithromycin, ceftriaxone, cefuroxime, levofloxacin, and moxifloxacin. This list encompassed all recommended treatments for community-acquired lower respiratory tract infection across all study sites. The rate of respiratory antibiotic prescribing in DOT/1,000 PD for each wave was compared to the baseline period (March 2019–February 2020). Wave 1 occurred between March and June 2020; wave 2 occurred between October 2020 and February 2021; and wave 3 occurred between March and June 2021. We also measured the number of admissions with COVID-19 to each hospital during each wave of the pandemic. The number of COVID-19 admissions was standardized per 1,000 PD to account for fluctuations in hospital occupancy throughout the pandemic.

Data sources

Antibiotic use data were collected from the electronic medical records of each participating institution. Patient-day data and number of COVID-19 admission numbers were obtained from administrative data.

Statistical analysis

An interrupted time-series analysis was used to analyze the aggregate rate of respiratory antibiotic use in all 3 institutions. Two separate analyses were performed: one examining the monthly DOT/1,000 PD on medical wards and one for ICUs. A segmented regression analysis was performed that compared each wave of the pandemic to the baseline. A level-only model was chosen due to the short duration of each wave. Monthly data were modeled using Poisson regression with the total number of patient days set as the offset variable. Seasonality was accounted for by including the calendar month in the model. Testing for autocorrelation was carried out by inspecting the residuals from the autocorrelation and partial autocorrelation plots. No evidence of autocorrelation was detected. Weighted empirical adaptive variance estimators were used to account for heteroscedasticity. All statistical analyses were performed using R version 3.4.3 statistical software (R Foundation for Statistical Computing, Vienna, Austria).

Ethical considerations

This initiative was formally reviewed by the Review of Quality Improvement Studies (ReQuIST) at St Michael’s Hospital and St Joseph’s Health Centre and was evaluated using the Ethics Review Self-Assessment (ER-SAT) at Sunnybrook Health Sciences Centre. Both entities indicated that neither research ethics board approval nor written informed consent from participants was required.

Results

COVID-19 admissions

All 3 hospitals had large volumes of COVID-19 admissions during all 3 waves of the pandemic which were relatively well distributed (Table 1). With each successive wave, all hospitals saw an increase in the proportion of patients they cared for with COVID-19, with the exception of hospital 1, which had a slight decrease in the volume of patients they cared for in wave 2 (14.4 COVID-19 admissions per 1,000 PD) compared to wave 1 (19.9 COVID-19 admissions per 1,000 PD). All 3 hospitals saw the largest volumes of COVID-19 admissions in wave 3.

Table 1. COVID-19 Admissions Compared Between Study Sites

Note. PD, patient days.

a Includes intensive care units and medical units.

Baseline respiratory antibiotic use

All 3 institutions had comparable rates of respiratory antibiotic usage at baseline. In the medical wards, the monthly usage ranged from 98 to 210 DOT/1,000 PD. The baseline monthly means in medical wards for hospitals 1, 2, and 3 were 139, 150, and 138 DOT/1,000 PD, respectively. In ICUs, monthly usage ranged from 95 to 286 DOT/1,000 PD. The baseline monthly means in ICUs for hospitals 1, 2, and 3 were 162, 178, and 195 DOT/1,000 PD, respectively.

Respiratory antibiotic use during the pandemic

All 3 institutions observed a statistically significant increase (rate ratio [RR], 1.76; 95% confidence interval [CI], 1.38–2.25) in respiratory antimicrobial use during the first wave of the pandemic in their medical wards (Fig. 1 and Table 2). The rates did not significantly differ when compared to the pre–COVID-19 baseline period for the following 2 waves, despite having more patients admitted with COVID-19. This change was temporally associated with the publication of the systematic review by Langford et al. Reference Langford, So and Raybardhan9

Fig. 1. Respiratory antibiotic use in general medicine. *Regional COVID-19 therapeutic guidelines were released that recommended against antibiotic use in patients with mild-to-moderate disease 20 **Langford et al Reference Langford, So and Raybardhan9 was published identifying a low rate of bacterial coinfection on admission.

Table 2. Segmented Regression Analysis of Combined Respiratory Antibiotic Days of Therapy (DOT) per 1,000 Patient Days (PD) during the First Three Pandemic Waves Compared to the Baseline

Note. CI, confidence interval.

A similar trend was observed in the ICUs. Respiratory antibiotic use increased by 30% in wave 1 (RR, 1.30; 95% CI, 1.16–1.46). This increase persisted in the second wave of the pandemic (RR, 1.21; 95% CI, 1.11–1.33). After regional COVID-19 therapeutic guidelines were modified to discourage the use of antibiotics in critically ill patients admitted with COVID-19, respiratory antibiotic use returned to the baseline in the third wave, which saw the highest number of admitted patients with COVID-19 (Fig. 2 and Table 2).

Fig. 2. Respiratory antibiotic use in intensive care units. *Regional COVID-19 therapeutic guidelines were released that recommended antibiotic use in critically ill patients when bacterial coinfection was suspected. 20 **Langford et al Reference Langford, So and Raybardhan9 was published identifying a low rate of bacterial coinfection on admission. ***Regional COVID-19 therapeutic guidelines were revised to highlight the low rate of bacterial coinfection on admission and recommended against antibiotic use in critically ill patients unless bacterial coinfection was strongly suspected. 10

Discussion

We examined the use of antibiotics commonly used for community-onset respiratory infections throughout the first 3 waves of the COVID-19 pandemic in Toronto, Ontario. In the medical wards, a 76% increase in respiratory antibiotic prescribing was observed in wave 1 but not in waves 2 or 3, despite higher numbers of patients admitted to the hospital with COVID-19 in the latter 2 waves. In ICUs, respiratory antibiotic use increased by 30% and 21% in waves 1 and 2, respectively; however, respiratory antibiotic use returned to the baseline in wave 3. Respiratory antibiotic use was similar between institutions (Figs. 1 and 2), and antibiotic use data were compared to a baseline period to adjust for seasonal and institution-specific prescribing trends.

Throughout the COVID-19 pandemic, significant healthcare resource strain has been described, leading to reduced or suspended ASP interventions. Reference Ashiru-Oredope, Kerr and Hughes6Reference Ng, Tan and Heng8 However, data describing the use of antibiotics in hospitalized patients throughout the many waves of the current pandemic are limited, especially in North America. In our study, clear prescribing trends evolved similarly in 3 large, acute-care hospitals that continued core ASP activities and followed the same regional COVID-19 therapeutic guidelines. Similar to existing publications, we noted an increased use of antibiotics during the pandemic. Reference Stevens, Jensen, Kooda, Mara, O’Horo and Shah16Reference Henig, Kehat and Meijer19 Compared to existing publications, our antibiotic use metrics were normalized with the use of patient day data, and we adjusted for prior antibiotic prescribing trends and seasonality with the use of an interrupted time-series analysis. We also analyzed antibiotic use between different pandemic waves to examine the evolution of antibiotic prescribing as new publications and guidelines were developed throughout the first 3 waves of the pandemic.

In this study, we observed a large initial increase in respiratory antibiotic prescribing, followed by reduced prescribing in subsequent pandemic waves even though COVID-19 admissions increased with every wave. All authors were involved in the clinical care of COVID-19 patients during the pandemic, and through our experiences, we identified several potential mechanisms and drivers of appropriate antibiotic prescribing. Firstly, the generation of timely scientific research to inform clinical practice and to develop evidence-based guidelines was essential. For example, the systematic living review published in July 20209 was the first large-scale meta-analysis describing the low incidence of bacterial coinfection in patients with COVID-19. Secondly, ASPs benefitted from the rapid development of regional COVID-19 treatment guidelines, which began as an informal initiative among hospitals in the Greater Toronto Area and later was incorporated into an advisory body to the government (Ontario COVID-19 Science Advisory Table). In contrast to some major international guidelines, Reference Bhimraj, Morgan and Shumaker21,22 the Ontario COVID-19 Science Advisory Table guidelines include explicit recommendations against the use of antibiotics unless there is a specific concern for bacterial coinfection. Contributors to these regional consensus guidelines included frontline healthcare clinicians across the province, with diverse backgrounds regarding practice setting (rural and urban centers) and clinical specialty (infectious diseases, antimicrobial stewardship, critical care, ambulatory care, and patient partners). Finally, involvement of ASPs in regional guideline development and as local content experts facilitated knowledge translation and implementation of evidence-based guidelines. This process occurred both at the individual patient level via prospective audit and feedback and at the system level via interventions such as order sets and institution-wide continuing education initiatives. Each of these potential mechanisms are closely linked and act in tandem; new research is needed to inform the development of evidence-based guidelines, which then empowers individual ASP initiatives to optimize antibiotic use.

Although our results do not prove causation, our findings may indicate that local and regional ASP initiatives and resources were successful in reducing unnecessary antibiotic use in patients with COVID-19. Despite the pandemic-associated challenges for each institution’s ASP, all programs maintained some form of prospective audit and feedback (the gold standard, and guideline-recommended approach/cornerstone for ASPs) Reference Barlam, Cosgrove and Abbo23 throughout the pandemic, and we observed that prescribing trends changed similarly across all study sites despite the local variations in ASP activities. Thus, we hypothesize that the combinations of a variety of ASP approaches were successful at changing prescribing behavior and that regional guidelines also contributed to improving antibiotic prescribing practices throughout the pandemic. Notably, a Public Health Ontario survey of all hospitals in the province reported that the pandemic may have had less adverse impact on core ASP activities and ASP funding in Ontario, compared to programs in other jurisdictions. Reference So and Leung24

Although our study observed similar trends of local respiratory antibiotic prescribing during the pandemic, it had several limitations. Although our results are hypothesis generating, our descriptive study could not identify the causative factors specifically responsible for the initial increase, and subsequent normalization of respiratory antibiotic prescribing during the first 3 waves of the COVID-19 pandemic across our institutions. We only included antibiotics recommended for community-acquired lower respiratory infection to best capture the direct impact of COVID-19 on antimicrobial prescribing. We did not have access to indications for antimicrobial therapy, thus our utilization data may have included antibiotics used for indications other than respiratory tract infection and may have excluded some patients who received broader antimicrobial coverage for bacterial coinfection. We were also unable to identify and exclude a small amount of study-related antibiotic prescribing (eg, REMAP-CAP Reference Angus, Berry and Lewis25 ). In addition, we were not able to restrict our study population solely to patients with COVID-19, due to limitations of administrative data. Thus, we selected a nonconventional metric of COVID-19 admissions per 1,000 PD. Our selected study units were chosen because they represent the admitting units for most COVID-19 patients at our institutions. Another factor that may have influenced our study results is the possible change in patient demographics across our study units throughout the pandemic (eg, surgical units may have taken patients who would usually be admitted to a medicine ward for bed-spacing purposes). Patient demographics may also have varied between our institutions, which could have contributed to variances from observed baseline antibiotic prescribing patterns. We attempted to control for these variances by including a local baseline use period and adjustment for seasonality, which provided a local historical comparator. Our chosen metric (DOT/1,000 PD) did not specifically assess appropriateness of antibiotic prescribing; however, the continuation of our local prospective audit-and-feedback programs regularly assessed antibiotic appropriateness in real time throughout the pandemic. Furthermore, as all 3 sites had comprehensive ASPs consisting of a variety of interventions (both prior to and during the pandemic), we were not able to directly identify which specific ASP intervention(s) may have driven our observations or whether additive or synergistic effects exist with multiple ASP interventions. Finally, it is unclear whether our observations are representative of other regional or international institutions, which may have had differing prepandemic ASP resources and may have faced different pandemic-related limitations or local pressures.

In summary, after an initial surge in respiratory antibiotic prescribing, we observed the normalization of prescribing trends at 3 large hospitals throughout the first 3 waves of the COVID-19 pandemic in Toronto, Ontario. Although exact causation could not be established, our results suggest that our ASPs were successful at decreasing respiratory antibiotic use by maintaining core antimicrobial stewardship activities, despite significant resource strains throughout the pandemic. Timely generation of new research and evidence, and rapid knowledge translation into guidelines with the involvement of frontline clinicians and local stakeholders, may have contributed to the success of our ASPs. Our study illustrates the essential nature of ASPs for both monitoring and influencing antibiotic prescribing trends; therefore, it is important to support the growth and development of ASPs, especially in situations in which the overuse of antibiotics is likely to occur.

Supplementary material

To view supplementary material for this article, please visit https://doi.org/10.1017/ash.2022.268

Acknowledgments

Financial support

No funding was received for this project.

Conflicts of interest

E.L., J.L., L.T., M.E., M.W., and P.W.L. are members of the Toronto Antimicrobial Resistance Research Network (TARRN). E.L. is a voting member of the Ontario COVID-19 Science Advisory Table’s Clinical Practice Guidelines Working Group.

References

Marchand-Senécal, X, Kozak, R, Mubareka, S, et al. Diagnosis and management of first case of COVID-19 in Canada: lessons applied from SARS-CoV-1. Clin Infect Dis 2020;71:22072210.10.1093/cid/ciaa227CrossRefGoogle ScholarPubMed
Accreditation Canada. Required Organizational Practices: 2020 Handbook. Ottawa, Canada: Accreditation Canada; 2020.Google Scholar
Peragine, C, Walker, SAN, Simor, A, Walker, SE, Kiss, A, Leis, JA. Impact of a comprehensive antimicrobial stewardship program on institutional burden of antimicrobial resistance: a 14-year controlled interrupted time-series study. Clin Infect Dis 2020;71:28972904.10.1093/cid/ciz1183CrossRefGoogle ScholarPubMed
Dellit, TH, Owens, RC, McGowan, JE, et al. Infectious Diseases Society of America and the Society for Healthcare Epidemiology of America guidelines for developing an institutional program to enhance antimicrobial stewardship. Clin Infect Dis 2007;44:159177.10.1086/510393CrossRefGoogle Scholar
Ashiru-Oredope, D, Kerr, F, Hughes, S, et al. Assessing the impact of COVID-19 on antimicrobial stewardship activities/programs in the United Kingdom. Antibiotics 2021;10:110.10.3390/antibiotics10020110CrossRefGoogle ScholarPubMed
Murgadella-Sancho, A, Coloma-Conde, A, Oriol-Bermúdez, I. Impact of the strategies implemented by an antimicrobial stewardship program on the antibiotic consumption in the coronavirus disease 2019 (COVID-19) pandemic. Infect Control Hosp Epidemiol 2021. doi: 10.1017/ice.2021.237.CrossRefGoogle Scholar
Ng, TM, Tan, SH, Heng, ST, et al. Effects of coronavirus disease 2019 (COVID-19) pandemic on antimicrobial prevalence and prescribing in a tertiary hospital in Singapore. Antimicrob Resist Infect Control 2021;10:18.CrossRefGoogle Scholar
Langford, BJ, So, M, Raybardhan, S, et al. Bacterial coinfection and secondary infection in patients with COVID-19: a living rapid review and meta-analysis. Clin Microbiol Infect 2020;26:16221629.10.1016/j.cmi.2020.07.016CrossRefGoogle ScholarPubMed
Clinical practice guideline summary: recommended drugs and biologics in adult patients with COVID-19. Ontario COVID-19 Science Advisory Table website. https://covid19-sciencetable.ca/sciencebrief/clinical-practice-guideline-summary-recommended-drugs-and-biologics-in-adult-patients-with-covid-19-version-10-0/. Published 2022. Accessed February 25, 2022.Google Scholar
Getahun, H, Smith, I, Trivedi, K, Paulin, S, Balkhy, HH. Tackling antimicrobial resistance in the COVID-19 pandemic. Bull World Health Organ 2020;98:442442A.10.2471/BLT.20.268573CrossRefGoogle ScholarPubMed
King, LM, Lovegrove, MC, Shehab, N, et al. Trends in US outpatient antibiotic prescriptions during the coronavirus disease 2019 pandemic. Clin Infect Dis 2021;73:e652e660.10.1093/cid/ciaa1896CrossRefGoogle ScholarPubMed
Rezel-Potts, E, L’Esperance, V, Gulliford, MC. Antimicrobial stewardship in the UK during the COVID-19 pandemic: a population-based cohort study and interrupted time-series analysis. Br J Gen Pract 2021;71:e331e338.10.3399/BJGP.2020.1051CrossRefGoogle ScholarPubMed
Zhu, N, Aylin, P, Rawson, T, Gilchrist, M, Majeed, A, Holmes, A. Investigating the impact of COVID-19 on primary care antibiotic prescribing in north west London across two epidemic waves. Clin Microbiol Infect 2021;27:762768.10.1016/j.cmi.2021.02.007CrossRefGoogle Scholar
Kitano, T, Brown, KA, Daneman, N, et al. The impact of COVID-19 on outpatient antibiotic prescriptions in Ontario, Canada: an interrupted time-series analysis. Open Forum Infect Dis 2021;8:ofab533.10.1093/ofid/ofab533CrossRefGoogle ScholarPubMed
Stevens, RW, Jensen, K, Kooda, K, Mara, K, O’Horo, JC, Shah, A. A retrospective antibiotic prescribing assessment and examination of potential antibiotic stewardship targets in patients with COVID-19. JAC Antimicrob Resist 2021;3:dlab170.CrossRefGoogle ScholarPubMed
So, M, Morris, AM, Walker, AM. Antibiotic prescribing patterns among patients admitted to an academic teaching hospital for COVID-19 during the first wave of the pandemic in Toronto: a retrospective, controlled study. JAMMI 2021;30:dlab085.Google Scholar
Calderón-Parra, J, Muiño-Miguez, A, Bendala-Estrada, AD, et al. Inappropriate antibiotic use in the COVID-19 era: factors associated with inappropriate prescribing and secondary complications. Analysis of the registry SEMI-COVID. PLoS One 2021;16(5):e0251340.10.1371/journal.pone.0251340CrossRefGoogle ScholarPubMed
Henig, O, Kehat, O, Meijer, SE, et al. Antibiotic Use during the COVID-19 pandemic in a tertiary hospital with an ongoing antibiotic stewardship program. Antibiotics (Basel) 2021;10(9):1056.10.3390/antibiotics10091056CrossRefGoogle Scholar
Greater Toronto Area (GTA) clinical practice guidelines for antimicrobial and immunomodulatory therapy in patients with COVID-19. University Health Network website. https://www.antimicrobialstewardship.com/covid-19. Accessed March 16, 2022.Google Scholar
Bhimraj, A, Morgan, RL, Shumaker, AH, et al. IDSA guidelines on the treatment and management of patients with COVID-19. Infectious Diseases Society of America website. https://www.idsociety.org/practice-guideline/covid-19-guideline-treatment-and-management/. Accessed February 25, 2022.Google Scholar
Therapeutic management of hospitalized adults with COVID-19. National Institutes of Health website. https://www.covid19treatmentguidelines.nih.gov/management/clinical-management/hospitalized-adults--therapeutic-management/. Accessed February 25, 2022.Google Scholar
Barlam, TF, Cosgrove, SE, Abbo, LM, et al. Implementing an antibiotic stewardship program: guidelines by the Infectious Diseases Society of America and the Society for Healthcare Epidemiology of America. Clin Infect Dis 2016;62:e51e77.10.1093/cid/ciw118CrossRefGoogle Scholar
So, M, Leung, V. Spread awareness, stop resistance: antimicrobial stewardship amid the COVID-19 pandemic. Public Health Ontario website. https://www.publichealthontario.ca/-/media/event-presentations/2021/antimicrobial-stewardship-covid-19.pdf?sc_lang=en. Published 2021. Accessed March 16, 2022.Google Scholar
Angus, DC, Berry, S, Lewis, RJ, et al. The REMAP-CAP (Randomized Embedded Multifactorial Adaptive Platform for Community-Acquired Pneumonia) study. Rationale and design. Ann Am Thorac Soc 2020;17:879891.10.1513/AnnalsATS.202003-192SDCrossRefGoogle ScholarPubMed
Figure 0

Table 1. COVID-19 Admissions Compared Between Study Sites

Figure 1

Fig. 1. Respiratory antibiotic use in general medicine. *Regional COVID-19 therapeutic guidelines were released that recommended against antibiotic use in patients with mild-to-moderate disease20 **Langford et al9 was published identifying a low rate of bacterial coinfection on admission.

Figure 2

Table 2. Segmented Regression Analysis of Combined Respiratory Antibiotic Days of Therapy (DOT) per 1,000 Patient Days (PD) during the First Three Pandemic Waves Compared to the Baseline

Figure 3

Fig. 2. Respiratory antibiotic use in intensive care units. *Regional COVID-19 therapeutic guidelines were released that recommended antibiotic use in critically ill patients when bacterial coinfection was suspected.20 **Langford et al9 was published identifying a low rate of bacterial coinfection on admission. ***Regional COVID-19 therapeutic guidelines were revised to highlight the low rate of bacterial coinfection on admission and recommended against antibiotic use in critically ill patients unless bacterial coinfection was strongly suspected.10

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