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Evaluating the impact of mandatory indications on antibiotic utilization in a community hospital

Published online by Cambridge University Press:  15 July 2022

April J. Chan*
Affiliation:
Unity Health Toronto, Ontario, Canada
Rosane Nisenbaum
Affiliation:
University of Toronto, Ontario, Canada Li Ka Shing Knowledge Institute, Ontario, Canada Applied Health Research Centre and MAP Centre for Urban Solutions, Ontario, Canada
Mark Downing
Affiliation:
Unity Health Toronto, Ontario, Canada University of Toronto, Ontario, Canada
Bradley J. Langford
Affiliation:
Public Health Ontario, Ontario, Canada Hotel Dieu Shaver Health and Rehabilitation Centre, Ontario, Canada
*
Author for correspondence: April J Chan, PharmD, Inpatient Pharmacy, Glendale Wing, St Joseph’s Health Centre, 30 The Queensway, Toronto, ON, CanadaM6R 1B5. E-mail: [email protected]

Abstract

Objective:

We evaluated the impact of introducing a mandatory indication field into electronic order entry for targeted antibiotics in adult inpatients.

Design:

Retrospective, before-and-after trial.

Setting:

A 400-bed community hospital.

Interventions:

All adult electronic intravenous (IV) and enteral orders for targeted antibiotics (moxifloxacin, ciprofloxacin, clindamycin, vancomycin, and metronidazole) had a mandatory indication field added. Control antibiotics (amoxicillin-clavulanate, ceftriaxone and piperacillin-tazobactam) were chosen to track shifts in antibiotic prescribing due to the introduction of mandatory indication field.

Methods:

Descriptive statistics were used to summarize the primary outcome, measured in Defined Daily Doses (DDD) per 1000 patient days (PD). Interrupted time-series (ITS) analysis was performed to compare levels and trends in antibiotic usage of targeted and control antibiotics during 24 months before and after the intervention. Additionally, a descriptive analysis of mandatory indication fields for targeted antibiotics in the postintervention period was conducted.

Results:

In total, 4,572 study antibiotic orders were evaluated after the intervention. Preset mandatory indications were selected for 30%–55% of orders. There was decreased usage of targeted antibiotics (mean, 92.02 vs 72.07 DDD/1000-PD) with increased usage of control antibiotics (mean, 102.73 vs 119.91 DDD/1000-PD). ITS analysis showed no statistically significant difference in overall antibiotic usage before and after the intervention for all targeted antibiotics.

Conclusion:

This study showed moderate use of preset mandatory indications, suggesting that the preset list of indications can be optimized. There was no impact on overall antibiotic usage with the use of mandatory indications. More prospective research is needed to study the utility of this intervention in different contexts.

Type
Original Article
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), 2022. Published by Cambridge University Press on behalf of The Society for Healthcare Epidemiology of America

Recent evidence suggests that 30%–40% of prescribed antibiotics in hospital are inappropriate. Reference Fridkin, Baggs and Fagan1 Unnecessary usage of antibiotics can lead to selection for antimicrobial resistant pathogens, Clostridioides difficile infection, and other adverse events such as nephrotoxity. Reference Tamma, Avdic and Li2 Documentation of indications for antibiotics is recommended to facilitate antimicrobial stewardship interventions such as prospective audit and feedback. 3 Some studies have shown to reduce rates of inappropriate prescribing and improve medication safety Reference Nomura, Garcia and Child4Reference Heil, Pineles and Mathur7 ; however, more studies are needed to confirm the impact on overall antibiotic usage and shifts in antibiotic prescribing.

In October 2015, St. Joseph’s Health Centre introduced mandatory indication fields into electronic order entry for selected antibiotics. These fields acted as a force function, requiring prescribers to provide a reason for prescribing at the time of order entry before the order can be processed. We evaluated the impact of introducing this intervention on antibiotic utilization and characterized the use of predefined indications by prescribers.

Methods

The study was conducted at a 400-bed community hospital in Toronto, Canada. An antimicrobial stewardship program (ASP) was established at our institution in 2011, with a multimodal approach including prospective audit and feedback, development of guidelines and order sets, microbiology laboratory report optimization and education. Staffing consisted of a lead ASP physician and 2 full-time equivalent ASP-trained pharmacists during the study period of October 1, 2013, to October 31, 2017.

All adult electronic intravenous (IV) and enteral orders for targeted antibiotics (moxifloxacin, ciprofloxacin, clindamycin, vancomycin, and metronidazole) had a mandatory indication field added on October 22, 2015. The first three antibiotics (ciprofloxacin, moxifloxacin, clindamycin) were selected based of risk for causing Clostridioides difficile infection and being not first line agents for most infections in our setting so there is higher potential for inappropriate use. The latter two antibiotics (metronidazole and vancomycin) were selected as they had more clear-cut indications. Each mandatory indication field had predefined indications tailored to the selected antibiotics as determined by the ASP team and a free-text field (Table 1). Only a single mandatory indication or free text can be selected at the time of order entry. Discrete preset indications of each antibiotic were discussed and chosen by the antimicrobial stewardship team. A descriptive analysis of the mandatory indication fields for the study antibiotics was conducted.

Table 1. Usage of Predefined and Free-Text Indications for Selected Antibiotics

Note. CDI, Clostridioides difficile infection; CNS, central nervous system; CNST, coagulase-negative Staphylococci; GI, gastrointestinal; GPC, gram-positive cocci; GU, genitourinary; IV, intravenous; MRSA, methicillin-resistant Staphylococcus aureus; NPO, nothing by mouth; OM, osteomyelitis; SSTI, skin and soft-tissue infection.

a Additional criterion of NPO in preset list of indications.

Control antibiotics (amoxicillin-clavulanate, ceftriaxone, and piperacillin-tazobactam) were chosen to track shifts in antibiotic prescribing due to the introduction of mandatory indication field because there were no specific initiatives addressing these control antibiotics during the study period.

The preintervention period was defined as October 1, 2013, to October 31, 2015, and the postintervention period was from November 1, 2015, to October 31, 2017. October 2015 was assigned to the preintervention period because the intervention started 1 week before the end of October and the assumption was that effect on antibiotic usage would be small after only a week of intervention.

Data on antibiotics were collected monthly as Defined Daily Doses (DDD) per 1000 patient days (PD). DDD was the available metric at the time and provided a longer history of antibiotic usage prior to the intervention. Descriptive statistics were used to summarize the antibiotic data. Interrupted time-series (ITS) analysis was performed to compare changes in level and slope with regard to the primary outcome. We used the regression model proposed by Wagner et al. Reference Wagner, Soumerai, Zhang and Ross-Degnan8 We used Stata version 15 software (StataCorp, College Station, TX) for these analyses. ITS analysis was used to estimate regression parameters by ordinary least-squares regression-based models which accommodated ITS data. These models estimate ordinary least-squares regression coefficients with Newey-West standard errors, which handle autocorrelation and heteroscedasticity. The command “actest” was used to perform the Cumby-Huizinga tests for autocorrelation and the specific lag order up to 12.

This study was approved by the research ethics board at St. Joseph’s Health Centre on January 20, 2017.

Results

In total, 8,399 orders were evaluated in the 1-year postintervention period, of which 4,572 orders were for targeted antibiotics and 3,287 were for control antibiotics. The preset mandatory indications were selected 30%–55% of the time, depending on targeted antibiotic (Table 1). When the free-form field was selected, the most common indication noted was a specific infection (eg, urinary tract infection-pyelonephritis for ciprofloxacin oral and intra-abdominal-gastrointestinal for ciprofloxacin IV) with very few indications that were incomprehensible (0–4 instances for each study antibiotic with examples such as a dot and a comma).

After mandatory indication field was introduced, there was decreased usage of targeted antibiotics (mean, 92.02 vs 72.07 DDD/1000-PD), driven by decreased usage of metronidazole (mean, 24.76 vs 18.44 DDD/1000-PD), ciprofloxacin (mean, 27.68 vs 21.30 DDD/1000-PD) and moxifloxacin (mean, 17.70 vs 11.89 DDD/1000-PD). We noted increased usage of control antibiotics (mean, 102.73 vs 119.91 DDD/1000-PD) driven by increased usage of amoxicillin-clavulanate (mean, 37.31 vs 43.14 DDD/1000-PD) and ceftriaxone (mean, 37.50 vs 46.88 DDD/1000-PD).

The ITS analysis showed levels were not different before and after the intervention for targeted antibiotics with mandatory indications. The difference in antibiotic usage (DDD/1000-PD) before the intervention (83.58; 95% CI, 77.21–89.95) and after the intervention (80.07; 95% CI, 70.62–89.51) was 3.51 (95% CI, −7.88 to 14.90; P = .538). Similarly, the preintervention slope (−0.92 per month) was not different from the postintervention slope (−1.00 per month) (change, −0.08; P = .821) (Table 2 and Fig. 1). Considering ITS analysis for individual targeted antibiotics, moxifloxacin levels were significantly different before and after the intervention. The difference between the postintervention level (16.98; 95% CI, 14.25–19.72) and the preintervention level (11.96; 95% CI, 9.00–14.93) was 5.02 (95% CI, 1.10–8.94; P = .013). There was no significant change in levels or slopes for other targeted antibiotics. Similarly, ITS analysis for control antibiotics showed that levels were not different before and after the intervention. The difference between postintervention levels (110.85; 95% CI, 101.03–120.66) and preintervention levels (102.25; 95% CI, 94.74–109.76) was 8.60 (95% CI, −3.76 to 20.95; P = .168). However, the preintervention slope (−0.04 per month) was different from postintervention slope (0.79 per month; change, 0.82; P = .051). Nonetheless, given the small change in DDD/1000-PD, this is likely not clinically significant (Table 3 and Fig. 2). This trend toward increased control antibiotic prescribing was driven by a significant level change seen with piperacillin-tazobactam. The difference between the postintervention level (30.03; 95% CI, 26.67–33.38) and the preintervention level (24.41; 95% CI, 21.61–27.21) was 5.62 (95% CI, 1.25–9.99; P = .013).

Table 2. ITS Analysis (Rate of Change)

Fig. 1. Mandatory indication antibiotic utilization pre and postintervention.

Table 3. ITS Analysis (Level Change)

Fig. 2. Control antibiotic utilization pre and postintervention.

Discussion

Although the use of prescriber-entered indications to track antibiotic prescribing has been described in literature and has been shown to improve appropriate antibiotic prescribing, Reference Nomura, Garcia and Child4Reference Heil, Pineles and Mathur7 our institution is one of few hospitals in Canada that have adopted mandatory indications in practice. To our knowledge, this is the first study to evaluate the impact of prescriber-selected indications on antibiotic usage of targeted antibiotics and potential shifts in prescribing. The introduction of mandatory fields led to moderate uptake of the predefined indications. Additionally, the use of mandatory indications did not have any significant impact to overall targeted and control antibiotic prescribing. We hypothesized that in the context of an already established ASP and concurrent other ASP interventions such as electronic order sets on common infections and high-intensity prospective audit and feedback, the true impact of mandatory indications may have been diminished. At our institution, ciprofloxacin is listed as 3rd line option for urinary tract infection and is not listed as an option for intra-abdominal infections. High-intensity prospective audit and feedback (PAF) at our institution comprise of twice weekly interdisciplinary rounds on our four internal medicine wards with a review of all internal medicine patients receiving any antimicrobial agent. High-intensity PAF was associated with a reduction in antibiotic use compared to our previous low-intensity PAF which consisted of ad-hoc review of patients on targeted antimicrobials.Reference Langford, Brown, Chan and Downing 10 The antibiotic usage reduction from high-intensity PAF would have some overlap with the reduction in targeted antibiotics seen with mandatory indications. Additionally, perhaps more time was needed to see the impact of this intervention, given we saw more changes in trends than levels.

This study had several limitations. Given its retrospective design, unaccounted confounding factors may have mitigated the change in antibiotic usage. However, our time-series analysis accounted for seasonal and secular (consistent) trends in antibiotic use to reduce the impact of any confounder. Secondly, we did not evaluate the accuracy of indication selection nor appropriateness of therapy. However, previous studies have shown high accuracy of selected indication (74%–100%) Reference Patel, Esterly, Scheetz and Postelnick5Reference Heil, Pineles and Mathur7,Reference Saini, Leung, Si and Ho11 for antimicrobials. We infer, based on these studies, that there was moderate to high accuracy and clinical appropriateness in the selection and use of our predefined mandatory indications. This finding was supported by the observations of specific infections noted when the free-text field was used and almost no incomprehensible rationale provided by prescribers.

Our next steps based on our findings include (1) optimizing the predefined list of indications to reflect the most commonly used free-form indications and (2) removing mandatory indications from oral vancomycin and indications pertaining to Clostridioides difficile infection from IV and oral metronidazole given the Infectious Diseases Society of America guideline update in 2017.

Acknowledgments

Financial support

Funding for statistical support was funded by the Department of Pharmacy, Unity Health Toronto (St. Joseph’s Health Centre site).

Conflicts of interest

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

Footnotes

PREVIOUS PRESENTATION. These findings were presented as a poster at IDWeek 2018 on October 4, 2018, in San Francisco, California.

References

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Figure 0

Table 1. Usage of Predefined and Free-Text Indications for Selected Antibiotics

Figure 1

Table 2. ITS Analysis (Rate of Change)

Figure 2

Fig. 1. Mandatory indication antibiotic utilization pre and postintervention.

Figure 3

Table 3. ITS Analysis (Level Change)

Figure 4

Fig. 2. Control antibiotic utilization pre and postintervention.