Lines represent linear regression lines of best fit, and dots represent the monthly UCs per 100 patient-days for each month of study.
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Taylor MT, McCready J, Havey T, Kaur S, Powis J. Assessment of a 2-Step Urine Culture Ordering Process for Detecting Asymptomatic Bacteruria Among Hospitalized Patients. JAMA Netw Open. 2020;3(2):e1921665. doi:10.1001/jamanetworkopen.2019.21665
Educational interventions attempting to reduce the treatment of asymptomatic bacteruria and candiduria (ASB/C) have been largely unsuccessful. Modifying how urine cultures (UCs) are ordered, processed, and reported may be a more effective strategy for reducing the overdiagnosis of ASB/C.1 A 2-step UC ordering process was associated with a reduction in the number of UCs and antimicrobial treatments of ASB/C in the emergency department,2 and we evaluated a similar intervention among patients hospitalized in an acute care setting.
This quality improvement study was approved by the Michael Garron Hospital research ethics board. Because the project was deemed a quality improvement evaluation with minimal risk, patient consent was waived. This report was structured according to the Standards for Quality Improvement Reporting Excellence (SQUIRE) reporting guideline for quality improvement studies.3
A time series analysis was conducted to evaluate the association of a 2-step UC ordering process with the number of processed UCs per 100 patient-days (primary outcome) and antimicrobial use, intensive care unit transfers, critical care outreach assessment, in-hospital mortality, length of stay, and 7-day readmission rates (secondary outcomes) at an urban community hospital with 515 beds. Before the intervention, UCs could be submitted by nurses, according to medical directives, or by physicians, based on clinical suspicion of urinary tract infection, and all UCs were processed by the microbiology laboratory. The 2-step process involved collection of UCs by nurses based on clinical symptoms. The sample was stored in a container with preservatives, allowing it to be held for 48 hours in the laboratory until a separate physician order triggered processing. Urine cultures were not processed unless a separate physician order was received. Urinalysis was not required at the time of UC but could be ordered at the discretion of the physician. Education was provided to nurses and physicians regarding the ordering process, but no specific education was provided regarding indications for urine culturing. All catheter and noncatheter urine specimens collected from May 2015 to April 2016 (ie, the preintervention period) and May 2016 to April 2017 (ie, the postintervention period) were eligible for analysis. A random medical record audit was conducted with records from 100 patients in both the preintervention and postintervention periods to determine ordering clinician, indication for ordering the UC, and antimicrobial use. The postintervention population was stratified to ensure proportions of processed UCs were the same as the entire postintervention population.
Analyses were conducted via linear regression and a χ2 test of independence using R version 3.0.2 (R Project for Statistical Computing) with P < .05 considered significant. All tests were 2-tailed.
A total of 1344 ordered UCs were included in the preintervention analysis, and 866 ordered UCs were included in the postintervention analysis. Preintervention and postintervention populations were comparable (UCs from patients aged 18-65 years: 327 [32.1%] vs 224 [30.8%]; women: 561 [55.0%] vs 387 [53.2%]; patients located in medical units: 316 [31.0%] vs 241 [33.1%]); however, there were more pediatric cases in the postintervention period than the preintervention period (56 [7.7%] vs 49 [4.8%]; P = .02) (Table). There was no change in secondary outcomes (Table). Comparing the preintervention period with the postintervention period, the intervention was associated with a significant reduction in processed UCs per 100 patient-days (2.29 vs 1.17 per 100 patient-days; P = .001) (Figure). In the first month of the intervention, the modeled rate was 1.03 (95% CI, 0.85 to 1.21). The amount of change associated with the intervention (adjusted for the estimated temporal trend) was −0.03 per month (95% CI, −0.10 to −0.05; P = .02). This represents a 0.93 absolute reduction (95% CI, 0.59 to 1.27; P < .001). Compared with the preintervention period, the postintervention period saw a reduction in monthly processed UCs in all clinical areas except the pediatric unit (UCs per 100 patient-days from medical wards: 1.92 vs 0.78; P < .001; surgical wards: 2.11 vs 0.96; P < .001; intensive care unit: 3.11 vs 1.64; P < .005; pediatric ward: 3.08 vs 4.06; P = .68). In the preintervention period, nurses ordered 45 of 100 UCs (45.0%), based on medical directive, of which 32 (71.1%) had no indication based on accepted guidelines.4,5 Similar proportions of patients in the preintervention and postintervention periods had empirical antimicrobials initiated (38 of 100 [38.0%] vs 37 of 100 [37.0%]), mostly for nonurinary indications (28 of 38 [73.7%] vs 30 of 37 [81.1%]). Among patients not receiving empirical antimicrobials, the intervention was associated with a significant decrease in the detection of ASB/C (18 of 62 [29.0%] in the preintervention period; 7 of 63 [11.1%] in the postintervention period; P = .01). Treatment of ASB/C was infrequent (3 of 18 episodes [16.7%] in the preintervention period; 1 of 7 episodes [14.3%] in the postintervention period) and did not change significantly (P = .90).
Before the intervention, patients who were hospitalized often had UCs completed by nursing staff for nonspecific symptoms. In this quality improvement study, a 2-step UC ordering process was associated with a nearly 50% reduction in the number of UCs processed and a reduction in the detection of ASB/C. Our intervention avoided unnecessary UCs while maintaining nurses’ autonomy to collect them. Not culturing urine maximizes cost avoidance compared with analytical or postanalytical interventions. The advantage of our 2-step ordering process compared with a reflex policy based on pyuria is that the decision to process a UC in our intervention was based on clinical assessment by a physician rather than the result of urinalysis alone. Asymptomatic pyuria can occur in as many as 90% of elderly patients, for whom processing UCs is likely to yield a diagnosis of ASB/C and unnecessary antimicrobial therapy.
There was no significant change in overall antimicrobial use or treatment of ASB/C. We attribute this to the fact that most empirical antimicrobials were provided for nonurinary indications and that the treatment of ASB/C was far lower than expected from the literature because of our antimicrobial stewardship program.6
Our study has several limitations. First, it was conducted at a single community hospital, with a medical directive for nurses to order UCs. Therefore, it may not apply to all acute care settings. Additionally, we conducted a medical record audit on a random sample of patients who, by chance, may not be representative of the larger sample. Although pediatric cases made up a small proportion of our study population, the 2-step UC ordering process was not associated with reductions in the number of UCs processed in this population, and as a result, our intervention would be anticipated to have a smaller association with reductions in the number of processed UCs if the population under evaluation included a larger proportion of pediatric patients. Furthermore, a computer-order entry system is required to help physicians order UCs after clinical assessment.
This 2-step UC ordering process for patients in an acute care setting was associated with a reduction in the number of UCs processed as well as a reduction in the detection of ASB/C. Our intervention was not associated with the elimination of the detection of ASB/C and, therefore, should be considered part of broader strategy to prevent antimicrobial use for ASB/C. Further evaluation would be necessary to determine whether the intervention was associated with reductions in antimicrobial treatment of ASB/C in an acute care setting where ASB/C is treated at usual rates.
Accepted for Publication: December 20, 2019.
Published: February 21, 2020. doi:10.1001/jamanetworkopen.2019.21665
Open Access: This is an open access article distributed under the terms of the CC-BY License. © 2020 Taylor MT et al. JAMA Network Open.
Corresponding Author: Maureen T. Taylor, BHSc, Division of Infectious Diseases, Department of Medicine, Michael Garron Hospital, 825 Coxwell Ave, Room D306, Toronto, ON M4C 3E7, Canada (firstname.lastname@example.org).
Author Contributions: Dr Powis had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Concept and design: McCready, Havey, Powis.
Acquisition, analysis, or interpretation of data: Taylor, Havey, Kaur, Powis.
Drafting of the manuscript: Taylor, Havey, Kaur, Powis.
Critical revision of the manuscript for important intellectual content: Taylor, McCready, Powis.
Statistical analysis: Kaur, Powis.
Administrative, technical, or material support: Taylor, McCready, Havey, Powis.
Supervision: McCready, Powis.
Conflict of Interest Disclosures: Dr Powis reported receiving grants from Gilead Pharmaceuticals outside the submitted work. No other disclosures were reported.
Additional Contributions: John Matelski, MSc (Biostatistics Research Unit, University Health Network, Toronto, Ontario, Canada), provided statistical analysis support. He was compensated for his time.