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. Author manuscript; available in PMC: 2019 Apr 19.
Published in final edited form as: Infect Control Hosp Epidemiol. 2017 Jan 5;38(4):455–460. doi: 10.1017/ice.2016.311

Inpatient urine cultures are frequently performed without urinalysis or microscopy: Findings from a large academic medical center

Abigail L Carlson 1, Satish Munigala 1, Anthony J Russo 2, Kathleen M McMullen 2,*, Helen Wood 2, Ronald Jackups 3, David K Warren 1
PMCID: PMC6474665  NIHMSID: NIHMS1004693  PMID: 28052781

Abstract

Objective:

To describe the frequency of urine cultures performed in inpatients without additional testing for pyuria.

Design:

Retrospective cohort study.

Setting:

A 1250-bed academic tertiary referral center.

Patients:

Hospitalized adults.

Methods:

We included urine cultures drawn on four medical and two surgical wards from 2009–2013 and in the medical and surgical intensive care units (ICUs) from 2012–2013. Patient and laboratory data were abstracted from the hospital’s medical informatics database. We identified catheter-associated urinary tract infections (CAUTIs) in the ICUs by routine infection prevention surveillance. Cultures without urinalysis or urine microscopy were defined as “isolated”. The primary outcome was the proportion of isolated urine cultures obtained. We used multivariable logistic regression to assess predictors of isolated cultures.

Results:

14,743 urine cultures were obtained (63.5 cultures/1000 patient-days) during 11,820 patient admissions. 2973 cultures (20.2%) were isolated cultures. 31 (50.8%) of 61 CAUTIs were identified by an isolated culture. Predictors for having an isolated culture included male gender [adjusted odds ratio (aOR)=1.22, 95% Confidence Interval (CI): 1.11, 1.35], urinary catheterization (aOR=2.15, 95%CI: 1.89, 2.46), ICU admission (medical ICU aOR=1.72, 95%CI: 1.47, 2.00; surgical ICU aOR=1.82, 95%CI: 1.51, 2.19), and obtaining the urine culture ≥1 calendar day after admission (1–7 days aOR=1.91, 95%CI 1.71, 2.12; >7 days after admission aOR=2.81, 95%CI: 2.37, 3.34).

Conclusions:

Isolated urine cultures are common in hospitalized patients, particularly in patients with urinary catheters and in ICUs. Interventions targeting inpatient culturing practices may improve the diagnosis of urinary tract infections.

Introduction

Differentiating asymptomatic bacteriuria from urinary tract infection (UTI) is a common diagnostic challenge among hospitalized patients. Data on the epidemiology of bacteriuria and pyuria in the inpatient setting are limited. For patients with urinary catheters, the incidence of bacteriuria is 3–8% per day, with nearly all catheterized patients becoming bacteriuric after one month.13 In one study of hospitalized patients, the rate of bacteriuria in catheterized patients was 51% versus 18.6% among non-catheterized patients.4

Because the diagnosis of UTI relies on clinical and laboratory findings, a positive urine culture alone is insufficient. Urine culture interpretation in hospitalized patients is complicated by concurrent illnesses, thus findings from urinalysis and/or urine microscopy can be a useful diagnostic aid. In a study of outpatient women with uncomplicated UTI symptoms, the combination of negative leukocyte esterase and nitrite on urinalysis had a negative predictive value of 98.3% for bacteriuria of ≥105 colony forming units (CFU)/mL.5 In another study of inpatients and outpatients, the same combination had a 100% negative predictive value for bacteriuria of ≥105 CFU/mL.6

Guidelines support using urinalysis and/or urine microscopy to help differentiate UTI from asymptomatic bacteriuria.1;7 However, data on the use of these tests in inpatients are limited. Most studies have been performed either among outpatients or catheterized inpatients, populations that differ significantly from the general inpatient population.814 Our objective in this study is to describe the frequency of urine cultures performed in inpatients without additional testing for pyuria by urinalysis or urine microscopy.

Methods

Study Design and Participants

We conducted a retrospective, cohort study at Barnes-Jewish Hospital (BJH), a 1250-bed academic hospital in St. Louis, Missouri. The study cohort comprised patients who had at least one urine culture performed during admission. Patients were selected from four general medical wards, two surgical wards, the medical intensive care unit (MICU), and the surgical intensive care unit (SICU). We included patients admitted to the medical or surgical wards between January 2008 and December 2013, or to the MICU or SICU between January 2012 and December 2013.

Data Collection

We abstracted urine diagnostic data from the BJH electronic medical informatics database, including culture collection date, location (the unit on which the culture was obtained), culture result, and specimen type (clean catch versus catheterized), as well as any urinalysis and urine microscopy with test date, location and results. For cultures with accompanying urinalysis or microscopy, the difference in calendar days between the culture and urinalysis and/or microscopy was calculated. The presence of a urinary catheter at the time of culture was identified based on specimen type per the hospital’s computerized provider order entry (CPOE) system.

Patient data abstracted from the medical informatics database included demographic data and length of stay. Admission-associated comorbidities and genito-urologic procedures were identified by abstracted International Classification of Diseases 9th Revision Clinical Modification (ICD-9-CM) codes (Supplementary Table).

Outcomes and Definitions

The primary study outcome was the proportion of urine cultures obtained as isolated cultures. We defined an isolated urine culture as a one without an associated urinalysis and/or urine microscopy performed within one calendar day before or after the culture. The secondary outcome was the proportion of catheter-associated urinary tract infections (CAUTIs) identified among ICU patients with isolated urine cultures.

The first urine culture obtained from the patient during the hospital admission was termed the “initial” culture. Urine cultures performed after the first culture of an admission were “subsequent” cultures. A positive culture was defined as any bacterial or fungal growth as per routine hospital laboratory protocols. The primary analysis included both initial and subsequent cultures.

CAUTI surveillance was conducted by the hospital’s infection prevention department and was initiated in BJH ICUs in January 2012. CAUTI was defined per National Healthcare Safety Network definitions.15;16

Statistical analysis

Data were analyzed using SAS version 9.3 (SAS Institute, Cary, NC). Descriptive statistics described the proportion of isolated urine cultures in patient subgroups. For categorical variables, between-group differences were analyzed using χ2 or univariable logistic regression where appropriate. For continuous variables, differences were assessed using Student t-test and Wilcoxon signed rank test.

To determine independent risk factors associated with performance of isolated urine cultures, we conducted a per-patient analysis. We categorized patients based on their initial culture of the admission to limit bias from over-representation of patients with multiple urine cultures. Forward, stepwise, multivariable logistic regression analysis was used to identify risk factors for isolated culture. A p ≤0.15 was used to allow variable entrance into the model, with p ≤0.05 required to remain in the final model.

We determined the proportion of CAUTIs identified by an isolated urine culture within the MICU and SICU. For the CAUTI assessment, we again only used the initial culture of the admission to avoid bias from over-representation.

Values of p <0.05 were considered statistically significant for all tests. This study was approved by the Washington University Human Research Protection Office.

Results

11,826 admissions met inclusion criteria. Six admissions were excluded due to incomplete data. 14,743 cultures (11,820 initial and 2923 subsequent cultures) performed during 11,820 admissions were analyzed (range, 1–12 cultures per admission) (Figure 1).

Figure 1. Summary of urine cultures performed in the study units.

Figure 1.

Subsequent cultures were more likely to come from patients with urinary catheters as compared to initial cultures (27.1% versus 12.2%, p<0.001). 6452 urine cultures (43.8%) were positive for microbial growth, with initial cultures more likely to be positive versus subsequent cultures (44.4% versus 41.2%, p=0.002).

The overall urine culture rate was 63.5 cultures/1000 patient-days. The MICU had the greatest frequency of urine cultures (133.5/1000 patient-days), followed by the medical wards (63.5/1000 patient-days), SICU (53.8/1000 patient-days), and surgical wards (53.6/1000 patient-days). ICUs had a higher incidence of urine cultures compared to non-ICU units (85.7 versus 58.8/1000 patient-days; p<0.001), as did medical versus surgical units (63.5 versus 53.6/1000 patient-days; p<0.001).

2973 urine cultures (20.2%) were isolated cultures, (i.e., sent without urinalysis and/or urine microscopy), for a rate of 12.8 isolated cultures/1000 patient-days (Table 1). Isolated cultures were most common in the SICU (37.9% of urine cultures obtained), followed by the MICU (32.9%), surgical wards (18.9%), and medical wards (15.9%). Subsequent cultures were more likely to be isolated cultures compared to initial cultures (28.2% versus 18.2%, p<0.001). In catheterized patients, 878 cultures (39.3%) were isolated, and 30 cultures (25.6 %) in patients with genito-urologic procedures were isolated. 1050 isolated cultures (35.3%) were positive for microbial growth.

Table 1.

Characteristics of 14,743 urine cultures obtained from patients on study units

Variable Total cultures n=14743 Urine cultures with urinalysis and/or microscopy n=11770 Isolated urine culturesa n = 2973 p
n (% of column) n (% of column) n (% of column)
Male 6829 (46.3) 5300 (45.0) 1529 (51.4) <0.001
Age in years, mean ± standard deviation 60 ± 18.4 60 ± 0.2 57 ± 0.3 <0.001
Race
 Caucasian 8812 (59.8) 6876 (58.4) 1936 (65.1) <0.001
 Other 5931 (40.2) 4894 (41.6) 1037 (34.9) <0.001
Congestive heart failure 1098 (7.4) 892 (7.6) 206 (6.9) 0.23
Chronic obstructive pulmonary disease 1641 (11.1) 1342 (11.4) 299 (10.1) 0.04
Malignancy 1174 (8.0) 898 (7.6) 276 (9.3) 0.003
HIV infection 165 (1.1) 129 (1.1) 36 (1.2) 0.60
Diabetes mellitus 2991 (20.3) 2483 (21.1) 508 (17.1) <0.001
Cirrhosis 581 (3.9) 417 (3.5) 164 (5.5) <0.001
End-stage renal disease 678 (4.6) 571 (4.9) 107 (3.6) 0.004
Urinary catheterization 2234 (15.2) 1356 (11.5) 878 (29.5) <0.001
Genito-urologic procedureb 117 (0.8) 87 (0.7) 30 (1.0) 0.14
Positive urine culturec 6450 (43.7) 5400 (45.9) 1050 (35.3) <0.001
Service
 Medicine 8220 (55.8) 6914 (58.7) 1306 (43.9) Reference
 Surgery 3782 (25.7) 3068 (26.1) 714 (24.0) <0.001
 Medical ICU 1710 (11.6) 1148 (9.8) 562 (18.9) <0.001
 Surgical ICU 1031 (7.0) 640 (5.4) 391 (13.2) <0.001
Days from Admission to Culture
 Same day 5798 (39.3) 5136 (43.6) 662 (22.3) Reference
 Within 1–7 days 7022 (47.6) 5394 (45.8) 1628 (54.8) <0.001
 >7 days 1923 (13.0) 1240 (10.5) 683 (23.0) <0.001

Note: HIV, Human Immunodeficiency Virus; ICU, intensive care unit

a

Cultures without associated urinalysis or urine microscopy performed within one calendar day of the culture

b

As defined by the National Healthcare Safety Network,15;16 based on ICD-9-CM procedure codes; Includes kidney and prostate procedures, and vaginal hysterectomy

c

Culture positive for bacterial or fungal growth

2150 (18.2%) initial urine cultures of each admission were isolated (Table 2). Factors independently associated with isolated initial urine culture include male sex, Caucasian race, ICU admission, urinary catheterization, and culture sent ≥1 calendar day after admission. Older age and diabetes mellitus conferred a lower risk of isolated urine cultures being obtained. A sensitivity analysis performed to re-define isolated urine cultures as those without a urinalysis and/or microscopy sent within 2 calendar days versus 1 calendar day found only a small decline in the proportion of isolated cultures [1984 (16.8%) versus 2150 (18.2%)]. We also compared patients who had only isolated cultures obtained during their admission to those having at least one culture sent with accompanying urinalysis or microscopy, with no significant change in our findings (data not shown).

Table 2.

Comparison of patient risk factors for isolated initial urine cultures

Variable Initial urine culture with urinalysis and/or microscopy n=9670 Isolated initial urine culturesa n=2150 p Multivariable analysisb
n (% of column) n (% of column) Adjusted odds ratio (95% CI) p
Male Sex 4338 (44.9) 1113 (51.8) <0.001 1.22 (1.11, 1.35) <0.001
Caucasian racec 5606 (58.0) 1410 (65.6) <0.001 1.22 (1.10, 1.35) <0.001
Age in years, mean ± standard deviation 60 ± 18.5 57 ± 18.4 <0.001 0.990 (0.987, 0.992) <0.001
CHF 746 (7.7) 139 (6.5) 0.05
COPD 1133 (11.7) 220 (10.2) 0.05
Malignancy 764 (7.9) 199 (9.3) 0.04
HIV 111 (1.1) 28 (1.3) 0.55
Diabetes mellitus 2057 (21.3) 374 (17.4) <0.001 0.87 (0.77, 0.99) 0.03
Cirrhosis 328 (3.4) 102 (4.7) 0.003
ESRD 476 (4.9) 94 (4.4) 0.28
Urinary catheterization 921 (9.5) 520 (24.2) <0.001 2.15 (1.89, 2.46) <0.001
Genito-urologic procedured 62 (0.6) 24 (1.1) 0.02
Positive urine culturee 4512 (46.7) 735 (34.2) <0.001 NA NA
Service
 Medicine 5845 (60.4) 984 (45.8) Reference Reference NA
 Surgery 2576 (26.6) 585 (27.2) <0.001 1.10 (0.98, 1.24) 0.15
 MICU 787 (8.2) 327 (15.2) <0.001 1.72 (1.47, 2.00) <0.001
 SICU 462 (4.8) 254 (11.8) <0.001 1.82 (1.51, 2.19) <0.001
ICU Admission 1249 (12.9) 581 (27.0) <0.001 NA NA
Days from Admission to Culture
  Same day 4850 (50.1) 636 (29.6) Reference Reference NA
  1–7 days 4247 (43.9) 1210 (56.3) <0.001 1.91 (1.71, 2.12) 0.02
  >7 days 573 (5.9) 304 (14.1) <0.001 2.81 (2.37, 3.34) <0.001

Note: CHF, congestive heart failure; CI, confidence interval; COPD, chronic obstructive pulmonary disease; ESRD, end-stage renal disease; HIV, Human Immunodeficiency Virus; ICU, intensive care unit; MICU, medical intensive care unit; NA, not applicable; SICU, surgical intensive care unit

a

Isolated cultures were defined as cultures without associated urinalysis or urine microscopy performed within one calendar day of the culture. Initial cultures were defined as the first culture drawn in a given admission.

b

Variables with a significance of ≤0.15 were considered for entry into the model, with a significance level of ≤0.05 required to stay in the model. The variables “Positive urine culture” and “ICU admission” were not used in constructing the model. All other variables without adjusted odds ratios reported were not included in the final model. See methods for full description.

c

Other races, as number (%) of total initial urine cultures: 3982 (33.7%) Black, 695 (5.9%) other unspecified, 104 (0.9%) Asian, 17 (0.1%) Native American, 4 Hispanic, 1 Pacific Islander, 1 Alaskan Native

d

As defined by the National Healthcare Safety Network,15;16 based on ICD-9-CM procedure codes. Includes kidney and prostate procedures, and vaginal hysterectomy.

e

Culture positive for bacterial or fungal growth

Sixty-one CAUTIs were identified in the ICUs during the study period, representing 2.2% of all ICU cultures performed. The SICU had significantly more CAUTIs identified per culture than the MICU (37/1031 versus 24/1710, p=0.002). Thirty-one (50.8%) of 61 CAUTIs identified by infection prevention surveillance were based upon an isolated culture. There was no difference between the MICU and SICU in the proportion of isolated urine cultures identified as CAUTIs [14/562 (2.5%) versus 17/391 (4.3%), p=0.112].

Discussion

Urine culturing was a frequent practice in our study units. Though the majority of urine cultures were accompanied by orders for urinalysis and/or urine microscopy, 1 in 5 cultures was sent without additional workup. Among catheterized patients, over a third of cultures were sent without an associated urinalysis or microscopy. About 50% of CAUTIs identified in the ICUs during the two-year study period were identified on the basis of an isolated culture.

Urine culture rates varied by unit type, with higher rates noted on medicine versus surgical units. The MICU had a urine culture rate more than double the composite rate. A recently published study from two Veterans Affairs hospitals reported baseline urine culture rates of 41.2 and 43.9/1000 patient-days, while a study of adult ICUs at an academic medical center in Maryland found a baseline rate of 139 cultures/1000 patient-days.17;18 These reports suggest highly variable culture rates between and within institutions.

In our study, male sex, Caucasian race, ICU admission, catheterization, and culture performed ≥1 calendar day after admission were all independent risk factors for an isolated urine culture, with the largest differences seen in the later three categories. Interventions targeted to ICUs, catheterized patients and post-admission cultures may therefore be of highest yield in decreasing isolated culture rates. Positive urine cultures were more common among initial cultures versus subsequent cultures, and in cultures sent with urinalysis and/or microscopy. Interpretation of this finding is limited by the inability to assess the clinical indications for culture. However, these data suggest a potential positive relationship between the clinical assessment of UTI and the ordering of an appropriate workup.

The odds of a culture being performed without urinalysis or microscopy may also be affected by the structure of the hospital’s CPOE system. The presentation of testing options to the provider by the CPOE system may alter ordering practices. For example, at the time of the study, the medicine service’s admission order set for non-ICU patients contained check boxes for urine microscopy and urine culture, potentially prompting providers to order both tests simultaneously. We were unable to assess specific methods of order entry in our study, such as the use of order sets or provider responses to presented order options. However, further research on provider behaviors within CPOE systems could improve the design of such interventions.

With the increasing focus on reimbursement of healthcare-acquired infections, it is concerning that half of the CAUTIs identified in study ICUs were based on an isolated urine culture. Even adjusting for catheterization status, ICU patients were at greater risk of having isolated cultures. Without chart review, we cannot comment on concordance between CAUTI surveillance definitions and clinical illness or infer how performing urinalysis or microscopy may impact CAUTI rates. We also could not directly assess providers’ rationale for ordering isolated cultures in the ICU. Given the higher proportion of ICU patients with urinary catheters and the surveillance focus on ICU CAUTIs, a better understanding of provider practices in this context is needed.

Our study was limited by the absence of chart review, preventing us from evaluating testing indications, treatment, provider characteristics (e.g., level of training), and other aspects of provider behavior. Certain cultures may have been performed for reasons other than UTI diagnosis, such as in pregnant women and in certain pre-procedure protocols. Though we attempted to limit such cultures by excluding gynecologic, obstetric, and urology wards, we were unable to assess all cultures for these indications. Additionally, comorbidities and genito-urologic procedures were identified based only on ICD-9-CM codes. CAUTI surveillance was not routine on medical and surgical floors during the study period, so CAUTI rates for these units were unavailable. We did not include data on antibiotic use and are thus unable to assess what impact a positive culture with or without urinalysis may have had on treatment. The setting of a single academic hospital also limits the generalizability of results. Strengths of our study include a large sample size and the inclusion of key clinical data, such as catheterization status and recent genito-urologic procedures. By using electronically available data, automated tracking of future interventions is feasible.

Our data suggest that interventions aimed at improving culturing practices may result in better diagnosis of inpatient UTIs. Knowledge of the variability of culturing practices across wards and patients assists in identifying those groups where interventions may be most beneficial. Further research is needed on testing practices across institutions, provider-related variables impacting urine culturing practices, and the effects of testing variability on antibiotic usage and clinical outcomes.

Supplementary Material

Supp. File 1

Acknowledgements

The authors wish to thank Dr. Carey-Ann Burnham, Dr. Jane Garbutt, and the staff of Barnes-Jewish Hospital Infection Prevention for their assistance and critical review of the manuscript. They also thank the staff of Barnes-Jewish Hospital Clinical Laboratories, who performed all laboratory and microbiological testing.

Financial Support. Research reported in this publication was supported by the Washington University Institute of Clinical and Translational Sciences Grant (UL1 TR000448), the Division of Infectious Diseases Institutional Training Grant (T32 AI007172–35) (ALC), and the CDC Prevention Epicenter Program (1U 54CK000162) (DKW). The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH or CDC.

Footnotes

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

Presented in part at the Society for Healthcare Epidemiology of America Spring 2015 Conference; Orlando, Florida; May 16, 2015 (Abstract #7155)

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