Literature DB >> 30946373

Utility of point-of-care Gram stain by physicians for urinary tract infection in children ≤36 months.

Toshifumi Yodoshi1,2,3, Masato Matsushima2, Tomohiro Taniguchi4, Saori Kinjo1.   

Abstract

Urinary tract infection (UTI) in children requires early diagnosis and treatment to prevent repeated UTI and renal scarring. This study aimed to evaluate the usefulness of the point-of-care Gram stain by physicians for suspected UTI in children at Okinawa Chubu Hospital as a rapid diagnostic test.A single-center, retrospective study was undertaken between January 2011 and December 2015. Patients aged 36 months or younger who were reviewed had suspected UTI in the emergency room or outpatient clinic. Urine culture, urinalysis, and point-of-care Gram stain were performed on a single specimen. Patients with structural or functional urological defects requiring routine catheterization were excluded. We compared the diagnostic performance among the rapid diagnostic tests (i.e., pyuria, point-of-care Gram stain, or both). Kappa statistics were used to evaluate the agreement between the results of point-of-care Gram stain and morphotypes of urine culture with the 95% CI (bias corrected bootstrap interval). We also analyzed which antibiotics were more susceptible to the bacteria of urine culture results, selected by the results of point-of-care Gram stain or empirical treatment based on the Japanese guidelines by McNemar test.Of 1594 patients reviewed in the study, 1546 were eligible according to our inclusion criteria. Using urine culture as the gold standard for UTI, the sensitivity and specificity of pyuria were 73.2% and 95.1%, whereas those of the point-of-care Gram stain were 81.4% and 98.2%, respectively. The concordance rate between the morphotypes of bacteria detected by point-of-care Gram stain and those of urine culture was 0.784 (kappa coefficient) (95% CI 0.736-0.831). Furthermore, the proportion of "susceptible" in the minimum inhibitory concentration of pathogen-targeted treatment based on the point-of-care Gram stain was higher than that of empirical therapy (exact McNemar significance probability: .0001).Our analysis suggests that the point-of-care Gram stain is a useful rapid diagnostic tool for suspected UTI in young children. Pathogen-targeted treatment based on the point-of-care Gram stain would lead to better antibiotic selection compared with empirical therapy.

Entities:  

Mesh:

Substances:

Year:  2019        PMID: 30946373      PMCID: PMC6456128          DOI: 10.1097/MD.0000000000015101

Source DB:  PubMed          Journal:  Medicine (Baltimore)        ISSN: 0025-7974            Impact factor:   1.817


Introduction

Urinary tract infection (UTI) represents one of the most significant causes of serious bacterial infection in the pediatric population.[ A delay in treatment may result in repeated UTI and scarring of the urinary tract, leading to renal failure.[ Therefore, appropriate use of antibiotics for UTI immediately after diagnosis is imperative. However, diagnosing UTI utilizing medical history or a physical examination alone is difficult because symptoms may not be specific, especially for infants and young children.[ The American Academy of Pediatrics guidelines suggests that the diagnosis of UTI should be made on the basis of quantitative urine culture results in addition to evidence of pyuria, with a threshold of 5 white blood cells per high-power field in microscopic analysis.[ In contrast, the UK's National Institute for Health and Clinical Excellence guideline[ and the Japanese Association for Infectious Disease/Japanese Society of Chemotherapy (JAID/JSC) Guide to Clinical Management of Infectious Diseases 2015[ suggests that excluding UTI is not possible, even if pyuria is not present and emphasizes urine culture as the gold standard for diagnosing UTI. Our research group previously reported that 21% of patients with UTIs did not present with pyuria at the time of diagnosis.[ Because results of urine cultures take a few days, an accurate rapid test for bed-side diagnosis of UTI can be valuable. A recent meta-analysis for rapid urine tests for UTI in children included 95 clinical studies and 95,703 children (<18 years of age), with urine culture as the gold standard test.[ Sensitivity and specificity was 91% and 96% for urine Gram stain, 74% and 86% for pyuria, 79% and 87% for leukocyte esterase test, and 49% and 98% for a nitrite test, respectively. While a urine Gram stain is useful, the guidelines do not include the results of Gram stains as part of the diagnosis of UTI[ because its utility compared to pyuria on urinalysis (UA) is still controversial.[ Nevertheless, no clinical studies have been conducted to evaluate point-of-care Gram stains performed by physicians for the diagnosis of UTI in young children. This study aimed to determine the usefulness of a point-of-care Gram stain by physicians for suspected UTI in children in a large hospital in Japan.[ The specific aims were to compare the validity of point-of-care Gram stain compared with urine cultures (gold standard test) and to evaluate the appropriateness of the antibiotic selection based on the results of the Gram stain compared with empirical therapy.

Materials and methods

Study design

This was a retrospective study of patients with suspected UTI in a single-center from January 2011 to December 2015.

Study setting

Our hospital in Okinawa, Japan is a 550-bed acute care general hospital, including 41 pediatric beds. Approximately 20,000 children visit the Emergency Department (ED) annually and nearly 1500 are hospitalized in a pediatric ward. Okinawa Chubu Hospital has a Postgraduate Medical Education Program since 1966 and is affiliated with the University of Hawaii.[ All physicians perform Gram stain tests in the ED and pediatric outpatient clinic, immediately after urine samples are obtained. They then select antibiotics based on the results of Gram staining.[ Our practice endorses catheterization of children younger than 36 months old. UA, urine culture, and point-of-care Gram stain were done on a single urine specimen obtained by catheter before administering antibiotics. The Gram stain was performed and interpreted by trained resident physicians as soon as possible after obtaining the urine samples. The technique of Gram staining was regularly instructed and evaluated by the members of infectious disease division in our facility.

Inclusion criteria and exclusion criteria

We reviewed patients 0 to 36 months of age visiting our hospital between January 2011 and December 2015 with suspected bacterial UTI and all febrile infants younger than 2 months. Because diagnosing UTI at an age younger than 2 months with a medical history or physical examination is difficult, these inclusion criteria were necessary to measure the accuracy of a rapid test for UTI in young children.[ Patients with structural or functional urological defects requiring routine catheterization were excluded from the study. Those who were not submitted either Gram stain or UA were also excluded.

Clinical management of patients

In our hospital, antibiotics for UTI were selected after point-of-care Gram stains in the ED or the pediatric outpatient clinic. The antibiotic regimen in our facility was based on Japanese[ or USA[ guidelines; the first-line therapy was based on local antibiotic-resistance patterns, updated annually by our hospital's microbiology lab.[ A second-generation cephalosporin is recommended for Gram-negative rods (Enterobacteriaceae, such as Escherichia coli, Klebsiella spp., Enterobacter spp., and Proteus mirabilis). Ampicillin and gentamicin are recommended for Gram-positive cocci (Enterococcus faecalis and Streptococcus agalactiae). First-line therapy based on the JAID/JSC[ is ampicillin and gentamicin for neonates and first to third generation cephalosporins for infants and young children.

Data collection

Medical records were reviewed in order to obtain pertinent demographics, clinical and laboratory information, all bacteria that were isolated, and the prescribed antibiotics. All point-of-care Gram stains were done by physicians.

Variable definitions

Point-of-care Gram stain, and urine culture were performed from un-centrifuged urine and UA was performed from centrifuged urine on a single urine specimen. Urine culture was considered positive if 104 colony forming unit of uropathogens were identified.[ Urine culture results were used as the gold standard of diagnosis of UTI for comparison. Urine cultures were evaluated by laboratory technicians without clinical information, pyuria on UA or Gram stain results. Pyuria was defined as positive when five leukocytes per oil immersion field were observed by using an automated urine analyzer (Aution Hybrid, Arkray, Kyoto, Japan). Point-of-care Gram stains were performed and interpreted by physicians soon after urine samples were obtained. A point-of-care Gram stain was deemed positive if white blood cells were present, and any organisms were observed. Morphotypes and the presumptive bacteria were as follows: Gram-positive cocci for E faecalis, S agalactiae, or Staphylococcus aureus and Gram-negative rods for E coli, Klebsiella spp., Enterobacter spp., P mirabilis, or Pseudomonas aeruginosa.

Statistical analysis

The median and interquartile ranges were used when data were non-normally distributed. Categorical variables were reported as percentages. To compare performance among the rapid diagnostic tests, we calculated sensitivity, specificity, positive likelihood ratio (LR), negative LR, and positive and negative predictive values (PPVs and NPVs) with the 95% confidence interval (95% CI) for each testing method (i.e., pyuria, point-of-care Gram stain, or both). Kappa statistics were used to evaluate the agreement between the results of point-of-care Gram stain and morphotypes of urine culture with the 95% CI (bias corrected bootstrap interval).[ These were calculated by bootstrap methods with options of 1000 replications and a random-number seed (1234321). We also analyzed which antibiotics were more susceptible to the bacteria of urine culture results, selected by the results of point-of-care Gram stain or empirical treatment based on the Japanese guidelines 2015[ by McNemar test. The drug susceptibility test was classified by the minimum inhibitory concentration (MIC). The MIC is the standard of the United States Clinical and Laboratory Standards Institute (CLSI; S: susceptible, I: intermediate, R: resistant). The data were analyzed with Stata software, version 14.2 (Stata Corp., College Station, TX).

Sample size calculation

According to Cantey et al,[ when a urine culture test is regarded as the gold standard for diagnosis of UTI, the sensitivity of the Gram stain is 97.3% and specificity 73.8%. Assuming that the predicted value of the sensitivity in the point-of-care Gram stain was 0.973, the expected proportion was 0.027 (= 1 − 0.973), the width of the interval was 0.05, and the confidence level was 95%, the sample size of patients with a positive urine culture needed for sensitivity calculation was 162. Additionally, assuming that the estimated value of specificity in the point-of-care Gram stain was 0.738, the expected proportion was 0.262 (= 1 − 0.738), the width of the interval was 0.05, and the confidence level was 95%, the number of negative urine cultures required was 1189. A total of 1351 people would be required. In our hospital, because 350 urine cultures are annually submitted and approximately 35 patients aged younger than 3 years with UTI are hospitalized, we set the research period as 5 years.

Ethics

The study was approved by the Institutional Review Board of Okinawa Chubu Hospital (No. 28-70), and the need for written informed consent was waived. This study was conducted in accordance with Ethical Guidelines for Medical and Health Research Involving Human Subjects in Japan. We were not required to obtain individual informed consent from the patients included in the study. We posted information on our research on the institution's website and a bulletin board at the hospital.

Results

Urine cultures of 1594 patients were processed during the study period (Fig. 1). Forty-six (2.9%) patients did not have urine cultures, UA, and/or point-of-care Gram stain from a single urine specimen. Two (0.1%) patients were excluded because of routine catheterization. Of the remaining 1546 patients, 696 (45%) were girls and the median age was 3 months (interquartile range, 1–15 months) (Table 1). Of these, 183 (12%) patients had a pathogen detected in urine culture. Among urine culture-positive patients, 63 (34%) were girls and the median age was 3 months (interquartile range, 2–11 months).
Figure 1

Flowchart for the selection of patients.

Table 1

Clinical and laboratory characteristics of this study.

Flowchart for the selection of patients. Clinical and laboratory characteristics of this study. We calculated the sensitivity, specificity, PPV, NPV, positive LR, and negative LR of pyuria on UA, point-of-care Gram stain, and combination of pyuria and point-of-care Gram stain, and positive combination of either pyuria or point-of-care Gram stain (Table 2). Urine culture was considered a gold standard test for comparison. The sensitivity and specificity of pyuria were 73.2% and 95.1% respectively, whereas the point-of-care Gram stain had a sensitivity and specificity of 81.4% and 98.2%, respectively. Furthermore, the sensitivity and specificity of combined pyuria and point-of-care Gram stain had a sensitivity and specificity of 70.0% and 99.6% respectively, while the sensitivity and specificity of either pyuria or point-of-care Gram stain had a sensitivity and specificity of 100% and 95.8%, respectively.
Table 2

Properties of rapid tests for UTI.

Properties of rapid tests for UTI. Of the 183 positive urine cultures, bacteria isolated from the urine culture were E coli, Klebsiella spp., E faecalis, P mirabilis, and multiple identified bacteria, including E faecalis (Table 3). Extended-spectrum beta-lactamases were confirmed in 12 (9.5%) cases in E coli, 2 (9.1%) cases in Klebsiella spp., and 2 (50%) cases in P mirabilis.
Table 3

Bacteria isolated from urine cultures.

Bacteria isolated from urine cultures. The kappa coefficient between the morphotypes of bacteria detected by the point-of-care Gram stain, and those detected by urine culture was 0.784 (95% CI 0.736–0.831) (Table 4). For the bacteria detected by urine culture, 87.4% of the pathogen-targeted treatments based on the point-of-care Gram stain were “susceptible” at MIC. In contrast, 79% of the empirical therapy based on the guideline was “susceptible” at MIC (exact McNemar significance probability was .0001). All cultured bacteria could be covered with antibiotics based on the point-of-care Gram stain except multidrug-resistant bacteria, such as extended-spectrum beta-lactamases.
Table 4

Concordance rate of the point-of-care gram stain and urine culture.

Concordance rate of the point-of-care gram stain and urine culture.

Discussion

We found that point-of-care Gram stain was superior to pyuria on UA as a rapid diagnostic test for UTI. Specifically, the sensitivity and positive LR were higher with Gram stain. Positive LR was 158.9 when both pyuria and the point-of-care Gram stain were positive, and sensitivity was 100% when either pyuria or the point-of-care Gram stain was positive. The agreement of bacterial morphology between the point-of-care Gram stain by physicians and results of the cultures was substantial by evaluating the kappa coefficient. Furthermore, the proportion of “susceptible” at MIC of the pathogen-targeted treatment based on the point-of-care Gram stain was higher than that of empirical therapy according to current Japanese guidelines.[ Our study shows that the point-of-care Gram stain and pyuria on UA had a very high specificity. This resulted in a higher positive LR, hence a positive test makes UTI extremely likely and that moderate sensitivity does not rule out UTI even if each test is negative. Importantly, the NPVs for UTI of Gram stain together with pyuria were 100%. Cantey et al reported that the sensitivity and specificity of the Gram stain using centrifuged urine for UTI were 97.3% and 85%, while those of pyuria were 97.5% and 74%, respectively.[ This previous report showed a much higher sensitivity than that of our study. This difference is likely because urine was not centrifuged for pyuria and Gram stain in our study. Shaw et al[ also examined the sensitivity and specificity of the Gram stain using un-centrifuged urine for UTI by laboratory technicians. They found that the sensitivity and specificity were 81% and 97%, respectively.[ Point-of-care Gram stain in our study had as high a sensitivity as that in the study by Shaw et al[ using unspun urine for the Gram stain and the gold standard of 104 uropathogens in urine culture. The Gram stain is a rapid diagnostic test for UTI, which can be carried quickly at low cost. For clean-catch, unspun urine, the presence of at least one bacteria is likely to indicate a bacterial count of ≥105 CFU/mL,[ and the absence of bacteria in several fields on a Gram stain indicates the probability of fewer than 104 bacteria/mL.[ In our study, we used point-of-care Gram stain with unspun urine, a procedure that took 5-minute. In our study physicians, not laboratory technicians, performed the Gram stain, and the kappa coefficient suggests that they were accurate in their reading. There have been no reports on the validity of the point-of-care urine Gram stain by physicians. Furthermore, we show that choice of antibiotics based on point-of-care Gram stain was better than recommended empirical therapy. In empirical therapy based on the Japanese guideline or local susceptibility patterns in Japan, the first-line drug of UTI for neonates is ampicillin plus gentamicin, and the first-line antibiotics after infancy are cephalosporins. However, cephalosporins, such as cefixime and cefotaxime, are used in most UTI cases in children living in North America.[ Except during the neonatal period, such empirical antibiotics do not cover E faecalis, which accounts for 9% to 10% of childhood infections.[ In our study, the rate of detection of E faecalis in the whole culture was 9.8%. Additionally, antibiotics that were selected based on point-of-care Gram stain were 8.4% more sensitive to culture results than those by empirical therapy based on the Japanese guidelines. These results suggest that the point-of-care Gram stain enabled selection of antibiotics that can cover E faecalis more accurately than empirical therapy. Furthermore, in our study, bacteria that were not covered by point-of-care Gram stain would not have been covered by empirical therapy. Limitations of our study include the retrospective nature of this study. It is also possible that despite clear guidelines in our hospital to do a Gram stain before sending a sample for a UA testing, in some children, the physician knew the results of a pyuria on UA before performing the Gram stain test, possibly resulting in biased reporting. In addition, we used unspun urine for testing, different than the technique used in the lab. However, we report similar sensitivity and specificity of the Gram stain as when performed by laboratory technicians.[ Finally, there may be limited applicability of this study to all patient populations. Although the recommendation of this study is that physicians perform Gram stains on urine samples, federal regulatory standards in some countries, such as the United States, may restrict physicians from carrying out urine Gram stains in non-certified settings. In conclusion, our analysis suggests that the point-of-care Gram stain is a useful rapid diagnostic tool for suspected UTI in children less than 36 months of age. Antibiotic selection based on point-of-care Gram stain is preferable compared to empirical therapy recommendations.

Acknowledgments

We would like to thank all staff members of the Okinawa Chubu Hospital who performed Gram staining to determine appropriate therapy for our patients. We also thank Professor Ran D Goldman (University of British Columbia) and Dr Thomas L. Hurt (Mary Bridge Children's Hospital) for their review of this manuscript.

Author contributions

Conceptualization: Toshifumi Yodoshi, Tomohiro Taniguchi. Data curation: Toshifumi Yodoshi, Masato Matsushima, Saori Kinjo. Formal analysis: Toshifumi Yodoshi, Masato Matsushima. Funding acquisition: Toshifumi Yodoshi. Investigation: Toshifumi Yodoshi, Masato Matsushima, Tomohiro Taniguchi, Saori Kinjo. Methodology: Toshifumi Yodoshi, Masato Matsushima, Tomohiro Taniguchi, Saori Kinjo. Project administration: Toshifumi Yodoshi. Resources: Toshifumi Yodoshi, Masato Matsushima, Tomohiro Taniguchi, Saori Kinjo. Software: Toshifumi Yodoshi, Masato Matsushima. Supervision: Masato Matsushima, Tomohiro Taniguchi, Saori Kinjo. Validation: Masato Matsushima, Tomohiro Taniguchi, Saori Kinjo. Visualization: Toshifumi Yodoshi, Masato Matsushima. Writing – original draft: Toshifumi Yodoshi. Writing – review & editing: Masato Matsushima, Tomohiro Taniguchi, Saori Kinjo. Toshifumi Yodoshi orcid: 0000-0001-7260-731X.
  20 in total

1.  Antibiotics for acute pyelonephritis in children.

Authors:  Jennifer M Walton
Journal:  Paediatr Child Health       Date:  2015-10       Impact factor: 2.253

2.  Gram staining by physicians: an invaluable practice still seen in East Asia.

Authors:  Kentaro Iwata
Journal:  Clin Infect Dis       Date:  2004-12-01       Impact factor: 9.079

3.  JAID/JSC Guidelines for Clinical Management of Infectious Disease 2015 - Urinary tract infection/male genital infection.

Authors:  Shingo Yamamoto; Kiyohito Ishikawa; Hiroshi Hayami; Tadahiro Nakamura; Isao Miyairi; Tadashi Hoshino; Masafumi Hasui; Kazushi Tanaka; Hiroshi Kiyota; Soichi Arakawa
Journal:  J Infect Chemother       Date:  2017-10-12       Impact factor: 2.211

4.  The measurement of observer agreement for categorical data.

Authors:  J R Landis; G G Koch
Journal:  Biometrics       Date:  1977-03       Impact factor: 2.571

5.  Antibiotic resistance of urinary pathogens in female general practice patients.

Authors:  Eva Hummers-Pradier; Matthias Koch; Ann Marit Ohse; Wolfgang R Heizmann; Michael M Kochen
Journal:  Scand J Infect Dis       Date:  2005

6.  Lack of clinical utility of urine gram stain for suspected urinary tract infection in pediatric patients.

Authors:  Joseph B Cantey; Claudia Gaviria-Agudelo; Erin McElvania TeKippe; Christopher D Doern
Journal:  J Clin Microbiol       Date:  2015-02-04       Impact factor: 5.948

7.  Urinary tract infection in boys.

Authors:  K A Burbige; A B Retik; A H Colodny; S B Bauer; R Lebowitz
Journal:  J Urol       Date:  1984-09       Impact factor: 7.450

Review 8.  Update on the approach of urinary tract infection in childhood.

Authors:  Ana Cristina Simões e Silva; Eduardo Araújo Oliveira
Journal:  J Pediatr (Rio J)       Date:  2015-09-07       Impact factor: 2.197

9.  Neonatal urinary tract infections: analysis of the patients and recurrences.

Authors:  Nese Karaaslan Biyikli; Harika Alpay; Eren Ozek; Ipek Akman; Hulya Bilgen
Journal:  Pediatr Int       Date:  2004-02       Impact factor: 1.524

10.  Use of urinary gram stain for detection of urinary tract infection in infants.

Authors:  G R Lockhart; W J Lewander; D M Cimini; S L Josephson; J G Linakis
Journal:  Ann Emerg Med       Date:  1995-01       Impact factor: 5.721

View more
  3 in total

Review 1.  Unmet Need of Antenatal Screening for Asymptomatic Bacteriuria: A Risk Factor for Adverse Outcomes of Pregnancy.

Authors:  Manish Gehani; Suman Kapur; Pankaj Bhardwaj; Vijayalakshmi Nag; Sudharsanam Manni Balasubramaniam; Nagamani Kammili; Sudha D Madhuri
Journal:  Indian J Community Med       Date:  2019 Jul-Sep

2.  Exploiting open source 3D printer architecture for laboratory robotics to automate high-throughput time-lapse imaging for analytical microbiology.

Authors:  Sarah H Needs; Tai The Diep; Stephanie P Bull; Anton Lindley-Decaire; Partha Ray; Alexander D Edwards
Journal:  PLoS One       Date:  2019-11-19       Impact factor: 3.240

3.  Point-of-care urine Gram stain led to narrower-spectrum antimicrobial selection for febrile urinary tract infection in adolescents and adults.

Authors:  Tomohiro Taniguchi; Sanefumi Tsuha; Soichi Shiiki; Masashi Narita
Journal:  BMC Infect Dis       Date:  2022-03-01       Impact factor: 3.090

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.