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Articoli di riviste sul tema "Urine Analysis"

Autore: Grafiati

Pubblicato: 4 giugno 2021

Ultima modifica: 25 luglio 2025

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1

Starcher, Barry, and Marti Scott. "Fractionation of Urine to Allow Desmosine Analysis by Radioimmunoassay." Annals of Clinical Biochemistry: International Journal of Laboratory Medicine 29, no. 1 (1992): 72–78. http://dx.doi.org/10.1177/000456329202900111.

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The present study was designed to re-evaluate the radioimmunoassay for desmosine in urine, which is currently used as a measure of elastin metabolism. Using ion exchange chromatography, gel filtration and affinity chromatography it was shown that at least five other compounds in hydrolysates of human urine competed for desmosine in the RIA. Fractionating the urine prior to hydrolysis with acetone removed one of the major contaminants. The other contaminants could subsequently be removed by extracting the urine hydrolysate with a mixture of chloroform/ethanol (60:40). Samples from nine normal a

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2

Örd, Lenna, Toomas Marandi, Marit Märk, et al. "Evaluation of DOAC Dipstick Test for Detecting Direct Oral Anticoagulants in Urine Compared with a Clinically Relevant Plasma Threshold Concentration." Clinical and Applied Thrombosis/Hemostasis 28 (January 2022): 107602962210843. http://dx.doi.org/10.1177/10760296221084307.

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Measuring direct oral anticoagulant (DOAC) concentrations might be necessary in certain clinical situations but is not routinely performed. The DOAC Dipstick is a new rapid test for detecting DOACs in urine. The aim of this study was to evaluate the possible uses and limitations of the DOAC Dipstick and to compare visual analysis and DOASENSE Reader analysis of DOAC Dipstick pads. Plasma and urine samples were collected from 23 patients taking DOACs. DOAC concentrations in plasma and urine were measured by chromogenic substrate assays and in urine also by the DOAC Dipstick. Plasma concentratio

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3

Clark, D. R., and T. M. Hajar. "Detection and confirmation of cocaine use by chromatographic analysis for methylecgonine in urine." Clinical Chemistry 33, no. 1 (1987): 118–19. http://dx.doi.org/10.1093/clinchem/33.1.118.

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Abstract Methylecgonine is a common metabolite of cocaine in man. We prepared methylecgonine and developed thin-layer chromatographic and gas-chromatographic methods for its detection in urine. Seventy urine specimens from our drug screening laboratory were tested by our method and by EMIT. Both methods were positive for 26 urines, and both were negative for 42 urines. The other two urines were shown to contain cocaine by GC/MS, and no detectable metabolites. We thus demonstrated that detection of methylecgonine and cocaine is as sensitive a test for cocaine use as EMIT.

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4

Peelen, G. O., J. G. de Jong, and R. A. Wevers. "HPLC analysis of oligosaccharides in urine from oligosaccharidosis patients." Clinical Chemistry 40, no. 6 (1994): 914–21. http://dx.doi.org/10.1093/clinchem/40.6.914.

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Abstract Analysis of urinary oligosaccharides by thin-layer chromatography (TLC) is used as screening procedure for 10 different lysosomal diseases. We tested the usefulness of HPLC in screening, using a CarboPac PA1 column (Dionex), pulsed amperometric detection (PAD), and post-column derivatization (PCD). Patterns from six types of oligosaccharidoses were compared with normal urinary patterns and with the TLC patterns. PAD appeared to be nonspecific and therefore is applicable only to desalted urine samples. PCD was more specific and applicable to nondesalted urine samples, albeit with a low

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5

van Kuilenburg, André B. P., Henk van Lenthe, Monika Löffler, and Albert H. van Gennip. "Analysis of Pyrimidine Synthesis “de Novo” Intermediates in Urine and Dried Urine Filter- Paper Strips with HPLC–Electrospray Tandem Mass Spectrometry." Clinical Chemistry 50, no. 11 (2004): 2117–24. http://dx.doi.org/10.1373/clinchem.2004.038869.

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Abstract Background: The concentrations of the pyrimidine “de novo” metabolites and their degradation products in urine are useful indicators for the diagnosis of an inborn error of the pyrimidine de novo pathway or a urea-cycle defect. Until now, no procedure was available that allowed the analysis of all of these metabolites in a single analytical run. We describe a rapid, specific method to measure these metabolites by HPLC–tandem mass spectrometry. Methods: Urine or urine-soaked filter-paper strips were used to measure N-carbamyl-aspartate, dihydroorotate, orotate, orotidine, uridine, and

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6

Monferdini, Donna, Margaret Joinville, and William Grove. "Improving Urine Sediment Analysis." Laboratory Medicine 26, no. 10 (1995): 660–64. http://dx.doi.org/10.1093/labmed/26.10.660.

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7

SERA, K., Y. MIURA, and S. FUTATSUGAWA. "APPLICATION OF A STANDARD-FREE METHOD TO QUANTITATIVE ANALYSIS OF URINE SAMPLES." International Journal of PIXE 11, no. 03n04 (2001): 149–58. http://dx.doi.org/10.1142/s0129083501000207.

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A standard-free method of quantitative analysis, which is based on the fact that the total yield of continuous x-rays from the sample approximately corresponds to effective weight of the sample, was developed and has been applied to some typical bio-samples such as serum, whole blood, hair and untreated bone. In this work, the standard-free method was applied to untreated urine samples. This method allows us to perform sample preparation only by dropping 5 μl of urine sample onto a backing film. It requires neither a large amount of urine nor the internal standard. As the results, values of co

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8

Hamid Saad Mohmoud1, Marai. "Dipstick urine analysis screening among asymptomatic dogs of k9 units." Iraqi Journal of Veterinary Medicine 42, no. 1 (2018): 61–64. http://dx.doi.org/10.30539/011.

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9

Abeje, Abebayehu. "Urine test strip analysis, concentration range and its interpretations of the parameters." GSC Biological and Pharmaceutical Sciences 22, no. 2 (2023): 001–13. https://doi.org/10.5281/zenodo.7919313.

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Urinalysis is a simple urine analysis performed in many healthcare settings and at home that reveals important diagnostic information. Diabetes mellitus, kidney failure, renal, liver diseases, hydration, urinary tract infection, and metabolic abnormalities are among the diseases studied. Urinalysis is simple to perform using a urine test strip, but the results must be correctly interpreted. Urinalysis is a noninvasive, widely available, and reasonably priced method. A urine test strip is a paper or plastic dipstick with a chemically impregnated pad that is one of the simplest, cheapest, and mo

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Al Ayoubi, Manar, Mohammad Salman, Lucia Gambacorta, Nada El Darra, and Michele Solfrizzo. "Assessment of Dietary Exposure to Ochratoxin A in Lebanese Students and Its Urinary Biomarker Analysis." Toxins 13, no. 11 (2021): 795. http://dx.doi.org/10.3390/toxins13110795.

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The present study investigated the dietary and urinary OTA occurrence among 44 Lebanese children. Relying on HPLC-FLD analysis, OTA was found in all the urine samples and in 46.5% and 25% of the 24 h duplicate diet and dinner samples, respectively. The means of OTA levels in positive samples were 0.32 ± 0.1 ng/g in 24 h diet, 0.32 ± 0.18 ng/g in dinner and 0.022 ± 0.012 ng/mL in urines. These values corresponded to margin of exposure (MOE) means of 7907 ± 5922 (neoplastic) and 2579 ± 1932 (non-neoplastic) calculated from positive 24 h diet, while 961 ± 599 (neoplastic) and 313 ± 195 (non-neopl

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Nowrousian, M. R., D. Brandhorst, C. Sammet, et al. "Relationship between Serum Concentrations and Urinary Excretions of Monoclonal Free Light Chains (mFLC) Detectable as Bence Jones Proteins (BJP) by Immunofixation Electrophoresis (IFE) in Patients with Multiple Myeloma (MM)." Blood 106, no. 11 (2005): 5060. http://dx.doi.org/10.1182/blood.v106.11.5060.5060.

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Abstract Introduction. mFLC are important markers for the diagnosis and monitoring of MM. This study for the first time determines serum concentrations of mFLC which are required to produce renal overflow and BJP in urine detectable by IFE and evaluates the relationship between urinary excretions of mFLC and renal function. Patients and methods. 378 paired samples of serum and 24-h-urine from 82 patients were evaluated during the course of their disease. Serum FLC concentrations were measured nephelometrically using an automated immunoassay. Urine samples were tested for clonal bands using aga

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Bauer, H., M. Jarvis, E. Hoffberg, A. Hijaz, and D. Sheyn. "Urine Gene Analysis Compared to Urine Culture for Pathogen Detection." Obstetrics & Gynecology 145, no. 5S (2025): 52S. https://doi.org/10.1097/aog.0000000000005851.85.

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Degen, Gisela H., Jörg Reinders, Martin Kraft, et al. "Citrinin Exposure in Germany: Urine Biomarker Analysis in Children and Adults." Toxins 15, no. 1 (2022): 26. http://dx.doi.org/10.3390/toxins15010026.

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Citrinin (CIT), a mycotoxin known to exert nephrotoxicity, is a contaminant in food and feed. Since CIT contamination is not regularly analyzed, data on its occurrence and especially levels in food commodities are insufficient for conducting a conventional exposure assessment. Yet, human biomonitoring, i.e., an analysis of CIT and its metabolite dihydrocitrinone (DH-CIT) in urine samples allows to estimate exposure. This study investigated CIT exposure in young (2–14 years) and adult (24–61 years) residents of three federal states in Germany. A total of 179 urine samples from children and 142

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14

Dr, Mahmood Ahmad Zahid Dr Muhammad Ufeen Akram Dr Muzzamal Hussain. "ANALYSIS OF SPOT URINE PROTEIN TO CREATININE RATIO AS AN INDICATOR OF 24-HOUR URINARY PROTEIN EXCRETION IN NEPHROTIC SYNDROME." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES o6, no. 04 (2019): 7432–38. https://doi.org/10.5281/zenodo.2636654.

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<strong><em>Introduction: </em></strong><em>Analysis of urine protein plays an important role in the evaluation of patients with suffering from renal disease. Analysis of 24h urine gathering was for quite a while the strategy for decision for measuring proteinuria however is never again suggested on the grounds of burden and imprecision because of human blunder in accumulation. </em> <strong><em>Aims and objectives: </em></strong><em>The basic aim of the study is to analyze spot urine protein vs creatinine ratio as a predictor of 24hr urinary protein excretion in nephrotic syndrome. </em> <str

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Moreno, Ana María Jiménez, and María José Navas Sánchez. "Luminol Chemiluminescence in Urine Analysis." Applied Spectroscopy Reviews 41, no. 6 (2006): 549–74. http://dx.doi.org/10.1080/05704920600899980.

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16

Lin, Chun-Che, Chin-Chung Tseng, Tsung-Kai Chuang, Der-Seang Lee, and Gwo-Bin Lee. "Urine analysis in microfluidic devices." Analyst 136, no. 13 (2011): 2669. http://dx.doi.org/10.1039/c1an15029d.

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17

Jandke, Joachim, and Gerhard Spiteller. "Dipeptide analysis in human urine." Journal of Chromatography B: Biomedical Sciences and Applications 382 (January 1986): 39–45. http://dx.doi.org/10.1016/s0378-4347(00)83502-1.

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18

Carey, John L. "Urine protein analysis: An overview." Clinical Immunology Newsletter 10, no. 7 (1990): 103–6. http://dx.doi.org/10.1016/0197-1859(90)90039-b.

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19

Naik, S., A. Mathew, and P. Chauhan. "Sigma metrics and urine analysis." Clinica Chimica Acta 558 (May 2024): 118709. http://dx.doi.org/10.1016/j.cca.2024.118709.

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Ann Pereira, Loretta, Hilda Fernandes, and Amritha Chidambaram. "Implementing the Paris System into Reclassifying Urine Cytology: A Descriptive Analysis." International Journal of Science and Research (IJSR) 10, no. 11 (2021): 399–403. https://doi.org/10.21275/art20193124.

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Mancarella, Daniela, Julia Rutsch, Lisa Erkelenz, et al. "Abstract 5039: Preanalytical workflow enabling cfDNA analysis from urine samples." Cancer Research 84, no. 6_Supplement (2024): 5039. http://dx.doi.org/10.1158/1538-7445.am2024-5039.

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Abstract Introduction: Urine has become an important source of information in the liquid biopsy field. In contrast to blood, specifications for the collection, storage, transport and processing of urine intended for molecular examination are not widely established. Preanalytical specifications were published for urine cell-free DNA (cfDNA) only recently (CEN/TS 17811:2022). In this study, we investigated post-collection changes to cfDNA profiles in urine samples and present the performance of an optimized preanalytical workflow for cfDNA analysis. Methods: Urine from apparently healthy, consen

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22

Čabarkapa, Velibor, Mirjana Đerić, and Zoran Stošić. "Testing of IQ™ 200 Automated Urine Analyzer Analytical Performances in Comparison with Manual Techniques." Journal of Medical Biochemistry 28, no. 2 (2009): 122–28. http://dx.doi.org/10.2478/v10011-009-0001-3.

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Testing of IQ™ 200 Automated Urine Analyzer Analytical Performances in Comparison with Manual Techniques Automation is necessary in laboratory systems. It enables reduction of time required for sample analysis, as well as standardization of methods. However, automation of urine control in laboratories is much less common than in hematological analyses. Not long ago, the necessary automated systems for urine analysis have also been developed. The objective of this study is a comparison of the IQ™ 200 automated system for urine analyzing with standardized manual urine analyzing techniques. Compa

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23

Ali, Nurshad, Ahsan Habib, Firoz Mahmud, Humaira Rashid Tuba, and Gisela H. Degen. "Aflatoxin M1 Analysis in Urine of Mill Workers in Bangladesh: A Pilot Study." Toxins 16, no. 1 (2024): 45. http://dx.doi.org/10.3390/toxins16010045.

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Presence of aflatoxin B1 (AFB1) in food and feed is a serious problem, especially in developing countries. Human exposure to this carcinogenic mycotoxin can occur through dietary intake, but also through inhalation or dermal contact when handling and processing AFB1-contaminated crops. A suitable biomarker of AFB1 exposure by all routes is the occurrence of its hydroxylated metabolite aflatoxin M1 (AFM1) in urine. To assess mycotoxin exposure in mill workers in Bangladesh, we analyzed AFM1 levels in urine samples of this population group who may encounter both dietary and occupational AFB1 exp

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Sreedharan, Shilpa, John A. Petros, Viraj A. Master, et al. "Aquaporin-1 Protein Levels Elevated in Fresh Urine of Renal Cell Carcinoma Patients: Potential Use for Screening and Classification of Incidental Renal Lesions." Disease Markers 2014 (2014): 1–6. http://dx.doi.org/10.1155/2014/135649.

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Introduction and Objectives. There are over 65,000 new cases of renal cell carcinoma (RCC) each year, yet there is no effective clinical screening test for RCC. A single report claimed no overlap between urine levels of aquaporin-1 (AQP1) in patients with and without RCC (Mayo Clin Proc. 85:413, 2010). Here, we used archived and fresh RCC patient urine to validate this report.Methods. Archived RCC, fresh prenephrectomy RCC, and non-RCC negative control urines were processed for Western blot analysis. Urinary creatinine concentrations were quantified by the Jaffe reaction (Nephron 16:31, 1976).

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McGrotty, Yvonne. "Getting the most from urine and sediment analysis." Companion Animal 29, no. 10 (2024): 2–7. http://dx.doi.org/10.12968/coan.2023.0052.

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Urine sediment examination is an integral part of urinalysis which is frequently overlooked as it can be time consuming and requires a functional microscope, a centrifuge and staff with both the time and expertise to perform the exam. Sediment examination allows the operator to identify crystals, casts, cells and bacteria in a urine sample. Failure to perform sediment examination promptly can lead to ageing artefacts which may negatively affect case management. Examination of the urine sediment should ideally be performed within 1–2 hours of urine collection.

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McGrotty, Yvonne. "Getting the most from urine and sediment analysis." Veterinary Nurse 15, no. 8 (2024): 326–32. http://dx.doi.org/10.12968/vetn.2024.0051.

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Urine sediment examination is an integral part of urinalysis which is frequently overlooked as it can be time consuming and requires a functional microscope, a centrifuge and staff with both the time and expertise to perform the exam. Sediment examination allows the operator to identify crystals, casts, cells and bacteria in a urine sample. Failure to perform sediment examination promptly can lead to ageing artefacts which may negatively affect case management. Examination of the urine sediment should ideally be performed within 1–2 hours of urine collection.

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Young, David C., Sandra Craft, Mary-Clare Day, Barbara Davis, Elizabeth Hartwell, and Song Tong. "Comparison of Abbott LCxChlamydia trachomatisAssay With Gen-Probe PACE2 and Culture." Infectious Diseases in Obstetrics and Gynecology 8, no. 2 (2000): 112–15. http://dx.doi.org/10.1155/s1064744900000119.

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In this study the LCx assay (a nucleic acid amplification assay) forChlamydia trachomatisin endocervical samples was compared with the Gen-Probe PACE2 assay (a nucleic acid probe assay) for endocervical samples, and with endocervical culture. In addition, the efficacy of the LCx assay was determined for midstream clean-catch urine samples because it is often necessary to obtain such a sample for routine urine culture and it is simpler to collect only a single sample without also collecting a first-void urine for LCx. Endocervical specimens from 205 patients were tested forC. trachomatisvia LCx

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Perkins, S. L., and P. M. Johnson. "Loss of porphyrins from solution during analysis: effect of sample pH and matrix on porphyrin quantification in urine by "high-performance" liquid chromatography." Clinical Chemistry 35, no. 7 (1989): 1508–12. http://dx.doi.org/10.1093/clinchem/35.7.1508.

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Abstract We report the effect of sample matrix and pH on quantification of porphyrins by HPLC with fluorimetric detection. For aqueous solutions of pH less than 2.5, HPLC peak heights of the porphyrins increased with decreasing pH, reaching a plateau at pH less than 1.0. This loss of porphyrins from solutions with pH greater than 1.0 appeared to be due to a combination of microprecipitation and aggregation effects. No such "pH effect" was observed for urine samples supplemented with mixed-porphyrin standards. Addition of trace amounts of albumin to aqueous solutions also decreased these pH-rel

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Naik, Dr Preeta. "A Study of Dipstick and Microscopic Analysis of Formed Elements in Urine." Journal of Medical Science And clinical Research 05, no. 04 (2017): 20485–88. http://dx.doi.org/10.18535/jmscr/v5i4.122.

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x, Sonu, Ruby Rani Agarwal, and Shashi Kant Tiwari. "Correlation of Urine Analysis with Mutrakriccha Types: A Modern and Ayurvedic Approach." International Journal of Science and Research (IJSR) 13, no. 10 (2024): 539–43. http://dx.doi.org/10.21275/sr241006205629.

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ZORBOZAN, Nergiz, İlker AKARKEN, and Orçun ZORBOZAN. "The performance of the urine strip test for predicting microscopic urine analysis." Turkish Bulletin of Hygiene and Experimental Biology 78, no. 1 (2021): 61–68. http://dx.doi.org/10.5505/turkhijyen.2020.98105.

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Uwamino, Yoshifumi, Mika Nagata, Wataru Aoki, et al. "Efficient automated semi-quantitative urine culture analysis via BD Urine Culture App." Diagnostic Microbiology and Infectious Disease 102, no. 1 (2022): 115567. http://dx.doi.org/10.1016/j.diagmicrobio.2021.115567.

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Shapiro, Rochel, and Eileen Yaney. "Analysis of Urinalysis and Urine Culture Methods: Preventing False Positive Urine Specimens." American Journal of Infection Control 43, no. 6 (2015): S32. http://dx.doi.org/10.1016/j.ajic.2015.04.080.

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Blijdorp, Charles J., Omar A. Z. Tutakhel, Thomas A. Hartjes, et al. "Comparing Approaches to Normalize, Quantify, and Characterize Urinary Extracellular Vesicles." Journal of the American Society of Nephrology 32, no. 5 (2021): 1210–26. http://dx.doi.org/10.1681/asn.2020081142.

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BackgroundUrinary extracellular vesicles (uEVs) are a promising source for biomarker discovery, but optimal approaches for normalization, quantification, and characterization in spot urines are unclear.MethodsUrine samples were analyzed in a water-loading study, from healthy subjects and patients with kidney disease. Urine particles were quantified in whole urine using nanoparticle tracking analysis (NTA), time-resolved fluorescence immunoassay (TR-FIA), and EVQuant, a novel method quantifying particles via gel immobilization.ResultsUrine particle and creatinine concentrations were highly corr

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Medintz, I., L. Chiriboga, L. McCurdy, and L. Kobilinsky. "DNA Analysis of Urine Stained Material." Analytical Letters 28, no. 11 (1995): 1937–45. http://dx.doi.org/10.1080/00032719508000015.

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Chard, J., M. Richardson, and S. Murphy. "Inclusion of urine analysis not justified." BMJ 347, jul10 2 (2013): f2331. http://dx.doi.org/10.1136/bmj.f2331.

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Barakat, M. Z., and M. M. El-Guindi. "Biochemical Analysis of Normal Goat Urine." Zentralblatt für Veterinärmedizin Reihe A 15, no. 1 (2010): 60–68. http://dx.doi.org/10.1111/j.1439-0442.1968.tb00416.x.

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Debrabandere, Lode, Maurits Van Boven, and Paul Daenens. "Analysis of Buprenorphine in Urine Specimens." Journal of Forensic Sciences 37, no. 1 (1992): 13214J. http://dx.doi.org/10.1520/jfs13214j.

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Lepowsky, Eric, Fariba Ghaderinezhad, Stephanie Knowlton, and Savas Tasoglu. "Paper-based assays for urine analysis." Biomicrofluidics 11, no. 5 (2017): 051501. http://dx.doi.org/10.1063/1.4996768.

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Soriano, C., J. Muñoz-Guerra, D. Carreras, C. Rodríguez, A. F. Rodríguez, and R. Cortés. "Automated analysis of drugs in urine." Journal of Chromatography B: Biomedical Sciences and Applications 687, no. 1 (1996): 183–87. http://dx.doi.org/10.1016/s0378-4347(96)00147-8.

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Wiwanitkit, Viroj, and Prapawadee Ekawong. "Urine Sample Stability for Pregnancy Analysis." Sexuality and Disability 25, no. 1 (2007): 37–39. http://dx.doi.org/10.1007/s11195-006-9031-7.

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Miyata, Hiroshi, Takashi Yamamoto, Ryogo Murata, Tomohiro Kinoshita, and Sunao Maki. "Analysis of Proteins in Unconcentrated Urine." Pediatrics International 29, no. 5 (1987): 727–36. http://dx.doi.org/10.1111/j.1442-200x.1987.tb00369.x.

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Bolann, B. J. "Urine analysis: Old and new algorithms." Scandinavian Journal of Clinical and Laboratory Investigation 65, no. 3 (2005): 177–79. http://dx.doi.org/10.1080/00365510510025737.

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Morgan, A. "Urine analysis for glucose and protein." BMJ 300, no. 6736 (1990): 1401. http://dx.doi.org/10.1136/bmj.300.6736.1401-a.

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Yudkin, J. S., R. D. Forrest, and C. Jackson. "Urine analysis for glucose and protein." BMJ 300, no. 6737 (1990): 1463–64. http://dx.doi.org/10.1136/bmj.300.6737.1463-b.

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Toren, Peter C. "Fake Urine Samples for Drug Analysis." JAMA: The Journal of the American Medical Association 259, no. 23 (1988): 3408. http://dx.doi.org/10.1001/jama.1988.03720230020016.

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Friedberg, Michael A., and Zakariya K. Shihabi. "Urine protein analysis by capillary electrophoresis." Electrophoresis 18, no. 10 (1997): 1836–41. http://dx.doi.org/10.1002/elps.1150181019.

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Premasiri, W. Ranjith, Richard H. Clarke, and M. Edward Womble. "Urine analysis by laser Raman spectroscopy." Lasers in Surgery and Medicine 28, no. 4 (2001): 330–34. http://dx.doi.org/10.1002/lsm.1058.

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Olszowy, Pawel, and Boguslaw Buszewski. "Urine sample preparation for proteomic analysis." Journal of Separation Science 37, no. 20 (2014): 2920–28. http://dx.doi.org/10.1002/jssc.201400331.

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Reddy, Kalyani Raman, and Archana M. Joshi. "Accuracy of Automated Urine Analysis versus Manual Microscopic Examination for Routine Urine Analysis – A Cross-sectional Study." Journal of the Scientific Society 52, no. 1 (2025): 38–42. https://doi.org/10.4103/jss.jss_93_24.

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Abstract (sommario):

Introduction: Urinary tract diseases are a global health concern. The gold standard for urinary tract infection diagnosis is pathogen detection in urine alongside symptoms. Manual microscopic examination of centrifuged urine is time-consuming and labor-intensive, requiring skilled interpretation. Automated urine analyzers provide better standardization, improve the certainty of measurement, and save staff time. Hence, there is a need to evaluate the concordance between automated and microscopic urine analysis in urinary tract diseases. Methodology: Five hundred urine samples received at the ce

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