ORIGINAL ARTICLE EVALUATION OF RAPID METHOD FOR THE DETECTION OF BACTERIURIA USING CONVENTIONAL CULTURE AS REFERENCE STANDARD Lakshmi N1, Maheswaran R2 HOW TO CITE THIS ARTICLE: Lakshmi N, Maheswaran R. “Evaluation Of Rapid Method For The Detection Of Bacteriuria Using Conventional Culture As Reference Standard”. Journal Of Evolution Of Medical And Dental Sciences 2013; Vol2, Issue 50, December 16; Page: 9798-9800. ABSTRACT:INTRODUCTION: A new commercially available method for detection of bacteriuria is compared to a conventional semi-quantitative bacteriology method. Screening methods are used to detect significant level of pathogenic microorganisms in urine specimens. This rapid method offers the advantages of both rapidly reporting the result as well as controlling costs1. On the basis of these findings, it is recommended to test the urine samples of all patients with suspected urinary tract infections by the rapid method and confirm and obtain the sensitivity pattern for the positive findings. Using this method we can get instant results and the patient would receive prompt appropriate treatment2.MATERIALS & METHODS: 600 mid-stream specimens of urine were tested by using Urocolor dipstick strips. Results for three infection associated markers- glucose,nitrite and pus cells were compared with the results of conventional laboratory culture & microscopy.RESULTS: Of the 600 urine samples obtained 136 were positive and 464 negative for infection associated markers whereas 166 were positive and 434 negative by culture. CONCLUSION: This study had shown that the combination of strip test for nitrite, glucose and pus cells raised the sensitivity to 97%, and among the strip negative results there is a high probability that the patient does not have UTI. INTRODUCTION:Urine is one of the most common samples submitted to the microbiology laboratory for testing. Quantitative urine culture represents the gold standard3 for the laboratory diagnosis ofurinary tract infection which is a labour-intensive, time consuming & expensive activity. Over 60% of all samples processed show no evidence of significant bacterial growth. Generation of a final negative culture report within a short time of specimen receipt is beneficial. A positive result requires urine culture and sensitivity for confirmation and treatment. Use of a rapid screen would be beneficial to the patient and the physician and reduce laboratory workload. MATERIALS & METHODS:600 mid-stream specimens of urine were received over a five month period (between 1.2.2011 and 1.7.2011) from the departments of Medicine, Surgery, Obstetrics and Gynaecology at the Kempegowda Institute of Medical Sciences and Research Hospital (KIMSH) Laboratory. Samples were also received from general practitioners of that area. These samples were tested by using the SD urocolor dipstick strips (Standard Diagnostics Inc). Urine obtained in a clean dry container was mixed well before testing. The test area of the strip was charged with fresh urine sample and removed immediately to avoid dissolving out of reagents. The strip was placed on tissue paper to remove excess urine and was kept in a horizontal position to prevent possible mixing of chemicals from adjacent test areas. The test areas were compared with Journal of Evolution of Medical and Dental Sciences/Volume 2/Issue 50/ December 16, 2013 Page 9798 ORIGINAL ARTICLE the corresponding colour chart on the bottle label and read visually at 60 seconds. The used strips were discarded. RESULTS:Out of the 600 samples 136 were positive for three infective markers, 25 were nitrate negative but glucose and pus cells positive, five were indeterminate and 434 were negative for all three infective markers. 72.3% (434/600) all specimens were strip negative for nitrite, glucose and pus cells. The positive cases were confirmed with culture. Of the 600 samples 166 were culture positive, 70 samples shows no significant bacteriuria and 63 samples shows contamination (more than three organisms). ISOLATE CULTURE GRAM BTS GLUCOSE NITRATE PUS CELLS E. coli Total [166] 28% [52] 9% [40] 76% Total [136] 22.7% [44] 85% [50] 96% [34] 65% [47] 90% Klebsiella [56] 93% [53] 5% [50] 92.5% Citrobacter [12] 2% [10] 83.3% [11] 92% [44] 85% [55] 98% [48] 86% [50] 92.5% [45] 80% [12] 105% [11] 92% [11] 92% [11] 92% [4] 100% Nil Proteus [4] 75% [2] 50% [2.6] 67% [2.6] 6% Pseudomonas [3] 5% [3] 100% [2.6] 67% [3] 100% [2] 67% 67% Staph. aureus [13] 2% [6] 46% [8] 62% [12] 92% [6] 62% CONS [9] 115% [8] 89% [6] 69% [9] 100% 67% [17] 100% [3] 8% Enterococci [17] 3% [13] 76% [12] 76% [12] 76% TOTAL 166 135 136 162 104 Comparison of conventional culture & biochemical test strip (BTS Urocolor) for significant isolates [4] 100% [3] 100% [12] 92% [9] 100% [16] 94% 147 DISCUSSION:With the present problem of constantly increasing laboratory workflow, there is a real need to economize on the time spent performing unnecessary testing3. Two- thirds of all urine specimens sent to the laboratory in this study comes from various departments, and only 28% of all the specimens received were subsequently confirmed to have significantly bacteriuria. 72.3% of all specimens were strip negative for nitrite, glucose and pus cells. The cost of the reagent strip test is approximately Rs6.50 much less than the cost of processing the specimen in the laboratory. The method is therefore cost effective with the advantages,that a negative urine sample is rapidly identified and unnecessary drug treatment is avoided with consequent cost saving. Through this method the general practitioner would have instant results thus the patient would receive immediate and appropriate treatment. Conventional culture technique requires more than 18 - 24 hours for obtaining an accurate colony count. It represents a labor-intensive, time consuming and expensive activity in which over 60% of all samples processed show no evidence of significant Journal of Evolution of Medical and Dental Sciences/Volume 2/Issue 50/ December 16, 2013 Page 9799 ORIGINAL ARTICLE bacterial growth. Negative culture report after several hours of receipt of specimen is a disadvantage of conventional culture. So a rapid report of a negative result can be decisive in improving patient management. Use of screens to detect significant levels of pathogenic micro organisms in urine specimens offers the advantages to both rapidly reporting results and controlling costs, and also beneficial to the patients, the physician and the laboratory. Nitrite, glucose, protein were all negative for clear urine. Positive test strips compared with conventional culture good correlation seen in BTS and only culture for positive strips. The aim of this study was to reduce the proportion of culture negative urines arriving in the laboratory by producing local evidence based guidelines for the use of urine dipstick testing. No special equipments are needed for screening urine samples so it can also be done in field conditions. BIBLIOGRAPHY: 1. Clinical relevance of culture versus screens for the detection of microbial pathogens in urine specimens. The American Journal of Medicine. Volume 83,Issue 4, October 1987,pages 739745. 2. Diagnostic value and cost utility analysis for urine Grams stain and urine microscopic examination as screening test for UTI. Department of laboratory medicine, Faculty of medicine, Chulalongkorn University. 1030 Bangkok, 25-10-2004. 3. Validation of a method for the rapid diagnosis of UTI suitable for use in general practice. Br J Gen - Pract- 1990. Oct: 40(339): 403-405. AUTHORS: 1. Lakshmi N. 2. Maheswaran R. PARTICULARS OF CONTRIBUTORS: 1. Associate Professor, Department of Microbiology, Sapthagiri Institute of Medical Sciences and Research Centre, Bangalore. 2. HOD & Professor, Department of Community Medicine, Sapthagiri Institute of Medical Sciences and Research Centre, Bangalore. NAME ADRRESS EMAIL ID OF THE CORRESPONDING AUTHOR: Dr. Lakshmi N. Associate Professor, Department of Microbiology, Sapthagiri Institute of Medical Sciences and Research Centre, Bangalore – 560090. Email –drlakshmi53@gmail.com Date of Submission: 11/11/2013. Date of Peer Review: 12/11/2013. Date of Acceptance: 20/11/2013. Date of Publishing: 12/12/2013 Journal of Evolution of Medical and Dental Sciences/Volume 2/Issue 50/ December 16, 2013 Page 9800