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Diagnosing bacterial peritonitis made easy by use of leukocyte esterase dipsticks

INTRODUCTION: Spontaneous bacterial peritonitis (SBP) requires rapid diagnosis for the initiation of antibiotics. Its diagnosis is usually based on manual examination of ascitic fluid (AF) having long reporting time. AF infection is diagnosed when the fluid polymorphonuclear leukocyte (PMNL) concent...

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Autores principales: Chugh, Kiran, Agrawal, Yuthika, Goyal, Vipin, Khatri, Vinod, Kumar, Pradeep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4366826/
https://www.ncbi.nlm.nih.gov/pubmed/25810962
http://dx.doi.org/10.4103/2229-5151.152337
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author Chugh, Kiran
Agrawal, Yuthika
Goyal, Vipin
Khatri, Vinod
Kumar, Pradeep
author_facet Chugh, Kiran
Agrawal, Yuthika
Goyal, Vipin
Khatri, Vinod
Kumar, Pradeep
author_sort Chugh, Kiran
collection PubMed
description INTRODUCTION: Spontaneous bacterial peritonitis (SBP) requires rapid diagnosis for the initiation of antibiotics. Its diagnosis is usually based on manual examination of ascitic fluid (AF) having long reporting time. AF infection is diagnosed when the fluid polymorphonuclear leukocyte (PMNL) concentration ≥250 cells/mm(3). AIMS AND OBJECTIVES: Aim was to evaluate the diagnostic utility of leukocyte esterase (LE) reagent strip for rapid diagnosis of SBP in patients who underwent abdominal paracentesis and to calculate the sensitivity, specificity, positive, and negative predictive values. MATERIALS AND METHODS: The study was carried out on 103 patients with ascites. Cell count of AF as determined by colorimetric scale of Multistix 10 SG reagent strip was compared with counting chamber method (PMNL count ≥250 cells/mm(3) was considered positive). RESULTS AND OBSERVATIONS: Of the 103 patients SBP was diagnosed in 20 patients, 83 patients were negative for SBP by manual cell count. The sensitivity and specificity of the LE test for detecting neutrocytic SBP taking grade 2 as cut off were 95% and 96.4% respectively, with a positive predictive value of 86.4% and a negative predictive value of 98.8%. Diagnostic accuracy of LE test was 96.1%. DISCUSSION: There was a good correlation between the reagent strip result and PMNL count. The LE strip test is based on the esterase activity of activated granulocytes which reacts with an ester-releasing hydroxyphenylpyrrole causing a colour change in the azo dye of reagent strip. It is a very sensitive and specific method for the prompt detection of elevated PMNL count, and represents a convenient, inexpensive, simple, and bedside method for diagnosis of SBP. A negative LE test result excludes SBP with a high degree of certainty.
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spelling pubmed-43668262015-03-25 Diagnosing bacterial peritonitis made easy by use of leukocyte esterase dipsticks Chugh, Kiran Agrawal, Yuthika Goyal, Vipin Khatri, Vinod Kumar, Pradeep Int J Crit Illn Inj Sci Original Article INTRODUCTION: Spontaneous bacterial peritonitis (SBP) requires rapid diagnosis for the initiation of antibiotics. Its diagnosis is usually based on manual examination of ascitic fluid (AF) having long reporting time. AF infection is diagnosed when the fluid polymorphonuclear leukocyte (PMNL) concentration ≥250 cells/mm(3). AIMS AND OBJECTIVES: Aim was to evaluate the diagnostic utility of leukocyte esterase (LE) reagent strip for rapid diagnosis of SBP in patients who underwent abdominal paracentesis and to calculate the sensitivity, specificity, positive, and negative predictive values. MATERIALS AND METHODS: The study was carried out on 103 patients with ascites. Cell count of AF as determined by colorimetric scale of Multistix 10 SG reagent strip was compared with counting chamber method (PMNL count ≥250 cells/mm(3) was considered positive). RESULTS AND OBSERVATIONS: Of the 103 patients SBP was diagnosed in 20 patients, 83 patients were negative for SBP by manual cell count. The sensitivity and specificity of the LE test for detecting neutrocytic SBP taking grade 2 as cut off were 95% and 96.4% respectively, with a positive predictive value of 86.4% and a negative predictive value of 98.8%. Diagnostic accuracy of LE test was 96.1%. DISCUSSION: There was a good correlation between the reagent strip result and PMNL count. The LE strip test is based on the esterase activity of activated granulocytes which reacts with an ester-releasing hydroxyphenylpyrrole causing a colour change in the azo dye of reagent strip. It is a very sensitive and specific method for the prompt detection of elevated PMNL count, and represents a convenient, inexpensive, simple, and bedside method for diagnosis of SBP. A negative LE test result excludes SBP with a high degree of certainty. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4366826/ /pubmed/25810962 http://dx.doi.org/10.4103/2229-5151.152337 Text en Copyright: © International Journal of Critical Illness and Injury Science http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Chugh, Kiran
Agrawal, Yuthika
Goyal, Vipin
Khatri, Vinod
Kumar, Pradeep
Diagnosing bacterial peritonitis made easy by use of leukocyte esterase dipsticks
title Diagnosing bacterial peritonitis made easy by use of leukocyte esterase dipsticks
title_full Diagnosing bacterial peritonitis made easy by use of leukocyte esterase dipsticks
title_fullStr Diagnosing bacterial peritonitis made easy by use of leukocyte esterase dipsticks
title_full_unstemmed Diagnosing bacterial peritonitis made easy by use of leukocyte esterase dipsticks
title_short Diagnosing bacterial peritonitis made easy by use of leukocyte esterase dipsticks
title_sort diagnosing bacterial peritonitis made easy by use of leukocyte esterase dipsticks
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4366826/
https://www.ncbi.nlm.nih.gov/pubmed/25810962
http://dx.doi.org/10.4103/2229-5151.152337
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