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Performance evaluation of point-of-care test for detection of Cryptosporidium stool antigen in children and HIV infected adults

BACKGROUND: Gastro-enteritis is associated with significant morbidity and mortality in patients with HIV/AIDS and children, and Cryptosporidium is the most important parasite implicated. To date, several commercial companies have developed simple and rapid point-of-care tests for the detection of Cr...

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Autores principales: Shimelis, Techalew, Tadesse, Endale
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4030457/
https://www.ncbi.nlm.nih.gov/pubmed/24885394
http://dx.doi.org/10.1186/1756-3305-7-227
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author Shimelis, Techalew
Tadesse, Endale
author_facet Shimelis, Techalew
Tadesse, Endale
author_sort Shimelis, Techalew
collection PubMed
description BACKGROUND: Gastro-enteritis is associated with significant morbidity and mortality in patients with HIV/AIDS and children, and Cryptosporidium is the most important parasite implicated. To date, several commercial companies have developed simple and rapid point-of-care tests for the detection of Cryptosporidium infection; however, information is scarce regarding their diagnostic significance in Ethiopia. This study aimed at evaluating the performance of a rapid diagnostic test (RDT) for the detection of Cryptosporidium stool antigen. METHODS: A hospital-based cross-sectional study was conducted in Hawassa University Hospital, southern Ethiopia from May to November 2013. Faecal samples were collected from a total of 100 children and 250 HIV infected individuals with diarrhea or CD4 T-cell count lower than 200 cells/μl. Specimens were processed using direct, formol-ether concentration and modified Ziehl-Neelsen techniques for diagnosis of Cryptosporidium and other parasites. One hundred faecal samples (50 positives for Cryptosporidium, 35 positives for other parasites and 15 negatives for any intestinal parasites) were tested using the CoproStrip™Cryptosporidium kit (Savyon Diagnostics Ltd, Israel). Test parameters were calculated using microscopy of the modified Ziehl-Neelsen stained stool smear as reference method. RESULTS: The performance of the RDT was first compared to routine microscopic analysis (examination ≤10 min). The CoproStrip™Cryptosporidium RDT correctly detected 31 of 42 positive samples and 49 of 50 negative samples (i.e., 11 false negatives and 1 false positive). Sensitivity, specificity, PPV, NPV and accuracy were calculated to be 74, 98, 97, 84 and 88%, respectively. Upon thorough microscopic analysis (examination >10 min), 8 more samples with very low oocyst density were found. However, these were missed by the kit and lower the sensitivity and NPV to 62 and 72%, respectively. No cross-reactivity was observed with any of the helminthic or other protozoan parasites including Isospora and Cyclospora species. CONCLUSION: Based on the results described herein, the CoproStrip™Cryptosporidium test could be used as an alternative to conventional microscopy especially where diagnosis of Cryptosporidium is limited due to time constraints, lack of experienced microscopists or unavailability of appropriate equipment/electricity.
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spelling pubmed-40304572014-05-23 Performance evaluation of point-of-care test for detection of Cryptosporidium stool antigen in children and HIV infected adults Shimelis, Techalew Tadesse, Endale Parasit Vectors Research BACKGROUND: Gastro-enteritis is associated with significant morbidity and mortality in patients with HIV/AIDS and children, and Cryptosporidium is the most important parasite implicated. To date, several commercial companies have developed simple and rapid point-of-care tests for the detection of Cryptosporidium infection; however, information is scarce regarding their diagnostic significance in Ethiopia. This study aimed at evaluating the performance of a rapid diagnostic test (RDT) for the detection of Cryptosporidium stool antigen. METHODS: A hospital-based cross-sectional study was conducted in Hawassa University Hospital, southern Ethiopia from May to November 2013. Faecal samples were collected from a total of 100 children and 250 HIV infected individuals with diarrhea or CD4 T-cell count lower than 200 cells/μl. Specimens were processed using direct, formol-ether concentration and modified Ziehl-Neelsen techniques for diagnosis of Cryptosporidium and other parasites. One hundred faecal samples (50 positives for Cryptosporidium, 35 positives for other parasites and 15 negatives for any intestinal parasites) were tested using the CoproStrip™Cryptosporidium kit (Savyon Diagnostics Ltd, Israel). Test parameters were calculated using microscopy of the modified Ziehl-Neelsen stained stool smear as reference method. RESULTS: The performance of the RDT was first compared to routine microscopic analysis (examination ≤10 min). The CoproStrip™Cryptosporidium RDT correctly detected 31 of 42 positive samples and 49 of 50 negative samples (i.e., 11 false negatives and 1 false positive). Sensitivity, specificity, PPV, NPV and accuracy were calculated to be 74, 98, 97, 84 and 88%, respectively. Upon thorough microscopic analysis (examination >10 min), 8 more samples with very low oocyst density were found. However, these were missed by the kit and lower the sensitivity and NPV to 62 and 72%, respectively. No cross-reactivity was observed with any of the helminthic or other protozoan parasites including Isospora and Cyclospora species. CONCLUSION: Based on the results described herein, the CoproStrip™Cryptosporidium test could be used as an alternative to conventional microscopy especially where diagnosis of Cryptosporidium is limited due to time constraints, lack of experienced microscopists or unavailability of appropriate equipment/electricity. BioMed Central 2014-05-16 /pmc/articles/PMC4030457/ /pubmed/24885394 http://dx.doi.org/10.1186/1756-3305-7-227 Text en Copyright © 2014 Shimelis and Tadesse; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Shimelis, Techalew
Tadesse, Endale
Performance evaluation of point-of-care test for detection of Cryptosporidium stool antigen in children and HIV infected adults
title Performance evaluation of point-of-care test for detection of Cryptosporidium stool antigen in children and HIV infected adults
title_full Performance evaluation of point-of-care test for detection of Cryptosporidium stool antigen in children and HIV infected adults
title_fullStr Performance evaluation of point-of-care test for detection of Cryptosporidium stool antigen in children and HIV infected adults
title_full_unstemmed Performance evaluation of point-of-care test for detection of Cryptosporidium stool antigen in children and HIV infected adults
title_short Performance evaluation of point-of-care test for detection of Cryptosporidium stool antigen in children and HIV infected adults
title_sort performance evaluation of point-of-care test for detection of cryptosporidium stool antigen in children and hiv infected adults
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4030457/
https://www.ncbi.nlm.nih.gov/pubmed/24885394
http://dx.doi.org/10.1186/1756-3305-7-227
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