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Association between oral candidiasis and low CD4+ count among HIV positive patients in Hoima Regional Referral Hospital
BACKGROUND: The aim of this study was to determine the prevalence of Human Immune Virus (HIV) related oral lesions and their association with Cluster of Differentiation 4 (CD4(+)) count among treatment naïve HIV positive patients. METHODS: This was a descriptive and analytical cross sectional study....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4280738/ https://www.ncbi.nlm.nih.gov/pubmed/25432363 http://dx.doi.org/10.1186/1472-6831-14-143 |
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author | Nanteza, Martina Tusiime, Jayne B Kalyango, Joan Kasangaki, Arabat |
author_facet | Nanteza, Martina Tusiime, Jayne B Kalyango, Joan Kasangaki, Arabat |
author_sort | Nanteza, Martina |
collection | PubMed |
description | BACKGROUND: The aim of this study was to determine the prevalence of Human Immune Virus (HIV) related oral lesions and their association with Cluster of Differentiation 4 (CD4(+)) count among treatment naïve HIV positive patients. METHODS: This was a descriptive and analytical cross sectional study. Participants were 346 treatment naïve HIV positive adult patients. These were consecutively recruited from Hoima Regional Referral hospital between March and April 2012. Data collection involved interviews, oral examinations and laboratory analysis. RESULTS: A total of 168(48.6%) participants had oral lesions. The four commonest lesions were oral candidiasis (24.9%, CI = 20.6-29.7%), melanotic hyperpigmentation (17.3%, CI = 13.7-21.7%), kaposi sarcoma (9.3%, CI = 6.6-12.8%) and Oral Hairy Leukoplakia (OHL) (5.5%, CI = 3.5-8.4%). There was significant association between oral candidiasis and immunosuppression measured as CD4+ less than 350 cells/mm(3) (OR = 2.69, CI = 1.608-4.502, p < 0.001). Oral candidiasis was the only oral lesion significantly predictive of immunosuppression (OR = 2.56, CI = 1.52-4.30, p < 0.001) with a Positive Predictive Value (PPV) of 48.2%, Negative Predictive Value (NPV) of 74.3%, 38.1% sensitivity and specificity of 81.4%. CONCLUSION: Oral candidiasis can be considered as a marker for immunesuppression, making routine oral examinations essential in the management of HIV positive patients. |
format | Online Article Text |
id | pubmed-4280738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42807382015-01-01 Association between oral candidiasis and low CD4+ count among HIV positive patients in Hoima Regional Referral Hospital Nanteza, Martina Tusiime, Jayne B Kalyango, Joan Kasangaki, Arabat BMC Oral Health Research Article BACKGROUND: The aim of this study was to determine the prevalence of Human Immune Virus (HIV) related oral lesions and their association with Cluster of Differentiation 4 (CD4(+)) count among treatment naïve HIV positive patients. METHODS: This was a descriptive and analytical cross sectional study. Participants were 346 treatment naïve HIV positive adult patients. These were consecutively recruited from Hoima Regional Referral hospital between March and April 2012. Data collection involved interviews, oral examinations and laboratory analysis. RESULTS: A total of 168(48.6%) participants had oral lesions. The four commonest lesions were oral candidiasis (24.9%, CI = 20.6-29.7%), melanotic hyperpigmentation (17.3%, CI = 13.7-21.7%), kaposi sarcoma (9.3%, CI = 6.6-12.8%) and Oral Hairy Leukoplakia (OHL) (5.5%, CI = 3.5-8.4%). There was significant association between oral candidiasis and immunosuppression measured as CD4+ less than 350 cells/mm(3) (OR = 2.69, CI = 1.608-4.502, p < 0.001). Oral candidiasis was the only oral lesion significantly predictive of immunosuppression (OR = 2.56, CI = 1.52-4.30, p < 0.001) with a Positive Predictive Value (PPV) of 48.2%, Negative Predictive Value (NPV) of 74.3%, 38.1% sensitivity and specificity of 81.4%. CONCLUSION: Oral candidiasis can be considered as a marker for immunesuppression, making routine oral examinations essential in the management of HIV positive patients. BioMed Central 2014-11-28 /pmc/articles/PMC4280738/ /pubmed/25432363 http://dx.doi.org/10.1186/1472-6831-14-143 Text en © Nanteza et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. 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 Article Nanteza, Martina Tusiime, Jayne B Kalyango, Joan Kasangaki, Arabat Association between oral candidiasis and low CD4+ count among HIV positive patients in Hoima Regional Referral Hospital |
title | Association between oral candidiasis and low CD4+ count among HIV positive patients in Hoima Regional Referral Hospital |
title_full | Association between oral candidiasis and low CD4+ count among HIV positive patients in Hoima Regional Referral Hospital |
title_fullStr | Association between oral candidiasis and low CD4+ count among HIV positive patients in Hoima Regional Referral Hospital |
title_full_unstemmed | Association between oral candidiasis and low CD4+ count among HIV positive patients in Hoima Regional Referral Hospital |
title_short | Association between oral candidiasis and low CD4+ count among HIV positive patients in Hoima Regional Referral Hospital |
title_sort | association between oral candidiasis and low cd4+ count among hiv positive patients in hoima regional referral hospital |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4280738/ https://www.ncbi.nlm.nih.gov/pubmed/25432363 http://dx.doi.org/10.1186/1472-6831-14-143 |
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