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Appropriate Time to Start Antiretroviral Therapy in HIV-infected Patients with Penicilliosis marneffei
BACKGROUND: Penicilliosis marneffei (PM) is endemic disease in many areas in Southeast Asia, South China, Hong Kong, Taiwan, and India. This disease is also the fourth most common opportunistic infection in human immunodeficiency virus (HIV)-infected patients in northern Thailand, after tuberculosis...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631984/ http://dx.doi.org/10.1093/ofid/ofx163.408 |
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author | Utkham, Thongchai Salee, Parichat Supparatpinyo, Khuanchai |
author_facet | Utkham, Thongchai Salee, Parichat Supparatpinyo, Khuanchai |
author_sort | Utkham, Thongchai |
collection | PubMed |
description | BACKGROUND: Penicilliosis marneffei (PM) is endemic disease in many areas in Southeast Asia, South China, Hong Kong, Taiwan, and India. This disease is also the fourth most common opportunistic infection in human immunodeficiency virus (HIV)-infected patients in northern Thailand, after tuberculosis, pneumocystis carinii pneumonia and cryptococcal meningitis. However, the optimal time to start antiretroviral therapy (ART) in HIV-infected patients with PM is still not clear. METHODS: This Retrospective cohort study was done by reviewing the medical records of HIV-infected patients with PM at Chiang Mai University Hospital from January 1, 2001 to October 31, 2015. Patients were allocated to early ART (<30 days of starting PM treatment) or delayed ART (>30 days of starting PM treatment) and followed until 48 weeks after starting ART. Demographic and clinical data were recorded. The primary endpoints were mortality or hospitalization rate at 24 weeks after starting ART. Prevalence of new AIDS-defining illness, relapse of PM, immune reconstitution inflammatory syndrome (IRIS) or virological failure at 24 and 48 weeks after starting ART were recorded. RESULTS: A total of 81 patients were enrolled to the study (20 patients in the early ART group and 61 patients in the delayed ART group). The median of absolute CD4 cell count at enrollment in the early vs. delayed ART group were 17.00 and 25.50 cells/mm(3), respectively (P = 0.07). There were no reports of deaths in both groups. The hospitalization rates were not statistically different between the early and delayed ART groups at 24 (10.00% vs. 8.20%; P = 0.56). The prevalence of opportunistic infections (such as CMV infection) differed between the early and delayed ART groups at 24 weeks after ART, but it was not statistically significant (0.00% vs. 13.11%; P = 0.09). There were no statistical difference of the prevalence of other opportunistic infections, relapse of PM, IRIS and virological failure at 24 and 48 weeks after ART between both groups. CONCLUSION: There were no differences in mortality, hospitalization rate, relapse of PM, IRIS, and virological failure between early and delayed ART groups. Although there was a trend for higher rate of other opportunistic infections in the delayed ART group; this was not statistically significant. Further prospective study is needed. DISCLOSURES: All authors: No reported disclosures. |
format | Online Article Text |
id | pubmed-5631984 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56319842017-11-07 Appropriate Time to Start Antiretroviral Therapy in HIV-infected Patients with Penicilliosis marneffei Utkham, Thongchai Salee, Parichat Supparatpinyo, Khuanchai Open Forum Infect Dis Abstracts BACKGROUND: Penicilliosis marneffei (PM) is endemic disease in many areas in Southeast Asia, South China, Hong Kong, Taiwan, and India. This disease is also the fourth most common opportunistic infection in human immunodeficiency virus (HIV)-infected patients in northern Thailand, after tuberculosis, pneumocystis carinii pneumonia and cryptococcal meningitis. However, the optimal time to start antiretroviral therapy (ART) in HIV-infected patients with PM is still not clear. METHODS: This Retrospective cohort study was done by reviewing the medical records of HIV-infected patients with PM at Chiang Mai University Hospital from January 1, 2001 to October 31, 2015. Patients were allocated to early ART (<30 days of starting PM treatment) or delayed ART (>30 days of starting PM treatment) and followed until 48 weeks after starting ART. Demographic and clinical data were recorded. The primary endpoints were mortality or hospitalization rate at 24 weeks after starting ART. Prevalence of new AIDS-defining illness, relapse of PM, immune reconstitution inflammatory syndrome (IRIS) or virological failure at 24 and 48 weeks after starting ART were recorded. RESULTS: A total of 81 patients were enrolled to the study (20 patients in the early ART group and 61 patients in the delayed ART group). The median of absolute CD4 cell count at enrollment in the early vs. delayed ART group were 17.00 and 25.50 cells/mm(3), respectively (P = 0.07). There were no reports of deaths in both groups. The hospitalization rates were not statistically different between the early and delayed ART groups at 24 (10.00% vs. 8.20%; P = 0.56). The prevalence of opportunistic infections (such as CMV infection) differed between the early and delayed ART groups at 24 weeks after ART, but it was not statistically significant (0.00% vs. 13.11%; P = 0.09). There were no statistical difference of the prevalence of other opportunistic infections, relapse of PM, IRIS and virological failure at 24 and 48 weeks after ART between both groups. CONCLUSION: There were no differences in mortality, hospitalization rate, relapse of PM, IRIS, and virological failure between early and delayed ART groups. Although there was a trend for higher rate of other opportunistic infections in the delayed ART group; this was not statistically significant. Further prospective study is needed. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2017-10-04 /pmc/articles/PMC5631984/ http://dx.doi.org/10.1093/ofid/ofx163.408 Text en © The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Utkham, Thongchai Salee, Parichat Supparatpinyo, Khuanchai Appropriate Time to Start Antiretroviral Therapy in HIV-infected Patients with Penicilliosis marneffei |
title | Appropriate Time to Start Antiretroviral Therapy in HIV-infected Patients with Penicilliosis marneffei |
title_full | Appropriate Time to Start Antiretroviral Therapy in HIV-infected Patients with Penicilliosis marneffei |
title_fullStr | Appropriate Time to Start Antiretroviral Therapy in HIV-infected Patients with Penicilliosis marneffei |
title_full_unstemmed | Appropriate Time to Start Antiretroviral Therapy in HIV-infected Patients with Penicilliosis marneffei |
title_short | Appropriate Time to Start Antiretroviral Therapy in HIV-infected Patients with Penicilliosis marneffei |
title_sort | appropriate time to start antiretroviral therapy in hiv-infected patients with penicilliosis marneffei |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631984/ http://dx.doi.org/10.1093/ofid/ofx163.408 |
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