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Contributions to early HIV diagnosis among patients linked to care vary by testing venue
OBJECTIVE: Early HIV diagnosis reduces transmission and improves health outcomes; screening in non-traditional settings is increasingly advocated. We compared test venues by the number of new diagnoses successfully linked to the regional HIV treatment center and disease stage at diagnosis. METHODS:...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2443802/ https://www.ncbi.nlm.nih.gov/pubmed/18578881 http://dx.doi.org/10.1186/1471-2458-8-220 |
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author | Lyons, Michael S Lindsell, Christopher J RN, DeAnna A Hawkins RN, Dana L Raab Trott, Alexander T Fichtenbaum, Carl J |
author_facet | Lyons, Michael S Lindsell, Christopher J RN, DeAnna A Hawkins RN, Dana L Raab Trott, Alexander T Fichtenbaum, Carl J |
author_sort | Lyons, Michael S |
collection | PubMed |
description | OBJECTIVE: Early HIV diagnosis reduces transmission and improves health outcomes; screening in non-traditional settings is increasingly advocated. We compared test venues by the number of new diagnoses successfully linked to the regional HIV treatment center and disease stage at diagnosis. METHODS: We conducted a retrospective cohort study using structured chart review of newly diagnosed HIV patients successfully referred to the region's only HIV treatment center from 1998 to 2003. Demographics, testing indication, risk profile, and initial CD4 count were recorded. RESULTS: There were 277 newly diagnosed patients meeting study criteria. Mean age was 33 years, 77% were male, and 46% were African-American. Median CD4 at diagnosis was 324. Diagnoses were earlier via partner testing at the HIV treatment center (N = 8, median CD4 648, p = 0.008) and with universal screening by the blood bank, military, and insurance companies (N = 13, median CD4 483, p = 0.05) than at other venues. Targeted testing by health care and public health entities based on patient request, risk profile, or patient condition lead to later diagnosis. CONCLUSION: Test venues varied by the number of new diagnoses made and the stage of illness at diagnosis. To improve the rate of early diagnosis, scarce resources should be allocated to maximize the number of new diagnoses at screening venues where diagnoses are more likely to be early or alter testing strategies at test venues where diagnoses are traditionally made late. Efforts to improve early diagnosis should be coordinated longitudinally on a regional basis according to this conceptual paradigm. |
format | Text |
id | pubmed-2443802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-24438022008-07-08 Contributions to early HIV diagnosis among patients linked to care vary by testing venue Lyons, Michael S Lindsell, Christopher J RN, DeAnna A Hawkins RN, Dana L Raab Trott, Alexander T Fichtenbaum, Carl J BMC Public Health Research Article OBJECTIVE: Early HIV diagnosis reduces transmission and improves health outcomes; screening in non-traditional settings is increasingly advocated. We compared test venues by the number of new diagnoses successfully linked to the regional HIV treatment center and disease stage at diagnosis. METHODS: We conducted a retrospective cohort study using structured chart review of newly diagnosed HIV patients successfully referred to the region's only HIV treatment center from 1998 to 2003. Demographics, testing indication, risk profile, and initial CD4 count were recorded. RESULTS: There were 277 newly diagnosed patients meeting study criteria. Mean age was 33 years, 77% were male, and 46% were African-American. Median CD4 at diagnosis was 324. Diagnoses were earlier via partner testing at the HIV treatment center (N = 8, median CD4 648, p = 0.008) and with universal screening by the blood bank, military, and insurance companies (N = 13, median CD4 483, p = 0.05) than at other venues. Targeted testing by health care and public health entities based on patient request, risk profile, or patient condition lead to later diagnosis. CONCLUSION: Test venues varied by the number of new diagnoses made and the stage of illness at diagnosis. To improve the rate of early diagnosis, scarce resources should be allocated to maximize the number of new diagnoses at screening venues where diagnoses are more likely to be early or alter testing strategies at test venues where diagnoses are traditionally made late. Efforts to improve early diagnosis should be coordinated longitudinally on a regional basis according to this conceptual paradigm. BioMed Central 2008-06-25 /pmc/articles/PMC2443802/ /pubmed/18578881 http://dx.doi.org/10.1186/1471-2458-8-220 Text en Copyright © 2008 Lyons et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Lyons, Michael S Lindsell, Christopher J RN, DeAnna A Hawkins RN, Dana L Raab Trott, Alexander T Fichtenbaum, Carl J Contributions to early HIV diagnosis among patients linked to care vary by testing venue |
title | Contributions to early HIV diagnosis among patients linked to care vary by testing venue |
title_full | Contributions to early HIV diagnosis among patients linked to care vary by testing venue |
title_fullStr | Contributions to early HIV diagnosis among patients linked to care vary by testing venue |
title_full_unstemmed | Contributions to early HIV diagnosis among patients linked to care vary by testing venue |
title_short | Contributions to early HIV diagnosis among patients linked to care vary by testing venue |
title_sort | contributions to early hiv diagnosis among patients linked to care vary by testing venue |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2443802/ https://www.ncbi.nlm.nih.gov/pubmed/18578881 http://dx.doi.org/10.1186/1471-2458-8-220 |
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