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Verbal autopsy-assigned causes of death among adults being investigated for TB in South Africa
BACKGROUND: Adults being investigated for TB in South Africa experience high mortality, yet causes of death (CoD) are not well defined. We determined CoD in this population using verbal autopsy (VA), and compared HIV- and TB-associated CoD using physician-certified verbal autopsy (PCVA) and InterVA-...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5091329/ https://www.ncbi.nlm.nih.gov/pubmed/27794093 http://dx.doi.org/10.1093/trstmh/trw058 |
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author | Maraba, Noriah Karat, Aaron S McCarthy, Kerrigan Churchyard, Gavin J Charalambous, Salome Kahn, Kathleen Grant, Alison D Chihota, Violet |
author_facet | Maraba, Noriah Karat, Aaron S McCarthy, Kerrigan Churchyard, Gavin J Charalambous, Salome Kahn, Kathleen Grant, Alison D Chihota, Violet |
author_sort | Maraba, Noriah |
collection | PubMed |
description | BACKGROUND: Adults being investigated for TB in South Africa experience high mortality, yet causes of death (CoD) are not well defined. We determined CoD in this population using verbal autopsy (VA), and compared HIV- and TB-associated CoD using physician-certified verbal autopsy (PCVA) and InterVA-4 software. METHODS: All contactable consenting caregivers of participants who died during a trial comparing Xpert MTB/RIF to smear microscopy were interviewed using the WHO VA tool. CoD were assigned using PCVA and InterVA-4. Kappa statistic (K) and concordance correlation coefficient (CCC) were calculated for comparison. RESULTS: Among 231 deaths, relatives of 137 deceased were interviewed. Of the 137 deceased 76 (55.4%) were males, median age 41 years (IQR 33–50). PCVA assigned 70 (51.1%) TB immediate CoD (44 [62.8%] pulmonary TB; 26 [37.1%] extra-pulmonary TB); 21 (15.3%) HIV/AIDS-related; and 46 (33.5%) other CoD. InterVA-4 assigned 48 (35.0%) TB deaths; 49 (35.7%) HIV/AIDS-related deaths; and 40 (29.1%) other CoD. Agreement between PCVA and InterVA-4 CoD was slight at individual level (K=0.20; 95% CI 0.10–0.30) and poor at population level (CCC 0.67; 95% CI 0.38–0.99). CONCLUSIONS: TB and HIV are leading CoD among adults being investigated for TB. PCVA and InterVA agreement at individual level was slight and poor at population level. VA methodology needs further development where TB and HIV are common. |
format | Online Article Text |
id | pubmed-5091329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50913292016-11-03 Verbal autopsy-assigned causes of death among adults being investigated for TB in South Africa Maraba, Noriah Karat, Aaron S McCarthy, Kerrigan Churchyard, Gavin J Charalambous, Salome Kahn, Kathleen Grant, Alison D Chihota, Violet Trans R Soc Trop Med Hyg Original Articles BACKGROUND: Adults being investigated for TB in South Africa experience high mortality, yet causes of death (CoD) are not well defined. We determined CoD in this population using verbal autopsy (VA), and compared HIV- and TB-associated CoD using physician-certified verbal autopsy (PCVA) and InterVA-4 software. METHODS: All contactable consenting caregivers of participants who died during a trial comparing Xpert MTB/RIF to smear microscopy were interviewed using the WHO VA tool. CoD were assigned using PCVA and InterVA-4. Kappa statistic (K) and concordance correlation coefficient (CCC) were calculated for comparison. RESULTS: Among 231 deaths, relatives of 137 deceased were interviewed. Of the 137 deceased 76 (55.4%) were males, median age 41 years (IQR 33–50). PCVA assigned 70 (51.1%) TB immediate CoD (44 [62.8%] pulmonary TB; 26 [37.1%] extra-pulmonary TB); 21 (15.3%) HIV/AIDS-related; and 46 (33.5%) other CoD. InterVA-4 assigned 48 (35.0%) TB deaths; 49 (35.7%) HIV/AIDS-related deaths; and 40 (29.1%) other CoD. Agreement between PCVA and InterVA-4 CoD was slight at individual level (K=0.20; 95% CI 0.10–0.30) and poor at population level (CCC 0.67; 95% CI 0.38–0.99). CONCLUSIONS: TB and HIV are leading CoD among adults being investigated for TB. PCVA and InterVA agreement at individual level was slight and poor at population level. VA methodology needs further development where TB and HIV are common. Oxford University Press 2016-09 2016-10-28 /pmc/articles/PMC5091329/ /pubmed/27794093 http://dx.doi.org/10.1093/trstmh/trw058 Text en © The Author 2016. Published by Oxford University Press on behalf of Royal Society of Tropical Medicine and Hygiene. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Articles Maraba, Noriah Karat, Aaron S McCarthy, Kerrigan Churchyard, Gavin J Charalambous, Salome Kahn, Kathleen Grant, Alison D Chihota, Violet Verbal autopsy-assigned causes of death among adults being investigated for TB in South Africa |
title | Verbal autopsy-assigned causes of death among adults being investigated for TB in South Africa |
title_full | Verbal autopsy-assigned causes of death among adults being investigated for TB in South Africa |
title_fullStr | Verbal autopsy-assigned causes of death among adults being investigated for TB in South Africa |
title_full_unstemmed | Verbal autopsy-assigned causes of death among adults being investigated for TB in South Africa |
title_short | Verbal autopsy-assigned causes of death among adults being investigated for TB in South Africa |
title_sort | verbal autopsy-assigned causes of death among adults being investigated for tb in south africa |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5091329/ https://www.ncbi.nlm.nih.gov/pubmed/27794093 http://dx.doi.org/10.1093/trstmh/trw058 |
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