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Venous thromboembolic disease in adults admitted to hospital in a setting with a high burden of HIV and TB

BACKGROUND: HIV and tuberculosis (TB) independently cause an increased risk for venous thromboembolic disease (VTE): deep vein thrombosis (DVT) and/or pulmonary embolism (PE). Data from high HIV and TB burden settings describing VTE are scarce. The Wells’ DVT and PE scores are widely used but their...

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Autores principales: Moodley, P, Martinson, N A, Joyimbana, W, Otwombe, K N, Abraham, P, Motlhaoleng, K, Naidoo, V A, Variava, E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: South African Medical Association 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8573812/
https://www.ncbi.nlm.nih.gov/pubmed/34761207
http://dx.doi.org/10.7196/AJTCCM.2021.v27i3.155
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author Moodley, P
Martinson, N A
Joyimbana, W
Otwombe, K N
Abraham, P
Motlhaoleng, K
Naidoo, V A
Variava, E
author_facet Moodley, P
Martinson, N A
Joyimbana, W
Otwombe, K N
Abraham, P
Motlhaoleng, K
Naidoo, V A
Variava, E
author_sort Moodley, P
collection PubMed
description BACKGROUND: HIV and tuberculosis (TB) independently cause an increased risk for venous thromboembolic disease (VTE): deep vein thrombosis (DVT) and/or pulmonary embolism (PE). Data from high HIV and TB burden settings describing VTE are scarce. The Wells’ DVT and PE scores are widely used but their utility in these settings has not been reported on extensively. OBJECTIVES: To evaluate new onset VTE, compare clinical characteristics by HIV status, and the presence or absence of TB disease in our setting. We also calculate the Wells’ score for all patients. METHODS: A prospective cohort of adult in-patients with radiologically confirmed VTE were recruited into the study between September 2015 and May 2016. Demographics, presence of TB, HIV status, duration of treatment, CD4 count, viral load, VTE risk factors, and parameters to calculate the Wells’ score were collected. RESULTS: We recruited 100 patients. Most of the patients were HIV-infected (n=59), 39 had TB disease and 32 were HIV/TB co-infected. Most of the patients had DVT only (n=83); 11 had PE, and 6 had both DVT and PE. More than a third of patients on antiretroviral treatment (ART) (43%; n=18/42) were on treatment for <6 months. Half of the patients (51%; n=20/39) were on TB treatment for <1 month. The median (interquartile range (IQR)) DVT and PE Wells’ score in all sub-groups was 3.0 (1.0 - 4.0) and 3.0 (2.5 - 4.5), respectively. CONCLUSION: HIV/TB co-infection appears to confer a risk for VTE, especially early after initiation of ART and/or TB treatment, and therefore requires careful monitoring for VTE and early initiation of thrombo-prophylaxis.
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spelling pubmed-85738122021-11-09 Venous thromboembolic disease in adults admitted to hospital in a setting with a high burden of HIV and TB Moodley, P Martinson, N A Joyimbana, W Otwombe, K N Abraham, P Motlhaoleng, K Naidoo, V A Variava, E Afr J Thorac Crit Care Med Research BACKGROUND: HIV and tuberculosis (TB) independently cause an increased risk for venous thromboembolic disease (VTE): deep vein thrombosis (DVT) and/or pulmonary embolism (PE). Data from high HIV and TB burden settings describing VTE are scarce. The Wells’ DVT and PE scores are widely used but their utility in these settings has not been reported on extensively. OBJECTIVES: To evaluate new onset VTE, compare clinical characteristics by HIV status, and the presence or absence of TB disease in our setting. We also calculate the Wells’ score for all patients. METHODS: A prospective cohort of adult in-patients with radiologically confirmed VTE were recruited into the study between September 2015 and May 2016. Demographics, presence of TB, HIV status, duration of treatment, CD4 count, viral load, VTE risk factors, and parameters to calculate the Wells’ score were collected. RESULTS: We recruited 100 patients. Most of the patients were HIV-infected (n=59), 39 had TB disease and 32 were HIV/TB co-infected. Most of the patients had DVT only (n=83); 11 had PE, and 6 had both DVT and PE. More than a third of patients on antiretroviral treatment (ART) (43%; n=18/42) were on treatment for <6 months. Half of the patients (51%; n=20/39) were on TB treatment for <1 month. The median (interquartile range (IQR)) DVT and PE Wells’ score in all sub-groups was 3.0 (1.0 - 4.0) and 3.0 (2.5 - 4.5), respectively. CONCLUSION: HIV/TB co-infection appears to confer a risk for VTE, especially early after initiation of ART and/or TB treatment, and therefore requires careful monitoring for VTE and early initiation of thrombo-prophylaxis. South African Medical Association 2021-10-04 /pmc/articles/PMC8573812/ /pubmed/34761207 http://dx.doi.org/10.7196/AJTCCM.2021.v27i3.155 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution - NonCommercial Works License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Moodley, P
Martinson, N A
Joyimbana, W
Otwombe, K N
Abraham, P
Motlhaoleng, K
Naidoo, V A
Variava, E
Venous thromboembolic disease in adults admitted to hospital in a setting with a high burden of HIV and TB
title Venous thromboembolic disease in adults admitted to hospital in a setting with a high burden of HIV and TB
title_full Venous thromboembolic disease in adults admitted to hospital in a setting with a high burden of HIV and TB
title_fullStr Venous thromboembolic disease in adults admitted to hospital in a setting with a high burden of HIV and TB
title_full_unstemmed Venous thromboembolic disease in adults admitted to hospital in a setting with a high burden of HIV and TB
title_short Venous thromboembolic disease in adults admitted to hospital in a setting with a high burden of HIV and TB
title_sort venous thromboembolic disease in adults admitted to hospital in a setting with a high burden of hiv and tb
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8573812/
https://www.ncbi.nlm.nih.gov/pubmed/34761207
http://dx.doi.org/10.7196/AJTCCM.2021.v27i3.155
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