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Burden of influenza A (H1N1)pdm09 infection among tuberculosis patients: a prospective cohort study

BACKGROUND: Influenza and tuberculosis both cause significant morbidity and mortality worldwide. Therefore, this study aimed to estimate the burden of influenza A (H1N1)pdm09 virus infection among human tuberculosis patients and the general population. METHODS: A prospective cohort study was conduct...

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Autores principales: Umbreen, Gulshan, Rehman, Abdul, Avais, Muhammad, Jabeen, Chanda, Sadiq, Shakera, Maqsood, Rubab, Rashid, Hamad Bin, Afzal, Saira, Chaudhry, Mamoona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10413717/
https://www.ncbi.nlm.nih.gov/pubmed/37563563
http://dx.doi.org/10.1186/s12879-023-08441-3
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author Umbreen, Gulshan
Rehman, Abdul
Avais, Muhammad
Jabeen, Chanda
Sadiq, Shakera
Maqsood, Rubab
Rashid, Hamad Bin
Afzal, Saira
Chaudhry, Mamoona
author_facet Umbreen, Gulshan
Rehman, Abdul
Avais, Muhammad
Jabeen, Chanda
Sadiq, Shakera
Maqsood, Rubab
Rashid, Hamad Bin
Afzal, Saira
Chaudhry, Mamoona
author_sort Umbreen, Gulshan
collection PubMed
description BACKGROUND: Influenza and tuberculosis both cause significant morbidity and mortality worldwide. Therefore, this study aimed to estimate the burden of influenza A (H1N1)pdm09 virus infection among human tuberculosis patients and the general population. METHODS: A prospective cohort study was conducted among a cohort group (TB positive patients) as exposed and a comparison group (general population) as non-exposed. A total of 304 participants were recruited in both groups and followed for a period of 12 weeks. Of the 304 concurrently enrolled individuals, 152 were TB-positive patients (cohort group) and 152 were from the general population (comparison group).To calculate the sample size, the power of study was kept at 80% for detecting a difference at 5% alpha level assuming the 25% prevalence of respiratory viruses in cohort group compared to 12.5% in general population. An oropharyngeal swab was taken from a participant with symptoms of influenza-like illness (ILI). Samples were tested by conventional reverse transcription polymerase chain reaction (RT-PCR) for the detection of influenza A (H1N1)pdm09. All statistical analyses were conducted using R software. RESULTS: A total of 95 participants developed influenza-like illness (ILI) symptoms. Among these, 64 tested positive for influenza A(H1N1)pdm09, of which 39 were from the exposed group and 25 were from the non-exposed group. During the 12-week period of follow-up, the influenza A (H1N1)pdm09 incidence rate was 20 per 1000 people. The risk of testing positive for influenza A (H1N1)pdm09 was 1.66 times higher in the exposed group compared to the non-exposed group. The cumulative incidence indicated that 25% of the TB cohort and 16% of the comparison group were at risk of getting influenza A (H1N1)pdm09 during the 12 weeks of follow-up. CONCLUSION: Participants from the TB cohort had a higher incidence of influenza A (H1N1)pdm09 than the general population suggesting that they should be prioritized for influenza vaccination. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08441-3.
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spelling pubmed-104137172023-08-11 Burden of influenza A (H1N1)pdm09 infection among tuberculosis patients: a prospective cohort study Umbreen, Gulshan Rehman, Abdul Avais, Muhammad Jabeen, Chanda Sadiq, Shakera Maqsood, Rubab Rashid, Hamad Bin Afzal, Saira Chaudhry, Mamoona BMC Infect Dis Research BACKGROUND: Influenza and tuberculosis both cause significant morbidity and mortality worldwide. Therefore, this study aimed to estimate the burden of influenza A (H1N1)pdm09 virus infection among human tuberculosis patients and the general population. METHODS: A prospective cohort study was conducted among a cohort group (TB positive patients) as exposed and a comparison group (general population) as non-exposed. A total of 304 participants were recruited in both groups and followed for a period of 12 weeks. Of the 304 concurrently enrolled individuals, 152 were TB-positive patients (cohort group) and 152 were from the general population (comparison group).To calculate the sample size, the power of study was kept at 80% for detecting a difference at 5% alpha level assuming the 25% prevalence of respiratory viruses in cohort group compared to 12.5% in general population. An oropharyngeal swab was taken from a participant with symptoms of influenza-like illness (ILI). Samples were tested by conventional reverse transcription polymerase chain reaction (RT-PCR) for the detection of influenza A (H1N1)pdm09. All statistical analyses were conducted using R software. RESULTS: A total of 95 participants developed influenza-like illness (ILI) symptoms. Among these, 64 tested positive for influenza A(H1N1)pdm09, of which 39 were from the exposed group and 25 were from the non-exposed group. During the 12-week period of follow-up, the influenza A (H1N1)pdm09 incidence rate was 20 per 1000 people. The risk of testing positive for influenza A (H1N1)pdm09 was 1.66 times higher in the exposed group compared to the non-exposed group. The cumulative incidence indicated that 25% of the TB cohort and 16% of the comparison group were at risk of getting influenza A (H1N1)pdm09 during the 12 weeks of follow-up. CONCLUSION: Participants from the TB cohort had a higher incidence of influenza A (H1N1)pdm09 than the general population suggesting that they should be prioritized for influenza vaccination. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08441-3. BioMed Central 2023-08-10 /pmc/articles/PMC10413717/ /pubmed/37563563 http://dx.doi.org/10.1186/s12879-023-08441-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Umbreen, Gulshan
Rehman, Abdul
Avais, Muhammad
Jabeen, Chanda
Sadiq, Shakera
Maqsood, Rubab
Rashid, Hamad Bin
Afzal, Saira
Chaudhry, Mamoona
Burden of influenza A (H1N1)pdm09 infection among tuberculosis patients: a prospective cohort study
title Burden of influenza A (H1N1)pdm09 infection among tuberculosis patients: a prospective cohort study
title_full Burden of influenza A (H1N1)pdm09 infection among tuberculosis patients: a prospective cohort study
title_fullStr Burden of influenza A (H1N1)pdm09 infection among tuberculosis patients: a prospective cohort study
title_full_unstemmed Burden of influenza A (H1N1)pdm09 infection among tuberculosis patients: a prospective cohort study
title_short Burden of influenza A (H1N1)pdm09 infection among tuberculosis patients: a prospective cohort study
title_sort burden of influenza a (h1n1)pdm09 infection among tuberculosis patients: a prospective cohort study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10413717/
https://www.ncbi.nlm.nih.gov/pubmed/37563563
http://dx.doi.org/10.1186/s12879-023-08441-3
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