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Morbidity burden, seasonality and factors associated with the human respiratory syncytial virus, human parainfluenza virus, and human adenovirus infections in Kenya
BACKGROUND: Human respiratory syncytial viruses (HRSV), human parainfluenza viruses (HPIV), and human adenoviruses (HAdVs) cause a substantial morbidity burden globally. OBJECTIVE: We sought to estimate morbidity burden, assess seasonality, and determine factors associated with these respiratory vir...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9216343/ https://www.ncbi.nlm.nih.gov/pubmed/35757823 http://dx.doi.org/10.1016/j.ijregi.2021.10.001 |
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author | Umuhoza, Therese Oyugi, Julius Mancuso, James D. Ahmed, Anwar Bulimo, Wallace D. |
author_facet | Umuhoza, Therese Oyugi, Julius Mancuso, James D. Ahmed, Anwar Bulimo, Wallace D. |
author_sort | Umuhoza, Therese |
collection | PubMed |
description | BACKGROUND: Human respiratory syncytial viruses (HRSV), human parainfluenza viruses (HPIV), and human adenoviruses (HAdVs) cause a substantial morbidity burden globally. OBJECTIVE: We sought to estimate morbidity burden, assess seasonality, and determine factors associated with these respiratory viruses in Kenya. METHODS: The data were obtained from Kenyan sites included in the Köppen-Geiger climate classification system. We defined the proportion of morbidity burden by descriptive analysis and visualized time-series data for January 2007–December 2013. Logistic regression was used to identify factors associated with infection outcomes. RESULTS: The morbidity burden for HRSV was 3.1%, HPIV 5.3% and HAdVs 3.3%. Infants were more likely to be infected than other age groups. HRSV exhibited seasonality with high occurrence in January–March (odds ratio[OR] = 2.73) and April–June (OR = 3.01). Hot land surface temperature (≥40 °C) was associated with HRSV infections (OR = 2.75), as was warmer air temperature (19-22.9 °C) (OR = 1.68), compared with land surface temperature (<30) and cooler air temperature (<19 °C) respectively. Moderate rainfall (150-200 mm) areas had greater odds of HRSV infection (OR = 1.32) than low rainfall (<150 mm). CONCLUSION: HRSV, HPIV and HAdVs contributed to morbidity burden, and infants were significantly affected. HRSV had a clear seasonal pattern and were associated with climate parameters, unlike HPIV and HAdVs. |
format | Online Article Text |
id | pubmed-9216343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-92163432022-06-24 Morbidity burden, seasonality and factors associated with the human respiratory syncytial virus, human parainfluenza virus, and human adenovirus infections in Kenya Umuhoza, Therese Oyugi, Julius Mancuso, James D. Ahmed, Anwar Bulimo, Wallace D. IJID Reg Original Report BACKGROUND: Human respiratory syncytial viruses (HRSV), human parainfluenza viruses (HPIV), and human adenoviruses (HAdVs) cause a substantial morbidity burden globally. OBJECTIVE: We sought to estimate morbidity burden, assess seasonality, and determine factors associated with these respiratory viruses in Kenya. METHODS: The data were obtained from Kenyan sites included in the Köppen-Geiger climate classification system. We defined the proportion of morbidity burden by descriptive analysis and visualized time-series data for January 2007–December 2013. Logistic regression was used to identify factors associated with infection outcomes. RESULTS: The morbidity burden for HRSV was 3.1%, HPIV 5.3% and HAdVs 3.3%. Infants were more likely to be infected than other age groups. HRSV exhibited seasonality with high occurrence in January–March (odds ratio[OR] = 2.73) and April–June (OR = 3.01). Hot land surface temperature (≥40 °C) was associated with HRSV infections (OR = 2.75), as was warmer air temperature (19-22.9 °C) (OR = 1.68), compared with land surface temperature (<30) and cooler air temperature (<19 °C) respectively. Moderate rainfall (150-200 mm) areas had greater odds of HRSV infection (OR = 1.32) than low rainfall (<150 mm). CONCLUSION: HRSV, HPIV and HAdVs contributed to morbidity burden, and infants were significantly affected. HRSV had a clear seasonal pattern and were associated with climate parameters, unlike HPIV and HAdVs. Elsevier 2021-10-09 /pmc/articles/PMC9216343/ /pubmed/35757823 http://dx.doi.org/10.1016/j.ijregi.2021.10.001 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Report Umuhoza, Therese Oyugi, Julius Mancuso, James D. Ahmed, Anwar Bulimo, Wallace D. Morbidity burden, seasonality and factors associated with the human respiratory syncytial virus, human parainfluenza virus, and human adenovirus infections in Kenya |
title | Morbidity burden, seasonality and factors associated with the human respiratory syncytial virus, human parainfluenza virus, and human adenovirus infections in Kenya |
title_full | Morbidity burden, seasonality and factors associated with the human respiratory syncytial virus, human parainfluenza virus, and human adenovirus infections in Kenya |
title_fullStr | Morbidity burden, seasonality and factors associated with the human respiratory syncytial virus, human parainfluenza virus, and human adenovirus infections in Kenya |
title_full_unstemmed | Morbidity burden, seasonality and factors associated with the human respiratory syncytial virus, human parainfluenza virus, and human adenovirus infections in Kenya |
title_short | Morbidity burden, seasonality and factors associated with the human respiratory syncytial virus, human parainfluenza virus, and human adenovirus infections in Kenya |
title_sort | morbidity burden, seasonality and factors associated with the human respiratory syncytial virus, human parainfluenza virus, and human adenovirus infections in kenya |
topic | Original Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9216343/ https://www.ncbi.nlm.nih.gov/pubmed/35757823 http://dx.doi.org/10.1016/j.ijregi.2021.10.001 |
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