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Comparing age and sex trends of chlamydia, gonorrhoea, hepatitis and syphilis infections in Samoa in 2012 and 2017

In Samoa, the seroprevalence rates of sexually transmitted infections other than HIV have been endemically high over the past decade, despite years of prevention programming. Odds ratio and χ(2) tests were conducted to compare the rates of positivity of chlamydia, gonorrhoea, hepatitis B and C, and...

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Autores principales: Carney, Robert, Howells, Michaela, Tanumafili, Aaone, Matalavea, Athena, Gafa, Judith, Leausa Toleafoa, Dr Take Naseri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: World Health Organization 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7485517/
https://www.ncbi.nlm.nih.gov/pubmed/32963885
http://dx.doi.org/10.5365/wpsar.2019.10.2.004
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author Carney, Robert
Howells, Michaela
Tanumafili, Aaone
Matalavea, Athena
Gafa, Judith
Leausa Toleafoa, Dr Take Naseri
author_facet Carney, Robert
Howells, Michaela
Tanumafili, Aaone
Matalavea, Athena
Gafa, Judith
Leausa Toleafoa, Dr Take Naseri
author_sort Carney, Robert
collection PubMed
description In Samoa, the seroprevalence rates of sexually transmitted infections other than HIV have been endemically high over the past decade, despite years of prevention programming. Odds ratio and χ(2) tests were conducted to compare the rates of positivity of chlamydia, gonorrhoea, hepatitis B and C, and syphilis across age groups from 2012 and 2017 surveillance data in Samoa. Young people aged 15–19 years were significantly more likely to have a chlamydia infection compared to all other age groups in both 2012 and 2017. Hepatitis B infections were more common in males and those aged 30 and above in both 2012 and 2017. Hepatitis C had no significant differences in age, but it was more common in males in 2012 and more common in females in 2017. Older age groups (aged 45 and above) were more likely to have a positive syphilis test in both 2014 and 2017 when compared to those aged 15–24 years. The results of this analysis confirm previously observed trends in Samoa for younger age groups’ prevalence of chlamydia and gonorrhoea, and for older age groups’ prevalence of hepatitis B and C. But the analysis also unexpectedly found that older age groups (aged 45 and above) are more likely to test positive for syphilis (for years 2014 and 2017). Further studies are needed to assess behavioural risk factors associated with older populations to explain the increase in risk and to design interventions suited to this demographic.
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spelling pubmed-74855172020-09-21 Comparing age and sex trends of chlamydia, gonorrhoea, hepatitis and syphilis infections in Samoa in 2012 and 2017 Carney, Robert Howells, Michaela Tanumafili, Aaone Matalavea, Athena Gafa, Judith Leausa Toleafoa, Dr Take Naseri Western Pac Surveill Response J Non Theme Issue In Samoa, the seroprevalence rates of sexually transmitted infections other than HIV have been endemically high over the past decade, despite years of prevention programming. Odds ratio and χ(2) tests were conducted to compare the rates of positivity of chlamydia, gonorrhoea, hepatitis B and C, and syphilis across age groups from 2012 and 2017 surveillance data in Samoa. Young people aged 15–19 years were significantly more likely to have a chlamydia infection compared to all other age groups in both 2012 and 2017. Hepatitis B infections were more common in males and those aged 30 and above in both 2012 and 2017. Hepatitis C had no significant differences in age, but it was more common in males in 2012 and more common in females in 2017. Older age groups (aged 45 and above) were more likely to have a positive syphilis test in both 2014 and 2017 when compared to those aged 15–24 years. The results of this analysis confirm previously observed trends in Samoa for younger age groups’ prevalence of chlamydia and gonorrhoea, and for older age groups’ prevalence of hepatitis B and C. But the analysis also unexpectedly found that older age groups (aged 45 and above) are more likely to test positive for syphilis (for years 2014 and 2017). Further studies are needed to assess behavioural risk factors associated with older populations to explain the increase in risk and to design interventions suited to this demographic. World Health Organization 2020-03-31 /pmc/articles/PMC7485517/ /pubmed/32963885 http://dx.doi.org/10.5365/wpsar.2019.10.2.004 Text en (c) 2020 The authors; licensee World Health Organization. This is an open access article distributed under the terms of the Creative Commons Attribution IGO License (http://creativecommons.org/licenses/by/3.0/igo/legalcode), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. In any reproduction of this article there should not be any suggestion that WHO or this article endorse any specific organization or products. The use of the WHO logo is not permitted. This notice should be preserved along with the article's original URL.
spellingShingle Non Theme Issue
Carney, Robert
Howells, Michaela
Tanumafili, Aaone
Matalavea, Athena
Gafa, Judith
Leausa Toleafoa, Dr Take Naseri
Comparing age and sex trends of chlamydia, gonorrhoea, hepatitis and syphilis infections in Samoa in 2012 and 2017
title Comparing age and sex trends of chlamydia, gonorrhoea, hepatitis and syphilis infections in Samoa in 2012 and 2017
title_full Comparing age and sex trends of chlamydia, gonorrhoea, hepatitis and syphilis infections in Samoa in 2012 and 2017
title_fullStr Comparing age and sex trends of chlamydia, gonorrhoea, hepatitis and syphilis infections in Samoa in 2012 and 2017
title_full_unstemmed Comparing age and sex trends of chlamydia, gonorrhoea, hepatitis and syphilis infections in Samoa in 2012 and 2017
title_short Comparing age and sex trends of chlamydia, gonorrhoea, hepatitis and syphilis infections in Samoa in 2012 and 2017
title_sort comparing age and sex trends of chlamydia, gonorrhoea, hepatitis and syphilis infections in samoa in 2012 and 2017
topic Non Theme Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7485517/
https://www.ncbi.nlm.nih.gov/pubmed/32963885
http://dx.doi.org/10.5365/wpsar.2019.10.2.004
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