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Association between route of illicit drug administration and hospitalizations for infective endocarditis

OBJECTIVE: This study examined the association between the route of drug administration and being hospitalized for infective endocarditis among 4817 treatment-seeking illicit drug users in Finland. METHODS: Cox regression models were used to examine the association between the route of drug administ...

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Autores principales: Olubamwo, Olubunmi, Onyeka, Ifeoma N, Aregbesola, Alex, Ronkainen, Kimmo, Tiihonen, Jari, Föhr, Jaana, Kauhanen, Jussi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5734445/
https://www.ncbi.nlm.nih.gov/pubmed/29276587
http://dx.doi.org/10.1177/2050312117740987
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author Olubamwo, Olubunmi
Onyeka, Ifeoma N
Aregbesola, Alex
Ronkainen, Kimmo
Tiihonen, Jari
Föhr, Jaana
Kauhanen, Jussi
author_facet Olubamwo, Olubunmi
Onyeka, Ifeoma N
Aregbesola, Alex
Ronkainen, Kimmo
Tiihonen, Jari
Föhr, Jaana
Kauhanen, Jussi
author_sort Olubamwo, Olubunmi
collection PubMed
description OBJECTIVE: This study examined the association between the route of drug administration and being hospitalized for infective endocarditis among 4817 treatment-seeking illicit drug users in Finland. METHODS: Cox regression models were used to examine the association between the route of drug administration and infective endocarditis hospitalization, adjusted for age, gender, and homelessness. Cases of infective endocarditis as a primary/main diagnosis were tracked using the 10th version of the International Classification of Disease code I33. RESULTS: In all, 47 persons had a primary diagnosis of infective endocarditis. These 47 persons contributed a total of 95 hospitalizations and their total length of hospital stay was 1393 days. There was a statistically significant difference in hospitalizations between injectors and non-injectors (Log-Rank test p = 0.018). Univariate Cox model showed that injectors had higher hazard or risk for infective endocarditis hospitalization compared to non-injectors (hazard ratio: 2.04, 95% confidence interval: 1.12–3.73, p = 0.020). After adjusting for age, gender, and homelessness in the multivariate model, the elevated hazard among injectors compared to non-injectors remained statistically significant with adjusted hazard ratio of 2.12 (95% confidence interval: 1.11–4.07, p = 0.024). CONCLUSION: The study findings suggested a need to boost harm reduction measures targeting high-risk injecting and other health behaviors among injecting drug users in order to reduce their hospitalizations for infective endocarditis.
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spelling pubmed-57344452017-12-22 Association between route of illicit drug administration and hospitalizations for infective endocarditis Olubamwo, Olubunmi Onyeka, Ifeoma N Aregbesola, Alex Ronkainen, Kimmo Tiihonen, Jari Föhr, Jaana Kauhanen, Jussi SAGE Open Med Original Article OBJECTIVE: This study examined the association between the route of drug administration and being hospitalized for infective endocarditis among 4817 treatment-seeking illicit drug users in Finland. METHODS: Cox regression models were used to examine the association between the route of drug administration and infective endocarditis hospitalization, adjusted for age, gender, and homelessness. Cases of infective endocarditis as a primary/main diagnosis were tracked using the 10th version of the International Classification of Disease code I33. RESULTS: In all, 47 persons had a primary diagnosis of infective endocarditis. These 47 persons contributed a total of 95 hospitalizations and their total length of hospital stay was 1393 days. There was a statistically significant difference in hospitalizations between injectors and non-injectors (Log-Rank test p = 0.018). Univariate Cox model showed that injectors had higher hazard or risk for infective endocarditis hospitalization compared to non-injectors (hazard ratio: 2.04, 95% confidence interval: 1.12–3.73, p = 0.020). After adjusting for age, gender, and homelessness in the multivariate model, the elevated hazard among injectors compared to non-injectors remained statistically significant with adjusted hazard ratio of 2.12 (95% confidence interval: 1.11–4.07, p = 0.024). CONCLUSION: The study findings suggested a need to boost harm reduction measures targeting high-risk injecting and other health behaviors among injecting drug users in order to reduce their hospitalizations for infective endocarditis. SAGE Publications 2017-12-15 /pmc/articles/PMC5734445/ /pubmed/29276587 http://dx.doi.org/10.1177/2050312117740987 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (http://www.creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Olubamwo, Olubunmi
Onyeka, Ifeoma N
Aregbesola, Alex
Ronkainen, Kimmo
Tiihonen, Jari
Föhr, Jaana
Kauhanen, Jussi
Association between route of illicit drug administration and hospitalizations for infective endocarditis
title Association between route of illicit drug administration and hospitalizations for infective endocarditis
title_full Association between route of illicit drug administration and hospitalizations for infective endocarditis
title_fullStr Association between route of illicit drug administration and hospitalizations for infective endocarditis
title_full_unstemmed Association between route of illicit drug administration and hospitalizations for infective endocarditis
title_short Association between route of illicit drug administration and hospitalizations for infective endocarditis
title_sort association between route of illicit drug administration and hospitalizations for infective endocarditis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5734445/
https://www.ncbi.nlm.nih.gov/pubmed/29276587
http://dx.doi.org/10.1177/2050312117740987
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