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Risk of long-term infection-related death in clinical osteoporotic vertebral fractures: A hospital-based analysis

BACKGROUND: Osteoporotic vertebral fractures adversely impact quality of life and also increase the risk of infection and mortality. Alendronate treatment increases bone mass and reduces the risk of fractures in patients with osteoporosis by suppressing bone resorption. We investigated the relations...

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Autores principales: Chen, Ying-Chou, Lin, Wei-Che
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5549923/
https://www.ncbi.nlm.nih.gov/pubmed/28793342
http://dx.doi.org/10.1371/journal.pone.0182614
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author Chen, Ying-Chou
Lin, Wei-Che
author_facet Chen, Ying-Chou
Lin, Wei-Che
author_sort Chen, Ying-Chou
collection PubMed
description BACKGROUND: Osteoporotic vertebral fractures adversely impact quality of life and also increase the risk of infection and mortality. Alendronate treatment increases bone mass and reduces the risk of fractures in patients with osteoporosis by suppressing bone resorption. We investigated the relationship between alendronate treatment and infection-related death in patients with osteoporotic vertebral fractures. METHODS: We retrospectively reviewed patients with osteoporosis and vertebral fractures from January 2001 to December 2007. The use of alendronate, glucocorticoid and medical factors including smoking, alcohol consumption, diabetes, hypertension, stroke, liver disease, heart disease, and pulmonary disease were analyzed. Cox regression was used to analyze the factors associated with life-threatening infections. RESULTS: A total of 210 patients (161 females and 49 males) were included with a mean age of 74.06±7.43 years. Among them, 87 had life-threatening infections and 123 did not. In Cox regression analysis, the patients who used alendronate had a significantly lower risk of life-threatening infections (p = 0.006, HR = 0.845, 95% CI 0.750–0.954), while glucocorticoid users had higher risk of death (p = 0.010, HR = 2.037, 95% CI 1.187–3.498). CONCLUSIONS: Osteoporosis was associated with a high rate of life-threatening infections, and the use of alendronate had a lower rate of infection-related death. Therefore, we suggest that alendronate be used after vertebral fractures in these patients.
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spelling pubmed-55499232017-08-15 Risk of long-term infection-related death in clinical osteoporotic vertebral fractures: A hospital-based analysis Chen, Ying-Chou Lin, Wei-Che PLoS One Research Article BACKGROUND: Osteoporotic vertebral fractures adversely impact quality of life and also increase the risk of infection and mortality. Alendronate treatment increases bone mass and reduces the risk of fractures in patients with osteoporosis by suppressing bone resorption. We investigated the relationship between alendronate treatment and infection-related death in patients with osteoporotic vertebral fractures. METHODS: We retrospectively reviewed patients with osteoporosis and vertebral fractures from January 2001 to December 2007. The use of alendronate, glucocorticoid and medical factors including smoking, alcohol consumption, diabetes, hypertension, stroke, liver disease, heart disease, and pulmonary disease were analyzed. Cox regression was used to analyze the factors associated with life-threatening infections. RESULTS: A total of 210 patients (161 females and 49 males) were included with a mean age of 74.06±7.43 years. Among them, 87 had life-threatening infections and 123 did not. In Cox regression analysis, the patients who used alendronate had a significantly lower risk of life-threatening infections (p = 0.006, HR = 0.845, 95% CI 0.750–0.954), while glucocorticoid users had higher risk of death (p = 0.010, HR = 2.037, 95% CI 1.187–3.498). CONCLUSIONS: Osteoporosis was associated with a high rate of life-threatening infections, and the use of alendronate had a lower rate of infection-related death. Therefore, we suggest that alendronate be used after vertebral fractures in these patients. Public Library of Science 2017-08-09 /pmc/articles/PMC5549923/ /pubmed/28793342 http://dx.doi.org/10.1371/journal.pone.0182614 Text en © 2017 Chen, Lin http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Chen, Ying-Chou
Lin, Wei-Che
Risk of long-term infection-related death in clinical osteoporotic vertebral fractures: A hospital-based analysis
title Risk of long-term infection-related death in clinical osteoporotic vertebral fractures: A hospital-based analysis
title_full Risk of long-term infection-related death in clinical osteoporotic vertebral fractures: A hospital-based analysis
title_fullStr Risk of long-term infection-related death in clinical osteoporotic vertebral fractures: A hospital-based analysis
title_full_unstemmed Risk of long-term infection-related death in clinical osteoporotic vertebral fractures: A hospital-based analysis
title_short Risk of long-term infection-related death in clinical osteoporotic vertebral fractures: A hospital-based analysis
title_sort risk of long-term infection-related death in clinical osteoporotic vertebral fractures: a hospital-based analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5549923/
https://www.ncbi.nlm.nih.gov/pubmed/28793342
http://dx.doi.org/10.1371/journal.pone.0182614
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