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Frailty and osteoporosis in patients with hip fractures under the age of 60—a prospective cohort of 218 individuals

SUMMARY: Research on younger patients with hip fractures is limited. This study adds knowledge on patient and injury characteristics, and DXA was investigated at the time of the fracture. Risk factors for osteoporosis and fractures were numerous among young patients, and osteoporosis was markedly mo...

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Autores principales: Strøm Rönnquist, Sebastian, Viberg, Bjarke, Kristensen, Morten Tange, Palm, Henrik, Jensen, Jens-Erik Beck, Madsen, Carsten Fladmose, Åkesson, Kristina E., Overgaard, Søren, Rogmark, Cecilia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer London 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007814/
https://www.ncbi.nlm.nih.gov/pubmed/35029719
http://dx.doi.org/10.1007/s00198-021-06281-y
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author Strøm Rönnquist, Sebastian
Viberg, Bjarke
Kristensen, Morten Tange
Palm, Henrik
Jensen, Jens-Erik Beck
Madsen, Carsten Fladmose
Åkesson, Kristina E.
Overgaard, Søren
Rogmark, Cecilia
author_facet Strøm Rönnquist, Sebastian
Viberg, Bjarke
Kristensen, Morten Tange
Palm, Henrik
Jensen, Jens-Erik Beck
Madsen, Carsten Fladmose
Åkesson, Kristina E.
Overgaard, Søren
Rogmark, Cecilia
author_sort Strøm Rönnquist, Sebastian
collection PubMed
description SUMMARY: Research on younger patients with hip fractures is limited. This study adds knowledge on patient and injury characteristics, and DXA was investigated at the time of the fracture. Risk factors for osteoporosis and fractures were numerous among young patients, and osteoporosis was markedly more prevalent than in the general population. INTRODUCTION: Knowledge on younger patients with hip fractures is limited. Common preconceptions are that they suffer fractures due to high-energy trauma, alcohol or substance use disorder but not associated to osteoporosis. We aimed to descriptively analyze the characteristics of young and middle-aged patients with hip fractures and examine bone mineral density (BMD) by dual-energy x-ray absorptiometry (DXA) at the time of the fracture. METHODS: A prospective multicenter cohort study on adult patients with hip fractures below age 60 collected detailed information on patient characteristics regarding demographics, trauma mechanism, previous fractures, comorbidity and medication, and lifestyle factors. DXA results were compared to population-based reference data. RESULTS: The cohort contains 91 women and 127 men, median age 53 (IQR 47–57). Most fractures, 83%, occurred in patients aged 45–59. Two-thirds of all fractures resulted from low-energy trauma. Half of the patients had prior fractures after age 20. Thirty-four percent were healthy, 31% had one previous disease, and 35% had multiple comorbidities. Use of medication associated with increased fracture risk was 32%. Smoking was prevalent in 42%, harmful alcohol use reported by 29%, and signs of drug-related problems by 8%. Osteoporosis according to WHO criteria was found in 31%, osteopenia in 57%, and normal BMD in 12%. CONCLUSION: In patients with hip fractures below age 60, risk factors for osteoporosis and fractures were numerous. Moreover, the prevalence of osteoporosis was markedly higher than in the general population. We suggest that young and middle-aged patients with hip fractures undergo a thorough health investigation including DXA, regardless of trauma mechanism.
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spelling pubmed-90078142022-04-19 Frailty and osteoporosis in patients with hip fractures under the age of 60—a prospective cohort of 218 individuals Strøm Rönnquist, Sebastian Viberg, Bjarke Kristensen, Morten Tange Palm, Henrik Jensen, Jens-Erik Beck Madsen, Carsten Fladmose Åkesson, Kristina E. Overgaard, Søren Rogmark, Cecilia Osteoporos Int Original Article SUMMARY: Research on younger patients with hip fractures is limited. This study adds knowledge on patient and injury characteristics, and DXA was investigated at the time of the fracture. Risk factors for osteoporosis and fractures were numerous among young patients, and osteoporosis was markedly more prevalent than in the general population. INTRODUCTION: Knowledge on younger patients with hip fractures is limited. Common preconceptions are that they suffer fractures due to high-energy trauma, alcohol or substance use disorder but not associated to osteoporosis. We aimed to descriptively analyze the characteristics of young and middle-aged patients with hip fractures and examine bone mineral density (BMD) by dual-energy x-ray absorptiometry (DXA) at the time of the fracture. METHODS: A prospective multicenter cohort study on adult patients with hip fractures below age 60 collected detailed information on patient characteristics regarding demographics, trauma mechanism, previous fractures, comorbidity and medication, and lifestyle factors. DXA results were compared to population-based reference data. RESULTS: The cohort contains 91 women and 127 men, median age 53 (IQR 47–57). Most fractures, 83%, occurred in patients aged 45–59. Two-thirds of all fractures resulted from low-energy trauma. Half of the patients had prior fractures after age 20. Thirty-four percent were healthy, 31% had one previous disease, and 35% had multiple comorbidities. Use of medication associated with increased fracture risk was 32%. Smoking was prevalent in 42%, harmful alcohol use reported by 29%, and signs of drug-related problems by 8%. Osteoporosis according to WHO criteria was found in 31%, osteopenia in 57%, and normal BMD in 12%. CONCLUSION: In patients with hip fractures below age 60, risk factors for osteoporosis and fractures were numerous. Moreover, the prevalence of osteoporosis was markedly higher than in the general population. We suggest that young and middle-aged patients with hip fractures undergo a thorough health investigation including DXA, regardless of trauma mechanism. Springer London 2022-01-14 2022 /pmc/articles/PMC9007814/ /pubmed/35029719 http://dx.doi.org/10.1007/s00198-021-06281-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial 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-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Article
Strøm Rönnquist, Sebastian
Viberg, Bjarke
Kristensen, Morten Tange
Palm, Henrik
Jensen, Jens-Erik Beck
Madsen, Carsten Fladmose
Åkesson, Kristina E.
Overgaard, Søren
Rogmark, Cecilia
Frailty and osteoporosis in patients with hip fractures under the age of 60—a prospective cohort of 218 individuals
title Frailty and osteoporosis in patients with hip fractures under the age of 60—a prospective cohort of 218 individuals
title_full Frailty and osteoporosis in patients with hip fractures under the age of 60—a prospective cohort of 218 individuals
title_fullStr Frailty and osteoporosis in patients with hip fractures under the age of 60—a prospective cohort of 218 individuals
title_full_unstemmed Frailty and osteoporosis in patients with hip fractures under the age of 60—a prospective cohort of 218 individuals
title_short Frailty and osteoporosis in patients with hip fractures under the age of 60—a prospective cohort of 218 individuals
title_sort frailty and osteoporosis in patients with hip fractures under the age of 60—a prospective cohort of 218 individuals
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007814/
https://www.ncbi.nlm.nih.gov/pubmed/35029719
http://dx.doi.org/10.1007/s00198-021-06281-y
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