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Bilateral femoral neck fractures resulting from a grand mal seizure in an elderly man with Down syndrome

Simultaneous bilateral hip fractures are exceedingly rare and usually occur following a seizure. To our knowledge, only 22 cases of such injuries have been reported in the literature during the past forty years and the majority of fractures are treated with open reduction and internal fixation. We p...

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Autores principales: Marsh, Jonathan P., Leiter, Jeff R.S., MacDonald, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3143951/
https://www.ncbi.nlm.nih.gov/pubmed/21808693
http://dx.doi.org/10.4081/or.2010.e10
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author Marsh, Jonathan P.
Leiter, Jeff R.S.
MacDonald, Peter
author_facet Marsh, Jonathan P.
Leiter, Jeff R.S.
MacDonald, Peter
author_sort Marsh, Jonathan P.
collection PubMed
description Simultaneous bilateral hip fractures are exceedingly rare and usually occur following a seizure. To our knowledge, only 22 cases of such injuries have been reported in the literature during the past forty years and the majority of fractures are treated with open reduction and internal fixation. We present a case of a 66-year old man with Down syndrome and severe dementia who was diagnosed with bilateral displaced femoral neck fractures following an epileptic seizure. He was treated with single staged bilateral uncemented monopolar hemi-arthroplasties through lateral Hardinge approaches. The treatment choice was governed by fracture displacement, the lack of pre-existing osteoarthritis, length of time to diagnosis, the patient's age, ambulatory status and mental impairment, with the intention to minimize post-operative complications such as avascular necrosis, non-union and hip dislocation.
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spelling pubmed-31439512011-08-01 Bilateral femoral neck fractures resulting from a grand mal seizure in an elderly man with Down syndrome Marsh, Jonathan P. Leiter, Jeff R.S. MacDonald, Peter Orthop Rev (Pavia) Case Report Simultaneous bilateral hip fractures are exceedingly rare and usually occur following a seizure. To our knowledge, only 22 cases of such injuries have been reported in the literature during the past forty years and the majority of fractures are treated with open reduction and internal fixation. We present a case of a 66-year old man with Down syndrome and severe dementia who was diagnosed with bilateral displaced femoral neck fractures following an epileptic seizure. He was treated with single staged bilateral uncemented monopolar hemi-arthroplasties through lateral Hardinge approaches. The treatment choice was governed by fracture displacement, the lack of pre-existing osteoarthritis, length of time to diagnosis, the patient's age, ambulatory status and mental impairment, with the intention to minimize post-operative complications such as avascular necrosis, non-union and hip dislocation. PAGEPress Publications 2010-03-20 /pmc/articles/PMC3143951/ /pubmed/21808693 http://dx.doi.org/10.4081/or.2010.e10 Text en ©Copyright J.P. Marsh et al., 2010 This work is licensed under a Creative Commons Attribution 3.0 License (by-nc 3.0). Licensee PAGEPress, Italy
spellingShingle Case Report
Marsh, Jonathan P.
Leiter, Jeff R.S.
MacDonald, Peter
Bilateral femoral neck fractures resulting from a grand mal seizure in an elderly man with Down syndrome
title Bilateral femoral neck fractures resulting from a grand mal seizure in an elderly man with Down syndrome
title_full Bilateral femoral neck fractures resulting from a grand mal seizure in an elderly man with Down syndrome
title_fullStr Bilateral femoral neck fractures resulting from a grand mal seizure in an elderly man with Down syndrome
title_full_unstemmed Bilateral femoral neck fractures resulting from a grand mal seizure in an elderly man with Down syndrome
title_short Bilateral femoral neck fractures resulting from a grand mal seizure in an elderly man with Down syndrome
title_sort bilateral femoral neck fractures resulting from a grand mal seizure in an elderly man with down syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3143951/
https://www.ncbi.nlm.nih.gov/pubmed/21808693
http://dx.doi.org/10.4081/or.2010.e10
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