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A classification method for neurogenic heterotopic ossification of the hip
BACKGROUND: Existing classifications for heterotopic ossification (HO) do not include all HO types; nor do they consider the anatomy of the involved joint or the neurological injury. Therefore, we performed this study to propose and evaluate a classification according to the location of neurogenic H...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3349026/ https://www.ncbi.nlm.nih.gov/pubmed/22476356 http://dx.doi.org/10.1007/s10195-012-0193-z |
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author | Mavrogenis, Andreas F. Guerra, Giovanni Staals, Eric Lodwijk Bianchi, Giuseppe Ruggieri, Pietro |
author_facet | Mavrogenis, Andreas F. Guerra, Giovanni Staals, Eric Lodwijk Bianchi, Giuseppe Ruggieri, Pietro |
author_sort | Mavrogenis, Andreas F. |
collection | PubMed |
description | BACKGROUND: Existing classifications for heterotopic ossification (HO) do not include all HO types; nor do they consider the anatomy of the involved joint or the neurological injury. Therefore, we performed this study to propose and evaluate a classification according to the location of neurogenic HO and the neurological injury. MATERIALS AND METHODS: We studied the files of 24 patients/33 hips with brain or spinal cord injury and neurogenic HO of the hip treated with excision, indomethacin, and radiation therapy. We classified patients according to the Brooker classification scheme as well as ours. Four types of neurogenic HO were distinguished according to the anatomical location of HO: type 1, anterior; type 2, posterior; type 3, anteromedial; type 4, circumferential. Subtypes of each type were added based on the neurological injury: a, spinal cord; b, brain injury. Mean follow-up was 2.5 years (1–8 years). RESULTS: The Brooker classification scheme was misleading—all hips were class III or IV, corresponding to ankylosis, even though only 14 hips had ankylosis. On the other hand, our classification was straightforward and easy to assign in all cases. It corresponded better to the location of the heterotopic bone, and allowed for preoperative planning of the appropriate surgical approach and evaluation of the prognosis; recurrence of neurogenic HO was significantly higher in patients with brain injury (subtype b), while blood loss was higher for patients with anteromedial (type 3) and circumferential (type 4) neurogenic HO. CONCLUSIONS: Our proposed classification may improve the management and evaluation of the prognosis for patients with neurogenic HO. |
format | Online Article Text |
id | pubmed-3349026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-33490262012-05-30 A classification method for neurogenic heterotopic ossification of the hip Mavrogenis, Andreas F. Guerra, Giovanni Staals, Eric Lodwijk Bianchi, Giuseppe Ruggieri, Pietro J Orthop Traumatol Original Article BACKGROUND: Existing classifications for heterotopic ossification (HO) do not include all HO types; nor do they consider the anatomy of the involved joint or the neurological injury. Therefore, we performed this study to propose and evaluate a classification according to the location of neurogenic HO and the neurological injury. MATERIALS AND METHODS: We studied the files of 24 patients/33 hips with brain or spinal cord injury and neurogenic HO of the hip treated with excision, indomethacin, and radiation therapy. We classified patients according to the Brooker classification scheme as well as ours. Four types of neurogenic HO were distinguished according to the anatomical location of HO: type 1, anterior; type 2, posterior; type 3, anteromedial; type 4, circumferential. Subtypes of each type were added based on the neurological injury: a, spinal cord; b, brain injury. Mean follow-up was 2.5 years (1–8 years). RESULTS: The Brooker classification scheme was misleading—all hips were class III or IV, corresponding to ankylosis, even though only 14 hips had ankylosis. On the other hand, our classification was straightforward and easy to assign in all cases. It corresponded better to the location of the heterotopic bone, and allowed for preoperative planning of the appropriate surgical approach and evaluation of the prognosis; recurrence of neurogenic HO was significantly higher in patients with brain injury (subtype b), while blood loss was higher for patients with anteromedial (type 3) and circumferential (type 4) neurogenic HO. CONCLUSIONS: Our proposed classification may improve the management and evaluation of the prognosis for patients with neurogenic HO. Springer International Publishing 2012-04-04 2012-06 /pmc/articles/PMC3349026/ /pubmed/22476356 http://dx.doi.org/10.1007/s10195-012-0193-z Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Article Mavrogenis, Andreas F. Guerra, Giovanni Staals, Eric Lodwijk Bianchi, Giuseppe Ruggieri, Pietro A classification method for neurogenic heterotopic ossification of the hip |
title | A classification method for neurogenic heterotopic ossification of the hip |
title_full | A classification method for neurogenic heterotopic ossification of the hip |
title_fullStr | A classification method for neurogenic heterotopic ossification of the hip |
title_full_unstemmed | A classification method for neurogenic heterotopic ossification of the hip |
title_short | A classification method for neurogenic heterotopic ossification of the hip |
title_sort | classification method for neurogenic heterotopic ossification of the hip |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3349026/ https://www.ncbi.nlm.nih.gov/pubmed/22476356 http://dx.doi.org/10.1007/s10195-012-0193-z |
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