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Initial intramuscular perfusion pressure predicts early skeletal muscle function following isolated tibial fractures

BACKGROUND: The severity of associated soft tissue trauma in complex injuries of the extremities guides fracture treatment and decisively determines patient's prognosis. Trauma-induced microvascular dysfunction and increased tissue pressure is known to trigger secondary soft tissue damage and s...

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Autores principales: Müller, Michael, Disch, Aleaxander C, Zabel, Nicole, Haas, Norbert P, Schaser, Klaus D
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2358881/
https://www.ncbi.nlm.nih.gov/pubmed/18419823
http://dx.doi.org/10.1186/1749-799X-3-14
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author Müller, Michael
Disch, Aleaxander C
Zabel, Nicole
Haas, Norbert P
Schaser, Klaus D
author_facet Müller, Michael
Disch, Aleaxander C
Zabel, Nicole
Haas, Norbert P
Schaser, Klaus D
author_sort Müller, Michael
collection PubMed
description BACKGROUND: The severity of associated soft tissue trauma in complex injuries of the extremities guides fracture treatment and decisively determines patient's prognosis. Trauma-induced microvascular dysfunction and increased tissue pressure is known to trigger secondary soft tissue damage and seems to adversely affect skeletal muscle function. METHODS: 20 patients with isolated tibial fractures were included. Blood pressure and compartment pressure (anterior and deep posterior compartment) were measured continuously up to 24 hours. Corresponding perfusion pressure was calculated. After 4 and 12 weeks isokinetic muscle peak torque and mean power of the ankle joint in dorsal and plantar flexion were measured using a Biodex dynamometer. RESULTS: A significant inverse correlation between the anterior perfusion pressure at 24 hours and deficit in dorsiflexion at 4 weeks was found for both, the peak torque (R = -0.83; p < 0.01) and the mean power (R = -0.84; p < 0.01). The posterior perfusion pressure at 24 h and the plantar flexion after 4 weeks in both, peak torque (R = -0.73, p =< 0.05) and mean power (R = -0.7, p =< 0.05) displayed a significant correlation. CONCLUSION: The functional relationship between the decrease in intramuscular perfusion pressures and muscle performance in the early rehabilitation period indicate a causative and prognostic role of early posttraumatic microcirculatory derangements and skeletal muscle function. Therapeutic concepts aimed at effective muscle recovery, early rehabilitation, and decreased secondary tissue damage, should consider the maintenance of an adequate intramuscular perfusion pressure.
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spelling pubmed-23588812008-04-29 Initial intramuscular perfusion pressure predicts early skeletal muscle function following isolated tibial fractures Müller, Michael Disch, Aleaxander C Zabel, Nicole Haas, Norbert P Schaser, Klaus D J Orthop Surg Research Article BACKGROUND: The severity of associated soft tissue trauma in complex injuries of the extremities guides fracture treatment and decisively determines patient's prognosis. Trauma-induced microvascular dysfunction and increased tissue pressure is known to trigger secondary soft tissue damage and seems to adversely affect skeletal muscle function. METHODS: 20 patients with isolated tibial fractures were included. Blood pressure and compartment pressure (anterior and deep posterior compartment) were measured continuously up to 24 hours. Corresponding perfusion pressure was calculated. After 4 and 12 weeks isokinetic muscle peak torque and mean power of the ankle joint in dorsal and plantar flexion were measured using a Biodex dynamometer. RESULTS: A significant inverse correlation between the anterior perfusion pressure at 24 hours and deficit in dorsiflexion at 4 weeks was found for both, the peak torque (R = -0.83; p < 0.01) and the mean power (R = -0.84; p < 0.01). The posterior perfusion pressure at 24 h and the plantar flexion after 4 weeks in both, peak torque (R = -0.73, p =< 0.05) and mean power (R = -0.7, p =< 0.05) displayed a significant correlation. CONCLUSION: The functional relationship between the decrease in intramuscular perfusion pressures and muscle performance in the early rehabilitation period indicate a causative and prognostic role of early posttraumatic microcirculatory derangements and skeletal muscle function. Therapeutic concepts aimed at effective muscle recovery, early rehabilitation, and decreased secondary tissue damage, should consider the maintenance of an adequate intramuscular perfusion pressure. BioMed Central 2008-04-17 /pmc/articles/PMC2358881/ /pubmed/18419823 http://dx.doi.org/10.1186/1749-799X-3-14 Text en Copyright © 2008 Müller et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Müller, Michael
Disch, Aleaxander C
Zabel, Nicole
Haas, Norbert P
Schaser, Klaus D
Initial intramuscular perfusion pressure predicts early skeletal muscle function following isolated tibial fractures
title Initial intramuscular perfusion pressure predicts early skeletal muscle function following isolated tibial fractures
title_full Initial intramuscular perfusion pressure predicts early skeletal muscle function following isolated tibial fractures
title_fullStr Initial intramuscular perfusion pressure predicts early skeletal muscle function following isolated tibial fractures
title_full_unstemmed Initial intramuscular perfusion pressure predicts early skeletal muscle function following isolated tibial fractures
title_short Initial intramuscular perfusion pressure predicts early skeletal muscle function following isolated tibial fractures
title_sort initial intramuscular perfusion pressure predicts early skeletal muscle function following isolated tibial fractures
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2358881/
https://www.ncbi.nlm.nih.gov/pubmed/18419823
http://dx.doi.org/10.1186/1749-799X-3-14
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