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Short-term perioperative parecoxib is not detrimental to shaft fracture healing in a rat model

OBJECTIVES: Experimental studies indicate that non-steroidal anti-inflammatory drugs (NSAIDs) may have negative effects on fracture healing. This study aimed to assess the effect of immediate and delayed short-term administration of clinically relevant parecoxib doses and timing on fracture healing...

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Autores principales: Hjorthaug, G. A., Søreide, E., Nordsletten, L., Madsen, J. E., Reinholt, F. P., Niratisairak, S., Dimmen, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825043/
https://www.ncbi.nlm.nih.gov/pubmed/31728186
http://dx.doi.org/10.1302/2046-3758.810.BJR-2018-0341.R1
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author Hjorthaug, G. A.
Søreide, E.
Nordsletten, L.
Madsen, J. E.
Reinholt, F. P.
Niratisairak, S.
Dimmen, S.
author_facet Hjorthaug, G. A.
Søreide, E.
Nordsletten, L.
Madsen, J. E.
Reinholt, F. P.
Niratisairak, S.
Dimmen, S.
author_sort Hjorthaug, G. A.
collection PubMed
description OBJECTIVES: Experimental studies indicate that non-steroidal anti-inflammatory drugs (NSAIDs) may have negative effects on fracture healing. This study aimed to assess the effect of immediate and delayed short-term administration of clinically relevant parecoxib doses and timing on fracture healing using an established animal fracture model. METHODS: A standardized closed tibia shaft fracture was induced and stabilized by reamed intramedullary nailing in 66 Wistar rats. A ‘parecoxib immediate’ (Pi) group received parecoxib (3.2 mg/kg bodyweight twice per day) on days 0, 1, and 2. A ‘parecoxib delayed’ (Pd) group received the same dose of parecoxib on days 3, 4, and 5. A control group received saline only. Fracture healing was evaluated by biomechanical tests, histomorphometry, and dual-energy x-ray absorptiometry (DXA) at four weeks. RESULTS: For ultimate bending moment, the median ratio between fractured and non-fractured tibia was 0.61 (interquartile range (IQR) 0.45 to 0.82) in the Pi group, 0.44 (IQR 0.42 to 0.52) in the Pd group, and 0.50 (IQR 0.41 to 0.75) in the control group (n = 44; p = 0.068). There were no differences between the groups for stiffness, energy, deflection, callus diameter, DXA measurements (n = 64), histomorphometrically osteoid/bone ratio, or callus area (n = 20). CONCLUSION: This study demonstrates no negative effect of immediate or delayed short-term administration of parecoxib on diaphyseal fracture healing in rats. Cite this article: G. A. Hjorthaug, E. Søreide, L. Nordsletten, J. E. Madsen, F. P. Reinholt, S. Niratisairak, S. Dimmen. Short-term perioperative parecoxib is not detrimental to shaft fracture healing in a rat model. Bone Joint Res 2019;8:472–480. DOI: 10.1302/2046-3758.810.BJR-2018-0341.R1.
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spelling pubmed-68250432019-11-14 Short-term perioperative parecoxib is not detrimental to shaft fracture healing in a rat model Hjorthaug, G. A. Søreide, E. Nordsletten, L. Madsen, J. E. Reinholt, F. P. Niratisairak, S. Dimmen, S. Bone Joint Res Bone Biology OBJECTIVES: Experimental studies indicate that non-steroidal anti-inflammatory drugs (NSAIDs) may have negative effects on fracture healing. This study aimed to assess the effect of immediate and delayed short-term administration of clinically relevant parecoxib doses and timing on fracture healing using an established animal fracture model. METHODS: A standardized closed tibia shaft fracture was induced and stabilized by reamed intramedullary nailing in 66 Wistar rats. A ‘parecoxib immediate’ (Pi) group received parecoxib (3.2 mg/kg bodyweight twice per day) on days 0, 1, and 2. A ‘parecoxib delayed’ (Pd) group received the same dose of parecoxib on days 3, 4, and 5. A control group received saline only. Fracture healing was evaluated by biomechanical tests, histomorphometry, and dual-energy x-ray absorptiometry (DXA) at four weeks. RESULTS: For ultimate bending moment, the median ratio between fractured and non-fractured tibia was 0.61 (interquartile range (IQR) 0.45 to 0.82) in the Pi group, 0.44 (IQR 0.42 to 0.52) in the Pd group, and 0.50 (IQR 0.41 to 0.75) in the control group (n = 44; p = 0.068). There were no differences between the groups for stiffness, energy, deflection, callus diameter, DXA measurements (n = 64), histomorphometrically osteoid/bone ratio, or callus area (n = 20). CONCLUSION: This study demonstrates no negative effect of immediate or delayed short-term administration of parecoxib on diaphyseal fracture healing in rats. Cite this article: G. A. Hjorthaug, E. Søreide, L. Nordsletten, J. E. Madsen, F. P. Reinholt, S. Niratisairak, S. Dimmen. Short-term perioperative parecoxib is not detrimental to shaft fracture healing in a rat model. Bone Joint Res 2019;8:472–480. DOI: 10.1302/2046-3758.810.BJR-2018-0341.R1. 2019-11-02 /pmc/articles/PMC6825043/ /pubmed/31728186 http://dx.doi.org/10.1302/2046-3758.810.BJR-2018-0341.R1 Text en © 2019 Author(s) et al. Open Access This is an open-access article distributed under the terms of the Creative Commons Attributions licence (CC-BY-NC), which permits unrestricted use, distribution, and reproduction in any medium, but not for commercial gain, provided the original author and source are credited.
spellingShingle Bone Biology
Hjorthaug, G. A.
Søreide, E.
Nordsletten, L.
Madsen, J. E.
Reinholt, F. P.
Niratisairak, S.
Dimmen, S.
Short-term perioperative parecoxib is not detrimental to shaft fracture healing in a rat model
title Short-term perioperative parecoxib is not detrimental to shaft fracture healing in a rat model
title_full Short-term perioperative parecoxib is not detrimental to shaft fracture healing in a rat model
title_fullStr Short-term perioperative parecoxib is not detrimental to shaft fracture healing in a rat model
title_full_unstemmed Short-term perioperative parecoxib is not detrimental to shaft fracture healing in a rat model
title_short Short-term perioperative parecoxib is not detrimental to shaft fracture healing in a rat model
title_sort short-term perioperative parecoxib is not detrimental to shaft fracture healing in a rat model
topic Bone Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825043/
https://www.ncbi.nlm.nih.gov/pubmed/31728186
http://dx.doi.org/10.1302/2046-3758.810.BJR-2018-0341.R1
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