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Teriparatide improves early callus formation in distal radial fractures: Analysis of a subgroup of patients within a randomized trial

Background Teriparatide (parathyreoid hormone; PTH 1-34) increases skeletal mass in humans and improves fracture healing in animals. A recent randomized multicenter trial of nonoperated distal radial fractures showed a moderate shortening of the time to restoration of cortical continuity by treatmen...

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Autores principales: Aspenberg, Per, Johansson, Torsten
Formato: Texto
Lenguaje:English
Publicado: Informa Healthcare 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2895344/
https://www.ncbi.nlm.nih.gov/pubmed/20367417
http://dx.doi.org/10.3109/17453671003761946
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author Aspenberg, Per
Johansson, Torsten
author_facet Aspenberg, Per
Johansson, Torsten
author_sort Aspenberg, Per
collection PubMed
description Background Teriparatide (parathyreoid hormone; PTH 1-34) increases skeletal mass in humans and improves fracture healing in animals. A recent randomized multicenter trial of nonoperated distal radial fractures showed a moderate shortening of the time to restoration of cortical continuity by treatment with 20 μg (low-dose) teriparatide per day, but not with 40 μg (high-dose). As radiographic cortical continuity appears late in the healing process, perhaps too late for clinical relevance, we studied the qualitative appearance of the callus 5 weeks after fracture. Methods One third of the patients of the international trial were treated at Linköping University Hospital. The multicenter trial did not evaluate early callus formation. We therefore made a blinded qualitative scoring of the callus at 5 weeks in our 27 patients. Callus formation was arbitrarily classified as rich, intermediate, or poor. Results 9 patients were classified as rich (none had received placebo, 3 low-dose teriparatide, and 6 high-dose teriparatide). 9 patients were classified as intermediate (1 had received placebo, 5 low-dose, and 3 high-dose). 9 patients were classified as poor (7 had received placebo, 1 low-dose, and 1 high-dose) (p < 0.001). Interpretation This is a post hoc subgroup analysis of an outcome variable, which was not in the official protocol. The results must therefore be interpreted with caution. However, in combination with the results of the larger trial, the data suggest that radiographic quality at an early time point might be a sensitive variable, perhaps better than time to cortical continuity. Moreover, teriparatide appeared to improve early callus formation in distal radial fractures.
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spelling pubmed-28953442010-09-03 Teriparatide improves early callus formation in distal radial fractures: Analysis of a subgroup of patients within a randomized trial Aspenberg, Per Johansson, Torsten Acta Orthop Research Article Background Teriparatide (parathyreoid hormone; PTH 1-34) increases skeletal mass in humans and improves fracture healing in animals. A recent randomized multicenter trial of nonoperated distal radial fractures showed a moderate shortening of the time to restoration of cortical continuity by treatment with 20 μg (low-dose) teriparatide per day, but not with 40 μg (high-dose). As radiographic cortical continuity appears late in the healing process, perhaps too late for clinical relevance, we studied the qualitative appearance of the callus 5 weeks after fracture. Methods One third of the patients of the international trial were treated at Linköping University Hospital. The multicenter trial did not evaluate early callus formation. We therefore made a blinded qualitative scoring of the callus at 5 weeks in our 27 patients. Callus formation was arbitrarily classified as rich, intermediate, or poor. Results 9 patients were classified as rich (none had received placebo, 3 low-dose teriparatide, and 6 high-dose teriparatide). 9 patients were classified as intermediate (1 had received placebo, 5 low-dose, and 3 high-dose). 9 patients were classified as poor (7 had received placebo, 1 low-dose, and 1 high-dose) (p < 0.001). Interpretation This is a post hoc subgroup analysis of an outcome variable, which was not in the official protocol. The results must therefore be interpreted with caution. However, in combination with the results of the larger trial, the data suggest that radiographic quality at an early time point might be a sensitive variable, perhaps better than time to cortical continuity. Moreover, teriparatide appeared to improve early callus formation in distal radial fractures. Informa Healthcare 2010-04 2010-04-06 /pmc/articles/PMC2895344/ /pubmed/20367417 http://dx.doi.org/10.3109/17453671003761946 Text en Copyright: © Nordic Orthopedic Federation http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the source is credited.
spellingShingle Research Article
Aspenberg, Per
Johansson, Torsten
Teriparatide improves early callus formation in distal radial fractures: Analysis of a subgroup of patients within a randomized trial
title Teriparatide improves early callus formation in distal radial fractures: Analysis of a subgroup of patients within a randomized trial
title_full Teriparatide improves early callus formation in distal radial fractures: Analysis of a subgroup of patients within a randomized trial
title_fullStr Teriparatide improves early callus formation in distal radial fractures: Analysis of a subgroup of patients within a randomized trial
title_full_unstemmed Teriparatide improves early callus formation in distal radial fractures: Analysis of a subgroup of patients within a randomized trial
title_short Teriparatide improves early callus formation in distal radial fractures: Analysis of a subgroup of patients within a randomized trial
title_sort teriparatide improves early callus formation in distal radial fractures: analysis of a subgroup of patients within a randomized trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2895344/
https://www.ncbi.nlm.nih.gov/pubmed/20367417
http://dx.doi.org/10.3109/17453671003761946
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