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I-ONE therapy in patients undergoing total knee arthroplasty: a prospective, randomized and controlled study

BACKGROUND: Total knee arthroplasty (TKA) is often associated with a severe local inflammatory reaction which, unless controlled, leads to persistent pain up to one year after surgery. Standard and accelerated rehabilitation protocols are currently being implemented after TKA, but no consensus exist...

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Autores principales: Moretti, Biagio, Notarnicola, Angela, Moretti, Lorenzo, Setti, Stefania, De Terlizzi, Francesca, Pesce, Vito, Patella, Vittorio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3476962/
https://www.ncbi.nlm.nih.gov/pubmed/22672794
http://dx.doi.org/10.1186/1471-2474-13-88
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author Moretti, Biagio
Notarnicola, Angela
Moretti, Lorenzo
Setti, Stefania
De Terlizzi, Francesca
Pesce, Vito
Patella, Vittorio
author_facet Moretti, Biagio
Notarnicola, Angela
Moretti, Lorenzo
Setti, Stefania
De Terlizzi, Francesca
Pesce, Vito
Patella, Vittorio
author_sort Moretti, Biagio
collection PubMed
description BACKGROUND: Total knee arthroplasty (TKA) is often associated with a severe local inflammatory reaction which, unless controlled, leads to persistent pain up to one year after surgery. Standard and accelerated rehabilitation protocols are currently being implemented after TKA, but no consensus exists regarding the long-term effects. Biophysical stimulation with pulsed electromagnetic fields (PEMFs) has been demonstrated to exert an anti-inflammatory effect, to promote early functional recovery and to maintain a positive long-term effect in patients undergoing joint arthroscopy. The aim of this study was to evaluate whether PEMFs can be used to limit the pain and enhance patient recovery after TKA. METHODS: A prospective, randomized, controlled study in 30 patients undergoing TKA was conducted. Patients were randomized into experimental PEMFs or a control group. Patients in the experimental group were instructed to use I-ONE stimulator 4hours/day for 60days. Postoperatively, all patients received the same rehabilitation program. Treatment outcome was assessed using the Knee Society Score, SF-36 Health-Survey and VAS. Patients were evaluated pre-operatively and one, two, six and 12 months after TKA. Joint swelling and Non Steroidal Anti Inflammatory Drug (NSAID) consumption were recorded. Comparisons between the two groups were carried out using a two-tail heteroschedastic Student’s t-test. Analysis of variance for each individual subject during the study was performed using ANOVA for multiple comparisons, applied on each group, and a Dunnet post hoc test. A p value < 0.05 was considered statistically significant. RESULTS: Pre-operatively, no differences were observed between groups in terms of age, sex, weight, height, Knee-Score, VAS, SF-36 and joint swelling, with the exception of the Functional Score. The Knee-Score, SF-36 and VAS demonstrated significantly positive outcomes in the I-ONE stimulated group compared with the controls at follow-ups. In the I-ONE group, NSAID use was reduced and joint swelling resolution was more rapid than in controls. The effect of I-ONE therapy was maintained after use of the device was discontinued. CONCLUSIONS: The results of the study show early functional recovery in the I-ONE group. I-ONE therapy should be considered after TKA to prevent the inflammatory reaction elicited by surgery, for pain relief and to speed functional recovery. TRIAL REGISTRATION: Current Controlled Trials ISRCTN10526056
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spelling pubmed-34769622012-10-23 I-ONE therapy in patients undergoing total knee arthroplasty: a prospective, randomized and controlled study Moretti, Biagio Notarnicola, Angela Moretti, Lorenzo Setti, Stefania De Terlizzi, Francesca Pesce, Vito Patella, Vittorio BMC Musculoskelet Disord Research Article BACKGROUND: Total knee arthroplasty (TKA) is often associated with a severe local inflammatory reaction which, unless controlled, leads to persistent pain up to one year after surgery. Standard and accelerated rehabilitation protocols are currently being implemented after TKA, but no consensus exists regarding the long-term effects. Biophysical stimulation with pulsed electromagnetic fields (PEMFs) has been demonstrated to exert an anti-inflammatory effect, to promote early functional recovery and to maintain a positive long-term effect in patients undergoing joint arthroscopy. The aim of this study was to evaluate whether PEMFs can be used to limit the pain and enhance patient recovery after TKA. METHODS: A prospective, randomized, controlled study in 30 patients undergoing TKA was conducted. Patients were randomized into experimental PEMFs or a control group. Patients in the experimental group were instructed to use I-ONE stimulator 4hours/day for 60days. Postoperatively, all patients received the same rehabilitation program. Treatment outcome was assessed using the Knee Society Score, SF-36 Health-Survey and VAS. Patients were evaluated pre-operatively and one, two, six and 12 months after TKA. Joint swelling and Non Steroidal Anti Inflammatory Drug (NSAID) consumption were recorded. Comparisons between the two groups were carried out using a two-tail heteroschedastic Student’s t-test. Analysis of variance for each individual subject during the study was performed using ANOVA for multiple comparisons, applied on each group, and a Dunnet post hoc test. A p value < 0.05 was considered statistically significant. RESULTS: Pre-operatively, no differences were observed between groups in terms of age, sex, weight, height, Knee-Score, VAS, SF-36 and joint swelling, with the exception of the Functional Score. The Knee-Score, SF-36 and VAS demonstrated significantly positive outcomes in the I-ONE stimulated group compared with the controls at follow-ups. In the I-ONE group, NSAID use was reduced and joint swelling resolution was more rapid than in controls. The effect of I-ONE therapy was maintained after use of the device was discontinued. CONCLUSIONS: The results of the study show early functional recovery in the I-ONE group. I-ONE therapy should be considered after TKA to prevent the inflammatory reaction elicited by surgery, for pain relief and to speed functional recovery. TRIAL REGISTRATION: Current Controlled Trials ISRCTN10526056 BioMed Central 2012-06-06 /pmc/articles/PMC3476962/ /pubmed/22672794 http://dx.doi.org/10.1186/1471-2474-13-88 Text en Copyright ©2012 Moretti 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
Moretti, Biagio
Notarnicola, Angela
Moretti, Lorenzo
Setti, Stefania
De Terlizzi, Francesca
Pesce, Vito
Patella, Vittorio
I-ONE therapy in patients undergoing total knee arthroplasty: a prospective, randomized and controlled study
title I-ONE therapy in patients undergoing total knee arthroplasty: a prospective, randomized and controlled study
title_full I-ONE therapy in patients undergoing total knee arthroplasty: a prospective, randomized and controlled study
title_fullStr I-ONE therapy in patients undergoing total knee arthroplasty: a prospective, randomized and controlled study
title_full_unstemmed I-ONE therapy in patients undergoing total knee arthroplasty: a prospective, randomized and controlled study
title_short I-ONE therapy in patients undergoing total knee arthroplasty: a prospective, randomized and controlled study
title_sort i-one therapy in patients undergoing total knee arthroplasty: a prospective, randomized and controlled study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3476962/
https://www.ncbi.nlm.nih.gov/pubmed/22672794
http://dx.doi.org/10.1186/1471-2474-13-88
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