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Reduced patient restrictions following total hip arthroplasty: study protocol for a randomized controlled trial
BACKGROUND: Total hip arthroplasty (THA) is a very common procedure in orthopedic surgery. In the Netherlands, 25,642 primary THAs were performed in 2013. Postoperative hip dislocation is one of the major complications and has been reported in 0.5 to 10.6 % of patients after primary THA. Several rep...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539699/ https://www.ncbi.nlm.nih.gov/pubmed/26283079 http://dx.doi.org/10.1186/s13063-015-0901-0 |
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author | Peters, Anil Tijink, Miranda Veldhuijzen, Anne Huis in ‘t Veld, Rianne |
author_facet | Peters, Anil Tijink, Miranda Veldhuijzen, Anne Huis in ‘t Veld, Rianne |
author_sort | Peters, Anil |
collection | PubMed |
description | BACKGROUND: Total hip arthroplasty (THA) is a very common procedure in orthopedic surgery. In the Netherlands, 25,642 primary THAs were performed in 2013. Postoperative hip dislocation is one of the major complications and has been reported in 0.5 to 10.6 % of patients after primary THA. Several reports regarding the use of an anterolateral surgical approach have shown that a non-restriction or reduced restriction protocol does not increase the dislocation rate. For the posterolateral surgical approach it has been suggested that patient restrictions might be unnecessary but the amount of available literature is scarce. As such, randomized controlled trials aimed at investigating restrictions following THA using a posterior approach are strongly recommended. The aim of this prospective randomized controlled trial is to investigate the non-inferiority hypothesis concerning the early dislocation rate after THA in patients with and without the use of a reduced restriction protocol. METHODS/DESIGN: After providing informed consent a group of 456 patients with symptomatic coxarthrosis will be randomized to receive a THA either with care as usual, i.e. receiving postoperative restrictions including the advice to sleep in a supine position for the first 8 weeks postoperatively, or reduced restrictions with no recommendations regarding the position during sleeping. Primary outcome measure will be the percentage of early dislocations within the first 8 weeks after THA. Secondary outcome measures will be patient satisfaction, time to functional recovery, quality of sleep and patient’s self-reported compliance with postoperative instructions. DISCUSSION: To our knowledge this will be the first randomized controlled trial that compares a reduced restriction protocol with a restricted protocol following THA using a posterolateral surgical approach. Our hypothesis is that a reduced restriction protocol following THA with use of a posterolateral surgical approach has no influence on the early dislocation rate compared to a restricted protocol. Instead, embracing a reduced restriction protocol might even contribute to a higher quality of sleep, thereby facilitating a faster uptake and return to daily functions in patients after THA. TRIAL REGISTRATION: ClinicalTrials.gov NCT02107248, registration date 3 April 2014. |
format | Online Article Text |
id | pubmed-4539699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45396992015-08-19 Reduced patient restrictions following total hip arthroplasty: study protocol for a randomized controlled trial Peters, Anil Tijink, Miranda Veldhuijzen, Anne Huis in ‘t Veld, Rianne Trials Study Protocol BACKGROUND: Total hip arthroplasty (THA) is a very common procedure in orthopedic surgery. In the Netherlands, 25,642 primary THAs were performed in 2013. Postoperative hip dislocation is one of the major complications and has been reported in 0.5 to 10.6 % of patients after primary THA. Several reports regarding the use of an anterolateral surgical approach have shown that a non-restriction or reduced restriction protocol does not increase the dislocation rate. For the posterolateral surgical approach it has been suggested that patient restrictions might be unnecessary but the amount of available literature is scarce. As such, randomized controlled trials aimed at investigating restrictions following THA using a posterior approach are strongly recommended. The aim of this prospective randomized controlled trial is to investigate the non-inferiority hypothesis concerning the early dislocation rate after THA in patients with and without the use of a reduced restriction protocol. METHODS/DESIGN: After providing informed consent a group of 456 patients with symptomatic coxarthrosis will be randomized to receive a THA either with care as usual, i.e. receiving postoperative restrictions including the advice to sleep in a supine position for the first 8 weeks postoperatively, or reduced restrictions with no recommendations regarding the position during sleeping. Primary outcome measure will be the percentage of early dislocations within the first 8 weeks after THA. Secondary outcome measures will be patient satisfaction, time to functional recovery, quality of sleep and patient’s self-reported compliance with postoperative instructions. DISCUSSION: To our knowledge this will be the first randomized controlled trial that compares a reduced restriction protocol with a restricted protocol following THA using a posterolateral surgical approach. Our hypothesis is that a reduced restriction protocol following THA with use of a posterolateral surgical approach has no influence on the early dislocation rate compared to a restricted protocol. Instead, embracing a reduced restriction protocol might even contribute to a higher quality of sleep, thereby facilitating a faster uptake and return to daily functions in patients after THA. TRIAL REGISTRATION: ClinicalTrials.gov NCT02107248, registration date 3 April 2014. BioMed Central 2015-08-18 /pmc/articles/PMC4539699/ /pubmed/26283079 http://dx.doi.org/10.1186/s13063-015-0901-0 Text en © Peters et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Peters, Anil Tijink, Miranda Veldhuijzen, Anne Huis in ‘t Veld, Rianne Reduced patient restrictions following total hip arthroplasty: study protocol for a randomized controlled trial |
title | Reduced patient restrictions following total hip arthroplasty: study protocol for a randomized controlled trial |
title_full | Reduced patient restrictions following total hip arthroplasty: study protocol for a randomized controlled trial |
title_fullStr | Reduced patient restrictions following total hip arthroplasty: study protocol for a randomized controlled trial |
title_full_unstemmed | Reduced patient restrictions following total hip arthroplasty: study protocol for a randomized controlled trial |
title_short | Reduced patient restrictions following total hip arthroplasty: study protocol for a randomized controlled trial |
title_sort | reduced patient restrictions following total hip arthroplasty: study protocol for a randomized controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539699/ https://www.ncbi.nlm.nih.gov/pubmed/26283079 http://dx.doi.org/10.1186/s13063-015-0901-0 |
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