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Ultrasound imaging to tailor the treatment of acute shoulder pain: a randomised controlled trial in general practice
OBJECTIVE: To determine the clinical effectiveness of ultrasound tailored treatment in patients with acute subacromial disorders. DESIGN: Pragmatic randomised controlled trial. SETTING: Dutch general practice. PARTICIPANTS: Patients aged 18–65 years with acute (duration <3 months) unilateral shou...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128954/ https://www.ncbi.nlm.nih.gov/pubmed/27872111 http://dx.doi.org/10.1136/bmjopen-2016-011048 |
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author | Ottenheijm, Ramon P G Cals, Jochen W L Winkens, Bjorn Weijers, René E de Bie, Rob A Dinant, Geert-Jan |
author_facet | Ottenheijm, Ramon P G Cals, Jochen W L Winkens, Bjorn Weijers, René E de Bie, Rob A Dinant, Geert-Jan |
author_sort | Ottenheijm, Ramon P G |
collection | PubMed |
description | OBJECTIVE: To determine the clinical effectiveness of ultrasound tailored treatment in patients with acute subacromial disorders. DESIGN: Pragmatic randomised controlled trial. SETTING: Dutch general practice. PARTICIPANTS: Patients aged 18–65 years with acute (duration <3 months) unilateral shoulder pain and no previous treatment, in whom the general practitioner suspected a subacromial disorder was enrolled. INTERVENTIONS: All patients underwent ultrasound imaging of the affected shoulder. Patients who were still symptomatic after a qualification period of 2 weeks with standard treatment were randomised to treatment tailored to ultrasound diagnosis (disclosure of the ultrasound diagnosis) or usual care (non-disclosure of the ultrasound diagnosis). PRIMARY OUTCOME MEASURE: Patient-perceived recovery using the Global Perceived Effect questionnaire at 1 year. RESULTS: 129 patients were included. 18 patients recovered during the 2-week qualification period, resulting in 111 randomised patients; 56 were allocated to ultrasound tailored treatment and 55 to usual care. After 1 year, no statistically significant differences in recovery were found between the ultrasound tailored treatment group (72.5% (37/51)) and the usual care group (60% (30/50), OR 2.24 (95% CI 0.72 to 6.89; p=0.16)). Also, healthcare use was similar. CONCLUSIONS: This study has shown no clinically significant difference in the primary outcome measure between the ultrasound tailored treatment and usual care groups. Furthermore, there was no overall difference in healthcare resources used between groups. Although no formal cost data are included, one can only assume that the ultrasound examinations are additional costs for the intervention group, which cannot be justified in routine practice based on this trial. Based on this study, no change in current pragmatic guidelines to incorporate early ultrasound imaging can be recommended. TRIAL REGISTRATION NUMBER: NTR2403; Results. |
format | Online Article Text |
id | pubmed-5128954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51289542016-12-02 Ultrasound imaging to tailor the treatment of acute shoulder pain: a randomised controlled trial in general practice Ottenheijm, Ramon P G Cals, Jochen W L Winkens, Bjorn Weijers, René E de Bie, Rob A Dinant, Geert-Jan BMJ Open General practice / Family practice OBJECTIVE: To determine the clinical effectiveness of ultrasound tailored treatment in patients with acute subacromial disorders. DESIGN: Pragmatic randomised controlled trial. SETTING: Dutch general practice. PARTICIPANTS: Patients aged 18–65 years with acute (duration <3 months) unilateral shoulder pain and no previous treatment, in whom the general practitioner suspected a subacromial disorder was enrolled. INTERVENTIONS: All patients underwent ultrasound imaging of the affected shoulder. Patients who were still symptomatic after a qualification period of 2 weeks with standard treatment were randomised to treatment tailored to ultrasound diagnosis (disclosure of the ultrasound diagnosis) or usual care (non-disclosure of the ultrasound diagnosis). PRIMARY OUTCOME MEASURE: Patient-perceived recovery using the Global Perceived Effect questionnaire at 1 year. RESULTS: 129 patients were included. 18 patients recovered during the 2-week qualification period, resulting in 111 randomised patients; 56 were allocated to ultrasound tailored treatment and 55 to usual care. After 1 year, no statistically significant differences in recovery were found between the ultrasound tailored treatment group (72.5% (37/51)) and the usual care group (60% (30/50), OR 2.24 (95% CI 0.72 to 6.89; p=0.16)). Also, healthcare use was similar. CONCLUSIONS: This study has shown no clinically significant difference in the primary outcome measure between the ultrasound tailored treatment and usual care groups. Furthermore, there was no overall difference in healthcare resources used between groups. Although no formal cost data are included, one can only assume that the ultrasound examinations are additional costs for the intervention group, which cannot be justified in routine practice based on this trial. Based on this study, no change in current pragmatic guidelines to incorporate early ultrasound imaging can be recommended. TRIAL REGISTRATION NUMBER: NTR2403; Results. BMJ Publishing Group 2016-11-21 /pmc/articles/PMC5128954/ /pubmed/27872111 http://dx.doi.org/10.1136/bmjopen-2016-011048 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | General practice / Family practice Ottenheijm, Ramon P G Cals, Jochen W L Winkens, Bjorn Weijers, René E de Bie, Rob A Dinant, Geert-Jan Ultrasound imaging to tailor the treatment of acute shoulder pain: a randomised controlled trial in general practice |
title | Ultrasound imaging to tailor the treatment of acute shoulder pain: a randomised controlled trial in general practice |
title_full | Ultrasound imaging to tailor the treatment of acute shoulder pain: a randomised controlled trial in general practice |
title_fullStr | Ultrasound imaging to tailor the treatment of acute shoulder pain: a randomised controlled trial in general practice |
title_full_unstemmed | Ultrasound imaging to tailor the treatment of acute shoulder pain: a randomised controlled trial in general practice |
title_short | Ultrasound imaging to tailor the treatment of acute shoulder pain: a randomised controlled trial in general practice |
title_sort | ultrasound imaging to tailor the treatment of acute shoulder pain: a randomised controlled trial in general practice |
topic | General practice / Family practice |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128954/ https://www.ncbi.nlm.nih.gov/pubmed/27872111 http://dx.doi.org/10.1136/bmjopen-2016-011048 |
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