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Dry needling for the treatment of acute myofascial pain syndrome in general practitioners’ clinics: a cohort study

BACKGROUND: Musculoskeletal pain is one of the leading complaints in the ambulatory setting. There are many ways to treat it, including pharmacologic and non-pharmacologic approaches. Dry needling (DN) is an option that is easy to learn, cheap and has a good safety profile. The aim of this study was...

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Autores principales: Yehoshua, Ilan, Rimon, Oded, Mizrahi Reuveni, Miri, Peleg, Roni, Adler, Limor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9792314/
https://www.ncbi.nlm.nih.gov/pubmed/36572860
http://dx.doi.org/10.1186/s12875-022-01951-0
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author Yehoshua, Ilan
Rimon, Oded
Mizrahi Reuveni, Miri
Peleg, Roni
Adler, Limor
author_facet Yehoshua, Ilan
Rimon, Oded
Mizrahi Reuveni, Miri
Peleg, Roni
Adler, Limor
author_sort Yehoshua, Ilan
collection PubMed
description BACKGROUND: Musculoskeletal pain is one of the leading complaints in the ambulatory setting. There are many ways to treat it, including pharmacologic and non-pharmacologic approaches. Dry needling (DN) is an option that is easy to learn, cheap and has a good safety profile. The aim of this study was to assess the association between DN performed by GPs for acute myofascial pain syndrome (MPS) and pain relief and to evaluate factors associated with treatment success. METHODS: In this prospective cohort study, two GPs performed DN in their clinics. Patients were asked to rank their pain using the Short-Form McGill Pain Questionnaire (SF-MPQ) before, 10-min and 1-week after the procedure. The SF-MPQ index consists of 3 parts; visual analog scale (VAS), pain rating index (PRI) and present pain intensity (PPI). Logistic regressions were performed to assess the variables associated with short- and medium- term success. RESULTS: Fifty two patients were recruited from September 2019 until August 2020. VAS was 6.0 ± 2.3 (before), 4.1 ± 2.5 (10-min after) and 2.6 ± 2.71 (1-week after), P < 0.05. PRI was 17 ± 9.1 (before), 10.8 ± 8.5 (10-min after) and 5.1 ± 6.5 (1-week after), P < 0.05. PPI was 2.6 ± 1.0 (before), 1.7 ± 1.0 (10-min after) and 1.1 ± 1.2 (1-week after), P < 0.05. Short-term success was associated with the physician who performed the procedure (OR 10.08, 95% CI 1.15,88.4) and with the use of a single needle (vs. multiple needles inserted) (OR 4.55, 95% CI 1.03,20.11). Medium-term success was associated with being a native born (non-immigrant), OR 8.59, 95% CI 1.11,66.28 and with high level of initial pain, OR 11.22, 95% CI 1.82,69.27. CONCLUSION: Our study demonstrated improvement in acute pain 10-min and 1-week after DN performed by a GP, in all parts of the SF-MPQ. Therefore, we believe DN is a good therapeutic option for GPs to aid patients suffering from MPS. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12875-022-01951-0.
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spelling pubmed-97923142022-12-27 Dry needling for the treatment of acute myofascial pain syndrome in general practitioners’ clinics: a cohort study Yehoshua, Ilan Rimon, Oded Mizrahi Reuveni, Miri Peleg, Roni Adler, Limor BMC Prim Care Research BACKGROUND: Musculoskeletal pain is one of the leading complaints in the ambulatory setting. There are many ways to treat it, including pharmacologic and non-pharmacologic approaches. Dry needling (DN) is an option that is easy to learn, cheap and has a good safety profile. The aim of this study was to assess the association between DN performed by GPs for acute myofascial pain syndrome (MPS) and pain relief and to evaluate factors associated with treatment success. METHODS: In this prospective cohort study, two GPs performed DN in their clinics. Patients were asked to rank their pain using the Short-Form McGill Pain Questionnaire (SF-MPQ) before, 10-min and 1-week after the procedure. The SF-MPQ index consists of 3 parts; visual analog scale (VAS), pain rating index (PRI) and present pain intensity (PPI). Logistic regressions were performed to assess the variables associated with short- and medium- term success. RESULTS: Fifty two patients were recruited from September 2019 until August 2020. VAS was 6.0 ± 2.3 (before), 4.1 ± 2.5 (10-min after) and 2.6 ± 2.71 (1-week after), P < 0.05. PRI was 17 ± 9.1 (before), 10.8 ± 8.5 (10-min after) and 5.1 ± 6.5 (1-week after), P < 0.05. PPI was 2.6 ± 1.0 (before), 1.7 ± 1.0 (10-min after) and 1.1 ± 1.2 (1-week after), P < 0.05. Short-term success was associated with the physician who performed the procedure (OR 10.08, 95% CI 1.15,88.4) and with the use of a single needle (vs. multiple needles inserted) (OR 4.55, 95% CI 1.03,20.11). Medium-term success was associated with being a native born (non-immigrant), OR 8.59, 95% CI 1.11,66.28 and with high level of initial pain, OR 11.22, 95% CI 1.82,69.27. CONCLUSION: Our study demonstrated improvement in acute pain 10-min and 1-week after DN performed by a GP, in all parts of the SF-MPQ. Therefore, we believe DN is a good therapeutic option for GPs to aid patients suffering from MPS. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12875-022-01951-0. BioMed Central 2022-12-27 /pmc/articles/PMC9792314/ /pubmed/36572860 http://dx.doi.org/10.1186/s12875-022-01951-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Yehoshua, Ilan
Rimon, Oded
Mizrahi Reuveni, Miri
Peleg, Roni
Adler, Limor
Dry needling for the treatment of acute myofascial pain syndrome in general practitioners’ clinics: a cohort study
title Dry needling for the treatment of acute myofascial pain syndrome in general practitioners’ clinics: a cohort study
title_full Dry needling for the treatment of acute myofascial pain syndrome in general practitioners’ clinics: a cohort study
title_fullStr Dry needling for the treatment of acute myofascial pain syndrome in general practitioners’ clinics: a cohort study
title_full_unstemmed Dry needling for the treatment of acute myofascial pain syndrome in general practitioners’ clinics: a cohort study
title_short Dry needling for the treatment of acute myofascial pain syndrome in general practitioners’ clinics: a cohort study
title_sort dry needling for the treatment of acute myofascial pain syndrome in general practitioners’ clinics: a cohort study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9792314/
https://www.ncbi.nlm.nih.gov/pubmed/36572860
http://dx.doi.org/10.1186/s12875-022-01951-0
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