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Ultrasound-guided rhomboid intercostal block for myofascial pain syndrome: a prospective clinical study
BACKGROUND/AIM: Myofascial pain syndrome (MPS) is a common chronic pain syndrome that may affect quality of life, daily living activities, and psychological status. Ultrasound (US)-guided rhomboid intercostal block (RIB) is a recently defined plane block and used for chronic pain such as postmastect...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Scientific and Technological Research Council of Turkey (TUBITAK)
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10395676/ https://www.ncbi.nlm.nih.gov/pubmed/36422491 http://dx.doi.org/10.55730/1300-0144.5517 |
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author | GÜVEN KÖSE, Selin KÖSE, Halil Cihan TULGAR, Serkan AKKAYA, Ömer Taylan |
author_facet | GÜVEN KÖSE, Selin KÖSE, Halil Cihan TULGAR, Serkan AKKAYA, Ömer Taylan |
author_sort | GÜVEN KÖSE, Selin |
collection | PubMed |
description | BACKGROUND/AIM: Myofascial pain syndrome (MPS) is a common chronic pain syndrome that may affect quality of life, daily living activities, and psychological status. Ultrasound (US)-guided rhomboid intercostal block (RIB) is a recently defined plane block and used for chronic pain such as postmastectomy syndrome and MPS. Our aim was to evaluate the efficacy of US-guided RIB for the management of pain, quality of life, physical disability, and patient satisfaction in MPS. MATERIALS AND METHODS: In this prospective study, between February and March 2021, a total of 30 patients who applied with the diagnosis of MPS, were included. The patients received US-guided RIB. Pain intensity was evaluated using a numerical rating scale (NRS) at pretreatment, and just after the intervention, at day 1, and 1, 2, 4, and 6 weeks after the intervention. At pretreatment and 6 weeks after treatment, Short Form-36 Health Survey (SF-36) for health-related quality of life, Neck Disability Index (NDI), and patient satisfaction were evaluated. RESULTS: There was a statistically significant decrease in average NRS immediately after treatment, at day 1 and week 1,2,4, and 6 compared to the pretreatment (p < 0.0001). The average SF-36 scores advanced at 6 weeks after treatment. There was a statistically significant reduction in mean NDI scores throughout the follow-up period (p < 0.001). CONCLUSION: Our study demonstrated that RIB had improved neck function, physical and mental quality of life, and patient satisfaction in MPS. Therefore, we think US-guided RIB could be an alternative treatment modality in patients suffering from MPS. |
format | Online Article Text |
id | pubmed-10395676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Scientific and Technological Research Council of Turkey (TUBITAK) |
record_format | MEDLINE/PubMed |
spelling | pubmed-103956762023-08-03 Ultrasound-guided rhomboid intercostal block for myofascial pain syndrome: a prospective clinical study GÜVEN KÖSE, Selin KÖSE, Halil Cihan TULGAR, Serkan AKKAYA, Ömer Taylan Turk J Med Sci Research Article BACKGROUND/AIM: Myofascial pain syndrome (MPS) is a common chronic pain syndrome that may affect quality of life, daily living activities, and psychological status. Ultrasound (US)-guided rhomboid intercostal block (RIB) is a recently defined plane block and used for chronic pain such as postmastectomy syndrome and MPS. Our aim was to evaluate the efficacy of US-guided RIB for the management of pain, quality of life, physical disability, and patient satisfaction in MPS. MATERIALS AND METHODS: In this prospective study, between February and March 2021, a total of 30 patients who applied with the diagnosis of MPS, were included. The patients received US-guided RIB. Pain intensity was evaluated using a numerical rating scale (NRS) at pretreatment, and just after the intervention, at day 1, and 1, 2, 4, and 6 weeks after the intervention. At pretreatment and 6 weeks after treatment, Short Form-36 Health Survey (SF-36) for health-related quality of life, Neck Disability Index (NDI), and patient satisfaction were evaluated. RESULTS: There was a statistically significant decrease in average NRS immediately after treatment, at day 1 and week 1,2,4, and 6 compared to the pretreatment (p < 0.0001). The average SF-36 scores advanced at 6 weeks after treatment. There was a statistically significant reduction in mean NDI scores throughout the follow-up period (p < 0.001). CONCLUSION: Our study demonstrated that RIB had improved neck function, physical and mental quality of life, and patient satisfaction in MPS. Therefore, we think US-guided RIB could be an alternative treatment modality in patients suffering from MPS. Scientific and Technological Research Council of Turkey (TUBITAK) 2022-08-30 /pmc/articles/PMC10395676/ /pubmed/36422491 http://dx.doi.org/10.55730/1300-0144.5517 Text en © TÜBİTAK https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License. |
spellingShingle | Research Article GÜVEN KÖSE, Selin KÖSE, Halil Cihan TULGAR, Serkan AKKAYA, Ömer Taylan Ultrasound-guided rhomboid intercostal block for myofascial pain syndrome: a prospective clinical study |
title | Ultrasound-guided rhomboid intercostal block for myofascial pain syndrome: a prospective clinical study |
title_full | Ultrasound-guided rhomboid intercostal block for myofascial pain syndrome: a prospective clinical study |
title_fullStr | Ultrasound-guided rhomboid intercostal block for myofascial pain syndrome: a prospective clinical study |
title_full_unstemmed | Ultrasound-guided rhomboid intercostal block for myofascial pain syndrome: a prospective clinical study |
title_short | Ultrasound-guided rhomboid intercostal block for myofascial pain syndrome: a prospective clinical study |
title_sort | ultrasound-guided rhomboid intercostal block for myofascial pain syndrome: a prospective clinical study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10395676/ https://www.ncbi.nlm.nih.gov/pubmed/36422491 http://dx.doi.org/10.55730/1300-0144.5517 |
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