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WALANT versus intravenous regional anesthesia for carpal tunnel syndrome: a randomized clinical trial
BACKGROUND: There are several anesthetic techniques for surgical treatment of carpal tunnel syndrome (CTS). Results from this surgery using the “wide awake local anesthesia no tourniquet” (WALANT) technique have been described. However, there is no conclusive evidence regarding the effectiveness of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação Paulista de Medicina - APM
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9634845/ https://www.ncbi.nlm.nih.gov/pubmed/34644765 http://dx.doi.org/10.1590/1516-3180.2020.0583.R2.0904221 |
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author | Okamura, Aldo de Moraes, Vinicius Ynoe Fernandes, Marcela Raduan-Neto, Jorge Belloti, João Carlos |
author_facet | Okamura, Aldo de Moraes, Vinicius Ynoe Fernandes, Marcela Raduan-Neto, Jorge Belloti, João Carlos |
author_sort | Okamura, Aldo |
collection | PubMed |
description | BACKGROUND: There are several anesthetic techniques for surgical treatment of carpal tunnel syndrome (CTS). Results from this surgery using the “wide awake local anesthesia no tourniquet” (WALANT) technique have been described. However, there is no conclusive evidence regarding the effectiveness of the WALANT technique, compared with the usual techniques. OBJECTIVE: To evaluate the effectiveness of the WALANT technique, compared with intravenous regional anesthesia (IVRA; Bier’s block), for surgical treatment of CTS. DESIGN AND SETTING: Randomized clinical trial, conducted at Hospital Alvorada Moema and the Discipline of Hand Surgery, Universidade Federal de São Paulo (UNIFESP), São Paulo (SP), Brazil. METHODS: Seventy-eight patients were included. The primary outcome was measurement of perioperative pain through a visual analogue scale (VAS). The secondary outcomes were the Boston Questionnaire score, Hospital Anxiety and Depression Scale (HADS) score, need for use of analgesics, operating room times, remission of paresthesia, failures and complications. RESULTS: The WALANT technique (n = 40) proved to be superior to IVRA (n = 38), especially for controlling intraoperative pain (0.11 versus 3.7 cm; P < 0.001) and postoperative pain (0.6 versus 3.9 cm; P < 0.001). Patients spent more time in the operating room in the IVRA group (59.5 versus 46 minutes; P < 0.01) and needed to use more analgesics (10.8 versus 5.7 dipyrone tablets; P = 0.02). Five IVRA procedures failed (5 versus 0; P = 0.06). CONCLUSIONS: The WALANT technique is more effective than IVRA for CTS surgery. |
format | Online Article Text |
id | pubmed-9634845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Associação Paulista de Medicina - APM |
record_format | MEDLINE/PubMed |
spelling | pubmed-96348452022-11-04 WALANT versus intravenous regional anesthesia for carpal tunnel syndrome: a randomized clinical trial Okamura, Aldo de Moraes, Vinicius Ynoe Fernandes, Marcela Raduan-Neto, Jorge Belloti, João Carlos Sao Paulo Med J Original Article BACKGROUND: There are several anesthetic techniques for surgical treatment of carpal tunnel syndrome (CTS). Results from this surgery using the “wide awake local anesthesia no tourniquet” (WALANT) technique have been described. However, there is no conclusive evidence regarding the effectiveness of the WALANT technique, compared with the usual techniques. OBJECTIVE: To evaluate the effectiveness of the WALANT technique, compared with intravenous regional anesthesia (IVRA; Bier’s block), for surgical treatment of CTS. DESIGN AND SETTING: Randomized clinical trial, conducted at Hospital Alvorada Moema and the Discipline of Hand Surgery, Universidade Federal de São Paulo (UNIFESP), São Paulo (SP), Brazil. METHODS: Seventy-eight patients were included. The primary outcome was measurement of perioperative pain through a visual analogue scale (VAS). The secondary outcomes were the Boston Questionnaire score, Hospital Anxiety and Depression Scale (HADS) score, need for use of analgesics, operating room times, remission of paresthesia, failures and complications. RESULTS: The WALANT technique (n = 40) proved to be superior to IVRA (n = 38), especially for controlling intraoperative pain (0.11 versus 3.7 cm; P < 0.001) and postoperative pain (0.6 versus 3.9 cm; P < 0.001). Patients spent more time in the operating room in the IVRA group (59.5 versus 46 minutes; P < 0.01) and needed to use more analgesics (10.8 versus 5.7 dipyrone tablets; P = 0.02). Five IVRA procedures failed (5 versus 0; P = 0.06). CONCLUSIONS: The WALANT technique is more effective than IVRA for CTS surgery. Associação Paulista de Medicina - APM 2021-10-11 /pmc/articles/PMC9634845/ /pubmed/34644765 http://dx.doi.org/10.1590/1516-3180.2020.0583.R2.0904221 Text en © 2022 by Associação Paulista de Medicina https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons license. |
spellingShingle | Original Article Okamura, Aldo de Moraes, Vinicius Ynoe Fernandes, Marcela Raduan-Neto, Jorge Belloti, João Carlos WALANT versus intravenous regional anesthesia for carpal tunnel syndrome: a randomized clinical trial |
title | WALANT versus intravenous regional anesthesia for carpal tunnel syndrome: a randomized clinical trial |
title_full | WALANT versus intravenous regional anesthesia for carpal tunnel syndrome: a randomized clinical trial |
title_fullStr | WALANT versus intravenous regional anesthesia for carpal tunnel syndrome: a randomized clinical trial |
title_full_unstemmed | WALANT versus intravenous regional anesthesia for carpal tunnel syndrome: a randomized clinical trial |
title_short | WALANT versus intravenous regional anesthesia for carpal tunnel syndrome: a randomized clinical trial |
title_sort | walant versus intravenous regional anesthesia for carpal tunnel syndrome: a randomized clinical trial |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9634845/ https://www.ncbi.nlm.nih.gov/pubmed/34644765 http://dx.doi.org/10.1590/1516-3180.2020.0583.R2.0904221 |
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