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Therapy With Local Anesthetics to Treat Vulvodynia. A Pilot Study
INTRODUCTION: Vulvodynia (chronic vulvar pain) is a sexually debilitating disorder with a prevalence of ∼10%. AIM: To investigate the effectiveness of therapy with local anesthetics (TLA) in women with severe vulvodynia, we conducted a prospective, non-controlled observational study. METHODS: 45 pat...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023246/ https://www.ncbi.nlm.nih.gov/pubmed/35063914 http://dx.doi.org/10.1016/j.esxm.2021.100482 |
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author | Weinschenk, Stefan Benrath, Justus Kessler, Eugen Strowitzki, Thomas Feisst, Manuel |
author_facet | Weinschenk, Stefan Benrath, Justus Kessler, Eugen Strowitzki, Thomas Feisst, Manuel |
author_sort | Weinschenk, Stefan |
collection | PubMed |
description | INTRODUCTION: Vulvodynia (chronic vulvar pain) is a sexually debilitating disorder with a prevalence of ∼10%. AIM: To investigate the effectiveness of therapy with local anesthetics (TLA) in women with severe vulvodynia, we conducted a prospective, non-controlled observational study. METHODS: 45 patients with severe chronic vulvodynia (primary and secondary vulvodynia, 0–10 numeric analogue scale (NAS) ≥6, median 7.9, duration ≥6 months, median 65.2 months) in an outpatient practice in Germany were treated with TLA in 3–12 sessions using procaine 1% as local anesthetic. Effectiveness was analyzed with Wilcoxon signed rank tests and Wilcoxon rank sum tests. OUTCOMES: Therapeutic success as a reduction of pain to ≤4 NAS lasting for ≥6 months after end of therapy. RESULTS: TLA successfully reduced vulvodynia in 36 of 45 patients (80 %, responders). The NAS reduction was from 7.9 to 2.4 (P < .001). Even patients denominated as non-responders experienced a significant reduction in NAS (P = .03). In responders, long-term success was observed for 6.8–125 months (median 24.1 months). No adverse events occurred. CLINICAL TRANSLATION: A promising new treatment for a hard-to-treat chronic female pain disorder. STRENGTHS AND LIMITATIONS: Limitation: Monocentric, non-controlled observational design; Strength: the high number of patients treated. CONCLUSION: The high success rate of TLA in this investigation offers new perspectives on the etiology of vulvodynia as a complex pain syndrome affecting several nerves of the pelvic floor, and also provides early insight into the effectiveness of TLA in women with vulvodynia. Weinschenk S, Benrath J, Kessler E, et al. Therapy With Local Anesthetics to Treat Vulvodynia. A Pilot Study. Sex Med 2022;10:100482. |
format | Online Article Text |
id | pubmed-9023246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-90232462022-04-22 Therapy With Local Anesthetics to Treat Vulvodynia. A Pilot Study Weinschenk, Stefan Benrath, Justus Kessler, Eugen Strowitzki, Thomas Feisst, Manuel Sex Med Original Research INTRODUCTION: Vulvodynia (chronic vulvar pain) is a sexually debilitating disorder with a prevalence of ∼10%. AIM: To investigate the effectiveness of therapy with local anesthetics (TLA) in women with severe vulvodynia, we conducted a prospective, non-controlled observational study. METHODS: 45 patients with severe chronic vulvodynia (primary and secondary vulvodynia, 0–10 numeric analogue scale (NAS) ≥6, median 7.9, duration ≥6 months, median 65.2 months) in an outpatient practice in Germany were treated with TLA in 3–12 sessions using procaine 1% as local anesthetic. Effectiveness was analyzed with Wilcoxon signed rank tests and Wilcoxon rank sum tests. OUTCOMES: Therapeutic success as a reduction of pain to ≤4 NAS lasting for ≥6 months after end of therapy. RESULTS: TLA successfully reduced vulvodynia in 36 of 45 patients (80 %, responders). The NAS reduction was from 7.9 to 2.4 (P < .001). Even patients denominated as non-responders experienced a significant reduction in NAS (P = .03). In responders, long-term success was observed for 6.8–125 months (median 24.1 months). No adverse events occurred. CLINICAL TRANSLATION: A promising new treatment for a hard-to-treat chronic female pain disorder. STRENGTHS AND LIMITATIONS: Limitation: Monocentric, non-controlled observational design; Strength: the high number of patients treated. CONCLUSION: The high success rate of TLA in this investigation offers new perspectives on the etiology of vulvodynia as a complex pain syndrome affecting several nerves of the pelvic floor, and also provides early insight into the effectiveness of TLA in women with vulvodynia. Weinschenk S, Benrath J, Kessler E, et al. Therapy With Local Anesthetics to Treat Vulvodynia. A Pilot Study. Sex Med 2022;10:100482. Elsevier 2022-01-18 /pmc/articles/PMC9023246/ /pubmed/35063914 http://dx.doi.org/10.1016/j.esxm.2021.100482 Text en Copyright © 2022 The Authors. Published by Elsevier Inc. on behalf of the International Society for Sexual Medicine. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Research Weinschenk, Stefan Benrath, Justus Kessler, Eugen Strowitzki, Thomas Feisst, Manuel Therapy With Local Anesthetics to Treat Vulvodynia. A Pilot Study |
title | Therapy With Local Anesthetics to Treat Vulvodynia. A Pilot Study |
title_full | Therapy With Local Anesthetics to Treat Vulvodynia. A Pilot Study |
title_fullStr | Therapy With Local Anesthetics to Treat Vulvodynia. A Pilot Study |
title_full_unstemmed | Therapy With Local Anesthetics to Treat Vulvodynia. A Pilot Study |
title_short | Therapy With Local Anesthetics to Treat Vulvodynia. A Pilot Study |
title_sort | therapy with local anesthetics to treat vulvodynia. a pilot study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023246/ https://www.ncbi.nlm.nih.gov/pubmed/35063914 http://dx.doi.org/10.1016/j.esxm.2021.100482 |
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