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Efficacy of Botulinum Toxin Type A in Trigeminal Neuralgia in a South Asian Cohort

INTRODUCTION: The antinociceptive effect of botulinum toxin-A (BTX-A) in trigeminal neuralgia (TN) has been described. We evaluated effects of BTX-A in relieving pain in patients with refractory TN at National Hospital of Sri Lanka. MATERIALS AND METHODS: Pain in patients with TN was assessed using...

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Autores principales: Caldera, Manjula Chandragomi, Senanayake, Sameera Jayan, Perera, Sujith Priyankara, Perera, Nadeeke Nidhan, Gamage, Ranjanie, Gooneratne, Inuka Kishara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5812131/
https://www.ncbi.nlm.nih.gov/pubmed/29456352
http://dx.doi.org/10.4103/jnrp.jnrp_346_17
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author Caldera, Manjula Chandragomi
Senanayake, Sameera Jayan
Perera, Sujith Priyankara
Perera, Nadeeke Nidhan
Gamage, Ranjanie
Gooneratne, Inuka Kishara
author_facet Caldera, Manjula Chandragomi
Senanayake, Sameera Jayan
Perera, Sujith Priyankara
Perera, Nadeeke Nidhan
Gamage, Ranjanie
Gooneratne, Inuka Kishara
author_sort Caldera, Manjula Chandragomi
collection PubMed
description INTRODUCTION: The antinociceptive effect of botulinum toxin-A (BTX-A) in trigeminal neuralgia (TN) has been described. We evaluated effects of BTX-A in relieving pain in patients with refractory TN at National Hospital of Sri Lanka. MATERIALS AND METHODS: Pain in patients with TN was assessed using a visual analog from 0 to 10. Three months after commencement of drug therapy with ≥2 drugs including one first-line drug (carbamazepine/oxcarbazepine), pain scores were re-assessed. Twenty-two patients who did not report improvement of ≥50% at 90 days’ posttreatment were recruited. They were given adjunct BTX-A directly to the trigger point (if identified) or intradermal. Pain scores were assessed at 10, 20, 30, 60, and 90 days’ posttreatment. RESULTS: There was a statistically significant improvement in mean pain scores at 10, 20, 30, 60, and 90 days’ posttreatment (5.59 [standard deviation (SD) = 2.7], 5.68 [SD = 2.6], 5.27 [SD = 3.2], 4.77 [SD = 3.7], and 5.32 [SD = 4.0]) compared to pre-BTX-A treatment (7.14, SD = 2.2). Percentage reduction in mean pain score ranged from 20.4% to 33.1%. Maximum response was at day 60 post-BTX-A (50% had ≥50% reduction in pain). No significant difference was found in response with higher doses and injection strategy. CONCLUSION: Consistent statistically significant reductions in pain scores at the aforesaid intervals compared to pretreatment means that there is a place for BTX in refractory TN.
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spelling pubmed-58121312018-02-16 Efficacy of Botulinum Toxin Type A in Trigeminal Neuralgia in a South Asian Cohort Caldera, Manjula Chandragomi Senanayake, Sameera Jayan Perera, Sujith Priyankara Perera, Nadeeke Nidhan Gamage, Ranjanie Gooneratne, Inuka Kishara J Neurosci Rural Pract Original Article INTRODUCTION: The antinociceptive effect of botulinum toxin-A (BTX-A) in trigeminal neuralgia (TN) has been described. We evaluated effects of BTX-A in relieving pain in patients with refractory TN at National Hospital of Sri Lanka. MATERIALS AND METHODS: Pain in patients with TN was assessed using a visual analog from 0 to 10. Three months after commencement of drug therapy with ≥2 drugs including one first-line drug (carbamazepine/oxcarbazepine), pain scores were re-assessed. Twenty-two patients who did not report improvement of ≥50% at 90 days’ posttreatment were recruited. They were given adjunct BTX-A directly to the trigger point (if identified) or intradermal. Pain scores were assessed at 10, 20, 30, 60, and 90 days’ posttreatment. RESULTS: There was a statistically significant improvement in mean pain scores at 10, 20, 30, 60, and 90 days’ posttreatment (5.59 [standard deviation (SD) = 2.7], 5.68 [SD = 2.6], 5.27 [SD = 3.2], 4.77 [SD = 3.7], and 5.32 [SD = 4.0]) compared to pre-BTX-A treatment (7.14, SD = 2.2). Percentage reduction in mean pain score ranged from 20.4% to 33.1%. Maximum response was at day 60 post-BTX-A (50% had ≥50% reduction in pain). No significant difference was found in response with higher doses and injection strategy. CONCLUSION: Consistent statistically significant reductions in pain scores at the aforesaid intervals compared to pretreatment means that there is a place for BTX in refractory TN. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC5812131/ /pubmed/29456352 http://dx.doi.org/10.4103/jnrp.jnrp_346_17 Text en Copyright: © 2018 Journal of Neurosciences in Rural Practice http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Caldera, Manjula Chandragomi
Senanayake, Sameera Jayan
Perera, Sujith Priyankara
Perera, Nadeeke Nidhan
Gamage, Ranjanie
Gooneratne, Inuka Kishara
Efficacy of Botulinum Toxin Type A in Trigeminal Neuralgia in a South Asian Cohort
title Efficacy of Botulinum Toxin Type A in Trigeminal Neuralgia in a South Asian Cohort
title_full Efficacy of Botulinum Toxin Type A in Trigeminal Neuralgia in a South Asian Cohort
title_fullStr Efficacy of Botulinum Toxin Type A in Trigeminal Neuralgia in a South Asian Cohort
title_full_unstemmed Efficacy of Botulinum Toxin Type A in Trigeminal Neuralgia in a South Asian Cohort
title_short Efficacy of Botulinum Toxin Type A in Trigeminal Neuralgia in a South Asian Cohort
title_sort efficacy of botulinum toxin type a in trigeminal neuralgia in a south asian cohort
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5812131/
https://www.ncbi.nlm.nih.gov/pubmed/29456352
http://dx.doi.org/10.4103/jnrp.jnrp_346_17
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