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Refractory burning mouth syndrome: clinical and paraclinical evaluation, comorbidities, treatment and outcome

BACKGROUND: Burning Mouth Syndrome (BMS) is a chronic pain condition characterized by persistent intraoral burning without related objective findings and unknown etiology that affects elderly females mostly. There is no satisfactory treatment for BMS. We aimed to observe the long-term efficacy of hi...

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Autores principales: Mitsikostas, Dimos D., Ljubisavljevic, Srdjan, Deligianni, Christina I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371535/
https://www.ncbi.nlm.nih.gov/pubmed/28357703
http://dx.doi.org/10.1186/s10194-017-0745-y
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author Mitsikostas, Dimos D.
Ljubisavljevic, Srdjan
Deligianni, Christina I.
author_facet Mitsikostas, Dimos D.
Ljubisavljevic, Srdjan
Deligianni, Christina I.
author_sort Mitsikostas, Dimos D.
collection PubMed
description BACKGROUND: Burning Mouth Syndrome (BMS) is a chronic pain condition characterized by persistent intraoral burning without related objective findings and unknown etiology that affects elderly females mostly. There is no satisfactory treatment for BMS. We aimed to observe the long-term efficacy of high velanfaxine doses combined with systemic and topical administered clonazepam in a particular subgroup of BMS patients who do not respond to current clinical management. RESULTS: Eight (66.1 ± 6.2 years old females) out of 14 BMS patients fulfilled the inclusion criteria and were treated with venlafaxine (300 mg/d) and clonazepam (5 mg/d) for 35.4 ± 12.1 (mean ± SD) months. The average duration of the symptoms at baseline was 4.3 ± 1.4 years and the overall mean daily pain intensity score was 8.6 ± 1.3 (VAS); pain was in tongue and within the oral mucosa, accompanying by oral and facial dysesthesia. In five patients tasting was abnormal. All patients had positive history of concomitant primary headache. The average score of Hamilton Rating scale for Anxiety and Depression was 21 ± 4.2, and 26.1 ± 2.9, respectively. Previous ineffective treatments include anticonvulsants and anti-depressants. All patients responded (more than 50% decrease in VAS) after three months treatment (mean VAS 3.2 ± 2.2) with no remarkable adverse events. CONCLUSION: BMS deserves bottomless psychiatric evaluation and management when current available treatments fail. Treatment with venlafaxine combined with topical and systemic clonazepam may be effective in refractory BMS cases but further investigation in a large-scale controlled study is needed to confirm these results.
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spelling pubmed-53715352017-04-12 Refractory burning mouth syndrome: clinical and paraclinical evaluation, comorbidities, treatment and outcome Mitsikostas, Dimos D. Ljubisavljevic, Srdjan Deligianni, Christina I. J Headache Pain Research Article BACKGROUND: Burning Mouth Syndrome (BMS) is a chronic pain condition characterized by persistent intraoral burning without related objective findings and unknown etiology that affects elderly females mostly. There is no satisfactory treatment for BMS. We aimed to observe the long-term efficacy of high velanfaxine doses combined with systemic and topical administered clonazepam in a particular subgroup of BMS patients who do not respond to current clinical management. RESULTS: Eight (66.1 ± 6.2 years old females) out of 14 BMS patients fulfilled the inclusion criteria and were treated with venlafaxine (300 mg/d) and clonazepam (5 mg/d) for 35.4 ± 12.1 (mean ± SD) months. The average duration of the symptoms at baseline was 4.3 ± 1.4 years and the overall mean daily pain intensity score was 8.6 ± 1.3 (VAS); pain was in tongue and within the oral mucosa, accompanying by oral and facial dysesthesia. In five patients tasting was abnormal. All patients had positive history of concomitant primary headache. The average score of Hamilton Rating scale for Anxiety and Depression was 21 ± 4.2, and 26.1 ± 2.9, respectively. Previous ineffective treatments include anticonvulsants and anti-depressants. All patients responded (more than 50% decrease in VAS) after three months treatment (mean VAS 3.2 ± 2.2) with no remarkable adverse events. CONCLUSION: BMS deserves bottomless psychiatric evaluation and management when current available treatments fail. Treatment with venlafaxine combined with topical and systemic clonazepam may be effective in refractory BMS cases but further investigation in a large-scale controlled study is needed to confirm these results. Springer Milan 2017-03-29 /pmc/articles/PMC5371535/ /pubmed/28357703 http://dx.doi.org/10.1186/s10194-017-0745-y Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research Article
Mitsikostas, Dimos D.
Ljubisavljevic, Srdjan
Deligianni, Christina I.
Refractory burning mouth syndrome: clinical and paraclinical evaluation, comorbidities, treatment and outcome
title Refractory burning mouth syndrome: clinical and paraclinical evaluation, comorbidities, treatment and outcome
title_full Refractory burning mouth syndrome: clinical and paraclinical evaluation, comorbidities, treatment and outcome
title_fullStr Refractory burning mouth syndrome: clinical and paraclinical evaluation, comorbidities, treatment and outcome
title_full_unstemmed Refractory burning mouth syndrome: clinical and paraclinical evaluation, comorbidities, treatment and outcome
title_short Refractory burning mouth syndrome: clinical and paraclinical evaluation, comorbidities, treatment and outcome
title_sort refractory burning mouth syndrome: clinical and paraclinical evaluation, comorbidities, treatment and outcome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371535/
https://www.ncbi.nlm.nih.gov/pubmed/28357703
http://dx.doi.org/10.1186/s10194-017-0745-y
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