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Long-Term Management of Generalised Anxiety Disorder with Low-Dose Continuous Infusions of Flumazenil: A Case Series

Background: Generalised anxiety disorder (GAD) is a common anxiety disorder associated with social and occupational impairment. Recently, a theory was postulated that dysfunctional gamma aminobutyric acid type A receptors (GABA(A)) are implicated in anxiety symptomology, which could be corrected by...

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Autores principales: Gallo, Alexander T., Addis, Stephen, Martyn, Vlad, Ramanathan, Hishani, Wilkerson, Grace K., Hood, Sean D., Stampfer, Hans, Hulse, Gary K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687673/
https://www.ncbi.nlm.nih.gov/pubmed/36354407
http://dx.doi.org/10.3390/bs12110430
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author Gallo, Alexander T.
Addis, Stephen
Martyn, Vlad
Ramanathan, Hishani
Wilkerson, Grace K.
Hood, Sean D.
Stampfer, Hans
Hulse, Gary K.
author_facet Gallo, Alexander T.
Addis, Stephen
Martyn, Vlad
Ramanathan, Hishani
Wilkerson, Grace K.
Hood, Sean D.
Stampfer, Hans
Hulse, Gary K.
author_sort Gallo, Alexander T.
collection PubMed
description Background: Generalised anxiety disorder (GAD) is a common anxiety disorder associated with social and occupational impairment. Recently, a theory was postulated that dysfunctional gamma aminobutyric acid type A receptors (GABA(A)) are implicated in anxiety symptomology, which could be corrected by flumazenil, an antagonist at the benzodiazepine binding site on the GABA(A) receptor. Method: Participants had a primary diagnosis of GAD and were treated initially with an eight-day continuous low-dose flumazenil infusion (total 32 mg at a rate of 4 mg/24 h). Some participants were re-treated with a further four- or eight-day infusion. Treatment response was measured as a 50% reduction in anxiety or stress scores on the Depression Anxiety Stress Scale—21 (DASS-21). Remission was measured as scores ≤3 or ≤7 on the anxiety and stress subscales of the DASS-21, respectively. Results: Eight cases are reported. All cases met the criteria for treatment response on the anxiety and stress subscale of the DASS-21. Remission was achieved in seven participants on the anxiety subscale and in five on the stress subscale. No changes in hepatic, renal, or haematological function were likely attributed to flumazenil. Conclusion: Data suggest that low-dose continuous flumazenil infusion manages GAD symptoms and is safe. Although these results are promising, future randomised control trials are required to confirm these results.
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spelling pubmed-96876732022-11-25 Long-Term Management of Generalised Anxiety Disorder with Low-Dose Continuous Infusions of Flumazenil: A Case Series Gallo, Alexander T. Addis, Stephen Martyn, Vlad Ramanathan, Hishani Wilkerson, Grace K. Hood, Sean D. Stampfer, Hans Hulse, Gary K. Behav Sci (Basel) Article Background: Generalised anxiety disorder (GAD) is a common anxiety disorder associated with social and occupational impairment. Recently, a theory was postulated that dysfunctional gamma aminobutyric acid type A receptors (GABA(A)) are implicated in anxiety symptomology, which could be corrected by flumazenil, an antagonist at the benzodiazepine binding site on the GABA(A) receptor. Method: Participants had a primary diagnosis of GAD and were treated initially with an eight-day continuous low-dose flumazenil infusion (total 32 mg at a rate of 4 mg/24 h). Some participants were re-treated with a further four- or eight-day infusion. Treatment response was measured as a 50% reduction in anxiety or stress scores on the Depression Anxiety Stress Scale—21 (DASS-21). Remission was measured as scores ≤3 or ≤7 on the anxiety and stress subscales of the DASS-21, respectively. Results: Eight cases are reported. All cases met the criteria for treatment response on the anxiety and stress subscale of the DASS-21. Remission was achieved in seven participants on the anxiety subscale and in five on the stress subscale. No changes in hepatic, renal, or haematological function were likely attributed to flumazenil. Conclusion: Data suggest that low-dose continuous flumazenil infusion manages GAD symptoms and is safe. Although these results are promising, future randomised control trials are required to confirm these results. MDPI 2022-11-02 /pmc/articles/PMC9687673/ /pubmed/36354407 http://dx.doi.org/10.3390/bs12110430 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gallo, Alexander T.
Addis, Stephen
Martyn, Vlad
Ramanathan, Hishani
Wilkerson, Grace K.
Hood, Sean D.
Stampfer, Hans
Hulse, Gary K.
Long-Term Management of Generalised Anxiety Disorder with Low-Dose Continuous Infusions of Flumazenil: A Case Series
title Long-Term Management of Generalised Anxiety Disorder with Low-Dose Continuous Infusions of Flumazenil: A Case Series
title_full Long-Term Management of Generalised Anxiety Disorder with Low-Dose Continuous Infusions of Flumazenil: A Case Series
title_fullStr Long-Term Management of Generalised Anxiety Disorder with Low-Dose Continuous Infusions of Flumazenil: A Case Series
title_full_unstemmed Long-Term Management of Generalised Anxiety Disorder with Low-Dose Continuous Infusions of Flumazenil: A Case Series
title_short Long-Term Management of Generalised Anxiety Disorder with Low-Dose Continuous Infusions of Flumazenil: A Case Series
title_sort long-term management of generalised anxiety disorder with low-dose continuous infusions of flumazenil: a case series
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687673/
https://www.ncbi.nlm.nih.gov/pubmed/36354407
http://dx.doi.org/10.3390/bs12110430
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