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Pharmacological treatment of Generalised Anxiety Disorder

Pharmacological treatment of Generalised Anxiety Disorder
Pharmacological treatment of Generalised Anxiety Disorder
Generalized anxiety disorder (GAD) is common in community and clinical settings. The individual and societal burden associated with GAD is substantial, but many of those who could benefit from treatment are not recognised or treated. Recent evidence-based guidelines for the pharmacological management of patients with GAD have recommended initial treatment with either a selective serotonin reuptake inhibitor (SSRI) or a serotonin-norepinephrine reuptake inhibitor (SNRI), on the basis of their proven efficacy and reasonable tolerability in randomised placebo-controlled trials.
However, there is much room for improvement in both the efficacy and tolerability of treatment. Response rates to first-line treatment can be disappointing and it is hard to predict reliably which patients will respond well and which will have only a limited treatment response. Many patients worry about becoming dependent on medication, a substantial proportion experience troublesome adverse effects, and these problems limit the effectiveness of pharmacological treatments in clinical practice.
The relative lack of longitudinal studies of clinical outcomes in GAD and the small number of placebo-controlled relapse prevention studies lead to uncertainty about the optimal duration of treatment after a satisfactory initial response. There have been few investigations of the further management of patients who have not responded to first-line treatment and there is a pressing need for further augmentation studies, in patients who have not responded to an SSRI or SNRI, or to other initial pharmacological approaches.
Future treatment guidelines for GAD will be influenced by emerging data for established and novel pharmacological approaches, and possibly through the more accurate identification of certain patient sub-groups, that are likely to respond preferentially to particular interventions.
Springer
Baldwin, D.S.
1beaa192-0ef1-4914-897a-3a49fc2ed15e
Ajel, K.
68013000-04dd-4ecd-ac40-71beac545318
Garner, M.
3221c5b3-b951-4fec-b456-ec449e4ce072
Steckler, T.
Stein, M.B.
Baldwin, D.S.
1beaa192-0ef1-4914-897a-3a49fc2ed15e
Ajel, K.
68013000-04dd-4ecd-ac40-71beac545318
Garner, M.
3221c5b3-b951-4fec-b456-ec449e4ce072
Steckler, T.
Stein, M.B.

Baldwin, D.S., Ajel, K. and Garner, M. (2009) Pharmacological treatment of Generalised Anxiety Disorder. In, Steckler, T. and Stein, M.B. (eds.) Behavioral Neurobiology of Anxiety and its Treatment. Springer.

Record type: Book Section

Abstract

Generalized anxiety disorder (GAD) is common in community and clinical settings. The individual and societal burden associated with GAD is substantial, but many of those who could benefit from treatment are not recognised or treated. Recent evidence-based guidelines for the pharmacological management of patients with GAD have recommended initial treatment with either a selective serotonin reuptake inhibitor (SSRI) or a serotonin-norepinephrine reuptake inhibitor (SNRI), on the basis of their proven efficacy and reasonable tolerability in randomised placebo-controlled trials.
However, there is much room for improvement in both the efficacy and tolerability of treatment. Response rates to first-line treatment can be disappointing and it is hard to predict reliably which patients will respond well and which will have only a limited treatment response. Many patients worry about becoming dependent on medication, a substantial proportion experience troublesome adverse effects, and these problems limit the effectiveness of pharmacological treatments in clinical practice.
The relative lack of longitudinal studies of clinical outcomes in GAD and the small number of placebo-controlled relapse prevention studies lead to uncertainty about the optimal duration of treatment after a satisfactory initial response. There have been few investigations of the further management of patients who have not responded to first-line treatment and there is a pressing need for further augmentation studies, in patients who have not responded to an SSRI or SNRI, or to other initial pharmacological approaches.
Future treatment guidelines for GAD will be influenced by emerging data for established and novel pharmacological approaches, and possibly through the more accurate identification of certain patient sub-groups, that are likely to respond preferentially to particular interventions.

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Published date: 2009

Identifiers

Local EPrints ID: 65050
URI: http://eprints.soton.ac.uk/id/eprint/65050
PURE UUID: f668044b-8c0d-4997-aa3a-03853e6f1ec3
ORCID for D.S. Baldwin: ORCID iD orcid.org/0000-0003-3343-0907
ORCID for M. Garner: ORCID iD orcid.org/0000-0001-9481-2226

Catalogue record

Date deposited: 30 Jan 2009
Last modified: 10 Aug 2023 01:36

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Contributors

Author: D.S. Baldwin ORCID iD
Author: K. Ajel
Author: M. Garner ORCID iD
Editor: T. Steckler
Editor: M.B. Stein

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