Interventions for the reduction of prescribed opioid use in chronic non-cancer pain.

BACKGROUND: Patients with chronic non-cancer pain who are prescribed and are taking opioids can have a history of long term high dose opioid use without effective pain relief. In those without good pain relief, reduction of prescribed opioid dose may be the desired and shared goal of both patient an...

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Main Authors: Windmill, J, Fisher, E, Eccleston, C, Derry, S, Stannard, C, Knaggs, R, Moore, R
Format: Journal article
Language:English
Published: 2013
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author Windmill, J
Fisher, E
Eccleston, C
Derry, S
Stannard, C
Knaggs, R
Moore, R
author_facet Windmill, J
Fisher, E
Eccleston, C
Derry, S
Stannard, C
Knaggs, R
Moore, R
author_sort Windmill, J
collection OXFORD
description BACKGROUND: Patients with chronic non-cancer pain who are prescribed and are taking opioids can have a history of long term high dose opioid use without effective pain relief. In those without good pain relief, reduction of prescribed opioid dose may be the desired and shared goal of both patient and clinician. Simple unsupervised reduction of opioid use is clinically challenging, and very difficult to achieve and maintain. OBJECTIVES: To investigate the effectiveness of different methods designed to achieve reduction or cessation of prescribed opioid use for the management of chronic non-cancer pain. SEARCH METHODS: We searched the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, and EMBASE from inception to 8th April 2013, as well as bibliographies. SELECTION CRITERIA: Included studies had to be randomised controlled trials comparing opioid users receiving an intervention with a control group receiving treatment as usual, active control, or placebo. The aim of the study had to include a treatment goal of dose reduction or cessation of opioid medication. DATA COLLECTION AND ANALYSIS: We sought data relating to prescribed opioid use, adverse events of opioid reduction, pain, and psychological and physical function. MAIN RESULTS: Two studies provided information on 86 participants. One compared electroacupuncture with sham acupuncture for 20 minutes twice a week for six weeks; there was no difference between treatments. The other followed 11 weeks of cognitive behavioural therapy with either therapeutic interactive voice response through a computer for four months or usual treatment; the active group had a significant reduction in opioid use, while the usual care group had a significant increase. AUTHORS' CONCLUSIONS: Both included studies were at significant risk of bias because of their small size, together with other important issues, including blinding. Because of this risk and the paucity of relevant studies, no conclusions can be drawn regarding the effectiveness of interventions for opioid withdrawal in chronic non-cancer pain.
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spelling oxford-uuid:73832b5f-031b-434f-b891-64a50b4345682022-03-26T19:56:56ZInterventions for the reduction of prescribed opioid use in chronic non-cancer pain.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:73832b5f-031b-434f-b891-64a50b434568EnglishSymplectic Elements at Oxford2013Windmill, JFisher, EEccleston, CDerry, SStannard, CKnaggs, RMoore, RBACKGROUND: Patients with chronic non-cancer pain who are prescribed and are taking opioids can have a history of long term high dose opioid use without effective pain relief. In those without good pain relief, reduction of prescribed opioid dose may be the desired and shared goal of both patient and clinician. Simple unsupervised reduction of opioid use is clinically challenging, and very difficult to achieve and maintain. OBJECTIVES: To investigate the effectiveness of different methods designed to achieve reduction or cessation of prescribed opioid use for the management of chronic non-cancer pain. SEARCH METHODS: We searched the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, and EMBASE from inception to 8th April 2013, as well as bibliographies. SELECTION CRITERIA: Included studies had to be randomised controlled trials comparing opioid users receiving an intervention with a control group receiving treatment as usual, active control, or placebo. The aim of the study had to include a treatment goal of dose reduction or cessation of opioid medication. DATA COLLECTION AND ANALYSIS: We sought data relating to prescribed opioid use, adverse events of opioid reduction, pain, and psychological and physical function. MAIN RESULTS: Two studies provided information on 86 participants. One compared electroacupuncture with sham acupuncture for 20 minutes twice a week for six weeks; there was no difference between treatments. The other followed 11 weeks of cognitive behavioural therapy with either therapeutic interactive voice response through a computer for four months or usual treatment; the active group had a significant reduction in opioid use, while the usual care group had a significant increase. AUTHORS' CONCLUSIONS: Both included studies were at significant risk of bias because of their small size, together with other important issues, including blinding. Because of this risk and the paucity of relevant studies, no conclusions can be drawn regarding the effectiveness of interventions for opioid withdrawal in chronic non-cancer pain.
spellingShingle Windmill, J
Fisher, E
Eccleston, C
Derry, S
Stannard, C
Knaggs, R
Moore, R
Interventions for the reduction of prescribed opioid use in chronic non-cancer pain.
title Interventions for the reduction of prescribed opioid use in chronic non-cancer pain.
title_full Interventions for the reduction of prescribed opioid use in chronic non-cancer pain.
title_fullStr Interventions for the reduction of prescribed opioid use in chronic non-cancer pain.
title_full_unstemmed Interventions for the reduction of prescribed opioid use in chronic non-cancer pain.
title_short Interventions for the reduction of prescribed opioid use in chronic non-cancer pain.
title_sort interventions for the reduction of prescribed opioid use in chronic non cancer pain
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