Benefits and harms of pregabalin in the management of neuropathic pain: a rapid review and meta-analysis of randomised clinical trials
<strong>Objective</strong> To assess the benefits and harms of pregabalin in the management of neuropathic pain. <br/><br/> <strong>Design</strong> Rapid review and meta-analysis of phase III, randomised, placebo-controlled trials. <br/><br/> <stron...
| Main Authors: | , , , , |
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| Format: | Journal article |
| Language: | English |
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BMJ Publishing Group
2019
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| _version_ | 1797091753532063744 |
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| author | Onakpoya, I Thomas, E Lee, J Goldacre, B Heneghan, C |
| author_facet | Onakpoya, I Thomas, E Lee, J Goldacre, B Heneghan, C |
| author_sort | Onakpoya, I |
| collection | OXFORD |
| description | <strong>Objective</strong> To assess the benefits and harms of pregabalin in the management of neuropathic pain. <br/><br/> <strong>Design</strong> Rapid review and meta-analysis of phase III, randomised, placebo-controlled trials. <br/><br/> <strong>Participants</strong> Adults aged 18 years and above with neuropathic pain defined according to the International Association for the Study of Pain criteria. <br/><br/> <strong>Interventions</strong> Pregabalin or placebo. <br/><br/> <strong>Primary and secondary outcome measures</strong> Our primary outcomes were pain (as measured using validated scales) and adverse events. Our secondary outcomes were sleep disturbance, quality of life, Patient Global Impression of Change, Clinician Global Impression scale, anxiety and depression scores, overall discontinuations and discontinuations because of adverse events. <br/><br/> <strong>Results</strong> We included 28 trials comprising 6087 participants. The neuropathic pain conditions studied were diabetic peripheral neuropathy, postherpetic neuralgia, herpes zoster, sciatica (radicular pain), poststroke pain and spinal cord injury-related pain. Patients who took pregabalin reported significant reductions in pain (numerical rating scale (NRS)) compared with placebo (standardised mean difference (SMD) −0.49 (95% CI −0.66 to −0.32, p<0.00001), very low quality evidence). Pregabalin significantly reduced sleep interference scores (NRS) compared with placebo (SMD −0.38 (95% CI −0.50 to −0.26, p<0.00001), moderate quality evidence. Pregabalin significantly increased the risk of adverse events compared with placebo (RR 1.33 (95% CI 1.23 to 1.44, p<0.00001, low quality evidence)). The risks of experiencing weight gain, somnolence, dizziness, peripheral oedema, fatigue, visual disturbances, ataxia, non-peripheral oedema, vertigo and euphoria were significantly increased with pregabalin. Pregabalin was significantly more likely than placebo to lead to discontinuation of the drug because of adverse events (RR 1.91 (95% CI 1.54 to 2.37, p<0.00001), low quality evidence). <br/><br/> <strong>Conclusion</strong> Pregabalin has beneficial effects on some symptoms of neuropathic pain. However, its use significantly increases the risk of a number of adverse events and discontinuation due to adverse events. The quality of the evidence from journal publications is low. |
| first_indexed | 2024-03-07T03:37:06Z |
| format | Journal article |
| id | oxford-uuid:bcaba217-6b63-4581-9f84-fbd8a8dbba77 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T03:37:06Z |
| publishDate | 2019 |
| publisher | BMJ Publishing Group |
| record_format | dspace |
| spelling | oxford-uuid:bcaba217-6b63-4581-9f84-fbd8a8dbba772022-03-27T05:26:02ZBenefits and harms of pregabalin in the management of neuropathic pain: a rapid review and meta-analysis of randomised clinical trialsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:bcaba217-6b63-4581-9f84-fbd8a8dbba77EnglishSymplectic Elements at OxfordBMJ Publishing Group2019Onakpoya, IThomas, ELee, JGoldacre, BHeneghan, C<strong>Objective</strong> To assess the benefits and harms of pregabalin in the management of neuropathic pain. <br/><br/> <strong>Design</strong> Rapid review and meta-analysis of phase III, randomised, placebo-controlled trials. <br/><br/> <strong>Participants</strong> Adults aged 18 years and above with neuropathic pain defined according to the International Association for the Study of Pain criteria. <br/><br/> <strong>Interventions</strong> Pregabalin or placebo. <br/><br/> <strong>Primary and secondary outcome measures</strong> Our primary outcomes were pain (as measured using validated scales) and adverse events. Our secondary outcomes were sleep disturbance, quality of life, Patient Global Impression of Change, Clinician Global Impression scale, anxiety and depression scores, overall discontinuations and discontinuations because of adverse events. <br/><br/> <strong>Results</strong> We included 28 trials comprising 6087 participants. The neuropathic pain conditions studied were diabetic peripheral neuropathy, postherpetic neuralgia, herpes zoster, sciatica (radicular pain), poststroke pain and spinal cord injury-related pain. Patients who took pregabalin reported significant reductions in pain (numerical rating scale (NRS)) compared with placebo (standardised mean difference (SMD) −0.49 (95% CI −0.66 to −0.32, p<0.00001), very low quality evidence). Pregabalin significantly reduced sleep interference scores (NRS) compared with placebo (SMD −0.38 (95% CI −0.50 to −0.26, p<0.00001), moderate quality evidence. Pregabalin significantly increased the risk of adverse events compared with placebo (RR 1.33 (95% CI 1.23 to 1.44, p<0.00001, low quality evidence)). The risks of experiencing weight gain, somnolence, dizziness, peripheral oedema, fatigue, visual disturbances, ataxia, non-peripheral oedema, vertigo and euphoria were significantly increased with pregabalin. Pregabalin was significantly more likely than placebo to lead to discontinuation of the drug because of adverse events (RR 1.91 (95% CI 1.54 to 2.37, p<0.00001), low quality evidence). <br/><br/> <strong>Conclusion</strong> Pregabalin has beneficial effects on some symptoms of neuropathic pain. However, its use significantly increases the risk of a number of adverse events and discontinuation due to adverse events. The quality of the evidence from journal publications is low. |
| spellingShingle | Onakpoya, I Thomas, E Lee, J Goldacre, B Heneghan, C Benefits and harms of pregabalin in the management of neuropathic pain: a rapid review and meta-analysis of randomised clinical trials |
| title | Benefits and harms of pregabalin in the management of neuropathic pain: a rapid review and meta-analysis of randomised clinical trials |
| title_full | Benefits and harms of pregabalin in the management of neuropathic pain: a rapid review and meta-analysis of randomised clinical trials |
| title_fullStr | Benefits and harms of pregabalin in the management of neuropathic pain: a rapid review and meta-analysis of randomised clinical trials |
| title_full_unstemmed | Benefits and harms of pregabalin in the management of neuropathic pain: a rapid review and meta-analysis of randomised clinical trials |
| title_short | Benefits and harms of pregabalin in the management of neuropathic pain: a rapid review and meta-analysis of randomised clinical trials |
| title_sort | benefits and harms of pregabalin in the management of neuropathic pain a rapid review and meta analysis of randomised clinical trials |
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