TY - JOUR
T1 - Pharmacologic management of neuropathic pain
T2 - Evidence-based recommendations
AU - Dworkin, Robert H.
AU - O'Connor, Alec B.
AU - Backonja, Miroslav
AU - Farrar, John T.
AU - Finnerup, Nanna B.
AU - Jensen, Troels S.
AU - Kalso, Eija A.
AU - Loeser, John D.
AU - Miaskowski, Christine
AU - Nurmikko, Turo J.
AU - Portenoy, Russell K.
AU - Rice, Andrew S.C.
AU - Stacey, Brett R.
AU - Treede, Rolf Detlef
AU - Turk, Dennis C.
AU - Wallace, Mark S.
N1 - Funding Information:
Support for the consensus meeting on which this article is based was provided by the IASP Neuropathic Pain Special Interest Group and by the Neuropathic Pain Institute, both of which have received unrestricted support for their activities from multiple pharmaceutical companies. All authors received an honorarium for participation in the consensus meeting from the University of Rochester Office of Professional Education. RHD has received research support, consulting fees, or honoraria in the past year from Allergan, Balboa, CombinatoRx, Dara, Eli Lilly, Endo, EpiCept, Fralex, GlaxoSmithKline, GW Pharmaceuticals, Johnson & Johnson, KAI Pharmaceuticals, Merck, NeurogesX (also stock options), Ono, Organon, Pfizer, Supernus, US Food and Drug Administration, US National Institute of Health, US Veterans Administration, Wyeth, and XTL Biopharmaceuticals. ABO has received research support from Endo and the Mayday Fund, and is the recipient of an institutional career development award (T32 AG020493-02) from the National Institute on Aging. MB has received research support, consulting fees, or honoraria in the past year from Allergan, Astellas, Cephalon, Dov, Eli Lilly, Eisia, Endo, Johnson & Johnson, Merck, NeurogesX, Novartis, Pfizer, Schwarz, and Xenoport. JTF has received research support, consulting fees, or honoraria in the past year from Abbott, Adolor, Allergan, Celgene, Cephalon, Eli Lilly, GW Pharmaceuticals, Ortho McNeil, Pfizer, Philadelphia Health Care Trust, Purdue, and UCB Pharma. NBF has received research support or honoraria in the past year from Neurosearch A/S and UCB Nordic. TSJ has received research support, consulting fees, or honoraria in the past year from Eli Lilly, GlaxoSmithKline, Johnson & Johnson, Lundbeck Research Foundation, and Pfizer. JDL has received a grant from Purdue and honoraria from Endo, Medtronic, Pfizer, and US National Institute of Health. TJN has received research support, consulting fees, or honoraria in the past year from Eli Lilly, GW Pharmaceuticals, Medtronic, Pain Relief Foundation, Pfizer, Schwarz, UCB Pharma, and UK Department of Health. RKP has received research support, consulting fees, or honoraria in the past year from Abbott, Ametek, Bayer, Biovail, Cephalon, Cytogel, Endo, Forest, GlaxoSmithKline, GW Pharmaceuticals, Janssen, King, Ligand, Medgenex, Merck, Mylan, Neuromed, Organon, Ortho McNeil, Painceptor, Pfizer, Pharmos, Progenics, Sarentis, Solvay, UCB Pharma, Wex, and Xenon. ASCR has received research support, consulting fees, honoraria, or travel expenses in the past two years from Amgen, Boehringer Ingelheim, Eisai, Eli Lilly, GlaxoSmithKline, Novartis, Ono Pharma, Organon, Pfizer, Sanofi Pasteur/MSD, Solvay, Spinifex, Trophus, and UCB Pharma. BRS has received research support, consulting fees, or honoraria from Celgene, DepoMed, Eli Lilly, and Pfizer. RDT has received research support, consulting fees, or honoraria from Allergan, Boehringer Ingelheim, Bundesministerium für Bildung und Forschung, Deutsche Forschungsgemeinschaft, GlaxoSmithKline, Grünenthal, Merck Sharpe & Dohme, Pfizer, Schwarz, and US National Institute of Health. DCT has received consulting fees or honoraria in the past year from Abbott, Alpharma, AstraZeneca, Celgene, Eli Lilly, GlaxoSmithKline, PriCara/Ortho-McNeil, Schwarz, and Wyeth.
PY - 2007/12/5
Y1 - 2007/12/5
N2 - Patients with neuropathic pain (NP) are challenging to manage and evidence-based clinical recommendations for pharmacologic management are needed. Systematic literature reviews, randomized clinical trials, and existing guidelines were evaluated at a consensus meeting. Medications were considered for recommendation if their efficacy was supported by at least one methodologically-sound, randomized clinical trial (RCT) demonstrating superiority to placebo or a relevant comparison treatment. Recommendations were based on the amount and consistency of evidence, degree of efficacy, safety, and clinical experience of the authors. Available RCTs typically evaluated chronic NP of moderate to severe intensity. Recommended first-line treatments include certain antidepressants (i.e., tricyclic antidepressants and dual reuptake inhibitors of both serotonin and norepinephrine), calcium channel α2-δ ligands (i.e., gabapentin and pregabalin), and topical lidocaine. Opioid analgesics and tramadol are recommended as generally second-line treatments that can be considered for first-line use in select clinical circumstances. Other medications that would generally be used as third-line treatments but that could also be used as second-line treatments in some circumstances include certain antiepileptic and antidepressant medications, mexiletine, N-methyl-d-aspartate receptor antagonists, and topical capsaicin. Medication selection should be individualized, considering side effects, potential beneficial or deleterious effects on comorbidities, and whether prompt onset of pain relief is necessary. To date, no medications have demonstrated efficacy in lumbosacral radiculopathy, which is probably the most common type of NP. Long-term studies, head-to-head comparisons between medications, studies involving combinations of medications, and RCTs examining treatment of central NP are lacking and should be a priority for future research.
AB - Patients with neuropathic pain (NP) are challenging to manage and evidence-based clinical recommendations for pharmacologic management are needed. Systematic literature reviews, randomized clinical trials, and existing guidelines were evaluated at a consensus meeting. Medications were considered for recommendation if their efficacy was supported by at least one methodologically-sound, randomized clinical trial (RCT) demonstrating superiority to placebo or a relevant comparison treatment. Recommendations were based on the amount and consistency of evidence, degree of efficacy, safety, and clinical experience of the authors. Available RCTs typically evaluated chronic NP of moderate to severe intensity. Recommended first-line treatments include certain antidepressants (i.e., tricyclic antidepressants and dual reuptake inhibitors of both serotonin and norepinephrine), calcium channel α2-δ ligands (i.e., gabapentin and pregabalin), and topical lidocaine. Opioid analgesics and tramadol are recommended as generally second-line treatments that can be considered for first-line use in select clinical circumstances. Other medications that would generally be used as third-line treatments but that could also be used as second-line treatments in some circumstances include certain antiepileptic and antidepressant medications, mexiletine, N-methyl-d-aspartate receptor antagonists, and topical capsaicin. Medication selection should be individualized, considering side effects, potential beneficial or deleterious effects on comorbidities, and whether prompt onset of pain relief is necessary. To date, no medications have demonstrated efficacy in lumbosacral radiculopathy, which is probably the most common type of NP. Long-term studies, head-to-head comparisons between medications, studies involving combinations of medications, and RCTs examining treatment of central NP are lacking and should be a priority for future research.
KW - Evidence-based recommendations
KW - Neuropathic pain
KW - Pharmacologic management
KW - Randomized clinical trials
UR - http://www.scopus.com/inward/record.url?scp=35748943212&partnerID=8YFLogxK
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U2 - 10.1016/j.pain.2007.08.033
DO - 10.1016/j.pain.2007.08.033
M3 - Review article
C2 - 17920770
AN - SCOPUS:35748943212
SN - 0304-3959
VL - 132
SP - 237
EP - 251
JO - Pain
JF - Pain
IS - 3
ER -