TY - JOUR
T1 - Consensus guidelines
T2 - Treatment planning and options
AU - Argoff, Charles E.
AU - Backonja, Misha Miroslav
AU - Belgrade, Miles J.
AU - Bennett, Gary J.
AU - Clark, Michael R.
AU - Cole, B. Eliot
AU - Fishbain, David A.
AU - Irving, Gordon A.
AU - McCarberg, Bill H.
AU - McLean, Michael J.
N1 - Funding Information:
Dr Argoff receives grant and research support from Endo Pharmaceuticals, UCB Pharma, and Cephalon, Inc. He is a consultant to GlaxoWellcome, Eli Lilly and Company, Endo Pharmaceuticals, Pfizer Inc, UCB Pharma, and Allergan. Dr Backonja receives grant and research support from Pfizer Inc, NeurogesX Inc, and Avanir Pharmaceuticals. He is a consultant to Pfizer Inc and Eli Lilly and Company. Dr Bennett receives grant and research support from Endo Pharmaceuticals, Guilford Pharmaceuticals, and Pfizer Inc. He is a consultant to Amgen, Avigen Inc, NeurogesX Inc, Neuromed Technologies Inc, and Pfizer Pharmaceuticals Nagoya. He also receives honoraria from Eli Lilly and Company. Dr Belgrade receives honoraria from Eli Lilly and Company. Dr Clark receives honoraria from Eli Lilly and Company, Ligand Pharmaceuticals Inc, Organon, Pfizer Inc, and Wyeth. Dr Cole receives honoraria from Eli Lilly and Company and Ligand Pharmaceuticals, Inc. Dr Fishbain receives honoraria from Eli Lilly and Company and Endo Pharmaceuticals. Dr Irving receives grant and research support from Celgene Corporation and is a consultant to Pfizer Inc, Eli Lilly and Company, and Depomed, Inc. He also receives honoraria from Eli Lilly and Company and Pfizer Inc. Dr McCarberg receives honoraria from Janssen Pharmaceutica, Purdue Pharma LP, Eli Lilly and Company, Pfizer Inc, Ligand Pharmaceuticals Inc, Endo Pharmaceuticals, and Ortho-McNeil. Dr McLean receives grants and research support from Abbott, Pfizer Inc, Novartis, and Ortho-McNeil and is a consultant to Pfizer Inc, Xenoport, GlaxoWellcome, Novartis, Ortho-McNeil, and Shire Pharmaceuticals. He also receives honoraria from Pfizer Inc, Ortho-McNeil, Eisai, Novartis, and Shire Pharmaceuticals.
PY - 2006/4
Y1 - 2006/4
N2 - Despite the number of patients affected by diabetic peripheral neuropathic pain (DPNP), little consensus exists about the pathophysiology, best diagnostic tools, and primary treatment choices. Theories about tlie causes of DPNP are Inextricably linked with the causes of dietetic neuropathies, yet most patients with such neuropathies do not experience pain. The factors that differentiate patients with pain from those without remain unknown and are the subject of much research. When choosing treatment for patients with DPNP, physicians are confronted with a myriad of choices, none of which has been shown to be effective for all patients. This article reviews the evidence for these treatments and attempts to guide physicians in choosing those treatments based on evidence from well-designed clinical trials to support their use. Two agents, duioxetine and pregabalin, are formally approved by the Food and Drug Administration for the treatment of DPNIP. Dn addition, several other agents, Including the tricyclic class of antidepressants, have been effective in clinical trials. Ultimately, treatment choice must also Include consideration of adverse effects, individual patient factors such as comorbidities, and often cost.
AB - Despite the number of patients affected by diabetic peripheral neuropathic pain (DPNP), little consensus exists about the pathophysiology, best diagnostic tools, and primary treatment choices. Theories about tlie causes of DPNP are Inextricably linked with the causes of dietetic neuropathies, yet most patients with such neuropathies do not experience pain. The factors that differentiate patients with pain from those without remain unknown and are the subject of much research. When choosing treatment for patients with DPNP, physicians are confronted with a myriad of choices, none of which has been shown to be effective for all patients. This article reviews the evidence for these treatments and attempts to guide physicians in choosing those treatments based on evidence from well-designed clinical trials to support their use. Two agents, duioxetine and pregabalin, are formally approved by the Food and Drug Administration for the treatment of DPNIP. Dn addition, several other agents, Including the tricyclic class of antidepressants, have been effective in clinical trials. Ultimately, treatment choice must also Include consideration of adverse effects, individual patient factors such as comorbidities, and often cost.
UR - http://www.scopus.com/inward/record.url?scp=33645689140&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33645689140&partnerID=8YFLogxK
U2 - 10.1016/S0025-6196(11)61475-4
DO - 10.1016/S0025-6196(11)61475-4
M3 - Article
C2 - 16608049
AN - SCOPUS:33645689140
SN - 0025-6196
VL - 81
SP - S12-S25
JO - Mayo Clinic proceedings
JF - Mayo Clinic proceedings
IS - 4 SUPPL.
ER -