TY - JOUR
T1 - Evidence-based guidance for the management of postherpetic neuralgia in primary care.
AU - Harden, Robert N
AU - Kaye, Alan David
AU - Kintanar, Thomas
AU - Argoff, Charles E.
N1 - Funding Information:
R. Norman Harden, MD, discloses no conflicts of interest. Alan David Kaye, MD, discloses that he a recipient of research grants from and on the speakers bureau for Depomed, Inc. Thomas Kintanar, MD, discloses that he is on the speakers board for Ironwood Pharmaceuticals, Inc./Forest Pharmaceuticals, Inc., and Takeda Pharmaceuticals USA, Inc. Charles E. Argoff, MD, discloses that he is a consultant for Collegium Pharmaceutical, is an advisor and on the speakers bureau for Depomed, Inc., Janssen Pharmaceuticals, Inc., and Pfizer Inc.; an advisor for, receives research grants from, and is on the speakers bureau for Eli Lilly and Company, Endo Pharmaceuticals, Inc., and Forest Pharmaceuticals, Inc.
Copyright:
This record is sourced from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
PY - 2013/7
Y1 - 2013/7
N2 - This article aims to help primary care physicians negotiate gaps in current guidelines for postherpetic neuralgia (PHN). The objectives of this article are to: 1) briefly review the available guidelines and identify their strengths and weaknesses; 2) review the gaps in the guidelines; 3) review new data that were not included in the most recent guidelines; 4) provide expert opinion on how the new data and current guidelines can be used to make treatment decisions; and 5) review several important dimensions of care (eg, tolerability, dosing) and provide guidance. In general, all guidelines recognize the α2δ ligands, tricyclic antidepressants (TCAs), opioids, and tramadol as efficacious systemic options, with topical lidocaine serving as an efficacious nonsystemic approach for localized PHN treatment. The first-line treatment options typically recommended in the guidelines are α2δ ligands and TCAs, while opioids and tramadol are often recommended as second- or third-line options. Since the latest guidelines were published, newer agents (eg, topical capsaicin [8%] patch and gastroretentive gabapentin) have met the standard as first-line therapy with the publication of ≥ 1 randomized controlled trial. However, gabapentin enacarbil has not met this standard due to a lack of a published randomized controlled trial in PHN.
AB - This article aims to help primary care physicians negotiate gaps in current guidelines for postherpetic neuralgia (PHN). The objectives of this article are to: 1) briefly review the available guidelines and identify their strengths and weaknesses; 2) review the gaps in the guidelines; 3) review new data that were not included in the most recent guidelines; 4) provide expert opinion on how the new data and current guidelines can be used to make treatment decisions; and 5) review several important dimensions of care (eg, tolerability, dosing) and provide guidance. In general, all guidelines recognize the α2δ ligands, tricyclic antidepressants (TCAs), opioids, and tramadol as efficacious systemic options, with topical lidocaine serving as an efficacious nonsystemic approach for localized PHN treatment. The first-line treatment options typically recommended in the guidelines are α2δ ligands and TCAs, while opioids and tramadol are often recommended as second- or third-line options. Since the latest guidelines were published, newer agents (eg, topical capsaicin [8%] patch and gastroretentive gabapentin) have met the standard as first-line therapy with the publication of ≥ 1 randomized controlled trial. However, gabapentin enacarbil has not met this standard due to a lack of a published randomized controlled trial in PHN.
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U2 - 10.3810/pgm.2013.07.2690
DO - 10.3810/pgm.2013.07.2690
M3 - Review article
C2 - 23933906
AN - SCOPUS:84885943491
SN - 0891-5849
VL - 125
SP - 191
EP - 202
JO - Free Radical Biology and Medicine
JF - Free Radical Biology and Medicine
IS - 4
ER -