4.4 Article

The Pharmacological Therapy of Chronic Neuropathic Pain

Journal

DEUTSCHES ARZTEBLATT INTERNATIONAL
Volume 113, Issue 37, Pages 616-+

Publisher

DEUTSCHER AERZTE-VERLAG GMBH
DOI: 10.3238/arztebl.2016.0616

Keywords

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Funding

  1. Pfizer
  2. Grunenthal
  3. Astellas
  4. Mundipharma
  5. Genzyme
  6. Allergan
  7. Sanofi Pasteur
  8. Medtronic
  9. Eisai
  10. Lilly
  11. Boehringer Ingelheim
  12. Novartis
  13. Bristol Myers-Squibb
  14. Biogenidec
  15. AstraZeneca
  16. Merck
  17. Abbvie
  18. Daiichi Sankyo
  19. Glenmark Pharmaceuticals
  20. Seguris
  21. Teva
  22. Genentech
  23. Galapagos
  24. Desitin
  25. Teva Pharma
  26. Bayer-Schering MSD
  27. bioCSL

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Background: Chronic neuropathic pain, including painful peripheral polyneuropathy and post-herpetic neuralgia, affects 6.9-10% of the general population. Methods: In this article, we present current treatment recommendations on the basis of a selective review of the literature. Results: Neuropathic pain does not respond consistently to classic non-opioid analgesic drugs and is better treated with co-analgesic, antidepressant, and anticonvulsant drugs and topical agents. Under certain conditions, however, neuropathic pain can be treated with opioids, even chronically. It was concluded in a large-scale meta-analysis that tricyclic antidepressants, selective serotonin-norepinephrine reuptake inhibitors, and calcium-channel anticonvulsants are the drugs of first choice, with a number needed to treat (NNT) of 3.5-7.7 for a 50% reduction of pain. An analysis of all studies yielded an estimated publication bias of 10%. Treatment planning must include adequate consideration of the patient's age and comorbidities, concomitant medication, and potential side effects. Conclusion: Drugs are now chosen to treat neuropathic pain independently of the cause and symptoms of the pain. Topical agents are used only to treat peripheral neuropathy. The utility of a treatment approach based on the patient's symptoms and pathological mechanisms was recently demonstrated for the first time in a randomized trial. The goal of current research is to facilitate treatment planning on the basis of the clinical phenotype.

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