» Articles » PMID: 21695762

Painful Diabetic Peripheral Neuropathy: Consensus Recommendations on Diagnosis, Assessment and Management

Overview
Specialty Endocrinology
Date 2011 Jun 23
PMID 21695762
Citations 134
Authors
Affiliations
Soon will be listed here.
Abstract

Painful diabetic peripheral neuropathy (DPN) is common, is associated with significant reduction in quality of life and poses major treatment challenges to the practising physician. Although poor glucose control and cardiovascular risk factors have been proven to contribute to the aetiology of DPN, risk factors specific for painful DPN remain unknown. A number of instruments have been tested to assess the character, intensity and impact of painful DPN on quality of life, activities of daily living and mood. Management of the patient with DPN must be tailored to individual requirements, taking into consideration the co-morbidities and other factors. Pharmacological agents with proven efficacy for painful DPN include tricyclic anti-depressants, the selective serotonin and noradrenaline re-uptake inhibitors, anti-convulsants, opiates, membrane stabilizers, the anti-oxidant alpha-lipoic acid and topical agents including capsaicin. Current first-line therapies for painful DPN include tricyclic anti-depressants, the serotonin and noradrenaline re-uptake inhibitor duloxetine and the anti-convulsants pregabalin and gabapentin. When prescribing any of these agents, other co-morbidities and costs must be taken into account. Second-line approaches include the use of opiates such as synthetic opioid tramadol, morphine and oxycodone-controlled release. There is a limited literature with regard to combination treatment. In extreme cases of painful DPN unresponsive to pharmacotherapy, occasional use of electrical spinal cord stimulation might be indicated. There are a number of unmet needs in the therapeutic management of painful DPN. These include the need for randomized controlled trials with active comparators and data on the long-term efficacy of agents used, as most trials have lasted for less than 6 months. Finally, there is a need for appropriately designed studies to investigate non-pharmacological approaches.

Citing Articles

Correlation between Sirtuin 1 downregulation and reduced vitamin D receptor expression in patients with diabetic neuropathy.

Latini A, De Benedittis G, Morgante C, Gasperini B, DIppolito I, Lauro D Acta Diabetol. 2025; .

PMID: 39976627 DOI: 10.1007/s00592-025-02463-w.


Remote Monitoring of Chemotherapy-Induced Peripheral Neuropathy by the NeuroDetect iOS App: Observational Cohort Study of Patients With Cancer.

Chen C, Dorsch M, Alsomairy S, Griggs J, Jagsi R, Sabel M J Med Internet Res. 2025; 27:e65615.

PMID: 39908091 PMC: 11840369. DOI: 10.2196/65615.


E-52862-A selective sigma-1 receptor antagonist, in peripheral neuropathic pain: Two randomized, double-blind, phase 2 studies in patients with chronic postsurgical pain and painful diabetic neuropathy.

Galvez R, Mayoral V, Cebrecos J, Medel F, Morte A, Sust M Eur J Pain. 2024; 29(1).

PMID: 39629978 PMC: 11616472. DOI: 10.1002/ejp.4755.


Inter-trial Variation in the Sensitivity of Thermal Threshold Testing for the Diagnosis of Neuropathy in Type 2 Diabetes Mellitus.

Gaur A, Varatharajan S, Taranikanti M, John N, Kalpana M, Ganji V Int J Appl Basic Med Res. 2024; 14(3):182-186.

PMID: 39310082 PMC: 11412566. DOI: 10.4103/ijabmr.ijabmr_207_24.


Liquiritin ameliorates painful diabetic neuropathy in SD rats by inhibiting NLRP3-MMP-9-mediated reversal of aquaporin-4 polarity in the glymphatic system.

Jia S, Yin W, Xu W, Li J, Yan W, Lin J Front Pharmacol. 2024; 15:1436146.

PMID: 39295943 PMC: 11408323. DOI: 10.3389/fphar.2024.1436146.