4. Painful diabetic polyneuropathy

Author:

Zuidema Xander12,de Galan Bastiaan345,Brouwer Brigitte1,Cohen Steven P.6,Eldabe Sam7ORCID,Argoff Charles E.8,Huygen Frank910,Van Zundert Jan111ORCID

Affiliation:

1. Department of Anesthesiology and Pain Medicine Maastricht University Medical Centre Maastricht The Netherlands

2. Department of Anesthesiology and Pain Management Diakonessenhuis Utrecht/Zeist Utrecht The Netherlands

3. Division of Endocrinology, Department of Internal Medicine Maastricht University Medical Centre Maastricht The Netherlands

4. CARIM School for Cardiovascular Diseases Maastricht University Maastricht The Netherlands

5. Department of Internal Medicine Radboud University Medical Centre Nijmegen The Netherlands

6. Department of Anesthesiology, Pain Medicine Division Johns Hopkins School of Medicine Baltimore Maryland USA

7. Department of Pain Medicine and Anesthesiology Durham University Durham UK

8. Department of Neurology, New York University School of Medicine, and Pain Management Center North Shore University Hospital Manhasset New York USA

9. Department of Anesthesiology and Pain Management Erasmus Medical Centre Rotterdam The Netherlands

10. Department of Anesthesiology and Pain Management University Medical Center Utrecht Utrecht The Netherlands

11. Department of Anesthesiology, Intensive Care Emergency Medicine and Multidisciplinary Pain Center Ziekenhuis Oost‐Limburg Belgium

Abstract

AbstractIntroductionPain as a symptom of diabetic polyneuropathy (DPN) significantly lowers quality of life, increases mortality and is the main reason for patients with diabetes to seek medical attention. The number of people suffering from painful diabetic polyneuropathy (PDPN) has increased significantly over the past decades.MethodsThe literature on the diagnosis and treatment of diabetic polyneuropathy was retrieved and summarized.ResultsThe etiology of PDPN is complex, with primary damage to peripheral nociceptors and altered spinal and supra‐spinal modulation. To achieve better patient outcomes, the mode of diagnosis and treatment of PDPN evolves toward more precise pain‐phenotyping and genotyping based on patient‐specific characteristics, new diagnostic tools, and prior response to pharmacological treatments. According to the Toronto Diabetic Neuropathy Expert Group, a presumptive diagnosis of “probable PDPN” is sufficient to initiate treatment. Proper control of plasma glucose levels, and prevention of risk factors are essential in the treatment of PDPN. Mechanism‐based pharmacological treatment should be initiated as early as possible. If symptomatic pharmacologic treatment fails, spinal cord stimulation (SCS) should be considered. In isolated cases, where symptomatic pharmacologic treatment and SCS are unsuccessful or cannot be used, sympathetic lumbar chain neurolysis and/or radiofrequency ablation (SLCN/SLCRF), dorsal root ganglion stimulation (DRGs) or posterior tibial nerve stimulation (PTNS) may be considered. However, it is recommended that these treatments be applied only in a study setting in a center of expertise.ConclusionsThe diagnosis of PDPN evolves toward pheno‐and genotyping and treatment should be mechanism‐based.

Publisher

Wiley

Subject

Anesthesiology and Pain Medicine

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