» Articles » PMID: 22606406

Sympathetic Blocks Provided Sustained Pain Relief in a Patient with Refractory Painful Diabetic Neuropathy

Overview
Publisher Wiley
Specialty Anesthesiology
Date 2012 May 19
PMID 22606406
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

The sympathetic nervous system has been implicated in pain associated with painful diabetic neuropathy. However, therapeutic intervention targeted at the sympathetic nervous system has not been established. We thus tested the hypothesis that sympathetic nerve blocks significantly reduce pain in a patient with painful diabetic neuropathy who has failed multiple pharmacological treatments. The diagnosis of small fiber sensory neuropathy was based on clinical presentations and confirmed by skin biopsies. A series of 9 lumbar sympathetic blocks over a 26-month period provided sustained pain relief in his legs. Additional thoracic paravertebral blocks further provided control of the pain in the trunk which can occasionally be seen in severe diabetic neuropathy cases, consequent to extensive involvement of the intercostal nerves. These blocks provided sustained and significant pain relief and improvement of quality of life over a period of more than two years. We thus provided the first clinical evidence supporting the notion that sympathetic nervous system plays a critical role in painful diabetic neuropathy and sympathetic blocks can be an effective management modality of painful diabetic neuropathy. We concluded that the sympathetic nervous system is a valuable therapeutic target of pharmacological and interventional modalities of treatments in painful diabetic neuropathy patients.

Citing Articles

Lumbar Sympathetic Block Leading to Increased Arterial Diameter and Blood Flow: A Mechanism of Therapeutic Benefit.

Dickey Z, Sharma N Cureus. 2024; 16(6):e61755.

PMID: 38975506 PMC: 11227424. DOI: 10.7759/cureus.61755.


A Systematic Guideline by the ASPN Workgroup on the Evidence, Education, and Treatment Algorithm for Painful Diabetic Neuropathy: SWEET.

Sayed D, Deer T, Hagedorn J, Sayed A, DSouza R, Lam C J Pain Res. 2024; 17:1461-1501.

PMID: 38633823 PMC: 11022879. DOI: 10.2147/JPR.S451006.


Use of Bioelectrical Impedance Analysis to Explore the Effectiveness of Stellate Ganglion Block in Patients with Post-Stroke Complex Regional Pain Syndrome: A Retrospective Pilot Study.

Ryu J, Hwang I, Lim S J Pers Med. 2024; 14(3).

PMID: 38541000 PMC: 10971433. DOI: 10.3390/jpm14030258.


Effective sympathetic nerve block for chemotherapy-induced peripheral neuropathy: a case report.

Kuroyanagi A, Inano C, Adachi J, Kaneko G, Toyokawa H Oxf Med Case Reports. 2024; 2024(2):omae006.

PMID: 38370507 PMC: 10873712. DOI: 10.1093/omcr/omae006.


Efficacy of the lumbar sympathetic ganglion block in lower limb pain and its application prospects during the perioperative period.

Zhang J, Deng Y, Geng M Ibrain. 2023; 8(4):442-452.

PMID: 37786587 PMC: 10529158. DOI: 10.1002/ibra.12069.


References
1.
Tesfaye S, Stevens L, Stephenson J, Fuller J, Plater M, Ionescu-Tirgoviste C . Prevalence of diabetic peripheral neuropathy and its relation to glycaemic control and potential risk factors: the EURODIAB IDDM Complications Study. Diabetologia. 1996; 39(11):1377-84. DOI: 10.1007/s001250050586. View

2.
Singleton J, Smith A, Bromberg M . Increased prevalence of impaired glucose tolerance in patients with painful sensory neuropathy. Diabetes Care. 2001; 24(8):1448-53. DOI: 10.2337/diacare.24.8.1448. View

3.
Devor M, Raber P . Corticosteroids suppress ectopic neural discharge originating in experimental neuromas. Pain. 1985; 22(2):127-137. DOI: 10.1016/0304-3959(85)90173-3. View

4.
McCarthy B, Hsieh S, STOCKS A, Hauer P, Macko C, Cornblath D . Cutaneous innervation in sensory neuropathies: evaluation by skin biopsy. Neurology. 1995; 45(10):1848-55. DOI: 10.1212/wnl.45.10.1848. View

5.
WALL P, Gutnick M . Ongoing activity in peripheral nerves: the physiology and pharmacology of impulses originating from a neuroma. Exp Neurol. 1974; 43(3):580-93. DOI: 10.1016/0014-4886(74)90197-6. View