Neuromodulation Therapy for Chemotherapy-Induced Peripheral Neuropathy: A Systematic Review.
Ryan Steven D'SouzaYeng F HerMax Y JinMahmoud MorsiAlaa Abd-ElsayedPublished in: Biomedicines (2022)
Chemotherapy-induced peripheral neuropathy (CIPN) is a debilitating and painful condition in patients who have received chemotherapy. The role of neuromodulation therapy in treating pain and improving neurological function in CIPN remains unclear and warrants evidence appraisal. In compliance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, we performed a systematic review to assess change in pain intensity and neurological function after implementation of any neuromodulation intervention for CIPN. Neuromodulation interventions consisted of dorsal column spinal cord stimulation (SCS), dorsal root ganglion stimulation (DRG-S), or peripheral nerve stimulation (PNS). In total, 15 studies utilized SCS (16 participants), 7 studies utilized DRG-S (7 participants), and 1 study utilized PNS (50 participants). Per the Grading of Recommendations, Assessment, Development, and Evaluations (GRADE) criteria, there was very low-quality GRADE evidence supporting that dorsal column SCS, DRG-S, and PNS are associated with a reduction in pain severity from CIPN. Results on changes in neurological function remained equivocal due to mixed study findings on thermal sensory thresholds and touch sensation or discrimination. Future prospective, well-powered, and comparative studies assessing neuromodulation for CIPN are warranted.
Keyphrases
- chemotherapy induced
- neuropathic pain
- spinal cord
- meta analyses
- chronic pain
- spinal cord injury
- systematic review
- pain management
- end stage renal disease
- randomized controlled trial
- chronic kidney disease
- ejection fraction
- stem cells
- physical activity
- case control
- newly diagnosed
- prognostic factors
- quality improvement
- clinical practice
- peritoneal dialysis
- squamous cell carcinoma
- high resolution
- mesenchymal stem cells
- bone marrow
- high intensity
- mass spectrometry
- locally advanced
- drug induced