Table 1.
References | No. | Study | DBS target | Indication | FU | Outcome | SAE/AE |
---|---|---|---|---|---|---|---|
Invasive DBS (reversible) | |||||||
(Abdallat et al. 2021) [33] | 40 | PT | Unilateral VPM/VPL or CmPf alone | Facial pain | 63 months | Average pain relief 63 months > 50% in 10/18 patients | 11 hardware SAE |
CRPS | No differences between VPM/VPL and CmPf | ||||||
CPSP | |||||||
Spinal cord lesion | |||||||
Brachial plexus injury | |||||||
Postherpetic pain | |||||||
FBSS | |||||||
Nerve lesions | |||||||
Phantom limb | |||||||
(Ten Brinke et al. 2020) [51] | 1 | CR | Unilateral VS/ALIC | CPSP | NA | Mean pain relief at the end of observation (VAS): 50% | NA |
(Lempka et al. 2017) [12] | 10 | RCT | Bilateral VS/ALIC | CPSP | 24 months (6 months sham/verum + open-label phase 18 months) | Primary endpoint failure | Seizure (DBS “on”/“off”) |
Improvement in affective pain scores | |||||||
(Levi et al. 2019) [10] | 5 | PT | Bilateral ACC | Thalamic pain syndrome | 28 months | Mean pain relief 6 months (NRS): 37.9% | None |
Mean pain relief 18 months (VAS): 35% | |||||||
(Boccard et al. 2017) [43] | 22 | PT | Bilateral ACC | Neuropathic pain | 39 months | Mean pain relief 6 months (NRS): 60% | Seizure (DBS “on”/“off”) |
Mean pain relief 12 months (VAS): 43% |
DBS deep brain stimulation, PT pilot study, RCT randomized controlled trial, CR case report, VPL nucleus ventrolateralis of the thalamus, VPM nucleus ventromedialis of the thalamus, CmPf centromedian-parafascicular complex of the thalamus, PVG periventricular grey, PAG periaqueductal grey, VC ventrocaudal nucleus of the thalamus, PLIC posterior limb of the capsula interna, ACC anterior cingulate cortex, CRPS complex regional pain syndrome, CPSP chronic post-stroke pain, FBSS failed back surgery syndrome, VAS visual analogue scale, NRS numeric rating scale, FU follow-up, SAE/AE serious adverse event, NA not applicable