Table 1.
Reference number | Year of publication | Comments | Type of stimulation | Number of patients | Number of patients with long-term pain relief |
---|---|---|---|---|---|
[2] | 2017 | stSCS | 46 | 32 | |
[14] | 2002 | SCS | 28 | 23 | |
[15] | 2012 | stSCS | 33 | 21 | |
[16] | 2011 | SCS | 11 | 4 | |
[17] | 2019 | DRG focus trial | DRGS | 4 | 3 |
[18] | 2019 | DRGS | 3 | 0 | |
[19] | 2029 | DRGS | 2 | 1 | |
[20] | 2021 | hfSCS | 1 | 1 | |
[21] | 2018 | hfSCS | 1 | 1 | |
[22] | 2021 | burstSCS | 1 | 1 | |
[23] | 2021 | DRGS | 3 | 3 | |
[13] | 2021 | SCS + DRGS | 1 | 1 | |
% Of patients with long-term pain relief | Affected dermatomes | Average pain reduction (%) | Follow-up, mo | Medication usage after stimulation | |
69.6 | T5-L5 | 50.7 | 6–12 | Reduction or discontinuation in 11 patients | |
82.1 | C3-S1 | 89 | 29 average | Discontinuation in 13 patients | |
63.6 | Cervical and thoracic | 49 | 6 | No patient required changes in drug doses | |
36.3 | C5-L2 | N/A | 34.5 | N/A | |
75 | N/A | 82.5 | N/A | N/A | |
0 | T1-L2 | 16,00 | 8 | No changes | |
50 | C8-T7 | 37.5 | 12 | N/A | |
100 | T2 | 90 | 7 days | N/A | |
100 | C4-T1 | 78 | N/A | Reduction of oxycodone usage | |
100 | T2 | 62.5 | 6 | Reduction in opioid dose | |
100 | T5-T10 | 60 | 18 | Reduction or discontinuation in all patients | |
100 | C6-T1 | 60 | 2 | Discontinuation of fentanyl usage |