Table 1.
Basic characteristic | All implants (N = 955) |
---|---|
Age in years at implant | 53 [45–63] range 18–87 |
Female | 558 (58%) |
Male | 397 (42%) |
Indications for SCS | |
Prior spine surgery (FBSS/FNSS) | 700 (73%) |
CRPS type I or II | 60 (6%) |
Peripheral neuropathy | 130 (14%) |
Neuritis/Radiculitis | 17 (2%) |
Lumbosacral neuropathy with no prior surgery | 20 (2%) |
Radiculopathies | 42 (4%) |
Angina pectoris | 25 (3%) |
Abdominal, pelvic or cancer pain | 6 (1%) |
Peripheral vascular disease | 51 (5%) |
Predominant pain location | |
Low back and lower extremity | 599 (63%) |
Low back | 66 (7%) |
Lower extremity | 185 (19%) |
Upper extremity | 47 (5%) |
Thoracic | 33 (3%) |
Cervical | 42 (4%) |
Other | 23 (2%) |
Time from chronic pain diagnosis to implant (years) | 3.8 [1.0–8.4] |
First (de novo) SCS implant | 715 (75%) |
Trial performed | 568 of 715 (79%) |
Days from start of trial to permanent implant | 14 [10–31] |
One previous SCS pulse generator implant | 156 (16%) |
More than one previous SCS implant | 84 (9%) |
Type of SCS system | |
Conventional nonrechargeable | 462 (48%) |
Conventional rechargeable | 329 (34%) |
High‐frequency (10 kHz) rechargeable | 155 (16%) |
Other or not known | 9 (1%) |
One percutaneous lead | 615 (64%) |
Two percutaneous leads | 256 (27%) |
More than two percutaneous leads | 23 (3%) |
Paddle lead | 61 (6%) |
Lead 1 location | |
Cervical | 82 (9%) |
Upper thoracic (T1‐T5) | 15 (2%) |
Mid‐thoracic (T6‐T9) | 622 (67%) |
Lower thoracic (T10‐T12) | 171 (19%) |
Lumbar or sacral | 31 (3%) |
Note: Summary statistics are calculated on each implant. An individual subject may have more than one implant. Additionally, there may be more than one indication per implant.