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https://hdl.handle.net/11055/1211
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DC Field | Value | Language |
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dc.contributor.author | Verrills P | en_US |
dc.contributor.author | Salmon J | en_US |
dc.contributor.author | Russo M | en_US |
dc.contributor.author | Gliner B | en_US |
dc.contributor.author | Barnard A | en_US |
dc.contributor.author | Caraway D | en_US |
dc.date | 2020-06-30 | - |
dc.date.accessioned | 2024-05-02T06:01:03Z | - |
dc.date.available | 2024-05-02T06:01:03Z | - |
dc.date.issued | 2020-11 | - |
dc.identifier.citation | 29(11):2786-2794. | en_US |
dc.identifier.issn | 0940-6719 | en_US |
dc.identifier.uri | https://hdl.handle.net/11055/1211 | - |
dc.description.abstract | Purpose: Intractable upper limb and neck pain has traditionally been a challenging pain condition to treat, with conventional spinal cord stimulation (SCS) often inducing positional variation in paraesthesia and/or inadequate coverage of axial neck pain. The purpose of this Australian multi-centre prospective, clinical trial was to assess the safety and effectiveness of paraesthesia-independent 10 kHz SCS for the treatment of upper limb and neck pain. Methods: Subjects with chronic, intractable neck and/or upper limb pain of ≥ 5 cm (on a 0-10-cm visual analogue scale) were enrolled (ACTRN12614000153617) following human research ethics committee approval. Subjects were implanted with two epidural leads spanning C2-C6 vertebral bodies. Subjects with successful trial stimulation were implanted with a Senza® system (Nevro Corp., Redwood City, CA, USA) and included in the safety and effectiveness evaluation at 3 months post-implant (primary endpoint assessment, PEA) and followed to 12 months. Results: Overall, 31/38 (82.6%) subjects reported a successful 10 kHz SCS trial and proceeded to a permanent implant. Twenty-three of 30 subjects (76.7%) met the PEA. Subjects reported a reduction in neck pain and upper limb pain from baseline at the PEA (8.1 ± 0.2 cm vs. 2.9 ± 0.5 cm, 7.3 ± 0.3 cm vs. 2.5 ± 0.5 cm, respectively, p ≤ 0.0001). Disability, as measured by pain disability index score, decreased from 42.6 ± 2.6 at baseline to 22.7 ± 3.2 at PEA. Results were maintained 12 months post-implant. No neurological deficits, nor reports of paraesthesia, were observed. Conclusions: Stable, long-term results demonstrated that 10 kHz SCS is a promising therapy option for intractable chronic upper limb and neck pain. | en_US |
dc.subject | 10 kHz SCS | en_US |
dc.subject | chronic neck pain | en_US |
dc.subject | chronic upper limb pain | en_US |
dc.subject | VAS | en_US |
dc.title | 10 kHz spinal cord stimulation for chronic upper limb and neck pain: Australian experience | en_US |
dc.type | Journal Article | en_US |
dc.type.content | Text | en_US |
dc.identifier.journaltitle | European Spine Journal: Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society | en_US |
dc.identifier.doi | 10.1007/s00586-020-06480-x | en_US |
dc.description.affiliates | Metro Pain Group, Clayton, VIC, Australia | en_US |
dc.description.affiliates | PainCare, Perth, WA, Australia | en_US |
dc.description.affiliates | Genesis Research Services, Broadmeadow, NSW, Australia | en_US |
dc.description.affiliates | Nevro Corp, Redwood City, CA, USA | en_US |
dc.description.pubmeduri | https://pubmed.ncbi.nlm.nih.gov/32607784/ | en_US |
dc.type.studyortrial | Clinical Trial | en_US |
dc.type.specialty | Pain Medicine | en_US |
dc.identifier.fulltextlink | https://link.springer.com/article/10.1007/s00586-020-06480-x | en_US |
item.cerifentitytype | Publications | - |
item.grantfulltext | restricted | - |
item.openairetype | Journal Article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.fulltext | With Fulltext | - |
Appears in Collections: | Scholarly and Clinical |
Files in This Item:
File | Description | Size | Format | |
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10 kHz SCS for chronic upper limb and neck pain- Australian experience.pdf Restricted Access | 1.62 MB | Adobe PDF | View/Open Request a copy |
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