2015
DOI: 10.1155/2015/173872
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Clinical Performance and Safety of 108 SpineJack Implantations: 1-Year Results of a Prospective Multicentre Single-Arm Registry Study

Abstract: This prospective, consecutive, multicentre observational registry aimed to confirm the safety and clinical performance of the SpineJack system for the treatment of vertebral compression fractures (VCF) of traumatic origin. We enrolled 103 patients (median age: 61.6 years) with 108 VCF due to trauma, or traumatic VCF with associated osteoporosis. Primary outcome was back pain intensity (VAS). Secondary outcomes were Oswestry Disability Index (ODI), EuroQol-VAS, and analgesic consumption. 48 hours after surgery,… Show more

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Cited by 46 publications
(49 citation statements)
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References 33 publications
(40 reference statements)
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“…A significant improvement in back pain has been reported with a mean VAS score decreasing from 6.6 AE 2.6 at baseline to 1.4 AE 1.3 within 48 hours posttreatment and a mean ODI score improvement at 3-month follow-up decreasing from 76.2 AE 20.0 at baseline to 14.2 AE 16.6. 28 Compared with BKP, the SpineJack system did not show any significant loss of intraoperative height gain with durable vertebral fracture reduction. It demonstrated an increased height restoration > 300% better than BKP.…”
Section: Resultsmentioning
confidence: 80%
See 1 more Smart Citation
“…A significant improvement in back pain has been reported with a mean VAS score decreasing from 6.6 AE 2.6 at baseline to 1.4 AE 1.3 within 48 hours posttreatment and a mean ODI score improvement at 3-month follow-up decreasing from 76.2 AE 20.0 at baseline to 14.2 AE 16.6. 28 Compared with BKP, the SpineJack system did not show any significant loss of intraoperative height gain with durable vertebral fracture reduction. It demonstrated an increased height restoration > 300% better than BKP.…”
Section: Resultsmentioning
confidence: 80%
“…SpineJack was designed for the anatomical reduction of vertebral compression fractures of traumatic origin (VCF type A1, A2, and A3 in Magerl's classification). 28,29 The device must always be implanted bilaterally in each hemisection of the vertebral body to obtain a symmetrical restoration of the end-plate level. As for VBS, implant technique, indications, and contraindications are similar.…”
Section: Spinejackmentioning
confidence: 99%
“…No additional new fracture was observed at 12-month follow up. These results are higher than those reported in the literature with different devices: With the use of VBS, the risk of adjacent vertebral fracture was 9% [26] and 3% with SpineJack [29]. In these studies, the cohorts of patients were similar and these were performed on osteoporotic subjects with spontaneous fractures or minor trauma in osteoporosis.…”
Section: Discussionmentioning
confidence: 89%
“…The decade following these two publications witnessed further expansion of their technique and the introduction of additional devices including balloon kyphoplasty (BKP), which was developed as a tool intended for fracture reduction and vertebral height restoration 7. More recently, innovation has resulted in the availability of vertebral body implant-based technology (instrumented kyphoplasty), biologic cements, and radiofrequency ablative technologies, permitting the treatment of a wider array of patients with more complex presentations including osteoporotic, traumatic, and neoplastic lesions 8–10…”
Section: Introductionmentioning
confidence: 99%