R F M R Kersten1,2, F C Öner2, M P Arts3, M Mitroiu4, K C B Roes5, A de Gast1, S M van Gaalen1,6. 1. Department of Orthopedics, Clinical Orthopedic Research Center-midden Nederland (CORC-mN), Diakonessenhuis Utrecht/Zeist, The Netherlands. 2. Department of Orthopedics, 8124University Medical Center Utrecht, Utrecht University, The Netherlands. 3. Department of Neurosurgery, 2901Haaglanden Medical Center, the Hague, The Netherlands. 4. Department of Biostatistics and Research Support, Clinical Trial Methodology, 168086Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, The Netherlands. 5. Department of Health Evidence, Section Biostatistics, Radboud University Medical Center, Radboud University, The Netherlands. 6. Spinecenter.Amsterdam, Acibadem International Medical Center, Amsterdam, the Netherlands.
Abstract
STUDY DESIGN: Randomized controlled trial. OBJECTIVES: Lumbar interbody fusion with cages is performed to provide vertebral stability, restore alignment, and maintain disc and foraminal height. Polyetheretherketone (PEEK) is commonly used. Silicon nitride (Si3N4) is an alternative material with good osteointegrative properties. This study was designed to assess if Si3N4 cages perform similar to PEEK. METHODS: A non-inferiority double-blind multicenter RCT was designed. Patients presenting with chronic low-back pain with or without leg pain were included. Single- or double-level instrumented transforaminal lumbar interbody fusion (TLIF) using an oblique PEEK or Si3N4 cage was performed. The primary outcome was the Roland-Morris Disability Questionnaire (RMDQ). The non-inferiority margin for the RMDQ was 2.6 points on a scale of 24. Secondary outcomes included the Oswestry Disability Questionnaire (ODI), Visual Analogue Scales (VAS), SF-36 Physical Function, patient and surgeon Likert scores, radiographic evaluations for subsidence, segmental motion, and fusion. Follow-up was planned at 3, 6, 12, and 24-months. RESULTS: Ninety-two patients were randomized (i.e. 48 to PEEK and 44 to Si3N4). Both groups showed good clinical improvements on the RMDQ scores of up to 5-8 points during follow-up. No statistically significant differences were observed in clinical and radiographic outcomes. Mean operative time and blood loss were statistically significantly higher for the Si3N4 cohort. Although not statistically significant, there was a higher incidence of complications and revisions associated with the Si3N4 cage. CONCLUSIONS: There was insufficient evidence to conclude that Si3N4 was non-inferior to PEEK.
STUDY DESIGN: Randomized controlled trial. OBJECTIVES: Lumbar interbody fusion with cages is performed to provide vertebral stability, restore alignment, and maintain disc and foraminal height. Polyetheretherketone (PEEK) is commonly used. Silicon nitride (Si3N4) is an alternative material with good osteointegrative properties. This study was designed to assess if Si3N4 cages perform similar to PEEK. METHODS: A non-inferiority double-blind multicenter RCT was designed. Patients presenting with chronic low-back pain with or without leg pain were included. Single- or double-level instrumented transforaminal lumbar interbody fusion (TLIF) using an oblique PEEK or Si3N4 cage was performed. The primary outcome was the Roland-Morris Disability Questionnaire (RMDQ). The non-inferiority margin for the RMDQ was 2.6 points on a scale of 24. Secondary outcomes included the Oswestry Disability Questionnaire (ODI), Visual Analogue Scales (VAS), SF-36 Physical Function, patient and surgeon Likert scores, radiographic evaluations for subsidence, segmental motion, and fusion. Follow-up was planned at 3, 6, 12, and 24-months. RESULTS: Ninety-two patients were randomized (i.e. 48 to PEEK and 44 to Si3N4). Both groups showed good clinical improvements on the RMDQ scores of up to 5-8 points during follow-up. No statistically significant differences were observed in clinical and radiographic outcomes. Mean operative time and blood loss were statistically significantly higher for the Si3N4 cohort. Although not statistically significant, there was a higher incidence of complications and revisions associated with the Si3N4 cage. CONCLUSIONS: There was insufficient evidence to conclude that Si3N4 was non-inferior to PEEK.
Authors: Roel F M R Kersten; F Cumhur Öner; Mark P Arts; Marian Mitroiu; Kit C B Roes; Arthur de Gast; Steven M van Gaalen Journal: J Spine Surg Date: 2021-06