Clinical Outcomes Following Minimally Invasive Sacroiliac Joint Fusion With Decortication: The EVoluSIon Clinical Study.

BACKGROUND: This report documents 1-year results of 250 patients enrolled in a prospective, multicenter study of a minimally invasive (MI) sacroiliac joint fusion (SIJF) system that uses decortication, graft placement, and joint fixation. METHODS: The cohort includes all patients enrolled in the EVoluSIon (EVSI) clinical study who had MI SIJF surgery and completed 1-year follow-up. Average age at baseline was 60.5 years, and 70.8% were female. Sacroiliac (SI) joint-related pain duration was ≥2 years in 56% of patients. Visual analog scale (VAS) SI joint pain, Oswestry Disability Index (ODI), quality of life, and opioid use were assessed preoperatively and at 1 year. RESULTS: At 1 year, the mean VAS pain demonstrated a significant reduction of more than 43 points, from 76.4 at baseline to 33.0 (P < 0.0001), with 72.2% of patients attaining the minimal clinically important difference (MCID, ≥20-point improvement). Mean ODI scores also significantly improved from 54.4 at baseline to 30.5 at 1 year (P < 0.0001), with 62.5% of patients achieving the MCID (≥15-point improvement). Prior to surgery, 62.7% (126/201) of patients were taking opioids or other narcotics, but by 1 year postsurgery, only 26.9% (54/201) of patients reported using these medications, representing a significant 57.1% decrease in narcotic/opioid use (P < 0.0001). Fusion of the SI joint was seen in 68.7% of patients. Few procedural complications were reported. In all, there were 8 (8/250) serious procedure-related events, including 1 device malposition observed on the day of surgery that required replacing the superior screw with a shorter screw. CONCLUSIONS: Analysis of patients treated with MI SIJF in the EVSI study demonstrated that the procedure can be performed safely and results in significant improvements in pain, quality of life, and opioid use at 1 year as well as causing fusion in the majority of patients. CLINICAL RELEVANCE: MI SIJF differs from most procedures currently being performed in that it applies true orthopedic principles with decorticating, bone grafting, fusion, and placement of implants perpendicular to the joint for greatest stability. The 12-month data show improvement in functionality, reduction in pain, and, most notably, a reduction in narcotic usage, which is important considering the ongoing opioid epidemic.

Pain and Opioid use Outcomes Following Minimally Invasive Sacroiliac Joint Fusion with Decortication and Bone Grafting: The Evolusion Clinical Trial.

PURPOSE: This report documents six-month results of the first 50 patients treated in a prospective, multi-center study of a minimally invasive (MI) sacroiliac (SI) joint fusion system. PATIENTS AND METHODS: This cohort includes 50 patients who had MI SI joint fusion surgery and completed 6 month follow-up. Average age at baseline was 61.5, 58% were female, and SI joint-related pain duration was ≥2yrs in 54.0% of patients. Visual Analog Scale (VAS) SI joint pain, Oswestry Disability Index (ODI), quality of life and opioid use were assessed preoperatively and at 6 months. RESULTS: At 6 months, mean VAS pain demonstrated a significant reduction from 76.2 at baseline to 35.1 (54% reduction, p<0.0001), with 72% of patients attaining the minimal clinically important difference (MCID, ≥20 point improvement). Mean ODI improved from 55.5 to 35.3 at 6 months (p < 0.001), with 56% of patients achieving the MCID (≥15 point improvement). Prior to surgery 33/50 (66%) of patients were taking opioids, but by 6 months the number of patients taking opioids had decreased by 55% to 15/50 (30%). Few procedural complications were reported. Two procedure-related events required hospitalization: a revision procedure (2%) for nerve impingement and one case of ongoing low back pain. CONCLUSION: Analysis of patients treated with MI SI joint fusion using the SImmetry System demonstrated that the procedure can be performed safely and results in significant improvements in pain, disability, and opioid use at 6 months. Longer term follow-up in this study will determine whether these improvements are durable, as well as the associated radiographic fusion rates.

Biomechanical evaluation of a metal-on-metal cervical intervertebral disc prosthesis.

BACKGROUND CONTEXT: In vitro nondestructive flexibility testing of the CerviCore total disc replacement (TDR) was performed. It was hypothesized that TDR would not significantly alter biomechanics relative to intact, whereas rigid fixation would cause significant changes. PURPOSE: To assess the ability of a cervical metal-on-metal saddle-shaped TDR to replicate normal biomechanics in vitro. STUDY DESIGN: Human cadaveric flexibility experiment. METHODS: Nine human cadaveric C3-T1 specimens were tested intact, after TDR and after anterior plating. Flexion, extension, lateral bending, and axial rotation were induced by pure moments; flexion-extension was then repeated using a simplified muscle force model with 70-N follower load. Optical markers measured three-dimensional intervertebral motion, and eight points of laminar surface strain were recorded near the left and right C5-C6 facet joints. Biomechanical parameters studied included range of motion (ROM), lax zone (LZ), angular coupling pattern, sagittal instantaneous axis of rotation (IAR), and facet loads normal to the facet joint plane. Mean values of parameters were compared statistically using repeated measures analysis of variance and Holm-Sidak tests. RESULTS: Total disc replacement caused significant reduction in ROM during extension (p=.004) and significant reduction in LZ during lateral bending (p=.01). However, plating significantly reduced both ROM and LZ during flexion, extension, and lateral bending (p<.006). Sagittal IAR shifted relative to intact by 3.6 mm after TDR (p>.05) and 6.5 mm after plating (p>.05). Coupled axial rotation/degree lateral bending was 99% of intact after TDR but 76% of intact after plating (p=.15). Coupled lateral bending/degree axial rotation was 95% of intact after TDR but 85% of intact after plating (p=.43). Neither construct altered facet loads from intact. CONCLUSIONS: With regard to ROM, LZ, IAR, and coupling, deviations from intact biomechanics were less substantial after TDR than after plating. Facet load alterations were minimal with either construct. Our results show that this particular TDR permits ROM and maintains some measures of kinematics in a cadaver model.

Carpal tunnel syndrome: "no-stitch endoscopic surgery" as a treatment option.

Carpal tunnel syndrome (CTS) is the most common nerve entrapment disorder causing considerable discomfort, activity limitations and even a change in occupation. Appropriate medical and surgical treatment can interrupt the progression of the syndrome and avoid permanent disability. We report here a case of a woman who was unable to work because of persistent CTS. Her disabling symptoms were completely resolved and she was able to return to work after a successful endoscopic carpal tunnel release.

Importance of the C1 anterior tubercle depth and lateral mass geometry when placing C1 lateral mass screws.

OBJECTIVE: We measured the variability in the size of the anterior tubercle of C1 and the optimal depth and angle of placement of C1 lateral mass screws using axial and sagittal reconstructed computed tomographic scans to determine the utility of these parameters for preoperative planning and intraoperative guidance. METHODS: One hundred consecutive cervical spine computed tomographic scans were reviewed (mean patient age, 44.6 years; age range, 7-96 years). The size of the anterior tubercle of C1, bilateral depths of optimal screw placement in the axial and sagittal planes, and optimal angles of placement in the axial and sagittal planes were measured in a standardized manner using the measuring tool included in our radiology server software. These measurements were correlated with age and sex. RESULTS: The mean depth of the C1 tubercle was 6.9 mm (range, 2.7-11.2 mm; standard deviation, 1.7 mm). The depth of the C1 tubercle tended to increase with age, but the relationship was not significant. The optimal screw depth in the sagittal plane was significantly greater than in the axial plane (right 2.09 versus 1.93 cm; left 2.07 versus 1.91 cm). The depth of the right lateral mass increased significantly with age. No other relationships reached significance. CONCLUSION: The depth of the anterior tubercle of C1 varies considerably and should be studied carefully before using lateral fluoroscopy of this structure to guide depth of C1 lateral mass screw placement. Optimal angles and depths of placement of C1 lateral mass screws vary widely and should be examined preoperatively to plan appropriate depth and trajectory.

Craniovertebral instability with spinal cord compression in a 17-month-old boy with Sly syndrome (mucopolysaccharidosis type VII): a surgical dilemma.

STUDY DESIGN: A case study with review of surgical technique in craniovertebral stabilization for young children with mucopolysaccharidosis. OBJECTIVES: To describe an interesting patient with a rare metabolic disorder and review surgical technique for craniovertebral instability in this rare patient population. SUMMARY OF BACKGROUND DATA: Craniovertebral instability has been reported in patients with mucopolysaccharidosis and poses a problem for spinal surgery because of the inherent metabolic disorder and age at presentation. We present the first case of craniovertebral instability and spinal cord compression occurring in Sly syndrome (mucopolysaccharidosis type VII) who is the youngest patient afflicted with this metabolic disorder to undergo craniovertebral stabilization. METHODS: A 17-month-old boy presented with inability to support his head, decreasing muscle strength in all extremities, distended abdomen, and shortness of breath. The patient was found to have a dilated cardiomyopathy, hepatosplenomegaly, abnormal hepatobiliary function, corneal clouding, and a questionable tracheal anomaly. Genetic testing provided a diagnosis of Sly syndrome, mucopolysaccharidosis type VII. Magnetic resonance imaging revealed focal stenosis with significant spinal cord compression at the craniovertebral junction. Neurologic examination revealed normal muscle volume with strength 3/5 in all extremities and significant weakness in the neck muscles with instability at the craniovertebral junction. RESULTS: On a concerted preoperative medical clearance by pediatric intensive care, pediatric neuroanesthesia, pediatric cardiology, pediatric gastroenterology, and pediatric neurosurgery, the patient underwent occipital to C3 decompression and fusion with autogenous rib grafts. The patient was placed in a prefitted halo-vest after surgery and was neurologically intact. CONCLUSIONS: This case demonstrates the heterogeneity of cervical spine deformities among the mucopolysaccharidosis syndromes and confirms the propensity for deposition of glycosaminoglycans at the craniovertebral junction. Further studies should investigate the etiology for this propensity of glycosaminoglycan deposition at the craniovertebral junction. We think that this case demonstrates that, with appropriate preoperative planning, these patients can undergo successful posterior cervical arthrodesis despite their age or metabolic defects.