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1.
Neurochirurgie ; 69(2): 101419, 2023 Mar.
Article in English | MEDLINE | ID: mdl-36754146

ABSTRACT

OBJECTIVES: To determine the incidence of sacroiliac joint (SIJ) pain after lumbosacral spinal fusion. BACKGROUND: Persistent low back pain is a potential source of disability and poor outcomes following lumbar spine fusion. The SIJ has been described as a potential source. However, there is a paucity of data concerning its importance. METHODS: This is a PROSPERO registered systematic review. A systematic search of the English literature was performed in Medline, Embase and Cochrane Library databases. MeSH terms such as Lumbar vertebrae, Sacrum, Spinal Fusion, Pain, Sacrum, Ligaments, Sacroiliac Joint were utilized for the search. Key words such as "sacroiliac dysfunction.mp." and "sacroiliac complex.mp." were utilized for the search. Two independent reviewers reviewed articles to determine eligibility for final review and analysis. The Newcastle-Ottawa Scale was used to appraise the quality of all nonrandomized observational studies. Inverse variance weighting with random effects was used to pool data. The GRADE approach, PRISMA workflow and checklists was performed. RESULTS: Twelve studies were included. All studies were observational and of moderate to low quality. The pooled incidence of sacroiliac joint pain was 15.8%. The pooled incidence of SIJ pain for patients without fusion extending to the sacrum was 15.8%. The pooled incidence of SIJ pain for patients with fusion extending to the sacrum was 32.9%. There was high heterogeneity. CONCLUSION: SIJ pain is a potential cause of persistent pain after lumbar spine surgery. The current literature of poor quality. Patients presenting with pain after lumbosacral spine fusion should be evaluated for SIJ related pain.


Subject(s)
Low Back Pain , Spinal Fusion , Humans , Spinal Fusion/adverse effects , Sacroiliac Joint/surgery , Incidence , Low Back Pain/epidemiology , Low Back Pain/etiology , Low Back Pain/surgery , Lumbar Vertebrae/surgery
3.
Neurochirurgie ; 68(3): 289-292, 2022 Apr.
Article in English | MEDLINE | ID: mdl-34995565

ABSTRACT

INTRODUCTION: The relationship between obesity and outcome of spine surgery has been controversial. The impact of obesity on surgical outcomes of patients undergoing long- segment (6 vertebrae or more) spinal fusion have not been studied. This study was designed to define the influence of obesity on the outcomes of patients undergoing long-segment spinal fusion. METHODS AND MATERIALS: A retrospective study of patients undergoing long-segment (6 vertebrae or more) spinal fusion was realized. Patients were divided into non-obese group and obese group. Variables such as blood loss, operative time, length of stay, complications, reoperation rates, and clinical outcome were compared between the two groups. RESULTS: Thirty-four non-obese patients (BMI: 26.43±0.87) and 27 obese ones (BMI: 35.35±1.81) were recruited. Number of fused levels in non-obese group was not significantly different from obese group (9.06±0.57 vertebrae vs 8.85±0.68 vertebrae, P=0.65). There was no significant difference between non-obese group and obese group in the blood loss during surgery (P= 0.12), the operating time (P=0.46) and the length of hospitalization (P=0.64). Similarly, no significant difference was found in surgical complications (P=0.76) and medical complications (P=0.82) between the two groups. The rate of ambulatory improvement is similar between non-obese group and obese group (P=0.64). CONCLUSION: Our study showed that there was no relationship between obesity and adverse surgical outcomes in ADS surgery with long-segment (6 vertebrae or more) spinal fusion.


Subject(s)
Scoliosis , Spinal Fusion , Adult , Humans , Lumbar Vertebrae/surgery , Obesity/complications , Obesity/surgery , Postoperative Complications/epidemiology , Postoperative Complications/etiology , Retrospective Studies , Scoliosis/complications , Scoliosis/surgery , Spinal Fusion/adverse effects , Spinal Fusion/methods , Treatment Outcome
4.
Neurochirurgie ; 67(4): 346-349, 2021 Jul.
Article in English | MEDLINE | ID: mdl-33757775

ABSTRACT

STUDY DESIGN: Retrospective analysis. OBJECTIVE: To define C2-C3 vertebral disc angle (VDA) in patients with and without cervical spondylotic myelopathy. SUMMARY OF BACKGROUND DATA: C2-C3 VDA is a new radiological index of cervical spine alignment. Recent studies have suggested that high postoperative values are associated with greater mechanical complications in patients with cervical spondylotic myelopathy. However, normative values for patients without myelopathy has yet to be defined. METHODS: Patients with and without cervical myelopathy between 2017 and 2019 were included. Inclusion criteria were patients above 18 years of age with antero-posterior (AP) and lateral (LAT) cervical X-rays. In the non-myelopathic group, patients were excluded if they had neurological symptoms or deficits, presence of cervical axial pain, previous spinal surgery, or diagnosis of either spondylolisthesis or scoliosis. In the myelopathic group, patients were excluded if they had previous spinal surgery. Radiological indices evaluated include: C2-C3 disc angle, C2-C7 Cobb angle, C7 sagittal vertical axis, T1 slope. RESULTS: In total, 99 patients without myelopathy and 22 patients with myelopathy were identified and analyzed. In patients without myelopathy, the mean for C2-C3 VDA was 25.9±7.9. For patients with myelopathy, preoperative values were 24.4±10.0 and 27.1±7.9 postoperatively. No statistically significant differences were found between patients with and without myelopathy. C2-C3 disc angle was not correlated with age (R=-0.173). CONCLUSION: This study did not find statistically significant differences in C2-C3 VDA values between patients with and without cervical myelopathy. This study provides normative data for C2-C3 vertebral disc angle in patients with and without cervical spondylotic myelopathy. Furthermore, C2-C3 vertebral disc angle may be independent from age.


Subject(s)
Cervical Vertebrae/diagnostic imaging , Intervertebral Disc/diagnostic imaging , Spinal Cord Diseases/diagnostic imaging , Spondylosis/diagnostic imaging , Adolescent , Adult , Aged , Aged, 80 and over , Cervical Vertebrae/surgery , Female , Humans , Intervertebral Disc/surgery , Male , Middle Aged , Neck Pain/diagnostic imaging , Neck Pain/surgery , Retrospective Studies , Spinal Cord Diseases/surgery , Spondylosis/surgery , Young Adult
5.
Neurochirurgie ; 67(2): 157-164, 2021 Apr.
Article in English | MEDLINE | ID: mdl-33450269

ABSTRACT

Fungal spondylodiscitis is rare (0.5%-1.6% of spondylodiscitis) and mainly caused by Candida albicans. Surgical intervention in spondylodiscitis patients is indicated for compression of neural elements, spinal instability, severe kyphosis, failure of conservative management and intractable pain. However, there is no evidence-based optimal surgical approach for spondylodiscitis. There have been only case reports of surgical treatment for Candida spondylodiscitis. We evaluated the preliminary results of the efficacy and safety of one-stage debridement via oblique lateral corridor with interbody fusion (OLIF) using stand-alone cement reconstruction after debridement for the treatment of Candida spondylodiscitis in patients with major co-morbidities. Five patients (4 males, 1 female, mean age: 64.2 years) suffering from Candida albicans lumbar spondylodiscitis who underwent this procedure were studied. Their predominant symptoms were unremitting back and leg pain and all had pre and postoperative anti-fungal therapy under microbiologist supervision. The operative time ranged from 137minutes to 260minutes (mean: 213.4minutes). The mean blood loss was 160mL (range: 100-200mL). There were no perioperative complications. At follow-up all showed major improvement in pain and ambulatory status. CT scan showed radiological stability for all patients at 6-12 months. Our preliminary results showed stand-alone anterior debridement and spinal re-construction with cement through mini-open OLIF approach might be a safe and effective option for patients with spinal fungal infection and major comorbidities.


Subject(s)
Anti-Bacterial Agents/administration & dosage , Bone Cements/therapeutic use , Candidiasis/surgery , Debridement/methods , Discitis/surgery , Lumbar Vertebrae/surgery , Aged , Candida albicans/isolation & purification , Candidiasis/diagnostic imaging , Comorbidity , Debridement/trends , Discitis/diagnostic imaging , Female , Follow-Up Studies , Humans , Lumbar Vertebrae/diagnostic imaging , Male , Middle Aged , Retrospective Studies , Treatment Outcome
6.
Neurochirurgie ; 66(2): 85-90, 2020 Apr.
Article in English | MEDLINE | ID: mdl-32197973

ABSTRACT

BACKGROUND: Multiple surgical techniques and approaches exist to obtain lumbar interbody fusion. Anterolateral (oblique) is a relatively recent technique. Controversy exists for its use at the L5-S1 level. We performed this study in order to show the safety and efficacy of this technique. The aim of this study was to report the long-term complications and fusion rates of minimally-open (mini-open) anterolateral interbody fusion at the L5-S1 level. METHODS: We retrospectively analyzed all patients who underwent mini-open anterolateral interbody fusion for L5-S1 level in our department. The data collected were the following: age, sex, surgical indication, acute (less than four weeks) and long-term complications (>3 months), fusion at six months and length of follow-up. RESULTS: Seventeen patients (8M/9F) underwent mini-open anterolateral interbody fusion at L5-S1. The mean age was 64.5 years. The surgical indication was scoliosis in 10 cases, flat back in 4 cases, and spondylolisthesis in 3 cases. All patients underwent a complementary posterior procedure that included fixation. Mean blood loss was 252.9mL for the anterior procedure. Eight acute and minor complications occurred (anemia, delirium, and psoas paresis). Two acute complications required surgical intervention (cage displacement and hematoma). Long-term complications were observed in 2 cases and included proximal junction kyphosis and non-union. The fusion rate was evaluated at 88%. The mean follow-up period was 28.3 months. CONCLUSIONS: Mini-open anterolateral interbody fusion at the L5-S1 level is safe and results in fusion at the same rate as anterior interbody fusion. Most acute complications are minor and resolve spontaneously.


Subject(s)
Postoperative Complications/therapy , Spinal Fusion/adverse effects , Adult , Blood Loss, Surgical , Female , Follow-Up Studies , Humans , Lumbosacral Region/surgery , Male , Postoperative Complications/diagnostic imaging , Postoperative Complications/surgery , Retrospective Studies , Treatment Outcome , Young Adult
7.
Orthop Traumatol Surg Res ; 103(2): 295-299, 2017 04.
Article in English | MEDLINE | ID: mdl-28089666

ABSTRACT

STUDY DESIGN: Technical description and single institution retrospective case series. OBJECTIVE: Evaluate technical feasibility and evaluate complications of mini-open retroperitoneal oblique lumbar interbody fusion (OLIF) at the L5-S1 level. SUMMARY OF BACKGROUND: The mini-open retroperitoneal oblique lumbar interbody fusion (OLIF) approach was first described in 2012 as a surgical approach to achieve spinal fusion while limiting invasiveness of the exposure to the anterior lumbar spine. Surgeons who use this approach, along with those who described it in cadaveric studies describe it as a feasible approach in targeting the L2 down to the L5 level and recommend alternative approaches to the L5-S1 level due to the vascular challenges and possible complications. METHODS: Technical description and single institution case series of patients treated with the OLIF between 2013 and 2015 at the L5-S1 level. The previously described surgical approach was modified by identifying and ligating the iliolumbar vein before retracting the iliac artery and vein anteriorly instead of passing between the vessels. RESULTS: Six patients (3 males, 3 females, mean age 62 years) were operated between 2013 and 2015. There were no vascular injuries or peripheral nerve trauma associated with the surgical procedure. Complications associated with the procedure included: cage displacement immediately postoperative requiring re-operation in one patient, transient psoas weakness in one patient, extended hospital stay for pain control in one patient, and transfusion was required in one patient. CONCLUSIONS: Mini-open retroperitoneal oblique lumbar interbody fusion is feasible at the L5-S1 level with limited vascular complications through a technical modification for safe mobilization of the iliac vessels by first ligating the iliolumbar vein.


Subject(s)
Diskectomy , Lumbar Vertebrae/surgery , Sacrum/surgery , Spinal Fusion/methods , Adult , Aged , Feasibility Studies , Female , Humans , Length of Stay , Male , Middle Aged , Muscle Weakness/etiology , Pain, Postoperative/drug therapy , Pain, Postoperative/etiology , Postoperative Period , Prosthesis Failure/etiology , Psoas Muscles/physiopathology , Reoperation , Retroperitoneal Space , Retrospective Studies , Spinal Fusion/adverse effects , Treatment Outcome
8.
Orthop Traumatol Surg Res ; 102(4): 525-7, 2016 06.
Article in English | MEDLINE | ID: mdl-26965645

ABSTRACT

The Morel-Lavallée lesion (MLL) is a rarely reported closed degloving injury, in which shearing forces have lead to break off subcutaneous tissues from the underlying fascia. Lumbar MLL have been rarely reported to date, explaining that patients are frequently misdiagnosed. While patients could be treated conservatively or with non-invasive procedures, delayed diagnosis may require open surgery for its cure. Indeed, untreated lesions can cause pain, infection or growing subcutaneous mass that can be confused with a soft tissue tumor. We report the clinical and radiological features of a 45-year old man with voluminous lumbar MLL initially misdiagnosed. We also reviewed the relevant English literature to summarize the diagnostic tools and the main therapeutic options.


Subject(s)
Soft Tissue Injuries/surgery , Subcutaneous Tissue/injuries , Humans , Lumbosacral Region , Magnetic Resonance Imaging , Male , Middle Aged , Soft Tissue Injuries/diagnostic imaging , Subcutaneous Tissue/diagnostic imaging , Ultrasonography
9.
Gynecol Oncol ; 83(2): 400-4, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11606104

ABSTRACT

BACKGROUND: Granulosa cell tumors (GCT) of the ovary generally have a good prognosis. Recurrences tend to be late and are usually abdominopelvic. Bone metastases are extremely rare. CASE: A case of recurrent GCT with vertebral metastasis is presented. Radiologic studies were helpful in documenting the presence of an invasive tumor destroying the vertebral body of T7. Bone scintigraphy excluded other metastatic sites. Diagnosis could not be established by CT-scan-directed fine-needle aspiration cytology or trocar biopsies. Since the lesion was isolated and resectable, aggressive surgery with complete tumoral excision was performed followed by local radiation therapy. Megestrol acetate was given as systemic treatment. CONCLUSION: Multiple treatments of GCT may alter the pattern of recurrence. Every symptom should be thoroughly evaluated. Bone metastases may be treated aggressively.


Subject(s)
Bone Neoplasms/metabolism , Granulosa Cell Tumor/secondary , Ovarian Neoplasms/pathology , Thoracic Vertebrae/pathology , Bone Neoplasms/therapy , Female , Granulosa Cell Tumor/pathology , Granulosa Cell Tumor/therapy , Humans , Middle Aged , Ovarian Neoplasms/therapy
10.
J Spinal Disord ; 12(3): 234-9, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10382777

ABSTRACT

The Universal Spine System (USS) pedicle hook design includes a fixation screw that passes obliquely in the anterocranial direction in the pedicle. The addition of the fixation screw was to address concerns with rotation of the hook and hook disengagement. This study was designed to evaluate the safety of the USS screw locked pedicle hook. Eleven cadaveric thoracic spines were instrumented posteriorly with USS pedicle hooks from T1 to T12. Spinal instrumentation was performed by a spinal surgeon experienced with the USS system. Spinal deformity was created prior to instrumentation, ranging from 0 to 55 degrees in the horizontal plane (rotation) and from 0 to 50 degrees in the frontal plane (scoliosis). Radiographs, computed tomography (CT), and segmental dissection were used for data acquisition. Morphometric CT analysis before instrumentation demonstrated that the transverse pedicular diameter was the smallest at T5 with a mean of 3.7 mm. The transverse pedicular angle (TPA) was found to always point toward the midline. The largest TPA was observed at T1 with a mean TPA of 28.4 degrees. The pedicle with the least angular deviation from the midline was T11 with a mean TPA of 7 degrees. Postinstrumentation CT analysis and segmental dissection revealed perforations of the pedicle cortex by the fixation screw in 15% of instrumented pedicles (26/172). There were 6 medial and 20 lateral perforations. Medial perforations occurred exclusively in the three most proximal spinal segments, whereas the lateral perforations occurred throughout the thoracic spine. The mean encroachment of the fixation screw was 1.67 mm medially and 1.95 mm laterally. This study demonstrates the variation in caliber and direction of the thoracic pedicles. Medial and lateral perforations of the pedicle can occur with the USS pedicle hook instrumented system.


Subject(s)
Internal Fixators , Spinal Fusion/instrumentation , Thoracic Vertebrae/surgery , Aged , Aged, 80 and over , Bone Screws , Cadaver , Female , Humans , Male , Middle Aged
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