Neurospine Search

CLOSE


Neurospine > Volume 15(3); 2018 > Article
Kim, Ryu, Moon, and Lee: Clinical Outcomes and Prognostic Factors in Patients With Myelopathy Caused by Thoracic Ossification of the Ligamentum Flavum

Abstract

Objective

The objective of this study was to investigate the surgical outcomes and prognostic factors for thoracic ossification of the ligamentum flavum (OLF) after decompressive laminectomy, focusing on the quantitative signal intensity ratio (SIR) of preoperative magnetic resonance imaging (MRI) and its prognostic significance.

Methods

We retrospectively reviewed 24 patients who previously underwent total laminectomy to remove OLF from 2010 to 2015. MRI and computed tomography were performed to detect OLF. The SIR between the regions of interest of high signal intensity lesions and the normal cord at the T1–2 disc levels was calculated. We divided patients into 2 groups based on the extent of the modified Japanese Orthopaedic Association (JOA) recovery rate (RR): good (RR ≥ 50%) and poor (RR < 50%).

Results

The mean preoperative and postoperative modified JOA scores for thoracic myelopathy were 6.67 ± 1.73 and 8.63 ± 1.81, respectively (p < 0.001). The preoperative JOA score (7.5 vs. 5.83, p = 0.028), postoperative JOA score (9.83 vs. 7.42, p = 0.000), and SIR (1.16 vs. 1.41, p = 0.009) were significantly different between the good and poor RR groups. A higher preoperative JOA score and lower SIR were associated with a good RR according to the JOA criteria.

Conclusion

The clinical outcomes for thoracic OLF after decompressive laminectomy were favorable. A higher RR was correlated with a lower SIR and higher preoperative modified JOA score. Therefore, a relatively low SIR on MRI and a relatively high preoperative JOA score could be positive prognostic indicators for the JOA RR in patients with thoracic OLF.

INTRODUCTION

Ossification of the ligamentum flavum (OLF) is a rare disease that is characterized by replacement of the ligamentum flavum with mature and hypertrophic lamina bone [1]. OLF is increasingly recognized as a major cause of acquired thoracic spinal canal stenosis, which frequently results in thoracic myelopathy [2,3].
The prevalence of OLF has been reported to vary from 3.8% to 26% in East Asia, particularly in countries such as China, Japan, and Korea [4-6]. Recently in Korea, the prevalence of thoracic OLF based on magnetic resonance imaging (MRI) has been reported to be 16.9% [7]. OLF frequently affects the lower thoracic spine, T9–12, and often leads to slowly progressive thoracic radiculomyelopathy [8]. Patients eventually visit clinics when their myelopathic symptoms become aggravated owing to severe spinal cord compression. Decompressive surgery is considered the best treatment option for patients with OLF with radiculomyelopathy [9,10]. Patients with thoracic OLF have various symptoms, such as sensory abnormality of the trunk or lower extremities, gait disturbance, and urinary dysfunction [8]. Although decompressive surgery is an available treatment option for this disease, the surgical outcome is not always satisfactory [3,11]. Furthermore, prognostic factors are still controversial and it is very difficult for the surgeon to predict postoperative recovery.
Signal intensity (SI) changes of the spinal cord on MRI reflect pathological changes in the spinal cord and are indicative of prognosis in cervical compressive myelopathy [12]. Many researchers have reported a correlation between clinical outcomes and SI changes in MRI [13,14]. Furthermore, a previous study evaluated the correlation between surgical outcomes and signal changes on MRI by measuring the signal intensity ratio (SIR) of the spinal cord and comparing the signal change at the lesion and the normal area [15]. Therefore, in this study, we evaluated clinical outcomes for the thoracic OLF after decompressive laminectomy and focused on the quantitative SIR of preoperative MRI and their prognostic significance.

MATERIALS AND METHODS

1. Patients and Surgical Procedure

Approval for the current study was granted by the Institutional Review Board of Chonnam National University Hospital (approval number: 2016-127). Informed consents were waived by our IRB because of retrospective study. All patients were diagnosed using thoracic MRI and computed tomography (CT) scans to detect thoracic OLF. A total of 49 patients (21 men and 28 women), who underwent decompressive total laminectomy and OLF removal at index level from January 2010 to December 2015, were included initially in this study; however, we excluded 14 patients who had simultaneous cervical or lumbar decompressive surgery owing to coexisting cord compression or thecal sac compression at another spinal segment. Of the remaining of 35 patients, we excluded 11 patients because of previous spinal surgery, experience of trauma, and spinal tumor. Therefore, a total of 24 consecutive patients with pure thoracic OLF were enrolled in this study. Distributions and types of thoracic OLF, the type of initial symptom, and preoperative symptom duration were evaluated.

2. Radiologic Assessment: SIR

All patients underwent high-resolution MRI using the MAGENTOM Trio 3.0T (Siemens, Erlangen, Germany) or Discovery MR750 3.0T (GE, Little Chalfont, England), T2-weighted sagittal and axial imaging of the thoracic spine. The SI values of the spinal cord on the sagittal view of T2-weighted image (T2WI) were obtained, and the regions of interest (ROI) at high SI lesion by OLF were taken as 4.98 mm2. The normal cord SI, as reference SI, at the T1–2 disc levels was obtained and the ROIs were taken as 4.98 mm2. The SIR between ROIs of high SI lesion and normal cord at the T1–2 disc levels was calculated (Fig. 1). If no high SI change was noted on T2WI, the ROIs were taken as 4.98 mm2 in the area of most severe compression of the cord. The SIR on T2WI was calculated by the following equation [16]:
SIR=(ROI of high SI lesion [4.98 mm2])/(reference ROI of the sagittal normal cord between T1–2 disc levels [4.98 mm2])
The types of the axial configuration of thoracic OLF by lateral, extended, and fused type were also evaluated [7,17].

3. Clinical Outcome Assessment

The modified Japanese Orthopaedic Association (JOA) scoring system was used to evaluate the neurological status of patients before and after surgical decompression, which excluded the sections regarding upper extremity function [10]. The maximum score of 11 indicates normal function, total score ≤3 was considered severe neurological impairment, 4–6 was moderate, and ≥7 was mild [18]. Postoperative improvement of symptoms was estimated on the basis of the recovery rate (RR)=(postoperative JOA score−preoperative JOA score)/(11−preoperative JOA score)×100%. A score of 75 to 100% was designated as excellent, 50% to 74% as good, 25% to 49% as fair and 0% to 24% as poor [18-20]. Therefore, the extent of recovery was defined by RR, with good (RR≥50%), poor (RR<50%).

4. Statistical Analysis

Since the number of subjects were less than 30, we used the nonparametric analysis methods. Wilcoxon signed rank test was used to figure out the significant pairwise change between preoperative and postoperative JOA scores. Mann-Whitney Utest and Fisher exact test were used to compare the difference between good and poor RR groups. Spearman correlation analysis was used to examine the relationship between age, symptom duration, pre- and postoperative JOA scores, SIR on T2WI, and JOA RR. We performed the multiple linear regression analysis using the input method.

RESULTS

A summary of patients’ demographics, clinical characteristics, and neurologic outcome score are shown in Table 1. All 24 participants (10 men and 14 women; mean age, 63.83 years; age range, 34–83 years) underwent 1- or 2-level total laminectomy and OLF removal. The duration of preoperative symptoms ranged from 1 to 84 weeks (mean, 15.25±22.84 weeks). After the surgical operation, the mean follow-up period was 29.7±15.15 months (range, 12–56 months). The overall mean preoperative and postoperative modified JOA scores for thoracic myelopathy were 6.67±1.73 and 8.63±1.81, respectively (p<0.001) in Fig. 2. Neurological outcomes for all patients with thoracic OLF improved to a mean of 50.45%±24.37%, based on the JOA RR. The initial symptoms were paraparesis (14 patients), hypesthesia or leg pain (9 patients), and bladder dysfunction (1 patient) in Fig. 3. There were 35 affected levels of OLF in total, and the primarily involved segments were T11–12 (n=11, 31.4%), T9–10 (n=10, 28.5%), and T10–11 (n=8, 22.8%) in Fig. 4. Of 24 patients assessed, 8 (33.3%) patients had multilevel OLF.

1. Comparison of Clinical and Radiological Data Between “Good” and “Poor” Groups Based on JOA RR

As above mentioned in the methods part, we divided patients into 2 groups based on the extent of JOA RR: good (RR ≥50%) and poor (RR<50%). Between good and poor groups, the preoperative JOA score (7.5 vs. 5.83, p=0.028), postoperative JOA score (9.83 vs. 7.42, p=0.000), and SIR (1.16 vs. 1.41, p=0.009) had significant differences (Table 2). There were no significant differences between groups in age (p=0.563), sex (p=0.680), symptom duration (p=0.770), ROI of high SI (p=0.795), and reference of ROI (p=0.298).

2. Relationship Among Variables Affecting JOA RRs

Table 3 shows the correlation among the independent variables, which included age, symptom duration, pre- and postoperative JOA score, SIR, ROI, reference ROI, and JOA RR. We found significant correlations between pre- and postoperative JOA score, SIR, and JOA RR. Furthermore, multiple linear regression analysis using input method showed that preoperative JOA, and SIR were the significant contributors for predicting the JOA RR (Table 4). Higher preoperative JOA score (B=5.949, β=0.424, p=0.03) and lower SIR (B=-9.699, β=-0.195, p=0.038) were affecting factors of increased JOA RR.

DISCUSSION

OLF is generally observed in the lower thoracic spine and frequently results in thoracic myelopathy. The lower thoracic region (T9–12) was involved in 82.7% of patients in this study. Surgical intervention is generally necessary for patients with symptomatic thoracic OLF. Decompressive surgery is recommended and should be performed if paralysis has developed. Posterior decompressive laminectomy and removal of the OLF is commonly supported because thoracic OLF compresses the dorsal spinal cord, and the surgical procedure provides wide decompression of the spinal canal [3]. In the present study, the JOA scores of all patients with thoracic OLF after decompressive resection improved from 6.67±1.73 to 8.63±1.81 and the mean JOA RR improved to 50.45%±24.37%. Therefore, posterior decompressive laminectomy provided satisfactory neurological improvement in patients with thoracic OLF, similar to other studies [3,8].
There are various clinical and radiological factors such as age, gender, duration of symptoms, preoperative JOA score, SI changes, and OLF type in predicting the postsurgical prognosis of patients with thoracic OLF [1,3,8,10,13,20]. However, it is also uncertain whether these factors are predictive of surgical outcome, as our findings are inconsistent with the results of previous studies.
OLF located in multiple segments and tandem ossification is common [7]. In our series, 33.3% of total patients have also multiple segments of OLF. Some reports have mentioned that their surgical outcomes were not always satisfactory after laminectomy if tandem ossification exists [7,20]. Therefore, we exclude the tandem ossification that might have any impact on recovery. No significant difference was observed in the correlation between other factors (age, gender, and duration of symptoms), similar to the other results [1,20]. However, a shorter duration of preoperative symptoms, a thoracic canal less affected by stenosis and the absence of proximal stenosis are correlated with a better postoperative neurological recovery [13,21]. In this study, duration of symptoms did not affect the JOA RR. This might be due to the insidious onset of clinical symptoms and hypesthesia in leg which might have confused the patient’s recognition and progression of symptoms associated with thoracic OLF [8].
Preoperative severity of myelopathy was considered as the most important predictor of the postoperative outcome [11,20]. In our results, the preoperative JOA scores correlated with RR in the correlation analysis. Multiple linear analysis of RR revealed that higher preoperative JOA score correlated with increased overall RR. These results are in agreement with those of previous studies evaluating the prognostic factors of thoracic OLF [11,20,21].
The SI changes on T2WI indicates local pathologic changes in the spinal cord, and patients with thoracic OLF and high-SI on T2WI usually have a poor prognosis even after surgical intervention [13,14,22]. The SI changes on T2WI were presumed to be myelomalacia or cord gliosis secondary to a long-standing compressive effect of the spinal cord [22]. However, the presence and grading of the SI change did not always correlate with prognosis [8,23]. Only SI change on MRI as a poor prognostic factor is controversial. In this study, we attempted to use disinterested quantitative data to investigate the relationship between signal intensities, clinical manifestations, and prognosis. With recent developments and advances in MRI techniques and software, we can quantify various signal intensities of the spinal cord using ROIs in these patients. Zhang et al. [18] reported that preoperative SIR on T2WI of MRI could be potentially useful for the prediction of surgical outcomes in patients with thoracic OLF. Results of the present study corresponded with the results of an earlier study, which reported low SIR as a prognostic factor correlated with high JOA RR. Furthermore, 2 previous studies reported that patients with preoperative SIR greater than or equal to 1.54 or 1.55 are likely to experience poor postoperative recovery [12,18]. In accordance with previous studies [12,18], mean SIR (1.41±0.23) was higher in the poor RR group than (1.16±0.17) in the good RR group (p=0.009) (Table 2). The SIR value in the poor RR group differs because the area of the ROIs and the levels at which they are measured are different in this study than in previous studies. It is difficult to constantly obtain 3.00 mm2 of ROIs, measured in previous studies, in picture archiving and communication system. Therefore, it is possible to increase the reliability of SIR by uniformly measuring 4.98 mm2 of ROIs, which is relatively easy to measure in the thoracic spinal cord. Thus, the normal cord SI as reference SI at the disc level of T1–2 was obtained, and the ROIs were taken as 4.98 mm2. The SIR between ROIs of high SI lesion and normal cord at the T1–2 disc level was calculated.
OLF morphology might affect recovery or preoperative neurological status. Kuh et al. [24] introduced the beak and round type classification system and considered intramedullary cord signal change with a beak type lesion to be a poor prognostic factor in 2 patients. However, Kang et al. [4] observed that localized compression of the spinal cord could be better corrected than compression of a round type OLF. In our study, we did not find any statistical correlation between RR and OLF type in accordance with previous studies [8,17,25].
This study has some limitations. This study is retrospective and nonrandomized. Additionally, the number of patients in this study were relatively small. Thoracic OLF is often associated with coexisting spinal disorders, such as ossification of posterior longitudinal ligament, disc herniation, canal stenosis or OLF at other spinal levels. Hence, patients with these coexisting conditions were excluded because they were reported to make the surgical decision more complicated and the surgical outcome more unpredictable. Further investigation on prognostic factors utilizing a larger sample size will be performed in the future.

CONCLUSION

Clinical outcomes for thoracic OLF after decompressive laminectomy is favorable. The increase in RR was correlated with lower SIR and higher preoperative modified JOA score. Therefore, lower SIR on MRI and higher preoperative JOA score could be a good predictable factor of increasing JOA recovery rate in thoracic OLF.

Fig. 1.
Radiologic measurement of signal intensity ratio on T2-wighted sagittal image of thoracic magnetic resonance imaging. Mean regions of interests were measured as 4.98 mm2 at the spinal cord of T1–2 disc level (upper circle) and intramedullary high signal change area (lower circle) of pathologic level.
ns-1836128-064f1.tif
Fig. 2.
The preoperative and postoperative modified Japanese Orthopaedics Association (JOA) score in total patients with thoracic ossification of the ligamentum flavum after decompressive laminectomy.
ns-1836128-064f2.tif
Fig. 3.
Initial symptoms in patients with thoracic ossification of the ligamentum flavum.
ns-1836128-064f3.tif
Fig. 4.
Distributions of involved levels in thoracic ossification of the ligamentum flavum (OLF).
ns-1836128-064f4.tif
Table 1.
Overall patients’ demographics (n=24)
Variable Value
Age (yr) 63.83 ± 13.23
Sex, male:female 10:14
Symptom duration (wk) 15.25 ± 22.84
Preoperative JOA 6.67 ± 1.73*
Postoperative JOA 8.63 ± 1.81*
Follow-up period (mo) 29.7 ± 15.15
JOA recovery rate (%) 50.45 ± 24.37
OLF type
 Lateral 4 (16.7)
 Extended 13 (54.2)
 Fused 7 (29.2)
 Tuberous 0 (0)
Presence of HSI 21 (87.5)

Values are presented as mean±standard deviation or number (%).

JOA, Japanese Orthopaedics Association; OLF, ossification of ligamentum flavum; HSI, high signal intensity.

* Statistical significant difference between preoperative JOA and postoperative JOA by Wilcoxon signed rank test (p<0.001).

Table 2.
Factors affecting Japanese Orthopaedics Association (JOA) recovery rate
Variable Good (RR ≥ 50%) Poor (RR < 50%) p-value
No. of patients 12 12
Age (yr) 62.42 ± 13.74 65.25 ± 13.15 0.563
Sex, male: female 6:6 4:8 0.680
Symptom duration (wk) 12.08 ± 23.58 18.41 ± 22.65 0.770
Preoperative JOA 7.50 ± 1.00 5.83 ± 1.946 0.028*
Postoperative JOA 9.83 ± 0.83 7.42 ± 1.73 0.000*
ROI of HSI 244.92 ± 93.17 248.42 ± 49.89 0.795
Ref. ROI 210.50 ± 81.57 177.75 ± 32.07 0.298
SIR 1.16 ± 0.17 1.41 ± 0.23 0.009*
OLF type 0.355
 Lateral 2 (16.7) 2 (16.7)
 Extended 5 (41.7) 8 (66.7)
 Fused 5 (41.7) 2 (16.7)
Presence of signal change 11 (91.7) 10 (83.3) 1.000

Values are presented as mean±standard deviation or number (%).

RR, recovery rate; OLF, ossification of ligamentum flavum; ROI, regions of interest; HSI, high signal intensity; Ref., reference; SIR, signal intensity ratio.

* Statistical significant difference between the 2 groups by Mann-Whitney U-test.

Table 3.
Correlation analysis on relationship between variables affecting JOA recovery rate
Variable Value Recovery rate Age Sx duration Preop JOA Postop JOA ROI Ref. ROI SIR Signal change
Recovery rate Coefficient 1
p-value
Age Coefficient -0.112 1
p-value 0.602
Sx duration Coefficient -0.021 0.094 1
p-value 0.923 0.664
Preop JOA Coefficient 0.498 -0.362 0.126 1
p-value 0.013* 0.082 0.559
Postop JOA Coefficient 0.849 -0.339 0.035 0.863 1
p-value 0.000* 0.105 0.870 0.000*
ROI Coefficient -0.019 -0.128 0.256 0.117 0.005 1
p-value 0.929 0.550 0.228 0.585 0.982
Ref. ROI Coefficient 0.264 -0.117 0.237 0.171 0.239 0.682 1
p-value 0.212 0.586 0.265 0.425 0.261 0.000*
SIR Coefficient -0.598 0.071 -0.547 -0.314 -0.547 0.437 -0.160 1
p-value 0.002* 0.742 0.006* 0.135 0.006* 0.033* 0.456
Signal change Coefficient 0.028 0.328 -0.543 -0.168 -0.056 -0.228 -0.118 -0.191 1
p-value 0.898 0.117 0.006* 0.432 0.793 0.285 0.582 0.371

Coefficient: Spearman correlation coefficient; Sx, symptom; preop, preoperative; postop, postoperative; JOA, Japanese Orthopaedics Association; OLF, ossification of ligamentum flavum; HSI, high signal intensity; ROI, regions of interest; Ref., reference; SIR, signal intensity ratio.

* Statistical significance between variables by Spearman correlation analysis satisfied with p<0.05.

Table 4.
Association of Japanese Orthopaedics Association (JOA) recovery rate and affecting variables by multiple linear regression analyses with input method
Variable Multiple linear regression analysis model (R2 = 0.941)
B SE β t p-value
Age -0.314 0.314 -0.170 -0.999 0.330
Sx duration 0.121 0.186 0.114 0.651 0.523
Preop JOA 5.949 2.533 0.424 2.349 0.030*
SIR -19.699 8.861 -0.195 -2.223 0.038*

Sx, symptom; preop, preoperative; SIR, signal intensity ratio; SE, standard error.

* Statistical significance by multiple linear regression analysis satisfied with p<0.05.

REFERENCES

1. Miyakoshi N, Shimada Y, Suzuki T, et al. Factors related to long-term outcome after decompressive surgery for ossification of the ligamentum flavum of the thoracic spine. J Neurosurg 2003;99(3 Suppl):251-6.
crossref pmid
2. Aizawa T, Sato T, Sasaki H, et al. Thoracic myelopathy caused by ossification of the ligamentum flavum: clinical features and surgical results in the Japanese population. J Neurosurg Spine 2006;5:514-9.
crossref pmid
3. Zhong ZM, Wu Q, Meng TT, et al. Clinical outcomes after decompressive laminectomy for symptomatic ossification of ligamentum flavum at the thoracic spine. J Clin Neurosci 2016;28:77-81.
crossref pmid
4. Kang KC, Lee CS, Shin SK, et al. Ossification of the ligamentum flavum of the thoracic spine in the Korean population. J Neurosurg Spine 2011;14:513-9.
crossref pmid
5. Mori K, Kasahara T, Mimura T, et al. Prevalence, distribution, and morphology of thoracic ossification of the yellow ligament in Japanese: results of CT-based cross-sectional study. Spine (Phila Pa 1976) 2013;38:E1216-22.
crossref pmid
6. Guo JJ, Luk KD, Karppinen J, et al. Prevalence, distribution, and morphology of ossification of the ligamentum flavum: a population study of one thousand seven hundred thirty-six magnetic resonance imaging scans. Spine (Phila Pa 1976) 2010;35:51-6.
crossref pmid
7. Moon BJ, Kuh SU, Kim S, et al. Prevalence, distribution, and significance of incidental thoracic ossification of the ligamentum flavum in Korean patients with back or leg pain: MR-based cross sectional study. J Korean Neurosurg Soc 2015;58:112-8.
crossref pmid pmc
8. Hur H, Lee JK, Lee JH, et al. Thoracic myelopathy caused by ossification of the ligamentum flavum. J Korean Neurosurg Soc 2009;46:189-94.
crossref pmid pmc
9. Sun J, Zhang C, Ning G, et al. Surgical strategies for ossified ligamentum flavum associated with dural ossification in thoracic spinal stenosis. J Clin Neurosci 2014;21:2102-6.
crossref pmid
10. Wang H, Wei F, Long H, et al. Surgical outcome of thoracic myelopathy caused by ossification of ligamentum flavum. J Clin Neurosci 2017;45:83-88.
crossref pmid
11. Onishi E, Yasuda T, Yamamoto H, et al. Outcomes of surgical treatment for thoracic myelopathy: a single-institutional study of 73 patients. Spine (Phila Pa 1976) 2016;41:E1356-63.
crossref pmid
12. Shin JJ, Jin BH, Kim KS, et al. Intramedullary high signal intensity and neurological status as prognostic factors in cervical spondylotic myelopathy. Acta Neurochir (Wien) 2010;152:1687-94.
crossref pmid
13. Sanghvi AV, Chhabra HS, Mascarenhas AA, et al. Thoracic myelopathy due to ossification of ligamentum flavum: a retrospective analysis of predictors of surgical outcome and factors affecting preoperative neurological status. Eur Spine J 2011;20:205-15.
crossref pmid
14. Wang LF, Liu FJ, Zhang YZ, et al. Clinical results and intramedullary signal changes of posterior decompression with transforaminal interbody fusion for thoracic myelopathy caused by combined ossification of the posterior longitudinal ligament and ligamentum flavum. Chin Med J (Engl) 2013;126:3822-7.
pmid
15. Wang LF, Zhang YZ, Shen Y, et al. Using the T2-weighted magnetic resonance imaging signal intensity ratio and clinical manifestations to assess the prognosis of patients with cervical ossification of the posterior longitudinal ligament. J Neurosurg Spine 2010;13:319-23.
crossref pmid
16. Zhang YZ, Shen Y, Wang LF, et al. Magnetic resonance T2 image signal intensity ratio and clinical manifestation predict prognosis after surgical intervention for cervical spondylotic myelopathy. Spine (Phila Pa 1976) 2010;35:E396-9.
crossref pmid
17. Yoon SH, Kim WH, Chung SB, et al. Clinical analysis of thoracic ossified ligamentum flavum without ventral compressive lesion. Eur Spine J 2011;20:216-23.
crossref pmid
18. Zhang J, Wang L, Li J, et al. Predictors of surgical outcome in thoracic ossification of the ligamentum flavum: focusing on the quantitative signal intensity. Sci Rep 2016;6:23019.
crossref pmid pmc pdf
19. Ando K, Imagama S, Wakao N, et al. Examination of the influence of ossification of the anterior longitudinal ligament on symptom progression and surgical outcome of ossification of the thoracic ligamentum flavum: a multicenter study. J Neurosurg Spine 2012;16:147-53.
crossref pmid
20. Yu S, Wu D, Li F, et al. Surgical results and prognostic factors for thoracic myelopathy caused by ossification of ligamentum flavum: posterior surgery by laminectomy. Acta Neurochir (Wien) 2013;155:1169-77.
crossref pmid
21. He S, Hussain N, Li S, et al. Clinical and prognostic analysis of ossified ligamentum flavum in a Chinese population. J Neurosurg Spine 2005;3:348-54.
crossref pmid
22. Karpova A, Arun R, Cadotte DW, et al. Assessment of spinal cord compression by magnetic resonance imaging--can it predict surgical outcomes in degenerative compressive myelopathy? A systematic review. Spine (Phila Pa 1976) 2013;38:1409-21.
crossref pmid
23. Kawaguchi Y, Yasuda T, Seki S, et al. Variables affecting postsurgical prognosis of thoracic myelopathy caused by ossification of the ligamentum flavum. Spine J 2013;13:1095-107.
crossref pmid
24. Kuh SU, Kim YS, Cho YE, et al. Contributing factors affecting the prognosis surgical outcome for thoracic OLF. Eur Spine J 2006;15:485-91.
crossref pmid
25. Li Z, Ren D, Zhao Y, et al. Clinical characteristics and surgical outcome of thoracic myelopathy caused by ossification of the ligamentum flavum: a retrospective analysis of 85 cases. Spinal Cord 2016;54:188-96.
crossref pmid pdf


Editorial Office
Department of Neurosurgery, Yonsei University College of Medicine
50-1, Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea
Tel: +82-2-2228-2172  E-mail: theneurospine@gmail.com
The Korean Spinal Neurosurgery Society
#407, Dong-A Villate 2nd Town, 350 Seocho-daero, Seocho-gu, Seoul 06631, Korea
Tel: +82-2-585-5455  Fax: +82-2-2-523-6812  E-mail: ksns1987@gmail.com
Business License No.: 209-82-62443

Copyright © The Korean Spinal Neurosurgery Society. All rights reserved.

Developed in M2community

Close layer
prev next