Literature DB >> 29331977

Clinical outcomes and prognostic factors in patients with spinal dural arteriovenous fistulas : a prospective cohort study in two Chinese centres.

Yongjie Ma1,2, Sichang Chen1,2, Chao Peng1,2, Chunxiu Wang3, Guilin Li1,2, Chuan He1,2, Ming Ye1,2, Tao Hong1,2, Lisong Bian4, Jiang Liu4, Zhichao Wang4, Adnan I Qureshi5, Feng Ling1,2, Hongqi Zhang1,2.   

Abstract

BACKGROUND: The short-term outcomes and prognostic factors of patients with spinal dural arteriovenous fistulas (SDAVFs) have not been defined in large cohorts.
OBJECTIVE: To define the short-term clinical outcomes and prognostic factors in patients with SDAVFs.
METHODS: A prospective cohort of 112 patients with SDAVFs were included consecutively in this study. The patients were serially evaluated with the modified Aminoff and Logue's Scale (mALS) one day before surgery and at 3 months, 6 months and 12 months after treatment. Univariate and multivariate analyses were performed to identify demographic, clinical and procedural factors related to favourable outcome.
RESULTS: A total of 94 patients (mean age 53.5 years, 78 were men) met the criteria and are included in the final analyses. Duration of symptom ranged from 0.5 to 66 months (average time period of 12.7 months). The location of SDAVFs was as follows: 31.6% above T7 level, 48.4% between T7 and T12 level (including T7 and T12) and 20.0% below T12 level. A total of 81 patients (86.2%) underwent neurosurgical treatment, 10 patients (10.6%) underwent endovascular treatment, and 3 patients (3.2%) underwent neurosurgical treatment after unsuccessful embolisation. A total of 78 patients demonstrated an improvement in mALS score of one point or greater at 12 months. Preoperative mALS score was associated with clinical improvement after adjusting for age, gender, duration of symptoms, location of fistula and treatment modality using unconditional logistic regression analysis (p<0.05).
CONCLUSION: Approximately four fifths of the patients experienced clinical improvement at 12 months and preoperative mALS was the strongest predictor of clinical improvement in the cohort. © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

Entities:  

Keywords:  embolisation; neurosurgical treatment; outcome; prognostic factors; spinal dural arteriovenous fistula

Mesh:

Year:  2018        PMID: 29331977      PMCID: PMC5781161          DOI: 10.1136/bmjopen-2017-019800

Source DB:  PubMed          Journal:  BMJ Open        ISSN: 2044-6055            Impact factor:   2.692


The first prospective cohort study with a large sample size considering the incidence of spinal dural arteriovenous fistulas (SDAVFs). This study monitored a continuous change in spinal cord function post treatment. The modified Aminoff and Logue’s Scale focuses on motor and sphincter status. Validated quality of sensory function evaluation would be imperative. The study lacks imaging analysis For the time being, the study has been a short-term follow-up, while our long-term follow-up is still ongoing.

Introduction

Spinal dural arteriovenous fistulas (SDAVFs) are rare with an incidence of only 5–10 new cases per million persons per year.1 Neurosurgery and endovascular treatment are both effective options.2 According to a meta-analysis, 89% of patients showed improvement or stabilisation of symptoms after treatment.3 However, due to the low incidence rate of SDAVFs, previous studies that have been published reporting on the clinical outcome and prognostic factors of SDAVFs are limited due to small sample size and/or unstandardised outcome assessment due to their retrospective nature. In these studies, the preoperative severity of disability was identified to be the most important prognostic factor.4–7 Previous studies have demonstrated conflicting results regarding the relationship between age, gender and duration of symptoms prior to treatment and treatment outcome.4–8 In addition, small sample sizes of previous studies mean that they are unable to adequately address the relationship between angioarchitecture and location of the lesion, despite the recognition that lesions located in craniocervical and sacrococcygeal regions are more complex.9–12 Previous studies and meta-analyses have consistently identified the lack of standardised long-term follow-up data as a major limitation to better understanding of the natural history of SDAVFs. To address gaps in our understanding of SDAVFs, we conducted a prospective cohort study to evaluate the 1 year outcome of patients with cervical and thoracolumbar SDAVFs and identify the main prognostic factors.

Methods

Study design

We performed a prospective, longitudinal cohort study at two referral centres using the STROBE guideline.13 Both hospitals are the regional referral centres for SDAVFs and provide neurosurgical and endovascular treatments. This study was approved by the Institutional Ethics Committees at each site. Informed consent was obtained from each patient.

Participants and setting

We prospectively collected data on patients with SDAVFs located at the cervical and thoracolumbar regions, who underwent treatment at the two referral centres between March 2013 and December 2014 using a standard data collection form. All patients SDAVFs who were evaluated were considered for participation. Patients who had been previously treated with endovascular or surgical treatment, those with limb or sphincter dysfunction caused by other lesions, or those who refused treatment were excluded. The data were analysed by one of three designated investigators who did not participate in the treatment process. The treatment strategies (neurosurgery or endovascular) were decided by consensus after review by a team of experienced neurosurgeons and neuroradiologists.

Intervention

Spinal angiography was performed in all patients, including angiography of at least two segmental arteries above and below the target segmental artery bilaterally. Neurosurgical treatment was the preferred choice. All patients underwent hemilaminectomy in the location of the fistula followed by cauterisation. Indocyanine green angiography was used before and after coagulation to identify and confirm fistula obliteration between the arterial feeder and the draining vein. Endovascular treatment was considered for patients who were assessed as high risk of general anaesthesia, but did not have any arterial feeders from the radicular artery of Adamkiewicz. Embolisation was performed under local anaesthesia and a transfemoral approach was used. A Marathon 1.5-French microcatheter (ev3 Inc.) was used for selective catheterisation of the radiculomeningeal artery. Onyx (ev3 Inc.) was injected thorough the microcatheter as close as possible to the fistula until the proximal part of the draining vein was obliterated. However, if endovascular treatment was unsuccessful in achieving obliteration of SDAVFs, neurosurgical treatment was performed.

Data collection

Clinical data including age, gender, duration of symptoms, location of fistula, spinal functional status and treatment methods were collected. The onset of symptoms was considered to be when neurological deficits (gait disturbances, paresthesia, diffuse or patchy sensory loss, and bowel or bladder incontinence) were first noticed. We also recorded the time interval between symptom onset and treatment. The images of pre-procedure spinal angiogram were reviewed by one of two senior authors to identify the location of SDAVFs. The functional status of the patients was assessed using the modified Aminoff and Logue’s Scale (mALS, which grades gait, urinary incontinence and faecal continence/constipation, table 1) one  day before the procedure, and at 3, 6 and 12 months post procedure.14 An effort was made to perform spinal angiography and MRI during the follow-up period when feasible.
Table 1

Modified Aminoff and Logue’s Scale

Gait (G)
0Normal leg power, stance and gait
1Leg weakness with no restriction of walking
2Restricted exercise tolerance
3Requires one stick or some support for walking
4Requires crutches or two sticks for walking
5Requires a wheelchair
Modified Aminoff and Logue’s Scale

Bias

Loss to follow-up might bias the results. Nine patients were lost to follow-up; the follow-up rate was 87.4% and those lost to follow-up and those followed-up at 12 months had similar baseline demographics and characteristics (online supplementary file). Therefore, recall bias might affect data entry, but this was minimised by ensuring that data were entered in a timely fashion.

Statistical analysis

Formal sample size calculations were not performed. All data were descriptively presented using mean ±SD for continuous data and frequencies for categorical data. Paired t tests (with adjustment for multiple comparisons) were used to assess differences in means for the cohort between baseline and different follow-up time points. Pearson χ2 tests were used to find factors associated with preoperative status. Pearson χ2 tests and unconditional logistic regression were used to identify factors affecting clinical improvement at 12 months. Clinical improvement was defined as a decrease of at least one point on the mALS compared with baseline assessment at 12 months. In the multivariate model, age (<=55 y or >55 y), gender (men/women), time interval between symptom onset and treatment (≤6 months, >6 months and ≤12 months or >12 months), location (above T7, T7–T12 or below T12), treatment performed (neurosurgical treatment, endovascular treatment or both), and preoperative mALS were entered. The preoperative mALS was classified as follows: a total score of 0–3 indicated a mild disability, a score of 4–7 a moderate disability and a score of 8–11 a severe disability. Clinical improvement was entered as the dichotomous dependent variable. Interactions were tested in the model. The OR and 95% CI were determined for significant variables in the model. All analyses were performed under the conduct of the epidemiologist using SPSS software (version 21, IBM Corp., Armonk, New York, USA).

Results

Patient population

The baseline demographic characteristics of these 94 patients are presented in table 2. A total of 112 patients were screened for inclusion in the study; 18 patients were excluded (figure 1) due to previous history of treatment for the fistula (n=5, three underwent surgery and two underwent embolisation); with other lesions that induced neurological deficits (n=4); nine patients were lost to follow-up (two died due to unrelated events, lung cancer and intracranial haemorrhage, and seven were not accessible).
Table 2

Baseline demographics and characteristics of patients with SDAVFs*

CharacteristicsNumber (%)
Age at treatment, average (SD), years53.5 (10.7)
Men, n (%)78 (83.0)
Time interval between symptoms and treatment, average (SD), months12.7 (12.8)
 ≤6 months, n (%)37 (39.4)
 6–12 m, n (%)28 (29.8)
 >12 m, n (%)29 (30.8)
Location of the fistula, n (%)
 Above T730 (31.6%)
 T7–T1246 (48.4%)
 Below T1219 (20.0%)
Treatment method, n (%)
 Neurosurgery81 (86.2%)
 Endovascular10 (10.6%)
 Combination3 (3.2%)
Preoperative mALS, n (%)
 G score
  05 (5.3%)
  19 (9.6%)
  239 (41.5%)
  318 (19.1%)
  48 (8.5%)
  515 (16.0%)
  average (SD)2.6 (1.4)
 U score
  011 (11.7%)
  141 (43.6%)
  225 (26.6%)
  317 (18.1%)
  average (SD)1.5 (0.9)
 F score
  08 (8.5%)
  157 (60.6%)
  224 (25.5%)
  35 (5.4%)
  average (SD)1.3 (0.7)

*patient with two fistulas (T8, T10).

F, faeces; G, gait; mALS, modified Aminoff and Logue’s Scale; SDAVF, spinal dural arteriovenous fistula; T, thoracic; U, urination.

Figure 1

Flow diagram demonstrating inclusion and exclusion of screened patients. SDAVF, spinal dural arteriovenous fistula.

Baseline demographics and characteristics of patients with SDAVFs* *patient with two fistulas (T8, T10). F, faeces; G, gait; mALS, modified Aminoff and Logue’s Scale; SDAVF, spinal dural arteriovenous fistula; T, thoracic; U, urination. Flow diagram demonstrating inclusion and exclusion of screened patientsSDAVF, spinal dural arteriovenous fistula. A total of 94 patients were included (mean age 53.5±10.7 years; 78 were men) with 95 SDAVFs. The mean time interval between symptom onset and procedure was 12.7 months (range 0.5–66 months). The most common location for SDAVFs was lower thoracic (T7–12, 48.4%). Before treatment, the patients presented with median mALS of 5 (range 0–11), the median G score was 2 (range 0–5), U score was 1 (range 0–3) and F score was 1 (range 0–3). A total of 81 patients (86.2%) underwent neurosurgical treatment, 10 patients (10.6%) underwent endovascular treatment, and three patients (3.2%) underwent neurosurgical treatment after unsuccessful endovascular treatment. In one patient, the fistula was obliterated after first embolisation, but required neurosurgery for recurrence demonstrated on 8-month follow-up angiography.

Clinical outcome

The pattern of change in mALS scores at 3, 6 and 12 months post treatment is presented in figure 2. There was improvement in mALS scores at all time points compared with baseline mALS scores. The highest improvement in mALS scores was seen between baseline and 3 months post treatment evaluation. However, the differences between the two adjacent follow-up time points were significant (p<0.05), except the change of F score between 3 months and 6 months (p=0.09). At 1 year follow-up, 78 patients (83.0%) experienced improvement of their mALS, 70 patients (74.5%) experienced improvement of the gait disability, 55 patients (58.5%) experienced improvement of the urination function and only 41 patients (43.6%) experienced improvement of defecation function. In addition, 10 of the 18 patients (55.6%) with mild disability showed improvement, in 43 of the 60 patients (71.7%) with moderate disability the level decreased to mild, in 4 of the 16 patients (25.0%) with severe disability the level decreased to mild, while in 9 patients (56.2%) the level decreased to moderate. For patients with a motor score of 5, only 40% were able to ambulate independently at 1 year.
Figure 2

Change in modified Aminoff and Logue’s Scale (mALS) (A), gait (G) score (B), urine (U) score (C) and faeces (F) score (D) before and after surgery in patients with spinal dural arteriovenous fistula (SDAVFs) (mean and 95% CIs).

Change in modified Aminoff and Logue’s Scale (mALS) (A), gait (G) score (B), urine (U) score (C) and faeces (F) score (D) before and after surgery in patients with spinal dural arteriovenous fistula (SDAVFs) (mean and 95% CIs).

Prognostic factors

The preprocedural mALS was found to be related to the clinical improvement at 1 year. In the logistic regression model, a preprocedural mALS score of 4–7 (OR 8.98, 95% CI 2.1 to 38.4) and score of 8–11 (OR 20.8, 95% CI 1.6 to 269.2) were associated with higher rates of clinical improvement at 1 year. There was a trend towards an inverse relationship between age (when entered as a continuous variable) and higher rate of clinical improvement (OR 0.26, 95% CI 0.06 to 1.1). The duration of symptoms, location of fistula, and treatment method used were not related to the outcome (table 3).
Table 3

Factors associated with clinical improvement at 1 year: univariate and multivariate analysis

VariablePatients with improvement, n (%)Patients without improvement, n (%)Univariate modelMultivariate model
χ2 p ValueOR (95% CI)p Value
Age0.7340.3920.264 (0.064 to 1.084)0.065
 ≤55 years48 (85.7%)8 (14.3%)
 >55 years30 (78.9%)8 (21.1%)
Gender0.0001.0000.963 (0.174 to 5.314)0.965
 Men65 (83.3%)13 (16.7%)
 Women13 (81.3%)3 (18.8%)
Time interval between symptom onset and treatment2.0640.3560.374
 ≤6 months33 (89.2%)4 (10.8%)Reference
 6–12 months23 (82.1%)5 (17.9%)0.520 (0.093 to 2.925)0.458
 >12 months22 (75.9%)7 (24.1%)0.327 (0.068 to 1.562)0.161
Location of the fistula2.9770.2260.389
 Above T722 (73.3%)8 (26.7%)Reference
 T7–T1239 (86.7%)6 (13.3%)2.396 (0.571 to 10.049)0.232
 Below T1217 (89.5%)2 (10.5%)3.605 (0.377 to 37.427)0.265
Treatment method0.9180.6320.303
Neurosurgery67 (82.7%)14 (17.3%)Reference
Endovascular9 (90.0%)1 (10.0%)0.626 (0.045 to 8.649)0.726
Combination2 (66.7%)1 (33.3%)0.105 (0.006 to 1.831)0.122
Preoperative mALS12.1160.0020.006
 0–310 (55.6%)8 (44.4%)Reference
 4–753 (88.3%)7 (11.7%)8.983 (2.104 to 38.357)0.003
 8–1115 (93.8%)1 (6.3%)20.792 (1.606 to 269.164)0.020

mALS, modified Aminoff and Logue’s Scale; T, thoracic.

Factors associated with clinical improvement at 1 year: univariate and multivariate analysis mALS, modified Aminoff and Logue’s Scale; T, thoracic.

Discussion

Our study provides the pattern of recovery and prognostic factors using a large patient cohort with SDAVFs using prospective standardised evaluation.

Outcome of patients with SDAVFs

In an analysis of a large cohort study of surgically treated patients with myelopathy from SDAVFs, continuous improvement after hospital discharge was confirmed, and the process lasted a long time. Approximately 97% of patients experienced improvement (82.2%) or stabilisation (14.4%) of their motor symptoms, while the sphincter dysfunction improved after surgery in 45% of patients.15 16 We obtained similar results in this study; at 1-year follow-up, the percentage of patients who experienced improvement in their motor symptoms was 74.5%, and stabilisation was 22.3%. Only 58.5% of patients experienced recovery of their urination function, and in terms of defecation function, the percentage was 43.6%. We also confirmed the recovery would continue for a long period after the operation, but improvements in the first 3 months were more obvious. This may suggest early rehabilitation exercises. As we found in this study, age, sex, duration of symptom and location of fistula were not directly correlated to the postoperative outcome. Nagata et al suggested that outcome was better in younger patients6; however, in our cohort, younger age (≤55 years) did not correlate with improved clinical outcome at 1-year follow-up. Moreover, no correlation was found between duration of symptoms and short-term outcome; this was also found in various studies.4 6 8 17 Cenzato et al found that location of fistula could predict outcome; patients with a fistula between T9 and T12 improved more than those with a fistula elsewhere.5 8 In our results, most of the fistulas were located between T7 and T12; no association was found between clinical improvement and level of fistula. Besides, lower cervical SDAVFs are extremely rare.18 In our study, only one case located at the C5 level presented with congestive venous oedema at the thoracic cord. We also included a patient with double SDAVFs, which is also extremely rare.19 The two fistulas were separate; one was at T8 on the right and one at T10 on the left, the venous drainage was also separate. Regardless of the therapeutic method of choice, the primary goal of SDAVF treatment must be the interruption of the fistula. A meta-analysis has been performed showing an advantage of primary surgical treatment of SDAVFs over endovascular treatment in terms of initial fistula closure and fistula recurrence. In 2004, Steinmetz et al reported a success rate of 46% in the endovascular group,3 while in 2015, Bakker et al found the proportion to be 72.2%.20 This may reflect the advancement in endovascular techniques that has been made over the last decade. In this study, there were a total of 13 patients undergoing embolisation: 10 patients had obliteration, two patients not cured with embolisation were treated with microsurgery, and one patient experienced delayed recurrence at 8-month angiography. So the success rate of endovascular treatment in our study was 76.9%. As presented previously, either microsurgery occlusion or endovascular embolisation did not show statistical significance with regards to outcome. Complications were considered; at 3-month follow-up, nine patients who underwent neurosurgery experienced worsening of their mALS, and one patient who we lost to follow-up experienced surgical site infection. Venous thrombosis might be considered to cause aggravation, while anticoagulation therapy cannot be administrated during the early postoperative period. Prophylactic anticoagulation was suggested for patients who experienced secondary clinical deterioration after successful embolisation.21 This is the advantage of endovascular treatment. It seems to be widely recognised that preoperative functional status had an impact on clinical outcome,5 6 17 while one other study came to a different conclusion.3 Our results confirm that preoperative mALS was associated with functional outcome. Patients with more severe deficits before surgery were more likely to show improvement. Besides, in our cohort, we also found that age, gender, duration of symptoms and location of fistula were not correlated with preoperative mALS. It seems that longer duration may result in worse symptoms, but patients with SDAVFs could experience acute neurological deterioration,22 and also could be asymptomatic.23 Moreover, acute paraplegia could be induced by corticosteroid administration in misdiagnosed patients and could also be exacerbated by hydrostatic forces resulting from erect posture, abnormal compression, and the Valsalva manoeuvre.24 25 It is widely recognised that the pathophysiology of SDAVFs is chronic hypoxia and progressive myelopathy induced by venous hypertension.26 The acute aggravation showed that the change of blood flow in shunting cross the SDAVF or rapid infusion of saline solution could also be physiological factors affecting the disease course.27 SDAVFs are really rare diseases. Our prospective cohort recruited 94 consecutive patients; we hope to have presented generalisable results. The participants were from different provinces in China, and the inclusion criteria were set without age and gender limitations. Given the large series size and consecutive participants, we were able to reveal a result that was closer to the real situation.

Limitations

This study has some limitations. First, the investigator analyses the spinal function based on mALS which focuses only on motor and sphincter status. Validated quality of sensory function evaluation would be imperative. Second, the study lacks imaging analysis. The imaging features on MRI have been studied. Patients with enlarged draining veins (>10 spinal levels) had worse mALS scores, and more extensive draining veins were associated with more spinal cord T2 hyperintensity,28 and the extent of the hyperintensity area was relevant to preoperative neurological deficits.29 But the T2 signal abnormality of the spinal cord was not associated with clinical outcome.2 30 Finally, this is a short-term follow-up; long-term follow-up is ongoing.

Conclusion

This prospective cohort study shows that preoperative mALS is related to outcome in patients with SDAVFs. Most patients can recover after interruption of the fistula either by microsurgery or endovascular treatment, especially during the first 3 months during which the recovery is more obvious.
  30 in total

1.  Spinal dural arteriovenous fistulas: outcome and prognostic factors.

Authors:  Marco Cenzato; Alberto Debernardi; Roberto Stefini; Giuseppe D'Aliberti; Maurizio Piparo; Giuseppe Talamonti; Matteo Coppini; Pietro Versari
Journal:  Neurosurg Focus       Date:  2012-05       Impact factor: 4.047

2.  Factors that affect the surgical outcomes of spinal dural arteriovenous fistulas.

Authors:  Shinji Nagata; Takato Morioka; Yoshihiro Natori; Koichiro Matsukado; Tomio Sasaki; Tomomi Yamada
Journal:  Surg Neurol       Date:  2006-06

3.  Acute paraparesis following intravenous steroid therapy in a case of dural spinal arteriovenous fistula.

Authors:  Macarena Cabrera; Carmen Paradas; Celedonio Márquez; Alejandro González
Journal:  J Neurol       Date:  2008-09-03       Impact factor: 4.849

4.  Asymptomatic spinal dural arteriovenous fistulas: pathomechanical considerations.

Authors:  Kenichi Sato; Karel G Terbrugge; Timo Krings
Journal:  J Neurosurg Spine       Date:  2012-03-02

5.  Complex spinal arteriovenous fistula of the craniocervical junction with pial and dural shunts combined with contralateral dural arteriovenous fistula.

Authors:  Jin Pyeong Jeon; Young Dae Cho; Chi Heon Kim; Moon Hee Han
Journal:  Interv Neuroradiol       Date:  2015-10-13       Impact factor: 1.610

6.  Comparison of 3 Different Types of Spinal Arteriovenous Shunts below the Conus in Clinical Presentation, Radiologic Findings, and Outcomes.

Authors:  T Hong; J E Park; F Ling; K G terBrugge; M Tymianski; H Q Zhang; T Krings
Journal:  AJNR Am J Neuroradiol       Date:  2016-11-24       Impact factor: 3.825

Review 7.  Natural history and treatment of craniocervical junction dural arteriovenous fistulas.

Authors:  Joanna Y Wang; Joseph Molenda; Ali Bydon; Geoffrey P Colby; Alexander L Coon; Rafael J Tamargo; Judy Huang
Journal:  J Clin Neurosci       Date:  2015-07-17       Impact factor: 1.961

8.  Outcome and prognostic factors in the surgical treatment of spinal dural arteriovenous fistulas. A long-term study.

Authors:  L Tacconi; B C Lopez Izquierdo; L Symon
Journal:  Br J Neurosurg       Date:  1997-08       Impact factor: 1.596

9.  Spinal dural arteriovenous fistula: the pathology of venous hypertensive myelopathy.

Authors:  R W Hurst; L C Kenyon; E Lavi; E C Raps; P Marcotte
Journal:  Neurology       Date:  1995-07       Impact factor: 9.910

10.  Spinal dural arteriovenous fistulae: analysis of outcome in relation to pretreatment indicators.

Authors:  Marco Cenzato; Pietro Versari; Claudio Righi; Franco Simionato; Cecilia Casali; Massimo Giovanelli
Journal:  Neurosurgery       Date:  2004-10       Impact factor: 4.654

View more
  8 in total

1.  [Clinical outcomes following microsurgery and endovascular embolization in the management of spinal dural arteriovenous fistula: A meta-analysis study].

Authors:  C W Yuan; Y J Wang; S J Zhang; S L Shen; H Z Duan
Journal:  Beijing Da Xue Xue Bao Yi Xue Ban       Date:  2022-04-18

2.  Potential biomarkers of spinal dural arteriovenous fistula: C4BPA and C1QA.

Authors:  Yinqing Wang; Yongjie Ma; Chengbin Yang; Hongqi Zhang; Xiahe Huang; Kun Yang; Fei Lan; Jingxuan Fu; Zihao Song; An Tian; Yueshan Feng; Tianqi Tu; Haifeng Li; Tao Hong; Yingchun Wang
Journal:  J Neuroinflammation       Date:  2022-06-22       Impact factor: 9.587

3.  Treatment strategy to maximize the treatment outcome of spinal dural arteriovenous fistula after initial endovascular embolization attempt at diagnostic angiography.

Authors:  Heui Seung Lee; Hyun-Seung Kang; Sung Min Kim; Chi Heon Kim; Seung Heon Yang; Moon Hee Han; Chun Kee Chung
Journal:  Sci Rep       Date:  2021-05-11       Impact factor: 4.379

4.  Progressive Paraplegia Due to Spinal Dural Arteriovenous Fistula: A Rare but Treatable Diagnosis That Should Not Be Missed.

Authors:  Sajid Hameed; Bushra Taimuri; Marvi Sajid; Farah Siraj; Ayeesha Kamal
Journal:  Cureus       Date:  2019-10-11

5.  Long-term outcomes and prognostic factors in patients with treated spinal dural arteriovenous fistulas: a prospective cohort study.

Authors:  Chengbin Yang; Yongjie Ma; An Tian; Jiaxing Yu; Sichang Chen; Chao Peng; Kun Yang; Guilin Li; Chuan He; Ming Ye; Tao Hong; Lisong Bian; Zhichao Wang; Feng Ling; Hongqi Zhang
Journal:  BMJ Open       Date:  2022-01-03       Impact factor: 2.692

6.  Sudden-onset paraplegia in a 72-year-old male with a spinal dural arteriovenous fistula: illustrative case.

Authors:  Ikenna I Ogbu; Nikolaos Tzerakis; Zaineb Al-Shamary
Journal:  J Neurosurg Case Lessons       Date:  2021-08-30

7.  Spinal dural arteriovenous fistula: A rare but treatable disease that should not be missed by orthopedic surgeons.

Authors:  Baohui Yang; Teng Lu; Xijing He; Haopeng Li
Journal:  Front Neurol       Date:  2022-09-20       Impact factor: 4.086

8.  Microsurgery Versus Endovascular Treatment - Which Is Adequate for Initial Treatment of Spinal Dural Arteriovenous Fistula: A Case Series.

Authors:  Younggyu Oh; Yeon Heo; Sang Ryong Jeon; Sung Woo Roh; Jin Hoon Park
Journal:  Neurospine       Date:  2021-06-30
  8 in total

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