Abstract
Objective
The efficacy of preoperative embolization for hypervascular metastatic spine disease (MSD) such as renal cell and thyroid cancers has been reported. However, the debate on the efficacy of preoperative embolization for non-hypervascular MSD still remains unsettled. The purpose of this study is to determine whether preoperative embolization for non-hypervascular MSD decreases perioperative blood loss.
Methods
A total of 79 patients (36 cases of preoperative embolization and 43 cases of non-embolization) who underwent surgery for metastatic spine lesions were included. Representative hypervascular tumors such as renal cell and thyroid cancers were excluded. Intraoperative and perioperative estimated blood losses (EBL), total number of transfusion and calibrated EBL were recorded in the embolization and non-embolization groups. The differences in EBL were also compared along with the type of surgery. In addition, the incidence of Adamkiewicz artery and complications of embolization were assessed.
Results
The average age of 50 males and 29 females was 57.6±13.5 years. Lung (30), hepatocellular (14), gastrointestinal (nine) and others (26) were the primary cancers. The demographic data was not significantly different between the embolization and the non-embolization groups. There were no significant differences in intraoperative EBL, perioperative EBL, total transfusion and calibrated EBL between two groups. However, intraoperative EBL and total transfusion in patients with preoperative embolization were significantly lower than in non-embolization in the corpectomy group (1645.5 vs. 892.6 mL, p=0.017 for intraoperative EBL and 6.1 vs. 3.9, p=0.018 for number of transfusion). In addition, the presence of Adamkiewicz artery at the index level was noted in two patients. Disruption of this major feeder artery resulted in significant changes in intraoperative neuromonitoring.
Conclusion
Preoperative embolization for non-hypervascular MSD did not reduce perioperative blood loss. However, the embolization significantly reduced intraoperative bleeding and total transfusion in corpectomy group. Moreover, the procedure provided insights into the anatomy of tumor and spinal cord vasculature.
Keywords: Neoplasm metastasis, Spine, Embolization therapeutic, Postoperative hemorrhage, Complications
INTRODUCTION
The incidence of metastatic spine disease (MSD) is increasing due to improved survival of cancer patients. Surgical interventions for MSD have been increasingly performed, because MSD impairs the quality of life in terms of severe pain, pathologic fractures and risk of paraplegia [5,7,16,19,20,22]. However, spinal surgeries such as total en-bloc spondylectomy or corpectomy may cause severe perioperative bleeding resulting in postoperative complications and poor surgical outcomes. Moreover, highly vascularized tumors including renal and thyroid carcinoma are associated with a high risk of massive blood loss. In this regard, transarterial embolization has been reported to decrease perioperative bleeding in hypervascular tumors [5,8-10,12,15,16,21]. However, consensus regarding embolization in non-hypervascular spinal metastasis has yet to be achieved [3,8,16,17].
In addition to reduced perioperative bleeding, preoperative embolization has another advantage in evaluating the vascularity of the lesion and spinal cord [19]. However, simultaneous embolization and extensive surgery for MSD increase the risk of spinal cord injury and impairment although vascular insult following major spinal surgery has rarely been reported [2]. Therefore, the purpose of this study was to evaluate the efficacy of preoperative transarterial embolization in non-hypervascular MSD and the vascular safety of the spinal cord.
MATERIALS AND METHODS
Patients and surgical procedures
A clinical and radiological database from 2011 to 2016 was retrospectively reviewed at a single institution. This study was approved by the Institutional Review Board of Seoul St. Mary's Hosptial (IRB approval No. KC15RISE0947). We included patients with the following criteria : 1) adult patients diagnosed with metastatic spine lesion and 2) treatment with reconstructive surgery. The exclusion criteria were : 1) metastatic spine lesion with highly vascular tumor such as renal or thyroid carcinoma and 2) combined surgery for non-spinal metastatic tumors. One hundred eighty-two patients who underwent spinal surgery for MSD were screened and a total of 79 consecutive patients who met these criteria were included in this study. Nine patients were excluded because of known highly vascular tumors (three thyroid and six renal carcinomas). Ninety-four patients who underwent non-reconstruction surgery such as percutaneous vertebroplasty and kyphoplasty were also excluded. General condition of the patients (revised Tokuhashi score) [18] and instability of the spine (spinal instability neoplastic score, SINS) [4] were used to determine the surgical intervention, as well as location of the main lesions and history of radiation therapy. Three types of surgical intervention were performed : 1) posterior palliative laminectomy and excision of epidural extension of tumors with posterior reconstruction (n=41), 2) posterior vertebral column resection with posterior reconstruction (n=22), and 3) anterior corpectomy with anterior or posterior reconstruction (n=16).
Preoperative embolization
Pre-operative embolization was determined randomly considering the general condition and emergent surgery due to neurological status. Preoperative embolization was performed in 36 patients (45.6%). All embolization procedures were conducted within 48 hours prior to surgery. The embolization of the index segmental artery included the cephalad and caudal segmental arteries. Embolization was not performed if there was evidence of major blood supply to the spinal cord (the Adamkiewicz artery). In this series, two patients presented with major blood supply for the anterior spinal artery through the Adamkiewicz artery at the index level. A mechanical coil (Tornado® or Vortx®; Cook Medical, Bloomington, IN, USA) was used in most patients.
Estimated blood loss
Intraoperative (measured by the amount of suction drainage and soaked by gauze) and perioperative (the amount of drain for postoperative 2 days) estimated blood losses (EBLs) were recorded. Calibrated EBL was also computed using the following formula : (preoperative hemoglobin – hemoglobin on postoperative 2nd day) + total number of transfused packed red blood cell (PRC). One unit of PRC was considered to increase the hemoglobin rate by 1 g/dL.
Statistical analysis
Perioperative continuous variables in different groups presented with mean values and standard deviation were compared using Student’s t-test. Categorical variables were compared using Pearson’s chi-squared test. All statistical analysis was performed using SPSS software (IBM SPSS Statistics for Windows, version 24.0; IBM Corp., Armonk, NY, USA). The significance level was set at p value less than 0.05.
RESULTS
Patients
The mean age of the patients was 57.6±13.5 years (range, 21–84). Fifty patients were male and 29 patients were female. Lung (30, 38.0%), hepatocellular (14, 17.7%), gastrointestinal (9, 11.4%) and others including hematologic malignancy, breast, uterus, bladder, adrenal gland, hypopharynx, nasopharynx, tongue (26, 32.9%) were the primary sites of cancer. The lesion locations were : five cervical, 53 thoracic and 21 lumbosacral spines. The mean number of instrumented levels was 3.9±1.5. Demographic data such as age, sex, number of instrumented levels, bone mineral density and American society of anesthesiologists physical status classification were not significantly different between the two groups (Table 1). The revised Tokuhashi score and SINS were also not significantly different (7.9±2.5 vs. 6.5±2.2, p=0.111 for Tokuhashi score; 10.4±2.6 vs. 10.1±3.3, p=0.815 for SINS).
Table 1.
Non-embolization (n=43) | Embolization (n=36) | p-value | |
---|---|---|---|
Age (years) | 58.7±13.4 | 56.1±13.6 | 0.395 |
Sex (M : F) | 30 : 13 | 20 : 16 | 0.192 |
Primary | |||
Lung | 16 | 14 | |
HCC | 7 | 7 | |
GI | 5 | 4 | |
Others* | 15 | 11 | |
Number of instrumented levels | 4.1±1.5 | 3.7±1.3 | 0.177 |
BMD (T-score) | -2.5±1.1 | -2.3±1.4 | 0.623 |
ASA grade (1, 2 : 3, 4) | 36 : 7 | 29 : 7 | 0.714 |
Revised Tokuhashi score | 7.9±2.5 | 6.5±2.2 | 0.111 |
SINS | 10.4±2.6 | 10.1±3.3 | 0.815 |
Values are presented as mean±standard deviation unless otherwise indicated.
Others including hematologic malignancy, breast, uterus, bladder, adrenal gland, hypopharynx, nasopharynx, tongue cancer.
M : male, F : female, HCC : hepatocellular cancer, GI : gastrointestinal, BMD : bone mineral density, ASA : American Society Anesthesiologists physical status classification, SINS : spinal instability neoplastic score
Embolization vs. non-embolization
Table 2 shows the operation time, intraoperative EBL, perioperative EBL, total number of transfusion and calibrated EBL in the embolization and the non-embolization groups. The operation time was longer in embolization group without significance (219.9±77.7 vs. 231.9±79.9 minutes, p=0.501). The intraoperative EBL and perioperative EBL were not significantly different between the two groups (1069.8±869.7 vs. 862.5±526.2 mL, p=0.215 for intraoperative EBL; 529.0±287.3 vs. 513.9±415.6 mL, p=0.849 for perioperative EBL). The total number of transfusion and calibrated EBL were also similar in both groups (4.1±2.8 vs. 3.7±2.2, p=0.540 for total transfusion; 5.5±3.1 vs. 4.9±3.3, p=0.420 for calibrated EBL).
Table 2.
Non-embolization (n=43) | Embolization (n=36) | p-value | |
---|---|---|---|
Operation time | 219.9±77.7 | 231.9±79.9 | 0.501 |
Intraoperative EBL (mL) | 1069.8±869.7 | 862.5±526.2 | 0.215 |
Perioperative EBL (mL) | 529.0±287.3 | 513.9±415.6 | 0.849 |
No. of transfused PRC | 4.1±2.8 | 3.7±2.2 | 0.540 |
Cal. EBL* (g/dL) | 5.5±3.1 | 4.9±3.3 | 0.420 |
Values are presented as mean±standard deviation.
(preoperative hemoglobin – hemoglobin on postoperative 2nd day) + total number of transfused red blood cell (PRC). EBL : estimated blood loss, PRC : packed red blood cells, Cal. EBL : calibrated estimated blood loss
The EBL was compared according to the type of surgery. In patients who had undergone corpectomy, the operation time, perioperative EBL and calibrated EBL were not significantly different between the two groups. However, intraoperative EBL was significantly less in the embolization group compared with the non-embolization group (892.6±589.0 vs. 1645.5±1277.8 mL, p=0.017). Furthermore, the total number of transfusion was also significantly lower in the embolization group than in the non-embolization group (3.9±2.2 vs. 6.1±2.9, p=0.018). In laminectomy group, there were no significant differences in operation time, intraoperative EBL, perioperative EBL, the total number of transfusion and calibrated EBL (Table 3).
Table 3.
Corpectomy (n=38) |
Laminectomy (n=41) |
|||||
---|---|---|---|---|---|---|
Non-embol (n=11) | Embol (n=27) | p-value | Non-embol (n=32) | Embol (n=9) | p-value | |
Operation time | 276.3±89.3 | 200.5±63.9 | 196.0±24.5 | 0.838 | ||
Intraoperative EBL (mL) | 1645.5±1277.8 | 892.6±589.0 | 0.017 | 871.9±583.1 | 772.2±268.2 | 0.624 |
Perioperative EBL (mL) | 569.7±378.5 | 555.3±454.4 | 0.927 | 515.0±254.6 | 389.6±247.7 | 0.197 |
No. of transfused PRC | 6.1±2.9 | 3.9±2.2 | 0.018 | 3.3±2.4 | 3.0±2.2 | 0.698 |
Cal. EBL* (g/dL) | 7.5±3.4 | 5.5±3.5 | 0.117 | 4.8±2.7 | 3.1±1.6 | 0.084 |
Values are presented as mean±standard deviation.
(preoperative hemoglobin – hemoglobin on postoperative 2nd day) + total number of transfused red blood cell (PRC). Embol : embolization, EBL : estimated blood loss, PRC : packed red blood cells, Cal. EBL : calibrated estimated blood loss
Case illustrations : clinical significance of the artery of Adamkiewicz
Any complications directly related to preoperative embolization were not detected in patients. However, the Adamkiewicz artery was noted in two patients with thoracolumbar lesions. Disruption of this major feeder artery during surgery resulted in significant changes in intraoperative neuromonitoring.
Case 1
A 58-year-old woman presented with severe back pain due to spinal cord compression with T6 metastasis from lung carcinoma (Tokuhashi score, 10; SINS, 8). Thoracic aortography and intercostal arteriography showed extensive vascularization of the tumor and the major feeder artery from the left side 6th intercostal artery. Both the 7th and right 6th intercostal arteries supplying the tumor were unevenly embolized. Palliative surgery (T6 corpectomy, and T5–7 anterior interbody graft with allogenous fibular bone graft combined with posterior instrumentation and posterior fusion) was performed. The artery of Adamkiewicz was identified on the left 6th intercostal artery and temporary clipping showed significant changes on the motor evoked potentials (MEPs) in intraoperative neuromonitoring (Fig. 1, Supplementary Video 1). No postoperative complications or neurological compromise were detected.
Case 2
A 61-year-old male patient was diagnosed with hepatocellular carcinoma, which metastasized at L2. The patient presented with intractable back pain radiating to bilateral legs due to compression of the spinal cord at the L2 level even after radiotherapy (Tokuhashi score, 10; SINS, 13). The Adamkiewicz artery originating from the segmental artery supplying the tumor was identified during preoperative angiography. The segmental vessels except the left side at L2 level were successfully embolized. Palliative surgery (L2 corpectomy, and L1–3 anterior interbody graft with allogenous fibular bone graft combined with posterior instrumentation and posterolateral fusion) was performed. Despite attempts to avoid injury to the left segmental artery of the L2 during the procedures, the loss of MEP was noted after corpectomy (Fig. 2). The loss of MEP persisted until the end of the surgery. However, the preoperative complaint was relieved without any neurological deficits.
DISCUSSION
Debate on the efficacy of preoperative embolization for non-hypervascular MSD still persists. Studies reported a decrease in intraoperative blood loss with preoperative embolization while other studies demonstrated no significant differences in EBL after embolization [3,8,16,17]. In this study, although intraoperative EBL (862.5 vs. 1069.8 mL), perioperative EBL (513.9 vs. 529.0 mL), transfusion amount (3.7 vs. 4.1), and calibrated EBL (4.9 vs. 5.5) were less in the embolization group, no significant differences were detected between the two groups. Robial et al. [16] reported no significant differences in blood loss and transfusion in breast, lung cancer and metastasis other than renal cell carcinoma. Clausen et al. [3] also demonstrated that intraoperative blood loss (618 vs. 735 mL, p=0.270) and perioperative blood loss (902 vs. 985 mL, p=0.505) were not significantly different between the two groups. Previous studies included both hypervascular and non-hypervascular tumors and sub-group analysis of non-hypervascular tumors was performed. In this cohort, highly vascular metastatic tumors such as renal and thyroid cancers were excluded and the efficacy of preoperative transarterial embolization in non-hypervascular MSD was evaluated.
The degree of intraoperative blood loss in spinal metastasis may vary according to the operative procedure [8]. Since this study included both corpectomy and laminectomy, the EBL in the two groups was also compared along with the type of surgery. Preoperative embolization significantly decreased intraoperative EBL (892.6 vs. 1645.5 mL, p=0.017) and the total number of transfusion (3.9 vs. 6.1, p=0.018) in patients treated with corpectomy. Berkefeld et al. [2] reported that preoperative embolization using coils and particles significantly reduced mean blood loss in corpectomy (2379±1844 vs. 4770±3299 mL, p=0.05). Robial et al. [16] also demonstrated preoperative embolization in major surgeries such as corpectomies and vertebrectomies, while limited in palliative procedures such as decompression in all types of metastasis. Based on this study, patients with non-hypervascular MSD may not necessarily benefit from preoperative embolization. Preoperative embolization can be considered selectively for metastatic spinal lesions requiring extensive surgery such as corpectomy and en-bloc spondylectomy.
Preoperative embolization was conducted 2 days before surgery in all patients. Surgery performed within 72 hours of embolization has been shown to decrease perioperative blood loss compared with surgery performed beyond this time period [1,6]. In addition, any complication was not reported in the 36 patients with preoperative embolization, which was consistent with previous studies reporting that preoperative embolization was a safe procedure with a very low complication rate (0–1%) [12,21].
The clinical significance of the artery of Adamkiewicz was also interesting in this study. The artery of Adamkiewicz, also known as the great anterior radiculomedullary artery, is the most important feeding artery of the thoracolumbar spinal cord. It supplies the lower two-thirds of the spinal cord via the spinal artery. In spine surgery, sacrificing this artery can potentially result in severe neurological deficits. However, Murakami et al. [11] concluded that interruption of the artery of Adamkiewicz did not interfere with neurological function and even recommended that sacrifice of up to three pairs of segmental arteries including the artery of Adamkiewicz does not disrupt the circulation of the spinal cord, based on their study of 180 cases of total en-bloc sponydylectomy. In our study, disruption of the Adamkiewicz artery in two patients carrying thoracolumbar lesions during preoperative embolization led to significant changes in intraoperative neuromonitoring (amplitudes and latency in motor evoked potentials, MEPs), without any neurological deterioration in both patients after the surgery. MEP monitoring responds to loss of spinal cord perfusion by the anterior spinal artery [14]. The changes in the MEPs can be explained by the interruption of blood flow to the anterior two-thirds of the spinal cord supplied by the Adamkiewicz artery, which may not necessarily translate to neurological impairment because of the possible compensatory blood supply to the spinal cord. However, Orchowski et al. [13] reported that a small percentage of patients (0.75%) had major neurological deficits after ligation of a few segmental vessels on one side. Therefore, it is important to recognize the possibility of neurologic deficits after the vascular compromise of spinal cord during surgery. Preoperative angiography provides insights into the anatomy of major feeder artery of spinal cord.
This study has a few limitations. First, the primary sites of cancer were heterogeneous such as lung, hepatocellular, gastrointestinal cancers. Since the number of MSD treated with the surgery was limited, non-hypervascular tumors other than highly vascular tumors were included in this study to minimize tumor heterogeneity. Second, clinical outcomes such as pain and functional status were not evaluated in this study. However, clinical outcomes may be influenced by uncontrolled factors such as general conditions, activity of tumor or other concurrent metastasis. Third, our study showed that preoperative embolization is effective for corpectomy group. But, bias is thought to exist because it is a retrospective study and it is not randomization.
CONCLUSION
Preoperative embolization for non-hypervascular MSD other than renal and thyroid cancer failed to reduce perioperative blood loss in this study. However, the embolization significantly decreased intraoperative bleeding and total transfusion in the corpectomy group. Furthermore, the procedure provides anatomic insights for the surgeon to avoid vascular compromise of the spinal cord.
Acknowledgments
This study was supported by Research Fund of Seoul St. Mary’s Hospital, The Catholic University of Korea.
Footnotes
No potential conflict of interest relevant to this article was reported.
INFORMED CONSENT
This type of study does not require informed consent.
Supplementary Materials
The online-only data supplement is available with this article at https://doi.org/10.3340/jkns.2018.0073.
References
- 1.Barton PP, Waneck RE, Karnel FJ, Ritschl P, Kramer J, Lechner GL. Embolization of bone metastases. J Vasc Interv Radiol. 1996;7:81–88. doi: 10.1016/s1051-0443(96)70738-8. [DOI] [PubMed] [Google Scholar]
- 2.Berkefeld J, Scale D, Kirchner J, Heinrich T, Kollath J. Hypervascular spinal tumors: influence of the embolization technique on perioperative hemorrhage. AJNR Am J Neuroradiol. 1999;20:757–763. [PMC free article] [PubMed] [Google Scholar]
- 3.Clausen C, Dahl B, Frevert SC, Hansen LV, Nielsen MB, Lönn L. Preoperative embolization in surgical treatment of spinal metastases: singleblind, randomized controlled clinical trial of efficacy in decreasing intraoperative blood loss. J Vasc Interv Radiol. 2015;26:402–412.e1. doi: 10.1016/j.jvir.2014.11.014. [DOI] [PubMed] [Google Scholar]
- 4.Fisher CG, DiPaola CP, Ryken TC, Bilsky MH, Shaffrey CI, Berven SH, et al. A novel classification system for spinal instability in neoplastic disease: an evidence-based approach and expert consensus from the Spine Oncology Study Group. Spine (Phila Pa 1976) 2010;35:E1221–E1229. doi: 10.1097/BRS.0b013e3181e16ae2. [DOI] [PubMed] [Google Scholar]
- 5.Guzman R, Dubach-Schwizer S, Heini P, Lovblad KO, Kalbermatten D, Schroth G, et al. Preoperative transarterial embolization of vertebral metastases. Eur Spine J. 2005;14:263–268. doi: 10.1007/s00586-004-0757-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Heran MK. Preoperative embolization of spinal metastatic disease: rationale and technical considerations. Semin Musculoskelet Radiol. 2011;15:135–142. doi: 10.1055/s-0031-1275596. [DOI] [PubMed] [Google Scholar]
- 7.Jacobs WB, Perrin RG. Evaluation and treatment of spinal metastases: an overview. Neurosurg Focus. 2001;11:e10. doi: 10.3171/foc.2001.11.6.11. [DOI] [PubMed] [Google Scholar]
- 8.Kato S, Murakami H, Minami T, Demura S, Yoshioka K, Matsui O, et al. Preoperative embolization significantly decreases intraoperative blood loss during palliative surgery for spinal metastasis. Orthopedics. 2012;35:e1389–e1395. doi: 10.3928/01477447-20120822-27. [DOI] [PubMed] [Google Scholar]
- 9.Kobayashi K, Ozkan E, Tam A, Ensor J, Wallace MJ, Gupta S. Preoperative embolization of spinal tumors: variables affecting intraoperative blood loss after embolization. Acta Radiol. 2012;53:935–942. doi: 10.1258/ar.2012.120314. [DOI] [PubMed] [Google Scholar]
- 10.Manke C, Bretschneider T, Lenhart M, Strotzer M, Neumann C, Gmeinwieser J, et al. Spinal metastases from renal cell carcinoma: effect of preoperative particle embolization on intraoperative blood loss. AJNR Am J Neuroradiol. 2001;22:997–1003. [PMC free article] [PubMed] [Google Scholar]
- 11. doi: 10.1097/BRS.0b013e3181e215e5. Murakami H, Kawahara N, Tomita K, Demura S, Kato S, Yoshioka K : Does interruption of the artery of Adamkiewicz during total en bloc spondylectomy affect neurologic function? Spine (Phila Pa 1976) 35 : E1187-E1192, 2010. [DOI] [PubMed] [Google Scholar]
- 12.Nair S, Gobin YP, Leng LZ, Marcus JD, Bilsky M, Laufer I, et al. Preoperative embolization of hypervascular thoracic, lumbar, and sacral spinal column tumors: technique and outcomes from a single center. Interv Neuroradiol. 2013;19:377–385. doi: 10.1177/159101991301900317. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Orchowski J, Bridwell KH, Lenke LG. Neurological deficit from a purely vascular etiology after unilateral vessel ligation during anterior thoracolumbar fusion of the spine. Spine (Phila Pa 1976) 2005;30:406–410. doi: 10.1097/01.brs.0000153391.55608.72. [DOI] [PubMed] [Google Scholar]
- 14.Pajewski TN, Arlet V, Phillips LH. Current approach on spinal cord monitoring: the point of view of the neurologist, the anesthesiologist and the spine surgeon. Eur Spine J 16 Suppl. 2007;2:S115–S129. doi: 10.1007/s00586-007-0419-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Pikis S, Itshayek E, Barzilay Y, Hasharoni A, Kaplan L, Gomori M, et al. Preoperative embolization of hypervascular spinal tumors: current practice and center experience. Neurol Res. 2014;36:502–509. doi: 10.1179/1743132814Y.0000000361. [DOI] [PubMed] [Google Scholar]
- 16.Robial N, Charles YP, Bogorin I, Godet J, Beaujeux R, Boujan F, et al. Is preoperative embolization a prerequisite for spinal metastases surgical management? Orthop Traumatol Surg Res. 2012;98:536–542. doi: 10.1016/j.otsr.2012.03.008. [DOI] [PubMed] [Google Scholar]
- 17.Thiex R, Harris MB, Sides C, Bono CM, Frerichs KU. The role of preoperative transarterial embolization in spinal tumors. A large single-center experience. Spine J. 2013;13:141–149. doi: 10.1016/j.spinee.2012.10.031. [DOI] [PubMed] [Google Scholar]
- 18.Tokuhashi Y, Matsuzaki H, Oda H, Oshima M, Ryu J. A revised scoring system for preoperative evaluation of metastatic spine tumor prognosis. Spine (Phila Pa 1976) 2005;30:2186–2191. doi: 10.1097/01.brs.0000180401.06919.a5. [DOI] [PubMed] [Google Scholar]
- 19.Truumees E, Dodwad SN, Kazmierczak CD. Preoperative embolization in the treatment of spinal metastasis. J AM Acad Orthop Surg. 2010;18:449–453. doi: 10.5435/00124635-201008000-00001. [DOI] [PubMed] [Google Scholar]
- 20.White AP, Kwon BK, Lindskog DM, Friedlaender GE, Grauer JN. Metastatic disease of the spine. J AM Acad Orthop Surg. 2006;14:587–598. doi: 10.5435/00124635-200610000-00001. [DOI] [PubMed] [Google Scholar]
- 21.Wilson MA, Cooke DL, Ghodke B, Mirza SK. Retrospective analysis of preoperative embolization of spinal tumors. AJNR Am J Neuroradiol. 2010;31:656–660. doi: 10.3174/ajnr.A1899. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Wirbel RJ, Roth R, Schulte M, Kramann B, Mutschler W. Preoperative embolization in spinal and pelvic metastases. J Orthop Sci. 2005;10:253–257. doi: 10.1007/s00776-005-0900-1. [DOI] [PubMed] [Google Scholar]
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