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DOI: 10.1148/radiol.2261011911
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(Radiology 2003;226:119-124.)
© RSNA, 2003


Vascular and Interventional Radiology

Occurrence of New Vertebral Body Fracture after Percutaneous Vertebroplasty in Patients with Osteoporosis1

Anita A. Uppin, MD, Joshua A. Hirsch, MD, Luis V. Centenera, MD, Bernard A. Pfiefer, MD, Artemis G. Pazianos, MD and In Sup Choi, MD

1 From the Lahey Clinic Medical Center, Burlington, Mass. From the 2001 RSNA scientific assembly. Received November 27, 2001; revision requested January 7, 2002; revision received April 15; accepted May 24. Address correspondence to J.A.H., Department of Neurointerventional Radiology, Beth Israel Deaconess Medical Center, One Deaconess Rd, West Campus, Boston, MA 02215 (e-mail: jhirsch@caregroup.harvard.edu).


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
PURPOSE: To investigate the prevalence and findings of vertebral body compression fractures adjacent to those previously treated with percutaneous vertebroplasty.

MATERIALS AND METHODS: The findings in 177 patients treated with percutaneous vertebroplasty for more than 2 years were reviewed retrospectively. The following parameters were reviewed: primary diagnosis, patient age and sex, date of treatment with vertebroplasty, vertebral level(s) treated, pedicular approach, and amount of polymethylmethacrylate injected per vertebral body. Patients with acute compression fractures secondary to osteoporosis were selected.

RESULTS: Of 177 patients treated with percutaneous vertebroplasty, 22 (12.4%) developed a total of 36 new vertebral body fractures following treatment. Of the 36 newly documented fractures, 24 (67%) involved vertebrae adjacent to the previously treated vertebral level(s), whereas 12 (33%) involved the collapse of nonadjacent vertebrae. In addition, 24 (67%) of the 36 new vertebral fractures occurred within 30 days after treatment of the initial fracture(s).

CONCLUSION: A substantial number of patients with osteoporosis develop new fractures after undergoing percutaneous vertebroplasty; two-thirds of these new fractures occur in vertebrae adjacent to those previously treated.

© RSNA, 2003

Index terms: Osteoporosis, 321.56, 331.56 • Spine, fractures, 321.41, 331.41 • Spine, MR, 321.121411, 321.121413, 321.121416, 331.121411, 331.121413, 331.121416 • Spine, vertebroplasty


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Osteoporotic vertebral compression fractures are a major cause of morbidity and health care costs among elderly patients. Many patients lose their independence and have a poorer quality of life as a result of these fractures. In the past, the primary therapy for these fractures has been conservative and consisted of bed rest, analgesic medications, and physical therapy. Percutaneous vertebroplasty is now a therapeutic option for individuals in whom medical management has not been successful or who are at risk of developing complications secondary to immobilization.

The technique of percutaneous vertebroplasty with polymethylmethacrylate (PMMA) for the treatment of aggressive spinal angiomas was described by Deramond et al (1) in France in 1984. The indications for this procedure have increased to include the treatment of osteoporotic compression fractures and malignant vertebral neoplasms (1). In preliminary studies (14), percutaneous vertebroplasty has been shown to facilitate substantial pain relief and improve mobility in up to 90% of patients, with such results occurring as early as 24–48 hours following intervention.

The overall complication rate associated with percutaneous vertebroplasty for the treatment of osteoporotic compression fractures is reported to be 1%–3% (1,5). The findings of some authors (1,68) have indicated that there is a risk of collapse of a vertebral body adjacent to the one injected with PMMA in a subset of patients. To our knowledge, there have been no reports to date of a large series of compression fractures that developed within adjacent vertebral bodies. The purpose of our study was to investigate the development of compression fractures in vertebral bodies adjacent to those previously treated with percutaneous vertebroplasty. Herein we report our experiences.


    MATERIALS AND METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
We performed a retrospective review of the findings in patients treated with percutaneous vertebroplasty at our institution from September 15, 1998 to November 30, 2000. Of the patients who returned for multiple interventions, those with acute compression fractures secondary to osteoporosis were selected for retrospective analysis. Patients who were treated for metastatic disease or multiple myelomas were excluded. Primarily, two authors (A.A.U., J.A.H.) reviewed the following parameters: patient age, patient sex, primary diagnosis, date that vertebroplasty was performed, vertebral level(s) treated, amount of PMMA injected per vertebral body, pedicular approach (ie, unipedicular vs bipedicular), and date that and vertebral level(s) at which subsequent vertebral body fractures were diagnosed. The time (in months and days) from the date of the initial intervention with vertebroplasty to the development of subsequent fractures was then calculated. According to the policies of our institutional review board, its approval was not required for this retrospective analysis.

The vertebroplasty technique currently used at our institution is equivalent to the procedure (with the associated materials) that has been thoroughly described by Centenera et al (4). A multidisciplinary team that consists of an endocrinologist (A.G.P.), orthopedic surgeon (B.A.P.), and interventional neuroradiologist (J.A.H., I.S.C.) examines the patients referred to our vertebroplasty clinic. Complete medical history data and physical examination findings are supplemented with the results of diagnostic imaging, which may include anteroposterior and lateral radiography and magnetic resonance (MR) imaging of the spine or technetium 99m (99mTc)–labeled planar and single photon emission computed tomographic (CT) bone scintigraphy. Typical MR examinations include transverse and sagittal T1- and T2-weighted imaging, in addition to sagittal short inversion time inversion-recovery (STIR) imaging of the spine (Fig 1).



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Figure 1a. Images obtained in an 82-year-old woman with a history of T12 fracture and back pain of 1-month duration. (a) Sagittal fast spin-echo T1-weighted MR image (repetition time msec/echo time msec, 566/12.4) shows low signal intensity in the bone marrow, a loss of vertebral body height, and an end plate deformity at the L1 and L3 vertebral levels. A remote T12 fracture with acute kyphosis and a retropulsed fragment (*) also is seen. (b) Sagittal STIR MR image (3,716/17) shows high signal intensity within the L1 and L3 vertebral bodies, indicating acute compression at these levels. (c) Spot posteroanterior radiograph obtained after vertebroplasty at the L1 and L3 vertebral levels shows PMMA within the L1 and L3 vertebrae. The patient reported having complete relief of symptoms.

 


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Figure 1b. Images obtained in an 82-year-old woman with a history of T12 fracture and back pain of 1-month duration. (a) Sagittal fast spin-echo T1-weighted MR image (repetition time msec/echo time msec, 566/12.4) shows low signal intensity in the bone marrow, a loss of vertebral body height, and an end plate deformity at the L1 and L3 vertebral levels. A remote T12 fracture with acute kyphosis and a retropulsed fragment (*) also is seen. (b) Sagittal STIR MR image (3,716/17) shows high signal intensity within the L1 and L3 vertebral bodies, indicating acute compression at these levels. (c) Spot posteroanterior radiograph obtained after vertebroplasty at the L1 and L3 vertebral levels shows PMMA within the L1 and L3 vertebrae. The patient reported having complete relief of symptoms.

 


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Figure 1c. Images obtained in an 82-year-old woman with a history of T12 fracture and back pain of 1-month duration. (a) Sagittal fast spin-echo T1-weighted MR image (repetition time msec/echo time msec, 566/12.4) shows low signal intensity in the bone marrow, a loss of vertebral body height, and an end plate deformity at the L1 and L3 vertebral levels. A remote T12 fracture with acute kyphosis and a retropulsed fragment (*) also is seen. (b) Sagittal STIR MR image (3,716/17) shows high signal intensity within the L1 and L3 vertebral bodies, indicating acute compression at these levels. (c) Spot posteroanterior radiograph obtained after vertebroplasty at the L1 and L3 vertebral levels shows PMMA within the L1 and L3 vertebrae. The patient reported having complete relief of symptoms.

 
We have found MR imaging to be more conclusive than radiography in the evaluation of acute versus chronic compression fractures and thus include it as part of our initial imaging protocol. The MR imaging criteria that are positive for acute compression fracture include low signal intensity of bone marrow within the vertebral body on T1-weighted images and high signal intensity on T2-weighted and STIR images. Acute compression fractures can also be distinguished from chronic compression fractures at nuclear imaging. The positive nuclear imaging criteria include abnormal foci of increased radiotracer distributed within the affected vertebral segment.

The risks and complications of vertebroplasty, including bleeding; infection; pain; cement extravasation to the perivertebral venous plexus, epidural veins, or intervertebral disk space; nerve root compression; paralysis; and pulmonary embolization, are discussed with the patient. Informed consent is obtained. The procedure is performed with neuroleptic analgesia, which is induced by an anesthesiologist who is present during the procedure. The patient is placed in a prone position. With an aseptic technique, the skin and paravertebral soft tissues are anesthetized with lidocaine (1%) and sodium bicarbonate. With use of biplanar fluoroscopy—that is, in anteroposterior and lateral projections—the pedicle of interest is localized and an 11-gauge needle (Jamshedi Needle; Cook Medical, West Lafayette, Ind) is positioned at the anterior and middle one-third regions of the vertebral body. Transosseous venography with manual contrast agent injection is performed to identify the perivertebral venous plexus.

Next, PMMA is prepared by combining 6 g of sterile barium, 1.2 g of injectable tobramycin (Nebcin; Eli Lilly, Indianapolis, Ind), and one packet of cranioplastic cement (Codman Cranioplastic; Johnson & Johnson Medical, Bershire, United Kingdom) and then storing the mixture on ice to delay rapid polymerization. The PMMA mixture is then administered to the patient, with fluoroscopic visualization, in 0.2–0.3-mL increments. The vertebral body is filled as much as possible, and the process is stopped when there is filling in the posterior one-fourth of the vertebra, the epidural vein, the anterior or lateral disk space, or the intervertebral disk space. If PMMA does not extravasate to the opposite pedicle, the contralateral pedicle is localized and the procedure is repeated.

Multiple vertebral levels can be treated during a single session as long as the patient can tolerate the prone positioning and is not at risk of developing complications secondary to an underlying coexistent morbidity. In our initial experience, we obtained a nonenhanced CT scan of the area of interest to more clearly delineate the PMMA extravasation or associated complications. We no longer follow this practice, however. After the vertebroplasty procedure, the patient is observed in the recovery area for 3–4 hours and instructed at discharge to perform normal activities slowly within the next 48 hours. Three to 4 weeks after the procedure, patients either are contacted by telephone by a clinical nurse coordinator or undergo a follow-up examination at the vertebroplasty clinic, after which they are instructed to contact us on an as-needed basis.


    RESULTS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
One hundred seventy-seven patients were treated in our institution for more than 2 years. Twenty-eight of these 177 patients returned for subsequent interventions or because of the development of new vertebral body fractures. Six of these patients were excluded for the following reasons: One patient had non-Hodgkin lymphoma that involved multiple vertebral levels; one patient had multiple myelomas that involved multiple levels; two patients presented with symptoms of multilevel disease that necessitated more than one vertebroplasty session for complete treatment; one patient returned with a single-level compression fracture that necessitated two sessions to complete the intervention; and one patient died. Twenty-two (12.4%) of the 177 patients had developed new osteoporotic vertebral body fractures.

The mean age of the 22 patients was 77.5 years (age range, 54–88 years). Seventeen patients were women, and five were men. Although all of the patients had received a diagnosis of osteoporosis, seven of them had steroid-induced osteoporosis. Thirteen (59%) of the 22 patients had signs and symptoms of multiple vertebral level involvement—that is, acute or chronic fracture involving two or more segments—at presentation. The average number of treated vertebral segments was 3.2, and the new fractures involved segments of the thoracolumbar spine from the T6 through L4 vertebrae. A bipedicular approach was used in 60 (86%) of the 70 vertebroplasties performed, whereas a unipedicular approach was used in 10 (14%) vertebroplasties. The average amount of PMMA injected per vertebral body was 9.14 mL (range 5.0–14.5 mL).

The results of analysis with these 22 patients are summarized in Table 1. In this series of 22 patients, a total of 70 vertebral fractures were treated. Thirty-six (51%) of these fractures represented new compression fractures that developed after treatment of another vertebral level. Twenty-four (67%) of these 36 newly documented fractures involved vertebrae adjacent to the previously treated vertebral level(s), whereas 12 (33%) of the new fractures involved a collapse of a nonadjacent vertebral body. All patients who returned to our institution with new fractures underwent subsequent vertebroplasty for the treatment of newly involved vertebra(e).


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TABLE 1. Patients Who Developed New Compression Fractures after Undergoing Vertebroplasty

 
The interval of the development of new fractures was calculated on the basis of the time between the date of the initial vertebroplasty and the date of the diagnosis of a new compression fracture, which was based on positive MR imaging or 99mTc-labeled nuclear bone scan findings (Figs 1, 2). Twenty-four (67%) of the 36 new vertebral fractures occurred within 30 days after the initial treatment of another segment. The remaining 12 (33%) new vertebral fractures occurred more than 30 days after the initial treatment. Two of these 12 fractures occurred 31 days following treatment. The remaining 10 fractures occurred 48 days to 10 months after the initial treatment, as outlined in Table 1.



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Figure 2a. Images obtained in the patient described in Figure 1 after she returned with a new onset of back pain 13 days after treatment with vertebroplasty. (a) Sagittal fast spin-echo T1-weighted MR image (566/12.4) shows PMMA within the L1 and L3 vertebral bodies. There is a new deformity with depression of the superior end plate of the L2 vertebra (arrow). (b) Sagittal STIR MR image (3,716/17) shows increased signal intensity within the L2 vertebral body. This increased signal intensity represents a new compression fracture at this level. (c) Lateral radiograph obtained in the interventional suite immediately after the second vertebroplasty shows PMMA within the L1, L2, and L3 vertebral bodies. The patient reported having complete pain relief following treatment.

 


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Figure 2b. Images obtained in the patient described in Figure 1 after she returned with a new onset of back pain 13 days after treatment with vertebroplasty. (a) Sagittal fast spin-echo T1-weighted MR image (566/12.4) shows PMMA within the L1 and L3 vertebral bodies. There is a new deformity with depression of the superior end plate of the L2 vertebra (arrow). (b) Sagittal STIR MR image (3,716/17) shows increased signal intensity within the L2 vertebral body. This increased signal intensity represents a new compression fracture at this level. (c) Lateral radiograph obtained in the interventional suite immediately after the second vertebroplasty shows PMMA within the L1, L2, and L3 vertebral bodies. The patient reported having complete pain relief following treatment.

 


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Figure 2c. Images obtained in the patient described in Figure 1 after she returned with a new onset of back pain 13 days after treatment with vertebroplasty. (a) Sagittal fast spin-echo T1-weighted MR image (566/12.4) shows PMMA within the L1 and L3 vertebral bodies. There is a new deformity with depression of the superior end plate of the L2 vertebra (arrow). (b) Sagittal STIR MR image (3,716/17) shows increased signal intensity within the L2 vertebral body. This increased signal intensity represents a new compression fracture at this level. (c) Lateral radiograph obtained in the interventional suite immediately after the second vertebroplasty shows PMMA within the L1, L2, and L3 vertebral bodies. The patient reported having complete pain relief following treatment.

 

    DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
The indication for percutaneous vertebroplasty in patients with osteoporosis was proposed by Deramond et al: "incapacitating and persistent" back pain (1). In patients with osteoporosis, vertebral collapses may involve one or more levels. The goals of percutaneous vertebroplasty are pain relief and restoration of patient mobility. A potential qualitative goal of the procedure is to minimize the foreshortening and kyphosis of the spine that gradually evolve following repeated vertebral collapse. The results of in vitro biomechanical studies (911) support the strengthening effect of percutaneous vertebroplasty. The positive outcomes of percutaneous vertebroplasty for treatment of osteoporotic compression fractures, including immediate and complete relief of pain in up to 90% of patients, have also been reported in clinical studies (14).

Some of the earliest and most comprehensive results with percutaneous vertebroplasty have been reported by Deramond et al (1). Along with the frequently discussed complications of percutaneous vertebroplasty, including cement extravasation, infection, nerve root compression, and cement embolization, a risk of collapse of a vertebral body adjacent to one injected with PMMA also was proposed by these authors. They believed that this risk is low and probably an inherent risk for any patient with osteoporosis of the spine.

Other authors (2,3,68,1214) have observed and briefly discussed similar findings in small subsets of patients with osteoporosis; a summary of these observations in the English-language literature is provided in Table 2. Grados et al (7) evaluated 25 patients with osteoporosis (with 34 treated vertebrae) who were followed up for an average of 48 months (range 12–84 months). Although there was no progression of collapse within the vertebrae injected with PMMA, the authors reported an increased risk of adjacent vertebral body fractures as follows: 13 (52%) patients developed at least one new vertebral fracture, and the relative risk of fracture of a vertebral segment adjacent to a treated vertebral body was 2.27 (7).


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TABLE 2. Cases of New Vertebral Body Fractures Following Vertebroplasty Cited in the English Literature

 
A large population of patients with osteoporotic compression fractures is treated at our institution. In our early clinical experiences, marked or complete pain relief was achieved in more than 90% of patients (4). Some patients, who were initially pain free following treatment, returned with new symptoms that prompted clinical evaluation. The results of repeat MR imaging or bone scintigraphy, as compared with those of pretreatment repeat MR imaging and bone scintigraphy studies, confirmed the presence of new vertebral fractures (Figs 1, 2). We reviewed the data on these cases at our institution, which were collected for more than 2 years, and found that this phenomenon occurred in 22 (12.4%) of 177 treated patients.

In a clinical study of osteoporosis in women performed by Lindsay et al (15), the patients had a propensity to develop a second—even third—vertebral fracture within 1 year after an incident fracture; this phenomenon occurred in as many as 20% of the patients. The baseline bone mineral density and architecture inherent of osteoporosis of the spine are unfavorable; this assertion is supported by in vitro study results (8,9). Tohmeh et al (9) evaluated the strength and stiffness of the spine in cadavers with osteoporosis (bone mineral density t score, -3.7 to -8.8). Following compression, these vertebrae were observed to be structurally weaker and less stiff than they had been before the fracture (9). In addition, the fractured vertebrae that were not treated were weaker and less stiff than those that were treated with vertebroplasty (9).

The biomechanical forces that act on the spine are complex and beyond the focus of this article. Following a vertebral fracture, deformity and kyphosis alter the vectors of the forces that are in action throughout the spine (16). Load-bearing kinetics redistribute the forces to other vertebrae, particularly those vertebrae adjacent to the original fracture (8,16). An individual with a normal spine may be able to tolerate these altered biomechanics; however, a person with a diseased spine may tolerate these alterations poorly.

The goal of vertebroplasty is to strengthen and stabilize a collapsed vertebral body and, consequently, restore the integrity of the collapsed vertebral body so that it can support weight-bearing kinetics (9). Percutaneous vertebroplasty strengthens a vertebra, but it also increases the stiffness of the segment (9,11). This altered stiffness of the vertebral body may again alter the distribution of forces to nearby vertebrae and thus increase the risk of fracture of these bodies (7,8). Other investigators (1,6) suggest that the collapse of adjacent vertebrae may, to some extent, reflect the natural evolution of osteoporosis in the spine (1,6). In the present study, 67% (24 of 36) of the new vertebral fractures represented a collapse of a vertebra adjacent to a level initially treated with percutaneous vertebroplasty. Three of the 22 patients had multiple new fractures after vertebroplasty (Table 1).

It is also important to note that 24 (67%) of the 36 new fractures occurred within 30 days after treatment with vertebroplasty and two other fractures occurred within 31 days (Table 1). It appears that a majority of the patients developed this complication within a relatively short period. It has been postulated that bone loss may occur in vertebral bodies adjacent to an original fracture (16). Following treatment with vertebroplasty, patients may demonstrate rapid clinical improvement. As a result, they may become more active and engage in activities that they were unable to perform previously. This new axial load on the vertebra may be stressful and result in new compression on adjacent vertebrae. Other patients may resume full activity and fall, fracturing another vertebra, an extremity, or even a hip (17).

The current uses of percutaneous vertebroplasty include treatment of both benign and malignant disease. In this retrospective analysis, we limited our study population to patients with osteoporosis. We observed a recurrent phenomenon in our experience, the development of a new fracture after vertebroplasty, and then attempted to analyze it. This observation bias represents another limitation that was inherent to the design of this retrospective study: We performed all vertebroplasties as clinical cases. There was no random selection of patients or a control population of patients who did not receive treatment with vertebroplasty.

In terms of follow-up, the patients were contacted by telephone or seen in the vertebroplasty clinic in the 3–4-week interim after treatment. Most of these patients were instructed to contact us on an as-needed basis. Therefore, we were able to report on only those patients who returned to our institution for reevaluation if vertebral body compression recurred or new symptoms occurred. In addition, we were not able to obtain substantial long-term follow-up data to determine if more patients experience this phenomenon.

In conclusion, percutaneous vertebroplasty has become an option for the treatment of painful osteoporotic compression fractures in patients in whom conservative medical management has failed. The risks of complications with this procedure are low, and patients demonstrate marked improvement with a rapid return to normal activities (1). We recognize that a substantial number of patients with osteoporosis, 12.4% of the study population, experienced new fractures following treatment with vertebroplasty. It is our hope that further study and recognition of this phenomenon will facilitate pretreatment screening of individuals who are at higher risk of having this complication.


    FOOTNOTES
 
Abbreviations: PMMA = polymethylmethacrylate, STIR = short inversion time inversion recovery

Author contributions: Guarantor of integrity of entire study, J.A.H.; study concepts and design, A.A.U., J.A.H., L.V.C.; literature research, A.A.U.; clinical studies, J.A.H., L.V.C., I.S.C., B.A.P., A.G.P.,; data acquisition, A.A.U., J.A.H.; data analysis/interpretation, A.A.U.; manuscript preparation, A.A.U.; manuscript definition of intellectual content, A.A.U., J.A.H.; manuscript editing, A.A.U., J.A.H., L.V.C.; manuscript revision/review, J.A.H., L.V.C., B.A.P., A.G.P., I.S.C.; manuscript final version approval, A.A.U., J.A.H., L.V.C., B.A.P., I.S.C.


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 

  1. Deramond H, Depriester C, Galibert P, Le Gars D. Percutaneous vertebroplasty with polymethylmethacrylate: technique, indications, and results. Radiol Clin North Am 1998; 36:533-546.[CrossRef][Medline]
  2. Gangi A, Kastler BA, Dietemann JL. Percutaneous vertebroplasty guided by a combination of CT and fluoroscopy. AJNR Am J Neuroradiol 1994; 15:83-86.[Abstract]
  3. Jensen ME, Evans AJ, Mathis JM, Kallmes DF, Cloft HJ, Dion JE. Percutaneous polymethylmethacrylate vertebroplasty in the treatment of osteoporotic vertebral body compression fractures: technical aspects. AJNR Am J Neuroradiol 1997; 18:1897-1904.[Abstract]
  4. Centenera LV, Choi S, Hirsch JA. Percutaneous vertebroplasty treats compression fractures. Diagn Imaging (San Franc) 2000; 22:147-148, 153.
  5. Chiras J, Depriester C, Weill A, Sola-Martinez MT, Deramond H. Percutaneous vertebral surgery: technics and indications. J Neuroradiol 1997; 24:45-59[French].[Medline]
  6. Cyteval C, Sarrabere MP, Roux JO, et al. Acute osteoporotic vertebral collapse: open study on percutaneous injection of acrylic surgical cement in 20 patients. AJR Am J Roentgenol 1999; 173:1685-90.[Abstract]
  7. Grados F, Depriester C, Cayrolle G, Hardy N, Deramond H, Fardellone P. Long-term observations of vertebral osteoporotic fractures treated by percutaneous vertebroplasty. Rheumatology (Oxford) 2000; 39:1410-1414.[Abstract/Free Full Text]
  8. Barr JD, Barr MS, Lemley TJ, McCann RM. Percutaneous vertebroplasty for pain relief and spinal stabilization. Spine 2000; 25:923-928.[CrossRef][Medline]
  9. Tohmeh AG, Mathis JM, Fenton DC, Levine AM, Belkoff SM. Biomechanical efficacy of unipedicular versus bipedicular vertebroplasty for the management of osteoporotic compression fractures. Spine 1999; 24:1772-1776.[CrossRef][Medline]
  10. Dean JR, Ison KT, Gishen P. The strengthening effect of percutaneous vertebroplasty. Clin Radiol 2000; 55:471-476.[CrossRef][Medline]
  11. Belkoff SM, Maroney M, Fenton DC, Mathis JM. An in vitro biomechanical evaluation of bone cements used in percutaneous vertebroplasty. Bone 1999; 25:23S-26S.[Medline]
  12. Cortet B, Cotten A, Boutry N. Percutaneous vertebroplasty in the treatment of osteoporotic vertebral compression fractures: an open prospective study. J Rheumatol 1999; 26:2222-2228.[Medline]
  13. Mathis JM, Petri M, Naff N. Percutaneous vertebroplasty treatment of steroid-induced osteoporotic compression fractures. Arthritis Rheum 1998; 41:171-175.[CrossRef][Medline]
  14. Zoarski GH, Snow P, Olan WJ. Percutaneous vertebroplasty for osteoporotic compression fractures: quantitative prospective evaluation of long-term outcomes. J Vasc Interv Radiol 2002; 13:139-148.[Medline]
  15. Lindsay R, Silverman S, Cooper C, et al. Risk of new vertebral fracture in the year following a fracture. JAMA 2001; 285:320-323.[Abstract/Free Full Text]
  16. Wasnich U. Vertebral fracture epidemiology. Bone 1996; 18:179S-183S.[Medline]
  17. Jensen ME, Dion JE. Percutaneous vertebroplasty in the treatment of osteoporotic compression fractures. Neuroimaging Clin N Am 2000; 10:547-568.[Medline]



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A.T. Trout, D.F. Kallmes, J.I. Lane, K.F. Layton, and W.F. Marx
Subsequent Vertebral Fractures after Vertebroplasty: Association with Intraosseous Clefts
AJNR Am. J. Neuroradiol., August 1, 2006; 27(7): 1586 - 1591.
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JBJSHome page
N. A. Manson and F. M. Phillips
Minimally Invasive Techniques for the Treatment of Osteoporotic Vertebral Fractures
J. Bone Joint Surg. Am., August 1, 2006; 88(8): 1862 - 1872.
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JBJSHome page
H. Prather, L. Van Dillen, J. P. Metzler, K. D. Riew, and L. A. Gilula
Prospective Measurement of Function and Pain in Patients with Non-Neoplastic Compression Fractures Treated with Vertebroplasty
J. Bone Joint Surg. Am., February 1, 2006; 88(2): 334 - 341.
[Abstract] [Full Text] [PDF]


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Am. J. Neuroradiol.Home page
A.T. Trout, D.F. Kallmes, and T.J. Kaufmann
New Fractures after Vertebroplasty: Adjacent Fractures Occur Significantly Sooner
AJNR Am. J. Neuroradiol., January 1, 2006; 27(1): 217 - 223.
[Abstract] [Full Text] [PDF]


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RadiologyHome page
A. K. Singh, T. K. Pilgram, and L. A. Gilula
Osteoporotic Compression Fractures: Outcomes after Single- versus Multiple-Level Percutaneous Vertebroplasty
Radiology, January 1, 2006; 238(1): 211 - 220.
[Abstract] [Full Text] [PDF]


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J Bone Joint Surg BrHome page
A. G. Hadjipavlou, M. N. Tzermiadianos, P. G. Katonis, and M. Szpalski
Percutaneous vertebroplasty and balloon kyphoplasty for the treatment of osteoporotic vertebral compression fractures and osteolytic tumours
J Bone Joint Surg Br, December 1, 2005; 87-B(12): 1595 - 1604.
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RadiologyHome page
A. Hiwatashi, R. Sidhu, R. K. Lee, R. R. deGuzman, D. T. Piekut, and P.-L. A. Westesson
Kyphoplasty versus Vertebroplasty to Increase Vertebral Body Height: A Cadaveric Study
Radiology, December 1, 2005; 237(3): 1115 - 1119.
[Abstract] [Full Text] [PDF]


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Am. J. Neuroradiol.Home page
M. I. Syed, N. A. Patel, S. Jan, M. S. Harron, K. Morar, and A. Shaikh
New Symptomatic Vertebral Compression Fractures within a Year Following Vertebroplasty in Osteoporotic Women
AJNR Am. J. Neuroradiol., June 1, 2005; 26(6): 1601 - 1604.
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J Am Acad Orthop SurgHome page
J. M. Spivak and M. G. Johnson
Percutaneous Treatment of Vertebral Body Pathology
J. Am. Acad. Ortho. Surg., January 1, 2005; 13(1): 6 - 17.
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F. Mckiernan, T. Faciszewski, and R. Jensen
Quality of Life Following Vertebroplasty
J. Bone Joint Surg. Am., December 1, 2004; 86(12): 2600 - 2606.
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RadiologyHome page
G. Baroud, P. Heini, J. Nemes, M. Bohner, S. Ferguson, T. Steffen, J. A. Hirsch, R. Alkaley, A. A. Uppin, A. Pazianos, et al.
Biomechanical Explanation of Adjacent Fractures Following Vertebroplasty [letter] * Dr Hirsch and colleagues respond:
Radiology, November 1, 2003; 229(2): 606 - 608.
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