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Vertebral augmentation

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Percutaneous vertebroplasty
ICD-9-CM81.65
MedlinePlus007512

Vertebroplasty and kyphoplasty are similar medical spinal procedures where bone cement is injected through a small hole in the skin (percutaneously) into a fractured vertebra with the goal of relieving the pain of vertebral compression fractures (VCF). There are 1587 vertebral augmention articles in the English language. The most recent meta-analysis published in 2012 by Dr. Ioannis Papanastassiou is the first meta-analysis of only Level I and Level II date and evaluated 27 studies including eight randomized studies. The authors concluded after analyzing this body of literature in great detail that both Vertebroplasty and Kyphoplasty provide significant pain relief and 50% reduced rate of additional fracture over nonsurgical management. They also concluded that BKP has better anatomy restoration, and may be more beneficial than VP for improving quality of life (QOL) and disability. There were two randomized controlled trials published in 2009 by Dr. David Kallmes and Dr. Rachael Buchbinder that concluded that Vertebroplasty was no better than a sham treatment at relieving the pain associate with vertebral compression fractures. This created controversy as the conclusions were not consistent with clinicians experience with this procedure. A meta-analysis published in 2012 by Dr. Ming-Min Shi was the first to include all available prospective evidence, including six of which were randomized control trials RCT’s. This meta-analysis concluded that compared with nonsurgical management (NSM), Vertebroplasty was more effective in relieving pain and in improving the QOL for patients with VCFs. The 2009 articles published in the New England Journal of Medicine have since been discredited due to the bulk of high quality data that has found Vertebroplasty to be safe and effective and because of design and excution problems with these articles. Some of the primary criticisms include that the 2009 triald were underpowered, suffered from selection bias, had unclear clinical and imaging diagnostic criteria for inclusion (i.e. no requirement for Magnetic Resonance (MR) imaging or nuclear bone scanning for diagnosing the fractures), that there was no description of a clinical exam used to determine if the pain came from a vertebral fracture or from another issue, and that the sham was actually an injection of local anesthetic into the area around the spine. Despite all of these limiting factors, when analyzing the structure and execution of the trial itself, if the same response rate for the 131 patients that were included had been carried out for the originally intended 250 patients, vertebroplasty would have been found to be significantly better than sham treatement at a p-value of < 0.01. Even with the 131 patients, if one patient had a different response (i..e a favorable response in the VP group or an unfavorable response in the sham group), VP would have been found to be significantly better than sham with a p-value of < 0.04. Given the near equivocal nature of this information and the presence of a large body of data with a different conclusion these studies should not be considered within a larger perspective. If the highest quality portion of that literature on Vertebroplasty and Kyphoplasty is analyzed the conclusions that can be drawn are that vertebral augmentation was significantly better than nonsurgical management for decreasing pain and if the fracture was treated in the first seven weeks, the pain reduction is better. This analysis also shows significantly less additional fractures for those patients treated with vertebral augmentation rather than those treated with nonsurgical management and those patients treated with Kyphoplasty had a significantly better improvement in their quality of life than those treated with Vertebroplasty. The data also shows a significantly higher mortality in those patients treated with nonsurgical management as compared with those patients treated with vertebral augmentation emphasizes the importance of offering the treatment most likely to benefit the patient.


History

The first percutaneous vertebroplasty was performed in 1984 at the University Hospital of Amiens, France to treat an aggressive vertebral hemangioma spinal tumor. A report of this and 6 other patients was published in 1987 and it was introduced in the United States in the early 1990s. Initially, the treatment was used primarily for tumors in Europe and VCF in the United States, although the distinction has largely gone away since then.[1]

Effectiveness

Out of the 27 articles on Vertebral Augmentation (including Vertebroplasty and Kyphoplasty) identified by Papanastassiou, et al in their summary of all Level I and Level II data, 18 of the studies involved Kyphoplasty. All of these studies by definition included over 20 patients and the Kyphoplasty articles included the FREE trial with 300 patients and a trial comparing Kyphoplasty and Vertebroplasty with 100 patients. The conclusion of Papanastassiou regarding Kyphoplasty was that it decreased pain to a greater degree than Vertebroplasty (5.07 vs 4.55 points on the VAS) and resulted in significantly better improvement in quality of life than both Vertebroplasty and non-surgical management. This meta-analysis was taken from 1587 articles on vertebral augmentation, more articles than in any other area of spine. A recent meta-analysis on Vertebroplasty by Dr. Ming-Min Shi which was the first to include all the available prospective evidence, including nine prospective controlled trials (six of which were RCT’s) concluded that compared with NSM, VP was more effective in relieving pain and in improving the QOL for patients with vertebral compression fractures. This meta-analysis was also substantially larger, quadrupling the sample size compared with previous meta-analysis.


Procedure

Vertebroplasty is typically performed by a spine surgeon or interventional radiologist. It is a minimally invasive procedure and patients usually go home the same or next day as the procedure. Patients are given local anesthesia and light sedation for the procedure, though it can be performed using only local anesthetic for patients with medical problems who cannot tolerate sedatives well.

During the procedure, bone cement is injected with a biopsy needle into the collapsed or fractured vertebra. The needle is placed with fluoroscopic x-ray guidance. The cement (most commonly PMMA, although more modern cements are used as well) quickly hardens and forms a support structure within the vertebra that provide stabilization and strength. The needle makes a small puncture in the patient's skin that is easily covered with a small bandage after the procedure.[2]

New Vertebral Fractures

In a study regarding this topic, Lin et al. it was hypothesized that the new vertebral fractures resulted from a combination of factors. The patient’s underlying spinal disease (e.g., osteoporosis or vertebral metastasis) in conjunction with the alteration in the biomechanics of force transmission through the augmented vertebral body were suspected of increasing the risk of subsequent vertebral fractures post-vertebroplasty. In addition, Lin et al. believe that there was increased stress placed on the adjacent vertebral body after vertebroplasty that may have contributed to new fractures, stating that pain reduction and subsequent increased activity by the patient were the contributing factors. Hu and Hart state that multiple retrospective reviews have shown an increased risk of adjacent vertebral body fractures after vertebroplasty and mention a study by Trout et al. in which 41.4% of 186 new fractures were adjacent to the treated level in 86 of 432 patients with new fractures. In Trout’s study, it was found that the relative risk of adjacent level was 4.62 times greater than that for nonadjacent level fractures however they could not prove that vertebroplasty was the cause of these adjacent vertebral fractures, stating that they could only suggest a strong association between the two events. In the meta-analysis of all of the level I data, subsequent fractures occurred more frequently in the nonsurgical management group (22 %) compared with Vertebroplasty (11 %, P = 0.04) and Kyphoplasty (11 %, P = 0.01).

Kyphoplasty

Cement in a vertebra as seen on plain Xray.

Kyphoplasty is a variation of a vertebroplasty that attempts to stop the pain caused by the bone fracture and attempts to restore the height and angle of kyphosis of a fractured vertebra (of certain types), followed by its stabilization using injected bone cement. The procedure typically includes the use of a small balloon that is inflated in the vertebral body to create a void within the cancellous bone prior to cement delivery.[3] Once the void is created, the procedure continues in a similar manner as a vertebroplasty, but the bone cement is typically delivered directly into the newly created void.


Risks

A CT image of cement used in kyphoplasty that has entered the spinal channel and is pressing on the spinal cord resulting in neurological symptoms

Some of the associated risks that can be produced are from the leak of acrylic cement outside of the vertebral body. Although severe complications are extremely rare, it is important to know that infection, bleeding, numbness, tingling, headache, and paralysis may ensue due to misplacement of the needle or cement. This particular risk is decreased by the use of x-ray or other radiological imaging to ensure proper placement of the cement.[2]



See also

References

  1. ^ Mathis, John M.; Deramond, Hervé; Belkoff, Stephen M., eds. (2006) [First edition published 2002]. Percutaneous Vertebroplasty and Kyphoplasty (2nd ed.). Springer Science+Business Media. pp. 3–5. ISBN 0-387-29078-8.
  2. ^ a b Nicole Berardoni M.D, Paul Lynch M.D, and Tory McJunkin M.D. "Vertebroplasty and Kyphoplasty" 2008. Accessed 7 Aug 2009. http://www.arizonapain.com/Vertebroplasty-W.html
  3. ^ Ty Thaiyananthan M.D and Bryan Oh M.D. "Kyphoplasty/Vertebroplasty Procedure Ilustrations" 2011. http://www.basicspine.com/conditions-procedures/spine-treatments/kyphoplasty.html

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