The Journal of Bone and Joint Surgery (American). 2008;90:1722-1725.
doi:10.2106/JBJS.G.00646
© 2008 The Journal of Bone and Joint Surgery, Inc.
Percutaneous Spine Biopsy: A Meta-Analysis
Ali Nourbakhsh, MD1,
James J. Grady, DrPH1 and
Kim J. Garges, MD1
1 Division of Spine Surgery, Department of Orthopaedic Surgery and Rehabilitation (A.N. and K.J.G.) and Division of Epidemiology and Biostatistics, Office of Biostatistics (J.J.G.), University of Texas Medical Branch, Galveston, TX 77555. E-mail address for A. Nourbakhsh: alnourba{at}utmb.edu. E-mail address for J.J. Grady: jgrady{at}utmb.edu. E-mail address for K.J. Garges: kjgarges{at}utmb.edu
Investigation performed at University of Texas Medical Branch, Galveston, Texas
Disclosure: The authors did not receive any outside funding or grants in support of their research for or preparation of this work. Neither they nor a member of their immediate families received payments or other benefits or a commitment or agreement to provide such benefits from a commercial entity. No commercial entity paid or directed, or agreed to pay or direct, any benefits to any research fund, foundation, division, center, clinical practice, or other charitable or nonprofit organization with which the authors, or a member of their immediate families, are affiliated or associated.
A commentary is available with the electronic versions of this article, on our web site (www.jbjs.org) and on our quarterly CD-ROM (call our subscription department, at 781-449-9780, to order the CD-ROM).
Background: Percutaneous spine biopsy has widely replaced open biopsy. We conducted a meta-analysis to evaluate the effect of the inner diameter of the biopsy needle and the method of imaging guidance on the adequacy and accuracy of tissue samples and to evaluate the complication rates associated with the different needle diameters and imaging guidance methods.
Methods: We searched MEDLINE for studies that evaluated either the adequacy (whether or not a diagnosis could be made on the basis of pathologic examination) or the accuracy (whether or not the primary diagnosis was correct) of samples obtained by means of percutaneous spine biopsy. These articles and their relevant references subsequently were reviewed twice and were evaluated against the inclusion criteria, yielding twenty-five studies. The inclusion criterion was the use of a biopsy instrument (a fine needle or trephine with an identifiable inner diameter) under the guidance of imaging (fluoroscopy or computed tomography) for the evaluation of an identified spine lesion, with the report of either adequacy or accuracy. Meta-analysis with use of the random-effects model was used to analyze the data.
Results: The adequacy, accuracy, and complication rates increased with the inner diameter of the needles, but, with the numbers available, only the complication rate increased significantly (p = 0.01). Although the use of a computed tomography scan slightly increased the adequacy and accuracy of the samples, these increases were not significant. The complication rate associated with the use of computed tomography was 3.3%, compared with 5.3% for fluoroscopy.
Conclusions: As the outcomes associated with computed tomography were not significantly different from those associated with fluoroscopy, the decision to use one or the other requires the consideration of other factors, such as the type, level, and vertebral location of the lesion as well as the expertise of the physician. In situations in which the use of a needle with a small inner diameter is highly effective (for example, in cases of metastatic lesions), the clinician should first consider using a needle with a smaller inner diameter to obtain the biopsy specimen because of the higher complication rate associated with large-bore needles. However, in cases of sclerotic lesions, in which obtaining an adequate sample can be difficult, the use of a needle with a larger inner diameter is desirable.
Level of Evidence: Therapeutic Level III. See Instructions to Authors for a complete description of levels of evidence.

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