Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/51854
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dc.contributor.authorEssibayi M.A.-
dc.contributor.authorMortezaei A.-
dc.contributor.authorAzzam A.Y.-
dc.contributor.authorBangash A.H.-
dc.contributor.authorEraghi M.M.-
dc.contributor.authorFluss R.-
dc.contributor.authorBrook A.-
dc.contributor.authorAltschul D.J.-
dc.contributor.authorYassari R.-
dc.contributor.authorChandra R.V.-
dc.contributor.authorCancelliere N.M.-
dc.contributor.authorPereira V.M.-
dc.contributor.authorJennings J.W.-
dc.contributor.authorGilligan C.J.-
dc.contributor.authorBono C.M.-
dc.contributor.authorHirsch J.A.-
dc.contributor.authorDmytriw A.A.-
dc.date.accessioned2024-06-17T03:32:47Z-
dc.date.available2024-06-17T03:32:47Z-
dc.date.copyright2024-
dc.date.issued2024-06-05en
dc.identifier.citationEuropean Radiology. 34(11) (pp 7185-7196), 2024. Date of Publication: November 2024.-
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/51854-
dc.description.abstractObjectives: Percutaneous vertebroplasty and kyphoplasty are common interventions for osteoporotic vertebral compression fractures. However, there is concern about an increased risk of adjacent-level fractures after treatment. This study aimed to compare the risk of adjacent-level fractures after vertebroplasty and kyphoplasty with the natural history after osteoporotic vertebral compression fractures. Material(s) and Method(s): A network meta-analysis of randomized controlled trials (RCTs) was conducted to evaluate the risk of adjacent-level fractures after vertebroplasty and kyphoplasty compared to the natural history after osteoporotic vertebral compression fractures. Frequentist network meta-analysis was conducted using the "netmeta" package, and heterogeneity was assessed using Q statistics. The pooled risk ratio (RR) and 95% confidence intervals (CI) were calculated using random effects. Result(s): Twenty-three RCTs with a total of 2838 patients were included in the analysis. The network meta-analysis showed comparable risks of adjacent-level fractures between vertebroplasty, kyphoplasty, and natural history after osteoporotic vertebral compression fractures with a mean follow-up of 21.2 (range: 3-49.4 months). The pooled RR for adjacent-level fractures after kyphoplasty compared to natural history was 1.35 (95% CI, 0.78-2.34, p = 0.23) and for vertebroplasty compared to natural history was 1.16 (95% CI, 0.62-2.14) p = 0.51. The risk of bias assessment showed a low to moderate risk of bias among included RCTs. Conclusion(s): There was no difference in the risk of adjacent-level fractures after vertebroplasty and kyphoplasty compared to natural history after osteoporotic vertebral compression fractures. The inclusion of a large patient number and network meta-analysis of RCTs serve evidence-based clinical practice. Clinical relevance statement: The risk of adjacent-level fracture following percutaneous vertebroplasty or kyphoplasty is similar to that observed in the natural history after osteoporotic vertebral compression fractures. Key Points: RCTs have examined the risk of adjacent-level fracture after intervention for osteoporotic vertebral compression fractures. There was no difference between vertebroplasty and kyphoplasty patients compared to the natural disease history for adjacent compression fractures. This is strong evidence that interventional treatments for these fractures do not increase the risk of adjacent fractures.Copyright © The Author(s), under exclusive licence to European Society of Radiology 2024.-
dc.publisherSpringer Science and Business Media Deutschland GmbH-
dc.relation.ispartofEuropean Radiology-
dc.subject.meshfracture-
dc.subject.meshkyphoplasty-
dc.subject.meshosteoporosis-
dc.titleRisk of adjacent level fracture after percutaneous vertebroplasty and kyphoplasty vs natural history for the management of osteoporotic vertebral compression fractures: a network meta-analysis of randomized controlled trials.-
dc.typeArticle-
dc.identifier.affiliationRadiology-
dc.type.studyortrialSystematic review and/or meta-analysis-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=https://dx.doi.org/10.1007/s00330-024-10807-3-
dc.publisher.placeGermany-
dc.identifier.pubmedid38811388 [https://www.ncbi.nlm.nih.gov/pubmed/?term=38811388]-
dc.identifier.institution(Essibayi, Fluss, Altschul, Yassari) Department of Neurological Surgery, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY, United States-
dc.identifier.institution(Essibayi) Department of Radiology, Mayo Clinic, Rochester, NY, United States-
dc.identifier.institution(Essibayi, Mortezaei, Azzam, Bangash, Eraghi, Altschul) Montefiore-Einstein Cerebrovascular Research Lab, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY, United States-
dc.identifier.institution(Brook) Department of Neuroradiology, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY, United States-
dc.identifier.institution(Yassari) Montefiore Spine Research Group, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY, United States-
dc.identifier.institution(Chandra) Department of Interventional Neuroradiology, Monash Health, Clayton, VIC, Australia-
dc.identifier.institution(Chandra) Department of Image, Monash University Faculty of Medicine Nursing and Health Sciences, Clayton, VIC, Australia-
dc.identifier.institution(Cancelliere, Pereira, Dmytriw) Neurovascular Centre, Divisions of Therapeutic Neuroradiology & amp; Neurosurgery, St. Michael's Hospital, University of Toronto, Toronto, ON, Canada-
dc.identifier.institution(Jennings) Musculoskeletal Radiology, Mallinckrodt Institute of Radiology, Washington University St. Louis School of Medicine, St. Louis, MO, United States-
dc.identifier.institution(Gilligan) Robert Wood Johnson University Hospital, New Brunswick, NJ, United States-
dc.identifier.institution(Bono) Department of Orthopedics, Massachusetts General Hospital & amp; Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States-
dc.identifier.institution(Hirsch, Dmytriw) Neuroendovascular Program, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States-
dc.identifier.institution(Hirsch) Senior affiliate research fellow, The Harvey L. Neiman Health Policy Institute, Reston, VA, United States-
dc.identifier.affiliationmh(Chandra) Department of Interventional Neuroradiology, Monash Health, Clayton, VIC, Australia-
item.openairetypeArticle-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
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