Safety and effectiveness of recombinant human bone morphogenetic protein-2 for spinal fusion: a meta-analysis of individual-participant data
- PMID: 23778905
- DOI: 10.7326/0003-4819-158-12-201306180-00005
Safety and effectiveness of recombinant human bone morphogenetic protein-2 for spinal fusion: a meta-analysis of individual-participant data
Abstract
Background: Recombinant human bone morphogenetic protein-2 (rhBMP-2) is widely used to promote fusion in spinal surgery, but its safety has been questioned.
Purpose: To evaluate the effectiveness and safety of rhBMP-2.
Data sources: Individual-participant data obtained from the sponsor or investigators and data extracted from study publications identified by systematic bibliographic searches through June 2012.
Study selection: Randomized, controlled trials of rhBMP-2 versus iliac crest bone graft (ICBG) in spinal fusion surgery for degenerative disc disease and related conditions and observational studies in similar populations for investigation of adverse events.
Data extraction: Individual-participant data from 11 eligible of 17 provided trials sponsored by Medtronic (Minneapolis, Minnesota) (n = 1302) and 1 of 2 other eligible trials (n = 106) were included. Additional aggregate adverse event data were extracted from 35 published observational studies.
Data synthesis: Primary outcomes were pain (assessed with the Oswestry Disability Index [ODI] or Short Form-36), fusion, and adverse events. At 24 months, ODI scores were 3.5% lower (better) with rhBMP-2 than with ICBG (95% CI, 0.5% to 6.5%) and radiographic fusion was 12% higher (CI, 2% to 23%). At or shortly after surgery, pain was more common with rhBMP-2 (odds ratio, 1.78 [CI, 1.06 to 2.95]). Cancer was more common after rhBMP-2 (relative risk, 1.98 [CI, 0.86 to 4.54]), but the small number of events precluded definite conclusions.
Limitation: The observational studies were diverse and at risk of bias.
Conclusion: At 24 months, rhBMP-2 increases fusion rates, reduces pain by a clinically insignificant amount, and increases early postsurgical pain compared with ICBG. Evidence of increased cancer incidence is inconclusive.
Primary funding source: Yale University Open Data Access Project.
Comment in
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A historic moment for open science: the Yale University Open Data Access project and medtronic.Ann Intern Med. 2013 Jun 18;158(12):910-1. doi: 10.7326/0003-4819-158-12-201306180-00009. Ann Intern Med. 2013. PMID: 23778908 Free PMC article. No abstract available.
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Meta-analysis of trials of recombinant human bone morphogenetic protein-2: what should spine surgeons and their patients do with this information?Ann Intern Med. 2013 Jun 18;158(12):912-3. doi: 10.7326/0003-4819-158-12-201306180-00010. Ann Intern Med. 2013. PMID: 23778909 No abstract available.
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The changing structure of industry-sponsored clinical research: pioneering data sharing and transparency.Ann Intern Med. 2013 Jun 18;158(12):914-5. doi: 10.7326/0003-4819-158-12-201306180-00011. Ann Intern Med. 2013. PMID: 23778910 No abstract available.
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Closing in on the truth about recombinant human bone morphogenetic protein-2: evidence synthesis, data sharing, peer review, and reproducible research.Ann Intern Med. 2013 Jun 18;158(12):916-8. doi: 10.7326/0003-4819-158-12-201306180-00012. Ann Intern Med. 2013. PMID: 23778911 No abstract available.
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