The minimally effective dose of bone morphogenetic protein in posterior lumbar interbody fusion: a systematic review and meta-analysis
•Fusion and complication rates did not differ significantly between doses of BMP.•The minimally effective dose of BMP for fusion was 1.28 mg/level.•The location of BMP placement does not significantly affect fusion and complication rates. The risks and benefits of recombinant human bone morphogeneti...
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Veröffentlicht in: | The spine journal 2020-08, Vol.20 (8), p.1286-1304 |
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Zusammenfassung: | •Fusion and complication rates did not differ significantly between doses of BMP.•The minimally effective dose of BMP for fusion was 1.28 mg/level.•The location of BMP placement does not significantly affect fusion and complication rates.
The risks and benefits of recombinant human bone morphogenetic protein-2 (BMP) in posterior lumbar interbody fusion (PLIF) and transforaminal lumbar interbody fusion (TLIF) have been widely reported. However, the BMP dose associated with such reports varied widely. Additionally, data on the location of BMP placement on complications and fusion are lacking.
To determine the minimally effective dose (MED) of BMP which results in optimal fusion rates while minimizing complications; to determine the effects of the location of BMP placement has on fusion rates and complications.
Systematic review and meta-analysis.
Adult patients undergoing PLIF/TLIF for degenerative indications.
Rates of radiculitis, fusion, osteolysis, heterotopic bone formation, and new cancer diagnosis.
PubMed, Embase, and Cochrane Database were used to identify studies published between January 1, 2011 and April 30, 2019 reporting BMP usage in adult patients who underwent PLIF/TLIF degenerative indications. A qualitative and quantitative synthesis was performed to evaluate the MED of BMP and the effect of location of BMP placement on fusion and complications. Complications were defined as osteolysis, heterotopic bone growth, radiculitis, and rate of new cancer diagnosis. Complications and fusion outcomes were each pooled according to commercially available BMP doses. Additionally, complications and fusion outcomes were pooled according to 4 location groups (interbody cage only, interbody cage + posterolateral gutter [PLG], cage + interspace, and interspace + PLG). Heterogeneity was assessed with Q and I2 statistics.
Twenty-two articles, totaling 2,729 patients were included. Sixteen studies reported fusion and 15 reported complications. Among fusion studies, the mean BMP/level ranged from 1.28 to 12 mg/level. Among complication studies, the mean BMP/level ranged from 6.7 to 23.6 mg/level. The pooled overall fusion rate was 94.0% (91.4–95.8 confidence intervals). There was no significant difference in fusion and complication rates between different BMP doses. Thirteen studies included data on the location of BMP placement with 1,823 patients. At each BMP location, the fusion rate was not significantly different across the dose ranges (1.28–12 mg/level). We |
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ISSN: | 1529-9430 1878-1632 |
DOI: | 10.1016/j.spinee.2020.04.012 |