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Erratum to: Clinical trial and in-vitro study comparing the efficacy of treating bony lesions with allografts versus synthetic or highly-processed xenogeneic bone grafts
BMC Musculoskeletal Disorders volume 17, Article number: 118 (2016)
The Original Article was published on 13 February 2016
Erratum
After publication of the original article [1], the authors noticed an error in the ‘Methods’ section. Within the ‘Patients’ sub-section, the first item in the list of synthetic or highly processed xenogeneic bone substitutes (SBS) should have been given as Orthoss®, rather than BioOss®. The sentence should therefore have read as follows:
“The following SBS were used: Orthoss® (Geistlich, Wolhusen, Switzerland) in 41.4 %, and at clearly lower percentages, respectively: Norian SRS® (Synthes) (8.6 %), Chronos® (Synthes) (1.7 %), Atlantik® (Argomedical) (2.6 %), Alaska® (Argomedical) (0.9 %), Endobone® (Biomet) (4.3 %), Pyrost® (Stryker) (0.9 %), Nanostim® (Medtronic) (37.1 %), Actifuse® (Baxter) (0.9 %), Tutobone® (Novomedics) (0.9 %) and PerOssal® (Botiss) (0.9 %).”
Reference
Kubosch EJ, Bernstein A, Wolf L, Fretwurst T, Nelson K, Schmal H. Clinical trial and in-vitro study comparing the efficacy of treating bony lesions with allografts versus synthetic or highlyprocessed xenogeneic bone grafts. BMC Musc Disord. 2016;17:77.
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The online version of the original article can be found under doi:10.1186/s12891-016-0930-1.
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Kubosch, E.J., Bernstein, A., Wolf, L. et al. Erratum to: Clinical trial and in-vitro study comparing the efficacy of treating bony lesions with allografts versus synthetic or highly-processed xenogeneic bone grafts. BMC Musculoskelet Disord 17, 118 (2016). https://doi.org/10.1186/s12891-016-0976-0
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DOI: https://doi.org/10.1186/s12891-016-0976-0