Evidence map›Paper›PMID 26873750›Full record

Trial reportBMC musculoskeletal disorders2016

Clinical trial and in-vitro study comparing the efficacy of treating bony lesions with allografts versus synthetic or highly-processed xenogeneic bone grafts.

Eva Johanna Kubosch, Anke Bernstein, Laura Wolf, Tobias Fretwurst, Katja Nelson, Hagen Schmal

Erratum issuedOpen access · goldAbstract readClinical TrialComparative Study
In one paragraph

Trial report in BMC musculoskeletal disorders, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.9field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 37 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Eva Johanna KuboschDepartment of Orthopedics and Trauma Surgery, Albert-Ludwigs University Medical Center, Freiburg, Germany. johanna.kubosch@uniklinik-freiburg.de.
Anke BernsteinDepartment of Orthopedics and Trauma Surgery, Albert-Ludwigs University Medical Center, Freiburg, Germany. anke.bernstein@uniklinik-freiburg.de.
Laura WolfDepartment of Orthopedics and Trauma Surgery, Albert-Ludwigs University Medical Center, Freiburg, Germany. wolflaura@web.de.
Tobias FretwurstDepartment of Craniomaxillofacial Surgery, Albert-Ludwigs University Medical Center, Freiburg, Germany. tobias.fretwurst@uniklinik-freiburg.de.
Katja NelsonDepartment of Craniomaxillofacial Surgery, Albert-Ludwigs University Medical Center, Freiburg, Germany. katja.nelson@uniklinik-freiburg.de.
Hagen SchmalDepartment of Orthopedics and Trauma Surgery, Albert-Ludwigs University Medical Center, Freiburg, Germany. hagen.schmal@freenet.de.
University of Freiburg · DEUniversity Medical Center Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOur study aim was to compare allogeneic cancellous bone (ACB) and synthetic or highly-processed xenogeneic bone substitutes (SBS) in the treatment of skeletal defects in orthopedic surgery.

methods232 patients treated for bony lesions with ACB (n = 116) or SBS (n = 116) within a 10-year time period were included in this case-control study. Furthermore, both materials were seeded with human osteoblasts (hOB, n = 10) and analyzed by histology, for viability (AlamarBlue®) and protein expression activity (Luminex®).

resultsThe complication rate was 14.2 %, proportion of defects without bony healing 3.6 %; neither outcome parameter differed comparing the intervention groups. Failed consolidation correlated with an increase in complications (p < 0.03). The rate of complications was further highly significant in association with the location of use (p < 0.001), but did not depend on age, ASA risk classification, BMI, smoking behavior or type of insurance. However, those factors did significantly influence the bony healing rate (p < 0.02). Complication and consolidation rates were independent of gender and the filling substances employed within the different locations. Histological examination revealed similar bone structures, whereas cell remnants were apparent only in the allografts. Both materials were biocompatible in-vitro, and seeded with human osteoblasts. The cells remained vital over the 3-week culture period and produced microscopically typical bone matrix. We observed initially increased expression of osteocalcin, osteopontin, and osteoprotegerin as well as leptin and adiponectin secretion declining after 1 week, especially in the ACB group.

conclusionAlthough both investigated materials appeared to be similarly suitable for the treatment of skeletal lesions in-vivo and in-vitro, outcome was decisively influenced by other factors such as the site of use or epidemiological parameters.

Indexed as

AllograftsHeterograftsAdultAgedBone DiseasesBone SubstitutesBone TransplantationCase-Control StudiesCells, CulturedCell SurvivalFemaleHumansMaleMiddle AgedOsseointegrationOsteoblastsBone Substitutes

Identifiers

PMID26873750
PMCPMC4752776
OpenAlexW4254140549

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.