Evidence map›Paper›PMID 27835935›Full record

ArticleTissue engineering. Part A2017

A New Vertebral Body Replacement Strategy Using Expandable Polymeric Cages.

Xifeng Liu, Alex Paulsen, Hugo Giambini, Ji Guo, A Lee Miller, Po-Chun Lin, Michael J Yaszemski, Lichun Lu

Abstract read
In one paragraph

Article in Tissue engineering. Part A, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Xifeng Liu1 Department of Physiology and Biomedical Engineering, Mayo Clinic , Rochester, Minnesota.
Alex Paulsen2 Department of Orthopedic Surgery, Mayo Clinic , Rochester, Minnesota.
Hugo Giambini2 Department of Orthopedic Surgery, Mayo Clinic , Rochester, Minnesota.
Ji Guo2 Department of Orthopedic Surgery, Mayo Clinic , Rochester, Minnesota.
A Lee Miller2 Department of Orthopedic Surgery, Mayo Clinic , Rochester, Minnesota.
Po-Chun Lin2 Department of Orthopedic Surgery, Mayo Clinic , Rochester, Minnesota.
Michael J Yaszemski1 Department of Physiology and Biomedical Engineering, Mayo Clinic , Rochester, Minnesota.
Lichun Lu1 Department of Physiology and Biomedical Engineering, Mayo Clinic , Rochester, Minnesota.
Mayo Clinic · US

Funding

Musculoskeletal Research Training ProgramT32AR056950 · NIAMS · MAYO CLINIC ROCHESTER · PI Jennifer J Westendorf · 2009 to 2026
$7.0M
Metastatic Spine Tumors: Minimally Invasive Fracture Risk Analysis and Treatment - MasterR01AR056212 · NIAMS · MAYO CLINIC ROCHESTER · PI Benjamin D Elder, Lichun Lu · 2008 to 2026
$6.2M
NIAMS NIH HHS R01 AR056212NIAMS NIH HHS T32 AR056950
6 · The paper itself

Abstract

We have developed a novel polymeric expandable cage that can be delivered via a posterior-only surgical approach for the treatment of noncontained vertebral defects. This approach is less invasive than an anterior-only or combined approach and much more cost-effective than currently used expandable metal cages. The polymeric expandable cage is composed of oligo poly(ethylene glycol) fumarate (OPF), a hydrogel that has been previously shown to have excellent nerve and bone tissue biocompatibility. OPF hydrogel cages can expand to twice their original diameter and length within a surgical time frame following hydration. Modulation of parameters such as polymeric network crosslink density or the introduction of charge to the network allowed for precise expansion kinetics. To meet specific requirements due to size variations in patient vertebral bodies, we fabricated a series of molds with varied diameters and explored the expansion kinetics of the OPF cages. Results showed a stable expansion ratio of approximately twofold to the original size within 20 min, regardless of the absolute value of the cage size. Following implantation of a dried OPF cage into a noncontained vertebral defect and its in situ expansion with normal saline, other augmentation biomaterials, such as poly(propylene fumarate) (PPF), can be injected to the lumen of the OPF cage and allowed to crosslink in situ. The OPF/PPF composite scaffold can provide the necessary rigidity and stability to the augmented spine.

Indexed as

SpineStress, MechanicalAnimalsBone SubstitutesHumansHydrogelsPolyethylene GlycolsBone SubstitutesHydrogelsPolyethylene Glycolsbiomaterialshydrogelspinetissue engineeringvertebral body reconstruction

Identifiers

PMID27835935
PMCPMC5346914
OpenAlexW2550928386

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.