Evidence map›Paper›PMID 30513305›Full record

ArticleJournal of neuroscience methods2019

MRI guidance technology development in a large animal model for hyperlocal analgesics delivery to the epidural space and dorsal root ganglion.

Timothy P Maus, Joel P Felmlee, Mark D Unger, Andreas S Beutler

Abstract read
In one paragraph

Article in Journal of neuroscience methods, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
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

4 authors at 1 institution in 1 country.

Timothy P MausDepartment of Radiology, Mayo Graduate School, Mayo Clinic, Rochester, MN, 55902, USA. Electronic address: maus.timothy@mayo.edu.
Joel P FelmleeDepartment of Radiology, Mayo Graduate School, Mayo Clinic, Rochester, MN, 55902, USA.
Mark D UngerDepartment of Anesthesiology, Mayo Graduate School, Mayo Clinic, Rochester, MN, 55902, USA; Department of Oncology, Mayo Clinic, Mayo Graduate School, Mayo Clinic, Rochester, MN, 55902, USA; Translational Science Track, Mayo Graduate School, Mayo Clinic, Rochester, MN, 55902, USA.
Andreas S BeutlerDepartment of Anesthesiology, Mayo Graduate School, Mayo Clinic, Rochester, MN, 55902, USA; Department of Oncology, Mayo Clinic, Mayo Graduate School, Mayo Clinic, Rochester, MN, 55902, USA; Translational Science Track, Mayo Graduate School, Mayo Clinic, Rochester, MN, 55902, USA. Electronic address: beutler.andreas@mayo.edu.
Mayo Clinic in Arizona · US

Funding

Intraganglionic Analgesic Adeno-Associated Virus (AAV) Gene Vector Optimization in Large AnimalsR01NS100725 · NINDS · MAYO CLINIC ROCHESTER · PI BEUTLER, ANDREAS S. · 2017 to 2021
$3.2M
NINDS NIH HHS R01 NS100725
6 · The paper itself

Abstract

backgroundDevelopment of new analgesic drugs or gene therapy vectors for spinal delivery will be facilitated by "hyperlocal" targeting of small therapeutic injectate volumes if spine imaging technology can be used that is ready for future clinical translation. NEW

methodThis study provides methods for MRI-guided drug delivery to the periganglionic epidural space and the dorsal root ganglion (DRG) in the Yucatan swine.

resultsPhantom studies showed artifact-corrected needle localization with frequency encoding parallel to the needle shaft, while maximizing bandwidth (125 KHz) minimized needle artifact. A custom constructed 8-12 element surface coil (phased array) wrapped over the spine in conjunction with lateral recumbent positioning achieved diagnostic quality signal to noise ratio at the depth of the DRG and afforded transforaminal access via anterolateral or posterolateral vectors, as well as interlaminar access. Swine epidural anatomy was homologous with human anatomy. Injectate containing 2% gadolinium allowed imaging of injectate volumes in increments as small as 10 microliters and discrimination of epidural flow from intraparenchymal injectate delivery into a DRG. All technical and technological elements of the procedure appear clinically translatable. COMPARISON WITH EXISTING

methodsComputed tomographic or fluoroscopic guidance cannot directly visualize drug delivery into the DRG due to contrast medium toxicity, nor reliably identify epidural injection volumes of < 50 microliters.

conclusionsMRI-guided hyperlocal delivery in swine provides a translatable and faithful model of future human spinal novel drug- or gene therapy vector delivery.

Indexed as

AnalgesicsAnimalsArtifactsDrug Delivery SystemsEpidural SpaceGanglia, SpinalInjections, EpiduralMagnetic Resonance ImagingNeuronavigationPhantoms, ImagingSwineSwine, MiniatureAnalgesicsAnimal modelEpiduralIntraganglionicMRI-guidanceSpinal injection

Identifiers

PMID30513305
PMCPMC6317369
OpenAlexW2902276612

What OpenQuestion holds

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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.