Evidence map›Paper›PMID 39241108›Full record

ArticleBrain : a journal of neurology2024

Intracerebral delivery of antiseizure medications by microinvasive neural implants.

Hannah D Jackson, Max J Cotler, Gerald W Saunders, Carena A Cornelssen, Peter J West, Cameron S Metcalf, Karen S Wilcox, Michael J Cima

Abstract read
In one paragraph

Article in Brain : a journal of neurology, 2024. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Hannah D JacksonHarvard-MIT Program in Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.ORCID 0000-0002-7243-6802
Max J CotlerHarvard-MIT Program in Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Gerald W SaundersAnticonvulsant Drug Development Program, University of Utah, Salt Lake City, UT 84112, USA.
Carena A CornelssenDepartment of Biomedical Engineering, University of Utah, Salt Lake City, UT 84112, USA.
Peter J WestAnticonvulsant Drug Development Program, University of Utah, Salt Lake City, UT 84112, USA.
Cameron S MetcalfAnticonvulsant Drug Development Program, University of Utah, Salt Lake City, UT 84112, USA.
Karen S WilcoxAnticonvulsant Drug Development Program, University of Utah, Salt Lake City, UT 84112, USA.ORCID 0000-0003-2660-8826
Michael J CimaDepartment of Materials Science and Engineering, Koch Institute of Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

Funding

Deshpande Center for Technological Innovation at MITNIH HHSUniversity of Utah
6 · The paper itself

Abstract

Focal epilepsy is a difficult disease to treat as two-thirds of patients will not respond to oral anti-seizure medications (ASMs) or have severe off-target effects that lead to drug discontinuation. Current non-pharmaceutical treatment methods (resection or ablation) are underutilized due to the associated morbidities, invasive nature and inaccessibility of seizure foci. Less invasive non-ablative modalities may potentially offer an alternative. Targeting the seizure focus in this way may avoid unassociated critical brain structures to preserve function and alleviate seizure burden. Here we report use of an implantable, miniaturized neural drug delivery system [microinvasive neural implant infusion platform (MINI)] to administer ASMs directly to the seizure focus in a mouse model of temporal lobe epilepsy. We examined the effect local delivery of phenobarbital and valproate had on focal seizures, as well as adverse effects, and compared this to systemic delivery. We show that local delivery of phenobarbital and valproate using our chronic implants significantly reduced focal seizures at all doses given. Furthermore, we show that local delivery of these compounds resulted in no adverse effects to motor function, whereas systemic delivery resulted in significant motor impairment. The results of this study demonstrate the potential of ASM micro dosing to the epileptic focus as a treatment option for people with drug resistant epilepsy. This technology could also be applied to a variety of disease states, enabling a deeper understanding of focal drug delivery in the treatment of neurological disorders.

Indexed as

AnticonvulsantsEpilepsy, Temporal LobePhenobarbitalValproic AcidAnimalsDisease Models, AnimalDrug Delivery SystemsMaleMiceMice, Inbred C57BLSeizuresAnticonvulsantsPhenobarbitalValproic Acidanti-seizure medicationbrainepilepsyintracerebral deliveryneural implant

Identifiers

PMID39241108
PMCPMC11731051

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.