Evidence map›Paper›PMID 35743425›Full record

ArticleJournal of clinical medicine2022

Exploring Contraindications for Thrombolysis: Risk of Hemorrhagic Transformation and Neurological Deterioration after Thrombolysis in Mice with Recent Ischemic Stroke and Hyperglycemia.

Sarah Gelhard, Roxane-Isabelle Kestner, Moritz Armbrust, Helmuth Steinmetz, Christian Foerch, Ferdinand O Bohmann

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Observational
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

6 authors at 1 institution in 1 country.

Sarah GelhardDepartment of Neurology, Goethe University, Schleusenweg 2-16, 60528 Frankfurt am Main, Germany.ORCID 0000-0001-5097-985X
Roxane-Isabelle KestnerDepartment of Neurology, Goethe University, Schleusenweg 2-16, 60528 Frankfurt am Main, Germany.
Moritz ArmbrustInstitute of Neurology (Edinger Institute), Goethe University, 60528 Frankfurt am Main, Germany.
Helmuth SteinmetzDepartment of Neurology, Goethe University, Schleusenweg 2-16, 60528 Frankfurt am Main, Germany.
Christian FoerchDepartment of Neurology, Goethe University, Schleusenweg 2-16, 60528 Frankfurt am Main, Germany.
Ferdinand O BohmannDepartment of Neurology, Goethe University, Schleusenweg 2-16, 60528 Frankfurt am Main, Germany.ORCID 0000-0001-6439-0667
Goethe University Frankfurt · DE

Funding

This study was supported in part by a grant from the Goethe University Hospital Frankfurt (Nachwuchsforscher). Goethe University Hospital Frankfurt (Nachwuchsforscher)
6 · The paper itself

Abstract

(1) Intravenous thrombolysis with recombinant tissue plasminogen activator (rt-PA) in patients with acute ischemic stroke is limited because of several contraindications. In routine clinical practice, patients with a recent stroke are typically not treated with rt-PA in case of a recurrent ischemic event. The same applies to its use in the context of pulmonary artery embolism and myocardial infarction with a recent stroke. In this translational study, we evaluated whether rt-PA treatment after experimental ischemic stroke with or without additional hyperglycemia increases the risk for hemorrhagic transformation (HT) and worsens functional outcome regarding the old infarct area. (2) In total, 72 male C57BL/6N mice were used. Ischemic stroke (index stroke) was induced by transient middle cerebral artery occlusion (tMCAO). Mice received either rt-PA or saline 24 h or 14 days after index stroke to determine whether a recent ischemic stroke predisposes to HT. In addition to otherwise healthy mice, hyperglycemic mice were analyzed to evaluate diabetes as a second risk factor for HT. Mice designated to develop hyperglycemia were pre-treated with streptozotocin. (3) The neurological outcome in rt-PA and saline-treated normoglycemic mice did not differ significantly, either at 24 h or at 14 days. In contrast, hyperglycemic mice treated with rt-PA had a significantly worse neurological outcome (at 24 h,

Indexed as

hemorrhagic transformationhyperglycemiastrokethrombolysis

Identifiers

PMID35743425
PMCPMC9225099
OpenAlexW4281789071

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.