Evidence map›Paper›PMID 25824317›Full record

ArticleJournal of vascular and interventional radiology : JVIR2015

Calibrated Bioresorbable Microspheres as an Embolic Agent: An Experimental Study in a Rabbit Renal Model.

Lihui Weng, Davis Seelig, Parinaz Rostamzadeh, Jafar Golzarian

Abstract read
In one paragraph

Article in Journal of vascular and interventional radiology : JVIR, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Polymeric materials for embolic and chemoembolic applications.Journal of controlled release : official journal of the Controlled Release Society · 2016
    Review
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.

Lihui WengDepartment of Radiology, University of Minnesota, Mayo B228, 420 Delaware Street SE, Minneapolis, MN 55455.
Davis SeeligDepartment of Veterinary Clinical Sciences, University of Minnesota, St Paul, Minnesota.
Parinaz RostamzadehDepartment of Radiology, University of Minnesota, Mayo B228, 420 Delaware Street SE, Minneapolis, MN 55455.
Jafar GolzarianDepartment of Radiology, University of Minnesota, Mayo B228, 420 Delaware Street SE, Minneapolis, MN 55455.. Electronic address: jafar@umn.edu.

Funding

University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR000114 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2012 to 2015
$35.0M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)KL2TR000113 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2012 to 2015
$5.4M
Pathogenesis of Chronic Wasting Disease in Transgenic MiceK01OD010987 · OD · UNIVERSITY OF MINNESOTA · PI SEELIG, DAVIS MARTIN · 2012 to 2014
$327k
NCATS NIH HHS KL2 TR000113NCATS NIH HHS UL1 TR000114NIH HHS K01 OD010987
6 · The paper itself

Abstract

purposeTo evaluate the time frame of resorption and tissue response of newly developed bioresorbable microspheres (BRMS) and vessel recanalization after renal embolization. MATERIALS AND

methodsEmbolization of lower poles of kidneys of 20 adult rabbits was performed with BRMS (300-500 µm). Two rabbits were sacrificed immediately after embolization (day 0). Three rabbits were sacrificed after follow-up angiography at 3, 7, 10, 14, 21, and 30 days. The pathologic changes in the renal parenchyma, BRMS degradation, and vessel recanalization were evaluated histologically and angiographically.

resultsEmbolization procedures were successfully performed, and all animals survived without complication. Infarcts were observed in all kidneys that received embolization harvested after day 0. Moderate degradation of BRMS (score = 1.07 ± 0.06) was observed by day 3. Of BRMS, 95% were resorbed before day 10 with scant BRMS materials remaining in the arteries at later time points. Partial vessel recanalization was observed by angiography starting on day 3, whereas new capillary formation was first identified histologically on day 7. Vascular inflammation associated with BRMS consisted of acute, heterophilic infiltrate at earlier time points (day 3 to day 10); this was resolved with the resorption of BRMS. Inflammation and fibrosis within infarcted regions were consistent with progression of infarction.

conclusionsBRMS were bioresorbable in vivo, and most BRMS were resorbed before day 10 with a mild tissue reaction. Vessel recanalization occurred secondary to the resorption of BRMS.

Indexed as

Absorbable ImplantsMicrospheresAnimalsBlood Flow VelocityEmbolization, TherapeuticHemostaticsParticle SizeRabbitsRenal ArteryTreatment OutcomeHemostatics

Identifiers

PMID25824317
PMCPMC5048746

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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.