Evidence map›Paper›PMID 39034338›Full record

ArticleCardiovascular intervention and therapeutics2024

Degradation of a novel magnesium alloy-based bioresorbable coronary scaffold in a swine coronary artery model.

Sho Torii, Akiko Yamamoto, Ayako Yoshikawa, Linhai Lu, Makoto Sasaki, Shoko Obuchi, Akira Wada, Hideo Tsukamoto, Gaku Nakazawa

Abstract read
In one paragraph

Article in Cardiovascular intervention and therapeutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. A hierarchical MgFBioactive materials · 2025
    Article
  4. Review
  5. 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

9 authors.

Sho ToriiDepartment of Cardiology, School of Medicine, Faculty of Medicine, Tokai University, 143 Shimokasuya, Kanagawa, 2591193, Japan.
Akiko YamamotoResearch Center for Macromolecules and Biomaterials, National Institute for Materials Science, Ibaraki, Japan.
Ayako YoshikawaDepartment of Cardiology, School of Medicine, Faculty of Medicine, Tokai University, 143 Shimokasuya, Kanagawa, 2591193, Japan.
Linhai LuShanghai Kepan Investment and Management CO., LTD, Shanghai, China.
Makoto SasakiFaculty of Advanced Science and Technology, Kumamoto University, Kumamoto, Japan.
Shoko ObuchiJapan Medical Device Technology Co., Ltd, Kumamoto, Japan.
Akira WadaJapan Medical Device Technology Co., Ltd, Kumamoto, Japan.
Hideo TsukamotoJapan Medical Device Technology Co., Ltd, Kumamoto, Japan.
Gaku NakazawaDepartment of Cardiology, Faculty of Medicine, Kindai University, Osaka, Japan. gnakazawa@med.kindai.ac.jp.ORCID http://orcid.org/0000-0002-6721-1342

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The objective of the study is to investigate the safety, feasibility, and degradation profile of a novel Mg alloy-based bioresorbable coronary scaffold (JFK-PRODUCT BRS) with thin struts (110 μm). Polymer- or Mg alloy-based BRSs have not replaced nondegradable metal stents because of the higher prevalence of scaffold thrombosis and restenosis in clinical practice; these poor clinical outcomes were due to inadequate scaffold designs, including thick struts (more than 150 μm) and their inappropriate degradation processes. Fourteen healthy pigs received 17 JFK-PRODUCT BRSs in the coronary arteries and were sacrificed at 1, 6, 12, 18, and 26 months after implantation. Angiography, optical coherence tomography, microfocus X-ray computed tomography (µCT), scanning electron microscopy with energy-dispersive X-ray spectrometry (SEM-EDX), and histopathological evaluation were performed. The JFK-PRODUCT had a median percent late recoil of 11.28% at 1 month. The µCT observation confirmed that scaffold discontinuity reached 64.8% at 12 months with increased scaffold inner area thereafter, suggesting artery positive remodeling. The inflammation was mild, peaked at 18 months, and decreased thereafter. The SEM-EDX analysis demonstrated gradual degradation of the scaffold with formation of inorganic deposits, presumed to be calcium phosphates. It also revealed the disappearance of calcium phosphates at 26 months, achieving almost complete replacement of the scaffold by biocomponents. The current study demonstrated the safety and feasibility of JFK-PRODUCT with a lower acute recoil rate despite its thin struts. The scaffolds were almost completely disappeared at 26 months after implantation.

Indexed as

Absorbable ImplantsAlloysCoronary VesselsMagnesiumTissue ScaffoldsTomography, Optical CoherenceAnimalsCoronary AngiographyMicroscopy, Electron, ScanningProsthesis DesignSwineX-Ray MicrotomographyAlloysMagnesiumBioabsorbable magnesium scaffoldsControlled degradation profileElemental mappingPercutaneous coronary interventionPreclinical study

Identifiers

PMID39034338
PMCPMC11436393

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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.