Evidence map›Paper›PMID 26685129›Full record

ArticleEuropean heart journal2017

Intravascular fibrin molecular imaging improves the detection of unhealed stents assessed by optical coherence tomography in vivo.

Tetsuya Hara, Giovanni J Ughi, Jason R McCarthy, S Sibel Erdem, Adam Mauskapf, Samantha C Lyon, Ali M Fard, Elazer R Edelman, Guillermo J Tearney, Farouc A Jaffer

Open access · bronzeAbstract read
In one paragraph

Article in European heart journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

31 citing papers in PubMed, 58 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Review
  6. Ultrathin-strut versus thin-strut stent healing and outcomes in preclinical and clinical subjects.EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology · 2024
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Intravascular Fluorescence Molecular Imaging of Atherosclerosis.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  12. Let's embrace optical imaging: a growing branch on the clinical molecular imaging tree.European journal of nuclear medicine and molecular imaging · 2021
    Article
  13. Article
  14. Article
  15. ACS sensors · 2021
    Article
  16. Intracoronary optical coherence tomography: state of the art and future directions.EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology · 2021
    Article
  17. Article
  18. Article
  19. Atorvastatin ReducesJournal of the American Society of Nephrology : JASN · 2020
    Article
  20. 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

10 authors at 4 institutions in 1 country.

Tetsuya HaraCardiovascular Research Center, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Giovanni J UghiWellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Jason R McCarthyCenter for System Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
S Sibel ErdemCenter for System Biology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Adam MauskapfCardiovascular Research Center, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Samantha C LyonWellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Ali M FardWellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Elazer R EdelmanMassachusetts Institute of Technology, Cambridge, MA, USA.
Guillermo J TearneyWellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA fjaffer@mgh.harvard.edu gtearney@mgh.harvard.edu.
Farouc A JafferCardiovascular Research Center, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA fjaffer@mgh.harvard.edu gtearney@mgh.harvard.edu.
Massachusetts General Hospital · USHarvard University · USCenter for Systems Biology · USMassachusetts Institute of Technology · US

Funding

Vascular Drug Delivery - Supplement for EquipmentR01GM049039 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI EDELMAN, ELAZER R · 1994 to 2019
$8.9M
Targeted inhibition of fibrosis for the prevention of heart failureR01HL122238 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI MCCARTHY, JASON R. · 2015 to 2019
$4.0M
Chemical analysis of coronary atherosclerosis in patientsR01HL093717 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI TEARNEY, GUILLERMO J · 2008 to 2011
$3.3M
Intravascular Fluorescence Molecular Imaging of Inflammation in AtherosclerosisR01HL108229 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI JAFFER, FAROUC AMIN · 2010 to 2014
$2.1M
NIRF-OFDI of Inflammation in Atheroma Progression and Stent ComplicationsR01HL122388 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI JAFFER, FAROUC AMIN · 2015 to 2018
$2.1M
NHLBI NIH HHS R01 HL093717NHLBI NIH HHS R01 HL108229NHLBI NIH HHS R01 HL122238NHLBI NIH HHS R01 HL122388NIGMS NIH HHS R01 GM049039
6 · The paper itself

Abstract

aimsFibrin deposition and absent endothelium characterize unhealed stents that are at heightened risk of stent thrombosis. Optical coherence tomography (OCT) is increasingly used for assessing stent tissue coverage as a measure of healed stents, but cannot precisely identify whether overlying tissue represents physiological neointima. Here we assessed and compared fibrin deposition and persistence on bare metal stent (BMS) and drug-eluting stent (DES) using near-infrared fluorescence (NIRF) molecular imaging in vivo, in combination with simultaneous OCT stent coverage. METHODS AND

resultsRabbits underwent implantation of one BMS and one DES without overlap in the infrarenal aorta (N = 20 3.5 × 12 mm). At Days 7 and/or 28, intravascular NIRF-OCT was performed following the injection of fibrin-targeted NIRF molecular imaging agent FTP11-CyAm7. Intravascular NIRF-OCT enabled high-resolution imaging of fibrin overlying stent struts in vivo, as validated by histopathology. Compared with BMS, DES showed greater fibrin deposition and fibrin persistence at Days 7 and 28 (P < 0.01 vs. BMS). Notably, for edge stent struts identified as covered by OCT on Day 7, 92.8 ± 9.5% of DES and 55.8 ± 23.6% of BMS struts were NIRF fibrin positive (P < 0.001). At Day 28, 18.6 ± 10.6% (DES) and 5.1 ± 8.7% (BMS) of OCT-covered struts remained fibrin positive (P < 0.001).

conclusionIntravascular NIRF fibrin molecular imaging improves the detection of unhealed stents, using clinically translatable technology that complements OCT. A sizeable percentage of struts deemed covered by OCT are actually covered by fibrin, particularly in DES, and therefore such stents might remain prothrombotic. These findings have implications for the specificity of standalone clinical OCT assessments of stent healing.

Indexed as

FibrinMolecular imagingOptical coherence tomographyStent thrombosis

Identifiers

PMID26685129
PMCPMC5837565
OpenAlexW2212419929

What OpenQuestion holds

Textmetadata
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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.