Evidence map›Paper›PMID 33714389›Full record

ArticleLancet (London, England)2021

Identification of vulnerable plaques and patients by intracoronary near-infrared spectroscopy and ultrasound (PROSPECT II): a prospective natural history study.

David Erlinge, Akiko Maehara, Ori Ben-Yehuda, Hans Erik Bøtker, Michael Maeng, Lars Kjøller-Hansen, Thomas Engstrøm, Mitsuaki Matsumura, Aaron Crowley, Ovidiu Dressler and 15 more

7 registry-linked trialsAbstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Lancet (London, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 7 registered trials, which are not on this map. Cited by 255 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
255citing papers in PubMed, 2 pooled it
39.1field-weighted citation impact, top 1% 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.

NCT06520904 phase4recruitingstarted 2024, after this paper: background citation

Effect of PCSK9 Inhibitors on Coronary Atherosclerotic Plaques Derived From Optical Coherence Tomography in Patients With Premature Coronary Artery Disease: a Randomized Controlled Trial

Ran2024Enrolled396Registered outcomes6Posted comparisons0ConditionsCoronary Artery Disease, Optical Coherence TomographyArmsPCSK9 inhibitor, Statin
Open the trial in the graph
NCT02171065 nacompletednot on this map

A Multicentre Prospective Natural History Study Using Multimodality Imaging in Patients With ACS- PROSPECT II (Natural History Study), Combined With a Randomized, Controlled, Intervention Study - PROSPECT ABSORB (Randomized Trial)

TypeinterventionalSponsorUppsala UniversityRan2014 to 2020Enrolled902ConditionsAcute Coronary Syndrome (ACS)Armssham, ABSORB BVS
NCT04857580 nawithdrawnnot on this map

Intracoronary Cryotherapy Effect for staBilization of vulnErable Plaque at Risk of Rupture as Assessed by imaGing

TypeinterventionalSponsorCryotherapeutics SARan2021 to 2022Enrolled0ConditionsAcute Coronary SyndromeArmsCTS Device
NCT05427786 phase4recruitingnot on this mapstarted 2022, after this paper: background citation

A Randomized, Open Label, Parallel-group Study to Evaluate the Impact of Pre-procedural Intracoronary Nicorandil Injection to PREVENT ReductioN of DecREased TIMI FLOW in Patients Who Undergoing Percutaneous Coronary Intervention for the Coronary Artery Disease

TypeinterventionalSponsorKorea University Anam HospitalRan2022 to 2026Enrolled460ConditionsNo-Reflow Phenomenon, Coronary Artery Disease, Percutaneous Coronary InterventionArmsNicorandil
NCT05599061 naactive not recruitingnot on this mapstarted 2023, after this paper: background citation

Treatment of Functionally Non-significant Vulnerable Plaques in Patients With Multivessel ST-elevation Myocardial Infarction The VULNERABLE Randomized Trial

TypeinterventionalSponsorFundación EPICRan2023 to 2028Enrolled609ConditionsCoronary Artery Disease, Coronary Disease, Ischemic Heart DiseaseArmsFFR>0.80+ OCT with findings indicative of vulnerable plaque
NCT05669222 nanot yet recruitingnot on this mapstarted 2023, after this paper: background citation

Functional and Angiography-Derived Strain Guided Multi-Vessel/Lesion Revascularization Strategy in Patients With Acute ST-Segment Elevation Myocardial Infarction (FAVOR V AMI)

TypeinterventionalSponsorChina National Center for Cardiovascular DiseasesRan2023 to 2028Enrolled5,000ConditionsST-Segment Elevation Myocardial Infarction, Multivessel Coronary Artery Disease, Percutaneous Coronary InterventionArmsFAST Technique, Angiography
NCT06681155 not yet recruitingnot on this mapstarted 2024, after this paper: background citation

A Prospective Cohort Study on the Identification of High-Risk Coronary Plaque by Multimodality Intravascular Imaging(PlaqueVision Study)

TypeobservationalSponsorChinese PLA General HospitalRan2024 to 2031Enrolled500ConditionsCoronary Arterial Disease (CAD), Acute Coronary SyndromesArmsAssessment of plaque morphology, structure, and stability in non-culprit lesions
3 · Its place in the literature

Who cites it

255 citing papers in PubMed, 2 syntheses or guidelines pooled it, 441 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Changes in non-culprit coronary lesions with PCSK9 inhibitors: the randomised, placebo-controlled FITTER trial.EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology · 2025
    Trial
  8. Incidence and pattern of urgent revascularization in acute coronary syndromes treated with ticagrelor or prasugrel.Clinical research in cardiology : official journal of the German Cardiac Society · 2024
    Trial
  9. Trial
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article

195 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 19 institutions in 4 countries.

David ErlingeLund University, Lund, Sweden. Electronic address: david.erlinge@med.lu.se.
Akiko MaeharaNewYork-Presbyterian Hospital/Columbia University Irving Medical Center, New York, NY, USA; Cardiovascular Research Foundation, New York, NY, USA.
Ori Ben-YehudaNewYork-Presbyterian Hospital/Columbia University Irving Medical Center, New York, NY, USA; Cardiovascular Research Foundation, New York, NY, USA; University of California San Diego, San Diego, CA, USA.
Hans Erik BøtkerAarhus University Hospital, Aarhus, Denmark.
Michael MaengAarhus University Hospital, Aarhus, Denmark.
Lars Kjøller-HansenZealand University Hospital, Roskilde, Denmark.
Thomas EngstrømUniversity of Copenhagen, Copenhagen, Denmark.
Mitsuaki MatsumuraCardiovascular Research Foundation, New York, NY, USA.
Aaron CrowleyCardiovascular Research Foundation, New York, NY, USA.
Ovidiu DresslerCardiovascular Research Foundation, New York, NY, USA.
Gary S MintzCardiovascular Research Foundation, New York, NY, USA.
Ole FröbertFaculty of Health, Örebro University, Sweden.
Jonas PerssonDanderyd Hospital, Karolinska Institutet, Stockholm, Sweden.
Rune WisethSt Olavs Hospital, Trondheim University Hospital, Norway.
Alf Inge LarsenStavanger University Hospital, Stavanger, Norway.
Lisette Okkels JensenOdense University Hospital, Odense, Denmark.
Jan Erik NordrehaugUniversity of Bergen, Bergen, Norway.
Øyvind BleieHaukeland University Hospital, Bergen, Norway.
Elmir OmerovicDepartment of Cardiology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Claes HeldUppsala University and Uppsala Clinical Research Center, Uppsala, Sweden.
Stefan K JamesUppsala University and Uppsala Clinical Research Center, Uppsala, Sweden.
Ziad A AliNewYork-Presbyterian Hospital/Columbia University Irving Medical Center, New York, NY, USA; Cardiovascular Research Foundation, New York, NY, USA.
James E MullerBrigham and Women's Hospital, Boston, MA, USA.
Gregg W StoneCardiovascular Research Foundation, New York, NY, USA; The Zena and Michael A Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
PROSPECT II Investigators
Aarhus University Hospital · DKCardiovascular Research Foundation · USUniversity of Bergen · NOÖrebro University · SEStavanger University Hospital · NOKarolinska Institutet · SENew York Hospital Queens · USOdense University Hospital · DKUniversity of Copenhagen · DKUppsala University · SEBrigham and Women's Hospital · USColumbia University · USHaukeland University Hospital · NOIcahn School of Medicine at Mount Sinai · USLund University · SENewYork–Presbyterian Hospital · USSahlgrenska University Hospital · SESt Olav's University Hospital · NOZealand University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNear-infrared spectroscopy (NIRS) and intravascular ultrasound are promising imaging modalities to identify non-obstructive plaques likely to cause coronary-related events. We aimed to assess whether combined NIRS and intravascular ultrasound can identify high-risk plaques and patients that are at risk for future major adverse cardiac events (MACEs).

methodsPROSPECT II is an investigator-sponsored, multicentre, prospective natural history study done at 14 university hospitals and two community hospitals in Denmark, Norway, and Sweden. We recruited patients of any age with recent (within past 4 weeks) myocardial infarction. After treatment of all flow-limiting coronary lesions, three-vessel imaging was done with a combined NIRS and intravascular ultrasound catheter. Untreated lesions (also known as non-culprit lesions) were identified by intravascular ultrasound and their lipid content was assessed by NIRS. The primary outcome was the covariate-adjusted rate of MACEs (the composite of cardiac death, myocardial infarction, unstable angina, or progressive angina) arising from untreated non-culprit lesions during follow-up. The relations between plaques with high lipid content, large plaque burden, and small lumen areas and patient-level and lesion-level events were determined. This trial is registered with ClinicalTrials.gov, NCT02171065.

findingsBetween June 10, 2014, and Dec 20, 2017, 3629 non-culprit lesions were characterised in 898 patients (153 [17%] women, 745 [83%] men; median age 63 [IQR 55-70] years). Median follow-up was 3·7 (IQR 3·0-4·4) years. Adverse events within 4 years occurred in 112 (13·2%, 95% CI 11·0-15·6) of 898 patients, with 66 (8·0%, 95% CI 6·2-10·0) arising from 78 untreated non-culprit lesions (mean baseline angiographic diameter stenosis 46·9% [SD 15·9]). Highly lipidic lesions (851 [24%] of 3500 lesions, present in 520 [59%] of 884 patients) were an independent predictor of patient-level non-culprit lesion-related MACEs (adjusted odds ratio 2·27, 95% CI 1·25-4·13) and non-culprit lesion-specific MACEs (7·83, 4·12-14·89). Large plaque burden (787 [22%] of 3629 lesions, present in 530 [59%] of 898 patients) was also an independent predictor of non-culprit lesion-related MACEs. Lesions with both large plaque burden by intravascular ultrasound and large lipid-rich cores by NIRS had a 4-year non-culprit lesion-related MACE rate of 7·0% (95% CI 4·0-10·0). Patients in whom one or more such lesions were identified had a 4-year non-culprit lesion-related MACE rate of 13·2% (95% CI 9·4-17·6).

interpretationCombined NIRS and intravascular ultrasound detects angiographically non-obstructive lesions with a high lipid content and large plaque burden that are at increased risk for future adverse cardiac outcomes.

fundingAbbott Vascular, Infraredx, and The Medicines Company.

Indexed as

AgedAngina, UnstableDeathFemaleHumansLipidsMaleMiddle AgedMyocardial InfarctionPlaque, AtheroscleroticProspective StudiesScandinavian and Nordic CountriesSpectroscopy, Near-InfraredUltrasonographyLipids

Identifiers

PMID33714389
OpenAlexW3135498932

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

and 1 more above

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 Socratic graph.