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The Full Revasc (Ffr-gUidance for compLete non-cuLprit REVASCularization) Registry-based randomized clinical trial
- Source :
- Böhm, F, Mogensen, B, Östlund, O, Engstrøm, T, Fossum, E, Stankovic, G, Angerås, O, Ērglis, A, Menon, M, Schultz, C, Berry, C, Liebetrau, C, Laine, M, Held, C, Rück, A & James, S K 2021, ' The Full Revasc (Ffr-gUidance for compLete non-cuLprit REVASCularization) Registry-based randomized clinical trial ', American Heart Journal, vol. 241, pp. 92-100 . https://doi.org/10.1016/j.ahj.2021.07.007
- Publication Year :
- 2021
- Publisher :
- Uppsala universitet, Uppsala kliniska forskningscentrum (UCR), 2021.
-
Abstract
- Publisher Copyright: © 2021 Background: Complete revascularization in ST elevation myocardial infarction (STEMI) patients with multivessel disease has resulted in reduction in composite clinical endpoints in medium sized trials. Only one trial showed an effect on hard clinical endpoints, but the revascularization procedure was guided by angiographic evaluation of stenosis severity. Consequently, it is not clear how Fractional Flow Reserve (FFR)-guided percutaneous coronary intervention (PCI) affects hard clinical endpoints in STEMI. Methods and Results: The Ffr-gUidance for compLete non-cuLprit REVASCularization (FULL REVASC) – is a pragmatic, multicenter, international, registry-based randomized clinical trial designed to evaluate whether a strategy of FFR-guided complete revascularization of non-culprit lesions, reduces the combined primary endpoint of total mortality, non-fatal MI and unplanned revascularization. 1,545 patients were randomized to receive FFR-guided PCI during the index hospitalization or initial conservative management of non-culprit lesions. We found that in angiographically severe non-culprit lesions of 90-99% severity, 1 in 5 of these lesions were re-classified as non-flow limiting by FFR. Considering lesions of intermediate severity (70%-89%), half were re-classified as non-flow limiting by FFR. The study is event driven for an estimated follow-up of at least 2.75 years to detect a 9.9%/year>7.425%/year difference (HR = 0.74 at 80% power (α = .05)) for the combined primary endpoint. Conclusion: This large randomized clinical trial is designed and powered to evaluate the effect of complete revascularization with FFR-guided PCI during index hospitalization on total mortality, non-fatal MI and unplanned revascularization following primary PCI in STEMI patients with multivessel disease. Enrollment completed in September 2019 and follow-up is ongoing.
- Subjects :
- Male
Emergency Medical Services
medicine.medical_treatment
Fractional flow reserve
030204 cardiovascular system & hematology
Coronary Angiography
GUIDELINES
Severity of Illness Index
ANGIOGRAPHY
DISEASE
law.invention
0302 clinical medicine
Randomized controlled trial
law
FRACTIONAL FLOW RESERVE
Clinical endpoint
Medicine
Cardiac and Cardiovascular Systems
030212 general & internal medicine
Registries
Kardiologi
Middle Aged
3. Good health
Fractional Flow Reserve, Myocardial
Outcome and Process Assessment, Health Care
Surgery, Computer-Assisted
Cardiology
Female
Cardiology and Cardiovascular Medicine
medicine.medical_specialty
Revascularization
Culprit
LESION
03 medical and health sciences
Percutaneous Coronary Intervention
Internal medicine
Humans
cardiovascular diseases
Mortality
ANGIOPLASTY
Aged
business.industry
Coronary Stenosis
ELEVATION MYOCARDIAL-INFARCTION
Percutaneous coronary intervention
medicine.disease
3126 Surgery, anesthesiology, intensive care, radiology
Stenosis
3121 General medicine, internal medicine and other clinical medicine
Conventional PCI
ST Elevation Myocardial Infarction
business
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Böhm, F, Mogensen, B, Östlund, O, Engstrøm, T, Fossum, E, Stankovic, G, Angerås, O, Ērglis, A, Menon, M, Schultz, C, Berry, C, Liebetrau, C, Laine, M, Held, C, Rück, A & James, S K 2021, ' The Full Revasc (Ffr-gUidance for compLete non-cuLprit REVASCularization) Registry-based randomized clinical trial ', American Heart Journal, vol. 241, pp. 92-100 . https://doi.org/10.1016/j.ahj.2021.07.007
- Accession number :
- edsair.doi.dedup.....2e8c134b7307098500da377c8ceb2fa1
- Full Text :
- https://doi.org/10.1016/j.ahj.2021.07.007