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Functional Assessment in Elderly MI Patients With Multivessel Disease (FIRE)

Primary Purpose

Myocardial Infarction

Status
Active
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Culprit-only revascularization
Complete functionally-guided revascularization
Sponsored by
Consorzio Futuro in Ricerca
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Myocardial Infarction focused on measuring older adults, multivessel coronary disease, intracoronary physiology, functional assessment

Eligibility Criteria

75 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients ≥75 years AND
  2. MI (ST-segment elevation or not ST.segment elevation MI) with indication to invasive management AND
  3. Multi-vessel disease defined as at least 1 non-culprit coronary artery lesion at least 2.5 mm in diameter deemed at visual estimation with a diameter stenosis % ranging from 50 to 99% amenable to successful treatment with PCI AND
  4. Successful treatment of culprit lesion

Exclusion Criteria:

  1. Planned surgical revascularization
  2. Non-cardiovascular co-morbidity reducing life expectancy to < 1 year
  3. Any factor precluding 1-year follow-up
  4. Prior Coronary Artery Bypass Graft (CABG) Surgery
  5. Impossibility to identify a clear culprit lesion
  6. Non culprit lesion located in the left main

Sites / Locations

  • Maria Cecilia Hospital
  • ASP Agrigento
  • Ospedale Maggiore
  • AOU Sant'Anna e San Sebastiano
  • Casa di Cura San Michele Maddaloni
  • AO Cannizzaro
  • AOU Ferrara
  • Ospedale della Misericordia
  • Ospedale Sant.Andrea
  • AOU Gaetano Martino
  • Ospedale dell'Angelo
  • Ospedale Civile di Baggiovara
  • Ospedale Santa Croce
  • AOU Giaccone
  • Ospedale Santa Maria delle Croci
  • Arcispedale Santa Maria Nuova
  • Ospedale Infermi
  • AOU Sant'Andrea
  • Ospedale SS Annunziata
  • Ospedale Umberto I
  • Ospedale di Rivoli
  • AOU Integrata di Verona
  • Centrum Kardiologii Inwazyjnej, Elektroterapii i Angiologii
  • Centrum Kardiologii Inwazyjnej, Elektroterapii i Angiologii
  • Centrum Kardiologii Inwazyjnej Elektroterapii i Angiologii
  • Centrum Kardiologii Inwazyjnej, Elektroterapii i Angiologii
  • Podkarpackie Centrum Interwencji Sercowo-Naczyniowych
  • Hospital General Universitario de Ciudad Real
  • Complejo Hospitalario de La Coruna
  • Hospital Universitario Lucus Augusti
  • Hospital Clinico San Carlos
  • Hospital General Universitario Gregorio Maranon
  • Hospital Universitario La Paz
  • Complejo Hospitalario Universitario de Santiago
  • Hospital Universitario La FE
  • Hospital Clinico Universitario
  • Hospital Alvaro Conqueiro de Vigo

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Culprit-only revascularization

Complete functionally-guided revascularization

Arm Description

All patients randomized to culprit only revascularization must not undergo percutaneous coronary intervention (PCI) any lesion except from the culprit lesion already treated at the moment of the randomization. Staged procedures are considered protocol violation.

Patients who are randomized to this strategy will receive revascularization of the culprit lesion and guided by functional assessment on all non-culprit lesions. Functional evaluation is mandatory for all stenosis with diameter stenosis % between 50 and 90% at visual estimation. Revascularization must be guided by functional assessment on all vessels. The system utilized to obtain functional evaluation is left to Operator's discretion. PCI is allowed only if functional evaluation is positive according to the threshold of the chosen functional system. It is suggested to achieve functional complete revascularization within the index procedure, while it is mandatory to obtain it within the index hospitalization.

Outcomes

Primary Outcome Measures

Patient oriented cardiac events
cumulative occurrence of all-cause death, any MI, any stroke, any revascularization

Secondary Outcome Measures

Patient oriented cardiac events
cumulative occurrence of all-cause death, any MI, any stroke, any revascularization
Patient oriented cardiac events
cumulative occurrence of all-cause death, any MI, any stroke, any revascularization
Device oriented composite endpoint
cumulative occurrence of Cardiovascular Death, MI or non-culprit target vessel revascularization
Device oriented composite endpoint
cumulative occurrence of Cardiovascular Death, MI or non-culprit target vessel revascularization
Device oriented composite endpoint
cumulative occurrence of Cardiovascular Death, MI or non-culprit target vessel revascularization
Cardiovascular Death or MI
cumulative occurrence of Cardiovascular Death or MI
Cardiovascular Death or MI
cumulative occurrence of Cardiovascular Death or MI
Cardiovascular Death or MI
cumulative occurrence of Cardiovascular Death or MI
All-cause death or MI
cumulative occurrence of All-cause Death or MI
All-cause death or MI
cumulative occurrence of All-cause Death or MI
All-cause death or MI
cumulative occurrence of All-cause Death or MI
All-cause death
cumulative occurrence of All-cause Death
All-cause death
cumulative occurrence of All-cause Death
All-cause death
cumulative occurrence of All-cause Death
MI
cumulative occurrence of MI
MI
cumulative occurrence of MI
MI
cumulative occurrence of MI
Any revascularization
cumulative occurrence of revascularization
Any revascularization
cumulative occurrence of revascularization
Any revascularization
cumulative occurrence of revascularization
Ischemic Adverse Events in patients interrupting DAPT
cumulative occurrence of CV death, MI, stroke and revascularization in patients interrupting DAPT
Ischemic Adverse Events in patients disrupting DAPT
cumulative occurrence of CV death, MI, stroke and revascularization in patients disrupting DAPT
Contrast-Induced Acute Kidney Injury
cumulative occurrence of Contrast-Induced Acute Kidney Injury

Full Information

First Posted
December 9, 2018
Last Updated
March 29, 2023
Sponsor
Consorzio Futuro in Ricerca
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1. Study Identification

Unique Protocol Identification Number
NCT03772743
Brief Title
Functional Assessment in Elderly MI Patients With Multivessel Disease
Acronym
FIRE
Official Title
Functional Versus Culprit-only Revascularization in Elderly Patients With Myocardial Infarction and Multivessel Disease
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 15, 2019 (Actual)
Primary Completion Date
October 30, 2022 (Actual)
Study Completion Date
October 3, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Consorzio Futuro in Ricerca

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Elderly patients presenting with myocardial infarction (MI) and multivessel disease are the highest risk population with the worst prognosis. No trial has ever been designed to optimize their outcome. The actual real-life standard of care is, in the best of the cases, culprit only revascularization. However, real-life registries show that outcome of MI elderly patients treated with this strategy is far from being optimal with at least a 15% rate of cardiac death or myocardial infarction at 1 year. To date, studies on this population have been focused on devices (bare metal stent vs biodegradable drug eluting stent) or on dual antiplatelet regimen (long vs short) and no study was focused on evaluating if complete revascularization is able to improve the prognosis in these patients. The contemporary complete revascularization is represented by a functionally-driven revascularization that recently showed to significantly reduce myocardial infarction rate and outperformed an angio-complete revascularization. Thus, our hypothesis is that a functionally-driven complete revascularization in elderly patients with MI and multivessel disease may improve prognosis compared to the actual standard of care in these patients, namely culprit only revascularization. Being a "strategy" trial, we identified the patient-oriented composite endpoint (POCE) as primary outcome of interest (all cause death, any MI, any stroke, any revascularization). Several pre-specified substudies have been planned. A detailed list of the substudies is available in the website of the trial (http://www.thefiretrial.com)
Detailed Description
BACKGROUND OF THE STUDY Acute myocardial infarction (AMI) is the most frequent clinical presentation in older adults (≥75 years). Registry data shows that up to 65% of patients ≥75 years with AMI has multivessel disease, namely at least one lesion beyond the culprit one with diameter stenosis >50% and located in a coronary artery different from the culprit vessel. Presence of multivessel disease is a marker of worse prognosis. The rate of adverse events, such as death and MI is 3-fold higher in multivessel disease patients if compared to single vessel disease patients. During a 3-5 years follow-up, the number of adverse events related to non-culprit lesions is double than the one related to culprit lesions (data from SWEDEHEART registry and PROSPECT trial). These adverse events are even more frequent in older adults reaching a 15-30% incidence at 1 year. Several studies were focused on older adults with AMI in order to optimize their treatment. The main focus of those studies were: optimal dual antiplatelet therapy (DAPT) duration and type of stent. As for DAPT, data is in favour of a short regimen (1-6 months) as it represents the best balance between ischemic protection and reduction of bleeding events. In both LEADERS FREE and ZEUS trials, age was the main criteria for enrollment and it was considered as a marker of high risk of bleeding event. In the ongoing XIENCE 28 study, age ≥75 years is considered a sufficient criteria to prescribe 28 days of DAPT after stent implantation. As for stent type, the recent SENIOR trial showed that biodegradable polymer second generation drug eluting stents (DES) are the gold standard in older adults receiving percutaneous coronary interventions (PCI). These stents clearly outperformed bare metal stents with a low event rate in presence of a short DAPT regimen. Thus, at the present time, we have sufficient data to consider biodegradable polymer DES and short DAPT as cornerstones of the treatment in older adults with MI. On the contrary, we have no scientific evidence regarding the best treatment strategy to apply in multivessel disease patients. It is not clear whether to prefer a culprit only strategy or if revascularization of non-culprit lesions is associated to a reduction of adverse events. Culprit lesion treatment with PCI and stent implantation in MI setting is universally agreed as gold standard since it reduces morbidity and mortality. In the last 10 years, several studies were focused on the treatment of non-culprit lesions. PRAMI, CULPRIT, DANAMI 3 PRIMULTI, COMPARE ACUTE trial tried to assess if a systematic treatment of non-culprit lesions was associated with an improved prognosis if compared to a culprit only strategy. All these studies showed that complete revascularization clearly reduce the risk of repeated revascularizations. However, no study showed a significant impact on death or MI. When pooled in a meta-analysis, we can observe a trend in favour of MI reduction but data cannot be considered as conclusive. In 2019, COMPLETE trial results will be disclosed. In COMPLETE trial, more than 4000 patients were enrolled with consequent power to detect a difference in terms of death and MI. The limits of all the above mentioned studies are that the mean age was around 60 years and that only ST-segment elevated MI (STEMI) patients were included. No study included a relevant portion of patients ≥75 years nor included no-STEMI (NSTEMI) patients. However, a culprit lesion is identifiable in more than 90% of NSTEMI patients and the issue on their management is similar to the one of the STEMI patients. In addiction, in older adults, clinical presentation is as NSTEMI in more than 70% of the cases. Consequently, it is mandatory to generate solid data on the correct treatment strategy in these patients. In younger adults (<65 years), in concordance with the solid scientific evidences, it is widespread a complete revascularization strategy. In older adults (≥75 years), also guidelines, in absence of clear data, suggest a case-by-case decision and suggest to consider age as one of the determinants of the final decision (Class IIa level of evidence C, ESC NSTEMI guidelines). Both European and American registry data shows clearly that the most frequently applied strategy is the culprit only one, both in STEMI and NSTEMI patients. Also in the LEADERS FREE trial, patients ≥75 years had multivessel disease in 65% of the cases, but in more than 80% of them, treatment was limited to the culprit lesion. In conclusion, the actual gold standard of treatment in older adults with MI and multivessel disease is the culprit-only strategy. The traditional concept of complete revascularization was based on angiography. Operator visually identified the lesions >50% and decided to treat or not each one of them. Contemporary data on fractional flow reserve and instantaneous free-wave ratio demonstrated that an angio-guided strategy is similar to a coin toss in terms of detection of lesions causing ischemia. This leads to unnecessary PCIs or avoided necessary PCIs in more than 50% of the cases. Studies on angio-complete revascularization probably failed to show an MI reduction because of this reason. In addition, long-term follow-up data of lesions functionally deferred shows that the rate of death and MI at 5 years is below 3%. As a consequence, functional revascularization should be considered as contemporary strategy to achieve a real complete revascularization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myocardial Infarction
Keywords
older adults, multivessel coronary disease, intracoronary physiology, functional assessment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
All comers, prospective, randomized, multicenter, open-label trial with blinded adjudicated evaluation of outcomes (PROBE).
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1445 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Culprit-only revascularization
Arm Type
Other
Arm Description
All patients randomized to culprit only revascularization must not undergo percutaneous coronary intervention (PCI) any lesion except from the culprit lesion already treated at the moment of the randomization. Staged procedures are considered protocol violation.
Arm Title
Complete functionally-guided revascularization
Arm Type
Other
Arm Description
Patients who are randomized to this strategy will receive revascularization of the culprit lesion and guided by functional assessment on all non-culprit lesions. Functional evaluation is mandatory for all stenosis with diameter stenosis % between 50 and 90% at visual estimation. Revascularization must be guided by functional assessment on all vessels. The system utilized to obtain functional evaluation is left to Operator's discretion. PCI is allowed only if functional evaluation is positive according to the threshold of the chosen functional system. It is suggested to achieve functional complete revascularization within the index procedure, while it is mandatory to obtain it within the index hospitalization.
Intervention Type
Other
Intervention Name(s)
Culprit-only revascularization
Intervention Description
Implantation of drug eluting stents with biodegradable polymer with struts ≤65 μ in the culprit lesion of the MI. Each patient should receive revascularization with Supraflex stent or its newer versions
Intervention Type
Other
Intervention Name(s)
Complete functionally-guided revascularization
Intervention Description
Implantation of drug eluting stents with biodegradable polymer with struts ≤65 μ in the culprit lesion of the MI and in all non culprit lesions with positive functional assessment. Each patient should receive revascularization with Supraflex stent or its newer versions
Primary Outcome Measure Information:
Title
Patient oriented cardiac events
Description
cumulative occurrence of all-cause death, any MI, any stroke, any revascularization
Time Frame
1-year
Secondary Outcome Measure Information:
Title
Patient oriented cardiac events
Description
cumulative occurrence of all-cause death, any MI, any stroke, any revascularization
Time Frame
3-year
Title
Patient oriented cardiac events
Description
cumulative occurrence of all-cause death, any MI, any stroke, any revascularization
Time Frame
5-year
Title
Device oriented composite endpoint
Description
cumulative occurrence of Cardiovascular Death, MI or non-culprit target vessel revascularization
Time Frame
1-year
Title
Device oriented composite endpoint
Description
cumulative occurrence of Cardiovascular Death, MI or non-culprit target vessel revascularization
Time Frame
3-year
Title
Device oriented composite endpoint
Description
cumulative occurrence of Cardiovascular Death, MI or non-culprit target vessel revascularization
Time Frame
5-year
Title
Cardiovascular Death or MI
Description
cumulative occurrence of Cardiovascular Death or MI
Time Frame
1-year
Title
Cardiovascular Death or MI
Description
cumulative occurrence of Cardiovascular Death or MI
Time Frame
3-year
Title
Cardiovascular Death or MI
Description
cumulative occurrence of Cardiovascular Death or MI
Time Frame
5-year
Title
All-cause death or MI
Description
cumulative occurrence of All-cause Death or MI
Time Frame
1-year
Title
All-cause death or MI
Description
cumulative occurrence of All-cause Death or MI
Time Frame
3-year
Title
All-cause death or MI
Description
cumulative occurrence of All-cause Death or MI
Time Frame
5-year
Title
All-cause death
Description
cumulative occurrence of All-cause Death
Time Frame
1-year
Title
All-cause death
Description
cumulative occurrence of All-cause Death
Time Frame
3-year
Title
All-cause death
Description
cumulative occurrence of All-cause Death
Time Frame
5-year
Title
MI
Description
cumulative occurrence of MI
Time Frame
1-year
Title
MI
Description
cumulative occurrence of MI
Time Frame
3-year
Title
MI
Description
cumulative occurrence of MI
Time Frame
5-year
Title
Any revascularization
Description
cumulative occurrence of revascularization
Time Frame
1-year
Title
Any revascularization
Description
cumulative occurrence of revascularization
Time Frame
3-year
Title
Any revascularization
Description
cumulative occurrence of revascularization
Time Frame
5-year
Title
Ischemic Adverse Events in patients interrupting DAPT
Description
cumulative occurrence of CV death, MI, stroke and revascularization in patients interrupting DAPT
Time Frame
1-year
Title
Ischemic Adverse Events in patients disrupting DAPT
Description
cumulative occurrence of CV death, MI, stroke and revascularization in patients disrupting DAPT
Time Frame
1-year
Title
Contrast-Induced Acute Kidney Injury
Description
cumulative occurrence of Contrast-Induced Acute Kidney Injury
Time Frame
1 month
Other Pre-specified Outcome Measures:
Title
Target Lesion Failure
Description
cumulative occurrence of Target Lesion Failure
Time Frame
1-year
Title
Target Lesion Failure
Description
cumulative occurrence of Target Lesion Failure
Time Frame
3-year
Title
Target Lesion Failure
Description
cumulative occurrence of Target Lesion Failure
Time Frame
5-year
Title
Ischemia-driven Revascularization
Description
cumulative occurrence of ischemia-driven revascularization
Time Frame
1-year
Title
Ischemia-driven Revascularization
Description
cumulative occurrence of ischemia-driven revascularization
Time Frame
3-year
Title
Ischemia-driven Revascularization
Description
cumulative occurrence of ischemia-driven revascularization
Time Frame
5-year
Title
EQ-5D scale
Description
quality of life as assessed by EQ-5D scale
Time Frame
1-year
Title
EQ-5D scale
Description
quality of life as assessed by EQ-5D scale
Time Frame
3-year
Title
EQ-5D scale
Description
quality of life as assessed by EQ-5D scale
Time Frame
5-year
Title
Short Physical Performance Battery
Description
Physical Performance as assessed by Short Physical Performance Battery
Time Frame
1-year
Title
Short Physical Performance Battery
Description
Physical Performance as assessed by Short Physical Performance Battery
Time Frame
3-year
Title
Short Physical Performance Battery
Description
Physical Performance as assessed by Short Physical Performance Battery
Time Frame
5-year
Title
Seattle Angina Questionnarie
Description
angina symptoms control as assessed by Seattle Angina Questionnarie
Time Frame
1-year
Title
Seattle Angina Questionnarie
Description
angina symptoms control as assessed by Seattle Angina Questionnarie
Time Frame
3-year
Title
Seattle Angina Questionnarie
Description
angina symptoms control as assessed by Seattle Angina Questionnarie
Time Frame
5-year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients ≥75 years AND MI (ST-segment elevation or not ST.segment elevation MI) with indication to invasive management AND Multi-vessel disease defined as at least 1 non-culprit coronary artery lesion at least 2.5 mm in diameter deemed at visual estimation with a diameter stenosis % ranging from 50 to 99% amenable to successful treatment with PCI AND Successful treatment of culprit lesion Exclusion Criteria: Planned surgical revascularization Non-cardiovascular co-morbidity reducing life expectancy to < 1 year Any factor precluding 1-year follow-up Prior Coronary Artery Bypass Graft (CABG) Surgery Impossibility to identify a clear culprit lesion Non culprit lesion located in the left main
Facility Information:
Facility Name
Maria Cecilia Hospital
City
Cotignola
State/Province
Ravenna
Country
Italy
Facility Name
ASP Agrigento
City
Agrigento
Country
Italy
Facility Name
Ospedale Maggiore
City
Bologna
Country
Italy
Facility Name
AOU Sant'Anna e San Sebastiano
City
Caserta
Country
Italy
Facility Name
Casa di Cura San Michele Maddaloni
City
Caserta
Country
Italy
Facility Name
AO Cannizzaro
City
Catania
Country
Italy
Facility Name
AOU Ferrara
City
Ferrara
ZIP/Postal Code
44124
Country
Italy
Facility Name
Ospedale della Misericordia
City
Grosseto
Country
Italy
Facility Name
Ospedale Sant.Andrea
City
La Spezia
Country
Italy
Facility Name
AOU Gaetano Martino
City
Messina
Country
Italy
Facility Name
Ospedale dell'Angelo
City
Mestre
Country
Italy
Facility Name
Ospedale Civile di Baggiovara
City
Modena
Country
Italy
Facility Name
Ospedale Santa Croce
City
Moncalieri
Country
Italy
Facility Name
AOU Giaccone
City
Palermo
Country
Italy
Facility Name
Ospedale Santa Maria delle Croci
City
Ravenna
Country
Italy
Facility Name
Arcispedale Santa Maria Nuova
City
Reggio Emilia
Country
Italy
Facility Name
Ospedale Infermi
City
Rimini
Country
Italy
Facility Name
AOU Sant'Andrea
City
Roma
Country
Italy
Facility Name
Ospedale SS Annunziata
City
Savigliano
Country
Italy
Facility Name
Ospedale Umberto I
City
Siracusa
Country
Italy
Facility Name
Ospedale di Rivoli
City
Torino
Country
Italy
Facility Name
AOU Integrata di Verona
City
Verona
Country
Italy
Facility Name
Centrum Kardiologii Inwazyjnej, Elektroterapii i Angiologii
City
Krosno
Country
Poland
Facility Name
Centrum Kardiologii Inwazyjnej, Elektroterapii i Angiologii
City
Nowy Sącz
Country
Poland
Facility Name
Centrum Kardiologii Inwazyjnej Elektroterapii i Angiologii
City
Oświęcim
Country
Poland
Facility Name
Centrum Kardiologii Inwazyjnej, Elektroterapii i Angiologii
City
Pińczów
Country
Poland
Facility Name
Podkarpackie Centrum Interwencji Sercowo-Naczyniowych
City
Sanok
Country
Poland
Facility Name
Hospital General Universitario de Ciudad Real
City
Ciudad Real
Country
Spain
Facility Name
Complejo Hospitalario de La Coruna
City
La Coruña
Country
Spain
Facility Name
Hospital Universitario Lucus Augusti
City
Lugo
Country
Spain
Facility Name
Hospital Clinico San Carlos
City
Madrid
Country
Spain
Facility Name
Hospital General Universitario Gregorio Maranon
City
Madrid
Country
Spain
Facility Name
Hospital Universitario La Paz
City
Madrid
Country
Spain
Facility Name
Complejo Hospitalario Universitario de Santiago
City
Santiago De Compostela
Country
Spain
Facility Name
Hospital Universitario La FE
City
Valencia
Country
Spain
Facility Name
Hospital Clinico Universitario
City
Valladolid
Country
Spain
Facility Name
Hospital Alvaro Conqueiro de Vigo
City
Vigo
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data will be available after motivated request to the Executive Committee of the study. All requests will be evaluated for acceptance. Positive evaluation by the Executive Committee is mandatory before data release
IPD Sharing Time Frame
After the publication of the manuscripts reporting the primary outcome and the prespecified substudies
IPD Sharing Access Criteria
Data will be available after motivated request to the Executive Committee of the study. All requests will be evaluated for acceptance. Positive evaluation by the Executive Committee is mandatory before data release
IPD Sharing URL
http://thefiretrial.com
Citations:
PubMed Identifier
32822656
Citation
Biscaglia S, Guiducci V, Santarelli A, Amat Santos I, Fernandez-Aviles F, Lanzilotti V, Varbella F, Fileti L, Moreno R, Giannini F, Colaiori I, Menozzi M, Redondo A, Ruozzi M, Gutierrez Ibanes E, Diez Gil JL, Maietti E, Biondi Zoccai G, Escaned J, Tebaldi M, Barbato E, Dudek D, Colombo A, Campo G. Physiology-guided revascularization versus optimal medical therapy of nonculprit lesions in elderly patients with myocardial infarction: Rationale and design of the FIRE trial. Am Heart J. 2020 Nov;229:100-109. doi: 10.1016/j.ahj.2020.08.007. Epub 2020 Aug 18.
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Functional Assessment in Elderly MI Patients With Multivessel Disease

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