FRACTIONAL FLOW RESERVE Step-by-step measurement, Practical tips & Pitfalls

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FRACTIONAL FLOW RESERVE Step-by-step measurement, Practical tips & Pitfalls Ahmed M ElGuindy, MSc, MRCP(UK) Division of Cardiology Aswan Heart Centre 2013 Fractional Flow Reserve Essential diagnostic tool in the modern cath-lab Based on sound physiological principles Supported by a large body of clinical outcome data (hard clinical end-points) Avoids the limitations of coronary angiography 2D luminogram 20% visual error margin Does not account for various pathophysiological factors Cost effective 1

Current Recommendations Wijns W et al. EHJ 2010 Current Recommendations 2

Landmark Studies DEFER 1ry endpoint: freedom from MACE 5-years follow up of the DEFER Study: Pijls et al JACC 2007 Landmark Studies FAME 1005 patients with MVD randomized to FFR-guided PCI or angiography-guided PCI 1ry endpoint: composite of Death, MI and repeat revascularization Tonino et al. NEJM 2009 3

Landmark Studies FAME 2 888 patients with SIHD and FFR < 0.8 randomized to PCI + OMT or OMT only 1ry endpoint: composite of Death, MI and urgent revascularization Registry: patients with FFR > 0.8 on OMT De Bruyne et al. NEJM 2012 Principles & theoretical background 4

The Role of Maximal Hyperemia Maximal hyperemia = minimal & steady microvascular resistance = linear relationship between perfusion pressure and flow Q=P/R P a Qs/Qn = (Pd/Rs) P d (Pa/Rn) If Rs=Rn, then Qs/Qn = Pd/Pa NHJ Pijls et al. Circulation 1993 5

Definition FFR = 0.75 means: Due to this particular stenosis, the maximum achievable blood flow to the myocardium supplied by this artery is only 75% of what it would be if this artery were completely normal Strengths FFR has a normal value of 1.0 for every patient, for every vessel, and in every segment. FFR accounts for body size, coronary segment and myocardial territory supplied Highly reproducible Not influenced by changes in contractility, loading conditions and/or heart rate 6

Strengths Accounts for myocardial mass supplied by vessel (perfusion area) Accounts for collateral flow Very high spatial resolution: ability to assess individual lesions within the same vessel (pullback) vs. diffuse disease Limitations Acute myocardial infarction (culprit vessel) Severe LVH (caution) Severe hypotension (outside autoregulatory range) Dynamic obstruction: spasm and/or myocardial bridges (caution) 7

Step-by-step measurement 1. Flush the wire while it still is in its sleeve 2. Connect the pressure wire to the analyzer 8

3. Calibrate the pressure wire (with the wire still in its sleeve) 4. Insert wire in guiding catheter. 5. Equalize guiding (Pa) pressure and wire (Pd) pressure with the pressure sensor placed at the tip of the guiding catheter. Caution: Do not change the height of the aortic transducer after pressure equalization Tip: removing the guidewire introduced needle is preferable if IV adenosine infusion is planned and mandatory with IC adenosine Tip: Ensure that the guiding is not deeply engaged with pressure damping 9

6. Advance pressure wire, place the sensor distal to the stenosis and give 200 mcg IC GTN Induce Maximal Hyperemia IV adenosine infusion (preferred method): 140 mcg/kg/min. NB. Central Vein preferred Or IC bolus: at least 180 mcg for left coronary system and 90 mcg for right system). N.B. ensure GC is properly engaged. Caution: - Do not use guiding catheter with side-holes - With IC adenosine: ensure that guiding catheter is properly engaged - With either method: ensure that guiding catheter does not become deeply engaged (sucked in) 10

Effect of Deep Engagement FFR = 87/96 = 90 FFR = 87/106 = 82 7. Repeat measurement. Further IC adenosine bolus is required if IC method is used. No need for extra GTN bolus. Tip: Checking maximal hyperemia 11

8. Check for signal drift. True pressure gradient Signal drift Special Situations Aorto-ostial lesions IV adenosine infusion preferred Place guiding catheter in aortic root and check that pressure does not become dampened With IC adenosine: engage to deliver adenosine, disengage before measurement. Check Pa waveform 12

Special Situations Tandem lesions vs. diffuse disease Strategy: Stent the area with maximal pressure drop then remeasure Pijls and Willens. JACC 2012 Special Situations In press 13

Special Situations In press Special Situations Others SVG grafts Not recommended: rate of progress unknown Bifurcations Valuable to detect a pinched SB with provisional stenting. Tip: 75/25 rule 1 1 Koo et al. EHJ 2008 14

Special Situations 29 yr old male patient FH and supravalvular AS One final tip: Grey zone Significant stenosis Non-significant 0 0.75 0.8 1.0 Vague symptoms, no other evidence of ischemia defer PCI Typical symptoms, non-invasive evidence of ischemia, diabetes > Perform PCI 15

FFR and clinical outcomes FFR and clinical outcomes Pijls and Willens. JACC 2012 16

Take home message Always look for explanations to abnormal findings Look at both the pressure waveforms carefully. Do not rely on the figures solely. Sensitivity is > 90%: True false negatives are rare Specificity is 100%: True false positive are extremely rare Take home message FFR is the current gold-standard for evaluating the physiological significance of epicardial coronary stenoses Intracoronary imaging is useful understanding the mechanism(s) of disease and in planning/optimizing PCI FFR tells you when to treat, IVUS and/or OCT tell you how to do so. 17

Trust your measurements: Coronary Pressure Never Lies Suggested reading Functional measurement of coronary stenosis. Piljs N et al. JACC 2012 Practice and potential pitfalls of coronary pressure measurement. Piljs N, Kern M, Yock P and De Bruyne B. Cath and cardiovasc interv 2000 Coronary pressure-derived fractional flow reserve measurements: recommendations for standardization, recording, and reporting as a core laboratory technique. Proposals for integration in clinical trials. Vranckx P. et al. Circ Cardiovasc interv. Coronary hemodynamics: Fractional flow reserve concept, pitfalls and special applications. In Hanna E and Glancy D, eds: Practical Cardiovascular hemodynamics. Demos Medical publishing, LLC, New York, 2013. 18

Thank you 19