Pd/Pa at rest, ifr, b-srv, resting gradient Why Can They Never Be As Good As Hyperemic Indexes

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CORONARY PHYSIOLOGY IN THE CATHLAB: Pd/Pa at rest, ifr, b-srv, resting gradient Why Can They Never Be As Good As Hyperemic Indexes Educational Training Program ESC European Heart House april 25th - 27th 2013 Nico H. J. Pijls, MD, PhD Catharina Hospital, Eindhoven, The Netherlands

Hyperemic indices: FFR ( Pijls, De Bruyne 1992 ) ihdpvr ( Di mario, Serruys 1994 ) hsrv ( Piek, Spaan, Siebes 1997) Resting indices ( FFR-light ): resting transtenotic gradient (Gruentzig, 1977) Pd/Pa at rest, +/- diastolic (Gould,Meier, 1981) ifr (Sen, Davies 2011) i-ffr (Andersson, 2013) bsrv (Verhoef, Siebes 2012) Virtual Hyperemic Index: FFR CT ( Min, Koo, 2009)

FFR - light A collection of older and newer resting indexes derived from pressure measurement at rest: Pd/Pa at rest, diastolic Pd/Pa, ifr, i-ffr which have in common that they all try to avoid hyperemia are not independently validated, and only have a moderate accuracy (70% -80%) compared to FFR

Why Are Resting Indices Insufficient? Limited Clinical Significance Limited Physiological Meaning - poor scientific background - no experimental validation - fluid-dynamic equation Resting Conditions Are Very Hard to Obtain - uncertainty if resting condition is present in cath lab, large variation - most resting indices vary with level of hyperemia - the only condition which can be reliably obtained, is maximum hyperemia

Why Are Resting Indices Insufficient? Limited Clinical Significance In patients with Coronary Artery Disease, resting flow and gradients have little meaning. Angina pectoris occurs and the myocardium becomes ischemic as soon as maximum achievable blood flow is insufficient to match oxygen demand Therefore, looking at maximum flow (as a fraction of normal maximum flow), makes most sense and is the basis of Fractional Flow Reserve (FFR)

Why Are Resting Indices Insufficient? Limited Clinical Significance Limited Physiological Meaning - poor scientific background - no experimental validation - deny the fluid-dynamic equation

Similar baseline gradients can lead to large differences during hyperemia as a result of: geometry of the stenosis (fluid dynamics equation) different extent of the distal perfusion area age of the patient hemodynamic conditions like blood pressure, heart rate and contractility

ΔP = f.q + s.q 2 f = friction coefficient s = separation coefficient Moderate gradient at rest Moderate increment at hyperemia Small gradient at rest Large gradient at hyperemia 70% long prox LAD stenosis 50% ostial left main stenosis ifr = 0.89 FFR = 0.85 ifr = 0.94 FFR = 0.57

In addition, some resting indexes have no or poor scientific basis and lack experimental validation

ifr = Pd / Pa at rest during WFP (Sen et al, JACC 2012) basic assumptions: 1. resistance during WFP at rest equals average hyperemic resistance 2. ifr is claimed to be hyperemia-free :

Volumetric coronary blood flow Qphasic 200 ml/min Qmean 0 20 sec occlusion

In the presence of constant coronary pressure R ~ 1 / Flow coronary pressure resting flow hyperemic coronary flow coronary occlusion

minimal myocardial resistance during the so-called wave-free period is ~ 250 % higher than average myocardial resistance at maximum hyperemia in all dogs and swine wfp coronary pressure resting flow hyperemic coronary flow coronary occlusion

ifr = Pd / Pa during WFP strongly dependent on hyperemia Colin et al, JACC 2012, in press Johnson et al JACC 2012, in press

profound influence of hyperemia on ifr: ifrhyp was already called diastolic FFR by Abe et al in Circulation, 1996) estimated decrease of resistance during wave-free period (1.0 0.64) (1.0 0.82) = 200% (ADENOSINE) VERIFY study,colin et al, JACC 2012, in press

Why Are Resting Indices Insufficient? Limited Clinical Significance Limited Physiological Meaning - poor scientific background - no experimental validation - fluid-dynamic equation Resting Conditions Are Very Hard to Obtain - uncertainty if resting condition is present in cath lab large fluctuations - most resting indices vary considerably - in fact, the only condition which can be reliably obtained in the cathlab, is maximum hyperemia

Mr M, born 26-03-1937, long mild/moderate proximal LAD lesion

equalization (PW at tip of guiding catheter) long moderate proximal LAD lesion; equalization

distal LAD; resting pressures PW in distal LAD; patient asleep (relaxed)

distal LAD; resting pressures PW in distal LAD; patient awake

distal LAD; resting pressures prior to adenosine: explanation to patient what is going to happen

distal LAD; resting pressures advancing the wire 2 cm and pulling it back again

adenosine i.v. infusion distal LAD; maximum hyperemia Measurement of FFR

distal LAD; (pseudo-)resting??? After waiting for 5 minutes, not touching anything

PW back to tip of guiding catheter verification of equal pressures and absence of drift

ifr = 0.89 P d /P a =0.90 ifr = 0.84 P d /P a =0.87 ifr = 0.76 P d /P a =0.80 FFR = 0.69 resting resting resting hyperemia what is resting? nothing is so variable in the cathlab as resting

obtaining true resting conditions in a conscious patient in the catheterization room, is often an illusion

..and as a consequence, large variation in cut-off values for resting indices are found Traditional CFR: 1.7 2.0 2.5 3.5 CFR = 4.0 / 1.0 = 4, but: 4.0 / 1.5 = 2.7 ifr: 0.83 (Advise study, Sen et al) 0.88 ( Koo et al) 0.90 ( Jeremias et al, resolve registry)) Similar for all indexes which rely upon resting value of flow

Jongen Egidius Resting flow in the cath lab is an illusion: Influence of the Resting Flow on CFR RR = 115/76 (mean 90) RR = 129/84 (mean 101) 56 cm.s -1 asleep 48 cm.s -1 awake 20 cm.s -1 10 cm.s -1 CFR = 4.8 CFR = 2.8

Jongen Egidius Resting flow in the cath lab is an illusion: FFR IS NOT AFFECTED! RR = 115/76 (mean 90) RR = 129/84 (mean 101) 56 cm.s -1 48 cm.s -1 +11% + 10% 20 cm.s -1 10 cm.s -1 CFR = 4.8 CFR = 2.8

Cut-off = 0.83 ADVISE STUDY (N= 131) FFR 0.55 From: Sen, Davies, et al JACC 2011

Retrospective analysis IFR versus FFR in 500 patients ( VERIFY study, Berry et al, JACC 2013) Prospective analysis IFR versus FFR in 205 patients ( VERIFY study, Berry et al, JACC 2013) Range 0.6-0.9 R 2 = 0.67 diagn accuracy = 66 % R 2 = 0.70 diagn accuracy = 67 %

~ FFR diast defined by Abe, Circulation 2000 threshold 0.76 Colin et al, JACC 2012, in press; Johnson et al JACC 2012, in press; Koo et al, JaccCVI

Reproducibilty of FFR and ifr From VERIFY study, Berry et al, JACC 2013

CALCULATION OF ifr: VOLCANO BOX vs MATLAB DOES IT MATTER? VERIFY STUDY: 705 resting and hyperemic tracings Calculation by Mathlab (free available computer program) blinded for results by the Volcano algorhitm (University of Technology, BME dept) Calculation by the Volcano algorhitm blinded for the results by Mathlab (CRF, New York)

ifr_resolve ifr by Volcano From: VERIFY N=705 1 ifr comparison 0,8 0,6 0,4 0,2 Berry et al JACC 2013; 0 0 0,2 0,4 0,6 0,8 1 ifr by ifr_matlab Mathlab

RESOLVE REGISTRY (TCT 2012, Jeremias et al)

R 2 = 65 %

necessity of hyperemia If Pd/Pa at rest (or comparable indices) is < 0.80, as a matter of fact FFR will also be < 0.80 and hyperemia in itself is not strictly mandatory to decide upon inducible ischemia But without hyperemia and FRR, you cannot judge how much a patient improved by stenting: did FFR go from 0.78 to 0.91 or from 0.65 to 0.91? And without hyperemia, you cannot make a meaningful pull-back recording and you are loosing a lot of valuable information

hyperemic pull back recording * in case of diffuse disease or multiple lesions: how would you believe to get this information without hyperemia? *

AVOIDING HYPEREMIA IS PROHIBITIVE FOR STENT EVALUATION After stenting, in the majority of patients no resting conditions are obtained anymore and semi-hyperemic status persists, with a lot of inter-individual variation. It often takes > 30 minutes to achieve baseline again As a consequence, resting Pd/Pa ( and ifr) are often lower after stenting than before ( paradoxical deterioration of ifr or resting Pd/Pa ). To evaluate improvement by stenting, you need to compare FFR after and before stenting

Correct Classification of Ischemic Stenosis 100 % certainty (holy grail) FFR 95 % hyperemia resting Pd/Pa, ifr, bsvr ( FFR-light ) resting indexes angio 80 % 70 % the piramid of diagnostic accuracy

CONCLUSIONS the physiologic basis for using resting indices is flawed and based upon unproven assumptions the experimental validation is lacking and experiments in dogs and swine in fact reject those assumptions none of these resting indexes has been independently validated the accuracy of all of these resting indices (whether ΔP, Pd/Pa at rest, or ifr) in clinical studies is similar for all of them and ~ < 80 % only when compared to FFR It is questionable if you should accept 80% certainty in your patients if you can get 95%

CONCLUSIONS using resting indices is like testing in a wind tunnel without wind the physiologic basis for using resting indices is flawed and based upon unproven assumptions the experimental validation is completely absent and in fact experiments in dogs and swine reject their validity incontrovertably the accuracy of all resting indices (whether ΔP, Pd/Pa at rest, or ifr) in clinical studies is similar and ~ 80 % only, versus 95 % for (hyperemic) FFR relying upon resting indexes only, means a wrong decision in 1 out of every 5 patients

The resting gradient is far from enough but unfortunately it s all I have now.

The resting gradient is far from enough but unfortunately it s all I have now. why guessing if you can have certainty?

Neem als basis TCT 2012 (soortgelijke voordracht) Budapest (soortgelijke voordracht) Latere data: Dia s met reprod heid Inaccuracy van 80% en van 70% tov die 80% (lijn met intervallen) Ook Nils Johnson

Hocus-pocus with statistics (1) true value = 100 o 100 measuring methodology #1 : accuracy = 80 % o 80 120 measured value between 80 and 120

measuring methodology #1 : accuracy = 80 % o 80 120 measuring methodology #2 : accuracy = 90 % compared to methodology #1 70 130 Range of uncertainty between 70 and 130 (and not between 90 and 110) o

Hocus-pocus with statistics (2) Accuracy of method #1 = 90 % compared to gold standard Accuracy of method #2 = 80 % compared to method #1 What is the accuracy of method #2 compared to gold standard? (0.8 x 0.9) = 0.72 (or 72 %) And NOT: (0.8 : 0.9) = 0.89 (or 89 %)

Hocus-pocus with statistics (3) About reproducibility and wrong decisions Or: confusing a-priori and a-posteriori knowledge In Catharina Hospital, 7000 invasive procedures (diagnostics and PCI) are performed annually Prior to a procedure, kidney function is checked If GFR < 60 ml/min prehydration Accuracy of GFR measurement is 3ml/min (rather good!, you don t think so?)

Hocus-pocus with statistics (3) About reproducibility and wrong decisions Or: confusing a-priori and a-posteriori knowledge In the year 2012, out of the 7000 patients GFR was between 57 and 63 ml/min in 387 of them. In ~ 50% of these 387 patients, a second measurement would have switched them from above 60 ml to below or vice versa Does this mean that you could better not determine renal function prior to PCI/ CAG, because it is wrong In the group of patients where it matters???

Of the total population you need to examine, only a small percentage is close to the cut-off value and might cross the border (387/7000 = 6 % in case of GFR & hydration) Hocus-pocus with statistics (3) About reproducibility and wrong decisions What is fundamentally wrong in this reasoning? confusing a-priori and a-posteriori knowledge You do not know beforehand who is close to the cut-off value (if you would know that, there would be no need to measure at all)

Reproducibility of FFR N=200 VERIFY study, Berry et al, JACC 2013 ( published februari 2013) There is not any other index in physiology so reproducible as FFR

Reproducibility of FFR gray zone 0.76-0.80 N=200 VERIFY study, Berry et al, JACC 2013 ( published februari 2013) There is not any other index in physiology so reproducible as FFR

At 1200 consecutive in-duplo measurements of FFR, there was NOT ANY cross-over across the gray zone FFR non-signif. stenosis significant 1.0 0.80 0.75 0 3% 2% 0%

Reproducibility ifr using matlab Data from Verify Study

ifr2 Reproducibility ifr 1 0,8 0,6 0,4 0,2 0 0 0,2 0,4 0,6 0,8 1 ifr1

Diff ifr Bland-Altman Reproducibility ifr 0,3 Mean difference (std): -0.007 ± 0.037 0,2 0,1 0 0 0,2 0,4 0,6 0,8 1-0,1-0,2-0,3 Mean ifr

Measurements compared ifr matlab vs ifr volcano Absolute difference 2 measurements > 0.3 (axes Bland-Altman are truncated) All 705 measurements

ifr_resolve ifr comparison 1 0,8 0,6 0,4 0,2 0 0 0,2 0,4 0,6 0,8 1 ifr_matlab

Diff ifr 0,3 Bland-Altman ifr Mean difference (std): -0.005 ± 0.034 0,2 0,1 0 0 0,1 0,2 0,3 0,4 0,5 0,6 0,7 0,8 0,9 1-0,1-0,2-0,3 Mean ifr

Measurements compared ifr matlab vs ifr volcano Difference of 18 measurements 0.1 (ifr volcano < ifr matlab ) Difference of 2 measurements 0.1 (ifr volcano > ifr matlab ) Remain 685 measurements

ifr_resolve ifr comparison 1 0,8 0,6 0,4 0,2 0 0 0,2 0,4 0,6 0,8 1 ifr_matlab

Diff ifr Bland-Altman ifr 0,3 Mean difference (std): -0.003 ± 0.020 0,2 0,1 0 0 0,1 0,2 0,3 0,4 0,5 0,6 0,7 0,8 0,9 1-0,1-0,2-0,3 Mean ifr

Diff ifr Diff ifr Summary 705 measurements 685 measurements Bland-Altman ifr Bland-Altman ifr 0,3 0,3 0,2 0,2 0,1 0,1 0 0 0,1 0,2 0,3 0,4 0,5 0,6 0,7 0,8 0,9 1 0 0 0,1 0,2 0,3 0,4 0,5 0,6 0,7 0,8 0,9 1-0,1-0,1-0,2-0,2-0,3 Mean ifr Mean difference (std): -0.005 ± 0.034-0,3 Mean ifr Mean difference (std): -0.003 ± 0.020 Reproducibility; difference between two ifr measurements (Verify) Mean difference (std): -0.007 ± 0.037

Cut-off = 0.83 ADVISE STUDY (N= 131) FFR 0.55 From: Sen, Davies, et al JACC 2011

ifr 0.91 ADVISE STUDY (N= 131) ifr 0.37 FFR FFR 0.55 0.55 From: Sen, Davies, et al JACC 2011

ADVISE STUDY (N= 131) ifr 0.58 FFR 0.34 FFR 0.87 From: Sen, Davies, et al JACC 2011

Retrospective analysis IFR versus FFR in retrospective analysis in 500 patients in Aalst and Eindhoven Range 0.6-0.9 all data: R 2 = 0.67 FFR range 0.6-0.9: R 2 = 0.39 diagn accuracy = 66 % diagn accuracy = 59 %

Correlation between ifr and FFR ( N=206) all data: R 2 = 0.70 FFR range 0.6-0.9: R 2 = 0.33 diagn accuracy = 67 % diagn accuracy = 58 % (diagnostic accuracy of flipping a coin = 50 %)

ifr 0.91 ADVISE STUDY (N= 131) ifr 0.37 FFR FFR 0.55 0.55 From: Sen, Davies, et al JACC 2011

ADVISE STUDY (N= 131) ifr 0.58 FFR 0.34 FFR 0.87 From: Sen, Davies, et al JACC 2011

ifr_resolve ifr by Volcano N=685 ifr comparison 1 0,8 0,6 0,4 0,2 Berry et al JACC 2013; 0 0 0,2 0,4 0,6 0,8 1 ifr_matlab ifr by Mathlab

Diff ifr Bland-Altman ifr 0,3 Mean difference (std): -0.003 ± 0.020 0,2 0,1 0 0 0,1 0,2 0,3 0,4 0,5 0,6 0,7 0,8 0,9 1-0,1-0,2-0,3 Mean ifr

FFR 0.55