7. Saito N, Matsuo H et al. J Invasive Cardiol. 2013 Dec;25(12):642-9..
In Vitro Assessment of Mathematically-Derived FFR
in Coronary Lesions With More Than Two Sequential Stenoses
PCI workshop 2017
9. FFR oriented intervention to the
tandem lesion in real world
• Step1 : The rule of delta PG
Stenosis A > Stenosis B → Fix stenosis A
Stenosis A < Stensois B → Fix stenosis B
Stenosis A = Stenosis B → Fix proximal stenosis
• Step2 : Re-evaluate PG after fixing the first stenosis
If FFRmyo <0.80 Fix another stenosis
If FFRmyo >=0.80 leave the stenosis without Tx
PCI workshop 2017
11. PCI workshop 2017
Cardiac event occurred very few, if treated by this strategy
during mean follow-up of 501±311 days.
Kim HL, Koo BW et al. JACC Cardiol Interv. 2012;110:1578-1584.
A total of 131 patients (141 vessels and 298 lesions) with multiple intermediate stenoses
within the same coronary artery were assessed by FFR with pullback pressure tracings.
12. Case
ID:138126
74y.o. Male
Diagnosis : effort angina
Risk factor : Dyslipidemia ,DM, CKD stage ⅢA
Present illness : Pt began to feel chest oppressive
sensation during 5minutes walking about 2 weeks
before the procedure.
PCI workshop 2017
21. Case History
• 78-year-old male
• Dyslipidemia
• Coronary angiography and physiological study using a pressure
wire, followed by LM and LAD PCI (Xience V, Abbott Vascular, CA,
USA) performed 6 years ago
• Presented to our hospital complaining of chest tightness
PCI workshop 2017
22. Coronary Angiography and FFR
• Coronary angiography revealed
tandem lesions: 50% lesion in LAD
and 75% lesion in LMCA
• FFR (Opsens Medical, Quebec,
Canada) in distal LAD within the gray
zone (FFR = 0.76)
• Hyperemic pull back revealed step-
ups over the two lesions of 0.12 and
0.06, respectively
Pre-PCI: tandem lesion in LAD and LMT
PCI workshop 2017
23. Treatment
Lesion with the larger ΔFFR treated first
and then FFR reassessed:
• Drug-eluting stent (Ultimaster, Terumo,
Tokyo, Japan) implanted in the LAD
over the pressure guidewire
• FFR performed immediately after
dilatation
• FFR corrected for drift ≈ 0.83
Park SJ, Ahn JM, Pijls NH, De Bruyne B, Shim EB, Kim YT, et al. Am J Cardiol. 2012;110:1578–84.
FFR correctd for drift ≈ 0.83
PCI workshop 2017
24. Summary
• All procedures in this patient were performed using one pressure guidewire
and no re-normalization was performed until the end of the case
• Device exchange was performed 6 times over the Optowire
• Total procedure time was 53 minutes
• Drift observed after the procedure was 2 mmHg
• The FFR corrected for drift was ≈ 0.83; unnecessary stenting of the lesion in
this patient’s LMCA was avoided
PCI workshop 2017
25. 102 lesions from 95 patients
Total procedure time (min) 98±29 min
Total contrast volume (ml) 110±43
Device exchange (times) 6±2
Max pressure (atm) 21±4
Rotablator/Jailed wire
(case)
10/13
Drift in FFR value 0.013±0.013 [-0.07 – 0.02]
Drift in mmHg 1.2±1.1 [-5.0 – 2.0]
Optic sensor Pressure wire use as the workhorse wire
(2016/1/20-2016/10/12)
Kawase Y, Matsuo H et al. Cardiovasc Interv Ther. 2017 Jul 3.
doi: 10.1007/s12928-017-0481-x. [Epub ahead of print]
PCI workshop 2017
26. 102 lesions from 95 patients
Total procedure time (min) 98±29 min
Total contrast volume (ml) 110±43
Device exchange (times) 6±2
Max pressure (atm) 21±4
Rotablator/Jailed wire
(case)
10/13
Drift in FFR value 0.013±0.013 [-0.07 – 0.02]
Drift in mmHg 1.2±1.1 [-5.0 – 2.0]
Optic fiber pressure wire
Pressure drift>3.0mmHg (4/102=4%)
FFR drift>0.03 (6/102=6%)
Assessed after whole procedure
Optic sensor Pressure wire use as the workhorse wire
(2016/1/20-2016/10/12)
Kawase Y, Matsuo H et al. Cardiovasc Interv Ther. 2017 Jul 3.
doi: 10.1007/s12928-017-0481-x. [Epub ahead of print]
PCI workshop 2017
30. In Vitro Assessment of Mathematically-Derived FFR
in Coronary Lesions With More Than Two Sequential Stenoses
iFR(X-)=iFRpre+ΔiFR(X)
iFR(X)Pred=1-ΔiFR(X)PCI workshop 2017
31. iFR Scout™ Pullback Software
• Significant
Features
– Live display of
single-cycle iFR
value
– Pullback
assessment of
multiple lesions
– Highlighting of
the Wave-Free
Period
601-0103.181/001
Internal Use Only. Do Not Distribute
PCI workshop 2017
32. Case: M.M. ID: 334928 74 y.o. female
Coronary risk factors: HTN (-), DM (+), HL (+), Family Hx (+), Smoking (+)
PH: none, FH: Brother (cardiac death)
PI: The patient was referred to our hospital due to the suspicion
of angina pectoris. Coronary angiogram performed on 2016/2/12 showed
severe coronary stenosis in her coronary artery showed diffuse calcified coronary stenosis
both in RCA and LCA.(#1: 90%, #2 90%, #3 75%, #6, #14 90%.
42. FOCAL
DIFFUSED
(low pressure drop intensity)
iFR pullback mapping to identify focal and diffuse
disease
FOCAL
(high pressure drop intensity)
PCI workshop 2017
43. Case presentation
75 years old male
Effort Angina
PI: The patient was referred to our hospital due to the
exaggerated chest pain during effort.
Risk factors : past smoker, HT,DM,Dyslipidemia
No prior intervention
LVEF 60% CKD class 2
Transient perfusion defect in anteroseptal wall by
SPECT
Angiography showed LAD proximal and mid stenosis.
52. Take home message
• In serial lesion assessment, Physiological pullback recording is very
important to identify the lesions where stenting is necessary.
• Delta FFR theory is practically helpful for the routine clinical
practice.
• New generation pressure wire system using optical-fiber sensor
may be useful to the repeat assessment of FFR in serial stenosis
because of less chance of pressure drift during procedures.
• iFR pullback curve with syncvision angiocoregistration system may
have large potentials for identifying lesions most likely to lead to an
improvement in coronary physiology and deferring those of lesser
importance, and could assist lesion selection and PCI planning in
the presence of multiple lesions.
PCI workshop 2017
Objectives
This study was performed to evaluate the physiological and clinical outcomes of fractional flow reserve (FFR)-guided revascularization strategy with drug-eluting stents in serial stenoses within the same coronary artery.
Background
Identifying a functionally significant stenosis is difficult when several stenoses exist within 1 coronary artery.
Methods
A total of 131 patients (141 vessels and 298 lesions) with multiple intermediate stenoses within the same coronary artery were assessed by FFR with pullback pressure tracings. In vessels with an FFR <0.8, the stenosis that caused the largest pressure step-up was stented first. Major adverse cardiac events were assessed during follow-up.
Results
FFR was measured 239 times and there were no procedure-related complications. There was a weak negative correlation between FFR and angiographic percent diameter stenosis (r = −0.282, p < 0.001). In total, 116 stents were implanted and revascularization was deferred in 61.1% (182 of 298) of lesions. When the vessels with an initial FFR <0.8 were divided into 2 groups according to FFR after first stenting (FFR ≥0.8 vs. FFR <0.8), there were no differences in baseline angiographic and physiological parameters between the 2 groups. During the mean follow-up of 501 ± 311 days, there was only 1 target vessel revascularization due to in-stent restenosis. There were no events related to deferred lesions.
Conclusions
FFR-guided revascularization strategy using pullback pressure tracing in serial stenoses was safe and effective. This strategy can reduce unnecessary intervention and maximize the benefit of percutaneous coronary intervention with drug-eluting stents in patients with multiple stenoses within 1 coronary artery.
ミリマーキュリー
ミリマーキュリー
Figure 3: Representative case of failed prediction by the residual pressure gradient across the implanted stent
Pre percutaneous coronary intervention: Blue arrows: Lesion, White number: iFR value at each point. Yellow number : Pressure gradient across the lesion
Post percutaneous coronary intervention: Blue arrow heads: Implanted stent, White number: iFR value at each point. Yellow number: Residual pressure gradient across the implanted stent
Figure 1: The scatter gram of each correlation
The correlation between predicted iFR and post iFR
The correlation between predicted FFR and post FFR
The correlation between predicted iFR-SPG and post iFR
The correlation between predicted FFR-SPG and post FFR