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Educational Training Program ESC European Heart House, Nice, April 19th –21st , 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD CORONARY STENOSIS Nico H.J. Pijls, MD, PhD, Catharina Hospital, Eindhoven, The Netherlands

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Page 1: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

Educational Training Program ESC European Heart House, Nice, April 19th –21st , 2007

CORONARY PHYSIOLOGY IN THE CATHLAB

LONG-TERM CLINICAL OUTCOME OF MILD CORONARY STENOSIS

Nico H.J. Pijls, MD, PhD, Catharina Hospital, Eindhoven, The Netherlands

Page 2: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

Any treatment in health care should be directedeither to

• Releave symptoms ( improve functional class )

or to

• Improve outcome ( prognosis, longevity)

No other justification for any treatment is possible !

NOTE

Page 3: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

In patients with coronary artery disease,the most important factor with respect to both

• functional class (symptoms)

• and prognosis (outcome)

Is the presence and extent of inducible ischemia

(many invasive & non-invasive studies in > 100,000 patients)

If a stenosis is responsible for reversible ischemia, revascularization improves symptoms(if present) and outcome…..

DEFER study: background (1)

Page 4: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

Davies et al, Circulation, 1997

0 4 8 12 16 20 24 mos0 4 8 12 16 20 24 mos00

22

44

66

88

%% 6.6%Cumulative MortalityCumulative Mortality

1.1%

Revascularization

4.1%

Medical treatment

No treatment

558 patients , functionally significant stenosis without symptoms: randomization in 3 treatments strategies

Is it useful to revascularize hemodynamically significant stenosis ? (ACIP study)

P < 0.05

Page 5: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

DEFER study: background (2)

If a stenosis is responsible for reversible ischemia, revascularization is justified……

……But what if a stenosis or “plaque” is NOT responsible for reversible ischemia ? (functionally “non-significant” , “non-culprit”)

PCI is often performed in such lesions,yet the benefit of such treatment is not clear

Page 6: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

158 vb38/interm.RCA/Buddem (1)

• female, 58-y-old• underwent PCI of severe LCX lesion a minute before • 50 % stenosis in mid RCA

Should this lesion be stented ??

Page 7: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

The DEFER Study: The DEFER Study: Background (3)Background (3)

• The incidence of coronary lesions The incidence of coronary lesions increases with age. About 40% of increases with age. About 40% of all 60-year-old “healthy” personsall 60-year-old “healthy” persons have one or more have one or more plaques ,plaques , “ “non-significant” , or equivocal stenosesnon-significant” , or equivocal stenoses (50-70 % by angiography) in (50-70 % by angiography) in their coronary arteries.their coronary arteries.

Page 8: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

Cardiac Death + Myocardial Infarction Rates Cardiac Death + Myocardial Infarction Rates at 9-12 Months after (DES)-stentingat 9-12 Months after (DES)-stenting

0 2 4 6 8 %

4.14.1

4.74.7

4.94.9

4.94.9

3.73.7

3.83.8SIRIUS SIRIUS

TAXUS IVTAXUS IV

ENDEAVORENDEAVOR

DES – stenting is not harmless !!

DESBMS

DESBMS

DESBMS

Page 9: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

• Fractional Flow Reserve, Fractional Flow Reserve, calculated fromcalculated from coronary pressure measurement, coronary pressure measurement, is an accurate, is an accurate, invasive, and lesion-specific invasive, and lesion-specific indexindex to demonstrate to demonstrate or exclude whether a particular coronary stenosisor exclude whether a particular coronary stenosis can cause can cause reversible ischemiareversible ischemia..

• FFRFFR can be determined easily, in the cath-lab, can be determined easily, in the cath-lab, immediately prior to a planned interventionimmediately prior to a planned intervention

DEFER study: background (4)

FFR based strategy for PCI in equivocal stenosis( DEFER – Study)

Page 10: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

The DEFER Study: DesignThe DEFER Study: Design

prospective randomized multicentric trial prospective randomized multicentric trial (14 centers) in 325 patients with stable (14 centers) in 325 patients with stable chest pain and an intermediate stenosis chest pain and an intermediate stenosis without objective evidence of ischemiawithout objective evidence of ischemia

AalstAmsterdamEindhoven Essen Gothenborg Hamburg Liège

Maastricht Madrid Osaka Rotterdam Seoul Utrecht Zwolle

data collection & analysis: Jan Willem Bech, MD, PhDPepijn van Schaardenburgh, MD

Page 11: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

The DEFER Study: The DEFER Study: ObjectivesObjectives

• to test to test safetysafety of deferring PCI of stenoses of deferring PCI of stenoses not responsible for inducible ischemia as not responsible for inducible ischemia as indicated by FFR > 0.75 ( indicated by FFR > 0.75 ( ““outcomeoutcome”” ))

Secondary objectiveSecondary objective

• to compare to compare quality of lifequality of life in such patients, in such patients, whether or not treated by PCI whether or not treated by PCI (CCS-class, need for anti-anginal drugs)(CCS-class, need for anti-anginal drugs) (“symptoms”)(“symptoms”)

Primary objective

Page 12: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

DEFER Group

REFERENCE Group PERFORM Group

The DEFER Study: Flow ChartPatients scheduled for PCI without Proof of Ischemia

(n=325)

performance of PTCA (158)

deferral of PTCA (167)

FFR 0.75 (91)

No PTCA

FFR 0.75(90)

PTCA

FFR < 0.75(76)

PTCA

FFR < 0.75(68)

PTCA

RandomizationRandomization

Page 13: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

THE DEFER STUDY: RANDOMIZATION

1 : 1 randomization

deferral of PCI

performance of PCI

If FFR < 0.75 performance anyway reference group

If FFR > 0.75 randomization followed

defer PCI perform PCI

Page 14: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

The DEFER Study: The DEFER Study: CatheterizationCatheterization

• 6 or 7 F guiding catheter for measurement of aortic pressure ( Pa)

• QCA from 2 orthogonal views

• Coronary pressure measurement (Pd ) by 0.014” pressure wire (Radi Medical Systems)

• Maximum hyperemia by i.v. adenosine (140 ug/kg/min)

• Calculation of Fractional Flow Reserve by:

FFR = Pd / Pa

Page 15: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

The DEFER Study: Base line data

Randomized to Randomized to Deferral of PTCA Performance of

PTCA N=167 N=158

Diabetes (%) 13 12Hypertension (%) 41 35Hyperlipidemia (%) 47 48Current Smoker (%) 30 25Family History CAD (%) 50 49

Age, (yr) 629 6310Female sex (%) 29 29Ejection Fraction (%) 6710 689

Page 16: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

The DEFER Study: Baseline QCA and FFR

Ref. diam. (mm) 2.960.63 2.980.57

MLD (mm) 1.420.40

DS (%) 5210

1.420.38 5211

Randomized to Randomized to Deferral of PTCA Performance of PTCA

N=167 N=158

FFR 0.720.19 0.730.19

All baseline characteristics were identical between both groups

Page 17: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

The DEFER Study: Diameter Stenosis versus FFR

20

30

40

50

60

70

80

90

FFR < 0.75FFR 0.75

DS

%

Page 18: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

No. at risk

Defer group 90 85 82 74 73 72

Perform group 88 78 73 70 67 65

Reference gr 135 105 103 96 90 88

78.8

72.7

64.4

0 1 2 3 4 50

25

50

75

100

Defer

Perform

Reference(FFR < 0.75)

p=0.52

p=0.17p=0.03

Years of Follow-up

event – free survival (%)

Page 19: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

72 %72 % 58 %58 %68 %68 %Pts free of angina(%)Pts free of angina(%)

52 (39 %)52 (39 %)24 (27 %)24 (27 %)19 (21 %)19 (21 %)Patients Patients ≥1 event (%)≥1 event (%)

707029292121Total eventsTotal events

2 (1.5)2 (1.5)1 (1.1)1 (1.1)00Other (%)Other (%)

11 (8.2)11 (8.2)6 (6.8)6 (6.8)6 (6.7)6 (6.7)Non-TLR(%)Non-TLR(%)

14 (10.4)14 (10.4)4 (4.5)4 (4.5)1 (1.1) 1 (1.1) CABG(%)CABG(%)

7 (5.2)7 (5.2)1 (1.1)1 (1.1)00Non-Q wave MI(%)Non-Q wave MI(%)

6 (4.5)6 (4.5)4 (4.5)4 (4.5)00Q wave MI (%)Q wave MI (%)

4 (3.0)4 (3.0)3 (3.4)3 (3.4)3 (3.3)3 (3.3)Non Cardiac Death(%)Non Cardiac Death(%)

8 (6.0)8 (6.0)2 (2.3)2 (2.3)3 (3.3)3 (3.3)Cardiac Death(%)Cardiac Death(%)

14414490909191Number of patientsNumber of patients

ReferenceReferencePerformPerformDeferDefer

FFR<0.75FFR<0.75FFR FFR ≥0.75≥0.75

18 (13.4)18 (13.4)8 (9.1)8 (9.1)8 (8.9)8 (8.9)TLR(%)TLR(%)

DEFER: Clinical Outcome at 5 YearsDEFER: Clinical Outcome at 5 Years

Lost to follow-up 1 2 10Lost to follow-up 1 2 10

Page 20: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

Cardiac Death And Acute MI After 5 Years

3.3

7.9

15.7

0

5

10

15

20 %

P=0.20

P< 0.03

P< 0.005

DEFER PERFORM REFERENCE

FFR > 0.75 FFR < 0.75

Page 21: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

0%

20%

40%

60%

80%

100%

baseline 1month 1 year 2 year 5 year

Defer group Perform group Reference group

freedom from chest pain

FFR > 0.75 FFR > 0.75 FFR < 0.75

* *

* *

* **

*

Page 22: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

DEFER: Summary and Conclusions (1)DEFER: Summary and Conclusions (1)

1.1. In patients with stable chest pain, the most important In patients with stable chest pain, the most important prognostic factor of a given coronary artery stenosis, prognostic factor of a given coronary artery stenosis, is its ability of inducing myocardial ischemia (as is its ability of inducing myocardial ischemia (as reflected by FFR < 0.75)reflected by FFR < 0.75)

2.2. In those patients, clinical outcome of such “ischemic” In those patients, clinical outcome of such “ischemic” stenosis, even when treated by PCI, is much worse stenosis, even when treated by PCI, is much worse than that of a functionally “non-significant” stenosis.than that of a functionally “non-significant” stenosis.

3. The prognosis of “non-ischemic” stenosis (FFR > 0.75) 3. The prognosis of “non-ischemic” stenosis (FFR > 0.75) is excellent and the risk of such “non-significant” is excellent and the risk of such “non-significant” stenosis or plaque to cause death or AMI is < 1% per stenosis or plaque to cause death or AMI is < 1% per year, year, and not decreased by stentingand not decreased by stenting

Page 23: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

DEFER: Summary and Conclusions (2)DEFER: Summary and Conclusions (2)

Message

Stenting an ischemic lesion makes sense becauseStenting an ischemic lesion makes sense because it improves symptoms and often also outcome.it improves symptoms and often also outcome.

Stenting a “non-ischemic” stenosis has no benefit Stenting a “non-ischemic” stenosis has no benefit compared to medical treatment, neither in compared to medical treatment, neither in prognostic nor symptomatic respect.prognostic nor symptomatic respect.

Importance of FFR programm of tomorrow

Page 24: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD
Page 25: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

What was wrong the wrong concept in the (mostly retrospective) studies performed so far ?!

e.g. ARTS-studies:

30% incomplete revascularization, but….

“arbitrary” choice of no revascularization, or even worse: no revascularization because of technical difficulties considerable number of the non-revascularized lesions were ischemic lesions

Whereas among the treated lesions, quite a bit ofnon-ischemic lesions must have been stented

Complete vs Incomplete Revascularization:

Page 26: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

What was wrong the wrong concept in the (mostly retrospective) studies performed so far ?!

e.g. ARTS-studies:

30% incomplete revascularization, but….

“arbitrary” choice of no revascularization, or even worse: no revascularization because of technical difficulties considerable number of the non-revascularized lesions were ischemic lesions

Whereas among the treated lesions, quite a bit ofnon-ischemic lesions must have been stented

Complete vs Incomplete Revascularization:

Page 27: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

DEFER: Summary and ConclusionsDEFER: Summary and Conclusions

Summary1.1. In patients with stable chest pain, the most important prognostic In patients with stable chest pain, the most important prognostic

factor of a given coronary artery stenosis, is its ability of inducing factor of a given coronary artery stenosis, is its ability of inducing myocardial ischemia (as reflected by FFR < 0.75)myocardial ischemia (as reflected by FFR < 0.75)

2.2. In these patients, clinical outcome of such “ischemic” stenosis, In these patients, clinical outcome of such “ischemic” stenosis, even when treated by PCI, is much worse than that of a even when treated by PCI, is much worse than that of a functionally “non-significant” stenosis.functionally “non-significant” stenosis.

3. The prognosis of “non-ischemic” stenosis (FFR > 0.75) is excellent 3. The prognosis of “non-ischemic” stenosis (FFR > 0.75) is excellent and the risk of such “non-significant” stenosis or plaque to cause and the risk of such “non-significant” stenosis or plaque to cause death or AMI is < 1% per year, and death or AMI is < 1% per year, and not decreased by stentingnot decreased by stenting

ConclusionStenting a “non-significant” stenosis does not benefit patients withStenting a “non-significant” stenosis does not benefit patients withstable chest pain, neither in prognostic nor symptomatic respectstable chest pain, neither in prognostic nor symptomatic respect

Page 28: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

No. at risk

FFR ≥ 0.75 178 162 154 143 138 136

FFR < 0.75 135 105 103 96 90 88

75.8

64.4

0 1 2 3 4 50

25

50

75

100

FFR 0.75

FFR < 0.75p=0.03

Years of Follow-up

event – free survival (%)

Page 29: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

7.47.4

0.60.600

11

22

33

44

55

66

77

88

12000 Patients12000 Patients( 2 x 6000)( 2 x 6000)

similar stenosissimilar stenosisseverity byseverity bycoronary angiocoronary angio

The risk for death or acute myocardial infarction in the next five years is 20 times higher for an ischemic lesion compared to a non-ischemic lesion !!!

Iskander S, Iskandrian A E JACC 1998

% d

eath

or

Acu

te M

I

no ischemia ischemia

Page 30: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

Simply stated:

Ischemia - guided PCI strategy versus “stent ‘m all strategy”

In single vessel disease

With respect to: outcome (adeverse events) , quality of life cost-efectiveness

The DEFER Study: The DEFER Study: ObjectivesObjectives

Page 31: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

The DEFER Study: Exclusion Criteria

documented myocardial ischemia related to the target vessel within the last 2 months

severe hypokinesia or akinesia of the myocardium supplied by the target vessel

open bypass graft distal to the target lesion

Page 32: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

DEFER: Clinical Outcome at 5 YearsDEFER: Clinical Outcome at 5 Years

Cardiac death and Acute Myoc Infarction

ReferenceReferencePerformPerformDeferDefer

FFR < 0.75FFR < 0.75 FFR FFR ≥ 0.75≥ 0.75

3.3 % 7.9 % 15.7 %

P = 0.20

P < 0.005

P < 0.003

Page 33: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

Death + Myocardial Infarction Rates at 9-12 MonthsDeath + Myocardial Infarction Rates at 9-12 Months

0 2 4 6 8 %

4.14.1

4.74.7

4.94.9

4.94.9

3.73.7

3.83.8SIRIUS SIRIUS DES DES

BMS BMS

TAXUS IV TAXUS IV DES DES

BMS BMS

ENDEAVORENDEAVOR DESDES

BMSBMS

DEFERDEFER ALL PCI ALL PCI

(BMS)(BMS)

(9 months)(9 months)

(9 months)(9 months)

(9 months)(9 months)

(12 months)(12 months)5.15.1

Page 34: Educational Training Program ESC European Heart House, Nice, April 19 th –21st, 2007 CORONARY PHYSIOLOGY IN THE CATHLAB LONG-TERM CLINICAL OUTCOME OF MILD

Death + Myocardial Infarction Rates at 9-12 MonthsDeath + Myocardial Infarction Rates at 9-12 Months

0 2 4 6 8 %

2.72.7

7.67.6

4.14.1

4.74.7

4.94.9

4.94.9

3.73.7

3.83.8SIRIUS SIRIUS DES DES

BMS BMS

TAXUS IV TAXUS IV DES DES

BMS BMS

ENDEAVORENDEAVOR DESDES

BMSBMS

DEFERDEFER FFR<0.75 FFR<0.75

FFRFFR≥≥0.750.75

(9 months)(9 months)

(9 months)(9 months)

(9 months)(9 months)

(12 months)(12 months)perform

1.11.1 defer