Oxford The John Radcliffe Hospital Multi-vessel disease… Le Mans implications Dr Adrian Banning.
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Transcript of Oxford The John Radcliffe Hospital Multi-vessel disease… Le Mans implications Dr Adrian Banning.
OxfordThe John Radcliffe Hospital
Multi-vessel disease…Le Mans implications
Dr Adrian Banning
Multi-vessel disease…Le Mans - implications ?
• Lemans trial J Am Coll Cardiol 2008
– Small randomised trial of CABG vs PCI for patients with left main disease
• Syntax Lemans– Subset of the Syntax trial – patients with left main disease – follow up angios at 15 months (both surgical and PCI)– To be reported at PCR 09
Why is the Left Main important?
It supplies at least 2/3 of the blood to the heart!!!It supplies at least 2/3 of the blood to the heart!!!
Why is the left main special?
• Large vessel– Prone to calcification– Large volume of plaque required to cause stenosis– Intubated by the diagnostic catheter –ostium?– By definition terminates in a bifurcation – at least
• Untreated LMS stenosis > 20% mortality at 1yr
Results of initial intervention on the LMS- the early years
• 1980s Hartzler using POBA– 10% procedural mortality in hospital– 64% 3yr mortality
• Early 1993-8 ULTIMA– 279 pts unprotected LMS– 14% procedural mortality in hospital– 25% mortality at one year
– NB if 46% inoperable are excluded –• 97% 1yr survival in these low risk pts
Can we predict risk when stenting the LMS?
Stent the LMS with BMS safe, but high rate of MACE due to restenosis
Am J Cardiol. 2003;91:12-6.
• 103 patients• BMS (n 50) or PES (n 53). • All IVUS guidance and Cutting balloon pretreatment x 3 to cover
entire lesion
• Ostium and body were treated with a single stent
Single stent 49/50 and 52/53Final kissing balloon dilation was performed only in cases with suboptimal result at the LCX ostium (6% and 19%)
• Follow-up: 6 months angio and IVUS
• No “late” stent thrombosis in either group
A Randomized Comparison of Paclitaxel-ElutingStents Versus Bare-Metal Stents for Treatment
of Unprotected Left Main Coronary Artery Stenosis
Erglis et al JACC 2007
A Randomized Comparison of Paclitaxel-ElutingStents Versus Bare-Metal Stents for Treatment
of Unprotected Left Main Coronary Artery Stenosis
Erglis et al JACC 2007
A Randomized Comparison of Paclitaxel-ElutingStents Versus Bare-Metal Stents for Treatment
of Unprotected Left Main Coronary Artery Stenosis
Erglis et al JACC 2007
A Randomized Comparison of Paclitaxel-ElutingStents Versus Bare-Metal Stents for Treatment
of Unprotected Left Main Coronary Artery Stenosis
Erglis et al JACC 2007
Erglis et al JACC 2007
A Randomized Comparison of Paclitaxel-ElutingStents Versus Bare-Metal Stents for Treatment
of Unprotected Left Main Coronary Artery Stenosis
Location matters
Distal- bifurcation
Shaft
OstiumOstium
What makes the left main special?
• Anatomy matters– Ostial Needs 1 stent– Body Needs 1 stent– Bifurcation Usually >1 stent, 2 wires, >6F
Preliminary DES in LMS disease?
Long-Term Outcome After DES in Nonbifurcation Lesions that involve Unprotected LMS
Chieffo et al Circulation 2007
• Population: 147 pts• elective (only) consecutive pts SES or PES in 5 centers• - stenosis in the ostium and/or the mid-shaft of an
unprotected LMCA
• PCI instead of surgery was considered either(1) suitable anatomy for stenting and preference patient and physician (2) suitable anatomy for stenting and EuroSCORE 6 and/or Parsonnet score 13 and/or prior bypass surgery with failure of all conduits (n=2).
Favorable Long-Term Outcome After Drug-Eluting Stent Implantation in Nonbifurcation Lesions That Involve
Unprotected Left Main Coronary
Chieffo et al Circulation 2007
• Medications: • IIb/IIIa inhibitors at the discretion of the operator. • Dual antiplatelet therapy for at least 6 months after. All patients
were advised to maintain lifelong use of aspirin (100 mg/d).
• Clinical follow-up: at 1, 6, 12, and 24 months. • Patients eligible for longer clinical follow-up were contacted at 36
and 48 months.
• Angio follow-up: 4 and 9 months or earlier if neccesary
• Total follow up mean 886 days
Favorable Long-Term Outcome After Drug-Eluting Stent Implantation in Nonbifurcation Lesions That Involve
Unprotected Left Main Coronary
Chieffo et al Circulation 2007
Favorable Long-Term Outcome After Drug-Eluting Stent Implantation in Nonbifurcation Lesions That Involve
Unprotected Left Main Coronary
Chieffo et al Circulation 2007
Favorable Long-Term Outcome After Drug-Eluting Stent Implantation in Nonbifurcation Lesions That Involve
Unprotected Left Main Coronary
Chieffo et al Circulation 2007
Favorable Long-Term Outcome After Drug-Eluting Stent Implantation in Nonbifurcation Lesions That Involve
Unprotected Left Main Coronary
Chieffo et al Circulation 2007
Favorable Long-Term Outcome After Drug-Eluting Stent Implantation in Nonbifurcation Lesions That Involve
Unprotected Left Main Coronary
Chieffo et al Circulation 2007
No proven late stent thrombosis
4 unexpected deaths
Favorable Long-Term Outcome After Drug-Eluting Stent Implantation in Nonbifurcation Lesions That Involve
Unprotected Left Main Coronary
Chieffo et al Circulation 2007
What about late stent thrombosis in LMS disease?
• Specific worries– Late thrombosis for all DES >BMS– Late thrombosis higher off label– Higher risk of incomplete expansion?– Left main occlusion will be fatal
• Reassurances– Big vessel
Late and very late stent thrombosis following DES in ULM. Chieffo et al, EHJ Sept 2008.
• Multicentre registry of 731 pts with Elective DES stenting of ULM disease.
• Definite ST • 4 pts (0.5%). 3 early (≤30d), 1 late (≤ 1 yr). No VLST.
• Probable ST = 3 pts. All early (≤30d)
• Definite or probable ST = 7 / 731 = 0.95%• All were on dual AP Rx.
• Possible ST• (8 late, 12 very late) in 20 (2.7%) pts.
Late and very late stent thrombosis following DES in ULM. Chieffo et al, EHJ Sept 2008.
• Outcomes after 29.5±13.7 months follow up:– Death: 6.2% (n=45).
– Cardiac death: 4.2% (n=31)
– TVR: 12.9% (n=95)
– TLR: 10.9% (n=76)
– Restenosis rate: 14.1% on angiographic follow-up of 548 pts.
(NB: 76% of lesions involved the distal LM.)
• Predictors of ST at logistic analysis:– Euroscore– LVEF
• Consistent with general PCI population. • No unique ST predictor among ULM pts identified in this analysis.• Conclusion: Elective DES stenting of ULM is safe - low rates of ST.
358 consecutive patients
7 centres
All DES
Elective Urgent
MACE free 74% 68%
Mortality 6% 21%
Reinfarction 8% 10%
TLR 7% 3%
TVR 16% 7%
Delft J Am Coll Cardiol 2008 ; 51 2212-9
So can stents replace surgeryin left main disease?
Unprotected left main stenting vs CABG
Seung et al, NEJM April 2008.
• Long term follow up of 1102 patients stenting for ULM disease,
• vs propensity-matched cohort of CABG patients
• No significant difference in the risk of death and the composite outcome of death, Q-wave MI, or stroke between the two groups.
• TVR higher in the stents group, even with DES.
Seung KB et al. N Engl J Med 2008;358:1781-1792
Study of unprotected LEft MAiN Stenting versus bypass surgery
J Am Coll Cardiol 2008; 51: 538-45
Lemans study design
PCI techniqueDirect stenting preferred
if not poss predil with 2 or 2.5
Bifurcation technique
Initial stent to LAD then Cullotte or Prov T if necessary
No crush stenting
IVUS advised
DES if diameter < 3.8mm (35%)
LeMans study 2008
Lemans trial 2008
Improved EF with PCIETT similar by 12 months
more angina PCI initially
LeMans survival
Left Main Disease(isolated, +1, +2 or +3
vessels)
3 Vessel Disease(revasc all 3 vascular territories)
SYNTAX Eligible SYNTAX Eligible PatientsPatients
De novo disease
Limited Exclusion Criteria Previous interventions
Acute MI with CPK>2x
Concomitant cardiac surgery
Syntax Lemans (reports PCR 09)
• All left main pts in the randomised Syntax n=710• Follow up angio at 15 months• Asses late angio outcomes with clinical outcomes• Asses utility of angio follow up
• Stats– Surgery occlusion rate rate 5-12%
• 100 surgery pts 95% confidence interval (+/-0.043) if occlusion is 5% or (+/-0.043) if occlusion is 12%
– PCI Expected Patency rate 74-97%• 100 PCI pts 95% confidence interval (+/-0.078) if patency is 80%
– Expected attrition 30%
12 Month LM Subgroup MACCE Rates
CABG TAXUSLeft Main Isolated
Left Main + 3VD
Left Main + 2VD
Left Main + 1VD
N=258(37%)
N=218(31%)
N=138(20%)
N=91(13%
)
All LMN=705
Pati
en
ts (
%)
12 Month Subgroup MACCE Rates
All LMN=705
LM+1VDN=138
LM isolatedN=91
LM+2VDN=218
LM+3VDN=258
Pati
en
ts (
%)
3VD (All)N=1095
CABG TAXUS
So why is the left main special?
• The left main is unforgiving during PCI– Because large volumes of myocardium are at risk – Large volumes of plaque may move– Calcification is restrictive to stent expansion– loss of “branches” will have immediate and profound
haemodynamic consequences
• The left main is unforgiving in the long term– All ostial disease has a very high restenosis
rate (particularly if the stent is incompletely expanded).
What do we know about left main PCI?
• Procedural risk fallen from 10-20% to <1%
(in all but shock cases)
• Ostial and shaft disease is different to terminal disease of the main
• Left main PCI should be definitely considered in all emergency cases and many urgent cases
What do we know about left main PCI in 2008?
• DES are almost certainly better than BMS
• Risks of treating left main disease with PCI or surgery are probably the same
• Long term results of DES in elective ostial and shaft disease are very encouraging – Those cases treatable with one properly
expanded stent
What do we know about left main PCI in 2008?
• However– How do we treat distal bifurcation disease
best?• Perhaps the cullotte? Not the crush for me
• LMS + 2VD / 3VD – surgery still has lower rates of TVR
particularly in diabetics
OSTIUM BODYDISTAL
1 STENT
DISTAL2
STENTCABG
UNSUITABLE
URGENT
ELECTIVE
Isolated left main stenting in 2008…Isolated left main stenting in 2008…