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Pietro Giorgio Malvindi, Joel Dunning, Nicola Vitale, For which patients with left main stem disease is percutaneous intervention rather than coronary artery bypass grafting the better option?, Interactive CardioVascular and Thoracic Surgery, Volume 7, Issue 2, April 2008, Pages 306–314, https://doi.org/10.1510/icvts.2007.169938
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Abstract
A best evidence topic in cardiac surgery was written according to a structured protocol. The topic addressed was to identify the patients with left main stem disease for which percutaneous intervention would be a better option than coronary artery bypass grafting. Altogether 665 papers were found using the reported search, of which 15 presented the best evidence to answer the clinical question. The authors, journal, date and country of publication, patient group studied, study type, relevant outcomes and results of these papers were tabulated. We conclude that if a bare metal stent is used for left main stenting the mortality at one year may be from 3% to over 28% in reported series. The restenosis rate of the bare metal stent in the left main position is around 20% at one year. There are some early series and randomized studies of drug eluting stents for left main stem lesions and the restenosis rate is reported to be around 10%. The European Society of Cardiology in their 2005 percutaneous intervention guidelines state that coronary bypass grafting is the procedure of choice for left main stem disease and only patients with a prohibitively high surgical risk should be considered. We consider that with such high restenosis rates, and with short-term follow-up in such low numbers and short periods compared to coronary artery bypass grafting, left main stenting should only be used as a last resort in patients turned down for coronary artery bypass grafting after full assessment by a cardiac surgeon due to prohibitive co-morbidities.
1. Introduction
A best evidence topic was constructed according to a structured protocol. This protocol is fully described in the ICVTS [1].
2. Clinical scenario
You are asked by the interventional cardiologist on-call to discuss a 73-year-old gentleman still on the table in the angiography lab. He was admitted with a non-ST myocardial infarction with a small troponin rise, has had clopidogrel, aspirin and reopro and is currently stable. The coronary angiogram shows a tight proximal left main stem lesion of about 70%. The patient is mildly obese and diabetic with some varicosities of the left leg and has prostate carcinoma, which is currently well controlled. The cardiologist would like to stent this lesion if you thought that he was not a good surgical candidate and asks for your opinion.
3. Three-part question
In a [patient with left main stem coronary disease] does [percutaneous stenting or CABG] result in the best [long-term survival].
4. Search strategy
Medline 1995 to Aug 2007 using Ovid Interface.
[LMS.mp or left main.mp] AND [exp Angioplasty/OR angioplasty.mp]
5. Search outcome
Using the reported search, 665 papers were identified from which 15 papers provided the best evidence to answer the question. These are summarized in Table 1 .
Author, date, | Patient group | Outcomes | Key results | Comments |
and country | ||||
Study type | ||||
(level of evidence) | ||||
ACC/AHA/SC | Report of the | CABG using IMA grafting is the ‘gold standard’ for treatment of ULM disease and has | ||
AI guidelines, | American | proven benefit on long-term outcomes. The use of DES has shown encouraging short-term | ||
(2005), J Am | College of | outcomes, but long-term follow-up is needed. Nevertheless, the use of PCI for | ||
Coll Cardiol, | Cardiology/ | patients with significant ULM stenosis who are candidates for revascularization | ||
USA, [2] | American Heart | but not suitable for CABG can improve cardiovascular outcomes and is a reasonable | ||
Association | revascularization strategy in carefully selected patients | |||
Guideline | Task Force on | |||
(level 2a) | Practice | PCI is not recommended in patients with asymptomatic ischemia or CCS class I or II | ||
Guidelines | angina, left main disease and eligibility for CABG | |||
Practice | Use of PCI is reasonable in patients with CCS class III angina with significant | |||
guideline group | left main CAD (>50% diameter stenosis) who are candidates for revascularization | |||
consisted entirely | but are not eligible for CABG. (Level of Evidence: B) | |||
of cardiologists | ||||
from the 3 | PCI is not recommended for patients with CCS class III angina and significant left | |||
organisations | main CAD and candidacy for CABG. (Level of Evidence: C) | |||
involved | ||||
Use of PCI is reasonable in patients with UA/NSTEMI with significant left main | ||||
CAD (>50% diameter stenosis) who are candidates for revascularization but are not | ||||
eligible for CABG. (Level of Evidence: B) | ||||
In patients with cardiogenic shock and significant left main disease or severe 3-vessel | ||||
disease and without right ventricular infarction or major comorbidities such as | ||||
renal insufficiency or severe pulmonary disease, CABG can be considered as the | ||||
revascularization strategy | ||||
European | Report of the | The presence of a left main (LM) coronary artery stenosis identifies an anatomic subset | ||
Society for | European Society | still requiring bypass surgery for revascularization. PCI of protected LMS (i.e. by a distal graft) | ||
Cardiology | of Cardiology | can be performed although a 1-year MACE of 25% is still rather high, which may | ||
guidelines, | reflect an increased mortality in patients with severe CAD with previous CABG. | |||
(2005), | ||||
Eur Heart J, [3] | Stenting for unprotected LM disease should only be considered in the absence of other | |||
revascularization options. Therefore, PCI can be recommended in these subsets | ||||
Guidelines | when bypass surgery has a very high perioperative risk (e.g. EuroSCORE >10%) | |||
(level 2a) | ||||
Until proved otherwise, PCI should be used only with reservation in diabetics with multi-vessel | ||||
disease and in patients with unprotected left main stenosis | ||||
Erglis et al., (2007), | 103 patients | Myocardial infarction | BMS 7/50 (14%) | Patient population |
J Am Coll | with unprotected | by 6 months | PES 5/53 (10%) | is those also ideal |
Cardiol, | LMS disease, | for surgery | ||
Australia and | 2004–2006 | Restenosis | BMS 11/50 patients | Mean age 62 |
Latvia, [4] | (22%) | Only 6 had previous | ||
All patients | PES 3/53 patients (6%) | CABG, mean | ||
PRCT | were good | P=0.021 | LVEF 54% | |
(level 1b) | candidates for | |||
CABG | 6 months adverse | BMS 15/50 (30%) | ||
cardiac-event free | PES 7/53 (13%) | |||
Randomized to | survival | P=0.036 | ||
express or | ||||
liberte BMS | Mortality at | BMS and PES 1 | ||
or Paclitaxel | 6 months | patient each (2%) | ||
eluting stent | ||||
(PES) with | ||||
cutting balloon | ||||
pre-treatment | ||||
under IVUS | ||||
control | ||||
Clopidogrel, | ||||
Heparin, | ||||
GpIIb/IIIa | ||||
given | ||||
BMS n=50 | ||||
PES n=53 | ||||
Palmerini et al., | 154 patients | 30 days | – Short-term | |
(2006), | underwent | follow-up | ||
Am J Cardiol, | CABG and | Overall mortality | CABG 4.5% | |
Italy, [6] | 157 patients | PCI 3.2% | – Early and | |
underwent PCI | P=NS | long-term | ||
Prospective | for left main | mortality were not | ||
cohort study | stenosis (94 DES) | Cardiac related | CABG 3.9% | significantly |
(level 2b) | mortality | PCI 2.5% | different between | |
From | P=NS | CABG and PCI | ||
2002–2005 | ||||
Myocardial | CABG 1.9% | – Target lesion | ||
Mean age±S.D.: | infarction at | PCI 4.5% | revascularization | |
CABG | 30 days | P=NS | was significantly | |
69.3±9.5 | higher in PCI-treated | |||
PCI 73.0±10.9 | Target lesion | CABG 0.6% | patients | |
revascularization | PCI 0.6% | |||
Left main | P=NS | – Although patients | ||
disease alone: | Follow-up | treated with drug-eluting | ||
CABG 5.2% | stents had a | |||
PCI 12.7% | Overall mortality | CABG 12.3% | 25% relative risk | |
P<0.001 | PCI 13.4% | reduction in the | ||
P=0.861 | rate of major adverse | |||
Left main lesions | cardiac events | |||
locations: | CABG 12.3% | compared with | ||
P=0.742 | PCI-DES 11.7% | patients treated | ||
P=0.968 | with bare metal | |||
Follow-up: | stents, event survival | |||
430 days | Cardiac related | CABG 9.7% | was still higher in | |
(105–730) | mortality | PCI 9.5% | the CABG group | |
P=0.994 | than in the drug | |||
eluting stent group | ||||
CABG 9.7% | ||||
PCI-DES 7.4% | ||||
P=0.667 | ||||
Myocardial | CABG 4.5% | |||
infarction | PCI 8.3% | |||
P=0.170 | ||||
CABG 4.5% | ||||
PCI-DES 5.3% | ||||
P=0.690 | ||||
Target lesion | CABG 2.6% | |||
revascularization | PCI 25.5% | |||
P=0.0001 | ||||
Chieffo et al., | 142 patients | 30 days | The patients | |
(2006), | underwent | receiving DES | ||
Circulation, | CABG (86 | Mortality | CABG 2.1% | were significantly |
Italy, [7] | patients had | PCI 0 | younger than | |
on-pump | CABG patients | |||
Prospective | CABG, 56 | Myocardial | CABG 26.5% | (64 vs. 68 years), |
Cohort study | patients | infarction | PCI 9.3% | had lower incidence |
(level 2b) | underwent off-pump | P=0.0009 | of smoking, | |
CABG) | significantly less | |||
Q-wave MI | CABG 3.5% | hypertension, less | ||
107 patients | PCI 0 | diabetes, and | ||
underwent | P=0.07 | significantly less | ||
PCI-DES for | renal failure | |||
left main | Target lesion | CABG 2.1% | ||
stenosis | revascularization | PCI 0 | The PCI patients | |
(2002–2004) | were therefore | |||
81.3% of | TVR | CABG 2.1% | fitter than the | |
patients | PCI 0 | CABG patients | ||
treated with | ||||
PCI had distal | Follow-up | 26% perioperative | ||
LMCA | MI rate after CABG is | |||
Mortality | CABG 6.4% | incredibly high, due to | ||
Mean age±S.D.: | PCI 2.8% | their definition of MI | ||
CABG | P=0.07 | |||
67.5±9.7 | ||||
PCI 63.6±10.3 | Myocardial | CABG 1.4% | ||
infarction | PCI 0.9% | |||
Renal failure: | ||||
CABG 8.4% | Target lesion | CABG 3.6% | ||
PCI 1.9% | revascularization | PCI 15.8% | ||
P=0.02 | P=0.001 | |||
Follow-up: | TVR | CABG 3.6% | ||
1-year | PCI 19.6% | |||
P=0.0001 | ||||
Lee et al., | 123 patients | 30 days | – PCI with DES is a | |
(2006), J Am | underwent | viable alternative | ||
Coll Cardiol, | CABG and 50 | Mortality | CABG 5% | to CABG for |
USA, [8] | patients PCI | PCI 2% | treatment of left | |
with DES for | P=0.34 | main coronary | ||
Prospective | left main stenosis | artery when | ||
cohort study | (2003–2006) | Myocardial | CABG 2% | clinical judgment |
(level 2b) | infarction | PCI 0 | was used for | |
Mean age±S.D.: | P>0.9 | patients allocation | ||
CABG 70±10 | ||||
PCI 72±15 | Target vessel | CABG 1% | – There may be an | |
revascularization | PCI 0 | incidence of late | ||
Parsonnet score: | P>0.9 | complications | ||
CABG 13.7±9.7 | associated with | |||
PCI 18.3±10.9 | In-hospital length | CABG 7.6±4.9 | DES that will be | |
P<0.01 | of stay (days | PCI 3.9±4.5 | defined with a | |
mean±S.D.) | longer-term | |||
Follow-up: | follow-up | |||
CABG 6.7±6.2 months | Follow-up | |||
PCI 5.6±3.9 | (Kaplan–Meier) | |||
Freedom from | 6 months | |||
mortality | CABG 87% | |||
PCI 96% | ||||
P=0.861 | ||||
1-year | ||||
CABG 85% | ||||
PCI 96% | ||||
P=0.18 | ||||
Freedom from TVR | 6 months | |||
CABG 99% | ||||
PCI 93% | ||||
1-year | ||||
CABG 93% | ||||
PCI 87% | ||||
P=0.22 | ||||
Target lesion | CABG 3.6% | |||
revascularization | PCI 15.8% | |||
P=0.001 | ||||
TVR | CABG 3.6% | |||
PCI 19.6% | ||||
P=0.0001 | ||||
Tan et al., | 279 patients who | 30 days | Complete data | |
(2001), | had ULMS | regarding RCA are | ||
Circulation, | PCI from 1 of | Mortality | 13.7% | unavailable |
USA, Europe, | 25 sites of | Follow-up | ||
Japan, Korea, [9] | multicenter study | CABG is the first | ||
(1993–1998) | Mortality | 12.2% | choice for ULMS | |
Prospective | ||||
multicenter | 46% of patients | Cardiac related | 9.1% | PCI is a viable |
cohort study | were deemed | mortality | option in AMI, | |
(level 2b) | inoperable or at | inoperable patients | ||
high surgical risk | AMI | 8.7% | or low-risk patients | |
50% had a post | CABG | 8.7% | ||
procedure IABP | ||||
Follow-up: | ||||
1-year (97.1% | ||||
complete) | ||||
Kelley et al., | 142 patients | 30 days | – Stenting for | |
(2003), Eur | treated with | unprotected | ||
Heart J, USA, | BMS for LMS | Mortality | LMS 2.1% | LMCA disease in |
France, [10] | (1997–2003) | ULMS 9.3% | a high risk | |
99 patients with | Follow-up | population is | ||
Retrospective | protected LMS | associated with a | ||
cohort study | 43 patients with | Mortality | LMS 5% | poor one-year |
(level 2b) | ULMS | ULMS 28% | survival and should | |
P<0.0001 | only be considered | |||
ULMS cohort | in the absence | |||
had significant | of other | |||
higher age and | revascularization | |||
percentage of | MI | LMS 3% | options | |
AMI and 20% | ULMS 7% | |||
were in cardiogenic | – BMS procedure | |||
shock | Target lesion | LMS 18% | for protected | |
revascularization | ULMS 23% | LMCA disease is | ||
MACE: | still associated | |||
death+non-fatal | MACE | LMS 25% | with increased | |
MI+TLR | ULMS 49% | mortality and | ||
P=0.005 | MACE rates | |||
Follow-up: | compared to PCI | |||
1-year (96% complete) | of other coronary | |||
lesions | ||||
Valgimigli et al., | 181 patients | 30 days | – The use of DES as | |
(2005), | underwent PCI for | a default strategy | ||
Circulation, | LMS (2002–2003) | Mortality | BMS 7% | to treat LM |
Italy, The | 95 patients were | DES 11% | disease was | |
Netherlands, | treated with DES | associated with a | ||
[12] | (52 SES, 43 PES) | MI | BMS 9% | significant |
DES 4% | reduction in | |||
Retrospective | 2 cohorts BMS | adverse events | ||
cohort study | (86 patients) and | Target vessel | BMS 2% | |
(level 2b) | DES (95 patients) | revascularization | DES 0 | – CABG should |
with no differences | remain the | |||
in clinical features | Follow-up | preferred | ||
revascularization | ||||
Higher prevalence | Mortality | BMS 16% | treatment in good | |
of 3-vessel disease | DES 14% | surgical candidates | ||
and bifurcation | presenting with | |||
stenting in the DES | AMI | BMS 12% | LM coronary | |
group | DES 4% | artery disease | ||
P=0.006 | ||||
Follow-up: mean | ||||
503 days (range | Target vessel | BMS 23% | ||
331–873) | revascularization | DES 6% | ||
P=0.004 | ||||
Agostoni et al., | 58 patients | 30 days | – When ostial or | |
(2005), Am J | electively treated | mid-LM disease is | ||
Cardiol, The | for ULMS | Mortality | 3% | treated with DESs, |
Netherlands, [13] | (2002–2003) | the rate of cardiac | ||
events is | ||||
24 procedures with | particularly low | |||
Retrospective | IVUS aid | |||
cohort study | Follow-up | – In patients with | ||
(level 2b) | FU: mean 433 days | (Kaplan–Meier) | distal LM involvement, | |
(range 178–780) | the rate of events | |||
Mortality | 5% | was significantly | ||
higher, but also in | ||||
AMI | 3% | this instance, no | ||
significant clinical | ||||
Target vessel | 7% | benefit occurred | ||
revascularization | in the IVUS subgroup | |||
Jonsson et al., | 1888 patients who | 30 days | During the period | |
(2006), Eur J | had CABG for LM | 1970–1999 there | ||
Cardiothorac | stenosis from | Mortality | Overall | was a decrease of |
Surg, Sweden, | (1970–1999) | (1970–1999) | LM 2.7% | early and five-year |
[19] | No LM 2% | mortality in | ||
8759 patients | Males | patients with LM | ||
Retrospective | undergone CABG | LM 2.2% | after CABG despite | |
cohort study | for coronary | No LM 1.9% | increases of patient | |
(level 2b) | disease with no | Females | age and risk factors | |
LM | LM 4.7% | |||
No LM 2.6% | An increased risk of | |||
Follow-up: 5 years | early and late | |||
Follow-up | deaths after CABG | |||
in patients with | ||||
5-year mortality | Overall | LM stenosis | ||
LM 10% | compared with | |||
No LM 8.1% | patients without | |||
Males | LM stenosis in the | |||
LM 10.1% | 1970s and 1980s | |||
No LM 8.2% | was neutralised | |||
Females | during the 1990s. | |||
LM 9.6% | There has been an | |||
No LM 7.8% | improvement of | |||
peri- and | ||||
postoperative | ||||
management of | ||||
patients undergoing | ||||
CABG during this | ||||
time period | ||||
Ellis et al., | 107 patients | In-hospital results | 4 deaths in Cath lab | Very small numbers |
(1997), | treated for LMS | 20% in-hospital death | from each centres | |
Circulation, | disease from 16 | 10% Q wave MI | ||
USA, [5] | centres | 5% CABG | ||
Cohort study | These patients | Event-free survival | 88.8±3.5% at 1 month | |
(level 2b) | represented 0.2% | 72.6±5% at 6 months | ||
of all procedures | 71±5% at 12 months | |||
performed in these | ||||
hospitals | >4 month | 22% had restenosis | ||
angioplasty | ||||
27% were | ||||
inoperable | ||||
30% high risk for | ||||
surgery | ||||
15% prev CABG | ||||
15% acute MI | ||||
Age mean 66 | ||||
50% BMS | ||||
24% atherectomy | ||||
20% balloon | ||||
angioplasty | ||||
All had aspirin, 26 | ||||
Ticlopidine, 2 | ||||
abciximab | ||||
Follow-up | ||||
15±8 months | ||||
Park et al., | 1995–2000, 270 | Hospital | 3 stent thromboses, | Pre-DES era |
(2003), Am J | consecutive | complications | 3 Q-Wave MIs | |
Cardiol, South | patients with | No deaths | ||
Korea, [14] | unprotected LMS | 3 emergency CABG | ||
and normal LV | ||||
Cohort study | at 4 centres | Angiographic | Restenosis rate | |
(level 2b) | follow-up | 21.1% | ||
Mean follow-up | ||||
32±18 months | Deaths over mean | 20 deaths | ||
3 years | 8 cardiac deaths | |||
Mean age | ||||
61 years | Target vessel | 45 patients (17%) | ||
revascularization | ||||
3-year freedom | 77.7%±2.7% | |||
from major | ||||
cardiac events | ||||
Price et al., | 50 patients with | In-lesion restenosis | 21/50 (42%) | 84% bifurcational |
(2006), J Am | unprotected left | LMS stenting | ||
Coll Cardiol, | main stenosis who | Target lesion | 19 (38%) | |
USA, [17] | had a Sirolimus | revascularization | ||
eluting stent | ||||
Cohort study | Death | 5 (10%) | ||
(level 2b) | Patients too high | |||
risk for CABG or | MACE, death, MI, | 22/50 (44%) | ||
refused CABG | TLR, Thormbosis | |||
58% had | ||||
EuroSCORE | ||||
predicted mortality | ||||
>5% | ||||
Repeat | ||||
angiography at 3 | ||||
and 9 months | ||||
Lee et al., | 187 patients | 6 months | Restenosis rate 33% | After 2 years there |
(2007), Int | undergoing elective | angiography | at 6 months on | were no further |
J Cardiol | BMS unprotected | angiography | MIs, deaths or | |
South Korea, | LMCA stenting | revascularization | ||
[16] | with normal LV | 5-year mortality | Mortality 7.6% | procedures |
function from 1995 | and MI rate | 6/13 cardiac deaths | ||
Cohort study | to 2001 | |||
(level 2b) | 2 non-fatal MIs | |||
Follow-up: 5 years | ||||
(71 months | Repeat | Target lesion | ||
45–117 months) | revascularization | 36 patients (21%) | ||
angiography at | New lesion | |||
6 months | 13 patients (7.6%) | |||
Mean age 56 | 20 had PCI, 16 had | |||
Prev MI 6% | CABG | |||
EF mean 62% | ||||
Freedom from | 1 year – 80% | |||
MACE | 3 years – 78% | |||
5 years – 78% |
Author, date, | Patient group | Outcomes | Key results | Comments |
and country | ||||
Study type | ||||
(level of evidence) | ||||
ACC/AHA/SC | Report of the | CABG using IMA grafting is the ‘gold standard’ for treatment of ULM disease and has | ||
AI guidelines, | American | proven benefit on long-term outcomes. The use of DES has shown encouraging short-term | ||
(2005), J Am | College of | outcomes, but long-term follow-up is needed. Nevertheless, the use of PCI for | ||
Coll Cardiol, | Cardiology/ | patients with significant ULM stenosis who are candidates for revascularization | ||
USA, [2] | American Heart | but not suitable for CABG can improve cardiovascular outcomes and is a reasonable | ||
Association | revascularization strategy in carefully selected patients | |||
Guideline | Task Force on | |||
(level 2a) | Practice | PCI is not recommended in patients with asymptomatic ischemia or CCS class I or II | ||
Guidelines | angina, left main disease and eligibility for CABG | |||
Practice | Use of PCI is reasonable in patients with CCS class III angina with significant | |||
guideline group | left main CAD (>50% diameter stenosis) who are candidates for revascularization | |||
consisted entirely | but are not eligible for CABG. (Level of Evidence: B) | |||
of cardiologists | ||||
from the 3 | PCI is not recommended for patients with CCS class III angina and significant left | |||
organisations | main CAD and candidacy for CABG. (Level of Evidence: C) | |||
involved | ||||
Use of PCI is reasonable in patients with UA/NSTEMI with significant left main | ||||
CAD (>50% diameter stenosis) who are candidates for revascularization but are not | ||||
eligible for CABG. (Level of Evidence: B) | ||||
In patients with cardiogenic shock and significant left main disease or severe 3-vessel | ||||
disease and without right ventricular infarction or major comorbidities such as | ||||
renal insufficiency or severe pulmonary disease, CABG can be considered as the | ||||
revascularization strategy | ||||
European | Report of the | The presence of a left main (LM) coronary artery stenosis identifies an anatomic subset | ||
Society for | European Society | still requiring bypass surgery for revascularization. PCI of protected LMS (i.e. by a distal graft) | ||
Cardiology | of Cardiology | can be performed although a 1-year MACE of 25% is still rather high, which may | ||
guidelines, | reflect an increased mortality in patients with severe CAD with previous CABG. | |||
(2005), | ||||
Eur Heart J, [3] | Stenting for unprotected LM disease should only be considered in the absence of other | |||
revascularization options. Therefore, PCI can be recommended in these subsets | ||||
Guidelines | when bypass surgery has a very high perioperative risk (e.g. EuroSCORE >10%) | |||
(level 2a) | ||||
Until proved otherwise, PCI should be used only with reservation in diabetics with multi-vessel | ||||
disease and in patients with unprotected left main stenosis | ||||
Erglis et al., (2007), | 103 patients | Myocardial infarction | BMS 7/50 (14%) | Patient population |
J Am Coll | with unprotected | by 6 months | PES 5/53 (10%) | is those also ideal |
Cardiol, | LMS disease, | for surgery | ||
Australia and | 2004–2006 | Restenosis | BMS 11/50 patients | Mean age 62 |
Latvia, [4] | (22%) | Only 6 had previous | ||
All patients | PES 3/53 patients (6%) | CABG, mean | ||
PRCT | were good | P=0.021 | LVEF 54% | |
(level 1b) | candidates for | |||
CABG | 6 months adverse | BMS 15/50 (30%) | ||
cardiac-event free | PES 7/53 (13%) | |||
Randomized to | survival | P=0.036 | ||
express or | ||||
liberte BMS | Mortality at | BMS and PES 1 | ||
or Paclitaxel | 6 months | patient each (2%) | ||
eluting stent | ||||
(PES) with | ||||
cutting balloon | ||||
pre-treatment | ||||
under IVUS | ||||
control | ||||
Clopidogrel, | ||||
Heparin, | ||||
GpIIb/IIIa | ||||
given | ||||
BMS n=50 | ||||
PES n=53 | ||||
Palmerini et al., | 154 patients | 30 days | – Short-term | |
(2006), | underwent | follow-up | ||
Am J Cardiol, | CABG and | Overall mortality | CABG 4.5% | |
Italy, [6] | 157 patients | PCI 3.2% | – Early and | |
underwent PCI | P=NS | long-term | ||
Prospective | for left main | mortality were not | ||
cohort study | stenosis (94 DES) | Cardiac related | CABG 3.9% | significantly |
(level 2b) | mortality | PCI 2.5% | different between | |
From | P=NS | CABG and PCI | ||
2002–2005 | ||||
Myocardial | CABG 1.9% | – Target lesion | ||
Mean age±S.D.: | infarction at | PCI 4.5% | revascularization | |
CABG | 30 days | P=NS | was significantly | |
69.3±9.5 | higher in PCI-treated | |||
PCI 73.0±10.9 | Target lesion | CABG 0.6% | patients | |
revascularization | PCI 0.6% | |||
Left main | P=NS | – Although patients | ||
disease alone: | Follow-up | treated with drug-eluting | ||
CABG 5.2% | stents had a | |||
PCI 12.7% | Overall mortality | CABG 12.3% | 25% relative risk | |
P<0.001 | PCI 13.4% | reduction in the | ||
P=0.861 | rate of major adverse | |||
Left main lesions | cardiac events | |||
locations: | CABG 12.3% | compared with | ||
P=0.742 | PCI-DES 11.7% | patients treated | ||
P=0.968 | with bare metal | |||
Follow-up: | stents, event survival | |||
430 days | Cardiac related | CABG 9.7% | was still higher in | |
(105–730) | mortality | PCI 9.5% | the CABG group | |
P=0.994 | than in the drug | |||
eluting stent group | ||||
CABG 9.7% | ||||
PCI-DES 7.4% | ||||
P=0.667 | ||||
Myocardial | CABG 4.5% | |||
infarction | PCI 8.3% | |||
P=0.170 | ||||
CABG 4.5% | ||||
PCI-DES 5.3% | ||||
P=0.690 | ||||
Target lesion | CABG 2.6% | |||
revascularization | PCI 25.5% | |||
P=0.0001 | ||||
Chieffo et al., | 142 patients | 30 days | The patients | |
(2006), | underwent | receiving DES | ||
Circulation, | CABG (86 | Mortality | CABG 2.1% | were significantly |
Italy, [7] | patients had | PCI 0 | younger than | |
on-pump | CABG patients | |||
Prospective | CABG, 56 | Myocardial | CABG 26.5% | (64 vs. 68 years), |
Cohort study | patients | infarction | PCI 9.3% | had lower incidence |
(level 2b) | underwent off-pump | P=0.0009 | of smoking, | |
CABG) | significantly less | |||
Q-wave MI | CABG 3.5% | hypertension, less | ||
107 patients | PCI 0 | diabetes, and | ||
underwent | P=0.07 | significantly less | ||
PCI-DES for | renal failure | |||
left main | Target lesion | CABG 2.1% | ||
stenosis | revascularization | PCI 0 | The PCI patients | |
(2002–2004) | were therefore | |||
81.3% of | TVR | CABG 2.1% | fitter than the | |
patients | PCI 0 | CABG patients | ||
treated with | ||||
PCI had distal | Follow-up | 26% perioperative | ||
LMCA | MI rate after CABG is | |||
Mortality | CABG 6.4% | incredibly high, due to | ||
Mean age±S.D.: | PCI 2.8% | their definition of MI | ||
CABG | P=0.07 | |||
67.5±9.7 | ||||
PCI 63.6±10.3 | Myocardial | CABG 1.4% | ||
infarction | PCI 0.9% | |||
Renal failure: | ||||
CABG 8.4% | Target lesion | CABG 3.6% | ||
PCI 1.9% | revascularization | PCI 15.8% | ||
P=0.02 | P=0.001 | |||
Follow-up: | TVR | CABG 3.6% | ||
1-year | PCI 19.6% | |||
P=0.0001 | ||||
Lee et al., | 123 patients | 30 days | – PCI with DES is a | |
(2006), J Am | underwent | viable alternative | ||
Coll Cardiol, | CABG and 50 | Mortality | CABG 5% | to CABG for |
USA, [8] | patients PCI | PCI 2% | treatment of left | |
with DES for | P=0.34 | main coronary | ||
Prospective | left main stenosis | artery when | ||
cohort study | (2003–2006) | Myocardial | CABG 2% | clinical judgment |
(level 2b) | infarction | PCI 0 | was used for | |
Mean age±S.D.: | P>0.9 | patients allocation | ||
CABG 70±10 | ||||
PCI 72±15 | Target vessel | CABG 1% | – There may be an | |
revascularization | PCI 0 | incidence of late | ||
Parsonnet score: | P>0.9 | complications | ||
CABG 13.7±9.7 | associated with | |||
PCI 18.3±10.9 | In-hospital length | CABG 7.6±4.9 | DES that will be | |
P<0.01 | of stay (days | PCI 3.9±4.5 | defined with a | |
mean±S.D.) | longer-term | |||
Follow-up: | follow-up | |||
CABG 6.7±6.2 months | Follow-up | |||
PCI 5.6±3.9 | (Kaplan–Meier) | |||
Freedom from | 6 months | |||
mortality | CABG 87% | |||
PCI 96% | ||||
P=0.861 | ||||
1-year | ||||
CABG 85% | ||||
PCI 96% | ||||
P=0.18 | ||||
Freedom from TVR | 6 months | |||
CABG 99% | ||||
PCI 93% | ||||
1-year | ||||
CABG 93% | ||||
PCI 87% | ||||
P=0.22 | ||||
Target lesion | CABG 3.6% | |||
revascularization | PCI 15.8% | |||
P=0.001 | ||||
TVR | CABG 3.6% | |||
PCI 19.6% | ||||
P=0.0001 | ||||
Tan et al., | 279 patients who | 30 days | Complete data | |
(2001), | had ULMS | regarding RCA are | ||
Circulation, | PCI from 1 of | Mortality | 13.7% | unavailable |
USA, Europe, | 25 sites of | Follow-up | ||
Japan, Korea, [9] | multicenter study | CABG is the first | ||
(1993–1998) | Mortality | 12.2% | choice for ULMS | |
Prospective | ||||
multicenter | 46% of patients | Cardiac related | 9.1% | PCI is a viable |
cohort study | were deemed | mortality | option in AMI, | |
(level 2b) | inoperable or at | inoperable patients | ||
high surgical risk | AMI | 8.7% | or low-risk patients | |
50% had a post | CABG | 8.7% | ||
procedure IABP | ||||
Follow-up: | ||||
1-year (97.1% | ||||
complete) | ||||
Kelley et al., | 142 patients | 30 days | – Stenting for | |
(2003), Eur | treated with | unprotected | ||
Heart J, USA, | BMS for LMS | Mortality | LMS 2.1% | LMCA disease in |
France, [10] | (1997–2003) | ULMS 9.3% | a high risk | |
99 patients with | Follow-up | population is | ||
Retrospective | protected LMS | associated with a | ||
cohort study | 43 patients with | Mortality | LMS 5% | poor one-year |
(level 2b) | ULMS | ULMS 28% | survival and should | |
P<0.0001 | only be considered | |||
ULMS cohort | in the absence | |||
had significant | of other | |||
higher age and | revascularization | |||
percentage of | MI | LMS 3% | options | |
AMI and 20% | ULMS 7% | |||
were in cardiogenic | – BMS procedure | |||
shock | Target lesion | LMS 18% | for protected | |
revascularization | ULMS 23% | LMCA disease is | ||
MACE: | still associated | |||
death+non-fatal | MACE | LMS 25% | with increased | |
MI+TLR | ULMS 49% | mortality and | ||
P=0.005 | MACE rates | |||
Follow-up: | compared to PCI | |||
1-year (96% complete) | of other coronary | |||
lesions | ||||
Valgimigli et al., | 181 patients | 30 days | – The use of DES as | |
(2005), | underwent PCI for | a default strategy | ||
Circulation, | LMS (2002–2003) | Mortality | BMS 7% | to treat LM |
Italy, The | 95 patients were | DES 11% | disease was | |
Netherlands, | treated with DES | associated with a | ||
[12] | (52 SES, 43 PES) | MI | BMS 9% | significant |
DES 4% | reduction in | |||
Retrospective | 2 cohorts BMS | adverse events | ||
cohort study | (86 patients) and | Target vessel | BMS 2% | |
(level 2b) | DES (95 patients) | revascularization | DES 0 | – CABG should |
with no differences | remain the | |||
in clinical features | Follow-up | preferred | ||
revascularization | ||||
Higher prevalence | Mortality | BMS 16% | treatment in good | |
of 3-vessel disease | DES 14% | surgical candidates | ||
and bifurcation | presenting with | |||
stenting in the DES | AMI | BMS 12% | LM coronary | |
group | DES 4% | artery disease | ||
P=0.006 | ||||
Follow-up: mean | ||||
503 days (range | Target vessel | BMS 23% | ||
331–873) | revascularization | DES 6% | ||
P=0.004 | ||||
Agostoni et al., | 58 patients | 30 days | – When ostial or | |
(2005), Am J | electively treated | mid-LM disease is | ||
Cardiol, The | for ULMS | Mortality | 3% | treated with DESs, |
Netherlands, [13] | (2002–2003) | the rate of cardiac | ||
events is | ||||
24 procedures with | particularly low | |||
Retrospective | IVUS aid | |||
cohort study | Follow-up | – In patients with | ||
(level 2b) | FU: mean 433 days | (Kaplan–Meier) | distal LM involvement, | |
(range 178–780) | the rate of events | |||
Mortality | 5% | was significantly | ||
higher, but also in | ||||
AMI | 3% | this instance, no | ||
significant clinical | ||||
Target vessel | 7% | benefit occurred | ||
revascularization | in the IVUS subgroup | |||
Jonsson et al., | 1888 patients who | 30 days | During the period | |
(2006), Eur J | had CABG for LM | 1970–1999 there | ||
Cardiothorac | stenosis from | Mortality | Overall | was a decrease of |
Surg, Sweden, | (1970–1999) | (1970–1999) | LM 2.7% | early and five-year |
[19] | No LM 2% | mortality in | ||
8759 patients | Males | patients with LM | ||
Retrospective | undergone CABG | LM 2.2% | after CABG despite | |
cohort study | for coronary | No LM 1.9% | increases of patient | |
(level 2b) | disease with no | Females | age and risk factors | |
LM | LM 4.7% | |||
No LM 2.6% | An increased risk of | |||
Follow-up: 5 years | early and late | |||
Follow-up | deaths after CABG | |||
in patients with | ||||
5-year mortality | Overall | LM stenosis | ||
LM 10% | compared with | |||
No LM 8.1% | patients without | |||
Males | LM stenosis in the | |||
LM 10.1% | 1970s and 1980s | |||
No LM 8.2% | was neutralised | |||
Females | during the 1990s. | |||
LM 9.6% | There has been an | |||
No LM 7.8% | improvement of | |||
peri- and | ||||
postoperative | ||||
management of | ||||
patients undergoing | ||||
CABG during this | ||||
time period | ||||
Ellis et al., | 107 patients | In-hospital results | 4 deaths in Cath lab | Very small numbers |
(1997), | treated for LMS | 20% in-hospital death | from each centres | |
Circulation, | disease from 16 | 10% Q wave MI | ||
USA, [5] | centres | 5% CABG | ||
Cohort study | These patients | Event-free survival | 88.8±3.5% at 1 month | |
(level 2b) | represented 0.2% | 72.6±5% at 6 months | ||
of all procedures | 71±5% at 12 months | |||
performed in these | ||||
hospitals | >4 month | 22% had restenosis | ||
angioplasty | ||||
27% were | ||||
inoperable | ||||
30% high risk for | ||||
surgery | ||||
15% prev CABG | ||||
15% acute MI | ||||
Age mean 66 | ||||
50% BMS | ||||
24% atherectomy | ||||
20% balloon | ||||
angioplasty | ||||
All had aspirin, 26 | ||||
Ticlopidine, 2 | ||||
abciximab | ||||
Follow-up | ||||
15±8 months | ||||
Park et al., | 1995–2000, 270 | Hospital | 3 stent thromboses, | Pre-DES era |
(2003), Am J | consecutive | complications | 3 Q-Wave MIs | |
Cardiol, South | patients with | No deaths | ||
Korea, [14] | unprotected LMS | 3 emergency CABG | ||
and normal LV | ||||
Cohort study | at 4 centres | Angiographic | Restenosis rate | |
(level 2b) | follow-up | 21.1% | ||
Mean follow-up | ||||
32±18 months | Deaths over mean | 20 deaths | ||
3 years | 8 cardiac deaths | |||
Mean age | ||||
61 years | Target vessel | 45 patients (17%) | ||
revascularization | ||||
3-year freedom | 77.7%±2.7% | |||
from major | ||||
cardiac events | ||||
Price et al., | 50 patients with | In-lesion restenosis | 21/50 (42%) | 84% bifurcational |
(2006), J Am | unprotected left | LMS stenting | ||
Coll Cardiol, | main stenosis who | Target lesion | 19 (38%) | |
USA, [17] | had a Sirolimus | revascularization | ||
eluting stent | ||||
Cohort study | Death | 5 (10%) | ||
(level 2b) | Patients too high | |||
risk for CABG or | MACE, death, MI, | 22/50 (44%) | ||
refused CABG | TLR, Thormbosis | |||
58% had | ||||
EuroSCORE | ||||
predicted mortality | ||||
>5% | ||||
Repeat | ||||
angiography at 3 | ||||
and 9 months | ||||
Lee et al., | 187 patients | 6 months | Restenosis rate 33% | After 2 years there |
(2007), Int | undergoing elective | angiography | at 6 months on | were no further |
J Cardiol | BMS unprotected | angiography | MIs, deaths or | |
South Korea, | LMCA stenting | revascularization | ||
[16] | with normal LV | 5-year mortality | Mortality 7.6% | procedures |
function from 1995 | and MI rate | 6/13 cardiac deaths | ||
Cohort study | to 2001 | |||
(level 2b) | 2 non-fatal MIs | |||
Follow-up: 5 years | ||||
(71 months | Repeat | Target lesion | ||
45–117 months) | revascularization | 36 patients (21%) | ||
angiography at | New lesion | |||
6 months | 13 patients (7.6%) | |||
Mean age 56 | 20 had PCI, 16 had | |||
Prev MI 6% | CABG | |||
EF mean 62% | ||||
Freedom from | 1 year – 80% | |||
MACE | 3 years – 78% | |||
5 years – 78% |
BMS, bare metal stent; BS, bifurcation stenting; DES, drug eluting stent; LMCA, left main coronary artery; MACE, major cardiac events; PCI, percutaneous coronary intervention; TLR, target lesion revascularization; SVS, single vessel stenting; TVR, target vessel revascularization; ULMS, unprotected left main stenosis.
Author, date, | Patient group | Outcomes | Key results | Comments |
and country | ||||
Study type | ||||
(level of evidence) | ||||
ACC/AHA/SC | Report of the | CABG using IMA grafting is the ‘gold standard’ for treatment of ULM disease and has | ||
AI guidelines, | American | proven benefit on long-term outcomes. The use of DES has shown encouraging short-term | ||
(2005), J Am | College of | outcomes, but long-term follow-up is needed. Nevertheless, the use of PCI for | ||
Coll Cardiol, | Cardiology/ | patients with significant ULM stenosis who are candidates for revascularization | ||
USA, [2] | American Heart | but not suitable for CABG can improve cardiovascular outcomes and is a reasonable | ||
Association | revascularization strategy in carefully selected patients | |||
Guideline | Task Force on | |||
(level 2a) | Practice | PCI is not recommended in patients with asymptomatic ischemia or CCS class I or II | ||
Guidelines | angina, left main disease and eligibility for CABG | |||
Practice | Use of PCI is reasonable in patients with CCS class III angina with significant | |||
guideline group | left main CAD (>50% diameter stenosis) who are candidates for revascularization | |||
consisted entirely | but are not eligible for CABG. (Level of Evidence: B) | |||
of cardiologists | ||||
from the 3 | PCI is not recommended for patients with CCS class III angina and significant left | |||
organisations | main CAD and candidacy for CABG. (Level of Evidence: C) | |||
involved | ||||
Use of PCI is reasonable in patients with UA/NSTEMI with significant left main | ||||
CAD (>50% diameter stenosis) who are candidates for revascularization but are not | ||||
eligible for CABG. (Level of Evidence: B) | ||||
In patients with cardiogenic shock and significant left main disease or severe 3-vessel | ||||
disease and without right ventricular infarction or major comorbidities such as | ||||
renal insufficiency or severe pulmonary disease, CABG can be considered as the | ||||
revascularization strategy | ||||
European | Report of the | The presence of a left main (LM) coronary artery stenosis identifies an anatomic subset | ||
Society for | European Society | still requiring bypass surgery for revascularization. PCI of protected LMS (i.e. by a distal graft) | ||
Cardiology | of Cardiology | can be performed although a 1-year MACE of 25% is still rather high, which may | ||
guidelines, | reflect an increased mortality in patients with severe CAD with previous CABG. | |||
(2005), | ||||
Eur Heart J, [3] | Stenting for unprotected LM disease should only be considered in the absence of other | |||
revascularization options. Therefore, PCI can be recommended in these subsets | ||||
Guidelines | when bypass surgery has a very high perioperative risk (e.g. EuroSCORE >10%) | |||
(level 2a) | ||||
Until proved otherwise, PCI should be used only with reservation in diabetics with multi-vessel | ||||
disease and in patients with unprotected left main stenosis | ||||
Erglis et al., (2007), | 103 patients | Myocardial infarction | BMS 7/50 (14%) | Patient population |
J Am Coll | with unprotected | by 6 months | PES 5/53 (10%) | is those also ideal |
Cardiol, | LMS disease, | for surgery | ||
Australia and | 2004–2006 | Restenosis | BMS 11/50 patients | Mean age 62 |
Latvia, [4] | (22%) | Only 6 had previous | ||
All patients | PES 3/53 patients (6%) | CABG, mean | ||
PRCT | were good | P=0.021 | LVEF 54% | |
(level 1b) | candidates for | |||
CABG | 6 months adverse | BMS 15/50 (30%) | ||
cardiac-event free | PES 7/53 (13%) | |||
Randomized to | survival | P=0.036 | ||
express or | ||||
liberte BMS | Mortality at | BMS and PES 1 | ||
or Paclitaxel | 6 months | patient each (2%) | ||
eluting stent | ||||
(PES) with | ||||
cutting balloon | ||||
pre-treatment | ||||
under IVUS | ||||
control | ||||
Clopidogrel, | ||||
Heparin, | ||||
GpIIb/IIIa | ||||
given | ||||
BMS n=50 | ||||
PES n=53 | ||||
Palmerini et al., | 154 patients | 30 days | – Short-term | |
(2006), | underwent | follow-up | ||
Am J Cardiol, | CABG and | Overall mortality | CABG 4.5% | |
Italy, [6] | 157 patients | PCI 3.2% | – Early and | |
underwent PCI | P=NS | long-term | ||
Prospective | for left main | mortality were not | ||
cohort study | stenosis (94 DES) | Cardiac related | CABG 3.9% | significantly |
(level 2b) | mortality | PCI 2.5% | different between | |
From | P=NS | CABG and PCI | ||
2002–2005 | ||||
Myocardial | CABG 1.9% | – Target lesion | ||
Mean age±S.D.: | infarction at | PCI 4.5% | revascularization | |
CABG | 30 days | P=NS | was significantly | |
69.3±9.5 | higher in PCI-treated | |||
PCI 73.0±10.9 | Target lesion | CABG 0.6% | patients | |
revascularization | PCI 0.6% | |||
Left main | P=NS | – Although patients | ||
disease alone: | Follow-up | treated with drug-eluting | ||
CABG 5.2% | stents had a | |||
PCI 12.7% | Overall mortality | CABG 12.3% | 25% relative risk | |
P<0.001 | PCI 13.4% | reduction in the | ||
P=0.861 | rate of major adverse | |||
Left main lesions | cardiac events | |||
locations: | CABG 12.3% | compared with | ||
P=0.742 | PCI-DES 11.7% | patients treated | ||
P=0.968 | with bare metal | |||
Follow-up: | stents, event survival | |||
430 days | Cardiac related | CABG 9.7% | was still higher in | |
(105–730) | mortality | PCI 9.5% | the CABG group | |
P=0.994 | than in the drug | |||
eluting stent group | ||||
CABG 9.7% | ||||
PCI-DES 7.4% | ||||
P=0.667 | ||||
Myocardial | CABG 4.5% | |||
infarction | PCI 8.3% | |||
P=0.170 | ||||
CABG 4.5% | ||||
PCI-DES 5.3% | ||||
P=0.690 | ||||
Target lesion | CABG 2.6% | |||
revascularization | PCI 25.5% | |||
P=0.0001 | ||||
Chieffo et al., | 142 patients | 30 days | The patients | |
(2006), | underwent | receiving DES | ||
Circulation, | CABG (86 | Mortality | CABG 2.1% | were significantly |
Italy, [7] | patients had | PCI 0 | younger than | |
on-pump | CABG patients | |||
Prospective | CABG, 56 | Myocardial | CABG 26.5% | (64 vs. 68 years), |
Cohort study | patients | infarction | PCI 9.3% | had lower incidence |
(level 2b) | underwent off-pump | P=0.0009 | of smoking, | |
CABG) | significantly less | |||
Q-wave MI | CABG 3.5% | hypertension, less | ||
107 patients | PCI 0 | diabetes, and | ||
underwent | P=0.07 | significantly less | ||
PCI-DES for | renal failure | |||
left main | Target lesion | CABG 2.1% | ||
stenosis | revascularization | PCI 0 | The PCI patients | |
(2002–2004) | were therefore | |||
81.3% of | TVR | CABG 2.1% | fitter than the | |
patients | PCI 0 | CABG patients | ||
treated with | ||||
PCI had distal | Follow-up | 26% perioperative | ||
LMCA | MI rate after CABG is | |||
Mortality | CABG 6.4% | incredibly high, due to | ||
Mean age±S.D.: | PCI 2.8% | their definition of MI | ||
CABG | P=0.07 | |||
67.5±9.7 | ||||
PCI 63.6±10.3 | Myocardial | CABG 1.4% | ||
infarction | PCI 0.9% | |||
Renal failure: | ||||
CABG 8.4% | Target lesion | CABG 3.6% | ||
PCI 1.9% | revascularization | PCI 15.8% | ||
P=0.02 | P=0.001 | |||
Follow-up: | TVR | CABG 3.6% | ||
1-year | PCI 19.6% | |||
P=0.0001 | ||||
Lee et al., | 123 patients | 30 days | – PCI with DES is a | |
(2006), J Am | underwent | viable alternative | ||
Coll Cardiol, | CABG and 50 | Mortality | CABG 5% | to CABG for |
USA, [8] | patients PCI | PCI 2% | treatment of left | |
with DES for | P=0.34 | main coronary | ||
Prospective | left main stenosis | artery when | ||
cohort study | (2003–2006) | Myocardial | CABG 2% | clinical judgment |
(level 2b) | infarction | PCI 0 | was used for | |
Mean age±S.D.: | P>0.9 | patients allocation | ||
CABG 70±10 | ||||
PCI 72±15 | Target vessel | CABG 1% | – There may be an | |
revascularization | PCI 0 | incidence of late | ||
Parsonnet score: | P>0.9 | complications | ||
CABG 13.7±9.7 | associated with | |||
PCI 18.3±10.9 | In-hospital length | CABG 7.6±4.9 | DES that will be | |
P<0.01 | of stay (days | PCI 3.9±4.5 | defined with a | |
mean±S.D.) | longer-term | |||
Follow-up: | follow-up | |||
CABG 6.7±6.2 months | Follow-up | |||
PCI 5.6±3.9 | (Kaplan–Meier) | |||
Freedom from | 6 months | |||
mortality | CABG 87% | |||
PCI 96% | ||||
P=0.861 | ||||
1-year | ||||
CABG 85% | ||||
PCI 96% | ||||
P=0.18 | ||||
Freedom from TVR | 6 months | |||
CABG 99% | ||||
PCI 93% | ||||
1-year | ||||
CABG 93% | ||||
PCI 87% | ||||
P=0.22 | ||||
Target lesion | CABG 3.6% | |||
revascularization | PCI 15.8% | |||
P=0.001 | ||||
TVR | CABG 3.6% | |||
PCI 19.6% | ||||
P=0.0001 | ||||
Tan et al., | 279 patients who | 30 days | Complete data | |
(2001), | had ULMS | regarding RCA are | ||
Circulation, | PCI from 1 of | Mortality | 13.7% | unavailable |
USA, Europe, | 25 sites of | Follow-up | ||
Japan, Korea, [9] | multicenter study | CABG is the first | ||
(1993–1998) | Mortality | 12.2% | choice for ULMS | |
Prospective | ||||
multicenter | 46% of patients | Cardiac related | 9.1% | PCI is a viable |
cohort study | were deemed | mortality | option in AMI, | |
(level 2b) | inoperable or at | inoperable patients | ||
high surgical risk | AMI | 8.7% | or low-risk patients | |
50% had a post | CABG | 8.7% | ||
procedure IABP | ||||
Follow-up: | ||||
1-year (97.1% | ||||
complete) | ||||
Kelley et al., | 142 patients | 30 days | – Stenting for | |
(2003), Eur | treated with | unprotected | ||
Heart J, USA, | BMS for LMS | Mortality | LMS 2.1% | LMCA disease in |
France, [10] | (1997–2003) | ULMS 9.3% | a high risk | |
99 patients with | Follow-up | population is | ||
Retrospective | protected LMS | associated with a | ||
cohort study | 43 patients with | Mortality | LMS 5% | poor one-year |
(level 2b) | ULMS | ULMS 28% | survival and should | |
P<0.0001 | only be considered | |||
ULMS cohort | in the absence | |||
had significant | of other | |||
higher age and | revascularization | |||
percentage of | MI | LMS 3% | options | |
AMI and 20% | ULMS 7% | |||
were in cardiogenic | – BMS procedure | |||
shock | Target lesion | LMS 18% | for protected | |
revascularization | ULMS 23% | LMCA disease is | ||
MACE: | still associated | |||
death+non-fatal | MACE | LMS 25% | with increased | |
MI+TLR | ULMS 49% | mortality and | ||
P=0.005 | MACE rates | |||
Follow-up: | compared to PCI | |||
1-year (96% complete) | of other coronary | |||
lesions | ||||
Valgimigli et al., | 181 patients | 30 days | – The use of DES as | |
(2005), | underwent PCI for | a default strategy | ||
Circulation, | LMS (2002–2003) | Mortality | BMS 7% | to treat LM |
Italy, The | 95 patients were | DES 11% | disease was | |
Netherlands, | treated with DES | associated with a | ||
[12] | (52 SES, 43 PES) | MI | BMS 9% | significant |
DES 4% | reduction in | |||
Retrospective | 2 cohorts BMS | adverse events | ||
cohort study | (86 patients) and | Target vessel | BMS 2% | |
(level 2b) | DES (95 patients) | revascularization | DES 0 | – CABG should |
with no differences | remain the | |||
in clinical features | Follow-up | preferred | ||
revascularization | ||||
Higher prevalence | Mortality | BMS 16% | treatment in good | |
of 3-vessel disease | DES 14% | surgical candidates | ||
and bifurcation | presenting with | |||
stenting in the DES | AMI | BMS 12% | LM coronary | |
group | DES 4% | artery disease | ||
P=0.006 | ||||
Follow-up: mean | ||||
503 days (range | Target vessel | BMS 23% | ||
331–873) | revascularization | DES 6% | ||
P=0.004 | ||||
Agostoni et al., | 58 patients | 30 days | – When ostial or | |
(2005), Am J | electively treated | mid-LM disease is | ||
Cardiol, The | for ULMS | Mortality | 3% | treated with DESs, |
Netherlands, [13] | (2002–2003) | the rate of cardiac | ||
events is | ||||
24 procedures with | particularly low | |||
Retrospective | IVUS aid | |||
cohort study | Follow-up | – In patients with | ||
(level 2b) | FU: mean 433 days | (Kaplan–Meier) | distal LM involvement, | |
(range 178–780) | the rate of events | |||
Mortality | 5% | was significantly | ||
higher, but also in | ||||
AMI | 3% | this instance, no | ||
significant clinical | ||||
Target vessel | 7% | benefit occurred | ||
revascularization | in the IVUS subgroup | |||
Jonsson et al., | 1888 patients who | 30 days | During the period | |
(2006), Eur J | had CABG for LM | 1970–1999 there | ||
Cardiothorac | stenosis from | Mortality | Overall | was a decrease of |
Surg, Sweden, | (1970–1999) | (1970–1999) | LM 2.7% | early and five-year |
[19] | No LM 2% | mortality in | ||
8759 patients | Males | patients with LM | ||
Retrospective | undergone CABG | LM 2.2% | after CABG despite | |
cohort study | for coronary | No LM 1.9% | increases of patient | |
(level 2b) | disease with no | Females | age and risk factors | |
LM | LM 4.7% | |||
No LM 2.6% | An increased risk of | |||
Follow-up: 5 years | early and late | |||
Follow-up | deaths after CABG | |||
in patients with | ||||
5-year mortality | Overall | LM stenosis | ||
LM 10% | compared with | |||
No LM 8.1% | patients without | |||
Males | LM stenosis in the | |||
LM 10.1% | 1970s and 1980s | |||
No LM 8.2% | was neutralised | |||
Females | during the 1990s. | |||
LM 9.6% | There has been an | |||
No LM 7.8% | improvement of | |||
peri- and | ||||
postoperative | ||||
management of | ||||
patients undergoing | ||||
CABG during this | ||||
time period | ||||
Ellis et al., | 107 patients | In-hospital results | 4 deaths in Cath lab | Very small numbers |
(1997), | treated for LMS | 20% in-hospital death | from each centres | |
Circulation, | disease from 16 | 10% Q wave MI | ||
USA, [5] | centres | 5% CABG | ||
Cohort study | These patients | Event-free survival | 88.8±3.5% at 1 month | |
(level 2b) | represented 0.2% | 72.6±5% at 6 months | ||
of all procedures | 71±5% at 12 months | |||
performed in these | ||||
hospitals | >4 month | 22% had restenosis | ||
angioplasty | ||||
27% were | ||||
inoperable | ||||
30% high risk for | ||||
surgery | ||||
15% prev CABG | ||||
15% acute MI | ||||
Age mean 66 | ||||
50% BMS | ||||
24% atherectomy | ||||
20% balloon | ||||
angioplasty | ||||
All had aspirin, 26 | ||||
Ticlopidine, 2 | ||||
abciximab | ||||
Follow-up | ||||
15±8 months | ||||
Park et al., | 1995–2000, 270 | Hospital | 3 stent thromboses, | Pre-DES era |
(2003), Am J | consecutive | complications | 3 Q-Wave MIs | |
Cardiol, South | patients with | No deaths | ||
Korea, [14] | unprotected LMS | 3 emergency CABG | ||
and normal LV | ||||
Cohort study | at 4 centres | Angiographic | Restenosis rate | |
(level 2b) | follow-up | 21.1% | ||
Mean follow-up | ||||
32±18 months | Deaths over mean | 20 deaths | ||
3 years | 8 cardiac deaths | |||
Mean age | ||||
61 years | Target vessel | 45 patients (17%) | ||
revascularization | ||||
3-year freedom | 77.7%±2.7% | |||
from major | ||||
cardiac events | ||||
Price et al., | 50 patients with | In-lesion restenosis | 21/50 (42%) | 84% bifurcational |
(2006), J Am | unprotected left | LMS stenting | ||
Coll Cardiol, | main stenosis who | Target lesion | 19 (38%) | |
USA, [17] | had a Sirolimus | revascularization | ||
eluting stent | ||||
Cohort study | Death | 5 (10%) | ||
(level 2b) | Patients too high | |||
risk for CABG or | MACE, death, MI, | 22/50 (44%) | ||
refused CABG | TLR, Thormbosis | |||
58% had | ||||
EuroSCORE | ||||
predicted mortality | ||||
>5% | ||||
Repeat | ||||
angiography at 3 | ||||
and 9 months | ||||
Lee et al., | 187 patients | 6 months | Restenosis rate 33% | After 2 years there |
(2007), Int | undergoing elective | angiography | at 6 months on | were no further |
J Cardiol | BMS unprotected | angiography | MIs, deaths or | |
South Korea, | LMCA stenting | revascularization | ||
[16] | with normal LV | 5-year mortality | Mortality 7.6% | procedures |
function from 1995 | and MI rate | 6/13 cardiac deaths | ||
Cohort study | to 2001 | |||
(level 2b) | 2 non-fatal MIs | |||
Follow-up: 5 years | ||||
(71 months | Repeat | Target lesion | ||
45–117 months) | revascularization | 36 patients (21%) | ||
angiography at | New lesion | |||
6 months | 13 patients (7.6%) | |||
Mean age 56 | 20 had PCI, 16 had | |||
Prev MI 6% | CABG | |||
EF mean 62% | ||||
Freedom from | 1 year – 80% | |||
MACE | 3 years – 78% | |||
5 years – 78% |
Author, date, | Patient group | Outcomes | Key results | Comments |
and country | ||||
Study type | ||||
(level of evidence) | ||||
ACC/AHA/SC | Report of the | CABG using IMA grafting is the ‘gold standard’ for treatment of ULM disease and has | ||
AI guidelines, | American | proven benefit on long-term outcomes. The use of DES has shown encouraging short-term | ||
(2005), J Am | College of | outcomes, but long-term follow-up is needed. Nevertheless, the use of PCI for | ||
Coll Cardiol, | Cardiology/ | patients with significant ULM stenosis who are candidates for revascularization | ||
USA, [2] | American Heart | but not suitable for CABG can improve cardiovascular outcomes and is a reasonable | ||
Association | revascularization strategy in carefully selected patients | |||
Guideline | Task Force on | |||
(level 2a) | Practice | PCI is not recommended in patients with asymptomatic ischemia or CCS class I or II | ||
Guidelines | angina, left main disease and eligibility for CABG | |||
Practice | Use of PCI is reasonable in patients with CCS class III angina with significant | |||
guideline group | left main CAD (>50% diameter stenosis) who are candidates for revascularization | |||
consisted entirely | but are not eligible for CABG. (Level of Evidence: B) | |||
of cardiologists | ||||
from the 3 | PCI is not recommended for patients with CCS class III angina and significant left | |||
organisations | main CAD and candidacy for CABG. (Level of Evidence: C) | |||
involved | ||||
Use of PCI is reasonable in patients with UA/NSTEMI with significant left main | ||||
CAD (>50% diameter stenosis) who are candidates for revascularization but are not | ||||
eligible for CABG. (Level of Evidence: B) | ||||
In patients with cardiogenic shock and significant left main disease or severe 3-vessel | ||||
disease and without right ventricular infarction or major comorbidities such as | ||||
renal insufficiency or severe pulmonary disease, CABG can be considered as the | ||||
revascularization strategy | ||||
European | Report of the | The presence of a left main (LM) coronary artery stenosis identifies an anatomic subset | ||
Society for | European Society | still requiring bypass surgery for revascularization. PCI of protected LMS (i.e. by a distal graft) | ||
Cardiology | of Cardiology | can be performed although a 1-year MACE of 25% is still rather high, which may | ||
guidelines, | reflect an increased mortality in patients with severe CAD with previous CABG. | |||
(2005), | ||||
Eur Heart J, [3] | Stenting for unprotected LM disease should only be considered in the absence of other | |||
revascularization options. Therefore, PCI can be recommended in these subsets | ||||
Guidelines | when bypass surgery has a very high perioperative risk (e.g. EuroSCORE >10%) | |||
(level 2a) | ||||
Until proved otherwise, PCI should be used only with reservation in diabetics with multi-vessel | ||||
disease and in patients with unprotected left main stenosis | ||||
Erglis et al., (2007), | 103 patients | Myocardial infarction | BMS 7/50 (14%) | Patient population |
J Am Coll | with unprotected | by 6 months | PES 5/53 (10%) | is those also ideal |
Cardiol, | LMS disease, | for surgery | ||
Australia and | 2004–2006 | Restenosis | BMS 11/50 patients | Mean age 62 |
Latvia, [4] | (22%) | Only 6 had previous | ||
All patients | PES 3/53 patients (6%) | CABG, mean | ||
PRCT | were good | P=0.021 | LVEF 54% | |
(level 1b) | candidates for | |||
CABG | 6 months adverse | BMS 15/50 (30%) | ||
cardiac-event free | PES 7/53 (13%) | |||
Randomized to | survival | P=0.036 | ||
express or | ||||
liberte BMS | Mortality at | BMS and PES 1 | ||
or Paclitaxel | 6 months | patient each (2%) | ||
eluting stent | ||||
(PES) with | ||||
cutting balloon | ||||
pre-treatment | ||||
under IVUS | ||||
control | ||||
Clopidogrel, | ||||
Heparin, | ||||
GpIIb/IIIa | ||||
given | ||||
BMS n=50 | ||||
PES n=53 | ||||
Palmerini et al., | 154 patients | 30 days | – Short-term | |
(2006), | underwent | follow-up | ||
Am J Cardiol, | CABG and | Overall mortality | CABG 4.5% | |
Italy, [6] | 157 patients | PCI 3.2% | – Early and | |
underwent PCI | P=NS | long-term | ||
Prospective | for left main | mortality were not | ||
cohort study | stenosis (94 DES) | Cardiac related | CABG 3.9% | significantly |
(level 2b) | mortality | PCI 2.5% | different between | |
From | P=NS | CABG and PCI | ||
2002–2005 | ||||
Myocardial | CABG 1.9% | – Target lesion | ||
Mean age±S.D.: | infarction at | PCI 4.5% | revascularization | |
CABG | 30 days | P=NS | was significantly | |
69.3±9.5 | higher in PCI-treated | |||
PCI 73.0±10.9 | Target lesion | CABG 0.6% | patients | |
revascularization | PCI 0.6% | |||
Left main | P=NS | – Although patients | ||
disease alone: | Follow-up | treated with drug-eluting | ||
CABG 5.2% | stents had a | |||
PCI 12.7% | Overall mortality | CABG 12.3% | 25% relative risk | |
P<0.001 | PCI 13.4% | reduction in the | ||
P=0.861 | rate of major adverse | |||
Left main lesions | cardiac events | |||
locations: | CABG 12.3% | compared with | ||
P=0.742 | PCI-DES 11.7% | patients treated | ||
P=0.968 | with bare metal | |||
Follow-up: | stents, event survival | |||
430 days | Cardiac related | CABG 9.7% | was still higher in | |
(105–730) | mortality | PCI 9.5% | the CABG group | |
P=0.994 | than in the drug | |||
eluting stent group | ||||
CABG 9.7% | ||||
PCI-DES 7.4% | ||||
P=0.667 | ||||
Myocardial | CABG 4.5% | |||
infarction | PCI 8.3% | |||
P=0.170 | ||||
CABG 4.5% | ||||
PCI-DES 5.3% | ||||
P=0.690 | ||||
Target lesion | CABG 2.6% | |||
revascularization | PCI 25.5% | |||
P=0.0001 | ||||
Chieffo et al., | 142 patients | 30 days | The patients | |
(2006), | underwent | receiving DES | ||
Circulation, | CABG (86 | Mortality | CABG 2.1% | were significantly |
Italy, [7] | patients had | PCI 0 | younger than | |
on-pump | CABG patients | |||
Prospective | CABG, 56 | Myocardial | CABG 26.5% | (64 vs. 68 years), |
Cohort study | patients | infarction | PCI 9.3% | had lower incidence |
(level 2b) | underwent off-pump | P=0.0009 | of smoking, | |
CABG) | significantly less | |||
Q-wave MI | CABG 3.5% | hypertension, less | ||
107 patients | PCI 0 | diabetes, and | ||
underwent | P=0.07 | significantly less | ||
PCI-DES for | renal failure | |||
left main | Target lesion | CABG 2.1% | ||
stenosis | revascularization | PCI 0 | The PCI patients | |
(2002–2004) | were therefore | |||
81.3% of | TVR | CABG 2.1% | fitter than the | |
patients | PCI 0 | CABG patients | ||
treated with | ||||
PCI had distal | Follow-up | 26% perioperative | ||
LMCA | MI rate after CABG is | |||
Mortality | CABG 6.4% | incredibly high, due to | ||
Mean age±S.D.: | PCI 2.8% | their definition of MI | ||
CABG | P=0.07 | |||
67.5±9.7 | ||||
PCI 63.6±10.3 | Myocardial | CABG 1.4% | ||
infarction | PCI 0.9% | |||
Renal failure: | ||||
CABG 8.4% | Target lesion | CABG 3.6% | ||
PCI 1.9% | revascularization | PCI 15.8% | ||
P=0.02 | P=0.001 | |||
Follow-up: | TVR | CABG 3.6% | ||
1-year | PCI 19.6% | |||
P=0.0001 | ||||
Lee et al., | 123 patients | 30 days | – PCI with DES is a | |
(2006), J Am | underwent | viable alternative | ||
Coll Cardiol, | CABG and 50 | Mortality | CABG 5% | to CABG for |
USA, [8] | patients PCI | PCI 2% | treatment of left | |
with DES for | P=0.34 | main coronary | ||
Prospective | left main stenosis | artery when | ||
cohort study | (2003–2006) | Myocardial | CABG 2% | clinical judgment |
(level 2b) | infarction | PCI 0 | was used for | |
Mean age±S.D.: | P>0.9 | patients allocation | ||
CABG 70±10 | ||||
PCI 72±15 | Target vessel | CABG 1% | – There may be an | |
revascularization | PCI 0 | incidence of late | ||
Parsonnet score: | P>0.9 | complications | ||
CABG 13.7±9.7 | associated with | |||
PCI 18.3±10.9 | In-hospital length | CABG 7.6±4.9 | DES that will be | |
P<0.01 | of stay (days | PCI 3.9±4.5 | defined with a | |
mean±S.D.) | longer-term | |||
Follow-up: | follow-up | |||
CABG 6.7±6.2 months | Follow-up | |||
PCI 5.6±3.9 | (Kaplan–Meier) | |||
Freedom from | 6 months | |||
mortality | CABG 87% | |||
PCI 96% | ||||
P=0.861 | ||||
1-year | ||||
CABG 85% | ||||
PCI 96% | ||||
P=0.18 | ||||
Freedom from TVR | 6 months | |||
CABG 99% | ||||
PCI 93% | ||||
1-year | ||||
CABG 93% | ||||
PCI 87% | ||||
P=0.22 | ||||
Target lesion | CABG 3.6% | |||
revascularization | PCI 15.8% | |||
P=0.001 | ||||
TVR | CABG 3.6% | |||
PCI 19.6% | ||||
P=0.0001 | ||||
Tan et al., | 279 patients who | 30 days | Complete data | |
(2001), | had ULMS | regarding RCA are | ||
Circulation, | PCI from 1 of | Mortality | 13.7% | unavailable |
USA, Europe, | 25 sites of | Follow-up | ||
Japan, Korea, [9] | multicenter study | CABG is the first | ||
(1993–1998) | Mortality | 12.2% | choice for ULMS | |
Prospective | ||||
multicenter | 46% of patients | Cardiac related | 9.1% | PCI is a viable |
cohort study | were deemed | mortality | option in AMI, | |
(level 2b) | inoperable or at | inoperable patients | ||
high surgical risk | AMI | 8.7% | or low-risk patients | |
50% had a post | CABG | 8.7% | ||
procedure IABP | ||||
Follow-up: | ||||
1-year (97.1% | ||||
complete) | ||||
Kelley et al., | 142 patients | 30 days | – Stenting for | |
(2003), Eur | treated with | unprotected | ||
Heart J, USA, | BMS for LMS | Mortality | LMS 2.1% | LMCA disease in |
France, [10] | (1997–2003) | ULMS 9.3% | a high risk | |
99 patients with | Follow-up | population is | ||
Retrospective | protected LMS | associated with a | ||
cohort study | 43 patients with | Mortality | LMS 5% | poor one-year |
(level 2b) | ULMS | ULMS 28% | survival and should | |
P<0.0001 | only be considered | |||
ULMS cohort | in the absence | |||
had significant | of other | |||
higher age and | revascularization | |||
percentage of | MI | LMS 3% | options | |
AMI and 20% | ULMS 7% | |||
were in cardiogenic | – BMS procedure | |||
shock | Target lesion | LMS 18% | for protected | |
revascularization | ULMS 23% | LMCA disease is | ||
MACE: | still associated | |||
death+non-fatal | MACE | LMS 25% | with increased | |
MI+TLR | ULMS 49% | mortality and | ||
P=0.005 | MACE rates | |||
Follow-up: | compared to PCI | |||
1-year (96% complete) | of other coronary | |||
lesions | ||||
Valgimigli et al., | 181 patients | 30 days | – The use of DES as | |
(2005), | underwent PCI for | a default strategy | ||
Circulation, | LMS (2002–2003) | Mortality | BMS 7% | to treat LM |
Italy, The | 95 patients were | DES 11% | disease was | |
Netherlands, | treated with DES | associated with a | ||
[12] | (52 SES, 43 PES) | MI | BMS 9% | significant |
DES 4% | reduction in | |||
Retrospective | 2 cohorts BMS | adverse events | ||
cohort study | (86 patients) and | Target vessel | BMS 2% | |
(level 2b) | DES (95 patients) | revascularization | DES 0 | – CABG should |
with no differences | remain the | |||
in clinical features | Follow-up | preferred | ||
revascularization | ||||
Higher prevalence | Mortality | BMS 16% | treatment in good | |
of 3-vessel disease | DES 14% | surgical candidates | ||
and bifurcation | presenting with | |||
stenting in the DES | AMI | BMS 12% | LM coronary | |
group | DES 4% | artery disease | ||
P=0.006 | ||||
Follow-up: mean | ||||
503 days (range | Target vessel | BMS 23% | ||
331–873) | revascularization | DES 6% | ||
P=0.004 | ||||
Agostoni et al., | 58 patients | 30 days | – When ostial or | |
(2005), Am J | electively treated | mid-LM disease is | ||
Cardiol, The | for ULMS | Mortality | 3% | treated with DESs, |
Netherlands, [13] | (2002–2003) | the rate of cardiac | ||
events is | ||||
24 procedures with | particularly low | |||
Retrospective | IVUS aid | |||
cohort study | Follow-up | – In patients with | ||
(level 2b) | FU: mean 433 days | (Kaplan–Meier) | distal LM involvement, | |
(range 178–780) | the rate of events | |||
Mortality | 5% | was significantly | ||
higher, but also in | ||||
AMI | 3% | this instance, no | ||
significant clinical | ||||
Target vessel | 7% | benefit occurred | ||
revascularization | in the IVUS subgroup | |||
Jonsson et al., | 1888 patients who | 30 days | During the period | |
(2006), Eur J | had CABG for LM | 1970–1999 there | ||
Cardiothorac | stenosis from | Mortality | Overall | was a decrease of |
Surg, Sweden, | (1970–1999) | (1970–1999) | LM 2.7% | early and five-year |
[19] | No LM 2% | mortality in | ||
8759 patients | Males | patients with LM | ||
Retrospective | undergone CABG | LM 2.2% | after CABG despite | |
cohort study | for coronary | No LM 1.9% | increases of patient | |
(level 2b) | disease with no | Females | age and risk factors | |
LM | LM 4.7% | |||
No LM 2.6% | An increased risk of | |||
Follow-up: 5 years | early and late | |||
Follow-up | deaths after CABG | |||
in patients with | ||||
5-year mortality | Overall | LM stenosis | ||
LM 10% | compared with | |||
No LM 8.1% | patients without | |||
Males | LM stenosis in the | |||
LM 10.1% | 1970s and 1980s | |||
No LM 8.2% | was neutralised | |||
Females | during the 1990s. | |||
LM 9.6% | There has been an | |||
No LM 7.8% | improvement of | |||
peri- and | ||||
postoperative | ||||
management of | ||||
patients undergoing | ||||
CABG during this | ||||
time period | ||||
Ellis et al., | 107 patients | In-hospital results | 4 deaths in Cath lab | Very small numbers |
(1997), | treated for LMS | 20% in-hospital death | from each centres | |
Circulation, | disease from 16 | 10% Q wave MI | ||
USA, [5] | centres | 5% CABG | ||
Cohort study | These patients | Event-free survival | 88.8±3.5% at 1 month | |
(level 2b) | represented 0.2% | 72.6±5% at 6 months | ||
of all procedures | 71±5% at 12 months | |||
performed in these | ||||
hospitals | >4 month | 22% had restenosis | ||
angioplasty | ||||
27% were | ||||
inoperable | ||||
30% high risk for | ||||
surgery | ||||
15% prev CABG | ||||
15% acute MI | ||||
Age mean 66 | ||||
50% BMS | ||||
24% atherectomy | ||||
20% balloon | ||||
angioplasty | ||||
All had aspirin, 26 | ||||
Ticlopidine, 2 | ||||
abciximab | ||||
Follow-up | ||||
15±8 months | ||||
Park et al., | 1995–2000, 270 | Hospital | 3 stent thromboses, | Pre-DES era |
(2003), Am J | consecutive | complications | 3 Q-Wave MIs | |
Cardiol, South | patients with | No deaths | ||
Korea, [14] | unprotected LMS | 3 emergency CABG | ||
and normal LV | ||||
Cohort study | at 4 centres | Angiographic | Restenosis rate | |
(level 2b) | follow-up | 21.1% | ||
Mean follow-up | ||||
32±18 months | Deaths over mean | 20 deaths | ||
3 years | 8 cardiac deaths | |||
Mean age | ||||
61 years | Target vessel | 45 patients (17%) | ||
revascularization | ||||
3-year freedom | 77.7%±2.7% | |||
from major | ||||
cardiac events | ||||
Price et al., | 50 patients with | In-lesion restenosis | 21/50 (42%) | 84% bifurcational |
(2006), J Am | unprotected left | LMS stenting | ||
Coll Cardiol, | main stenosis who | Target lesion | 19 (38%) | |
USA, [17] | had a Sirolimus | revascularization | ||
eluting stent | ||||
Cohort study | Death | 5 (10%) | ||
(level 2b) | Patients too high | |||
risk for CABG or | MACE, death, MI, | 22/50 (44%) | ||
refused CABG | TLR, Thormbosis | |||
58% had | ||||
EuroSCORE | ||||
predicted mortality | ||||
>5% | ||||
Repeat | ||||
angiography at 3 | ||||
and 9 months | ||||
Lee et al., | 187 patients | 6 months | Restenosis rate 33% | After 2 years there |
(2007), Int | undergoing elective | angiography | at 6 months on | were no further |
J Cardiol | BMS unprotected | angiography | MIs, deaths or | |
South Korea, | LMCA stenting | revascularization | ||
[16] | with normal LV | 5-year mortality | Mortality 7.6% | procedures |
function from 1995 | and MI rate | 6/13 cardiac deaths | ||
Cohort study | to 2001 | |||
(level 2b) | 2 non-fatal MIs | |||
Follow-up: 5 years | ||||
(71 months | Repeat | Target lesion | ||
45–117 months) | revascularization | 36 patients (21%) | ||
angiography at | New lesion | |||
6 months | 13 patients (7.6%) | |||
Mean age 56 | 20 had PCI, 16 had | |||
Prev MI 6% | CABG | |||
EF mean 62% | ||||
Freedom from | 1 year – 80% | |||
MACE | 3 years – 78% | |||
5 years – 78% |
BMS, bare metal stent; BS, bifurcation stenting; DES, drug eluting stent; LMCA, left main coronary artery; MACE, major cardiac events; PCI, percutaneous coronary intervention; TLR, target lesion revascularization; SVS, single vessel stenting; TVR, target vessel revascularization; ULMS, unprotected left main stenosis.
6. Comment
In 2005 the ACC/AHA Task Force on Practice Guidelines updated their guidelines for percutaneous intervention [2]. They provided extensive guidance for patients with left main stem disease. They reiterate that CABG remains the gold standard for the treatment of the unprotected left main coronary artery. PCI should only be considered for patients with or without angina if the patient is a candidate for revascularization but who is not eligible for CABG. They further state that patients with unstable angina or NSTEMI with cardiogenic shock and left main stem disease should still undergo CABG.
The European Society of Cardiology Task Force for percutaneous interventions also published practice guidelines in 2005 [3]. They recommended that patients with left main stem disease or diabetics with multivessel disease undergo CABG rather than PCI. They additionally state that PCI could be contemplated in patients with a prohibitively high risk and cited a EuroSCORE risk of over 10% as a guide figure. Of note, in the UK we now perform at around half the EuroSCORE and thus a risk of 10% for CABG would equate to a EuroSCORE of approaching 20.
The most recent study is by Erglis et al. [4] published in August 2007. They performed an RCT of Paclitaxel-eluting stent vs. bare-metal stent in 103 patients who were also good candidates for CABG with mean EF 54%. There were no immediate procedural complications. The 6-month mortality was 2% in both groups. MI rate at 6 months was 14% for BMS and 9% for PES. MACE at 6 months was 30% for BMS and 13% for PES.
Ellis et al. [5] reported the results of 107 patients not eligible for CABG who had LMS disease prior to 1997. Survival was 70% at 12 months and of those who survived to 4 months for an angiogram, 20% had restenosis >50%. Fifty per cent of these patients had BMS, with the remainder having angioplasty or atherectomy.
Palmerini et al. [6] reported a contemporary cohort study of patients with LMS disease. One hundred and fifty-four patients underwent CABG and 157 patients PCI. On mean follow-up of just over a year, 25% of patients undergoing PCI required target vessel revascularization compared to 2.6% in the CABG group (P=0.0001), and 8.3% had an MI compared to 4.5% (P=0.17). One-year PCI mortality was 13%.
Chieffo et al. [7] reported a similar cohort of LMS patients. One hundred and forty-two patients were treated with CABG and 107 a DES during PCI. Of note the PCI patients were younger, had less diabetes, hypertension and smoking than CABG patients. Also the perioperative-MI rate of the CABG patients was reported as 26% at 30 days which seems extraordinary. At one year there was a 20% revascularization rate with PCI vs. 3.6% for CABG. There was no mortality or MI difference at one year. Mortality in the PCI group was 2.8% at 1 year in this group of patients with a mean EuroSCORE of 4.4.
Lee et al. [8] published results of patients with LMS disease followed up for 6 months. The only significant differences between the 123 patients CABG group and the 50 patients DES-PCI group was for target vessel revascularization (CABG 3.6%; DES 19.6%; P=0.0001). Mortality and MI rates were similar. Mortality from PCI was 4% at six months in this group with mean Parsonnet score of 18.
Tan et al. [9] reported their results of BMS-PCI in 279 patients deemed too high risk for CABG from 25 centres. The 1-year mortality/MI/CABG rate in the PCI group was 24% and death was 12%. Their risk scores were not given but 20% were in cardiogenic shock at PCI and 50% had an IABP.
Kelley et al. [10] evaluated clinical outcomes of protected and unprotected left main coronary bare-metal stenting in patients unsuitable for CABG. At 1 year 43 ULMS stents had a 28% mortality and 48% MACE.
Valgimigli et al. [11,12] assessed clinical outcomes of left main stem stenting with 86 DES and 95 BMS patients over a mean of nearly two years. There were significant higher rates of myocardial infarction (DES 4%; BMS 12%; P=0.006) and target vessel revascularization (DES 6%; BMS 23%, P=0.004) for BMS. Mortality at a mean two years was DES 14% and BMS 16%. Mean Parsonnet in the DES group was 19.
Agostoni et al. [13] achieved a 2-year mortality of only 5% in 58 patients undergoing PCI for LMS disease.
Price et al. [17] reported the angiographic findings of LMS stenting with a serolimus stent in 50 patients. At nine months, 38% required revascularization and there was a 44% MACE.
LMS stenting is also not being commonly performed. In a registry of current practice of 7752 patients undergoing PCI treated in 140 centres over 6 months in 2005, 90% received drug-eluting stents but only 110 patients had LMS stenting (2%) [18].
The results of surgery of left main stenosis were reviewed by Jonsson et al. [19]. They compared 1888 patients who underwent CABG for left-main stenosis with 8759 patients who had CABG for coronary disease without left-main disease. During 1970–1984 early mortality was 5.8% in patients with left-main stenosis vs. 1.5% in patients without left-main stenosis. The corresponding rates during 1995–1999 were 2.0% vs. 2.2%. Five-year survival in males with left-main stenosis was 88% after operations performed during 1994–1999. The continuous decline of mortality during three decades most likely reflects improvement of the peri- and postoperative management of patients undergoing CABG during this period.
7. Clinical bottom line
If a bare-metal stent is used for left main stenting the mortality at 1 year may be from 3% to over 28% in reported series. The restenosis rate of the bare-metal stent in the left main position is around 20% at one year. There are some early series and RCTs of drug eluting stents for LMS lesions and the restenosis rate is reported to be around 10%. The European Society of Cardiology in their 2005 PCI guidelines state that CABG is the procedure of choice for left main stem disease and only patients with a prohibitively high surgical risk should be considered. We consider that with such prohibitively high restenosis rates, and with short-term follow-up in such low numbers and short periods compared to coronary artery bypass grafting, left main stenting should only be used as a last resort in patients turned down for coronary artery bypass grafting after full assessment by a cardiac surgeon due to prohibitive co-morbidities.