background image
CDK 169/vol.36 no.3/Mei - Juni 2009
167
TINJAUAN PUSTAKA
CDK 169/vol.36 no.3/Mei - Juni 2009
168
TINJAUAN PUSTAKA
Introduction
Coronary heart disease (CHD) becomes a major global public
health problem since the last two decades. Although there has
been recent decline in age-standardized cardiovascular mortality,
the prevalence of CHD remains high due to increased life expec-
tancy and changing in life-style of the population. CHD is the
leading cause of death in the United States, responsible for
nearly 20% of all deaths
(1)
. Currently, CHD has been also the
leading contributor for death and disability in developing countries.
The World Health Organization estimates that CHD will account
for 6% of the total global disease burden in 2020
(2)
.
The treatment for coronary heart disease aims to reduce the risk
of mortality and morbidity as well as to reduce or eliminate
angina pectoris, thus, allowing patients to return to normal
activities. Ideally, these end points should be accomplished with
minimal side effects and adequate long-term results. There are
currently three well-established treatment options for CHD:
medical therapy, coronary artery bypass grafting (CABG), and
percutaneous coronary intervention (PCI). Throughout the last 2
decades, number of clinical trials has been conducted to
compare those strategies. The last two options have been rapidly
evolving. Both techniques have their own strengths and inherent
weaknesses. Each is particularly beneficial in specific clinical
settings. This article aims to review the evidences from the clinical
trials which could provide a fair comparison for medical pro-
fessionals in objectively choosing the best treatment option for
patients with CHD.
Medical Therapy
The primary consideration in choosing pharmacological agents
for treatment of CHD should be to improve prognosis. Aspirin
and lipid-lowering therapy have been proved to reduce the risk
of death and non-fatal myocardial infarction (MI) in both primary
and secondary prevention setting. The data strongly suggest that
cardiac events will also be reduced among patients with chronic
stable angina. The ACC/AHA guidelines suggest that aspirin (75
to 325 mg daily) should be administered routinely to all patients
without contraindications. Clopidogrel can be prescribed in
those having absolute contraindication to aspirin
(1)
. The Choles-
terol and Recurrent Events (CARE) trial and Scandinavian Simvas-
tatin Survival Study (4S) have established the benefit of aggressive
lipid-lowering therapy for most patients with CHD, even when
LDL levels are within the considered acceptable range for
patients in primary prevention setting. In addition, the Medical
Research Council/British Heart Foundation (MRC/BHF) Heart
Protection Study conducted in 20,536 high-risk adults in the
United Kingdom revealed that adding simvastatin 40 mg to
existing treatments reduced the rates of MI, stroke, or revascula-
rization by approximately 24%. Angiotensin-converting enzyme
inhibitors are also recommended for all patients with CHD and
asymptomatic patients with CHD who also have diabetes or left
ventricular systolic dysfunction. The Heart Outcomes Prevention
Evaluation (HOPE) trial confirm that the use of ramipril (10
mg/day) can reduce the composite risk of cardiovascular death,
MI, and stroke by approximately 25% in patients at high risk for
or with current vascular disease without heart failure, regardless
of age, sex, or coexisting disease. On the basis of their beneficial
effects on morbidity and mortality, beta-blockers should be
strongly considered as initial therapy for chronic stable angina, as
secondary prevention in post-MI patients, and as a means to reduce
morbidity and mortality among patients with hypertension.
Long-acting or slow-release calcium antagonists are indicated to
relieve symptoms in patients with chronic stable angina without
enhancing the risk of adverse cardiac events. They are often
preferable than long-acting nitrates for maintenance therapy
due to their sustained effects. Short-acting nitrates do not lose
their effect on symptom relief, but long-acting nitrates may
produce tolerance
(1,3)
.
Coronary Artery Bypass Grafting
The first CABG to the right coronary artery using a reverse
segment of saphenous vein was performed by Sabiston in 1962.
Although the patient died due to cerebrovascular accident, the
procedure itself was successful. DeBakey performed the first
complete CABG as a bailout procedure after a carotid endar-
terectomy
(4)
. Subsequently, Favaloro in Cleveland Clinic refined
the use of reversed saphenous vein grafts for coronary bypass.
Kolessov and Green were the first who used internal mammary
artery as bypass graft. Subsequently, the number of CABG has
markedly increased. Currently, more than 500,000 operations
are performed in the United States every year with excellent
results
(5)
. Even so, many physicians still attempt to avoid recom-
mending CABG to their patients. This may be in part a result of
the perception that CABG is associated with high mortality risk.
This perception has recently been challenged with large
published studies demonstrating mortality risk of 1.2% to 1.7%
for isolated CABG
(6,7)
. Some limitations of CABG include costs
Current Treatment Options for
Coronary Heart Disease
Yanto Sandy Tjang, Lech Hornik, John Mantas, Richardus Budiman,
Andreas Bairaktaris, Reiner Körfer.
Department of Thoracic & Cardiovascular Surgery,Heart & Diabetes Center
NRW/University Hospital of Bochum,Bad Oeynhausen, Germany
Banyak studi membuktikan bahwa latihan fisik sangat berpengaruh
terhadap kesehatan pembuluh darah dan jantung. Latihan fisik
secara dinamik dan isometrik sama-sama dapat mempengaruhi
tekanan darah. Latihan fisik teratur menghasilkan penurunan
tekana darah yang bermakna dan akan menetap selama latihan
fisik terus dilakukan. Mekanisme perurunan darah tersebut karena
terjadi penurunan curah jantung, penurunan aktivitas sistem
saraf simpatis, penurunan resistensi pembuluh darah perifer dan
meningkatnya sensitivitas baroreflek.
Rujukan : ada pada penulis.
Pada penderita yang lebih tua penurunan tekanan darah juga
berkaitan dengan penurunan resistensi perifer namun individu
dengan curah jantung yang tinggi, mempunyai curah jantung yang
lebih rendah sesudah latihan.
49
Oleh karena itu umur, lamanya
hipertensi adanya LVH dan barangkali berbagai faktor mempe-
ngaruhi gambaran hemodinamik terhadap penurunan tekanan
darah sesudah latihan. Sirkulasi norepinephrine dan epinephrine
diketahui juga menurun.
41-45,71
Penurunan tekanan darah sesudah
latihan secara ambulatoar sering ditemukan pada saat aktifitas
simpatis relatif tinggi.
72
Somers dkk
52
, melaporkan bahwa latihan endurance menurunkan
tekanan darah harian, baik pada saat istirahat maupun pada saat
aktifitas; tetapi tidak menurunkan tekanan darah saat tidur.
Mereka juga melaporkan meningkatnya sensiitivitas barorefleks
dan menurunnya pengaturan untuk meningkatkan tekanan darah
pada peningkatan aktifitas fisik penderita hipertensi ringan
maupun borderline (prahipertensi ).
SIMPULAN
Hipertensi merupakan faktor risiko utama untuk kematian maupun
kesakitan dari penyakit kardiovaskular. Tiga perempat kejadian
kardiovaskular justru terjadi di negara berkembang. Prevalensi
hipertensi makin meningkat karena perubahan definisi hipertensi.
Pengobatan hipertensi sesuai JNC 7 dapat dimulai dari obat anti-
hipertensi semua golongan termasuk antagonis kalsium, penyekat
beta maupun ACE dan ARB.
cdk
.redaksi@
yah
o
o.co.id
Penyakit Infeksi
Penyakit Infeksi
Reumatologi
Reumatologi
Bedah & Anestesi
Bedah & Anestesi
background image
CDK 169/vol.36 no.3/Mei - Juni 2009
169
TINJAUAN PUSTAKA
CDK 169/vol.36 no.3/Mei - Juni 2009
170
TINJAUAN PUSTAKA
benefit more from initial CABG. They also show that the rates of
repeat revascularization tend to become similar for both strate-
gies on long-term follow-up, probably due to late vein graft
failure in the CABG group. The Stent or Surgery trial has demon-
strated an early survival advantage for CABG
(32)
. This finding is
supported by recent meta-analysis from 13 trials with 7,964
patients
(33)
. When compared with PCI, CABG is associated with
lower 5-year mortality, less angina, and fewer repeat revascular-
izations. CABG provided a survival advantage at 5 - 8 years for
patients with multi-vessel CHD, and at 4 years for diabetic
patients.
The recent development of anti-proliferative DES is a major break-
through in preventing restenosis after initial PCI. DES prevents
neointimal proliferation, thereby, decreasing restenosis and
repeat revascularization. Randomized trials using both sirolimus-and
paclitaxel-eluting stents have shown significant reductions of
repeat revascularization in target lesion. A meta-analysis confirms
these aggregate reductions in repeat revascularization, but it
does not detect any mortality benefit
(34)
. Although several different
drug-eluting stents are under investigation, sirolimus and pacli-
taxel account for the majority of existing clinical data, and are
now commercially available. Clearly, not all of DES is promising.
At least three clinical trials with alternative drug formulations
have been discontinued due to poor effects. The long-term
effects of DES implantation remain unknown. The growing use
of DES not only produces clinical benefits for certain patients, but
also creates financial crises for many health care systems. DES
cost 3 - 7 times higher than their uncoated predecessors.
Conclusion
Despite increased popularity of PCI, CABG remains an important
treatment option for CHD. Further evidence on long-term efficacy
and safety of some DES, especially in high-risk subgroups, is
warranted. Meanwhile, intensive communication between
medical professionals who involve in providing medical care, in
term of objectively choosing the best treatment option for
specified patients with CHD, is of highly necessary. One can be
sure that most of the patients with CHD will benefit from each
treatment options that continue to advance and improve.
References
1. American College of Cardiology/American Heart Association Task Force on Practice
Guidelines (Committee on the Management of Patients with Chronic Stable Angina).
ACC/AHA 2002 guideline update for the management of patients with chronic stable
angina-summary article. J Am Coll Cardiol 2003; 41:15968.
2. Murray CJ, Lopez AD. Alternative projections of mortality and disability by cause
1990-2020: Global Burden of Disease Study. Lancet 1997;349:1498504.
3. Sleight P. Current options in the management of coronary artery disease. Am J Cardiol 2003;
92(suppl):2N-8N.
4. Garrett HE, Dennis EW, DeBakey ME. Aortocoronary bypass with saphenous
vein graft. Seven-year follow-up. JAMA 1973; 223:7924.
5. American Heart Association, Heart Disease and Stroke Statistics-2003 Update.
American Heart Association, Dallas, TX, 2002.
6. Nalysnyk L, Fahrbach K, Reynolds MW, et al. Adverse events in coronary artery bypass graft
(CABG) trials: a systematic review and analysis. Heart 2003; 89:76772.
7. Zacharias A, Habib RH, Schwann TA, et al. Improved survival with radial artery versus vein
conduits in coronary bypass surgery with left internal thoracic artery to left anterior
descending artery grafting. Circulation 2004; 109:148996.
8. Grüntzig AR, Myler RK, Hanna EH, et al. Coronary transluminal angioplasty. Circulation
1977;
55:8491.
9. Landau C, Lange RA, Hillis LD. Percutaneous transluminal coronary angioplasty. N. Engl. J.
Med. 1994; 330:98193.
10. The Veterans Administration Coronary Artery Bypass Surgery Cooperative Study Group:
Eleven-year survival in the Veterans Administration randomized trial of coronary bypass
surgery for stable angina. N Engl J Med 1984; 311:13339.
11. Varnauskas E. Twelve-year follow-up of survival in the randomized European Coronary
Surgery Study. N Engl J Med 1988; 319:3327.
12. Alderman EL, Bourassa MG, Cohen LS, et al. Ten-year follow-up of survival and myocardial
infarction in the randomized Coronary Artery Surgery Study. Circulation 1990; 82:162946.
13. Yusuf S, Zucker D, Peduzzi P, et al. Effect of coronary artery bypass graft surgery on survival:
overview of 10-year results from randomised trials by the Coronary Artery Bypass Graft
Surgery Trialists Collaboration. Lancet 1994; 344:56370.
14. Hartigan PM, Giacomini JC, Folland ED, et al. Two-to three-year follow-up of patients with
single-vessel coronary artery disease randomized to PTCA or medical therapy (results of a VA
cooperative study). Veterans Affairs Cooperative Studies Program ACME investigators.
Angioplasty Compared to Medicine. Am J Cardiol 1998; 15:144550.
15. Pocock SJ, Henderson RA, Clayton T, et al. Quality of life after coronary angioplasty or
continued medical treatment for angina: three-year follow-up in the RITA-2 trial.
Randomized Intervention Treatment of Angina. J Am Coll Cardiol 2000; 34:90714.
16. Davies RF, Goldberg AD, Forman S, et al. Asymptomatic Cardiac Ischemia Pilot (ACIP) study
two-year follow-up: outcomes of patients randomized to initial strategies of medical therapy
versus revascularization. Circulation 1997; 95:203743.
17. Hueb WA, Soares PR, Almeida De Oliveira S, et al. Five-year follow-up of the medicine,
angioplasty, or surgery study (MASS): a prospective, randomized trial of medical therapy,
balloon angioplasty, or bypass surgery for single proximal left anterior descending artery
stenosis. Circulation 1999; 100:II-10713.
18. Pitt B, Waters D, Brown WV, et al. Aggressive lipid-lowering therapy compared with
angioplasty in stable coronary artery disease. Atorvastatin versus Revascularization Treatment
Investigators. N Engl J Med 1999; 341:706.
19. Boden WE, O»Rourke RA, Teo KK, et al. Optimal medical therapy with or without PCI for
stable coronary disease. N Engl J Med 2007; 356(15):1503-16.
20. Rodriguez A, Boullon F, Perez-Balino N, et al. Argentine randomized trial of percutaneous
transluminal coronary angioplasty versus coronary artery bypass surgery in multivessel disease
(ERACI): in-hospital results and 1-year follow-up. ERACI Group. J Am Coll Cardiol 1993;
22:10607.
21. Hamm CW, Reimers J, Ischinger T, et al. A randomized study of coronary angioplasty
compared with bypass surgery in patients with symptomatic multivessel coronary disease.
German Angioplasty Bypass Surgery Investigation. N Engl J Med 1994; 331:103743.
22. King 3rd, SB Lembo NJ, Weintraub WS, et al. A randomized trial comparing coronary
angioplasty with coronary bypass surgery. Emory Angioplasty versus Surgery Trial. N Engl J
Med 1994; 331:104450.
23. CABRI Trial Participants: First-year results of CABRI (Coronary Angioplasty versus Bypass
Revascularization Investigation). Lancet 1995, 346:117984.
24. The Bypass Angioplasty Revascularization Investigation (BARI) Investigators: Comparison of
coronary bypass surgery with angioplasty in patients with multivessel disease. N Engl J Med
1996;
335:21725.
25. Coronary angioplasty versus coronary artery bypass surgery: the Randomized Intervention
Treatment of Angina (RITA) trial. Lancet 1993; 341:57380.
26. Henderson RA, Pocock SJ, Sharp SJ, et al. Long-term results of RITA-1 trial: clinical and cost
comparisons of coronary angioplasty and coronary-artery bypass grafting. Randomised
Intervention Treatment of Angina. Lancet 1998; 352:141925.
27. Goy JJ, Eeckhout E, Moret C, et al. Five-year outcome in patients with isolated proximal left
anterior descending coronary artery stenosis treated by angioplasty or left internal mammary
artery grafting. A prospective trial. Circulation 1999; 99:32559.
28. Sim I, Gupta M, McDonald K, et al. A meta-analysis of randomized trials comparing coronary
artery bypass grafting with percutaneous transluminal coronary angioplasty in multivessel
coronary artery disease. Am J Cardiol 1995; 76:10259.
29. Pocock SJ, Henderson RA, Rickards AF, et al. Meta-analysis of randomised trials comparing
coronary angioplasty with bypass surgery. Lancet 1995; 346:11849.
30. King SB, Kosinski AS, Guyton RA, et al. Eight-year mortality in the Emory Angioplasty versus
Surgery Trial. J Am Coll Cardiol 2000; 35:111621.
31. Seven-year outcome in the Bypass Angioplasty Revascularization Investigation (BARI) by
treatment and diabetic status. J Am Coll Cardiol 2000; 35:11229.
32. Coronary artery bypass surgery versus percutaneous coronary intervention with stent
implantation in patients with multivessel coronary artery disease (the Stent or Surgery trial): a
randomised controlled trial. Lancet 2002; 360:96570.
33. Hoffman SN, TenBrook JA, Wolf MP, et al. A meta-analysis of randomized controlled trials
comparing coronary artery bypass graft with percutaneous transluminal coronary
angioplasty: one- to eight-year outcomes. J Am Coll Cardiol 2003; 41:1293304.
34. Babapulle MN, Joseph L, Bélisle P, et al. A hierarchical Bayesian meta-analysis of randomized
clinical trials of drug-eluting stents. Lancet 2004; 364:58391.
associated with preoperative and postoperative care, the need
for several days of hospitalization (including intensive care),
rehabilitation, and delayed or inability to return to work quickly.
Since the average patency time of venous bypass grafts is around
7 - 10 years; some patients may require repeat revascularization.
In the mid-1990s two new surgical techniques have been intro-
duced in attempts to reduce the invasiveness of the standard
CABG procedure. Revascularization either on an arrested heart
with peripheral cannulation through a small access incision (port
access) or on a beating heart with a limited access approach
(MIDCABG) becomes emerging. However, the lack of demon-
strated benefit and significant technical challenge associated
with the port access approach hamper its widely application.
Similar restriction also happens to MIDCABG procedure since it is
not only technically challenging but also its inability to perform
complete myocardial revascularization. However, the recognition
of improved outcomes in selected patients served as an impetus
to develop off-pump coronary artery bypass (OPCAB) procedure
as a treatment option for patients with multi-vessel CHD. Many
other techniques, such as: complete arterial revascularization,
mechanical anastomosis connector, robotic assist systems, stem
cell implantation and genetic therapy for preventing vein graft
disease are of current research interest.
Percutaneous Coronary Intervention
Werner Forssman inserted a catheter into his own basilic vein
and threaded it to his right atrium for the purpose of «intra-
cardiac drug injection» in 1929. Later on, diagnostic cardiac
catheterization was developed by Cournand, Sones, and Judkins.
In 1964, Dotter and Judkins successfully dilated peripheral
atherosclerotic lesions using progressively larger coaxial dilators.
In 1974, Grüntzig developed the double lumen catheter and
performed the first percutaneous dilation of a human coronary
artery in 1977
(8)
. PCI is considered providing less invasive
approach and offers shorter hospital stay or faster recovery.
During earlier period, the quality of PCI was limited by lack of
user-friendly and lesion-suitable technical equipment. Dissection
and acute or threatened closure result in major morbidity.
Mortality was sufficiently frequent and unpredictable. Therefore,
in many institutions a staffed operating room was always kept
empty for emergeny surgery in case complications exist. The
major limiting factor of PCI is the occurrence of restenosis in
about 3060% of patients, depending on clinical risk factors,
lesion characteristics and technical aspects of the intervention
(9)
.
Newer interventional techniques such as stents, directional,
rotational, laser atherectomy, thrombectomy devices and drug-
eluting stents (DES) have been introduced into clinical practice
with better results.
Medical Therapy versus CABG
Three large randomized trials
(10-12)
, which included patients with
stable angina and single - or multi - vessel CHD for either medical
or surgical therapy, along with several observational studies and
a meta-analysis
(13)
, have yielded consistent results and established
the role of CABG as a solid treatment option for CHD. CABG
resulted in substantially lower mortality rates at 5-, 7-, and 10-
years compared to medical therapy. Patients with left main
coronary artery disease, three-vessel CHD with impaired left
ventricular function, diabetes mellitus, and instable angina
pectoris derive the greatest benefit from CABG.
Medical Therapy versus PCI
Two randomized clinical trials
(14,15)
, including low-risk patients
who were randomized to either medical therapy or PTCA, have
been published. Mortality rates were similar in both groups.
Patients who underwent PTCA were more likely to be free of
angina. In the Asymptomatic Cardiac Ischemia Pilot trial
(16)
,
patients with CHD who were free of angina and had evidence of
ischemia on electrocardiography or stress testing were random-
ized to either medical therapy or revascularization (percutaneous
or surgical depending on the operator). Patients who underwent
revascularization had lower mortality, MI, and hospitalization
rates than the medically treated patients. The Medicine, Angio-
plasty or Surgery Study was a three-arm trial that compared
PTCA, medical therapy, and CABG using LIMA graft in patients
with isolated severe proximal LAD stenosis
(17)
. There were no
differences in mortality risk or MI among all three groups.
Patients who underwent CABG or PTCA were more likely to be
symptom-free than those medically treated. Repeat revascular-
izations were higher in the PTCA and medically treated groups.
In the Atorvastatin Versus Revascularization Treatment trial
(18)
,
low-risk patients who were randomized to aggressive lipid-
lowering therapy with atorvastatin tended to have fewer
ischemic events than those who received angioplasty along with
usual medical care. A recent randomized trial involving 2,287
patients who had objective evidence of MI and significant CHD
at 50 American and Canadian centers demonstrated that PCI did
not reduce the risk of death, MI, or other major cardiovascular
events when added to optimal medical therapy in patients with
stable CHD
(19)
.
PCI versus CABG
Several randomized trials, comprising more than 5,000 patients,
have compared PCI and CABG in the management of single-
and multi-vessel CHD
(17,20-27)
. Despite differences in design and
inclusion criteria, several conclusions can be drawn from these
trials, in addition to two meta-analyses performed later
(28,29)
.
There were no significant differences in mortality or combined
endpoint of death and non-fatal MI between PCI and CABG.
Patients undergoing initial PCI are more likely to require repeat
revascularization (either CABG or PCI) than patients undergoing
initial CABG. Initial costs are lower in the PCI group but tend to
equalize later, owing to the increased repeat revascularizations.
More importantly, patients with treated diabetes mellitus seem
to have better survival from initial CABG than PCI. Recent long-
term follow-up results have been published
(30,31)
. More recent
data emphasize previous findings and confirm the similar survival
achieved by both strategies, except in the diabetic patients who
background image
CDK 169/vol.36 no.3/Mei - Juni 2009
169
TINJAUAN PUSTAKA
CDK 169/vol.36 no.3/Mei - Juni 2009
170
TINJAUAN PUSTAKA
benefit more from initial CABG. They also show that the rates of
repeat revascularization tend to become similar for both strate-
gies on long-term follow-up, probably due to late vein graft
failure in the CABG group. The Stent or Surgery trial has demon-
strated an early survival advantage for CABG
(32)
. This finding is
supported by recent meta-analysis from 13 trials with 7,964
patients
(33)
. When compared with PCI, CABG is associated with
lower 5-year mortality, less angina, and fewer repeat revascular-
izations. CABG provided a survival advantage at 5 - 8 years for
patients with multi-vessel CHD, and at 4 years for diabetic
patients.
The recent development of anti-proliferative DES is a major break-
through in preventing restenosis after initial PCI. DES prevents
neointimal proliferation, thereby, decreasing restenosis and
repeat revascularization. Randomized trials using both sirolimus-and
paclitaxel-eluting stents have shown significant reductions of
repeat revascularization in target lesion. A meta-analysis confirms
these aggregate reductions in repeat revascularization, but it
does not detect any mortality benefit
(34)
. Although several different
drug-eluting stents are under investigation, sirolimus and pacli-
taxel account for the majority of existing clinical data, and are
now commercially available. Clearly, not all of DES is promising.
At least three clinical trials with alternative drug formulations
have been discontinued due to poor effects. The long-term
effects of DES implantation remain unknown. The growing use
of DES not only produces clinical benefits for certain patients, but
also creates financial crises for many health care systems. DES
cost 3 - 7 times higher than their uncoated predecessors.
Conclusion
Despite increased popularity of PCI, CABG remains an important
treatment option for CHD. Further evidence on long-term efficacy
and safety of some DES, especially in high-risk subgroups, is
warranted. Meanwhile, intensive communication between
medical professionals who involve in providing medical care, in
term of objectively choosing the best treatment option for
specified patients with CHD, is of highly necessary. One can be
sure that most of the patients with CHD will benefit from each
treatment options that continue to advance and improve.
References
1. American College of Cardiology/American Heart Association Task Force on Practice
Guidelines (Committee on the Management of Patients with Chronic Stable Angina).
ACC/AHA 2002 guideline update for the management of patients with chronic stable
angina-summary article. J Am Coll Cardiol 2003; 41:15968.
2. Murray CJ, Lopez AD. Alternative projections of mortality and disability by cause
1990-2020: Global Burden of Disease Study. Lancet 1997;349:1498504.
3. Sleight P. Current options in the management of coronary artery disease. Am J Cardiol 2003;
92(suppl):2N-8N.
4. Garrett HE, Dennis EW, DeBakey ME. Aortocoronary bypass with saphenous
vein graft. Seven-year follow-up. JAMA 1973; 223:7924.
5. American Heart Association, Heart Disease and Stroke Statistics-2003 Update.
American Heart Association, Dallas, TX, 2002.
6. Nalysnyk L, Fahrbach K, Reynolds MW, et al. Adverse events in coronary artery bypass graft
(CABG) trials: a systematic review and analysis. Heart 2003; 89:76772.
7. Zacharias A, Habib RH, Schwann TA, et al. Improved survival with radial artery versus vein
conduits in coronary bypass surgery with left internal thoracic artery to left anterior
descending artery grafting. Circulation 2004; 109:148996.
8. Grüntzig AR, Myler RK, Hanna EH, et al. Coronary transluminal angioplasty. Circulation
1977;
55:8491.
9. Landau C, Lange RA, Hillis LD. Percutaneous transluminal coronary angioplasty. N. Engl. J.
Med. 1994; 330:98193.
10. The Veterans Administration Coronary Artery Bypass Surgery Cooperative Study Group:
Eleven-year survival in the Veterans Administration randomized trial of coronary bypass
surgery for stable angina. N Engl J Med 1984; 311:13339.
11. Varnauskas E. Twelve-year follow-up of survival in the randomized European Coronary
Surgery Study. N Engl J Med 1988; 319:3327.
12. Alderman EL, Bourassa MG, Cohen LS, et al. Ten-year follow-up of survival and myocardial
infarction in the randomized Coronary Artery Surgery Study. Circulation 1990; 82:162946.
13. Yusuf S, Zucker D, Peduzzi P, et al. Effect of coronary artery bypass graft surgery on survival:
overview of 10-year results from randomised trials by the Coronary Artery Bypass Graft
Surgery Trialists Collaboration. Lancet 1994; 344:56370.
14. Hartigan PM, Giacomini JC, Folland ED, et al. Two-to three-year follow-up of patients with
single-vessel coronary artery disease randomized to PTCA or medical therapy (results of a VA
cooperative study). Veterans Affairs Cooperative Studies Program ACME investigators.
Angioplasty Compared to Medicine. Am J Cardiol 1998; 15:144550.
15. Pocock SJ, Henderson RA, Clayton T, et al. Quality of life after coronary angioplasty or
continued medical treatment for angina: three-year follow-up in the RITA-2 trial.
Randomized Intervention Treatment of Angina. J Am Coll Cardiol 2000; 34:90714.
16. Davies RF, Goldberg AD, Forman S, et al. Asymptomatic Cardiac Ischemia Pilot (ACIP) study
two-year follow-up: outcomes of patients randomized to initial strategies of medical therapy
versus revascularization. Circulation 1997; 95:203743.
17. Hueb WA, Soares PR, Almeida De Oliveira S, et al. Five-year follow-up of the medicine,
angioplasty, or surgery study (MASS): a prospective, randomized trial of medical therapy,
balloon angioplasty, or bypass surgery for single proximal left anterior descending artery
stenosis. Circulation 1999; 100:II-10713.
18. Pitt B, Waters D, Brown WV, et al. Aggressive lipid-lowering therapy compared with
angioplasty in stable coronary artery disease. Atorvastatin versus Revascularization Treatment
Investigators. N Engl J Med 1999; 341:706.
19. Boden WE, O»Rourke RA, Teo KK, et al. Optimal medical therapy with or without PCI for
stable coronary disease. N Engl J Med 2007; 356(15):1503-16.
20. Rodriguez A, Boullon F, Perez-Balino N, et al. Argentine randomized trial of percutaneous
transluminal coronary angioplasty versus coronary artery bypass surgery in multivessel disease
(ERACI): in-hospital results and 1-year follow-up. ERACI Group. J Am Coll Cardiol 1993;
22:10607.
21. Hamm CW, Reimers J, Ischinger T, et al. A randomized study of coronary angioplasty
compared with bypass surgery in patients with symptomatic multivessel coronary disease.
German Angioplasty Bypass Surgery Investigation. N Engl J Med 1994; 331:103743.
22. King 3rd, SB Lembo NJ, Weintraub WS, et al. A randomized trial comparing coronary
angioplasty with coronary bypass surgery. Emory Angioplasty versus Surgery Trial. N Engl J
Med 1994; 331:104450.
23. CABRI Trial Participants: First-year results of CABRI (Coronary Angioplasty versus Bypass
Revascularization Investigation). Lancet 1995, 346:117984.
24. The Bypass Angioplasty Revascularization Investigation (BARI) Investigators: Comparison of
coronary bypass surgery with angioplasty in patients with multivessel disease. N Engl J Med
1996;
335:21725.
25. Coronary angioplasty versus coronary artery bypass surgery: the Randomized Intervention
Treatment of Angina (RITA) trial. Lancet 1993; 341:57380.
26. Henderson RA, Pocock SJ, Sharp SJ, et al. Long-term results of RITA-1 trial: clinical and cost
comparisons of coronary angioplasty and coronary-artery bypass grafting. Randomised
Intervention Treatment of Angina. Lancet 1998; 352:141925.
27. Goy JJ, Eeckhout E, Moret C, et al. Five-year outcome in patients with isolated proximal left
anterior descending coronary artery stenosis treated by angioplasty or left internal mammary
artery grafting. A prospective trial. Circulation 1999; 99:32559.
28. Sim I, Gupta M, McDonald K, et al. A meta-analysis of randomized trials comparing coronary
artery bypass grafting with percutaneous transluminal coronary angioplasty in multivessel
coronary artery disease. Am J Cardiol 1995; 76:10259.
29. Pocock SJ, Henderson RA, Rickards AF, et al. Meta-analysis of randomised trials comparing
coronary angioplasty with bypass surgery. Lancet 1995; 346:11849.
30. King SB, Kosinski AS, Guyton RA, et al. Eight-year mortality in the Emory Angioplasty versus
Surgery Trial. J Am Coll Cardiol 2000; 35:111621.
31. Seven-year outcome in the Bypass Angioplasty Revascularization Investigation (BARI) by
treatment and diabetic status. J Am Coll Cardiol 2000; 35:11229.
32. Coronary artery bypass surgery versus percutaneous coronary intervention with stent
implantation in patients with multivessel coronary artery disease (the Stent or Surgery trial): a
randomised controlled trial. Lancet 2002; 360:96570.
33. Hoffman SN, TenBrook JA, Wolf MP, et al. A meta-analysis of randomized controlled trials
comparing coronary artery bypass graft with percutaneous transluminal coronary
angioplasty: one- to eight-year outcomes. J Am Coll Cardiol 2003; 41:1293304.
34. Babapulle MN, Joseph L, Bélisle P, et al. A hierarchical Bayesian meta-analysis of randomized
clinical trials of drug-eluting stents. Lancet 2004; 364:58391.
associated with preoperative and postoperative care, the need
for several days of hospitalization (including intensive care),
rehabilitation, and delayed or inability to return to work quickly.
Since the average patency time of venous bypass grafts is around
7 - 10 years; some patients may require repeat revascularization.
In the mid-1990s two new surgical techniques have been intro-
duced in attempts to reduce the invasiveness of the standard
CABG procedure. Revascularization either on an arrested heart
with peripheral cannulation through a small access incision (port
access) or on a beating heart with a limited access approach
(MIDCABG) becomes emerging. However, the lack of demon-
strated benefit and significant technical challenge associated
with the port access approach hamper its widely application.
Similar restriction also happens to MIDCABG procedure since it is
not only technically challenging but also its inability to perform
complete myocardial revascularization. However, the recognition
of improved outcomes in selected patients served as an impetus
to develop off-pump coronary artery bypass (OPCAB) procedure
as a treatment option for patients with multi-vessel CHD. Many
other techniques, such as: complete arterial revascularization,
mechanical anastomosis connector, robotic assist systems, stem
cell implantation and genetic therapy for preventing vein graft
disease are of current research interest.
Percutaneous Coronary Intervention
Werner Forssman inserted a catheter into his own basilic vein
and threaded it to his right atrium for the purpose of «intra-
cardiac drug injection» in 1929. Later on, diagnostic cardiac
catheterization was developed by Cournand, Sones, and Judkins.
In 1964, Dotter and Judkins successfully dilated peripheral
atherosclerotic lesions using progressively larger coaxial dilators.
In 1974, Grüntzig developed the double lumen catheter and
performed the first percutaneous dilation of a human coronary
artery in 1977
(8)
. PCI is considered providing less invasive
approach and offers shorter hospital stay or faster recovery.
During earlier period, the quality of PCI was limited by lack of
user-friendly and lesion-suitable technical equipment. Dissection
and acute or threatened closure result in major morbidity.
Mortality was sufficiently frequent and unpredictable. Therefore,
in many institutions a staffed operating room was always kept
empty for emergeny surgery in case complications exist. The
major limiting factor of PCI is the occurrence of restenosis in
about 3060% of patients, depending on clinical risk factors,
lesion characteristics and technical aspects of the intervention
(9)
.
Newer interventional techniques such as stents, directional,
rotational, laser atherectomy, thrombectomy devices and drug-
eluting stents (DES) have been introduced into clinical practice
with better results.
Medical Therapy versus CABG
Three large randomized trials
(10-12)
, which included patients with
stable angina and single - or multi - vessel CHD for either medical
or surgical therapy, along with several observational studies and
a meta-analysis
(13)
, have yielded consistent results and established
the role of CABG as a solid treatment option for CHD. CABG
resulted in substantially lower mortality rates at 5-, 7-, and 10-
years compared to medical therapy. Patients with left main
coronary artery disease, three-vessel CHD with impaired left
ventricular function, diabetes mellitus, and instable angina
pectoris derive the greatest benefit from CABG.
Medical Therapy versus PCI
Two randomized clinical trials
(14,15)
, including low-risk patients
who were randomized to either medical therapy or PTCA, have
been published. Mortality rates were similar in both groups.
Patients who underwent PTCA were more likely to be free of
angina. In the Asymptomatic Cardiac Ischemia Pilot trial
(16)
,
patients with CHD who were free of angina and had evidence of
ischemia on electrocardiography or stress testing were random-
ized to either medical therapy or revascularization (percutaneous
or surgical depending on the operator). Patients who underwent
revascularization had lower mortality, MI, and hospitalization
rates than the medically treated patients. The Medicine, Angio-
plasty or Surgery Study was a three-arm trial that compared
PTCA, medical therapy, and CABG using LIMA graft in patients
with isolated severe proximal LAD stenosis
(17)
. There were no
differences in mortality risk or MI among all three groups.
Patients who underwent CABG or PTCA were more likely to be
symptom-free than those medically treated. Repeat revascular-
izations were higher in the PTCA and medically treated groups.
In the Atorvastatin Versus Revascularization Treatment trial
(18)
,
low-risk patients who were randomized to aggressive lipid-
lowering therapy with atorvastatin tended to have fewer
ischemic events than those who received angioplasty along with
usual medical care. A recent randomized trial involving 2,287
patients who had objective evidence of MI and significant CHD
at 50 American and Canadian centers demonstrated that PCI did
not reduce the risk of death, MI, or other major cardiovascular
events when added to optimal medical therapy in patients with
stable CHD
(19)
.
PCI versus CABG
Several randomized trials, comprising more than 5,000 patients,
have compared PCI and CABG in the management of single-
and multi-vessel CHD
(17,20-27)
. Despite differences in design and
inclusion criteria, several conclusions can be drawn from these
trials, in addition to two meta-analyses performed later
(28,29)
.
There were no significant differences in mortality or combined
endpoint of death and non-fatal MI between PCI and CABG.
Patients undergoing initial PCI are more likely to require repeat
revascularization (either CABG or PCI) than patients undergoing
initial CABG. Initial costs are lower in the PCI group but tend to
equalize later, owing to the increased repeat revascularizations.
More importantly, patients with treated diabetes mellitus seem
to have better survival from initial CABG than PCI. Recent long-
term follow-up results have been published
(30,31)
. More recent
data emphasize previous findings and confirm the similar survival
achieved by both strategies, except in the diabetic patients who