Skip to main content
Journal of the Saudi Heart Association logoLink to Journal of the Saudi Heart Association
. 2020 Dec 18;33(2):109–116. doi: 10.37616/2212-5043.1245

Individual Versus Sequential Saphenous Vein Grafts for on-Pump Coronary Artery Bypass Grafting – Does Smaller Coronaries in Indians Affect Graft Choice? – A Mid-Term Patency Comparison Study

Manoj M Joshi a, Saptarshi Paul a,*, Krishnarao N Bhosle b, Suraj W Nagre a, Hrishikesh Parashi a, Manish Jadhao c, Kunal Rawekar d, Vignesh Ravikumar a, Vishal Sawkar a, Joshua A Selwyn e
PMCID: PMC8143723  PMID: 34183906

Abstract

Purpose

Although multiarterial grafting or bilateral mammary artery use is being increasingly emphasized for contemporary coronary artery bypass grafting (CABG) practice, saphenous vein graft (SVG) still accounts for 80% of all CABG conduits (Park et al., 2020) [1]. In India, both the individual and sequential saphenous grafting techniques are used arbitrarily, and there has not been a study that compares the mid-term patency of these two. This is specially relevant in view of smaller coronaries in Indians than the Caucasian counterparts. This study aims to compare the patency for on pump CABG’s.

Methods

In the present study, 323 patients underwent either sequential (group A, N = 151 grafts, each graft having two anastomoses each) or individual (group B, N = 344 grafts) saphenous vein CABG, between February 2014 and June 2017. The SVG anastomoses were created on obtuse marginal (OM1/OM2) and posterior descending artery (PDA). The graft patency of the vein grafts as well as the left internal mammary artery were assessed by serial coronary angiograms.

Results

Results were evaluated at 6 months, 1, 2 and 3 years post operatively. Group A showed a higher graft patency at 3 years at 80.8%, and group B, 67.1% (P = 0.002). Also, anastomoses on sequential conduits had overall better patency rates at three years (77.2% vs 67.2%, P = 0.005). The groups showed similar results at one year post operatively.

Conclusions

Sequential bypass grafts were associated with superior mid-term patency compared with individual grafts. These findings suggest the more favourable results of sequential bypass grafting to be attributed to the enhanced flow haemodynamics.

Keywords: Coronary artery bypass grafting, Sequential grafting, Individual grafting, Coronary arteries, Saphenous vein grafting technique

1. Introduction

Despite the introduction and popularisation of a variety of arterial grafts having supposedly superior long-term patency rates, saphenous vein grafts continue to be the backbone of daily coronary revascularisation practice [2]. There is an ample amount of controversy as to whether sequential or individual grafting should be performed in bypass grafting. Sequential grafting is a technique whereby more than one distal anastomosis is constructed per segment of conduit used, thus resulting in two or more distal anastomoses per single proximal anastomosis. The advocates of this technique describe the haemodynamic advantage of increased total graft flow through improved distal runoff and, by extension, increased graft patency rates [3,4]. Sequential grafting helps to minimise aortic manipulation and, in some cases, allows anastomoses to smaller coronary arteries [57]. Despite these purported advantages, the acceptance of sequential grafting amongst surgeons as their default choice has been less than unanimous. This is due to the dependence of multiple grafts on a common inflow with the possibility of conduit block in the event of a proximal occlusion [8,9]. Conversely, in case of individual grafts, in case of individual graft occlusion, a large segment of the myocardium gets spared. (Table IA,B,C,D) (Table IIA,B,C,D, E,F,G,H) (Table IIIA,B,C,D).

Table IA.

Overall comparison of the patency of sequential and individual venous conduits at 6 months post operatively.

A. At 6 months post operatively

Outcome No. of individual SVG No. of sequential SVG No. of LIMA pedicled grafts
Patent 298 133 321
Partially patent 10 7 1
Occluded 36 11 1
Total 344 151 323

Overall patency (including partial patency) in case of individual grafts = 89.5%.

Overall patency (including partial patency) in case of sequential grafts = 92.7%.

Overall patency (including partial patency) in case of LIMA = 99.7%.

P value is 0.266, implies there is no significant difference between individual and sequential graft patency.

Table IB.

Overall comparison of the patency of sequential and individual venous conduits at 1 year post operatively (data from 0 to 1 yr).

B. At 1 year post operatively (data from 0 to 1 yr)

Outcome No. of Individual SVG No. of Sequential SVG No. of LIMA pedicled grafts
Patent 241 112 315
Partially patent 24 19 3
Occluded 79 20 5
Total 344 151 323

Overall patency (including partial patency) in case of individual grafts = 77.03%.

Overall patency (including partial patency) in case of sequential grafts = 86.8%.

Overall patency (including partial patency) in case of LIMA = 98.5%.

P value is 0.013, implying that the sequential SVGs have superior patency than the individual ones (P < 0.05).

Table IC.

Overall comparison of the patency of sequential and individual venous conduits at 2 years post operatively (data from 0 to 2 yrs).

C. At 2 years post operatively (data from 0 to 2 years)

Outcome No. Of individual SVG No. Of sequential SVG No. Of LIMA pedicled grafts
Patent 219 107 309
Partially patent 28 19 4
Occluded 97 25 10
Total 344 151 323

Overall patency (including partial patency) in case of individual grafts = 71.8%.

Overall patency (including partial patency) in case of sequential grafts = 83.4%.

Overall patency (including partial patency) in case of LIMA = 96.9%.

P value is 0.006, implying that the sequential SVGs have markedly superior patency than the individual ones (P < 0.05).

Table ID.

Overall comparison of the patency of sequential and individual venous conduits at 3 years post operatively (data from 0 to 3 yrs).

D. At 3 years post operatively (data from 0 to 3 years)

Outcome No. of Individual SVG No. of Sequential SVG No. of LIMA pedicled grafts
Patent 197 100 298
Partially patent 34 22 6
Occluded 113 29 19
Total 344 151 323

Overall patency (including partial patency) in case of individual grafts = 67.1%.

Overall patency (including partial patency) in case of sequential grafts = 80.8%.

Overall patency (including partial patency) in case of LIMA = 94.1%.

P value is 0.002, implying that the sequential SVGs have markedly superior patency than the individual ones (P < 0.05).

Table IIAi.

Patency rates for anastomoses on sequential conduits at 6 months post operatively.

II. Overall comparison of the patency of anastomoses on Cx and PDA systems between sequential and individual conduits

A. At 6 months post operatively

i. Patency rates for anastomoses on sequential conduits

Coronary artery system Patent Occluded Total Percentage of patency
Cx (OM1/OM2) 138 13 151 91.4
PDA 137 14 151 90.7
Total 275 27 302

Overall patency for anastomoses on sequential conduits = 275/ 302 × 100 = 91.1%.

Table IIAii.

Patency rates for anastomoses on individual conduits at 6 months post operatively.

ii. Patency rates for anastomoses on individual conduits

Coronary artery system Patent Occluded Total Percentage of patency
Cx (OM1/OM2) 152 20 172 88.4
PDA 156 16 172 90.7
Total 308 36 344

Overall patency for anastomoses on individual conduits = 308/ 344 × 100 = 89.5%.

P value is 0.515, i.e., there is no significant difference between individual and sequential anastomoses.

Table IIBi.

Patency rates for anastomoses on sequential conduits at 1 year post operatively.

B. At 1 year post operatively (data from 0 to 1 year)

i) Patency rates for anastomoses on sequential conduits

Coronary artery system Patent Occluded Total Percentage of patency
Cx (OM1/OM2) 126 25 151 83.4
PDA 128 23 151 84.8
Total 254 48 302

Overall patency for anastomoses on sequential conduits = 254/ 302 × 100 = 84.1%.

Table IIBii.

Patency rates for anastomoses on individual conduits at 1 year post operatively.

ii) Patency rates for anastomoses on individual conduits

Coronary artery system Patent Occluded Total Percentage of patency
Cx (OM1/OM2) 129 43 172 75
PDA 136 36 172 79.1
Total 265 79 344

Overall patency for anastomoses on individual conduits = 265/ 344 × 100 = 77%.

P value is 0.024, implies there is significant difference between individual and sequential anastomoses.

Table IICi.

Patency rates for anastomoses on sequential conduits at 2 year post operatively.

C. At 2 years post operatively (data from 0 to 2 years)

i) Patency rates for anastomoses on sequential conduits

Coronary artery system Patent Occluded Total Percentage of patency
Cx (OM1/OM2) 122 29 151 80.8
PDA 125 26 151 82.8
Total 247 55 302

Overall patency for anastomoses on sequential conduits = 247/ 302 × 100 = 81.8%.

Table IICii.

Patency rates for anastomoses on individual conduits at 2 years post operatively.

ii) Patency rates for anastomoses on individual conduits

Coronary artery system Patent Occluded Total Percentage of patency
Cx (OM1/OM2) 117 55 172 68.0
PDA 130 42 172 75.6
Total 247 97 344

Overall patency for anastomoses on individual conduits = 247/ 344 × 100 = 71.8%.

P value is 0.0004, implies there is significant difference between individual and sequential anastomoses.

Table IIDi.

Patency rates for anastomoses on sequential conduits at 3 years post operatively.

D. At 3 years post operatively (data from 0 to 3 years)

i) Patency rates for anastomoses on sequential conduits

Coronary artery system Patent Occluded Total Percentage of patency
Cx (OM1/OM2) 115 36 151 76.2
PDA 118 33 151 78.1
Total 233 69 302

Overall patency for anastomoses on sequential conduits = 233/ 302 × 100 = 77.2%.

Table IIDii.

Patency rates for anastomoses on sequential conduits at 3 years post operatively.

ii) Patency rates for anastomoses on individual conduits

Coronary artery system Patent Occluded Total Percentage of patency
Cx (OM1/OM2) 105 67 172 61
PDA 126 46 172 73.3
Total 231 113 344

Overall patency for anastomoses on individual conduits = 231/ 344 × 100 = 67.2%.

Table IIIA.

Overall comparison between the patency of anastomoses based on individual coronary artery systems (irrespective of type of anastomoses) at 6 months post operatively.

A) At 6 months post operatively

Coronary artery system Outcome at 6 months P value

Patent Occluded Patency rate (%)
Cx (OM1/OM2) system 290 33 89.78 0.691
PDA system 293 30 90.71

Table IIIB.

Overall comparison between the patency of anastomoses based on individual coronary artery systems at 1 year post operatively.

B) At 1 year post operatively

Coronary artery system Outcome at 1 year P value

Patent Occluded Patency rate (%)
Cx (OM1/OM2) system 255 68 78.95 0.373
PDA system 264 59 81.73

Table IIIC.

Overall comparison between the patency of anastomoses based on individual coronary artery systems at 2 years post operatively.

C) At 2 years post operatively

Coronary artery system Outcome at 2 years P value

Patent Occluded Patency rate (%)
Cx (OM1/OM2) system 239 84 73.99 0.138
PDA system 255 68 78.95

Table IIID.

Overall comparison between the patency of anastomoses based on individual coronary artery systems at 3 years post operatively.

D) At 3 years post operatively

Coronary artery system Outcome at 3 years P value

Patent Occluded Patency rate (%)
Cx (OM1/OM2) system 220 103 68.11 0.036
PDA system 244 79 75.54

Interpretation: Anastomosis on the PDA system is superior to that on the Cx system, irrespective of the type of anastomosis, according to the mid term data; but the same does not hold true prior to that. Further follow up is required to analyse long term patency rates.

1.1. In this study we have attempted to

  1. Draw a comparison between the patency rates of the individual versus sequential conduits, documented 6 months, 1,2 and 3 years post coronary artery bypass surgery

  2. Compare between the patency of anastomoses on individual and sequential saphenous vein grafts, at 6 months, 1,2 and 3 years post surgery

  3. Compare between the patency of anastomoses based on individual coronary artery systems, at 6 months, 1,2 and 3 years post surgery

We are hereby publishing the results of mid term patency with comparison of the patency rates. The aim is to continue this study till ten years of follow up, and compare the long term patency rates.

2. Materials and methods

A total of 323 patients were considered for this prospective study, all had ischaemic heart disease with triple vessel disease. The study was conducted in a single centre, Grant Medical College and Sir JJ Group of Hospitals, Mumbai, India. Total number of female patients were 57 and male patients were 266. Mean age was 62.25 ± 8.62 (Range 42–80) years. Vessel involvements involved the left anterior descending artery (LAD) with or without left main (LM) coronary artery involvement, left circumflex (LCx) in the form of obtuse marginal (OM1/OM2) involvement and posterior descending artery (PDA) involvement. Vessels in which LAD and any other one vessel was involved (double vessel), and those requiring more than three distal anastomoses, were excluded. Documented comorbidities were diabetes mellitus, hypertension, raised creatinine, previous history of transient ischaemic attacks (TIA), chronic obstructive pulmonary disease (COPD), raised liver enzymes. Those with disorders like a severe unresolved cerebrovascular accident (CVA), advanced malignancies, end stage kidney disease, and also concomitant other cardiac abnormalities like valve lesions, aortic root enlargement were excluded. Patients were divided into two randomised cohorts based on Simple Randomisation by a coin flipping technique; undergoing either i) sequential (for heads) or, ii) individual (for tails) saphenous vein coronary artery bypass grafting. No age or sex predilection or ejection fraction predilection was chosen. The patients were operated between February 2014 and June 2017. No patient had simultaneous inclusion of both types of conduits in them.

2.1. Operative technique

Totally 3 surgeons had operated. The bypass surgery was performed on pump at a temperature of 30 °C. Saphenous veins were harvested from the left lower limb by open tecehnique, and in a few occasions, from the right lower limb as well. St. Thomas cardioplegia was used. After going on cardiopulmonary bypass, the heart was subjected to cardioplegic arrest and the distal anastomoses on OM1/OM2, PDA and LAD were performed. Pedicled graft was used for left internal mammary artery to the left anterior descending artery (LIMA-LAD) anastomosis. After rewarming and removing the cross clamp, the proximal anastomoses were performed on the ascending aorta with a side biting clamp; one anastomosis for sequential conduit cases and two, for individual conduits. Average cross clamp time was 47 min and average time on pump was 92 min. The suture material used was 7,0 blue monofilament polypropylene, double armed, for the distal anastomoses and 6,0 blue monofilament polypropylene, double armed, for the proximal anastomoses. The most distal anastomosis on a sequential graft was done in end-to-side fashion. OM anastomoses were constructed side-to-side. Side-to-side anastomoses were done in a diamond-shape (graft axis perpendicular to coronary arteriotomy) and end-to-side anastomoses were done parallel to the native coronary vessel axis.

2.1.1. Group A

Total number of patients who underwent sequential grafting was 151; each patient had two distal anastomoses performed with the sequential saphenous venous conduit - one in the left circumflex artery (LCX) system (Obtuse marginal, either OM 1 or OM 2), and the other in the posterior descending artery (PDA). The proximal anastomosis was done on the ascending aorta. The third anastomosis in each patient was the left internal mammary artery to the left anterior descending artery (LIMA-LAD). Hence the total number of distal anastomoses performed on each patient with the venous conduit was 2, totally 302 for 151 patients.

2.1.2. Group B

Total number of patients who underwent individual venous grafting was 172; each patient had two anastomoses performed with two individual saphenous venous conduits - one in the left circumflex artery (LCX) system (Obtuse marginal, either OM 1 or OM 2), and the other in the posterior descending artery (PDA). Two proximal anastomoses were done on the ascending aorta. The third distal anastomosis in each patient was the LIMA-LAD. Hence the total number of distal anastomoses performed on 172 patients, with the individual venous conduits, was 344.

The total number of distal anastomoses performed using venous conduits was 302 + 344 = 646. If we take the LIMA-LAD anastomoses into account for all the patients, along with the anastomoses performed with venous conduits, then the total number of distal anastomoses performed for all patients is 646 + 151+172 = 969. We have not taken into account the proximal anastomoses.

The patients were discharged by the tenth post operative day, and were followed up from post operative day 15 till date.

2.2. Coronary angiograms

Angiograms were performed at six months, and one, two and three years post operatively. For symptomatic patients post CABG, emergency angiograms were performed. Any emergency angiogram that was done in the interim period between two scheduled angiograms, had its results incorporated in the next scheduled one. The angiograms documented the flow in the conduits, the patency of the conduits and the patency at the anastomotic sites. Proper consent was obtained prior to the invasive modality. Venous conduits were categorized as follows:

  1. patent: no stenosis;

  2. occluded: non-opacified graft;

  3. partially patent: hemodynamically significant (>50%) stenosis, and/or newly developed plaques and/or one open anastomosis through a sequential graft. Graft patency rates included both patent and partially patent grafts.

Anastomotic patency rates were documented for each vessel group or coronary artery system; circumflex, PDA and LAD.

3. Results

The follow up duration has been the maximum for the patients operated in 2014, till date. The last patient considered for the study was operated in June 2017. We are presenting the conduit and anastomotic patency results for the patients who had been operated in 2014–2017.

Each patient underwent 3 distal anastomoses-LIMA-LAD, saphenous venous graft (SVG) - OM1/OM2 (any one) and SVG-PDA.

Total number of patients who underwent sequential SVG grafting was 151 - Group A.

Total number of patients who underwent individual SVG grafting was 172 - Group B.

Total number of anastomoses of sequential SVG grafting - 302 (151 grafts), 151 in OM1/OM2, 151 in PDA.

Total number of anastomoses of individual SVG grafts - 344 (344 grafts), 172 in OM1/OM2, 172 in PDA.

Total number of LIMA-LAD anastomoses - 323.

Hence, the total number of anastomoses evaluated (distal) for all patients = 302 + 344+323 = 969.

3.1. Statistical analysis: using SPSS, documented in the figures and tables section

We observed that:

  1. Sequential conduits tend to have better midterm patency than individual ones, though the difference is not conspicuous in the initial post operative period, viz. 6 months (Tables IA, IB, IC and ID).

  2. Anastomoses on the sequential conduits have better mid-term patency than individual conduits, irrespective of the location of anastomoses, except in the initial period, viz 6 months (Tables IIAi, IIAii, IIBi, IIBii, IICi, IICii, IIDi, IIDii).

  3. Comparison of anastomoses on the PDA system and Cx system (irrespective of the type of conduit), did not lead to conclusive data; requires long term follow up (Tables IIIA, IIIB, IIIC, IIID).

Totally, 67 patients left the study during the course of follow up of 3 years. 11 patients left post complete occlusion of LIMA only, due to presentation in the form of angina or acute coronary syndrome (ACS), when they were managed by graft intervention (redo CABG in 3, percutaneous coronary intervention (PCI) in 8 [10,11]). Post repeat revascularisation their clinical course was uneventful. 4 patients expired post complete single LIMA graft occlusion due to myocardial infarction. 4 patients had symptoms due to both LIMA and SVG graft occlusion, they were managed by PCI. Out of the remaining 48 patients, 10 patients died due to SVG graft occlusion and 38 had angina, ACS, heart failure or arrhythmias, managed by medication and PCI. Total mortality was 14 (4.33%).

4. Discussion

The use of side-to-side anastomoses between veins and additional coronary branches was described by Flemma and colleagues in 1971 [12] and reported in more detail a year later by Bartley and colleagues [13]. Sequential vein grafts have been criticized because occlusion in the most proximal anastomosis may affect several coronary branches and that will result in a large area involving myocardial infarction and jeopardise the patient’s life [14]. However, more authors did not agree with the opinion above. They found that a proximal occlusion of a sequential vein bypass might cause renewed angina, but without infarction in most instances [9,15]. The hypothesis was that in case of a proximal occlusion, the sequential conduit will function as a large collateral vessel [2]. O’Neill and colleagues [16] reported that the proximal segment of the sequential bypass graft has a higher velocity of blood flow than that seen in a single bypass graft, hence a decreased total resistance to graft flow, minimal impedance mismatch, and good long-term patency rate [2]. According to Rittgers et al. [17], there is a reverse relationship between the flow rate and intimal proliferation; increased flow rate transpires into a lesser rate of proliferation. Faulkner et al. [18] also reported that an increased flow rate was associated with less intimal proliferation.

The diameters of SVG segments are relatively constant for a given patient. Also, the resistance posed by the former is negligible when compared to that of its coronary counterpart and hence the native coronary vessel’s resistance remains as the principal determinant of the flow rate. If we assume individual resistances of the grafted coronary arteries to be equivalent, a double sequential graft possesses only half of the resistance of an individual graft. Thus, the individual SVGs are more resistant than the sequential ones [16,19,20].

This brings us to the rationale behind our study. There has been no similar study that has been carried out in the Indian population (though a few Chinese and Korean studies can be accessed) [1,2,21]. As per separate studies conducted by Makaryus et al. [22], and G Y H Lip et al. [23], the coronary arteries of Asian-Indian patients show statistically significantly smaller values in the mean diameters of the coronaries as compared with Caucasians; the values of the mean diameters were, left main (2.96 mm vs 4.04 mm, p = 0.0004), left anterior descending (2.48 mm vs 3.24 mm, p = 0.0005), left circumflex (2.52 mm vs 3.06 mm, p = 0.00002), and right coronary artery (2.71 mm vs 3.65 mm, p = 0.0008) as compared with Caucasians. Smaller diameters lead to more effects on flow than the same degree of stenosis in vessels of larger diameters, as the cross-sectional area would be highly reduced in the former. Thus, a moderate plaque would cause a more significant obstruction in a small vessel [23] and increased resistance by the narrow coronaries. In this scenario, taking the study by Rittgers et al. into consideration, we had hypothesised that an increased flow rate, thus enabling reduced resistance, is essential to ensure prolonged patency in narrower coronaries in the Indian context. The institutional study proved that the mid-term patency is better in case of sequential SVG conduits than the individual ones. Our results are specifically relevant, especially as coronary artery disease is on the brink of an epidemic in the Indian subcontinent, and we need to swiftly document preferred CABG protocols [24], that are alarmingly non existent. Our studies are still underway and long term patencies shall be documented in due course.

Conclusion

Sequential bypass grafts were associated with superior mid-term patency compared with individual grafts, in line with a significant number of studies in the West. Indian data is specifically relevant due to the increasing number of cases and the presence of narrower coronaries.

Abbreviations

CABG

coronary artery bypass grafting

SVG

saphenous venous grafting

OM

obtuse marginal

PDA

posterior descending artery

LM

left main

LCx

left circumflex

TIA

transient ischaemic attacks

COPD

chronic obstructive pulmonary disease

LIMA

left internal mammary artery

Cx

circumflex

Footnotes

Funding

None declared.

Author contributions

Manoj M. Joshi: Conception and design of Study; Literature review; Acquisition of data; Revising and editing the manuscript critically for important intellectual contents; Data preparation and presentation; Supervision of the research; Research coordination and management; Funding for the research.

Saptarshi Paul: Conception and design of Study; Literature review; Research investigation and analysis; Data collection; Drafting of manuscript; Revising and editing the manuscript critically for important intellectual contents; Data preparation and presentation; Supervision of the research; Research coordination and management; Funding for the research.

Krishnarao N. Bhosle: Literature review; Acquisition of data; Research investigation and analysis; Revising and editing the manuscript critically for important intellectual contents; Supervision of the research; Research coordination and management.

Suraj W. Nagre: Literature review; Research investigation and analysis; Drafting of manuscript; Revising and editing the manuscript critically for important intellectual contents; Funding for the research.

Hrishikesh Parashi: Literature review; Acquisition of data; Research investigation and analysis; Data collection; Drafting of manuscript; Revising and editing the manuscript critically for important intellectual contents; Funding for the research.

Vignesh Ravikumar: Acquisition of data; Data collection; Funding for the research.

Vishal Sawkar: Acquisition of data; Data collection; Drafting of manuscript; Funding for the research.

Joshua A Selwyn: Acquisition of data; Data collection; Drafting of manuscript; Funding for the research.

Conflict of interest

None declared.

References

  • 1.Park SJ, Kim HJ, Kim JB, Jung SH, Choo SJ, Lee JW, et al. Sequential versus individual saphenous vein grafting during coronary arterial bypass surgery. Ann Thorac Surg. 2020;109(4):1165–73. doi: 10.1016/j.athoracsur.2019.07.094. [DOI] [PubMed] [Google Scholar]
  • 2.Li J, Liu Y, Zheng J, Bai T, Liu Y, Wang X, et al. The patency of sequential and individual vein coronary bypass grafts: a systematic review. Ann Thorac Surg. 2011;92:1292–8. doi: 10.1016/j.athoracsur.2011.05.038. [DOI] [PubMed] [Google Scholar]
  • 3.Onorati F, Pezzo F, Esposito A, Impiombato B, Comi MC, Polistina M, et al. Single versus sequential saphenous vein grafting of the circumflex system: a flowmetric study. Scand Cardiovasc J. 2007;41(4):265–71. doi: 10.1080/14017430701283864. [DOI] [PubMed] [Google Scholar]
  • 4.Meurala H, Valle M, Hekali P, Somer K, Frick MH, Harjola PT. Patency of sequential versus single vein grafts in coronary bypass surgery. Thorac Cardiovasc Surg. 1982;30(3):147–51. doi: 10.1055/s-2007-1022233. [DOI] [PubMed] [Google Scholar]
  • 5.Lattouf OM, Thourani VH, Kilgo PD, Halkos ME, Baio KT, Myung R, et al. Influence of on-pump versus off-pump techniques and completeness of revascularization on long-term survival after coronary artery bypass. Ann Thorac Surg. 2008 Sep;86(3):797–805. doi: 10.1016/j.athoracsur.2008.04.065. [DOI] [PubMed] [Google Scholar]
  • 6.Synnergren MJ, Ekroth R, Odén A, Rexius H, Wiklund L. Incomplete revascularization reduces survival benefit of coronary artery bypass grafting: role of off-pump surgery. J Thorac Cardiovasc Surg. 2008;136(1):29–36. doi: 10.1016/j.jtcvs.2007.07.059. [DOI] [PubMed] [Google Scholar]
  • 7.Bell MR, Gersh BJ, Schaff HV, Holmes DR, Jr, Fisher LD, Alderman EL, et al. Effect of completeness of revascularization on long-term outcome of patients with three-vessel disease undergoing coronary artery bypass surgery. A report from the Coronary Artery Surgery Study (CASS) Registry. Circulation. 1992 Aug;86(2):446–57. doi: 10.1161/01.cir.86.2.446. [DOI] [PubMed] [Google Scholar]
  • 8.Ouzounian M, Hassan A, Yip AM, Buth KJ, Baskett RJF, Ali IS, et al. The impact of sequential grafting on clinical outcomes following coronary artery bypass grafting. Eur J Cardio Thorac Surg. 2010;38(5):579–84. doi: 10.1016/j.ejcts.2010.03.008. [DOI] [PubMed] [Google Scholar]
  • 9.Meeter K, Veldkamp R, Tijssen JGP, van Herwerden LL, Bos E. Clinical outcome of single versus sequential grafts in coronary bypass operations at ten years’ follow-up. J Thorac Cardiovasc Surg. 1991;101:1076–81. [PubMed] [Google Scholar]
  • 10.Zhao DX, Leacche M, Balaguer JM, Boudoulas KD, Damp JA, Greelish JP, et al. Routine intraoperative completion angiography after coronary artery bypass grafting and 1-stop hybrid revascularization results from a fully integrated hybrid catheterization laboratory/operating room. J Am Coll Cardiol. 2009;53:232–41. doi: 10.1016/j.jacc.2008.10.011. [DOI] [PubMed] [Google Scholar]
  • 11.Task Force on Myocardial Revascularization of the European Society of Cardiology (ESC) and the European Association for Cardio-Thoracic Surgery (EACTS); European Association for Percutaneous Cardiovascular Interventions (EAPCI) Wijns W, Kolh P, Danchin N, Di Mario C, Falk V, Folliguet T, et al. Guidelines on myocardial revascularization. 2555 Eur Heart J. 2010 Oct;31(20):2501. doi: 10.1093/eurheartj/ehq277. [DOI] [PubMed] [Google Scholar]
  • 12.Flemma RJ, Johnson WD, Lepley D., Jr Triple aorto-coronary vein bypass as treatment for coronary insufficiency. Arch Surg. 1971;103:82–3. doi: 10.1001/archsurg.1971.01350070108026. [DOI] [PubMed] [Google Scholar]
  • 13.Bartley TD, Bigelow JC, Page US. Aortocoronary bypass grafting with multiple sequential anastomoses to a single vein. Arch Surg. 1972;105:915–7. doi: 10.1001/archsurg.1972.04180120092017. [DOI] [PubMed] [Google Scholar]
  • 14.Kieser TM, FitzGibbon GM, Keon WJ. Sequential coronary bypass grafts. Long-term follow-up. J Thorac Cardiovasc Surg. 1986;91:767–72. [PubMed] [Google Scholar]
  • 15.Christenson JT, Schmuziger M. Sequential venous bypass grafts: results 10 years later. Ann Thorac Surg. 1997;63(2):371–6. doi: 10.1016/s0003-4975(96)01059-4. [DOI] [PubMed] [Google Scholar]
  • 16.O’Neill MJ, Jr, Wolf PD, O’Neill TK, Montesano RM, Waldhausen JA. A rationale for the use of sequential coronary artery bypass grafts. J Thorac Cardiovasc Surg. 1981;81:686–90. [PubMed] [Google Scholar]
  • 17.Rittgers SE, Karayannacos PE, Guy JF, Nerem RM, Shaw GM, Hostetler JR, et al. Velocity distribution and intimal proliferation in autologous vein grafts in dogs. Circ Res. 1978;42:792–801. doi: 10.1161/01.res.42.6.792. [DOI] [PubMed] [Google Scholar]
  • 18.Faulkner SL, Fisher RD, Conkle DM, Page DL, Bender HW., Jr Effect of blood flow rate on subendothelial proliferation in venous autografts used as arterial substitutes. Circulation. 1975;51&52(suppl I):163–72. [PubMed] [Google Scholar]
  • 19.Bandyk DF, Galbraith TA, Haasler GB, Almassi GH. Blood flow velocity of internal mammary artery and saphenous vein grafts to the coronary arteries. J Surg Res. 1988;44:342–51. doi: 10.1016/0022-4804(88)90176-x. [DOI] [PubMed] [Google Scholar]
  • 20.Vural KM, Senerşener E, Taşdemir O. Long-term patency of sequential and individual saphenous vein coronary bypass grafts. Eur J Cardio Thorac Surg. 2001;19(2):140–4. doi: 10.1016/s1010-7940(00)00629-1. [DOI] [PubMed] [Google Scholar]
  • 21.Kim HJ, Lee TY, Kim JB, Cho WC, Jung SH, Chung CH, et al. The impact of sequential versus single anastomoses on flow characteristics and mid-term patency of saphenous vein grafts in coronary bypass grafting. J Thorac Cardiovasc Surg. 2011 Mar;141(3):750–4. doi: 10.1016/j.jtcvs.2010.05.037. . Epub 2010 Jul 2. [DOI] [PubMed] [Google Scholar]
  • 22.Makaryus AN, Jauhar R, Tortez LM, Pekmezaris R. Comparison of the diameters of the major epicardial coronary arteries by angiogram in Asian-Indians versus European Americans <40 Years of age undergoing percutaneous coronary artery intervention. Am J Cardiol. 2017 Sep 15;120(6):924–6. doi: 10.1016/j.amjcard.2017.06.018. . Epub 2017 Jun 29. [DOI] [PubMed] [Google Scholar]
  • 23.Lip GYH, Rathore VS, Katira R, Watson R, Singh S. Do Indo-Asians have smaller coronary arteries? Postgrad Med. 1999 Aug;75(866):463–6. doi: 10.1136/pgmj.75.886.463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Krishnan MN.Coronary heart disease and risk factors in India - on the brink of an epidemic? Indian Heart J 2012. July-August644364–7. 10.1016/j.ihj.2012.07.001. Epub 2012 Jul 13 [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of the Saudi Heart Association are provided here courtesy of Saudi Heart Association

RESOURCES