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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 28, No 1, January/February 2017

AFRICA

31

Finally, 760 patientswere divided into two groups: ONBHCAB

(group 1) or OPCAB (group 2). To adjust for baseline differences

in parameters between the groups, a propensity score analysis

was carried out and a total of 398 patients were included:

ONBHCAB (

n

=

181), OPCAB (

n

=

217).

Patients’ pre-operative characteristics, such as age and

gender, smoking status, hypertension, diabetes mellitus (DM),

dyslipidaemia, obesity (body mass index

>

30 kg/m²), chronic

obstructivepulmonarydisease(COPD),historyof stroke,peripheral

vascular disease (PVD), history of myocardial infarction (MI),

unstable angina pectoris (USAP), EuroSCORE (European System

for Cardiac Operative Risk Evaluation) risk score, left ventricular

dysfunction, history of percutaneous coronory intervention (PCI),

number of diseased vessels, and the presence of left main coronary

artery (LMCA) stenosis were recorded.

Definitions

Vessel disease was defined as stenosis of more than 50% of

the major epicardial coronary arteries. Estimated creatinine

clearance (CrCl) rate was calculated using the Cockcroft–Gault

formula: CrCl (ml/min)

=

[(140–age)

×

weight (kg)]/[serum

creatinine (mg/dl)

×

72]

×

0.85 for women, from baseline blood

samples. PVD was defined as a stenosis of 50% or more affecting

any non-coronary vasculature.

Left ventricular dysfunction was defined as moderate [ejection

fraction (EF) 0.30–0.49%] or severe (EF

<

0.30%). Complete

revascularisation was defined as treatment of all major coronary

arteries [left anterior descending (LAD), circumflex (Cx) and

right coronary artery (RCA)]

50% diameter stenosis.

Total blood loss was defined as the sum of the mediastinal

and chest tube drainage in the first 48 hours. Consumed units

of red blood cells (RBC) was defined as the sum of the blood

units used during the hospital stay. Any inotropic support

started in the peri-operative period, even low doses of dopamine

infusion due to haemodynamical instability, was determined

as peri-operative need for inotropic support. Peri-operative MI

was defined as cTnI

>

5

µ

g/l during the hospital stay with new

ECG change or echocardiographic evidence of new

regional wall

motion abnormality.

8

Renal complication was defined as at least

100% increase

in basal serum creatinine level. Pulmonary complication was

defined as pleural effusion, atelectasis, phrenic nerve paralysis,

diaphragmatic dysfunction, pneumonia, acute respiratory

distress syndrome, pneumothorax or chylothorax. Neurological

complication was defined as any new transient ischaemic attack

(TIA), stroke or encephalopathy occurring in the peri-operative

period.

Early rehospitalisation was defined as any hospitalisation

due to CABG-related complications (such as sternal dehiscence,

mediastinitis) or cardiovascular problems (such as MI, congestive

heart failure, rhythm disturbance, neurological complications,

pulmonary embolism). Early re-operation was defined as

re-operation due to bleeding or cardiac tamponade and graft

failure.

Surgical procedures

All procedures were performed by the same surgeon, who

made the decision to perform OPCAB or ONBHCAB surgery.

Classic median sternotomy, left internal thoracic artery (LIMA)

harvesting and other conduit preparations were performed

according to a standard technique. In patients undergoing

OPCAB, heparin was administered to keep the activated clotting

time (ACT) greater than 300 seconds.

Distal anastomoses were performed by end-to-side or side-to-

side techniques with a running 7/0 Prolene suture, using a local

myocardial stabiliser (Octopus, Medtronic Inc, Minneapolis,

MN, US). Proximal coronary clamping of all target vessels

was performed with Mueller atraumatic vascular clamps (0.5

Newton); distal occlusion was never performed. Insufflation of

filtered room air (

<

5 l/min) was used to provide better visibility

during anastomosis. During distal anastomosis and reperfusion,

2 ml

/

kg 20%

mannitol was administered. All proximal

anastomoses were performed under single side clamping using

6/0 prolene sutures.

At the end of surgery, heparin was neutralised with protamine,

ensuring that the ACT was between 150 and 180 seconds. In

the early postoperative period (6–8 hours), low molecular-

weight heparin and 100 mg acetylsalicylic acid were commenced

routinely.

In patients undergoing ONBHCAB, heparin was administered

to keep the ACT above 450 seconds. CPB was established with

an ascending aortic arterial cannula and a right atrial two-stage

venous cannula, using a membrane oxygenator and a roller

pump. All patients were cooled to 32–34°C. Mean arterial blood

pressure was maintained in the range of 60–90 mmHg. Distal

anastomoses were performed by end-to-side or side-to-side

techniques with a running 7/0 prolene suture, using a myocardial

stabiliser device (Octopus, Medtronic Inc, Minneapolis, MN,

US). Proximal anastomoses were performed using a 6/0 prolene

suture during the heating period with the assistance of an

ascending aortic side-clamp. After the completion of CPB

and cannula removal, heparin was neutralised with protamine,

providing an ACT

<

150 seconds. Acetylsalicylic acid at a dose

of 100 mg and low molecular-weight heparin was initiated at the

postoperative 24th hour.

The primary endpoint of this study was to compare the early

and long-term MACE rates, defined as cardiac related or sudden

death, MI, the need for repeat revascularisation, and stroke

following ONBHCAB versus OPCAB. The secondary endpoint

was to identify independent predictors of long-term MACE

in these groups of patient. Long-term follow up was obtained

through out-patient clinic visits, hospital records and phone

calls. All-cause mortality (patient death reported by patients’

relatives or hospital records) and MACE were determined.

Statistical analysis

Continuous variables are expressed as mean

±

standard deviation.

Categorical variables are expressed as percentages. A propensity

score analysis was carried out to control selection based on

the baseline variables. The Mann–Whitney

U

-test was used to

compare non-parametric continuous variables, the Student’s

t

-test was used to compare parametric continuous variables, and

the chi-squared test was used to compare categorical variables.

Cumulative survival curves for long-term MACE were

constructed using the Kaplan–Meier method, whereas

differences between the groups were evaluated with log-rank

tests. Multivariate logistic regression analysis was used to identify