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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 28, No 3, May/June 2017

194

AFRICA

We know that renal dysfunction is a serious complication of

coronary revascularisation with CABG and results in increased

morbidity and mortality rates and prolonged hospital stay.

18

The injurious action of CABG on renal function is caused

by several mechanisms, including non-pulsatile perfusion and

increased levels of circulating catecholamines, cytokines and

free haemoglobin.

19

These effects result in damage to the

glomerular as well as tubular structures, which, in turn, may

cause renal dysfunction, especially in the presence of additional

risk factors.

20-21

Microalbuminuria is one of the sensitive markers of increased

capillary permeability and may be useful to study the systemic

inflammatory response after CABG.

6,22,23

According to previous

investigations, urinary microalbuminuria increased significantly

in the early postoperative period and one day after CABG.

In our study, peak increase in microalbuminuria was observed

in both groups but there was no statistically significant difference

(

p

=

0.071). These levels decreased, particularly on the fifth day in

our cases, and the decrease was statistically significantly different

in group T. In both groups, hsCRP increased and peaked on

the first postoperative day in both groups. However, in group

T, hsCRP, as one of the pro-inflammatory agents, decreased

significantly on the fifth day. Therefore, the increase in acute

inflammatory response was similar in both groups on the first

postoperative day, and in group T, both markers had decreased

by the fifth day.

Borch-Johnsen

et al

. showed the direct relationship between

proteinuria and cardiovascular mortality rate in insulin-

dependent diabetic patients after open-heart surgery in patients

undergoing CABG.

24

Telmisartan was also shown to reduce or

normalise microalbuminuria in 34% of patients with diabetes,

and in a second, smaller study including 64 hypertensive

and 60 normotensive patients, to reduce the incidence of

renal dysfunction. This confirmed that telmisartan reduced

microalbuminuria independently of its blood pressure-lowering

effects. Restoration of normal urine albumin levels has also been

demonstrated by telmisartan.

25

Our study showed that telmisartan reduced

microalbuminuria, not only pre-operatively, but also after

open-heart surgery. The return to baseline levels was also faster

than in group N-T. Angiotensin receptor blocking agents

decrease some of the postoperative acute inflammatory agents

in on-pump CABG patients with diabetes mellitus by lessening

the systemic consequences of renal dysfunction, and may have

additional cardiovascular effects by exerting beneficial effects

on endothelial tissue elsewhere in the body and within the

heart in this patients group. The cardiovascular benefits of

angiotensin receptor antagonists have been evaluated, not only

in terms of their ability to lower blood pressure, but also on

their ability to prevent strokes, cardiac events and target-organ

damage.

14,16

Limitations of our study are the relatively small size of our

series and the lack of definite criteria for selection of patients

for this study. As most coronary patients are already being

treated with angiotensin receptor blocking agents, the results

of our study will not have a major impact on clinical practice.

Furthermore, it would have been better to test the predictive

value of microalbuminuria on prognosis in this category of

patients. However, we hope that this study will pioneer further

studies on this method.

Conclusion

Our results showed that telmisartan decreased systemic

inflammation and urinary albumin excretion in diabetic patients

after CABG surgery, compared to those not taking angiotensin

receptor antagonists. These beneficial effects of telmisartan

treatment on diabetic patients after CABG should be investigated

further in prospective, randomised studies.

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