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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 27, No 6, November/December 2016

348

AFRICA

Discussion

Our study shows that BVS implantation in CTO lesions appeared

to be effective and safe in terms of acute procedural and short-

term clinical follow-up results.

Theoretically, complete resorption of BVS, which is used

for treating complex and calcific lesions, such as CTOs, seems

to be advantageous. Lack of a metallic cage in these lesions

can decrease the risk of restenosis, especially in the long term.

Restoration of the vessel’s vasomotor functions may be easier

with BVS implantation than with metallic stents.

Since patients with complex lesions such as CTOs have a

greater risk for future CABG surgery, resorption of BVS in the

treated segment may facilitate the performance of future graft

anastomosis. However, in practice, the real effectiveness and

safety of the use of BVS in CTO lesions are unclear and long-

term clinical results are lacking. A few records and case reports

have been published in the literature which analyse the role of

BVS implantation in CTO lesions.

14-17

The baseline characteristics of our patients were similar

to those in previous BVS studies including patients with

CTO lesions.

14-16

In addition the cardiovascular risk profile of

our patients was high and parallel with real-life records that

investigate the effect of regular PCI procedures in CTO lesions.

Our mean BVS length was shorter than in previous studies.

14,15

Most of our CTO lesions were within the treatable length of

one BVS. Only 11 patients were treated with double BVS and

no patients were treated with more than two BVSs. Although we

had similar TLR rates and short-term clinical results with the

BVS CTO studies, which included longer CTO lesions treated

with a larger number of BVSs, studies with longer follow up

beyond the resorption period of BVSs are needed in order to

clearly determine the effect of scaffolds.

It is known that longer CTOs treated with a larger number

of metallic stents have a greater risk of restenosis and worse

clinical outcomes during follow up.

18,19

Currently, we do not

know whether complete resorption of the implanted scaffolds

eliminates the risk of restenosis in long CTO segments in the

long term.

Although BVS has thick struts (150 µm), a low crossing

profile and less distensibility, our procedural success rate was

100% in our patient group. The main reasons for procedural

success are effective dilatation after wiring the lesions, exact

scaffold sizing with the aid of quantitative coronary angiography

(QCA) measurements, and a high rate of post-dilatation. Lesion

preparation before BVS implantation is a crucial factor, especially

for CTO lesions.

Since a non-compliant balloon (NCB) reduces the procedure

time compared with the compliant balloon,

20

and is advised by

many experienced centres,

21,22

we preferred NCB for effective

dilatation after pre-dilatation with lower-profile balloons. Also,

a cutting balloon and rotablator can be used if needed. We

performed post-dilatation in almost every lesion, mainly with a

non-compliant balloon. We did not use balloons that had a size

of more than 0.5 mm larger than the implanted BVS diameter.

Post-dilatation with an inappropriate size of balloon can lead to

fracture of the BVS in heavily calcific CTO lesions. We did not

experience BVS fracture in our patient group.

Despite our high procedural success rate, implanting BVS

in CTO lesions should be reserved for less complex CTO

lesions, since experience is still limited. The J-CTO score, which

characterises lesion complexity, could be a useful tool for

decision making on indication. According to previous studies,

CTO lesions that have a score of more than three (very difficult

category) are associated with an unsuccessful procedure.

14,23

The

majority of our lesions were within the intermediate category

according to the J-CTO score (56%). More complex lesions with

a higher J-CTO score could affect procedural success and clinical

outcomes.

During CTO procedures, jailing of the major side branches

could be a problem, affecting the success of the procedure.

14,15

Complete resorption of the BVS at the site of the bifurcation

could lessen the effect of jailing and help return the side branch

to normal vasomotor function. In our study, six side branch

occlusions and four side branch narrowings were observed

because of scaffold jailing. All of these lesions were treated with

a provisional strategy with final kissing balloon dilatation.

Intravascular ultrasound (IVUS) and optical coherence

tomography (OCT) are very valuable tools for evaluating the

apposition of BVS during implantation.

12

Not using IVUS

or OCT is a limitation of our study but we had used QCA

measurements for exact sizing of the BVS.

Since our study was non-randomised and lacked a control

group, one should be cautious when interpreting the clinical

data. A randomised study with a larger number of patients

would be more valuable for evaluating the clinical outcomes.

Our clinical follow-up results are too limited to evaluate the real

clinical effectiveness of the use of BVS in CTO lesions. One year

is a short follow-up period and cannot answer the question as

Table 2. Procedural characteristics

Procedure

n

= 41 patients

n =

52 BVS (%)

BVS diameter, mm

2.8

±

0.29

BVS length, mm

25.6

±

4.2

Post-dilatation

40 (97.5)

Post-dilatation with NCB

38 (92.6)

RVD post-procedure, mm

2.8

±

0.25

MLD post-procedure, mm

2.5

±

0.25

Side-branch occlusion

6 (11.5)

Side-branch narrowing

4 (7.6)

CTO technique

Antegrade

36 (87.8)

Retrograde

5 (12.1)

Microcathater use

13 (31.7)

Procedure time, min

92

±

35.6

Fluoro time, min

20.2

±

4.8

Contrast volume, ml

146.6

±

26.7

BVS: bioresorbable vascular scaffold, CTO: chronic total occlusion, MLD:

minimal lumen diameter, NCB: non-compliant balloon, RVD: reference vessel

diameter.

Table 3. Clinical outcomes

One-year outcome

n

= 41 patients (%)

Death

Myocardial infarction

1 (2.4)

Angina

11 (26.8)

Coronary artery bypass graft

Target-lesion revascularisation

1 (2.4)

Target-vessel revascularisation

5 (12.2)