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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 29, No 5, September/October 2018

AFRICA

281

35%.

10

Operators tend to overestimate severe stenosis, whereas

modest stenosis is underestimated.

11

In our study, we found a moderate degree of concordance

between visual operators in the categories 70–89 and 90–99%.

There was a low degree of concordance between visual operators

in the categories

<

50 and 50–69%. These results show that

especially in cases of moderate and low degree of stenosis, inter-

observer variability increases.

QCA of coronary stenosis eliminates inter-observer bias

and enables reproducible measurements. QCA is also useful

for prediction of coronary restenosis after different coronary

interventional techniques.

12

It may also be used to follow the

natural course of atherosclerosis. A decrease in the minimal

lumen diameter and an increase in the percentage diameter of

stenosis determined by QCA in follow-up coronary angiography

was associated with increased coronary events. Change in

minimal lumen diameter was the strongest predictor of coronary

events.

13

When we compared the results of visual estimation with

QCA, we found significant differences between visual estimation

and QCA in percentage diameter of stenosis and percentage area

of stenosis. We also found differences between implanted stent

diameter and reference diameter calculated by QCA and between

stent length and lesion length derived from QCA. That means

there is variability between implanted stent diameter and length

and true size of the lesion. Physicians tended to implant larger

and longer stents. The difference between mean diameter of

implanted stent and mean reference diameter was 0.22 mm and

the difference inmean length of the implanted stent and the lesion

was 1.79 mm. Although statistically significant, this difference

was not so great as to cause clinically important consequences.

The important point is to cover the whole atherosclerotic

segment with an optimal sized stent. Theoretically, choosing a

longer stent size may increase the risk of stent restenosis in the

future.

Twenty-three lesions considered significant according to visual

estimation were found not to be significant when determined by

QCA. This means that approximately 15% of patients, or one in

seven, underwent unnecessary intervention.

When comparing the difference between percentage diameter

of stenosis and percentage area of stenosis in determining the

severity of stenosis, there was a statistically significant difference

between the QCA-derived parameters (58.4

±

14.5 vs 80.6

±

11.2%). Percentage area of stenosis had a low to moderate grade

of concordance with visual estimation, whereas there was no

concordance between percentage diameter of stenosis and visual

estimation. Percentage diameter of stenosis may underestimate

the lesion.

In a study by Gottsauner-Wolf

et al

., it was shown that

percentage area of stenosis more closely reflected the visual

estimation of lesion severity than percentage diameter of

stenosis.

14

In another study, the authors used dobutamine stress

echocardiography to determine the cut-off values of QCA

parameters in estimation of the functional significance of

coronary lesions. Angiographic cut-off values were determined

as ≤ 1.07 mm, ≥ 75% and ≥ 52% for minimal lumen diameter,

percentage area of stenosis and percentage diameter of stenosis,

respectively. The cut-off value for percentage diameter of

stenosis was much less than the cut-off value for percentage area

of stenosis.

15

Similar to the results of our study, percentage area

of stenosis was prone to underestimate the lesion if the cut-off

value was accepted as 70%. If percentage diameter of stenosis is

used as QCA parameter, it may be more suitable to accept the

cut-off value as 50%.

There are a few early trials comparing visual assessment

with QCA. Older QCA software systems did not have the

technology that we have today.

2-8

Modern QCA software systems

have advanced digital technology enabling more accurate and

complex assessment.

There is only one recent study comparing visual assessment

of severity of coronary lesions and QCA measurement. In this

study, similar to our study, Nallamothu

et al

. showed that visual

assessment tended to overestimate the lesion more than QCA.

Inconsistency between QCA and visual assessment was high,

especially in cases of moderately severe coronary lesions.

9

QCA is a non-invasive and cheap method of quantification of

coronary stenosis and measurement of reference vessel diameter

for deciding the size of the stent. Despite its limitations, such as

vessel foreshortening, it enables well-correlated measurements of

lesion length, minimal lumen diameter and reference diameter. It

also may prevent unnecessary PCI.

Conclusion

Visual estimation may overestimate a coronary lesion and may

lead to unnecessary coronary intervention. There was low

concordance in the categories

<

50% and 50–69% between the

operators. Percentage area of stenosis had a low to moderate

grade of concordance with visual estimation. Percentage area

of stenosis more closely reflected the visual estimation of lesion

severity than percentage diameter of stenosis.

References

1.

Gensini GG, Kelly AE, Da Costa BCB. Quantitative angiography: the

measurement of coronary vasomobility in the intact animal and man.

Chest

1971;

60

: 522–530.

Table 5. Comparison of concordance between visual estimation and

percentage area of stenosis with kappa analysis

Visual percentage

of stenosis

Percentage area of stenosis by QCA,

n

(%)

Kappa

p

-value

50

69% 70

89% 90

99% Total

50

69%

2 (33.3) 4 (66.7) 0 (0)

6 (100)

0.300 0.000**

70

89%

17 (22.7) 53 (70.7) 5 (6.7) 75 (100)

90

99%

6 (8.1) 32 (43.2) 36 (48.6) 74 (100)

Total

25 (15.6) 89 (57.8) 41 (26.6) 155 (100)

**

p

<

0.01.

Table 6. Comparison of concordance between visual estimation and

percentage diameter of stenosis with kappa analysis

Visual percentage

of stenosis

Percentage diameter of stenosis by QCA,

n

(%)

Kappa

p

-value

< 50% 50–69% 70–89% 90–99%

< 50%

0 (0)

0 (0)

0 (0)

0 (0)

–0.061 0.000**

50–69%

3 (50)

3 (50)

0 (0)

0 (0)

70–89%

29 (53) 42 (56)

4 (38.7) 0 (0)

90–99%

11 (14.9) 31 (41.9) 27 (36.5) 5 (6.8)

Total

43 (27.7) 76 (49.0) 31 (20.0) 5 (3.2)

**

p

<

0.01.