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SA JOURNAL OF DIABETES & VASCULAR DISEASE

RESEARCH ARTICLE

VOLUME 13 NUMBER 2 • DECEMBER 2016

71

6A–C, the pooled OR was 0.28 (95% CI: 0.16–0.48,

p

< 0.01,

Fig. 6A) for SES versus BMS in studies whose sample size was

above 90, with heterogeneities between the studies (

Q

2

= 8.7,

I

2

= 77%,

p

< 0.1). The pooled OR was 0.61 (95% CI: 0.31–1.21,

p

> 0.05, Fig. 6A) in studies whose sample size was 90 or less,

without heterogeneities between the studies (

Q

2

= 2.39,

I

2

= 16%,

p

> 0.1).

The pooled OR was 0.45 (95%CI = 0.27–0.77,

p

< 0.01, Fig. 6B)

in studies whose subjects were European, without heterogeneities

between the studies (

Q

2

= 3.71,

I

2

= 46%,

p

> 0.1). The pooled OR

was 0.37 (95% CI: 0.11–1.27,

p

> 0.05, Fig. 6B) in studies whose

subjects were American and Asian, with heterogeneities between

the studies (

Q

2

= 15.55,

I

2

= 87%,

p

< 0.1).

The pooled OR was 0.28 (95% CI: 0.19–0.42,

p

< 0.01, Fig. 6C)

in studies whose study method was RCT, without heterogeneities

between the studies (

Q

2

= 2.4,

I

2

= 0%,

p

> 0.1). The pooled OR

was 0.87 (95% CI: 0.61–1.24,

p

> 0.05, Fig. 6C) in studies whose

method of study was non-RCT, without heterogeneities between

the studies (

Q

2

= 0.92,

I

2

= 0%,

p

> 0.1).

By removing one study at a time, a sensitivity analysis was

performed and the model was rerun to determine the effect on

each estimate. It showed that the above meta-analysis estimates

did not change significantly after removal of each study, implying

that these results were statistically reliable.

Discussion

A growing number of studies has shown the efficacy and safety

of SES versus BMS for treating CAD patients with diabetes,

9,29

but

the outcome has been controversial. In this analysis, we retrieved

six studies, which included 1 259 CAD subjects with diabetes, and

performed a meta-analysis. It showed that the SES group had a

significant reduction in major adverse cardiac events, as well as

target-lesion revascularisations, compared with the BMS group.

There was no significant difference for myocardial infarction or

mortality.

These results are consistent with a recent study that suggested

a significant reduction in target-vessel revascularisations with SES,

but with similar mortality rates.

9

Unlike this study, in which the

incidence of myocardial infarction was higher, our analysis showed

no difference for myocardial infarctions between the groups.

Another recent study conducted in Europeans confirmed the

efficacy of SES compared with BMS, along with comparable

Fig. 5.

Forest plots of studies with mortality events in the SES group versus the BMS group.

Fig. 6. A

: Forest plots of sample size subgroups.