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SA JOURNAL OF DIABETES & VASCULAR DISEASE

REVIEW

VOLUME 12 NUMBER 2 • NOVEMBER 2015

71

units. Patients selected for the studies included in the review were

treated to ‘moving targets’ and therefore studies conducted in the

past five years only (2009–2014) were included, as recent guidelines

have more similar targets.

Some eight out of the 14 studies provided information on the type

of methods used for clinical and laboratory-based measurements,

but with differing levels of detail. Notably, only two studies confirmed

use of DCCT-standardised laboratory analysers for HbA

1c

analysis.

By converting to similar units (e.g. LDL-C from mg/dl to mmol/l),

target values in this retrospective study (Table 1) were presented

in a format that would allow for comparison. Ideally, a centralised

laboratory should have been used for measurements included in

this study, however, we relied on previously obtained measurements

from other studies. We therefore cannot guarantee the accuracy or

precision of measurements in the studies selected for this review,

as methodologies may have differed. Studies from resourcerich

settings may have implemented newer, more sophisticated and

improved methods for A

1c

and LDL-C measurements, influencing

the results of those specific studies.

This review did not stratify the selected individual studies according

topatient profiles, severity of disease, clinical settings (clinic or hospital)

or involvement of specialists (factors affecting how individuals are

managed and able to reach guideline targets). Although smoking is

considered a critical risk factor in the prevention and management of

CVD, it was not included as a crucial study parameter for this review

(partly due to many studies not reporting this).

Although previously identified as a source of bias, we only

included studies published in English, which according to an

analysis, has little effect on summaries of treatment effect

estimates.

28

Publication bias may have occurred in our study in that

a single reviewer (author) carried out the searches without the use

of specific methodology (e.g. Cochrane data system).

Conclusion

The results presented in this study demonstrate that T2DM patients

remain inadequately controlled for their cardiovascular risk factors.

Our review revealed that control of major risk factors did not

differ significantly between countries or healthcare settings. There

is substantial room for improvement in the way T2DM patients

are being managed for their condition. Further efforts through

multidisciplinary action to improve guideline adherence is critical

for the prevention or delay of diabetesrelated complications.

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