2008 Clinical Practice Guidelines - Canadian Diabetes Association
2008 Clinical Practice Guidelines - Canadian Diabetes Association
2008 Clinical Practice Guidelines - Canadian Diabetes Association
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<strong>2008</strong> CLINICAL PRACTICE GUIDELINES<br />
S102<br />
Vascular Protection in People With <strong>Diabetes</strong><br />
<strong>Canadian</strong> <strong>Diabetes</strong> <strong>Association</strong> <strong>Clinical</strong> <strong>Practice</strong> <strong>Guidelines</strong> Expert Committee<br />
The initial draft of this chapter was prepared by David Fitchett MD FRCPC and Maria Kraw MD<br />
FRCPC<br />
KEY MESSAGES<br />
• The first priority in the prevention of macrovascular<br />
complications should be reduction of cardiovascular<br />
(CV) risk through a comprehensive, multifaceted<br />
approach, integrating both lifestyle and pharmacologic<br />
measures.<br />
• Treatment with angiotensin-converting enzyme (ACE)<br />
inhibitors has been shown to result in better outcomes<br />
for people with atherosclerotic vascular disease, recent<br />
myocardial infarction, left ventricular impairment and<br />
heart failure. In a similar population, angiotensin II<br />
receptor antagonists have been shown to be noninferior<br />
to ACE inhibitors for vascular protection.<br />
• Low-dose acetylsalicylic acid therapy may be considered<br />
in people with stable CVD.The decision to prescribe<br />
antiplatelet therapy for primary prevention of<br />
CV events, however, should be based on individual<br />
clinical judgment.<br />
VASCULAR PROTECTION<br />
In order to reduce the excessive cardiovascular disease<br />
(CVD) risk associated with diabetes, all coronary risk factors<br />
must be addressed and treated aggressively. The Steno-2<br />
studies (1,2) demonstrated that a target-driven, comprehensive,<br />
multifaceted approach to risk factor management<br />
applied to high-risk patients with type 2 diabetes and<br />
microalbuminuria over a period of 7 years resulted in a<br />
>50% reduction of CVD (HR 0.47, 95% CI, 0.24–0.73)<br />
*See also “Identification of Individuals at High Risk of Coronary Events,” p. S95<br />
BP = blood pressure<br />
CAD = coronary artery disease<br />
CV = cardiovascular<br />
and microvascular events (nephropathy HR 0.39, 95% CI,<br />
0.17–0.87; retinopathy HR 0.42, 95% CI, 0.21–0.86). It is<br />
likely that similar relative benefits would be achieved by<br />
applying a comprehensive, multifaceted approach to risk factor<br />
control in high-risk patients with diabetes who do not<br />
have microalbuminuria.<br />
Patients at the highest risk for CV events include those<br />
who have diabetes and atherosclerotic vascular disease that<br />
includes either clinically recognized disease (e.g. coronary<br />
artery disease [CAD], peripheral arterial disease [PAD] and<br />
cerebrovascular disease) or clinically silent disease (e.g.<br />
silent myocardial ischemia or infarction, and PAD identified<br />
by the presence of bruits or abnormal ultrasound or anklebrachial<br />
index). Other patients at high risk include those<br />
with microvascular disease and multiple risk factors or<br />
extreme levels of a single risk factor (Table 1) (see also<br />
“Identification of Individuals at High Risk of Coronary<br />
Events,” p. S95).<br />
When deciding on appropriate treatment strategies, it is<br />
important to prioritize treatment goals. Since some of the<br />
available treatments, such as angiotensin converting enzyme<br />
(ACE) inhibitors and angiotensin II receptor antagonists<br />
(ARBs), have potential uses in controlling blood pressure<br />
(BP) as well as reducing the risks for CVD and nephropathy,<br />
it can be challenging to integrate the data to make recommendations<br />
for one application over another.Table 2 summarizes<br />
the priorities for vascular and renal protection, while<br />
Table 3 summarizes recommended interventions for vascular<br />
protection.<br />
Table 1. People with diabetes considered at high risk of a CV event*<br />
• Men aged ≥45 years, women aged ≥50 years<br />
• Men 180 mm Hg)<br />
• Duration of diabetes >15 years with age >30 years<br />
LDL-C = low-density lipoprotein cholesterol<br />
MI = myocardial infarction<br />
PAD = peripheral arterial disease