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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Pharmacotherapy<br />
Pharmacotherapy for overweight people with diabetes not<br />
only improves glycemic control, but also results in a significant<br />
reduction in the doses of antihyperglycemic agents (26).<br />
Pharmacotherapy is an acceptable adjunct in the short- and<br />
long-term management of obesity when lifestyle measures<br />
fail to achieve the desired weight loss after an adequate trial<br />
of 3 to 6 months (20,35). Pharmacotherapy can be considered<br />
for people with BMI ≥30.0 kg/m 2 with no obesityrelated<br />
comorbidities or risk factors, or BMI ≥27.0 kg/m 2<br />
with obesity-related comorbidities or risk factors (20).<br />
Antiobesity drug therapy may be considered as an adjunct to<br />
nutrition therapy, physical activity and behaviour modification<br />
to achieve a target weight loss of 5 to 10% of initial body<br />
weight and for weight maintenance (20,35).<br />
Two medications, orlistat and sibutramine, have been<br />
approved in Canada for long-term management of obesity<br />
(Table 4). Drug therapy leads to even greater weight loss<br />
when coupled with lifestyle intervention and behaviour modification<br />
therapy. Both drugs have been shown to be effective<br />
in obese people with type 2 diabetes, improving glycemic and<br />
metabolic control, and resulting in favourable changes in lipid<br />
levels, BP profile and fat distribution (26,36,37). In obese<br />
people with impaired glucose tolerance (IGT), orlistat also<br />
improves glucose tolerance and reduces the progression to<br />
type 2 diabetes (38). <strong>Clinical</strong> trials with antiobesity agents<br />
have confirmed a smaller degree of weight loss in people with<br />
diabetes compared with obese people who do not have diabetes<br />
(14,26).<br />
When pharmacotherapy is being considered in the treatment<br />
of the obese or overweight person with type 2 diabetes,<br />
the choice of drug should be based on the individual’s<br />
CV risk profile, dietary habits and concomitant disease(s).<br />
People with irregular eating habits, such as those who “snack”<br />
frequently, may be better suited to sibutramine therapy<br />
because of its long-acting satiety-enhancing properties.<br />
Combining orlistat and sibutramine therapy is not advocated<br />
for clinical use. Sibutramine should be avoided in patients<br />
with ischemic heart disease, congestive heart failure or other<br />
major cardiac disease. Orlistat should be avoided in patients<br />
with inflammatory or other chronic bowel disease.<br />
Other available antiobesity drugs, such as diethylpropion<br />
and phentermine, are sympathomimetic noradrenergic<br />
appetite suppressants that are approved only for short-term<br />
use of a few weeks. They are not recommended because of<br />
modest efficacy and frequent adverse side effects.<br />
Currently, a number of new molecular entities that target<br />
receptors and metabolic processes relevant to energy<br />
metabolism are being developed for the treatment of obesity.<br />
Among these emerging strategies, cannabinoid type 1<br />
receptor antagonists currently appear to be the most promising<br />
(39).<br />
Surgery<br />
Individuals who are candidates for surgical procedures<br />
should be carefully selected after evaluation by an interdisciplinary<br />
team with medical, surgical, psychiatric and nutritional<br />
expertise. Surgery is usually reserved for people with<br />
class III obesity (BMI ≥40.0 kg/m 2 ), or class II obesity<br />
(BMI=35.0–39.9 kg/m 2 ) in the presence of comorbidities<br />
(40) and the inability to achieve weight-loss goals following<br />
an adequate trial of lifestyle intervention. Long-term, if not<br />
lifelong, medical surveillance after surgical therapy is necessary<br />
for most people. Preferred surgical options for weight<br />
loss include laparoscopic vertical banded gastroplasty and<br />
laparoscopic Roux-en-Y gastric bypass (41-43).<br />
Table 4. Medications approved for the treatment of obesity in type 2 diabetes<br />
Class Generic (trade)<br />
name<br />
Gastrointestinal lipase<br />
inhibitor<br />
Norepinephrine and<br />
serotonin reuptake<br />
inhibitor<br />
Recommended<br />
regimen<br />
orlistat (Xenical) 120 mg TID (during or<br />
up to 1 hour after each<br />
meal)<br />
sibutramine (Meridia) 10–15 mg OD<br />
(in the morning)<br />
Action Adverse<br />
effects<br />
• Nonsystemic pancreatic<br />
lipase inhibitor<br />
that exerts its therapeutic<br />
activity in the<br />
stomach and gastrointestinal<br />
tract by<br />
reducing dietary fat<br />
digestion and absorption<br />
by about 30%<br />
• Reduces food intake<br />
by enhancing satiety<br />
• May increase thermogenesis<br />
• May prevent decline<br />
in energy expenditure<br />
with weight loss<br />
• Abdominal bloating,<br />
pain and cramping<br />
• Steatorrhea<br />
• Fecal incontinence<br />
• Xerostomia<br />
• Increase heart rate<br />
and blood pressure<br />
• Constipation<br />
• Dizziness<br />
S79<br />
MANAGEMENT