DM Full Guideline (2010) - VA/DoD Clinical Practice Guidelines Home
DM Full Guideline (2010) - VA/DoD Clinical Practice Guidelines Home
DM Full Guideline (2010) - VA/DoD Clinical Practice Guidelines Home
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Version 4.0<br />
<strong>VA</strong>/<strong>DoD</strong> <strong>Clinical</strong> <strong>Practice</strong> <strong>Guideline</strong><br />
for the Management of Diabetes Mellitus<br />
Biguanides<br />
Metformin<br />
Metformin XR<br />
1.0-2.0% Negligible<br />
risk as<br />
monotherapy<br />
• Use well-established<br />
• May restore ovulation in<br />
premenopausal anovulatory<br />
females<br />
• Monitor renal function prior to<br />
and at least annually thereafter<br />
• Weight neutral or slight weight<br />
loss<br />
• Decrease LDL-C<br />
• Contraindicated in:<br />
o Renal dysfunction (serum<br />
creatinine ≥ 1.5mg/dL<br />
[males]; ≥ 1.4mg/dL<br />
[females] or abnormal<br />
creatinine clearance ,<br />
30ml/min)<br />
o Acute or chronic metabolic<br />
acidosis<br />
• Temporarily discontinue<br />
metformin at the time of or prior<br />
to intravascular iodinated radio<br />
contrast studies and withhold for<br />
48 hours after the procedure.<br />
Reinstitute only after renal<br />
function has been reevaluated and<br />
found to be normal.<br />
• Temporarily discontinue for<br />
surgical procedures (except minor<br />
procedures not associated with<br />
restricted intake of food or fluids).<br />
Do not restart until oral intake has<br />
resumed and renal function has<br />
been evaluated as normal.<br />
• Do not use if patient is ≥80 years<br />
of age unless measurement of<br />
creatinine clearance demonstrates<br />
that renal function is not reduced;<br />
do not titrate to maximum dose.<br />
• In general, avoid metformin in<br />
patients with clinical or laboratory<br />
evidence of hepatic disease<br />
• Patients should be warned against<br />
excessive acute or chronic alcohol<br />
use.<br />
• Discontinue metformin in the<br />
presence of cardiovascular<br />
collapse<br />
• Patients with unstable or acute<br />
congestive heart failure who are at<br />
risk of hypoperfusion and<br />
hypoxemia are at increased risk of<br />
lactic acidosis<br />
• Inexpensive<br />
• Potential for lactic<br />
acidosis when used<br />
in patients for whom<br />
the drug is<br />
contraindicated<br />
• Transient doserelated<br />
GI symptoms<br />
(nausea, vomiting,<br />
bloating, flatulence,<br />
anorexia)<br />
• Decrease in vitamin<br />
B12 levels<br />
Module G: Glycemic Control: Appendices Page 82