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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

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