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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 />

These studies also reveal that oral agents are often used rather than insulin, and when insulin is ordered, sliding scale<br />

monotherapy is common. Lastly, insulin is infrequently adjusted after the initial order.<br />

Hypoglycemia<br />

Hypoglycemia is the most common complication associated with inpatient glycemic control, and is one of the<br />

leading adverse outcomes limiting the quality of trials addressing the benefits of intensive glycemic control<br />

(Brunkhorst et al., 2008; Gandhi et al., 2008; Finfer et al., 2009). In a recent meta-analysis by Griesdale et al.,<br />

among the trials that reported hypoglycemia, the pooled relative risk with intensive insulin therapy was 6.0 (95% CI<br />

4.5-8.0)(Griesdale et al., 2009). As such, the fear of hypoglycemia remains one of the most common barriers to the<br />

implementation of inpatient diabetes care strategies. Studies of hypoglycemia during hospitalization have identified<br />

factors that increase the risk for hypoglycemia; some of these include heart failure, renal or liver disease,<br />

malignancy, infection, or sepsis. Additional precipitating factors which can further increase the likelihood of<br />

inducing hypoglycemia include changing clinical condition, reduction of corticosteroid dose, reduction in the<br />

amount of nutrition (e.g. interruption of enteral feeding or intravenous dextrose, NPO status), vomiting, and<br />

inappropriate timing of short- or rapid-acting insulin in relation to meals (Smith et al., 2005; Krinsley et al., 2007;<br />

Fischer et al., 1986). Therefore, in order to prevent and promptly manage hypoglycemia, standardized protocols to<br />

treat hypoglycemia should be in place for nurses to implement immediately without an additional order from the<br />

physician. As with other adverse events in the hospital, instances of severe hypoglycemia should be documented and<br />

a root-cause analysis can be helpful. Monitoring such episodes and analyzing their cause can be used to eliminate<br />

future occurrences of these episodes.<br />

Some studies have demonstrated a relationship between hypoglycemia and increased mortality, however it is unclear<br />

if hypoglycemia is a marker of severe illness that is frequently observed in individuals with serious comorbidities<br />

such as sepsis, hepatic and renal failure, or if it is a direct cause of adverse outcomes. Several recent studies that<br />

control for these comorbidities or segregate the analysis based on spontaneous versus iatrogenic hypoglycemia are<br />

reassuring in that they have demonstrated no association between iatrogenic hypoglycemia and mortality (Kagansky<br />

et al., 2003; Vriesendorp et al., 2006; Kosiborod et al., 2009). Nevertheless it remains unclear what the<br />

consequences of hypoglycemia are during severe illness and how these sequelae may vary based on acute vs.<br />

chronic complications or susceptibility in different disease states.<br />

Oral anti-hyperglycemic agents<br />

Various circumstances and conditions related to hospitalization increase the likelihood of adverse effects typically<br />

associated with the use of oral agents. These include derangements in renal, cardiovascular, and hepatic function;<br />

changes in hemodynamic and fluid status; frequent changes in nutritional status; a rapidly changing clinical<br />

condition; and imaging studies requiring contrast. Because of the safety concerns, the use of oral agents should be<br />

discouraged for most hospitalized patients. However, in some hospitalized patients who are medically stable and<br />

have been controlled prior to admission with oral agents, the continuation of these medications may be of less risk<br />

than the initiation of insulin.<br />

Insulin<br />

Insulin is encouraged as an anti-hyperglycemic agent for hospitalized patients because it is able to address both basal<br />

and nutritional needs separately and is the only anti-hyperglycemic agent that allows intravenous infusion for<br />

critically ill patients with poor subcutaneous absorption (e.g. edema, hypotension, vasopressors). Furthermore, the<br />

rapidity of onset of action as well as flexibility in a variety of conditions makes insulin an ideal medication for<br />

glycemic management in inpatient setting (Inzucchi, 2006).<br />

When given subcutaneously, insulin should be prescribed with specifications for a basal, nutritional, and correction<br />

dose. The basal insulin dose, which is meant to suppress hepatic gluconeogenesis in the non-fed state can be<br />

calculated based on body weight for the insulin–naïve patient or based on previously known total daily dose of<br />

insulin at home for patients who have been on insulin. A recent study suggests that decreasing the total daily insulin<br />

dose of the patient’s home regimen by 20-25% is prudent given the observation that initiating the total home insulin<br />

dose is associated with higher rates of hypoglycemia during hospitalization (Umpierrez et al., 2009). The nutritional<br />

insulin, meant to correct glycemic excursions related to meals, should be tailored to the nutritional regimen, which<br />

could be discrete meals, enteral or total parenteral nutrition. Basal insulin is an important component of an effective<br />

insulin regimen. It should not be withheld in those individuals with “NPO” status, and is critical for an individual<br />

with type 1 diabetes in whom withholding basal insulin can precipitate diabetic ketoacidosis (Clement et al., 2004;<br />

Inzucchi 2006). The “sliding scale” method of insulin delivery is an algorithm for insulin orders to treat<br />

Module G: Glycemic Control Page 72

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