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2008 Clinical Practice Guidelines - Canadian Diabetes Association

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<strong>2008</strong> CLINICAL PRACTICE GUIDELINES<br />

S72<br />

nutrition, dextrose infusions should be provided.<br />

To maintain effective blood levels of insulin, short- or<br />

rapid-acting insulin should be administered 30 minutes to 2<br />

hours before discontinuation of IV insulin infusion.The initial<br />

dose of subcutaneous insulin given after discontinuation<br />

of IV insulin infusion should be based on previously established<br />

dose requirements or the rate and pattern of inhospital<br />

IV insulin infusion. Other parameters that affect<br />

subcutaneous insulin dose determination include body<br />

weight, stress of illness and other comorbid conditions such<br />

as renal insufficiency.<br />

ORGANIZATION OF CARE<br />

Healthcare institutions should implement a program to<br />

improve glycemic control in the inpatient setting.This should<br />

include the formation of a multidisciplinary steering committee<br />

to provide educational programs, implement policies<br />

to assess and monitor the quality of glycemic management,<br />

and produce standardized order sets, protocols and algorithms<br />

for diabetes care within the institution. The timely<br />

consultation of such teams has been demonstrated to<br />

improve quality, reduce length of stay and lower costs (8,9).<br />

Self-management in the hospital may be appropriate for<br />

competent adult patients who successfully conduct selfmanagement<br />

of diabetes at home, have a stable level of consciousness,<br />

and have the physical skills needed to self-administer<br />

insulin and perform self-monitoring of blood glucose<br />

(SMBG). A physician order for self-management should be<br />

written with respect to selection of food, SMBG, self-determination<br />

and administration of insulin dose and type.<br />

Bedside BG monitoring<br />

No study has compared the effect of frequency of bedside BG<br />

testing on the incidence of hyper- or hypoglycemia in the<br />

hospital. The frequency and timing of bedside BG monitoring<br />

should be individualized. Healthcare institutions must<br />

implement and maintain a quality-control program to ensure<br />

the accuracy of bedside BG testing (10,11).<br />

Safety – hypoglycemia<br />

Hypoglycemia remains a major impediment to achieving<br />

optimal glycemic control in hospitalized patients. Healthcare<br />

institutions should have standardized treatment protocols<br />

that address mild, moderate and severe hypoglycemia.<br />

Healthcare workers should be educated about factors that<br />

increase the risk of hypoglycemia, such as sudden reduction<br />

in oral intake or discontinuation of enteral or parenteral<br />

nutrition, unexpected transfer from nursing unit after rapidacting<br />

insulin administration, and reduction in corticosteroid<br />

dose (12).<br />

Safety – insulin administration errors<br />

Insulin is identified as 1 of the top 5 “high-risk medications”<br />

in the hospital setting. A systems approach may work to<br />

reduce errors. This includes preprinted, approved, unambiguous<br />

standard orders for insulin administration, or<br />

computerized order entry (13).<br />

THE CRITICALLY ILL PATIENT<br />

Acute hyperglycemia in the intensive care setting is not<br />

unusual and results from a number of factors, including<br />

stress-induced counterregulatory hormone secretion, and<br />

possibly the effect of medications administered in the<br />

intensive care unit (ICU) (14). Hyperglycemia in this setting<br />

has effects on multiple systems, including the CV, neurologic<br />

and immune systems (14). Van den Berghe and<br />

colleagues (15) demonstrated impressive benefits of intensive<br />

glycemic control with IV insulin infusion among predominantly<br />

surgical patients admitted to the ICU and<br />

requiring mechanical ventilation. A subsequent analysis of<br />

a heterogeneous ICU population with predominantly medical<br />

patients and utilizing historical controls demonstrated<br />

a reduction in mortality, length of stay, renal dysfunction<br />

and requirement of transfusion among those receiving<br />

intensive glycemic control with an IV insulin infusion protocol<br />

(16).<br />

A meta-analysis of studies looking at the effects of insulin<br />

therapy for critically ill adult patients also demonstrated an<br />

overall reduction in mortality, particularly among those with<br />

diabetes and if glycemic control was a primary goal (17).<br />

However, this meta-analysis did not include any randomized<br />

controlled trials (RCTs) of intensive insulin therapy in a<br />

medical ICU.To date, there has been only 1 RCT of intensive<br />

insulin therapy and glycemic control among medical ICU<br />

patients (18). There was no difference in the primary outcome<br />

of in-hospital mortality between the groups. However,<br />

there was a significant reduction in the prespecified secondary<br />

outcomes of renal dysfunction, length of stay and prolonged<br />

mechanical ventilation. Mortality was increased<br />

among patients who stayed in the ICU for 3 days.<br />

Perioperative glycemic control<br />

The management of individuals with diabetes at the time of<br />

surgery poses a number of challenges. Acute hyperglycemia<br />

is common secondary to the physiologic stress associated<br />

with surgery. Pre-existing diabetes-related complications<br />

and comorbidities may also influence clinical outcomes.<br />

Acute hyperglycemia has been shown to adversely affect<br />

immune function (19) and wound healing (20) in animal<br />

models. Observational studies in humans have shown that<br />

hyperglycemia increases the risk of postoperative infections<br />

(21-23) and renal allograft rejection (24), and is associated<br />

with increased resource utilization (25).<br />

In patients undergoing coronary artery bypass surgery, a<br />

pre-existing diagnosis of diabetes has been identified as a risk<br />

factor for postoperative sternal wound infections, delirium,<br />

renal dysfunction, respiratory insufficiency and prolonged

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