safe insulin
TRANSCRIPT
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Safe Administration of Insulin
Prepared by Vicki Kraus, PhD, ARNP, CDE and
the Insulin Administration Task Force
May, 2005
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Insulin Administration Task
Force
• Linda Chase, RN• Rhonda Fruhling, RN
• Pam Group, RN
• Susan Huff, RN
• Linda Johnson, RN
• Vicki Kraus, RN
• Jennifer Long, RN• Michael Murray, RPh
• Mary Sauers, RN
• Jeanne Sheetz, RN
• William Sivitz, MD
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Insulin Administration Task
Force
• Reviewed significant and serious insulinerrors for July, 2003 to December, 2004
• Identified the issues involved in each one of
the errors, e.g, lack of knowledge• Developed a plan for reducing errors
– Provide education– Improve communication
– Develop policies and procedures as needed
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Overview
• Review of differences between type 1 and type 2diabetes
• Concepts of basal and bolus insulin
• Insulin types and action patterns
• Changing insulin requirements in the hospitalized
patient• Hypoglycemia prevention, detection and treatment
• Preventing and solving blood sugar problems
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Diabetes Mellitus
• Hyperglycemia caused by an absolute orrelative deficiency of insulin
• Body is unable to properly use
carbohydrates, proteins and fats
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Type 1 Diabetes (T1DM)
• Absolute deficiency of insulin due todestruction of the beta cells of the pancreas
• Immunologic or idiopathic, i.e., no known
etiology and no autoimmunity
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T1DM
• Onset at any age, usually before 30• Ketosis prone
• Insulin sensitive• Usually thin or normal weight
• Treatment consists of a balance of diet,insulin and exercise
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Type 2 Diabetes (T2DM)
• Relative insulin deficiency due to decreasedliver, muscle, and fat sensitivity to insulin
and impaired beta cell function
• Genetic and environmental
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T2DM
• Onset may be as early as during childhoodor adolescence, usually after age 30
• Not ketosis prone
• Normal or high insulin levels
• Insulin resistant
• Usually obese• Treatment consists of diet and exercise and
oral agents and/or insulin
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Blood Glucose Targets
• Critical Care Units– 110 mg/dl
• Non-Critical Care Units– 110 mg/dl preprandial (range 90-130
mg/dl)– 180 mg/dl maximal
American Diabetes Association, 2005
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Insulin Therapy
• Basal insulin– Controls glucose production by the liver
• Bolus insulin
– Food insulin
• Use and store carbohydrates eaten
– Correction (supplemental) insulin• Treat an acute elevation in blood glucose
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Basal
Bolus
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Insulin Preparations
• Rapid-acting Insulin Analogs
– Lispro (Humalog), Aspart (Novolog), Glulisine(Apidra)
• Short-acting Insulin
– Regular (Humulin R and Novolin R)
• Intermediate-acting Insulin
– NPH (Humulin N and Novolin N)• Long-acting Insulin Analog
– Glargine (Lantus)
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Look Alike Sound Alike Names
• NovoLOG• NovoLIN
• HumULIN• HumaLOG
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Insulin Action Patterns
Insulin
Preparation
Onset of
Action
Peak Action Effective
Duration
Rapid-acting
Analogs
5-15
minutes
30-90 minutes 3-5 hours
Short-acting 30-60
minutes
2-3 hours 5-8 hours
Intermediate-
acting
2-4 hours 4-10 hours 10-16 hours
Long-acting 2-4 hours Peakless 20-24 hours
American Diabetes Association, 2005
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Pre-Mixed Insulins
• Humulin/ Novolin 70/30 (human)– 70 % NPH and 30 % Regular
• Humalog Mix ® 75/25 (analog)
– 75 % lispro protamine and 25 % lispro
• NovoLog Mix® 70/30 (analog)
– 70 % aspart protamine suspension and 30 %
aspart
American Diabetes Association, 2005
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American Diabetes Association (2003). Insulin therapy in the 21st century.
Alexandria, VA: ADA.
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Administration of Insulin
• Pre-meal Insulin
– Fast-acting: 5-15 minutes before eating (tray should beon the unit and patient ready to eat it)
– Short-acting: 30 minutes before eating
• Basal Insulin
– NPH: once or twice daily before breakfast and beforesupper or at bedtime; at bedtime only
– Glargine: once or twice daily before breakfast and/or atbedtime
• Correction Insulin
– Fast-acting or short-acting with pre-meal insulin
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Insulin Injection Sites
• Rotation of sites is important to prevent tissuechanges, e.g., hypertrophy
• Rotate sites within one body area for each insulininjection/time of day, e.g., lispro abdomen, lantusarms
• Absorption varies by body area
– Abdomen– Arms
– Legs
– Buttocks
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Injecting Insulin
• Clean injection site with alcohol
• Gently pinch up tissue to pull fat away frommuscle
• Insert needle (full length) at a 45-90º angleinto subcutaneous tissue (most people 90º)
• Inject at slow, steady rate• Remove needle and apply gentle pressure;
DO NOT massage the site
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Increased Insulin Requirements
Related to Hospitalization
• Illness• Surgery
• Infection• Steroid Therapy
• Added calorie load (CVN, enteral feeding)
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Prevention of Hyperglycemia
• Continue basal insulin or replace with continuousintravenous insulin
• Give fast or short-acting insulin before meals
• Use correction or sliding scale insulin doses thatmatch the current blood sugar and the insulinsensitivity (algorithms)*
• Monitor blood sugars at least 5 times per daywhen eating (before meals, at bedtime and at0200) or every 4-6 hours if NPO
(*Use sliding Scale Insulin Order sheet: Adult H9131)
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Hypoglycemia: Common Risk
Factors
• Mismatch of insulin timing, amount or typefor carbohydrate intake
– Fast-acting insulin given and food delayed
– Unexpected transport after fast or short-acting
insulin
• Oral secretagogues, e.g., sulfonylureas,without appropriate carbohydrate intake
Tomky, D. (2005). Detection, prevention, and treatment of hypoglycemia in
the hospital, Diabetes Spectrum, 18(1), 39-43.
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Hypoglycemia: Common Risk
Factors
• Reduction in nutrient intake– NPO
– Nausea and vomiting
– Not finishing a meal or eating a snack
– Intravenous carbohydrate discontinued or rate
decreased– Interruption of enteral feeding
Tomky, D. (2005). Detection, prevention, and treatment of hypoglycemia in the
hospital, Diabetes Spectrum, 18(1), 39-43.
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Hypoglycemia: Common Risk
Factors
• History of severe hypoglycemia• General anesthesia or sedation that puts
patient in an altered state of consciousness
• Critical illnesses (hepatic, cardiac, and renal
failure; sepsis;and, severe trauma)
Tomky, D. (2005). Detection, prevention, and treatment of hypoglycemia in the
hospital, Diabetes Spectrum, 18(1), 39-43.
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Prevention of Hypoglycemia
• Hold food insulin when NPO
• Replace carbohydrates if mealcarbohydrates not eaten or vomiting occurs
• Give fast-acting insulin within 15 minutesof eating (food should be present)
• Give bedtime snack as specified by mealplan or if blood sugar at bedtime is less than100 mg/dl
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Prevention of Hypoglycemia
• Reduce dose/insulin infusion rate if enteralfeeding or CVN or intravenous glucose is
reduced or discontinued
• Use of intravenous glucose to replace
carbohydrates when NPO or vomiting as
indicated
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Prevention of Hypoglycemia
• Base correction or sliding scale doses on current
blood sugar levels
• Avoid using sliding scale insulin as a replacement
for scheduled basal and bolus insulin• Accurate insulin dosing: double checks in
accordance with hospital policy
• No secondary set connections above the infusion
pump on continuous IV infusions of insulin
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Hypoglycemia Management
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Hypoglycemia: Definition
• Any blood sugar level of 70 mg/dl or lower• Symptoms may or may not be present
• Symptoms may occur and hypoglycemia is
not present
• Blood sugar level does not describe the
severity of hypoglycemia
– Severity based on whether person can treat self
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Hypoglycemia: Symptoms
• Autonomic– Trembling/shaking, sweating, pounding heart,
fast pulse, changes in body temperature,
tingling in extremities, heavy breathing
• Neuroglycopenic
– Slow thinking, blurred vision, slurred speech,uncoordinated, numbness, trouble
concentrating, dizziness, fatigue/sleepiness
Gonder-Frederick, L. & Zrebiec, J (2003). Hypoglycemia. In M.J. Franz (Ed.),Core curriculum for diabetes education (pp. 277-310). Chicago: AADE.
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Hypoglycemia: Symptoms
• Unknown etiology– Hunger, nausea, weakness, headache, general
feeling of something not right
Gonder-Frederick, L. & Zrebiec, J (2003). Hypoglycemia. In M.J. Franz (Ed.),
Core curriculum for diabetes education (pp. 277-310). Chicago: AADE.
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Hypoglycemia: Emotional and
Social Behavior Changes
• Negative Moods: anxiety, nervousness,tension, irritation, frustration, anger,sadness, pessimism
• Positive Moods: giddiness, euphoria,disinhibition
• Behaviors: arguing, crying, resistingtreatment, aggressive acts, inappropriatesocial/sexual behaviors
Gonder-Frederick, L. & Zrebiec, J (2003). Hypoglycemia. In M.J. Franz (Ed.),
Core curriculum for diabetes education (pp. 277-310). Chicago: AADE.
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Hypoglycemia should beconsidered a potential etiology in
any patient who has a change in
level of consciousness.
University HealthSystem Consortium (2005). Safe use of insulin. Chicago:UHC.
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Hypoglycemia: Causes
• Excess of blood sugar lowering agents
(insulin or oral agents* that increase
insulin) in relation to food intake and
activity level
• More likely when food has not been eaten
for several hours or when activity hasincreased significantly
Gonder-Frederick, L. & Zrebiec, J (2003). Hypoglycemia. In M.J. Franz (Ed.),
Core curriculum for diabetes education (pp. 277-310). Chicago: AADE.
*glyburide, glipizide, glimepiride, repaglinide, nateglinide
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Hypoglycemia: Management• Test blood sugar. If less than 70 mg/dl treat even
if symptoms are absent
• Take 15 grams of carbohydrate. 20-30 grams maybe needed if blood sugar is less than 50 mg/dl
• Retest blood sugar in 15 minutes. Repeattreatment if still less than 70 mg/dl
• Provide snack if scheduled meal/snack not withinthe next 30-60 minutes (6 saltines, 3 grahamcrackers, or 1 slice of bread)
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Hypoglycemia: Management
15 Gram Carbohydrate Options
Fruit juice (1/3-1/2 cup)
Non-diet soft drink (4-6 ounces)
Skim milk (1 cup)
Honey/jelly/corn syrup (1 Tablespoon)
Sugar (3-4 Teaspoons)
Glucose tablets or gel
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Hypoglycemia Management
• Relief of symptoms lags behind return of
blood sugar to normal (more is not better)
• Recovery of motor and mental function
takes a while when blood sugar levels have
been < 45 mg/dl (may take 45-75 minutes to
regain cognitive function)
f
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Management of Severe
Hypoglycemia (Unable to self manage)
• If not at risk for aspiration, give oral
carbohydrates.
• If unconscious, provide treatment based on
level of care available
– Glucagon (1 mg IM)
– D50 intravenously (25 ml)– D5 (300 ml) or D10 (150 ml) intravenously
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Hypoglycemia: Follow Up
• Retest blood sugar levels during recovery
and retreat as necessary
• Determine cause of hypoglycemia and make
regimen adjustments as appropriate
P i d S l i Bl d
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Preventing and Solving Blood
Sugar Problems
• Blood sugar level
– Low, normal or high
• Carbohydrate
– Source (PO, IV Fluids, CVN)– Continuous or intermittent
• Insulin– Type (s) and action pattern (s) and dose
– Time and method of administration
C S d CVN ith t
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Case Study: CVN without
Added Insulin
Insulin Low Blood
Sugar
High Blood
Sugar
Continuous IV Insulin Follow IV insulin
guideline
Follow IV insulin
guideline
Sliding Scale Insulin
Only
Treat using adult
Hypoglycemia
Management protocol.
Call HO to considerrevising sliding scale
insulin and/or giving
IVF containing glucose
Call HO to consider
revising sliding scale
insulin, adding
scheduled subcutaneousbasal* insulin or
initiating continuous IV
insulin
*NPH or Glargine (Lantus)
C St d CVN ith t
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Case Study: CVN without
Added Insulin
Insulin Low Blood
Sugar
High Blood
Sugar
Scheduled Subcutaneous
Basal* Insulin
Treat using adult
Hypoglycemia
Management protocol.
Call HO to consider
decreasing scheduled
subcutaneous basal*
insulin or adding IVF
containing glucose
Call HO to consider
adding correction/sliding
scale insulin and/or
increasing scheduled
subcutaneous basal*
insulin
*NPH or Glargine (Lantus)
C St d CVN ith I li
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Case Study: CVN with Insulin
Added
Insulin Low Blood
Sugar
High Blood
Sugar
Continuous IV Insulin Follow IV insulin
guideline
Follow IV insulin
guideline
Sliding Scale Insulin
Only
Call HO to consider
decreasing sliding scale
insulin and/or
decreasing insulin innext CVN bag and/or
adding IVF containing
glucose
Call HO to consider
increasing sliding scale
insulin and/or increasing
the insulin in the nextCVN or adding
scheduled subcutaneous
basal* insulin or starting
continuous IV insulin.
*NPH or Glargine (Lantus)
C St d CVN ith I li
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Case Study: CVN with Insulin
Added
Insulin Low Blood
Sugar
High Blood
Sugar
Scheduled Subcutaneous
Basal* Insulin
Call HO to decrease
scheduled
subcutaneous basal*
insulin
Call HO to increase
scheduled subcutaneous
basal* insulin
*NPH or Glargine (Lantus)
C St d C ti T b
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Case Study: Continuous Tube
Feeding Rate Adjustment
Insulin Low Blood
Sugar
High Blood
Sugar
Continuous IV Insulin Decrease rate using IV
insulin guideline. Call
HO to consider adding
IVF containing
glucose.
Increase rate using IV
insulin guideline.
Case Study: Continuous Tube
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Case Study: Continuous Tube
Feeding Rate Adjustment
Insulin Low Blood
Sugar
High Blood
Sugar
Sliding Scale Insulin
Only
Call HO to consider
decreasing sliding scale
insulin
Call HO to to consider
increasing sliding scale
insulin or starting
continuous IV insulin
or starting scheduled
subcutaneous basal*
insulin
*NPH or Glargine (Lantus)
Case Study: Continuous Tube
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Case Study: Continuous Tube
Feeding Rate Adjustment
Insulin Low Blood
Sugar
High Blood
Sugar
Scheduled
Subcutaneous Basal*
Insulin
Call HO to consider
starting IVF containing
glucose and
decreasing scheduled
subcutaneous basal*
insulin
Call HO to consider
revising
correction/sliding scale
insulin and increasing
scheduled
subcutaneous basal*
insulin
*NPH or Glargine (Lantus)
C St d C ti T b F di
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Case Study: Continuous Tube Feeding
Discontinued
• Continuous intravenous insulin
– Call HO to reduce the rate and consider adding IVFcontaining glucose
– Check blood sugars every hour until stable
• Sliding scale insulin– Call HO to reduce sliding scale insulin if indicated
• Scheduled subcutaneous basal* insulin
– Call HO to consider reducing dose and adding IVFcontaining glucose
– Check blood sugars every hour until stabilized
*NPH or Glargine (Lantus)
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Case Study: Blood Sugar < 70 mg/dl
• NPO for a test
– Call HO for order to hold scheduled fast-acting insulin(prevention)
– Call HO to consider starting IVF containing glucose
• Continuous NPO– Call HO to add/adjust IVF containing glucose and/or
adjust insulin
• Able to take food/fluids– Follow adult Hypoglycemia Management protocol