Part of the ICU Emergencies Hub — browse every related guide in one place.
| Context | Target Range | Notes |
|---|---|---|
| Fasting (non-diabetic, non-ICU) | 70–99 mg/dL | Normal fasting glucose; prediabetes defined as 100–125; diabetes defined as 126+ on two occasions |
| Postprandial (2 hours after eating) | <140 mg/dL (non-diabetic) | 140–199 = impaired glucose tolerance; 200+ with symptoms = diabetes criteria met |
| General inpatient (non-critical) | 140–180 mg/dL | ADA/AACE inpatient target; tighter targets in selected patients at provider discretion |
| ICU (critically ill) | 140–180 mg/dL | NICE-SUGAR trial (2009) showed tight glycemic control (81–108) in ICU increased mortality — moderate control is now standard. Some protocols target 110–150 depending on institution and patient |
| Hypoglycemia threshold | <70 mg/dL | ADA definition; clinically significant hypoglycemia = <54 mg/dL; severe hypoglycemia = altered consciousness, seizure, or loss of consciousness |
Glucometer technique: Wash hands before obtaining the finger-stick sample (alcohol wipes may temporarily affect reading accuracy if not fully dried). Use the lateral aspects of the fingertips (less pain, better perfusion) rather than the fingertip pad. Avoid cold fingers — warm the hand first if circulation is poor, as cold peripheral blood may give falsely low readings. Discard the first drop of blood (may contain interstitial fluid that dilutes the sample); use the second drop. Apply blood to the test strip promptly and per the meter manufacturer's instructions.
Glucometer limitations: Point-of-care glucose meters are accurate within ±15–20% of laboratory glucose values in most cases, but this margin of error has clinical significance at the extremes. A meter reading of 65 mg/dL could reflect a true glucose of 50–80 mg/dL. For critical clinical decisions (insulin drip titration, treatment of severe hypoglycemia), a laboratory plasma glucose is more reliable than a bedside glucometer. Glucometers are also unreliable in patients with severe anemia, polycythemia, or extremes of hematocrit.
Monitoring frequency: Varies by patient situation and institutional protocol. Typical examples: pre-meal and bedtime for most diabetic patients on insulin; every 1–2 hours for patients on continuous insulin infusions; every 4–6 hours for NPO patients on sliding scale; every 1–2 hours during hypoglycemia treatment until glucose is confirmed above 70 mg/dL for two consecutive checks.
Adrenergic (early, typically 50–70 mg/dL): Tremors, diaphoresis, tachycardia, anxiety, pallor, hunger, nausea — symptoms from epinephrine/glucagon release as the body attempts to raise glucose. These symptoms allow the patient to self-recognize and self-treat if alert.
Neuroglycopenic (later, typically below 50 mg/dL): Confusion, difficulty concentrating, altered mental status, slurred speech, visual changes, personality changes, seizures, loss of consciousness — symptoms from inadequate glucose delivery to the brain. Patients cannot reliably self-treat at this stage. Important: Patients on beta-blockers may have blunted adrenergic symptoms and present with neuroglycopenic symptoms without the classic early warning signs.
For conscious patients with blood glucose 54–70 mg/dL who can swallow safely:
Give 15 grams of fast-acting carbohydrates. Examples: 4 oz (120 mL) of fruit juice; 4 oz regular (not diet) soda; 3–4 glucose tablets; 15 mL (1 tablespoon) of honey or corn syrup; glucose gel per package directions.
Wait 15 minutes, then recheck blood glucose.
If still below 70 mg/dL, repeat 15 grams of fast-acting carbohydrate and recheck in another 15 minutes.
Once glucose is above 70 mg/dL and the next meal is more than 1 hour away, give a small snack containing protein and complex carbohydrate to prevent rebound hypoglycemia.
If the patient cannot swallow safely: call the provider immediately and prepare to administer IV dextrose per order. D50W (50% dextrose, 25 grams dextrose in 50 mL) is the rapid IV treatment. Administer through a large, patent peripheral IV or central line — D50W is highly concentrated and causes significant vein irritation; confirm patency before administration. In the ICU or for patients without IV access, glucagon 1 mg IM/SQ may be administered (stimulates hepatic glycogen release; less effective in patients with liver disease or prolonged fasting). Recheck glucose 15 minutes after IV dextrose administration.
| Insulin Type | Examples | Onset | Peak | Duration | Clinical Use |
|---|---|---|---|---|---|
| Rapid-acting | Lispro (Humalog), Aspart (NovoLog), Glulisine (Apidra) | 10–15 min | 1–2 hrs | 3–5 hrs | Given immediately before or at start of meal; covers postprandial glucose rise; also used in insulin pumps |
| Short-acting (regular) | Regular insulin (Humulin R, Novolin R) | 30–60 min | 2–3 hrs | 5–8 hrs | Mealtime coverage (give 30 min before meal); IV insulin infusions in ICU; sliding scale correction; DKA treatment IV |
| Intermediate-acting | NPH (Humulin N, Novolin N) | 1–2 hrs | 4–6 hrs | 10–16 hrs | Basal coverage; typically given twice daily; less commonly used since long-acting analogs became available |
| Long-acting | Glargine (Lantus, Basaglar), Detemir (Levemir), Degludec (Tresiba) | 1–2 hrs | Relatively flat (minimal peak) | 20–24+ hrs | Basal insulin; given once or twice daily for background coverage; do NOT mix with other insulins; continue through hospitalization unless eating is severely impaired |
DKA (Diabetic Ketoacidosis): Initial target is NOT normoglycemia — it is stopping ketone production. IV regular insulin infusion typically runs until the anion gap closes, even if glucose falls below 250 mg/dL. When glucose drops to 200–250 mg/dL during DKA treatment, D5W is added to the IV to maintain the insulin infusion without causing hypoglycemia while ketoacidosis continues to resolve. The insulin infusion is transitioned to subcutaneous insulin only after anion gap closes and patient can eat.
HHS (Hyperosmolar Hyperglycemic State): Very high glucose (often above 600 mg/dL) without significant ketoacidosis. Treatment focuses on aggressive fluid resuscitation first, then cautious insulin administration. Glucose should not be corrected faster than 50–75 mg/dL/hour — rapid correction risks cerebral edema.
Corticosteroid-induced hyperglycemia: Common pattern: glucose rises in the afternoon/evening (following morning prednisone dose) while fasting morning glucose may be near-normal. Insulin regimen should be timed to address the peak hyperglycemia period, not just fasting coverage. Patients discharged on steroids often need temporary insulin prescriptions.
Related guides: Diabetes nursing guide | Medication safety | Nursing prioritization
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