Inpatient diabetes management
Basal-bolus insulin is the standard for the non-critical inpatient with hyperglycemia. Sliding-scale alone is discouraged. This page walks total-daily-dose (TDD) sizing, correction scales, insulin products, and how to handle non-insulin diabetes medications on admission — including which SGLT-2 and GLP-1 agents to hold and why.
Build a starting insulin regimen
Have your insulin order reviewed
Paste the exact insulin order set you would enter into the EMR. The AI is tuned for insulin-specific errors: "u" vs "units", missing correction scale, sliding-scale-only, wrong basal timing, missing hypoglycemia protocol, product-strength ambiguity, wrong TDD split.
Basal-bolus initiation (the standard)
For persistent hyperglycemia (BG > 180 mg/dL) or a known diabetic admitted with active orders, initiate a scheduled basal + prandial + correction regimen. Estimate TDD from weight (or home dose), split it 50/50, then re-titrate every 24–48 h based on trends.
| Step | How | Example (82 kg adult, insulin-naïve) |
|---|---|---|
| Estimate TDD | 0.3–0.5 u/kg/day (0.3 if sensitive, 0.5 if resistant) | 82 × 0.4 = 33 u/day |
| Split 50/50 | Half as basal, half as prandial | Basal 16 u · Prandial 17 u |
| Divide prandial across 3 meals | Prandial ÷ 3, round to whole unit | 5–6 u with each meal |
| Add correction scale | Pre-meal + bedtime (or Q6H if NPO) | Mild scale (see below) |
| Re-titrate at 24–48 h | If pre-meal BG > 180 x 2, increase basal 10–20 % | 16 u → 18–19 u |
Correction (supplemental) scales
Correction is additional rapid-acting insulin layered on top of scheduled prandial. Pick a scale based on the patient's insulin sensitivity. Do not use correction alone — that's sliding-scale monotherapy and is discouraged in modern inpatient care.
| BG mg/dL | Extra units |
|---|---|
| < 70 | Hypoglycemia protocol |
| 70–149 | 0 units (baseline) |
| 150–199 | +1 u |
| 200–249 | +2 u |
| 250–299 | +3 u |
| 300–349 | +4 u |
| ≥ 350 | +5 u + notify |
| BG mg/dL | Extra units |
|---|---|
| < 70 | Hypoglycemia protocol |
| 70–149 | 0 units |
| 150–199 | +2 u |
| 200–249 | +4 u |
| 250–299 | +6 u |
| 300–349 | +8 u |
| ≥ 350 | +10 u + notify |
| BG mg/dL | Extra units |
|---|---|
| < 70 | Hypoglycemia protocol |
| 70–149 | 0 units |
| 150–199 | +3 u |
| 200–249 | +6 u |
| 250–299 | +9 u |
| 300–349 | +12 u |
| ≥ 350 | +15 u + notify |
Sliding-scale insulin — why alone is discouraged
Sliding-scale-only responds after the BG is already high. It doesn't cover carbohydrate intake proactively, causes glucose roller-coasters, and is associated with longer LOS in retrospective inpatient data.
- Very short admission < 24 h with mild hyperglycemia
- Diet-controlled T2DM with occasional BG > 180
- As the correction layer added to a scheduled basal + prandial regimen
NPO and tube-feed patients
| Scenario | Basal | Prandial | Correction | Monitoring |
|---|---|---|---|---|
| NPO (short-term, < 24 h) | Continue full dose | HOLD | Q6H rapid-acting | Q6H BG |
| NPO (prolonged) — T2DM | Reduce basal 20 % | HOLD | Q6H rapid-acting | Q6H BG |
| NPO — T1DM | NEVER hold basal — reduce 10–20 % only | HOLD | Q6H rapid-acting | Q4–6H BG |
| Continuous tube feed | Full basal + consider NPH q12h to match feed | HOLD (no discrete meals) | Q6H rapid-acting | Q6H BG |
| Bolus tube feed | Full basal | Give with each bolus feed | Pre-feed + HS | Q6H BG |
| Cyclic tube feed (nocturnal) | Basal small · add NPH at feed start | HOLD | Q6H rapid-acting | During + 4 h post-feed |
Steroid-induced hyperglycemia
Systemic glucocorticoids cause a post-prandial, afternoon-predominanthyperglycemia that classic once-daily basal misses. Match the insulin to the steroid's pharmacokinetics.
| Steroid pattern | Insulin strategy | Why |
|---|---|---|
| Prednisone AM daily | Add NPH 0.1 u/kg SC in the morning WITH the steroid | NPH peaks 4–8 h → matches prednisone glucose peak |
| Dexamethasone BID / continuous | Weight-based basal + higher prandial (60/40 split favouring prandial) | Long half-life ≈ 24-hour effect |
| Methylprednisolone IV pulse | Consider IV insulin infusion during pulse days | High-dose steroids cause severe insulin resistance |
| Steroid taper | Reduce insulin ≈ 20 % per dose reduction step | Prevents hypoglycemia as resistance falls |
IV insulin drip → subcutaneous transition
After DKA/HHS resolution (anion gap closed, HCO₃⁻ ≥ 18, patient tolerating PO), transition before the drip is stopped — never stop the drip without overlap or the patient re-enters ketosis.
- Estimate 24-h TDD from drip: last 6 h average rate × 4 × 0.8 (the 0.8 accounts for the more efficient SC absorption).
- Split 50/50 basal / prandial as above. Choose glargine or detemir for basal.
- Give the first SC basal dose 1–2 hours before stopping the drip.
- Stop the drip only after the first meal + prandial dose is given.
- Monitor BG Q1H × 4, then Q2H × 8, then Q4H. Continue home meds appropriately.
Home regimen reconciliation on admission
| Home therapy | On admission (eating) | On admission (NPO or acutely ill) |
|---|---|---|
| T1DM basal-bolus | Continue basal 100 % · prandial as ordered | Continue basal 80–100 % · HOLD prandial · correction Q6H |
| T2DM basal-bolus | Continue basal 80 % · prandial 50–80 % | Basal 50–80 % · HOLD prandial · correction Q6H |
| Basal-only (glargine) | Continue 80 % of home dose | Continue 50–80 % of home dose |
| Pre-mixed 70/30 or 75/25 | Convert to basal-bolus (safer inpatient) | Convert to basal only + correction |
| Oral agents / GLP-1 only | Hold metformin if AKI, contrast, sepsis · hold SGLT2 in AKI/DKA risk · hold GLP-1 if NPO | Same — start insulin as needed for BG > 180 |
Insulin pump on admission
Continue home pump only if all are true — otherwise transition to a standard basal-bolus regimen and store the pump with valuables.
- Patient is alert, cognitively intact, and physically able to operate the pump
- No DKA / HHS, ICU-level illness, or major surgery in the next 24 h
- Team has documented the basal profile + carb ratio + correction factor in the chart
- Institution has a pump-consent form on file and the primary team is comfortable co-managing
Red flags and hold parameters
- BG < 70 mg/dL → hypoglycemia protocol, hold next prandial + correction
- BG < 100 pre-meal → consider ↓ prandial 25–50 %
- NPO status → hold prandial (basal continues per T1/T2 rules above)
- Renal function drop (CrCl < 45) → reduce TDD 20–25 %
- Any hepatic decompensation → tighten monitoring, expect variable requirement
- Specific insulin product (glargine 100 vs. 300 u/mL, U-500 flagged separately)
- Dose in units — spell out, never "u"
- Route (SC), timing anchored to meal or fixed time (e.g., 22:00)
- Correction scale with hypoglycemia protocol reference
- BG monitoring frequency
- Indication and target BG range
Sample complete orders
Insulin glargine 16 units SC daily at 22:00 Insulin lispro 6 units SC with each meal (breakfast, lunch, dinner) Insulin lispro correction — mild scale — pre-meal + HS BG check: pre-meal + HS + PRN symptoms Target BG: 140–180 mg/dL Hypoglycemia protocol: institutional
Insulin glargine 20 units SC daily (80 % of 25 u home dose) Insulin lispro — HOLD prandial while NPO Insulin lispro correction — moderate scale — Q6H BG check: Q6H + pre-procedure Target BG: 140–180 mg/dL D5 ½NS at 75 mL/h while NPO
Insulin products cheatsheet
Choose the right family based on the job — basal covers fasting glucose, prandial covers meals, correction fixes real-time hyperglycemia. Always specify the exact product AND concentration in the order.
| Class | Products (generic · brand) | Onset · Peak · Duration | Inpatient use |
|---|---|---|---|
| Long-acting basal | glargine U-100 (Lantus, Basaglar) · glargine U-300 (Toujeo) · detemir (Levemir) · degludec (Tresiba) | 1–2 h · minimal peak · 20–42 h | Once daily basal. Toujeo & Tresiba more forgiving. NEVER hold in T1DM. |
| Intermediate basal | NPH (Humulin N, Novolin N) | 1–2 h · 4–8 h · 12–18 h | Twice daily, or matched to AM prednisone (peaks at steroid glucose spike). |
| Rapid-acting bolus | lispro (Humalog, Admelog) · aspart (Novolog, Fiasp) · glulisine (Apidra) | 10–15 min · 1–2 h · 3–5 h | Prandial + correction. Give within 15 min of meal. |
| Short-acting | regular insulin (Humulin R, Novolin R U-100) | 30 min · 2–4 h · 5–8 h | IV drip (DKA/HHS), K+ shift, TPN coverage. SC use largely replaced by rapid-acting. |
| Concentrated regular | regular U-500 (Humulin R U-500) | 30 min · 4–8 h · up to 24 h | Severe insulin resistance (TDD > 200 u/day). Flag SEPARATELY — dispense on dedicated protocol only. |
| Pre-mixed | 70/30 NPH-regular · 75/25 protamine-lispro · 70/30 protamine-aspart | Bi-modal | Home use — convert to basal-bolus on admission for tighter control. |
| Inhaled | insulin human (Afrezza) | 1–2 min · 12–15 min · 2–3 h | Uncommon inpatient. Contraindicated in asthma, COPD, active smoker. |
Non-insulin diabetes medications — inpatient rules
On admission, most oral / injectable agents are HELD in favor of insulin for glycemic control. The exceptions matter — SGLT-2s in particular can trigger euglycemic DKA if continued during acute illness.
| Class | Examples | Inpatient hold / continue | Why |
|---|---|---|---|
| Biguanide | metformin (Glucophage) | HOLD on admission | Lactic acidosis risk if AKI, sepsis, IV contrast, decompensated HF. Restart when eGFR stable & no contrast for 48 h. |
| Sulfonylurea | glipizide, glimepiride, glyburide | HOLD | Prolonged hypoglycemia risk in NPO / reduced PO / CKD. Glyburide worst offender — avoid. |
| Meglitinide | repaglinide, nateglinide | HOLD | Prandial — meaningless if NPO. Hypoglycemia risk. |
| DPP-4 inhibitor | sitagliptin (Januvia), linagliptin (Tradjenta), saxagliptin (Onglyza) | OK to continue if eating | Low hypoglycemia risk. Saxagliptin: HOLD in HF. Renal-adjust sitagliptin. |
| SGLT-2 inhibitor | empagliflozin (Jardiance), dapagliflozin (Farxiga), canagliflozin (Invokana), ertugliflozin | HOLD ≥ 3 days pre-op & during acute illness | EUGLYCEMIC DKA risk — patients present with normal glucose + gap acidosis. Also volume depletion, GU infections. |
| GLP-1 agonist | liraglutide (Victoza), semaglutide (Ozempic / Wegovy / Rybelsus PO), dulaglutide (Trulicity), exenatide | HOLD if NPO, ileus, gastroparesis, upcoming anesthesia | Delayed gastric emptying → aspiration risk during induction. ASA guidance: hold weekly agents ≥ 1 week pre-op. |
| Dual GIP/GLP-1 | tirzepatide (Mounjaro / Zepbound) | Same as GLP-1 — HOLD peri-op & if NPO | Same aspiration + gastroparesis concern; even stronger GI slowing. |
| Amylin analog | pramlintide (Symlin) | HOLD | Prandial adjunct — meaningless inpatient; nausea, hypoglycemia. |
| Thiazolidinedione | pioglitazone (Actos), rosiglitazone | HOLD in CHF / volume overload | Fluid retention, bone fracture risk. Slow onset — not useful for acute control. |
| α-glucosidase inhibitor | acarbose (Precose), miglitol | HOLD if NPO | Prandial only. GI side effects. Rarely inpatient. |
| Bile-acid sequestrant | colesevelam (Welchol) | OK to continue if eating | Minimal glycemic benefit. Watch drug absorption interactions. |
| Dopamine agonist | bromocriptine QR (Cycloset) | HOLD | Uncommon. Orthostasis, drug interactions. |
AI DM medication reconciliation
Paste the patient's home diabetes regimen and get a structured hold / continue / modify plan with a one-line rationale per drug. Brand names (Ozempic, Jardiance, Glucophage) are matched to their generics automatically.
Open the chat widget (bottom-right) and describe the patient — weight, home regimen, eating status, comorbidities — and the AI will walk through TDD, split, and correction scale with you.