Thiamine for Refeeding Syndrome
In patients at risk for refeeding syndrome, administer 300 mg IV thiamine immediately before initiating any nutrition, then continue 200–300 mg IV daily for at least 3 days. 1
Risk Identification
Patients requiring prophylactic thiamine include those with:
- **BMI <16 kg/m²** or unintentional weight loss >15% in 3–6 months 1, 2
- No nutritional intake for >10 days (or >5 days in some guidelines) 1, 2
- Chronic alcoholism – 30–80% have thiamine deficiency 1
- Low baseline electrolytes (potassium, phosphate, or magnesium) before feeding 1, 2
- Post-bariatric surgery with prolonged vomiting or poor intake 1
- Critical illness (sepsis, major surgery, severe burns) – >90% are thiamine deficient 1
- Chronic diuretic therapy or continuous renal replacement therapy 1
Thiamine Dosing Protocol
Pre-Feeding Phase (Critical)
- 300 mg IV thiamine as a single dose before any nutrition begins 1, 2
- Must be given before glucose-containing fluids – glucose loading in thiamine-depleted patients precipitates Wernicke's encephalopathy and acute heart failure 1, 2, 3
During Refeeding (Days 1–3 minimum)
- 200–300 mg IV daily for at least 3 days 1, 2
- Continue throughout the high-risk refeeding period 1
- Full B-complex vitamins IV should be given simultaneously 1, 2
Route Selection
- IV route is mandatory in refeeding syndrome prevention 1, 2
- Oral thiamine is inadequate for acute situations due to poor absorption in malnourished patients 1
- The FDA label confirms IV thiamine is indicated when rapid restoration is necessary and for patients who cannot take oral thiamine due to severe anorexia, nausea, vomiting, or malabsorption 3
Nutritional Reintroduction Strategy
Start nutrition at 5–10 kcal/kg/day in very high-risk patients (BMI <16, chronic alcoholism, prolonged starvation) and increase gradually over 4–7 days 1, 2. Standard high-risk patients can start at 10–20 kcal/kg/day 1, 2.
Macronutrient Distribution
- 40–60% carbohydrate, 30–40% fat, 15–20% protein 1, 2
- Protein intake should be ≥1.2 g/kg ideal body weight 2
Special Populations
- Severe acute pancreatitis: limit to 15–20 non-protein kcal/kg/day 1, 2
- Anorexia nervosa: start at the lower end (5–10 kcal/kg/day) with very slow progression 2
Concurrent Electrolyte Replacement
Thiamine alone is insufficient – aggressive electrolyte supplementation is mandatory:
- Phosphate: 0.3–0.6 mmol/kg/day IV 1, 2
- Potassium: 2–4 mmol/kg/day 1, 2
- Magnesium: 0.2 mmol/kg/day IV or 0.4 mmol/kg/day orally 1, 2
- Calcium: supplement as needed 2
The biochemical features of refeeding syndrome result from feeding-induced hormonal shifts regardless of baseline stability, so prophylactic replacement is essential even if pre-feeding electrolytes appear normal 2.
Monitoring Protocol
First 72 Hours (Critical Period)
- Daily electrolyte monitoring (phosphate, potassium, magnesium, calcium) 1, 2
- Strict glucose monitoring to avoid hyperglycemia 2
- Clinical surveillance for edema, arrhythmias, confusion, respiratory failure 1, 2
- Volume status and fluid balance monitoring 2
If Hypophosphatemia Develops
- Measure electrolytes 2–3 times daily 2
- Restrict energy to 5–10 kcal/kg/day for 48 hours before gradually increasing 2
- Intensify phosphate replacement while continuing thiamine 2
Critical Pitfalls to Avoid
Never start feeding without thiamine – carbohydrate loading precipitates Wernicke's encephalopathy, Korsakoff syndrome, acute heart failure, and sudden death 1, 2
Never use low-dose thiamine (10–100 mg) in high-risk patients – this is inadequate for refeeding syndrome prevention 1
Never stop thiamine prematurely – continue for the full minimum 3-day period even if symptoms improve 2
Never correct electrolytes alone before feeding – this provides false security without correcting massive intracellular deficits 2
Never stop feeding abruptly – taper gradually if necessary to avoid rebound hypoglycemia 1, 2
Duration of Thiamine Therapy
- Minimum 3 days of high-dose IV thiamine (200–300 mg daily) 1, 2
- Transition to oral thiamine 50–100 mg daily once stable oral intake is established 1
- Continue for 2–3 months in patients with chronic alcoholism or ongoing risk factors 1
- Lifelong supplementation (50–100 mg daily) may be necessary for post-bariatric surgery patients or those with chronic malabsorption 1
Evidence Quality Note
The benefit-risk ratio for prophylactic thiamine is overwhelmingly favorable – thiamine has no established upper toxicity limit, excess is excreted in urine, and high IV doses rarely cause anaphylaxis 1. Doses >400 mg may cause mild nausea, anorexia, or mild ataxia 1. The guideline recommendations are consistent across multiple societies despite limited high-quality randomized trials, reflecting the life-threatening nature of untreated deficiency and the safety of treatment 1, 2.