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Bedside Snapshot
- Essential vitamin in aerobic carbohydrate metabolism; deficiency impairs pyruvate dehydrogenase and other key enzymes → shunts metabolism toward lactate and energy failure in high-demand tissues (brain, heart)
- Core ED/ICU uses: treatment and prophylaxis of Wernicke encephalopathy, empiric supplementation in alcohol use disorder, severe malnutrition, and refeeding syndrome risk, and sometimes as an adjunct in septic shock with high lactate
- Thiamine is extremely safe, inexpensive, and often underused; many patients with alcohol use disorder or malnutrition have clinically significant deficiency
- Classic teaching: give thiamine before or with significant glucose loads in suspected deficiency to avoid worsening Wernicke encephalopathy (evidence imperfect, but high face validity and negligible downside)
- IV is preferred in acutely ill and malabsorptive patients; transition to oral thiamine once stable and able to absorb enterally
Brand & Generic Names
- Generic Name: Thiamine hydrochloride
- Brand Names: No single dominant brand; available as generic injection and tablets
Medication Class
Water-soluble vitamin (B1); cofactor in carbohydrate metabolism and neuronal function
Pharmacology
Mechanism of Action:
- Converted in tissues to thiamine pyrophosphate (TPP), an essential cofactor for multiple enzymes in carbohydrate metabolism including pyruvate dehydrogenase, α-ketoglutarate dehydrogenase, and transketolase
- These enzymes link glycolysis to the Krebs cycle and the pentose phosphate pathway; deficiency impairs ATP production and increases lactate generation
- Brain and myocardium are especially vulnerable, leading to Wernicke encephalopathy (ocular abnormalities, ataxia, confusion) and beriberi (cardiomyopathy, neuropathy)
- Repletion restores oxidative metabolism, improves lactate clearance, and can reverse early neurologic findings if given promptly
Pharmacokinetics:
- Absorption: Oral absorption is efficient at low doses but saturable; in severe deficiency, malabsorption, or critical illness, IV dosing is preferred initially
- Distribution: Widely distributed, with high uptake in heart, liver, kidneys, and brain; body stores are limited and can be depleted within 2–3 weeks of inadequate intake
- Metabolism: Thiamine is phosphorylated intracellularly to active coenzyme forms (TPP); excess is metabolized to inactive forms
- Elimination: Water-soluble; excess excreted in urine. No significant accumulation even with high parenteral doses for short courses
- Because stores are limited but turnover is modest, regular replacement is needed in ongoing high-risk states (alcohol use disorder, malnutrition, chronic diuretic use)
Indications
- Suspected or confirmed Wernicke encephalopathy (ocular abnormalities, ataxia, confusion) in patients with alcohol use disorder, malnutrition, or hyperemesis (including pregnancy)
- Empiric prophylaxis in patients with alcohol use disorder, especially when hospitalized or NPO, or during acute illness
- Severe malnutrition and refeeding syndrome risk, particularly when starting calories or parenteral nutrition
- Adjunctive therapy in septic shock or unexplained lactic acidosis in patients with possible deficiency, recognizing evidence is mixed but risk is low
- Supportive treatment in heart failure due to beriberi (rare in high-income settings but important in global and resource-limited contexts)
- Diseases & Conditions: Wernicke encephalopathy and Wernicke–Korsakoff syndrome, alcohol-related malnutrition, refeeding syndrome, hyperemesis gravidarum with prolonged vomiting, unexplained high lactate/anaplerotic failure states
Dosing & Administration
Available Forms:
- Injection: Typically 100 mg/mL in 1 mL vials or ampules for IV/IM use
- Oral tablets: Common strengths 50 mg and 100 mg
- Multivitamin preparations: Often contain small amounts of thiamine (e.g., 1–10 mg), which are inadequate to treat acute deficiency but helpful for maintenance
- Thiamine is often bundled in 'banana bags' or combination solutions, but high-dose replacement usually requires separate thiamine vials
Dosing – Thiamine (Adult ED/ICU):
Always follow local protocols and consult current drug references
| Indication / Scenario | Typical Dose | Route / Frequency | Notes |
|---|---|---|---|
| Suspected Wernicke encephalopathy (treatment) | 200–500 mg | IV q8h for 2–3 days | Then 250 mg IV/IM daily × 3–5 days; transition to PO 100 mg/day |
| High-risk alcohol use disorder (prophylaxis) | 100–200 mg | IV/IM/PO daily | Often part of 'rally pack' with folate and multivitamin |
| Severe malnutrition / refeeding risk | 100–200 mg | IV daily | Start before substantial carbohydrate load; continue for several days |
| Septic shock / lactic acidosis adjunct | 100–200 mg | IV q12–24h | Evidence mixed; very low toxicity and cost |
| Hyperemesis gravidarum with neurologic concern | 100 mg | IV/IM daily | Higher dosing (200–500 mg q8h) in overt Wernicke |
| Maintenance after IV course | 100 mg | PO daily | Duration based on ongoing risk factors |
| Pediatric dosing (outline only) | 10–50 mg | IV/IM/PO daily | Follow pediatric-specific references and weight-based protocols |
| Maximum common ICU dosing | 500 mg | IV q8h (short course) | Higher doses rarely needed; toxicity minimal |
Contraindications
- Known hypersensitivity to thiamine or formulation components (rare)
Adverse Effects
Common:
- Mild injection-site discomfort or irritation
- Transient flushing or pruritus (uncommon)
Serious (rare):
- Anaphylaxis or anaphylactoid reactions with IV administration (very rare)
Monitoring
- Clinical response in suspected Wernicke encephalopathy: improvement in ocular findings, gait/ataxia, and mental status over days
- Nutritional status, ongoing alcohol use, and risk of recurrent deficiency
- No routine serum thiamine level monitoring is required in most settings; deficiency is largely a clinical diagnosis in ED/ICU
Major Precautions
- Occasional anaphylactoid reactions reported with rapid IV injection; minimize risk by infusing slowly (e.g., over 30 minutes) rather than IV push in high doses
- No specific renal or hepatic dose adjustments are generally required; toxicity is extremely low even at high parenteral doses
Clinical Pearls
Low threshold for treatment: In any altered patient with alcohol use disorder or malnutrition, giving high-dose IV thiamine is almost never wrong and may be life-changing if Wernicke is present.
Refeeding syndrome prevention: When starting nutrition (especially in chronically malnourished patients), ensure thiamine is given early and regularly to reduce refeeding syndrome risk.
Persistent lactate: If lactate remains elevated despite apparent resuscitation, consider thiamine deficiency as a possible contributor, especially in high-risk patients.
Continuity of care: Thiamine is often omitted once the patient leaves the ICU; include it in your handoff and discharge planning for those with ongoing risk.
References
- Lexicomp. (2024). Thiamine: Drug information. Wolters Kluwer.
- Sechi, G., & Serra, A. (2007). Wernicke's encephalopathy: New clinical settings and recent advances in diagnosis and management. The Lancet Neurology, 6(5), 442–455.
- Farkas, J. (2022). Thiamine deficiency. EMCrit Project / IBCC. https://emcrit.org/