Vitamin

Thiamine

Reviewed by Alex G, BSN, RN, CEN, CCRN, CMC, NREMT-P · From the Reference tab of the app

Indications

Dosing

WhereDose
Metabolic and electrolyte bolusesThiamine: 100–500 mg IV before or with glucose in suspected deficiency

Mechanism of action

Thiamine enters cells on carriers (THTR-1 and THTR-2), and thiamine pyrophosphokinase converts it to thiamine pyrophosphate (TPP), the coenzyme for pyruvate dehydrogenase, α-ketoglutarate dehydrogenase, branched-chain keto acid dehydrogenase and transketolase in the pentose phosphate pathway. Without TPP, pyruvate backs up into lactate, ATP falls and neurons in high-demand areas (mammillary bodies, medial thalamus, periaqueductal gray, cerebellar vermis) swell and die. A glucose load pushes more flux through these enzymes and uses up the last TPP, so thiamine goes before or with glucose in anyone at risk.

Pharmacology

Pharmacokinetics

OnsetIV: immediate; clinical response in hours to days, eye signs first
Half-lifePlasma about 1.5 h (96 min after 50 mg IV, Tallaksen 1993); body pool 9–18 days
DistributionHighest in liver, heart, kidney and brain (label); body content 25–30 mg, about 80% as TPP
Protein bindingLoose, mainly albumin
MetabolismPhosphorylated in cells to TPP; about 1 mg a day is degraded, mainly to pyrimidine and thiazole fragments
EliminationUrine: little at normal intake; large doses spill unchanged (53% of a 50 mg IV dose in 24 h)
DialysisRemoved by hemodialysis and CRRT; long CRRT can cause deficiency
BioavailabilityOral about 5% of a 50 mg dose; carrier-limited and impaired by alcohol, so give IV for Wernicke

Chemistry

Adverse effects and cautions

In the one-pagers

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Sources

  1. FDA label: thiamine HCl injection, Fresenius Kabi (2019)
  2. Tallaksen 1993 (kinetics)
  3. Wrenn 1989 (IV safety)
  4. Harper 1986 (Wernicke autopsy series)

For education and exam preparation only. Follow your institution’s protocols. Typical adult values for study. Follow your local protocols and medical direction.