# Reversible Severe Acute Lactic Acidosis Caused by Thiamine Deficiency in Intensive Care Unit

**Authors:** Jisu Hong, Daehong Cho, Hong Jun Kim, Jaemin Jo, Gil Myeong Seong

PMC · DOI: 10.1155/crcc/3211626 · Case Reports in Critical Care · 2025-05-08

## TL;DR

A 50-year-old woman with severe lactic acidosis was found to have a reversible cause due to thiamine deficiency, which was treated successfully with high-dose thiamine.

## Contribution

This case highlights thiamine deficiency as a reversible cause of lactic acidosis in critically ill patients.

## Key findings

- High-dose intravenous thiamine rapidly improved mental status and normalized lactate levels.
- Thiamine deficiency was identified as the underlying cause of lactic acidosis, not an infection.
- Brain imaging revealed Wernicke's encephalopathy due to thiamine deficiency.

## Abstract

Lactic acidosis is a common cause of metabolic acidosis in hospitalized patients. It is typically caused by hypoperfusion and anaerobic metabolism and is often associated with sepsis. However, it can also result from impaired lactate metabolism, independent of hypoxemia. We report the case of a 50-year-old woman with severe lactic acidosis who was admitted to the intensive care unit. Lactic acidosis was initially attributed to an uncontrolled infection. However, brain magnetic resonance imaging revealed Wernicke's encephalopathy due to thiamine deficiency. The administration of high-dose intravenous thiamine rapidly improved the mental status and normalized serum lactate levels. This case highlights the importance of identifying thiamine deficiency as a reversible cause of lactic acidosis in critically ill patients.

## Linked entities

- **Chemicals:** thiamine (PubChem CID 1130)
- **Diseases:** lactic acidosis (MONDO:0006040), Wernicke's encephalopathy (MONDO:0007020)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** hyperlactatemia (MESH:D065906), septic shock (MESH:D012772), metabolic acidosis (MESH:D000138), WE (MESH:D014899), sepsis (MESH:D018805), malabsorption (MESH:D008286), fever (MESH:D005334), ophthalmoplegia (MESH:D009886), metabolic encephalopathy (MESH:D001928), Thiamine Deficiency (MESH:D013832), infection (MESH:D007239), cancer (MESH:D009369), impaired lactate metabolism (MESH:D007775), pneumonia (MESH:D011014), high-output cardiac failure (MESH:D006333), Korsakoff's syndrome (MESH:D020915), Decreased consciousness (MESH:D003244), inherited metabolic diseases (MESH:D030342), shock (MESH:D012769), respiratory distress (MESH:D012128), tachycardia (MESH:D013610), Coma (MESH:D003128), malnutrition (MESH:D044342), MV (MESH:D053717), confusion (MESH:D003221), gastric cancer (MESH:D013274), seizures (MESH:D012640), cognitive deficits (MESH:D003072), Critically ill (MESH:D016638), B lactic acidosis (MESH:D000140), liver dysfunction (MESH:D017093), hematological malignancies (MESH:D019337), ascites (MESH:D001201), memory loss (MESH:D008569), ataxia (MESH:D001259), anemia (MESH:D000740), polyneuropathy (MESH:D011115), hypoxemia (MESH:D000860), nystagmus (MESH:D009759), vitamin deficiencies (MESH:D014802)
- **Chemicals:** Pyruvate (MESH:D019289), glucose (MESH:D005947), Thiamine (MESH:D013831), acetyl coenzyme A. (MESH:D000105), ATP (MESH:D000255), lactate (MESH:D019344), inotropes (-), water (MESH:D014867)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12081139/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12081139/full.md

## References

14 references — full list in the complete paper: https://tomesphere.com/paper/PMC12081139/full.md

---
Source: https://tomesphere.com/paper/PMC12081139