# Increasing Hospitalizations for Wernicke Encephalopathy in Spain: A Nationwide Population-Based Study

**Authors:** David Puertas-Miranda, M. A. Ortiz-Pinto, F. Josue Cordero-Pérez, Luis Arribas-Pérez, P. Martinez-Rodríguez, Antonio-J. Chamorro, Miguel Marcos

PMC · DOI: 10.3390/jcm15041549 · 2026-02-15

## TL;DR

Hospitalizations for Wernicke encephalopathy in Spain have increased significantly, with higher mortality linked to comorbidities rather than the condition itself.

## Contribution

This study provides the first nationwide population-based analysis of Wernicke encephalopathy trends and outcomes in Spain.

## Key findings

- Hospital admission rates for Wernicke encephalopathy increased by 16% annually from 2016 to 2022.
- In-hospital mortality was 3.7%, primarily driven by comorbidities like cancer and infection.
- The proportion of foreign-born patients with Wernicke encephalopathy increased significantly over the study period.

## Abstract

Background/Objectives: Wernicke encephalopathy (WE) is an acute neurological syndrome caused by severe thiamine deficiency. Early detection is challenging due to the low sensitivity of the classic triad. Methods: This retrospective observational study used the Spanish Minimum Basic Data Set, including hospital admissions with a primary diagnosis of WE (2016–2022). Demographic, clinical, and economic variables were also analyzed. Severity of illness (SOI) and risk of mortality (ROM) were assessed using the All Patient Refined Diagnosis-Related Groups (APR–DRG) system. Results: A total of 2477 WE episodes were included (1864 men; mean age, 58.2 years; standard deviation [SD], 11.0). The hospital admission rate increased by an average of 16% per year (incidence rate ratio [IRR], 1.16; p < 0.001). The proportion of foreign-born patients increased significantly over the study period. Most patients were discharged home (1868; 75.4%), whereas transfers to residential care facilities increased over time. The mean hospital stay was 19.0 days (SD 36.5). In-hospital mortality was 3.7%. In multivariable analysis, malnutrition (odds ratio [OR] 1.64), cancer (OR 2.11), and active infection (OR 5.79) were independently associated with mortality. The incorporation of ROM into the mortality model markedly improved discrimination, and mortality increased progressively with higher ROM categories: moderate (OR 3.45), major (OR 11.76), and extreme (OR 38.76) (all p < 0.001). Conclusions: WE is an increasingly frequent cause of neurological hospitalization in Spain, associated with a substantial clinical and economic burden. In-hospital mortality is driven mainly by overall clinical complexity and comorbidity burden rather than by WE in isolation.

## Linked entities

- **Diseases:** Wernicke encephalopathy (MONDO:0007020), cancer (MONDO:0004992), infection (MONDO:0005550), malnutrition (MONDO:0006873)

## Full-text entities

- **Diseases:** Mortality (MESH:D003643), malnutrition (MESH:D044342), ataxia (MESH:D001259), alcohol use disorders (MESH:D000437), injury to (MESH:D014947), ophthalmoplegia (MESH:D009886), dietary deficiency (MESH:D000740), thiamine deficiency (MESH:D013832), cirrhosis (MESH:D005355), WE (MESH:D014899), neurological complications (MESH:D002493), infection (MESH:D007239), renal failure (MESH:D051437), psychiatric disorders (MESH:D001523), cancer (MESH:D009369), gastrointestinal surgery (MESH:D005767), diabetes mellitus (MESH:D003920), atrial fibrillation (MESH:D001281), MBDS (MESH:C564133), confusion (MESH:D003221), oculomotor abnormalities (MESH:D015840), hepatic encephalopathy (MESH:D006501), anorexia nervosa (MESH:D000856), alcoholic liver disease (MESH:D008108), obesity (MESH:D009765), heart failure (MESH:D006333), memory impairment (MESH:D008569), sepsis (MESH:D018805), chronic (MESH:D002908), neurological symptoms (MESH:D009461), HIV infection (MESH:D015658), amnesia (MESH:D000647), cerebellar dysfunction (MESH:D002526), Korsakoff's psychosis (MESH:D020915)
- **Chemicals:** thiamine (MESH:D013831), ethanol (MESH:D000431), alcohol (MESH:D000438)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12941529/full.md

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Source: https://tomesphere.com/paper/PMC12941529