# Factors associated with mortality in posterior reversible encephalopathy syndrome: a nationwide analysis

**Authors:** Ali Al-Salahat, Richard Cheung, Danielle B. Dilsaver, Amelia Pham, Ripudaman Kahlon, Muhammad Roshan Asghar, Rohan Sharma

PMC · DOI: 10.1007/s10072-026-08916-6 · Neurological Sciences · 2026-02-24

## TL;DR

This study identifies factors linked to higher in-hospital death rates in adults with posterior reversible encephalopathy syndrome using U.S. hospital data.

## Contribution

The study provides a nationwide analysis of risk factors for mortality in PRES patients using the National Inpatient Sample.

## Key findings

- Respiratory failure, sepsis, and ischemic stroke were the strongest predictors of in-hospital mortality in PRES patients.
- Conditions like cerebral edema, coma, and kidney disorders also independently increased mortality risk.
- Hypertensive crisis and a history of epilepsy were associated with lower odds of death.

## Abstract

To identify demographic and clinical factors associated with in-hospital mortality among hospitalizations of adults with posterior reversible encephalopathy syndrome (PRES) using the National Inpatient Sample (NIS) in the United States (US).

Hospitalizations for PRES in patients ≥ 18 years were abstracted from the NIS (2016–2022). To identify clinical factors associated with in-hospital mortality, univariable logistic regression models were estimated and significant predictors were retained in a multivariable logistic regression model. Collinearity was assessed via variance inflation factors. Association was quantified using adjusted odds ratios (aOR).

There were an estimated 75,830 PRES hospitalizations, of which, 3,665 in-hospital deaths occurred (4.8%). Decedents were older, had longer stays, and higher costs. In the adjusted model, the strongest factors associated with increased mortality were respiratory failure (aOR 5.43; 95% CI 4.40–6.71), sepsis (aOR 2.45; 95% CI 2.02–2.96), and ischemic stroke (aOR 2.25; 95% CI 1.86–2.72). Additional independent risk factors included cerebral edema, coma, intracerebral hemorrhage, severe liver disease, subarachnoid hemorrhage, kidney disorders, status epilepticus, encephalitis/encephalomyelitis, malignancy, complications of transplanted organs, and COVID-19. Documented hypertensive crisis (OR 0.63; 95% CI: 0.52 to 0.75) and history of epilepsy/seizures (OR 0.67; 95% CI: 0.55 to 0.81) were associated with lower odds of death.

Respiratory failure, sepsis, and cerebrovascular complications drive in-hospital mortality in PRES. Early airway protection, aggressive supportive care, and prompt neurovascular evaluation for high-risk patients may improve outcomes. Prospective studies with granular clinical and imaging data are needed to refine prognostic models.

The online version contains supplementary material available at 10.1007/s10072-026-08916-6.

## Linked entities

- **Diseases:** posterior reversible encephalopathy syndrome (MONDO:0044033), respiratory failure (MONDO:0021113), ischemic stroke (MONDO:1060198), coma (MONDO:0009764), intracerebral hemorrhage (MONDO:0013792), subarachnoid hemorrhage (MONDO:0005099), malignancy (MONDO:0004992), COVID-19 (MONDO:0100096)

## Full-text entities

- **Diseases:** Epilepsy (MESH:D004827), peripheral vascular disease (MESH:D016491), cerebral dysfunction (MESH:D002547), critical illness (MESH:D016638), RF (MESH:C538347), male reproductive disorders (MESH:D005832), headache (MESH:D006261), liver disease (MESH:D008107), inflammatory (MESH:D007249), ICH (MESH:D002543), SAH (MESH:D013345), skin (MESH:D012871), brain injury (MESH:D001930), encephalopathy (MESH:D001927), hypertension (MESH:D006973), Impaired level of consciousness (MESH:D003244), hematological disorders (MESH:D006402), hypertensive encephalopathy (MESH:D020343), connective tissue diseases (MESH:D003240), visual disturbance (MESH:D014786), PRES-RM (MESH:D003643), diabetes (MESH:D003920), neurovascular condition (MESH:D013901), COVID-19 (MESH:D000086382), peptic ulcers (MESH:D010437), Ear, nose and throat (MESH:D004427), IS (MESH:D002544), malignancy (MESH:D009369), renal failure (MESH:D051437), myocardial infarction (MESH:D009203), EM (MESH:D004679), mental conditions (MESH:D001523), encephalitis (MESH:D004660), toxic encephalopathy (MESH:D020258), hypertensive heart and chronic kidney disease (MESH:D051436), rheumatic disease (MESH:D012216), acute pancreatitis (MESH:D010195), cerebrovascular complications (MESH:D002561), urinary tract infection (MESH:D014552), congestive heart failure (MESH:D006333), essential hypertension (MESH:D000075222), Kidney disorders (MESH:D007674), aspiration (MESH:D011015), myelitis (MESH:D009187), CE (MESH:D001929), Respiratory compromise (MESH:D012131), musculoskeletal (MESH:D009140), SEP (MESH:D016472), dementia (MESH:D003704), acute kidney injury (MESH:D058186), stroke (MESH:D020521), paralysis (MESH:D010243), chronic obstructive pulmonary disease (MESH:D029424), KD (MESH:D009080), acute cerebrovascular complications (MESH:D000208), eye disorders (MESH:D005128), alcohol related disorders (MESH:D019973), EPS (MESH:D012640), sepsis (MESH:D018805), focal (MESH:D005490)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

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Source: https://tomesphere.com/paper/PMC12929328