# Hydrocortisone versus dexamethasone in cerebral salt-wasting after aneurysmal subarachnoid hemorrhage

**Authors:** Leander Steger, Benoit Liquet, Kevin Agyemang, Moritz Freistühler, Antonio Di Ieva, Walter Stummer, Christian Ertmer, Eric Suero Molina

PMC · DOI: 10.1016/j.bas.2026.105967 · Brain & Spine · 2026-02-12

## TL;DR

This study found that hydrocortisone is more effective than dexamethasone in preventing low sodium levels in patients with brain bleeding.

## Contribution

The study provides evidence that hydrocortisone reduces the risk of hyponatremia compared to dexamethasone in SAH patients.

## Key findings

- Hydrocortisone was associated with fewer cases of severe hyponatremia (12.4%) compared to dexamethasone (25%).
- Hydrocortisone reduced the occurrence of CSW proxy (35.4% vs. 47.3%) and fewer recurrences of hyponatremia.
- Higher steroid doses showed a protective trend against hyponatremia.

## Abstract

Cerebral salt wasting syndrome (CSW) is frequently observed in aneurysmal subarachnoid hemorrhage (SAH) patients and results in excessive natriuresis with decreased extracellular fluids, leading to hyponatremia and hypovolemia. Hyponatremia is associated with an increased complication rate and potential mortality.

This study compares hydrocortisone and dexamethasone for CSW-associated hyponatremia prophylaxis after non-traumatic SAH.

This retrospective cohort study analyzed data from 510 consecutive patients with non-traumatic SAH who were admitted to the University Hospital of Münster, Germany, between October 2009 and December 2019. Hyponatremia was defined as blood sodium levels <130 mmol/L. We compared 188 patients treated with dexamethasone and 322 with hydrocortisone, focusing on the incidence of hyponatremia (<130 mmol/L) and CSW, defined as sodium levels <135 mmol/L with a negative fluid balance.

Hyponatremia (Na(p) < 130 mmol/L) developed in 87 patients (25.0% dexamethasone, 12.4% hydrocortisone; p = 0.0004). Median treatment durations were 9.0 days for dexamethasone (IQR, 5.0-15.0 days) and 10.0 days for hydrocortisone (IQR, 8.0-12.8 days). Average daily doses were 9.2 mg (±4.3) of dexamethasone and 114.3 mg (±81.9) of hydrocortisone. Simultaneous negative fluid balance and hyponatremia (Na(p) < 135 mmol/L) occurred in 203 patients (39.8%) (47.3% dexamethasone vs. 35.4% hydrocortisone) (p=0.0079, OR: 1.64, 95% CI: 1.14-2.37). For hyponatremia alone (Na(p) < 130 mmol/L), multivariable analysis showed an OR of 0.21 (p=0.00021, 95%CI: 0.09-0.48) between both groups, indicating a 4.8 times higher risk in the dexamethasone group.

Our findings indicate that hydrocortisone is associated with a lower frequency of CSW-associated hyponatremia following non-traumatic SAH as compared to dexamethasone.

•Retrospective cohort of 510 non-traumatic SAH patients comparing hydrocortisone vs dexamethasone for CSW-related hyponatremia.•Severe hyponatremia (<130 mmol/L) occurred less often with hydrocortisone (12.4%) than deamethasone (25%), p ≈ 0.0002.•CSW proxy (Na<135 mmol/L + negative daily fluid balance) occurred less often with hydrocortisone(35.4% vs 47.3%, p = 0.008).•Hydrocortisone showed fewer recurrences: 95% remained hypoantremia-free by day 7 vs 79% with dexamethasone (p<0.0001).•Risk factors: lower sodium (p = 0.012) and older age (p = 0.034) raised risk; higher steroid dose trended protective (p = 0.058).

Retrospective cohort of 510 non-traumatic SAH patients comparing hydrocortisone vs dexamethasone for CSW-related hyponatremia.

Severe hyponatremia (<130 mmol/L) occurred less often with hydrocortisone (12.4%) than deamethasone (25%), p ≈ 0.0002.

CSW proxy (Na<135 mmol/L + negative daily fluid balance) occurred less often with hydrocortisone(35.4% vs 47.3%, p = 0.008).

Hydrocortisone showed fewer recurrences: 95% remained hypoantremia-free by day 7 vs 79% with dexamethasone (p<0.0001).

Risk factors: lower sodium (p = 0.012) and older age (p = 0.034) raised risk; higher steroid dose trended protective (p = 0.058).

## Linked entities

- **Chemicals:** hydrocortisone (PubChem CID 5754), dexamethasone (PubChem CID 5743)

## Full-text entities

- **Genes:** REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, NEDD4L (NEDD4 like E3 ubiquitin protein ligase) [NCBI Gene 23327] {aka NEDD4-2, NEDD4.2, PVNH7, RSP5, hNEDD4-2}, AVP (arginine vasopressin) [NCBI Gene 551] {aka ADH, ARVP, AVP-NPII, AVRP, VP}, NR3C2 (nuclear receptor subfamily 3 group C member 2) [NCBI Gene 4306] {aka MCR, MLR, MR, NR3C2VIT}, AGT (angiotensinogen) [NCBI Gene 183] {aka ANHU, SERPINA8, hFLT1}, NR3C1 (nuclear receptor subfamily 3 group C member 1) [NCBI Gene 2908] {aka GCCR, GCR, GCRST, GR, GRL}, NPPB (natriuretic peptide B) [NCBI Gene 4879] {aka BNP, Iso-ANP}, SGK1 (serum/glucocorticoid regulated kinase 1) [NCBI Gene 6446] {aka SGK}, NPPA (natriuretic peptide A) [NCBI Gene 4878] {aka ANF, ANP, ATFB6, ATRST2, CDD, CDD-ANF}
- **Diseases:** weight loss (MESH:D015431), RSNA disorder (MESH:D009358), gastrointestinal bleeding (MESH:D006471), traumatic brain injury (MESH:D000070642), Hyponatremia (MESH:D007010), hypoxia (MESH:D000860), vasospasm (MESH:D020301), hypovolemia (MESH:D020896), Asthma (MESH:D001249), CNS damage (MESH:D002493), SIADH (MESH:D007177), cardiovascular disease (MESH:D002318), infection (MESH:D007239), aneurysm (MESH:D000783), seizures (MESH:D012640), kidney failure (MESH:D051437), central nervous system (CNS) infections (MESH:D002494), adrenal insufficiency (MESH:D000309), anterior circulation (MESH:D020520), sodium and water loss (MESH:D000069578), DCI (MESH:D002545), blood (MESH:D006402), brain diseases (MESH:D001927), COPD (MESH:D029424), SAH (MESH:D013345), stroke (MESH:D020521), Brain damage (MESH:D001925), inflammatory (MESH:D007249), thyroid impairment (MESH:D013959), brain swelling (MESH:D001929), Trauma (MESH:D014947), renal impairment (MESH:D007674), critically ill (MESH:D016638), bleeding (MESH:D006470), cerebral disease (MESH:D002539), CSW (MESH:D013651), heart failure (MESH:D006333)
- **Chemicals:** Aldosterone (MESH:D000450), cortisone (MESH:D003348), blood glucose (MESH:D001786), Natriuretic peptides (MESH:D045265), Dexamethasone (MESH:D003907), hydrogen (MESH:D006859), Hydrocortisone (MESH:D006854), salt (MESH:D012492), potassium (MESH:D011188), fludrocortisone (MESH:D005438), Na(p (MESH:C043186), Na (MESH:D012964), water (MESH:D014867), CSW (-), steroid (MESH:D013256)
- **Species:** Canis lupus familiaris (dog, subspecies) [taxon 9615], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

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## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC12954284/full.md

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Source: https://tomesphere.com/paper/PMC12954284