# Hydrocortisone combined with fludrocortisone for treatment of adults with septic shock: an updated meta-analysis and systematic review

**Authors:** Alin Sun, Xiang Gao, Zhipeng Gao, Qinghai Zhang, Wenzheng He

PMC · DOI: 10.3389/fmed.2026.1755626 · Frontiers in Medicine · 2026-02-11

## TL;DR

This study finds that combining hydrocortisone and fludrocortisone may improve survival in septic shock compared to placebo, but not compared to hydrocortisone alone.

## Contribution

The study provides updated meta-analysis and systematic review on the combined use of hydrocortisone and fludrocortisone in septic shock.

## Key findings

- The combination of hydrocortisone and fludrocortisone significantly reduced 28-day, 90-day, and in-hospital mortality compared to placebo.
- No significant survival benefit was found when comparing the combination to hydrocortisone alone.
- The combination was associated with increased reinfection rates compared to placebo but not compared to hydrocortisone alone.

## Abstract

To evaluate the efficacy and safety of hydrocortisone combined with fludrocortisone in the treatment of septic shock in adults.

We searched PubMed, Embase, Web of Science, and the Cochrane Library for studies on hydrocortisone combined with fludrocortisone in the treatment of septic shock in adults. Two investigators independently screened studies, extracted data, and assessed the risk of bias of the included studies. A meta-analysis was performed using RevMan 5.3 and STATA 17.0 software.

A total of eight studies (5 RCTs and 3 N-RCTs) were included. Stratified analysis by study design and comparator type revealed that in the HC + FC vs. Placebo subgroup (derived solely from RCTs), the combination significantly reduced 28-day mortality [RR 0.84; 95% CI (0.76, 0.94); p = 0.002], 90-day mortality [RR 0.82; 95% CI (0.71, 0.94); p = 0.006], and in-hospital mortality [RR 0.85; 95% CI (0.77, 0.94); p = 0.002]. In contrast, for the HC + FC vs. HC alone subgroup (addressing incremental benefit), no significant survival advantage was observed in either RCTs (n = 553) or N-RCTs (n = 88,666, 28-day mortality RR 0.99, p = 0.79). Regarding safety, HC + FC was associated with a higher reinfection rate compared to placebo (RR 1.13, p = 0.03) but not when compared to HC alone (p = 0.19). No significant increase in gastrointestinal bleeding or reduction in ICU/hospital length of stay was identified across all tiers of evidence.

Evidence primarily from RCTs indicates that HC + FC is associated with improved survival compared to placebo in septic shock. However, large-scale observational data suggest no significant incremental benefit over hydrocortisone alone. While the combination appears safe regarding gastrointestinal bleeding, the increased reinfection risk compared to placebo warrants caution. Given the non-causal nature of observational findings, these results are suggestive rather than definitive. Future head-to-head trials are essential to confirm the marginal efficacy of fludrocortisone supplementation.

https://www.crd.york.ac.uk/PROSPERO/view/CRD420251001999, Identifier: CRD420251001999

## Linked entities

- **Chemicals:** hydrocortisone (PubChem CID 5754), fludrocortisone (PubChem CID 31378)

## Full-text entities

- **Genes:** REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}
- **Diseases:** death (MESH:D003643), re (MESH:D000084063), urinary tract infections (MESH:D014552), Infection (MESH:D007239), gastroduodenal bleeding (MESH:D010437), ischemic injury (MESH:D017202), immune dysfunction (MESH:D007154), vasoplegia (MESH:D056987), allergic (MESH:D004342), adrenal exhaustion (MESH:D006359), gastric and duodenal hemorrhage (MESH:D006471), cognitive impairment (MESH:D003072), mineralocorticoid deficiencies (MESH:C567596), Sepsis (MESH:D018805), Septic shock (MESH:D012772), septic (MESH:D001170), inflammatory (MESH:D007249), pulmonary infections (MESH:D012141), shock (MESH:D012769), Failure (MESH:D051437), glucocorticoid insufficiency (MESH:D000309), bleeding (MESH:D006470), MODS (MESH:D009102), gastric and duodenal bleeding (MESH:D004382)
- **Chemicals:** FC (MESH:C095424), sodium (MESH:D012964), catecholamines (MESH:D002395), steroid (MESH:D013256), aldosterone (MESH:D000450), epinephrine (MESH:D004837), HC (MESH:D006854), Fludrocortisone (MESH:D005438)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12932585/full.md

## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932585/full.md

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Source: https://tomesphere.com/paper/PMC12932585