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Gender-based Differences in the Outcome of the Treatment of Persistent Septic Shock With Hydrocortisone

A

Alexandria University

Status

Completed

Conditions

Septic Shock

Study type

Observational

Funder types

Other

Identifiers

NCT06537180
GBD-HYDRO

Details and patient eligibility

About

The aim of this study is to explore the gender-based differences in the outcomes of treatment with hydrocortisone in critically ill patients with persistent septic shock.

Full description

Because of their pleiotropic effects, corticosteroids are widely used as adjunctive therapy in sepsis for their anti-inflammatory, metabolic, and immune-suppressing actions. Moreover, the treatment benefits of corticosteroids in terms of hemodynamics and organ functions for septic shock were established. Hydrocortisone reduces the duration of mechanical ventilation and critical care treatment and reduces the time needed for shock reversal. Hydrocortisone use at a daily dose of ≤400 mg for at least 3 days was associated with survival benefits.

Interestingly, corticosteroid treatment was reported to be more cost-effective in females than in males with septic shock, compared with placebo. This may be explained by the fact that sex hormones modulate the expression and sensitivity of glucocorticoid receptors differently, potentially influencing the body's response to cortisol. To the best of our knowledge, the data available on whether females and males may be more or less likely to acquire a better or worse prognosis of persistent septic shock when treated with hydrocortisone is sparse.

The aim of this study is to explore the gender-based differences in the outcomes of treatment with hydrocortisone in critically ill patients with persistent septic shock.

Enrollment

621 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients of both sexes with persistent septic shock received hydrocortisone during their intensive care unit (ICU) stay.

Exclusion criteria

  • Patients with incomplete data sets.

Trial design

621 participants in 2 patient groups

The Female Group
Description:
Patients are categorized as females according to their apparent gender.
The Male Group
Description:
Patients are categorized as males according to their apparent gender.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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