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Impact of Ursodeoxycholic Acid in Critically Ill Patients With Sepsis: A Retrospective Study
Khalid Al Sulaiman1,2,3, Abdullah Kharbosh4, Khalid Bin Salah1,2,3
1Pharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Insights
Ursodeoxycholic acid (UDCA) did not improve sepsis severity in critically ill adults. However, UDCA use was linked to earlier extubation and reduced mechanical ventilation needs in these patients.
Area of Science:
- Critical Care Medicine
- Pharmacology
- Sepsis Research
Background:
- Ursodeoxycholic acid (UDCA) use in pediatric sepsis is debated.
- Limited data exists on UDCA for adult sepsis/septic shock.
- Investigating UDCA's role in critically ill adults is warranted.
Purpose of the Study:
- To evaluate UDCA's impact on early sepsis/septic shock resolution in critically ill adults.
- To assess UDCA's effect on shock severity and resolution by day three.
- To analyze secondary outcomes including mortality, ventilation duration, and ICU length of stay.
Main Methods:
- Retrospective study of 88 matched critically ill adult patients with sepsis/septic shock.
- Patients categorized into UDCA and control groups based on treatment.
- Analysis focused on day three outcomes and 30-day mortality.
Main Results:
- UDCA showed no significant improvement in SOFA scores, vasopressor needs, GCS, or bilirubin levels.
- A significant association was found between UDCA use and improved PaO2/FiO2 ratio.
- Early extubation by day three was significantly more likely in the UDCA group.
Conclusions:
- UDCA did not improve overall shock severity or resolution in critically ill adult sepsis patients.
- UDCA administration was associated with a higher likelihood of early extubation.
- Further research is needed to clarify UDCA's specific benefits in adult sepsis management.
Abstract:
Background: Using ursodeoxycholic acid (UDCA) in critically ill patients as adjunctive therapy for sepsis/septic shock in neonates and children is controversial, while it has not been extensively investigated in adults. This study aims to assess the effect of UDCA use on the early resolution of sepsis/septic shock in critically ill adult patients. Method: A retrospective study of critically ill adult patients in the intensive care unit (ICU) admitted with sepsis/septic shock at King Abdulaziz Medical City. Based on their usage of UDCA, patients were categorized into two groups. A total of 88 patients were included for analysis after matching, based on severity of illness scores within 24-hours of ICU admission. The primary outcome was to assess the effect of UDCA on the severity and resolution of shock at day three of ICU admission. The secondary outcomes were 30-day in-hospital mortality, mechanical ventilation (MV) duration, and ICU length of stay (LOS). Results: Out of the 88 patients matched, 44 patients (50%) received UDCA during the study period. Using UDCA was neither associated with improvement in Sequential Organ Failure Assessment (SOFA) score (p-value: 0.32), inotropes/vasopressors requirement (p-value: 0.79), Glasgow Coma Scale (GCS) (p-value: 0.59) nor total bilirubin levels (p-value: 0.79) at day three compared with the control. There was a significant association between using UDCA and improvement in PaO2/FiO2 ratio (p-value: 0.01) and early extubation at day three (p-value: 0.04). Conclusion: Using UDCA in critically ill patients with sepsis/septic shock was not associated with improvement in shock severity and resolution. However, patients who received UDCA were more likely to be extubated and not require MV on day three of ICU admission.
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