Quantification of Dilutional Anemia in the Initial Phase of Sepsis Management: Preliminary Retrospective Study: a Preliminary Retrospective Study
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 208
- Locations
- 1
- Primary Endpoint
- Total volume of fluids administered during the first 48 hours of ICU stay
Study Overview
Brief Summary
This is a single-center retrospective study conducted at Mercy hospital, aiming to investigate the correlation between changes in hemoglobin (Hb) levels and the volume of vascular refill administered during the first 48 hours.
Detailed Description
Vascular refill is central to the initial management of hypotension in sepsis, and is often started even before the patient is admitted to intensive care. Over the past 20 years, we have moved from ultraliberal fluid resuscitation to restrictive resuscitation. Indeed, in the early 2000s, the implementation of an early and aggressive hemodynamic optimization strategy, including liberal vascular filling, improved the survival of critically ill patients, and ushered in the era of the Surviving Sepsis Campaign. However, studies have shown increased morbidity and mortality associated with a positive fluid balance. Restrictive approaches to fluid resuscitation and/or deressuscitation were then tested. While these approaches failed to demonstrate any benefit in terms of mortality, they did have the merit of demonstrating their feasibility and good tolerability, albeit with a little-explored pathophysiology. Little is known about the problem of dilutional anemia in the acute phase of septic shock.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Retrospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Patients with septic shock, admitted to Mercy hospital between November 1, 2022 and July 31, 2023, with Noradrenaline administration for at least 6 hours and at least 2 hemoglobin measurements during the first 48 hours of resuscitation.
Exclusion Criteria
- •patients with acute bleeding or blood transfusion before or during the first 48 hours of resuscitation.
Outcomes
Primary Outcomes
Total volume of fluids administered during the first 48 hours of ICU stay
Time Frame: 48 hours from ICU admission
Total volume of fluids (ml)
Secondary Outcomes
- Length of hospital stay(at hospital discharge : an average of 15 days)
- In hospital mortality(at hospital discharge : an average of 15 days)
- Haemoglobinemia(48 hours from ICU admission)
- Volume of fluids administered before admission in ICU (ml)(at ICU admission)
- Type of fluids administered during the first 48 hours of ICU stay(48 hours from ICU admission)
