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Transfusion trigger in the critically ill with sepsis or septic shock: A prospective study
Mohd Mustahsin1, Souvik Maitra2, Rahul Kumar Anand2
1Department of Emergency Medicine & Critical Care, Era's Lucknow Medical College, Lucknow, Uttar Pradesh; Department of Anaesthesiology, Pain Medicine & Critical Care, All India Institute of Medical Sciences, New Delhi, India.
In critically ill sepsis patients, red blood cell transfusion triggers below 7 g/dL are common and do not appear to impact 28-day mortality. Further assessment is needed for other transfusion parameters and long-term outcomes.
Area of Science:
- Critical Care Medicine
- Hematology
- Transfusion Medicine
Background:
- Current transfusion trigger practices for critically ill sepsis patients lack clarity.
- The association between hemoglobin trigger, red blood cell age, and transfusion volume with mortality requires further investigation.
Purpose of the Study:
- To evaluate the current transfusion trigger practices in critically ill sepsis patients.
- To assess the impact of hemoglobin trigger and red blood cell transfusion parameters on mortality and adverse outcomes.
Main Methods:
- A prospective study included 108 critically ill sepsis patients (18-70 years).
- Data collected included baseline demographics, clinical parameters, and transfusion details (hemoglobin trigger, RBC age, units transfused).
- Outcomes measured were 28 and 90-day mortality, mechanical ventilation duration, vasopressor therapy, ICU/hospital stay, and renal replacement therapy.
Main Results:
- The median transfusion trigger was 6.9 g/dL.
- Predictors of 28-day mortality included APACHE II score, cumulative fluid balance, and admission platelet count.
- For 90-day mortality, predictors were APACHE II score, cumulative fluid balance, and the transfusion trigger (aOR: 3 [1.07, 8.34], P=0.035).
Conclusions:
- In critically ill sepsis patients, the current practice involves a transfusion trigger below 7 g/dL.
- This transfusion trigger level did not significantly affect 28-day mortality in the study population.
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