The effect of red blood cell transfusion on peripheral tissue oxygen delivery and consumption in septic patients

Author(s):  
L.C. Nicolescu ◽  
C.M. Nicolescu ◽  
A.G. Mihu ◽  
C. Balta
1990 ◽  
Vol 12 (2) ◽  
pp. 47-53
Author(s):  
Richard A. Molteni

In recent years a great deal of attention has been paid to the evaluation and treatment of conditions characterized by red blood cell excess (polycythemia). The debatable practice of routine newborn hematocrit screening was initiated and perpetuated by the still uncertain short-term and long-term complications of polycythemia and its commonly associated state of hyperviscosity. Previously unsuspected anemia is often identified during this same screening process. Unless profound (leading to hypovolemic shock) or associated with more visible signs of hemolysis (jaundice), the etiology of this state of diminished red blood cell mass is often ignored or evaluated incompletely. This review focuses on the effects of anemia in the fetus and neonate, discusses mechanisms of fetal red blood cell production, and provides a basic diagnostic approach for the clinician when anemia is recognized in the neonatal period. PHYSIOLOGIC EFFECTS OF RED CELL REDUCTION Tissue Oxygen Delivery Maintenance of adequate red blood cell numbers can be even more critical during fetal life than during the postnatal period. The fetus, dependent upon maternal oxygen sources, cannot raise tissue oxygen delivery acutely by increasing placental oxygen transfer, even when its red blood cell numbers are decreased. Total oxygen content (sum of oxygen dissolved in plasma and bound to hemoglobin) of the blood is dependent upon both the partial pressure of oxygen (Pao2) and the quantity of hemoglobin available.


2016 ◽  
Vol 26 (2) ◽  
pp. 247-255 ◽  
Author(s):  
Victoria A. McCredie ◽  
Simone Piva ◽  
Marlene Santos ◽  
Wei Xiong ◽  
Airton Leonardo de Oliveira Manoel ◽  
...  

Neurosurgery ◽  
2011 ◽  
Vol 68 (5) ◽  
pp. 1286-1292 ◽  
Author(s):  
Kevin N. Sheth ◽  
Aaron J. Gilson ◽  
Yuchiao Chang ◽  
Mona A. Kumar ◽  
Rosanna M. Rahman ◽  
...  

Abstract BACKGROUND: Accumulating data suggest that anemia worsens outcomes in critically ill patients, including those with subarachnoid and intracerebral hemorrhage (ICH). Although packed red blood cell (PRBC) transfusion appears to increase brain tissue oxygen, it is unknown whether such transfusions, which are commonly administered in patients with intracranial hemorrhage, alter outcome. OBJECTIVE: Following up on our observation that anemia is associated with poor outcome in patients with ICH, we investigated whether PRBC transfusion was associated with any benefit. METHODS: Five hundred forty-six consecutive subjects were identified from an ongoing single-center, prospective cohort study of nontraumatic ICH over a 6-year period. Clinical and radiographic characteristics, laboratory values including admission and daily mean hemoglobin values, and all instances of PRBC transfusion were recorded. Aggressiveness of care was assessed by whether the patient had a “do not resuscitate” order activated during hospitalization. The primary endpoint was 30-day survival. RESULTS: Anemia was present in 144 of 546 patients (26%) on admission and developed subsequently in an additional 250, leaving just 152 of 546 patients (28%) who never developed anemia. PRBC transfusion was administered to 100 patients (18%) during their hospital stay, 98% of whom were anemic. In multivariable analysis, PRBC transfusion was associated with improved survival at 30 days (odds ratio: 2.76; 95% confidence interval: 1.45-5.26; P = .002). CONCLUSION: Anemia develops in the majority of patients with ICH at some point during their hospitalization. PRBC transfusion was associated with improved outcome in these patients.


Transfusion ◽  
2020 ◽  
Vol 60 (3) ◽  
pp. 466-472
Author(s):  
Gregory P. Goldstein ◽  
Anoop Rao ◽  
Albee Y. Ling ◽  
Victoria Y. Ding ◽  
Irene J. Chang ◽  
...  

Stroke ◽  
2009 ◽  
Vol 40 (9) ◽  
pp. 3039-3044 ◽  
Author(s):  
Rajat Dhar ◽  
Allyson R. Zazulia ◽  
Tom O. Videen ◽  
Gregory J. Zipfel ◽  
Colin P. Derdeyn ◽  
...  

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