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Pediatric transfusions. Physiology differences neonate vs child/adultChildren have higher oxygen consumption and a higher cardiac output to blood volume ratio than adults The neonatal myocardium operates at near maximum level of performance as a baseline.The newborn's heart may be unable to compe
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1. 18/07/2012 Dr Gary Simon Blood issues Pediatric transfusions
Physiology
Transfusion reactions
Blood Conservation
2. Pediatric transfusions Physiology differences neonate vs child/adult
Children have higher oxygen consumption and a higher cardiac output to blood volume ratio than adults
The neonatal myocardium operates at near maximum level of performance as a baseline.
The newborns heart may be unable to compensate for a decreased oxygen carrying capacity by increasing cardiac output.
The neonatal myocardium will also suffer a greater degree of decompensation when exposed to decreased oxygen delivery. Age Heart Rate
Pretrem 150+/-20
Term 133 +/-18
6 mo 120 +/-20
12 mo 120 +/-20
2 yr 105 +/-25
5 yr 90 +/-10
12 yr 70 +/-5
Review article
Intraoperative pediatric blood transfusion therapy: a review of common issues. Part I: hematologic and physiologic differences from adults; metabolic and infectious risks
Pediatric Anesthesia 2005 15: 716726
Review article
Intraoperative pediatric blood transfusion therapy: a review of common issues. Part II: transfusion therapy, special considerations, and reduction of allogenic blood transfusions
Pediatric Anesthesia 2005 15: 814830
Age Heart Rate
Pretrem 150+/-20
Term 133 +/-18
6 mo 120 +/-20
12 mo 120 +/-20
2 yr 105 +/-25
5 yr 90 +/-10
12 yr 70 +/-5
Review article
Intraoperative pediatric blood transfusion therapy: a review of common issues. Part I: hematologic and physiologic differences from adults; metabolic and infectious risks
Pediatric Anesthesia 2005 15: 716726
Review article
Intraoperative pediatric blood transfusion therapy: a review of common issues. Part II: transfusion therapy, special considerations, and reduction of allogenic blood transfusions
Pediatric Anesthesia 2005 15: 814830
3. Pediatric transfusions Fetal hemoglobin (HbF) comprises 70% of full term and 97% of premature infants total hemoglobin at birth. Red blood cells (RBCs) containing HbF have a shorter life span (90 days) than those containing primarily adult hemoglobin (HbA) (120 days)
HbF interacts poorly with 2,3,DPG. Therefore the P50 decreases from 26 mmHg with HbA to 19 mmHg with HbF
The optimal hemoglobin values in the newborn are higher than those of older patients (14-20 g/dl).
Physiologic nadir for hemoglobin occurs at approximately 23 months of age (term -11, prem 9.5)
The threshold for transfusing RBCs to a neonate should be at a higher hemoglobin trigger than an older child or healthy adult.
1) HbF interacts poorly with 23-diphosphoglycerate (23 DPG). Therefore the P50 (the partial pressure of oxygen at which hemoglobin is 50% saturated)
decreases from 26 mmHg with HbA to 19 mmHg with HbF. This leftward displacement of the oxygenhemoglobin dissociation curve results in decreased
oxygen delivery to tissue because of the high affinity of HbF for oxygen.
2) HbF production diminishes during the first few months of life until only a trace is present at 6 months of age. In clinical terms, the younger the infant, the higher the fraction of HbF and thus the lower the oxygen carrying capacity. Premature infants have higher percentages of HbF than their full-term counterparts and decreased
erythropoietin production which inhibits them from responding to anemia appropriately
Normal hemoglobin values for full-term and premature infants
Full term(g/dl) of blood) Premature(g/dl) of blood)
Birth 19.3 Slightly less than full term
0.5 months 16.6 15.4
1 month 13.9 11.6
Age at Hb nadir 912 weeks 610 weeks
Mean Hb at nadir 11.2 9.4
4 months 12.2 11.7
6 months 12.5 12.4The threshold for transfusing RBCs to a neonate should be at a higher hemoglobin trigger than an older child or healthy adult.
1) HbF interacts poorly with 23-diphosphoglycerate (23 DPG). Therefore the P50 (the partial pressure of oxygen at which hemoglobin is 50% saturated)
decreases from 26 mmHg with HbA to 19 mmHg with HbF. This leftward displacement of the oxygenhemoglobin dissociation curve results in decreased
oxygen delivery to tissue because of the high affinity of HbF for oxygen.
2) HbF production diminishes during the first few months of life until only a trace is present at 6 months of age. In clinical terms, the younger the infant, the higher the fraction of HbF and thus the lower the oxygen carrying capacity. Premature infants have higher percentages of HbF than their full-term counterparts and decreased
erythropoietin production which inhibits them from responding to anemia appropriately
Normal hemoglobin values for full-term and premature infants
Full term(g/dl) of blood) Premature(g/dl) of blood)
Birth 19.3 Slightly less than full term
0.5 months 16.6 15.4
1 month 13.9 11.6
Age at Hb nadir 912 weeks 610 weeks
Mean Hb at nadir 11.2 9.4
4 months 12.2 11.7
6 months 12.5 12.4
4. Pediatric transfusions Figure 28-8 Hemoglobin switching during embryonic, fetal, and adult development. The ? and epsilon genes are transcribed during embryonic development and are soon replaced by the fetal ?- and adult a-globin gene. At birth, fetal hemoglobin forms about 75% and hemoglobin A forms 25% of the total. Transcription of the ? gene begins to fall before birth, and by 6 months of age, this gene is expressed only at very low levels. Expression of the d-globin gene begins near birth. In adults, hemoglobin A makes up about 97%, hemoglobin A2 about 2.5%, and fetal hemoglobin less than 1% of the total. (From Steinberg MH: Hemoglobinopathies and thalassemias. In Stein JH [ed]: Internal Medicine, 4th ed. St. Louis, Mosby-Year Book, 1994, p 852.)
Figure 28-8 Hemoglobin switching during embryonic, fetal, and adult development. The ? and epsilon genes are transcribed during embryonic development and are soon replaced by the fetal ?- and adult a-globin gene. At birth, fetal hemoglobin forms about 75% and hemoglobin A forms 25% of the total. Transcription of the ? gene begins to fall before birth, and by 6 months of age, this gene is expressed only at very low levels. Expression of the d-globin gene begins near birth. In adults, hemoglobin A makes up about 97%, hemoglobin A2 about 2.5%, and fetal hemoglobin less than 1% of the total. (From Steinberg MH: Hemoglobinopathies and thalassemias. In Stein JH [ed]: Internal Medicine, 4th ed. St. Louis, Mosby-Year Book, 1994, p 852.)
5. Pediatric transfusions The P50 decreases from 26 mmHg with HbA to 19 mmHg with HbF. This leftward displacement of the oxygenhemoglobin dissociation curve means decreased oxygen delivery to tissue because of the high affinity of HbF for oxygen.
HbF production diminishes until only a trace is present at 6 months of age.
The younger the infant, the higher the fraction of HbF and thus the lower the oxygen delivering capacity.
Hemoglobin levels that are adequate for the older patient may be suboptimal in the younger infant or neonate. P50 - the partial pressure of oxygen at which hemoglobin is 50% saturated
Premature infants have higher percentages of HbF than their full-term counterparts and decreased erythropoietin production which inhibits them from responding to anemia appropriately
The threshold for transfusing RBCs to a neonate should be at a higher hemoglobin trigger than an older child or healthy adult. In the operating room the decision to initiate RBC transfusion is based upon a constellation of factors such as the rapidity of the blood loss, the presence of impaired oxygenation (pulmonary or cardiac in origin), and the general medical condition of the patient.P50 - the partial pressure of oxygen at which hemoglobin is 50% saturated
Premature infants have higher percentages of HbF than their full-term counterparts and decreased erythropoietin production which inhibits them from responding to anemia appropriately
The threshold for transfusing RBCs to a neonate should be at a higher hemoglobin trigger than an older child or healthy adult. In the operating room the decision to initiate RBC transfusion is based upon a constellation of factors such as the rapidity of the blood loss, the presence of impaired oxygenation (pulmonary or cardiac in origin), and the general medical condition of the patient.
6. Pediatric transfusions