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Paediatric blood transfusion Dr. Chitra Rajeswari T Dr. Lokesh Kashyap www.anaesthesia.co.inwww.anaesthesia.co.in anaesthesia.co.in@gmail.comanaesthesia.co.in@gmail.com
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Why to transfuse blood Basic physiological function is to ensure adequate oxygenation of the tissues Physiology of oxygen transport
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Hypoxic hypoxia Anaemic hypoxia Histotoxic hypoxia Stagnant hypoxia
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Anaemic hypoxia
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Oxygen delivery DaO2 =Cardiac output X CaO2 [oxygen content] Oxygen content [Hb saturation X 1.34 X Hb conc] + 0.003 X PO2 Amount of oxygen carried by 100 ml of blood
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Fetal hemoglobin Cardiac reserve Increased metabolism
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Fetal hemoglobin HbF – 70-80% of full term and 97% of premature infants’ total hemoglobin at birth
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Fetal hemoglobin Shorter life span of 90 days (HbA- 120 days) HbF interacts poorly with 2,3,DPG P50 with HbF is 19 mmHg P50 with HbA is 27 mmHg Leftward shift of ODC
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ODC
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Hemoglobin for equivalent oxygen delivery P 50Hb Adult2710 Infants [>3 month] 308.2 Infants [<3 month] 2414.7 Motoyama et al. 1990
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6 months- 6 years 12 7-13 years 13 6 months- 6 years 12 7- 13 years 13
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Preoperative hemoglobin At the time of nadir Term infant with Hb < 9 g/dl Preterm infant <7 g/dl Haemoglobin levels that are adequate for the older patients may be suboptimal in the younger infant
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Fetal hemoglobin Cardiac reserve Increased metabolism
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Adult vs children - cardiac reserve Children have a higher cardiac output to blood volume ratio than adults Estimated circulating blood volume AgeBlood volume (ml/kg) Premature infant90-100 Term infant – 3 months80-90 Children older than 3 months70 Very obese children65 Sandra et al. Pediatric anesthesia 2005
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The neonatal myocardium operates at near maximum level of performance as a baseline The newborn’s 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 Adult vs children - cardiac reserve
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Metabolism Oxygen consumption
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When to transfuse blood?
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MABL MABL = Starting – Target hematocrit Blood loss more than this target value then RBC cell transfusion should be initiated 65 ml of packed RBC [Hct 70%] = 150 ml of whole blood [Hct 30%] 0.5 ml of PRBC for each ml of blood loss beyond the MABL 1 ml/kg PRBC raises the hematocrit by 1.5% Starting hematocrit X EBV
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May benefit from higher hematocrit Preterm and term infants Cyanotic congenital heart disease Large ventilation/ perfusion mismatch High metabolic demand Respiratory failure
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Guidelines for perioperative management of anemia Minimum acceptable hemoglobin Infants > 3 months8 g/dl Infants < 2 months Ex-premie <52 weeks PCA 10g/dl Infants in first week of life Weight < 1500 g With cardiopulmonary disease 12g/dl
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Guidelines contd… In an elective setting, anemia should be evaluated and treated,surgery may be postponed for a month or longer Cumulative record of blood loss should be kept for critically ill infants and loss replaced when it exceeds 10% of blood volume
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In an emergency setting, anesthesia administered with extreme caution Maintain high PaO2 Adequate cardiac output Adequate intravascular volume Avoid factors increasing oxygen consumption Avoid leftward shift of ODC Guidelines contd…
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Oxygen extraction ratio as hematocrit drops to 15%, OER increases from 38 to 60% Central venous Po2 - -Decline of pVo2 is the most sensitive indicator of anemia - -Normal => 38 mm Hg Holland et al. 1987 Guidelines contd…
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Pediatric transfusions – guidelines Platelet transfusions platelet count less than 50000 in acute bleeding Less than 1 lakh for intracranial and Subarachnoid or extra corporeal circulation procedures 5 mL/kg - 10 mL/kg causes a rise of platelets of 50 to 100 * 10 9 /L Fresh frozen plasma aPTT or PT > 1.5 times normal 10-15 ml/kg Cryoprecipitate Fibrinogen 100 mg/dl 1 unit /10 kg BW raises plasma fibrinogen by 50 mg/dl
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Acute transfusion reactions ( < 24 hours) Febrile nonhemolytic reaction Urticarial/allergic reaction Acute hemolytic reaction Bacterial contamination and sepsis Fluid overload Anaphylaxis TRALI Delayed transfusion reaction Infection Delayed hemolytic reaction Post transfusion purpura Graft Vs host disease Iron overload Transfusion reactions
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TRALI TRALI Acute hypoxemia Non-cardiogenic pulmonary edema During or after transfusion Leading cause of transfusion-related mortality in 2003 – FDA, TRALI conference Underdiagnosis & underreporting
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Incidence All plasma-containing blood & blood components 1/5,000 blood & blood component 1/2,000 plasma-containing component 1/7,900 units of FFP 1/432 units of whole blood derived platelets
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Pathophysiology Leukocyte antibodies Biologically active substance Lipids & cytokines Neutrophil priming activity Leukocyte Antibodies Neutrophil in pulmonary capillary → pulmonary damage & capillary leak Antibody to donor leukocyte Ab to HLA I, II, granulocyte, monocyte, IgA
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Management Supportive Stop transfusion if timely recognition Oxygen and ventilatory support as employed in ARDS Avoid blood from multiparous female donors
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Immunologic Transfusion related graft vs host disease Lymphocytes in transfused blood component proliferate and cause host tissue destruction Immunocompromised patient Premature infants Children with cancer or severe systemic illness Acute blood loss Cardiopulmonary bypass Prevented by irradiated blood
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Pediatric transfusions - neonates Neonates have some specific considerations with respect to anesthesia and blood products. Major hemolytic reaction (ABO) occurs less frequently in neonates compared with older children and adults. For the first 3–4 months of life, infants are unable to form alloantibodies to RBC antigens. After 4 months of age, hemolytic reactions become a potential factor
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Massive blood transfusion
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Definition Loss of one or more circulating blood volume in 24 hour 50% blood volume in 3 hours Loss occurring at the rate of 2-3 ml/kg/min
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Problems of massive transfusion Hypocalcemia Hyperkalemia Hypomagnesemia Hypothermia Volume overload Dilutional coagulopathy Acid base changes Shift of ODC curve Microaggregate delivery TRALI
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Hypocalcemia Degree of ionized hypocalcemia depends upon Blood product transfused Rate Hepatic blood flow Hepatic function
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Hypocalcemia Degree of ionized hypocalcemia depends upon Blood product transfused Rate Hepatic blood flow Hepatic function FFP Decreased ability to metabolise by neonate > 1 ml / kg / min
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Myocardial depression Hypocalcemia Decreased ability to metabolise by neonate Inhalational agents
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Prevention of hypocalcemia Rate should be < 1 ml / kg / min If more than > 1 ml / kg / min calcium should also be transfused Calcium infusion Calcium chloride 5-10 mg/kg Calcium gluconate 15-30 mg/kg Frequent measurement of ionised calcium
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Hyperkalemia Blood components with high potassium Whole blood Irradiated blood Near the expiry date
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Prevention of hyperkalemia Washing of erythrocytes Newer blood (< 7 days) Avoiding whole blood and prefer packed RBC
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Treatment CaCl 2 15-20 mg/kg Calcium gluconate 45-60 mg/kg 1-2 min intervals until the arrhythmia is resolved Glucose and insulin Hyperventilation Albuterol kayexalate
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Hypomagnesemia Result of citrate toxicity Stabilizes the resting membrane potential Life threatening arrhythmia that dose not respond to exogenous calcium therapy needs magnesium sulphate 25-50 mg/kg followed by 30-60 mg/kg/24 hours
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Acid-base changes RBC metabloism can elevate the dissolved CO 2 to 180-210 mmHg Anaerobic metabolism increases the lactic acid content Initial transient combined respiratory and metabolic acidosis Citrate metabolism leads to metabolic alkalosis
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Hypothermia Shift to left of ODC curve – decreased oxygen delivery Apnea Hypoglycemia Decreased drug metabolism Increased oxygen consumption Coagulopathy
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Coagulopathy Massive blood transfusion leads to thrombocytopenia 40%, 20% and 10% of starting platelet count is seen after 1 st, 2 nd and 3 rd blood volume loss Dilution and loss of clotting factors Clotting factor deficiency should be anticipated after one blood volume loss
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Recombinant factor VIIa Retrospective review of use of factor 7a in children undergoing major neurosurgical procedures experiencing massive uncontrollable hemorrhage Useful adjunct to control life threatening bleeding,but more extensive research is needed Uhring et al Ped crit care med, 2007
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Mechanism of action
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Blood Conservation Preoperative Autologous Donation Acute Normovolemic Hemodilution Intraoperative Blood Salvage Preoperative Erythropoietin Positioning Hypotensive anaesthesia Pharmacological enhancement of hemostasis Artificial blood www.anaesthesia.co.inwww.anaesthesia.co.in anaesthesia.co.in@gmail.comanaesthesia.co.in@gmail.com
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