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Folio edition · Set in Instrument Serif & Archivo

Paeds Vivashaematology-oncology-and-transfusion

Paeds Vivas · haematology-oncology-and-transfusion

Blood-component therapy in children: Viva

Branching clinical structured oral on blood-component therapy in children, covering the fractionation of whole blood into four components, the per-kilogram doses, the restrictive thresholds of the TRIPICU and PlaNeT-2 MATISSE trials, the special products, the prevention and recognition of transfusion reactions, and the massive-transfusion protocol, appraising the Lacroix, Curley, Kirpalani, Carson and Diab evidence.

branching clinical structured oral
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Target exams

RACP DWERACP DCEMRCPCH Clinical

Target exams

RACP DWERACP DCEMRCPCH Clinical
Prompt
A six-year-old girl is admitted to the paediatric intensive care unit after a motor vehicle accident with ongoing blood loss. The examiner asks you to outline the principles of blood-component therapy, to give the per-kilogram doses and the restrictive thresholds, to describe the massive-transfusion protocol and the role of tranexamic acid, to select the special products, and to recognise and manage the transfusion reactions.

Opening question: the principles and the doses

Blood-component therapy transfuses the specific component a child lacks at a weight-based dose, guided by the restrictive philosophy of patient blood management. One donation is centrifuged into four targeted components: red cells to carry oxygen, platelets to plug bleeding, fresh frozen plasma to supply clotting factors and cryoprecipitate to deliver fibrinogen. The per-kilogram doses are red cells 10 to 15 mL per kg over two to four hours, platelets 10 to 20 mL per kg, fresh frozen plasma 10 to 15 mL per kg and cryoprecipitate 5 to 10 mL per kg. A red cell transfusion of 10 to 15 mL per kg raises the haemoglobin by about 20 to 30 g per litre, and a platelet transfusion of 10 to 20 mL per kg raises the count by about 20 to 40 times ten to the nine per litre. [2]

Branch 1: the restrictive thresholds

The thresholds have fallen over three decades as the trials showed less is usually as good. The TRIPICU trial of Lacroix established the restrictive haemoglobin of 70 g per litre in the stable critically ill child, and the Cochrane review of Carson confirmed the safety of restrictive red cell thresholds across the populations studied. The prophylactic platelet threshold is 10 times ten to the nine per litre in the stable child, rising to 50 with bleeding or a procedure, and the neonatal platelet threshold is 25 rather than 50, because the PlaNeT-2 MATISSE trial of Curley found the higher threshold caused more death or major bleeding. [1][7][9]

Branch 2: the massive-transfusion protocol

This bleeding child needs the immediate activation of a massive-transfusion protocol, a pre-agreed pathway that delivers red cells, plasma and platelets in a balanced ratio while the source is controlled. Red cells are given at 10 to 20 mL per kg, fresh frozen plasma at 10 to 15 mL per kg and platelets at 10 to 20 mL per kg, with cryoprecipitate at 5 to 10 mL per kg for a fibrinogen under 1.5 g per litre. Tranexamic acid is given within three hours of the bleed, the child is warmed, the acidosis is corrected and the calcium is replaced, because the hypothermia, the acidosis and the hypocalcaemia each worsen the coagulopathy. [4][2]

Branch 3: special products and reactions

The special products are selected for the right child: leucodepleted components are the default, cytomegalovirus-negative components for the intrauterine, neonatal and immunocompromised recipient, and irradiated components for the profoundly immunocompromised to prevent graft-versus-host disease. K-negative red cells protect the girl from sensitisation, and phenotype-matched red cells prevent alloimmunisation in the chronically transfused. The commonest serious reaction is transfusion-associated circulatory overload, and the first step in any reaction is to stop the transfusion and keep the line open with saline, support the circulation, and return the unit to the laboratory. [2]

References

  1. [1]Lacroix J, Hebert PC, Hutchison JS Transfusion strategies for patients in pediatric intensive care units. N Engl J Med, 2007.PMID 17442904
  2. [2]New HV, Berryman J, Bolton-Maggs PH Guidelines on transfusion for fetuses, neonates and older children. Br J Haematol, 2016.PMID 27861734
  3. [4]Diab YA, Wong EC, Luban NL Massive transfusion in children and neonates. Br J Haematol, 2013.PMID 23432321
  4. [7]Carson JL, Stanworth SJ, Dennis JA Transfusion thresholds and other strategies for guiding red blood cell transfusion. Cochrane Database Syst Rev, 2025.PMID 41114449
  5. [9]Curley A, Stanworth SJ, Willoughby K Randomized Trial of Platelet-Transfusion Thresholds in Neonates. N Engl J Med, 2019.PMID 30387697