First Megan Delaney discussing the role of pathogen inactivation in platelets transfused to children and neonates.
Updating on the recent evidence supporting the safety of both Mirasol and Intercept products, but highlighting that both result in lower post transfusion platelet increments.
Then Marianne Nellis @mnellismd talking on transfusion in paediatric critical care, presenting the work of the TAXI (Transfusion and Anaemia eXpertise Initiative group), culminating in a series of best practice statements and a transfusion decision tree. ncbi.nlm.nih.gov/pmc/articles/P…
Following on from this will be TAXI-CAB (Control/Avoidance of Bleeding) – aiming for publication early next year. Amazing work!
Then @simonstanworth on the PlaNeT-2 study. Neonates were randomised to receiving platelets at 25 or 50 x10^9/L. Full study was published last year nejm.org/doi/10.1056/NE…
Paediatric practice has historically been to use more liberal thresholds in neonates versus adults (where 10 would be our standard in stable patients). @BritSocHaem guidelines state 25 for stable neonates. onlinelibrary.wiley.com/doi/full/10.11…
Bleeding/death composite outcome occurred in 19% in the restrictive group and 26% in the liberal group. OR 1.57 (1.06-2.32) i.e. outcomes worse in the patients receiving platelets at 50.
This was unexpected. Differences materialised from the second week after randomisation.
Why is this? Volume? Platelet donors are adults; are there physiological differences between adult and neonatal platelets and plasma? Is there an immune/inflammatory effect?
Other studies are also reporting worsening outcomes with platelet transfusion and a threshold of 25 is now recommended for neonatal platelet transfusions
I had a personal request to do a tweetorial for the #haemSpRs on haemovigilance. Here goes. A #blooducation 🧵
Haemovigilance is a systematic surveillance of adverse reactions and adverse events related to transfusion’ with the aim of improving transfusion safety. transfusionguidelines.org/transfusion-ha…
We are very lucky in the UK to have @SHOTHV1, one of the first in the world to collate adverse events relating to transfusion - since the 1990s.
This morning I met with the chair and vice chair of the Midlands Regional Transfusion Committee, the Midlands Patient Blood Management Practitioner and the Customer Services Manager. What are their roles and what does the RTC do?
A #blooducation 🧵
RTCs serve to bring together Hospital Transfusion Committees to discuss best practice, implement new guidance and provide educational resources and events. They are run by clinicians and scientists working in hospitals, supported by @NHSBT.
Teaching our incoming haematology doctors today about transfusion in haematology patients. So who needs irradiated blood and why? A #blooducation🧵
All blood in the UK is leucocyte reduced (except granulocytes, but that’s another story). Despite this, a unit of red cells or platelets can have around a million residual white cells, mostly lymphocytes.
Every doctor starting in a new trust does transfusion training as part of their mandatory training. But why?
50ml ABO incompatible blood can kill a patient. ABO antibodies are naturally occurring (“everyone” has them) and they are IgM; they can activate complement and cause *immediate* intravascular haemolysis, causing release of free haem, endothelial activation, renal failure and DIC.
In most hospitals, blood banks require 2 samples (one may be historic) before releasing group specific (non-O) blood for a patient. This is to increase the chances of identifying a *wrong blood in tube* (pt whose blood's in the tube is not the pt whose details are on the outside)
It can be difficult to know where to start with transfusion – you can’t go on a ward round to find patients. BUT you do start with lab induction and your helpful #BMSes will show you around.
Excellent session on emergency paediatric transfusion #AABB20. Cyril Jacquot talking on pre hospital transfusion and summarising the literature.
28 day mortality following haemorrhage is higher in children than adults (unpublished data and substudies from PROPPR and PROMMTT)
Observational studies of large numbers of patients but with only very small numbers of paediatric patients suggest that pre hospital blood is not associated with an excess of transfusion reactions and in some studies is thought to have improved survival.
Whole blood, group O, high titre neg, used in paediatrics in Pittsburgh appears to be safe with no haemolysin-mediated haemoylsis in non group O patients (Leeper et al JAMA Pediatrics 2018) ncbi.nlm.nih.gov/pmc/articles/P…