I’m spending a lot of time thinking about O D neg this week. R0 is something that often causes difficulties – for #haemSpRs and transfusion labs! So what is R0?
(also tempted to add a poll for how you say it! Will stick to "R oh" personally....)
and we have the correct answer! Capital R = D pos, then 0 means (to my mind) no C or E. R0 = cDe; R1 = CDe; R2 = cDE. r = cde which is of course D neg
R0 is the rh phenotype where c, D and e are expressed. These patients are D positive. 44% African Caribbean people will have this phenotype, but only 4% Caucasian people do.
Patients with sickle cell anaemia require blood that is fully Rh matched. Most patients with sickle cell anaemia are African Caribbean but 96% of UK blood donors are Caucasian.
The most common “C neg E neg” phenotype in Caucasians is cde (r). These donors are D negative (obviously). Hence to find Rh matched blood for pts with sickle cell anaemia can mean giving cde (r) blood to cDe (R0) pts, i.e. substituting D neg when there is no other indication!
*question time* #blooducation
Additional pressures are brought by the additional requirements for blood for patients with sickle cell anaemia. Q for #haemSpRs: what are these?
How to reduce the need to substitute D neg for D pos: 1. Clinicians: request blood for pts with SCD in good time 2. BMSs: only subst D neg when necessary, only give O when no other ABO compatible RBC available 3. Everyone: encourage people of BAME backgrounds to donate
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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…