First transfusion session of the day @BritSocHaem . BBTS session chaired by @mikefmurphy looking at red cell genotyping. Dr Megan Delaney is going to take us through when red cell genotyping should be undertaken #BSH2019
In the setting of AIHA, providing matched blood can avoid the need for multiple adsorptions (if pt only receiving blood in your institution) #BSH2019
Phenotyping may not be possible with a strong warm autoab therefore genotyping may be useful #BSH2019
Difficult to prove that matching for important antigens prevents alloimmunisation in AIHA #BSH2019
Daratumumab (antiCD38) targets red cells and causes panreactive antibody screens. Ideally need to phenotype patients prior to treatment #BSH2019
If no extended phenotype pre rx with dara, molecular typing will be useful #BSH2019
Can also treat cells with DTT to destroy the dara. BUT some blood group antigens are also destroyed #BSH2019 (K and k particularly) #BSH2019
Dr Delaney advocates
No prev abs : kell match
Prev abs : extended match
Genotyping also useful for patients with D variants. Some D variants can form anti D and others "can't". So important to know which variant the patient has #BSH2019
Markov model used by Kacker et al. to follow women through their lifetime and use genotyping to distinguish treatment approach. Found to be marginally cost saving #BSH2019 ncbi.nlm.nih.gov/pmc/articles/P…
In sickle cell anaemia we should be fully Rh matching in order to reduce risk of alloimmunisation. High rate of C/c and E/e variants in this population #BSH2019
D gene is thought to be a historical duplication of the CE gene; many similarities and parts of the genes have been 'exchanged' over time. RhD/CR hybrid allele in 24% sickle patients who are C positive, and 30% made anti-C #BSH2019
This is probably one of the most compelling reasons to genotype patients, argues Dr Delaney #BSH2019
Genotyping remains a tool for select groups of patients. No benefit still in the vast majority of patients #BSH2019
Dr Shubha Allard makes the point that dara is now being used for indications other than myeloma, and we need to find ways to reach non-haematology clinicians #BSH2019
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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…