This many moving haematologists need a name
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TeamHaem retweeted
#fASHion at #ASH22 (cc: @acweyand)
Reppin’ H&E and Giemsa colors in my tie today #PathAtash #hemepath
Normal bone marrow cells - what a joy to see! – at New Orleans, LA
Comin back soon...
Should we do Mastodon, Instagram or just stay here and see what happens?
Not LinkedIn obviously.
12%Mastodon
9%Instagram
52%Twitter
27%All of them
33 votes • Final resultsThis! LMWH often still given at 6pm which means anti-Xa at midnight. Not good for anyone. No need to routinely monitor levels. Only very specific situations e.g. extremes weight, thrombosis despite normal dose, bleeding, renal failure #TeamHaem
Will pre-exposure prophylaxis be the next step in protecting patients with CLL? #BSH2022
Pirtobrutinib - a non-covalent BTKi has efficacy in patients pre-treated with other BTKi #BSH2022
Would you like some blood film with your oil Dr T?! #TeamHaem
We do like a good Congo red too #TeamHaem
TeamHaem retweeted
#1 iStopMM RCT shows prevalence of MGUS in age >=40 is 5%. Importantly early results show that screening detects significantly higher number of people with MM, SMM. #ASH21 #ASH21VR @sykristinsson @SigrunThorstei1 @ThorvardurL @TBSsteharding @BrianDurieMD ash.confex.com/ash/2021/webp…
TeamHaem retweeted
Elevated plasma concentration of complement factor C5 is associated with risk of future venous thromboembolism loom.ly/Aab_WZ4
TeamHaem retweeted
It's your last chance to submit your entry for The Crucible Prize -an innovative trainee-led initiative with a £1000 prize.
The prize is open to doctors in training, nurses and other healthcare professionals (at any stage of their career).
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#BSH2022
TeamHaem retweeted
How I treat dysfibrinogenemia ashpublications.org/blood/ar…
Absolutely.. HLH is a possibility and marrow haemophagocytosis is not always seen.. but at times these things evolve and we may only have 3-4 of the 8 criteria.. here we would evaluate for both primary causes like perforin assay etc and also look at secondary causes..
Replying to @TeamHaem
Most likely HLH,5 out of 8 should be met,Hemopagocytosis is not necessary to be demonstrated in the bone marrow,can be genetic HLH as all infectious markers are negative,Perforin gene,sytaxin gene mutation
























