Most infections were P. falciparum, but we also detected a number of mixed infections. We were surprised to find three donors with quadruple infections (P. falciparum, P. malariae, P. ovale curtisi, P. ovale walikeri)! No P. vivax detected.
This has important public health implications as transfusion is a critical therapy for severe anemia. Severe anemia related to malaria is a common reason for transfusion in sub-Saharan Africa, and transfusion transmitted malaria can compromise recovery and increase mortality.
This study highlights the need for strategies to prevent transfusion transmitted malaria. Due to critical shortages in blood supply in many settings, testing blood and discarding infected units is endemic areas is problematic and would exacerbate shortages.
Pathogen reduction technology is another promising approach to prevent transfusion transmitted infections by broadly inactivating pathogens. The advantage is it can work against different classes of pathogens, and mitigate the risk of infection by new or emerging pathogens. 🦠
Studies are currently underway to assess the feasibility, efficacy and cost of implementing pathogen reduction technologies in Uganda. This could be an important tool in our arsenal to reduce the burden of malaria in endemic countries.
Thanks to our amazing collaborators @JohnsHopkinsSPH @JHUPath, Uganda Blood Transfusion Services, the CHILD lab @GHU_Official team ( @ivanmufumba @wasswar), and Kristin Murphy (who isn't on Twitter yet) for taking the lead. This officially our *first* CHILD lab publication 🎊🥂 🙏
And finally, thanks to @ChandyJohnLab and lab members @DibyaDatta, @KatrinaECo @AdnanGopinadhan and Giselle Lima-Cooper for their molecular expertise!
@womeninmalaria @WiParasitology @TransfusionNews @iupedsID @IUWellsCenter @pbangirana @IUGlobalHealth
You can follow @AndreaLConroy.
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