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Clinical and laboratory characterization of adult sickle cell anemia patients in Kinshasa.

Paul Kabuyi LumbalaGloire MbayaboMamy Nzita NgoleAimé Z LumakaValerie RaceGert MatthijsChris Van GeetProsper Tshilobo LukusaKoenraad DevriendtTite Minga Mikobi
Published in: PloS one (2022)
In this selected, hospital-based populations of adults with SCA, severe disease was rare, which may be due to survival bias. However, two thirds had moderate severity of the disease, mostly with a low HbF, and they may benefit from HU treatment. In the Central-African setting the separation between vaso-occlusive and hyperhemolytic sub-phenotypes was not applicable.
Keyphrases
  • end stage renal disease
  • chronic kidney disease
  • newly diagnosed
  • ejection fraction
  • sickle cell disease
  • prognostic factors
  • early onset
  • patient reported outcomes
  • mass spectrometry