「Anemia in the tropics」の版間の差分

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*malaria does not cause IDA directly; destruction of RBCs by ''Plasmodium'' does not cause iron loss
 
*malaria does not cause IDA directly; destruction of RBCs by ''Plasmodium'' does not cause iron loss
 
**anemia by malaria is mainly by inflammation, which suppresses iron absorption
 
**anemia by malaria is mainly by inflammation, which suppresses iron absorption
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==sickle cell anemia==
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*monogenetic recessive disorder
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*hemoglobin mutation
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*HbA mutated into HbS (sickle cell trait) or HbC (West Africa)
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*sickle cell trait protect against death from severe malaria
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**not prevent infection itself
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===clinical picture of SCD===
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*affects all organ systems
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*disease pattern and severity varies very much on patients
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===chronic management===
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*first to identify high risk groups
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==thalassemia==
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*decreased hemoglobin production
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**sickle cell trait is problem of hemoglobin destruction
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*beta thalassemia affects beta chain of hemoglobin
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*alpha thalassemia affects alpha chain of hemoglobin
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*major, media, minor

2021年5月6日 (木) 16:01時点における版

reference value/cut-off of Hb

  • adjust according to altitude of living

diagnosis

  • POC test kit: HemoCue
  • ferritin increases in inflammation in order to deliver more iron stimulated by inflammation itself as well as to avoid pathogens try to consume iron
  • serum transferrin (TIBC) increases in IDA, decreases in inflammation
  • zinc protoporphyrin (Zpp)
  • soluble transferrin receptor (sTfr)

cause

  • malaria does not cause IDA directly; destruction of RBCs by Plasmodium does not cause iron loss
    • anemia by malaria is mainly by inflammation, which suppresses iron absorption

sickle cell anemia

  • monogenetic recessive disorder
  • hemoglobin mutation
  • HbA mutated into HbS (sickle cell trait) or HbC (West Africa)
  • sickle cell trait protect against death from severe malaria
    • not prevent infection itself

clinical picture of SCD

  • affects all organ systems
  • disease pattern and severity varies very much on patients

chronic management

  • first to identify high risk groups

thalassemia

  • decreased hemoglobin production
    • sickle cell trait is problem of hemoglobin destruction
  • beta thalassemia affects beta chain of hemoglobin
  • alpha thalassemia affects alpha chain of hemoglobin
  • major, media, minor