Sowunmi Akin, Akano Kazeem, Ntadom Godwin, Ayede Adejumoke, Oguche Stephen, Agomo Chimere, Okafor Henrietta, Watila Ismaila, Meremikwu Martin, Ogala William, Agomo Philip, Adowoye Elsie, Fatunmbi Bayo, Aderoyeje Temitope, Happi Christian, Gbotosho Grace, Folarin Onikepe
Antimalarial Therapeutic Efficacy Monitoring Group, National Malaria Elimination Programme, The Federal Ministry of Health, Abuja, Nigeria.
Chemotherapy. 2017;62(4):231-238. doi: 10.1159/000449366. Epub 2017 Apr 28.
In severe malaria, intravenous artesunate may cause delayed haemolytic anaemia but there has been little evaluation of the propensity of oral artemisinin-based combination treatments (ACTs) to cause late-appearing anaemia.
The frequency of anaemia (haematocrit <30%), and temporal changes in haematocrit were evaluated in 1,191 malarious children following ACTs. "Haematocrit conservation" was evaluated by using the fall in haematocrit/1,000 asexual parasites cleared from the peripheral blood (FIH/1,000 asexual parasites cpb), and the ratio of the average haematocrit (on the first 3 days of starting treatment):total parasitaemia cleared.
The frequency of anaemia decreased significantly following treatment. FIH/1,000 asexual parasites cpb, average haematocrit:total parasitaemia cleared, and mean haematocrit 5 weeks after treatment began were significantly lower in hyperparasitaemic children than in children without hyperparasitaemia, suggesting haematocrit conservation during treatment followed later by a loss of haematocrit. Asymptomatic late-appearing anaemia occurred in 6% of the children.
Artesunate-amodiaquine and artemether-lumefantrine contribute to haematocrit conservation at high parasitaemias but may cause late-appearing anaemia.
在重症疟疾中,静脉注射青蒿琥酯可能会导致迟发性溶血性贫血,但对于基于青蒿素的口服联合疗法(ACTs)引发迟发性贫血的倾向,几乎没有相关评估。
对1191名接受ACTs治疗的疟疾患儿的贫血频率(血细胞比容<30%)以及血细胞比容的时间变化进行了评估。通过血细胞比容下降值/从外周血中清除的每1000个无性疟原虫(FIH/1000个无性疟原虫/cpb),以及起始治疗头3天的平均血细胞比容与清除的总疟原虫血症之比来评估“血细胞比容保留情况”。
治疗后贫血频率显著降低。高疟原虫血症患儿的FIH/1000个无性疟原虫/cpb、平均血细胞比容与清除的总疟原虫血症之比以及治疗开始5周后的平均血细胞比容,均显著低于无高疟原虫血症的患儿,这表明治疗期间血细胞比容得以保留,但随后会出现血细胞比容下降。6%的患儿出现了无症状的迟发性贫血。
青蒿琥酯 - 阿莫地喹和蒿甲醚 - 本芴醇在高疟原虫血症时有助于保留血细胞比容,但可能会导致迟发性贫血。