Sowunmi Akintunde, Akano Kazeem, Ayede Adejumoke I, Ntadom Godwin, Aderoyeje Temitope, Adewoye Elsie O, Fatunmbi Bayo
Department of Pharmacology and Therapeutics, University of Ibadan, Ibadan, Nigeria.
Institute for Medical Research and Training, University of Ibadan, Ibadan, Nigeria.
BMC Infect Dis. 2016 Jun 1;16:240. doi: 10.1186/s12879-016-1565-4.
Late-appearing anaemia (LAA) following treatment with artemisinins for severe malaria has been reported and well described, but there are limited clinical and parasitological data on LAA in African children with uncomplicated falciparum malaria following oral artemisinin-based combination therapies (ACTs).
This was an open label study with the main objectives of evaluating the clinical features, the risk factors for, the temporal changes in haematocrit and the outcomes of a LAA in malarious children treated with artesunate-amodiaquine (AA), artemether-lumefantrine (AL) or dihydroartemisinin-piperaquine (DHP). The diagnosis of LAA was made using the criteria: clearance of parasitaemia, fever and other symptoms within 1 week of commencing treatment; adequate clinical and parasitological response at 4-6 weeks after treatment began; haematocrit ≥30 % 1 and/or 2 weeks after treatment began; and haematocrit <30 %, parasite negativity by microscopy and polymerase chain reaction and absence of concomitant illness 3-6 weeks after treatment began.
LAA occurred in 84 of 609 children, was mild, moderate or severe in 77, 6 or 1 child, respectively and was relatively asymptomatic. Mean time elapsing from commencement of treatment to LAA was 27.1 days (95 % CI 25.3-28.9). In a multivariate analysis, an age <3 years (adjusted odd ratio [AOR] = 2.6, 95 % CI 1.3-5.2, P = 0.005), fever 1 day after treatment began (AOR = 3.8, 95 % CI 1.8-8.2, P < 0.0001), haematocrit <25 % at presentation (AOR = 2.2, 95 % CI 1.3-3.7, P = 0.003), haematocrit <30 % 1 day after treatment began (AOR = 2.1, 95 % CI 1.0-4.3, P = 0.04), parasite reduction ratio >10(4) 2 days after treatment began (AOR = 2.1, 95 % CI 1.1-3.9, P = 0.03) and spleen enlargement at presentation (AOR = 2.0, 95 % CI 1.1-3.9, P < 0.0001) were independent predictors of LAA. During 6 weeks of follow-up, uneventful recovery from anaemia occurred in 56 children [mean recovery time of 11.8 days (95 % CI 10.3-13.3)]. The only independent predictor of failure of recovery was LAA occurring 4 weeks after starting treatment (AOR = 7.5, 95 % CI 2.5-22.9, P < 0.0001).
A relatively asymptomatic LAA with uneventful recovery can occur in young malarious children following ACTs. Its occurrence may have implications for case and community management of anaemia and for anaemia control efforts in sub-Saharan Africa where ACTs have become first-line antimalarials.
Pan African Clinical Trial Registry PACTR201508001188143, 3 July 2015; PACTR201510001189370, 3 July 2015; PACTR201508001191898, 7 July 2015 and PACTR201508001193368, 8 July 2015 http://www.pactr.org .
青蒿素治疗重症疟疾后出现迟发性贫血(LAA)已有报道且描述详尽,但关于非洲单纯性恶性疟儿童口服青蒿素联合疗法(ACTs)后LAA的临床和寄生虫学数据有限。
这是一项开放标签研究,主要目的是评估接受青蒿琥酯 - 阿莫地喹(AA)、蒿甲醚 - 本芴醇(AL)或双氢青蒿素 - 哌喹(DHP)治疗的疟疾儿童LAA的临床特征、危险因素、血细胞比容的时间变化及结局。LAA的诊断标准为:治疗开始后1周内疟原虫血症、发热及其他症状消退;治疗开始后4 - 6周临床和寄生虫学反应良好;治疗开始后1周和/或2周血细胞比容≥30%;治疗开始后3 - 6周血细胞比容<30%,显微镜检查和聚合酶链反应检测寄生虫阴性且无合并疾病。
609名儿童中有84名发生LAA,分别有77例、6例和1例为轻度、中度或重度,且相对无症状。从治疗开始到发生LAA的平均时间为27.1天(95%置信区间25.3 - 28.9)。多因素分析显示,年龄<3岁(调整比值比[AOR]=2.6,95%置信区间1.3 - 5.2,P = 0.005)、治疗开始后1天发热(AOR = 3.8,95%置信区间1.8 - 8.2,P < 0.0001)、就诊时血细胞比容<25%(AOR = 2.2,95%置信区间1.3 - 3.7,P = 0.003)、治疗开始后1天血细胞比容<30%(AOR = 2.1,95%置信区间1.0 - 4.3,P = 0.04)、治疗开始后2天寄生虫减少率>10⁴(AOR = 2.1,95%置信区间1.1 - 3.9,P = 0.03)及就诊时脾肿大(AOR = 2.0,95%置信区间1.1 - 3.9,P < 0.0001)是LAA的独立预测因素。在6周的随访中,56名儿童贫血平稳恢复[平均恢复时间为11.8天(95%置信区间10.3 - 13.3)]。恢复失败的唯一独立预测因素是治疗开始后4周发生LAA(AOR = 7.5,95%置信区间2.5 - 22.9,P < 0.0001)。
接受ACTs治疗的疟疾患儿可能出现相对无症状且恢复平稳的LAA。其发生可能对贫血的病例和社区管理以及撒哈拉以南非洲地区的贫血控制工作产生影响,该地区ACTs已成为一线抗疟药物。
泛非临床试验注册中心PACTR201508001188143,2015年7月3日;PACTR201510001189370,2015年7月3日;PACTR201508001191898,2015年7月7日;PACTR201508001193368,2015年7月8日,http://www.pactr.org 。