Kinung'hi Safari M, Magnussen Pascal, Kishamawe Coleman, Todd Jim, Vennervald Birgitte J
National Institute for Medical Research (NIMR), Mwanza Centre, Isamilo Road, PO Box 1462, Mwanza, Tanzania.
Department of Veterinary Disease Biology, Faculty of Health and Medical Sciences, University of Copenhagen, Grønnegårdsvej 15 DK-1870 Frederiksberg C, Copenhagen, Denmark.
BMC Infect Dis. 2015 Mar 20;15:136. doi: 10.1186/s12879-015-0864-5.
Some studies have suggested that helminth infections increase the risk of malaria infection and are associated with increased number of malaria attacks and anaemia. Thus interventions to control helminth infections may have an impact on incidence of clinical malaria and anaemia. The current study assessed the impact of two anthelmintic treatment approaches on malaria infection and on anaemia in school and pre-school children in Magu district, Tanzania.
A total of 765 children were enrolled into a prospective randomized anthelmintic intervention trial following a baseline study of 1546 children. Enrolled children were randomized to receive either repeated treatment with praziquantel and albendazole four times a year (intervention group, 394 children) or single dose treatment with praziquantel and albendazole once a year (control group, 371 children). Follow up examinations were conducted at 12 and 24 months after baseline to assess the impact of the intervention. Stool and urine samples were collected and examined for schistosome and soil transmitted helminth infections. Blood samples were also collected and examined for malaria parasites and haemoglobin concentrations. Monitoring of clinical malaria attacks was performed at each school during the two years of the intervention.
Out of 1546 children screened for P. falciparum, S. mansoni, S. haematobium, hookworm and T. Trichiura at baseline, 1079 (69.8%) were infected with at least one of the four parasites. There was no significant difference in malaria infection (prevalence, parasite density and frequency of malaria attacks) and in the prevalence of anaemia between the repeated and single dose anthelmintic treatment groups at 12 and 24 months follow up (p>0.05). However, overall, there was significant improvement in mean haemoglobin concentrations (p<0.001) from baseline levels of 122.0 g/L and 123.0 g/L to 136.0 g/L and 136.8 g/L for the repeated and single dose treatment groups, respectively, at 24 months follow-up which resulted in significant reduction in prevalence of anaemia.
These results suggest that repeated anthelmintic treatment did not have an impact on malaria infection compared to single dose treatment. However, both treatment approaches had overall impact in terms of improvements of haemoglobin levels and hence reductions in prevalence of anaemia.
一些研究表明,蠕虫感染会增加疟疾感染风险,并与疟疾发作次数增加和贫血有关。因此,控制蠕虫感染的干预措施可能会对临床疟疾和贫血的发病率产生影响。本研究评估了两种驱虫治疗方法对坦桑尼亚马古区中小学及学龄前儿童疟疾感染和贫血的影响。
在对1546名儿童进行基线研究后,共有765名儿童被纳入一项前瞻性随机驱虫干预试验。入选儿童被随机分为两组,一组每年接受4次吡喹酮和阿苯达唑重复治疗(干预组,394名儿童),另一组每年接受1次吡喹酮和阿苯达唑单剂量治疗(对照组,371名儿童)。在基线后的12个月和24个月进行随访检查,以评估干预效果。收集粪便和尿液样本,检测血吸虫和土壤传播的蠕虫感染情况。还收集血样,检测疟原虫和血红蛋白浓度。在干预的两年期间,对每所学校的临床疟疾发作情况进行监测。
在基线时对1546名儿童进行恶性疟原虫、曼氏血吸虫、埃及血吸虫、钩虫和鞭虫筛查,其中1079名(69.8%)感染了四种寄生虫中的至少一种。在12个月和24个月随访时,重复给药组和单剂量给药组在疟疾感染(患病率、寄生虫密度和疟疾发作频率)和贫血患病率方面没有显著差异(p>0.05)。然而,总体而言,在24个月随访时,重复给药组和单剂量给药组的平均血红蛋白浓度分别从基线水平的122.0g/L和123.0g/L显著提高到136.0g/L和136.8g/L(p<0.001),这导致贫血患病率显著降低。
这些结果表明,与单剂量治疗相比,重复驱虫治疗对疟疾感染没有影响。然而,两种治疗方法在提高血红蛋白水平以及降低贫血患病率方面都有总体效果。