Assefa Mesfin, Eshetu Teferi, Biruksew Abdissa
Hossana Health Care Centre, Southern Nations, Nationalities, and Peoples' Region, Hossana, Ethiopia.
Department of Medical Laboratory Sciences and Pathology, Jimma University, P.O.Box: 878, Jimma, Ethiopia.
Malar J. 2015 Nov 17;14:458. doi: 10.1186/s12936-015-0983-x.
Plasmodium vivax accounts for about 44 % of all malaria infection in Ethiopia. Chloroquine (CQ) is the first-line treatment for vivax malaria in Ethiopia. Chloroquine-resistant (CQR) P. vivax has been emerging in different parts of the world to compromise the efficacy of the drug and pose both health and economic impact in the developing world. The current study was aimed at assessing the therapeutic efficacy of CQ for the treatment of vivax malaria among outpatients at Hossana Health Care Centre, southern Ethiopia.
A one-arm, 28-day follow-up, in vivo therapeutic efficacy study was conducted from 5 April to 25 June, 2014. Sixty-three patients aged between four and 59 years were enrolled with microscopically confirmed P. vivax infection. All patients were treated with CQ 25 mg/kg for 3 days. Recurrence of parasitaemia and clinical conditions of patients were assessed on days 1, 2, 3, 7, 14, 21, and 28 during the 28-day follow-up period. Haemoglobin (Hb) level was determined on day 0, day 28 and on day of recurrence of parasitaemia by using portable spectrophotometer.
Of the total 63 patients included in the study, 60 (95.2 %) completed their 28-day follow-up; three patients were excluded from the study: one patient due to vomiting of the second dose of drug, one patient due to Plasmodium falciparum infection and one patient lost to follow-up during the study. During enrolment, 35 (53.3 %) had a history of fever and 28 (46.7 %) had documented fever. The geometric mean of parasite density on day of enrolment was 3472 parasites/μl. Among these, two patients had recurrent parasitaemia within the 28-day follow-up. CQ was found to be efficacious in 96.7 % of the study participants except two treatment failures detected. The failure might be due to late parasitological failure among these two patients who had recurrent parasitaemia within the 28-day follow-up.
The current study revealed that CQ showed a high rate of efficacy (96.7 %) among the study participants even though some reports from previous studies elsewhere in Ethiopia showed an increase in CQR P. vivax. Thus, CQR molecular markers and regular monitoring of the pattern of resistance to CQ is needed for rapid and effective control measures of possible spread of drug resistance in the study area.
间日疟原虫占埃塞俄比亚所有疟疾感染病例的约44%。氯喹是埃塞俄比亚间日疟的一线治疗药物。耐氯喹的间日疟原虫已在世界不同地区出现,影响了该药物的疗效,并对发展中世界造成健康和经济影响。本研究旨在评估氯喹对埃塞俄比亚南部霍桑纳医疗中心门诊患者间日疟的治疗效果。
2014年4月5日至6月25日进行了一项单组、为期28天随访的体内治疗效果研究。纳入63名年龄在4至59岁之间、经显微镜确诊为间日疟原虫感染的患者。所有患者接受3天的氯喹治疗,剂量为25mg/kg。在28天的随访期内,于第1、2、3、7、14、21和28天评估患者的寄生虫血症复发情况和临床状况。使用便携式分光光度计在第0天、第28天以及寄生虫血症复发当天测定血红蛋白(Hb)水平。
纳入研究的63名患者中,60名(95.2%)完成了28天的随访;3名患者被排除在研究之外:1名患者因呕吐第二剂药物,1名患者因感染恶性疟原虫,1名患者在研究期间失访。入组时,35名(53.3%)有发热史,28名(46.7%)有发热记录。入组当天寄生虫密度的几何平均值为3472个寄生虫/μl。其中,2名患者在28天随访期内出现寄生虫血症复发。除检测到2例治疗失败外,氯喹在96.7%的研究参与者中显示有效。失败可能是由于这2例在28天随访期内出现寄生虫血症复发的患者存在晚期寄生虫学失败。
本研究表明,尽管埃塞俄比亚其他地方的一些先前研究报告显示耐氯喹间日疟原虫有所增加,但氯喹在研究参与者中显示出较高的有效率(96.7%)。因此,需要耐氯喹分子标记物并定期监测对氯喹的耐药模式,以便在研究区域迅速有效地控制耐药性可能的传播。