Skip to main content

Artemether–lumefantrine and dihydroartemisinin–piperaquine treatment outcomes among children infected with uncomplicated Plasmodium falciparum malaria in Mwanza, Tanzania



Artemisinin based combination therapies (ACTs) have been a cornerstone in the treatment of malaria in the world. A rapid decline in dihydroartemisinin piperaquine (DHP) and artemether lumefantrine (ALU) efficacies has been reported in some parts of South East Asia, the historical epicenter for the antimalarial drug resistance. Prolonged drug use is associated with selection of resistant parasites due to exposure to inadequate drug levels hence effects on treatment outcomes in malaria. ALU and DHP are used as first line and alternative first line, respectively, in Tanzania. This study was carried in Igombe, Tanzania to assess the efficacies of ALU and DHP in routine treatment of uncomplicated malaria among children.


This was a prospective study involving children up to 10 years and followed up for 28 and 35 days as per the WHO protocol, 2015 for monitoring antimalarial drug efficacy. The primary end points were crude and adjusted Adequate Clinical and Parasitological Response (ACPR), parasite clearance rate and reported adverse events.


A total of 205 children with uncomplicated malaria were enrolled. One hundred and sixteen participants were treated with ALU, while 89 participants were treated with DHP. Two participants in the ALU group were lost within the 24 h of follow-up. The PCR unadjusted ACPR was108 (94.7%) for ALU and 88 (98.9%) for DHP, while the PCR adjusted ACPR was 109(95.6%) and 88(98.9%) for ALU and DHP, respectively, at 28 day follow-up. No treatment failure was observed in both groups. Cumulative risk of recurrent parasitemia was similar in both groups (p = 0.32). Age and parasite density were strong predictors for persistent day 1 parasitemia (p = 0.034 and 0.026, respectively). Nausea and vomiting, abdominal pain and headache were the most clinical adverse events reported in both groups of patients.


The present study shows that ALU and DHP are still efficacious after more than a decade of use with PCR corrected efficacies greater than 95% implying a failure rate less than 5% which is below the WHO minimum threshold requirement for recommendation of a change in the treatment policy. Both drugs were well tolerated with no major adverse events reported.


The number of malaria cases has declined worldwide by 18% between 2000 and 2015 [1]. However, malaria still remains a public health challenge in Tanzania despite the reported decrease in prevalence by about 10% for the past 10 years. The proportion of children treated with ACT has increased in Sub-Saharan Africa [1] whereby Artemether–lumefantrine (ALU) is the most adopted Artemisinin based Combination Therapy (ACT) for the treatment of uncomplicated P.falciparum malaria [2]. Globally, ACT use is estimated to have played part in the decrease in malaria mortality rate by 48% since its introduction to 2015 [1, 3]. Tanzania mainland introduced ALU as the first line drug against uncomplicated malaria in 2006 after the transition from chloroquine (CQ) to Sulphadoxine–pyrimethamine (SP) to artemisinin monotherapy. Resistance has been a driving force for the above transition like in other malaria endemic countries [3,4,5,6]. Dihydroartemisinin–piperaquine (DHP) is used as an alternative first line drug in Tanzania. The drug provides longer prophylactic effect from re-infection after treatment up to 65 days due to the longer half-life of the partner drug piperaquine [7]. Piperaquine, a bisquinoline once used in China when chloroquine resistance was high has not been used as monotherapy in any country since 1990s [4, 8]. A rapid decline in DHP and ALU efficacies has been reported in some parts of South East Asia, the historical epicenter for the spread of antimalarial drug resistance [9]. Resistance to older antimalarials used as monotherapies emerged from the SEA and spread to Africa with overwhelming effects [10,11,12]. Limited update data are available on DHP clinical efficacy in WHO African region including Tanzania. The available data in some parts of the region indicate that DHP has retained high efficacy [13, 14], while in some parts, the drug has recorded inadequate efficacy [15]. No data is available for DHP efficacy and safety in the studied region in Tanzania. Studies on ALU from some parts of Tanzania mainland have reported treatment failure rate below 5% [16,17,18,19,20] which is less than the WHO recommended (10%) for change in the national antimalarial treatment policy [21].

Prolonged drug use is associated with selection of resistant parasites due to exposure to inadequate drug levels hence effects on treatment outcomes in malaria. ALU is the mostly used ACT in Tanzania because it is the first line drug whereas DHP is alternative first line. Therefore, DHP use is expected to be limited than ALU. This study evaluated clinical outcomes of ALU and DHP for the treatment of uncomplicated malaria in Igombe, Tanzania a decade after the introduction of ACTs in the country.


Study area

This was a prospective study conducted from April 2017 to May 2019 at Karume Health Centre in Igombe, a semi-urban and malaria meso-endemic area in Ilemela district, Mwanza region, Tanzania with a population of about 40,000. Igombe is one of the eight sentinel sites established for conducting therapeutic efficacy studies on antimalarial drugs as part of the recommendations of the World Health Organization.

Sample size determination

The sample size was determined based on the WHO standard protocol for conducting antimalarial efficacy studies [21, 22]. An expected treatment failure rate of 5% was assumed for both drugs used. With 95% confidence interval, 5% precision and 20% loss to follow-up or withdrawal, a minimum sample number of 88 was deemed sufficient for each group of patients.

Patient recruitment

The data for the study was prospectively collected from children with uncomplicated P. falciparum malaria attending the outpatient clinic. Upon seeing the clinician, a full medical history was recorded, followed by a clinical examination as per the Tanzania guideline for management of malaria. Children with signs or symptoms suggestive of uncomplicated malaria were sent to the laboratory where a rapid diagnostic test was done followed with microscopic examination. For those children who were P. falciparum positive after laboratory results and met the inclusion criteria as per the WHO protocol for assessment of antimalarial efficacy, a parent or guardian was consulted for the consent to participate in the study after a thorough explanation on the study aims, benefits and rights to reject or withdraw from the study.

Eligible patients were children up to 10 years with fever or history of fever above 37.5 in the past 24 h, microscopically confirmed P. falciparum mono-infection (parasite density of 1000–200,000 trophozoites/µL). Children with symptoms of severe malaria according to the WHO case definition, comorbid infection, epilepsy, malnutrition, chronic diseases, history of drug allergy, history of traditional herbs use in the past 4 weeks, any antimalarial drug use in the past 4 weeks, known liver dysfunction or disease and severe anaemia were excluded from this study. Children who had previously been allocated to ALU group were not included in the DHP group once they had malaria episode(s).

Drug administration and treatment

A clinician prescribed to the children enrolled in the two groups artemether–lumefantrine or dihydroartemisinin–piperaquine which are drugs used as first line and alternative first line, respectively, as per the Tanzania guideline for management of malaria. The first phase involved treatment of one hundred and sixteen children enrolled with artemether lumefantrine (ALU). A follow-up was done for 35 days. When the follow-up for patients on ALU was completed, a switch into treatment using DHP was done then a follow up was done for 35 days. A total of 89 children were treated with dihydroartemisinin–piperaquine (DHP). Artemether 20 mg–lumefantrine 120 mg (Lumartem, Cipla, India) was administered twice daily during three days, while dihydroartemisinin 20 mg—piperaquine 160 mg (Duocotexin® holley-cotec, Beijing) was given once daily as per manufacturer’s dosing schedule based on body weight. The first, third and fifth doses for ALU were administered as direct observation therapy (DOT). Evening/night doses were given at home. A nurse phoned parents and guardians to remind them it was time for taking the medication. To asses for compliance, parents or guardians were requested to bring the empty pill packages in the following morning. Mothers were insisted to breastfeed their children to increase bioavailability of lumefantrine. All doses for DHP were administered as DOT. Children were observed for 1 h after medication to monitor for vomiting. In case of vomiting within 30 min after medication administration, a full repeat dose was given. In the event of persistent vomiting or symptoms, the patient was excluded from the study and received rescue treatment in accordance to the national malaria treatment guideline.

Follow-up and sample collection

Guardians or parents were requested to return with the children for follow-up. Blood from finger pricks was collected on filter paper (FTA®Whatman paper) on day 0,1,2,3,7,14,21,28,35 for PCR genotyping of Merozoite Surface Protein 1(MSP1) and Merozoite Surface Protein (MSP2) to distinguish between recrudescence and reinfection, MSP1 and MSP2 alleles to establish genetic diversity and allele frequencies (to be published elsewhere) and CYP3A4*1B plus CYP3A5*3 to establish association with plasma concentrations. Venous blood (2mls) was also collected on day 0,1,2,3,7 and 14 for lumefantrine and piperaquine quantification (to be published elsewhere). Thick and thin blood smears were stained by Giemsa (on each day of the visit) according to the WHO standard protocol [23]. Parasite identification and counting were done by two independent experienced microscopists.

DNA extraction and molecular investigations

Capillary blood sample was collected on Whatman no 1 filter paper during the visits to the health center. The filter papers were then dried at room temperature and kept in sealed plastic bags. Parasite DNA was extracted from the dried blood spots (DBS) on day 0 and the respective days of reappearance of parasites using Life Sciences genomic DNA kit for dried spots according to the manufacture’s protocol. Nested PCR was done to identify MSP1 and MSP2 allele variants using a method described previously [24]. The results were classified as recrudescence or re-infection according to the WHO guideline [25].

Treatment outcomes

The WHO 2015 protocol [21, 22] was used to classify treatment outcomes as early treatment failure (ETF), late clinical failure (LCF), late parasitological failure (LPF) and adequate clinical and parasitological response (ACPR). Secondary outcomes included parasite clearance rate and occurrence of adverse events. Treatment failures were classified as recrudescence or re-infection after PCR correction.

Statistical analysis

We used Ms-Excel for data entry and cleaning. All statistical analyses were performed using STATA version 13.1(Statistical Corporation, College Station, TX, US). Categorical data were compared using chi square tests or fisher exact tests where appropriate. Student t test was used to compare continuous data for the two groups where necessary. Per-protocol analysis carried, patients who withdrew from the study or were lost to follow-up or had re-infection were not included in the denominator. Kaplan Meier analysis was done to determine the cumulative probability of recurrence-free survival over the 35 day follow-up. Univariate and multivariate analyses of risk factors associated with parasitemia persistence on day 1 were done using generalized linear model with link Poisson due to large variance.


Study subjects

Among 602 screened patients,336 patients were malaria positive. Thirty-six children were excluded because they had taken ALU before visiting the clinic and 44 children did not participate in the study because their parents or guardians did not give a consent. We excluded 14 children because they had taken traditional herbs before visiting the clinic and 33 children were excluded because they had severe malaria or mixed-species infections. Four children were excluded because of persistent nausea and vomiting. Therefore, total of 205 children with falciparum malaria were enrolled in the study. Two patients in the ALU group were lost within the 24 h of follow-up hence were not included in the analysis involving treatment outcomes.

In this study that investigated the efficacy, 116 and 89 participants were treated with ALU and DHP, respectively. Pre-treatment characteristics of the study participants are presented in Table 1

Table 1 Baseline characteristics of the study participants

Treatment outcomes

ETFs were not recorded in both groups of patients. The per protocol day 28 PCR corrected efficacies were high for both group of patients. Both drugs recorded lower LCF and LPF (Table 2).

Table 2 Crude and adjusted treatment outcomes

The percentage of parasite clearance at day1 were about 50% for both groups. All patients in both treatment groups were aparasitemic on day 3 (Table 2).

ETF Early Treatment Failure, LCF Late Clinical Failure, LPF Late Clinical and Parasitological Failure

The rate of parasite recurrence during 35 days follow-up was not different in the two treatment groups as suggested in Fig. 1.

Fig. 1
figure 1

Cumulative risk of recurrent parasitemia by 35 following treatment with artemether–lumefantrine and dihydroartemisinin–piperaquine–Cox-proportional hazards risk

Figure 2 shows the rate of parasite clearance by drugs in day1 and day2. The proportion of the parasite cleared in day1 was 80.44% and 96.41% for ALU and DHP, respectively, while by day 2, both drugs reached 99.99% clearance. In general, there was a rapid parasite clearance in both treatments although parasite clearance time was less in DHP than ALU.

Fig. 2
figure 2

Parasite clearance rate for DHP and ALU

Age and parasite density were strong predictors for persistent day 1 parasitemia. The patients aged 5 years and above were less likely to have parasitemia persistent in day 1 than those under five years. Higher pretreatment temperature (> 37.5), drug type, higher hemoglobin, sex and BMI were not predictors for persistent day 1 and 2 parasitemia (Table 3).

Table 3 Association between factors and a positive blood smear in day one

Adverse events Nausea and vomiting, abdominal pain and headache were the most clinical adverse events reported in both groups of patients. (Table 4).

Table 4 Patient-reported adverse events


The present study aimed at assessing the efficacy of ALU and DHP in routine treatment of uncomplicated malaria among children after more than a decade since the introduction of ACTs in Tanzania [26].

The per protocol day 28 PCR corrected efficacies were higher for both DHP and ALU. Several studies in other parts of Africa have reported high efficacy for DHP than ALU. Both drugs have shown higher efficacy than the cutoff value recommended by WHO for a change in the national antimalarial treatment policy [21, 22] similar to studies done in other parts of the country [16,17,18,19,20]. In general, this study shows that the two ACTs have retained high efficacies after about 14 years since the introduction of ACTs. Previous studies in the country have suggested the selection of Pfmdr1 N86 and PfcrtK76 does not affect the efficacy of ALU [20, 27]. Validated K13 mutants responsible for artemisinin resistance thus affecting treatment outcome have not been reported in the country [16, 17]. The contribution of the partner drug piperaquine to the parasite killing effect soon after drug administration may account for the high DHP efficacy observed [28]. Piperaquine has a longer half-life (2–3 weeks) than lumefantrine (4.5 days) which may also explain the lack of re-infection observed with DHP. In Tanzania, DHP is deployed as alternative first line treatment and its use is limited owing to the high cost as the drug is not subsidized unlike ALU. This may account for less drug pressure on P. falciparum and hence the high efficacy retained. However, experience from the Great Sub-Mekong region has shown a rapid decrease from the high DHP efficacy as a result of a rapid resistance selection to piperaquine [9, 29] possibly due to the long half-life of piperaquine thus warning us on the high efficacy we are enjoying now. This calls for close monitoring for DHP resistance.

Aparasitemia on day 3 in both treatment groups suggests an adequate response of P. falciparum to the artemisinin component and an indication of absence of artemisinin resistance in the study area as per the WHO’s indicator of day 3 parasitemia ≥ 10% [30]. Several factors related to drug, host and parasite determine the speed of parasite clearance [31,32,33]. The effect observed with age on persistent day 1 parasitemia in this study could be attributed to less acquired natural immunity among under-fives in the malaria endemic region. The present study also documents low rates of parasite recurrence for the two drugs (ALU and DHP) used for the treatment of P. falciparum malaria in Tanzania.

This study reports both ALU and DHP to be very well tolerated with comparable profiles. No patient experienced serious adverse event in both treatment groups during the follow-up whereby nausea and vomiting were observed more frequently in patients on ALU than DHP. This is not surprising since several studies have reported nausea and vomiting as the most common adverse event associated with ALU use [34]. The high tolerability observed in both drugs is consistent with other studies [16, 35]. The assessment of adverse events in malaria treated patients is complex because of the high background malaria signs and symptoms. To take care of this, clinical assessment was done prior administration of the ACTs. We only considered those events which occurred post start of treatment or worsened after the start of treatment as reported in previous studies [36].

Our study has some limitations. First, determination of the gametocytes clearance time was not done in both groups of patients. Secondly, molecular makers of resistance for both drugs were not studies; therefore, the association between these makers and recurrence of parasites was not done. The pill count method used to assess compliance of the night doses for artemether lumefantrine has some limitations, thus it could not be verified with certainty all children received the night doses which were not under DOT. However, previous studies done in similar settings indicated a high adherence to ALU under real-life situation and the non adherence was due to untimeliness rather than missing doses[37, 38]. The efficacy for the two drugs was based on followup up to 28 and 35 days only. Despite the limitations, our study provides an update on the efficacies of the ALU and DHP in the country.


ALU and DHP have retained a high efficacy in the treatment of uncomplicated plasmodium falciparum malaria. Age and parasite density were strong predictors for persistent day 1 parasitemia. The use of both ALU and DHP was associated with tolerable adverse effects.



Artemisinin-based combination therapy






Adequate clinical and parasitological response


Early treatment failure


Late clinical failure


Late parasitological failure


World Health Organization


  1. 1.

    Cibulskis RE, Alonso P, Aponte J, Aregawi M, Barrette A, Bergeron L, Fergus CA, Knox T, Lynch M, Patouillard E. Malaria: global progress 2000–2015 and future challenges. Infect Dis Poverty. 2016;5(1):1–8.

    Article  Google Scholar 

  2. 2.

    Kiaco K, Rodrigues AS. The drug transporter ABCB1 c 3435C> T SNP influences artemether–lumefantrine treatment outcome. Malaria J. 2017;16(1):1–6.

    Article  CAS  Google Scholar 

  3. 3.

    Organization WH: World malaria report 2015: World Health Organization; 2016.

  4. 4.

    Davis TM, Karunajeewa HA, Ilett KF. Artemisinin-based combination therapies for uncomplicated malaria. Med J Aust. 2005;182(4):181–5.

    Article  Google Scholar 

  5. 5.

    Organization WH: Guidelines for the treatment of malaria; 2006. Document no: WHO. In.: HTM/MAL; 2006.

  6. 6.

    Deressa T, Seid ME, Birhan W, Aleka Y, Tebeje BM. In vivo efficacy of artemether–lumefantrine against uncomplicated Plasmodium falciparum malaria in Dembia District, northwest ethiopia. Ther Clin Risk Manag. 2017;13:201.

    Article  CAS  Google Scholar 

  7. 7.

    Mohamed AO, Hamid MMA, Mohamed OS, Elkando NS, Suliman A, Adam MA, Elnour FAA, Malik EM. Efficacies of DHA–PPQ and AS/SP in patients with uncomplicated Plasmodium falciparum malaria in an area of an unstable seasonal transmission in Sudan. Malar J. 2017;16(1):1–6.

    Article  CAS  Google Scholar 

  8. 8.

    Davis TM, Hung T-Y, Sim K, Karunajeewa HA, Ilett KF. Piperaquine. Drugs. 2005;65(1):75–87.

    Article  CAS  Google Scholar 

  9. 9.

    Thanh NV, Thuy-Nhien N, Tuyen NTK, Tong NT, Nha-Ca NT, Quang HH, Farrar J, Thwaites G, White NJ, Wolbers M. Rapid decline in the susceptibility of Plasmodium falciparum to dihydroartemisinin–piperaquine in the south of Vietnam. Malar J. 2017;16(1):1–10.

    Article  CAS  Google Scholar 

  10. 10.

    Ariey F, Fandeur T, Durand R, Randrianarivelojosia M, Jambou R, Legrand E, Ekala MT, Bouchier C, Cojean S, Duchemin JB. Invasion of Africa by a single pfcrt allele of South East Asian type. Malar J. 2006;5(1):1–5.

    Article  CAS  Google Scholar 

  11. 11.

    Mita T, Venkatesan M, Ohashi J, Culleton R, Takahashi N, Tsukahara T, Ndounga M, Dysoley L, Endo H, Hombhanje F. Limited geographical origin and global spread of sulfadoxine-resistant dhps alleles in Plasmodium falciparum populations. J Infect Dis. 2011;204(12):1980–8.

    Article  CAS  Google Scholar 

  12. 12.

    Roper C, Pearce R, Nair S, Sharp B, Nosten F, Anderson T. Intercontinental spread of pyrimethamine-resistant malaria. Science. 2004;305(5687):1124–1124.

    Article  CAS  Google Scholar 

  13. 13.

    Yeka A, Wallender E, Mulebeke R, Kibuuka A, Kigozi R, Bosco A, Kyambadde P, Opigo J, Kalyesubula S, Senzoga J. Comparative efficacy of artemether-lumefantrine and dihydroartemisinin-piperaquine for the treatment of uncomplicated malaria in Ugandan children. J Infect Dis. 2019;219(7):1112–20.

    Article  CAS  Google Scholar 

  14. 14.

    Plucinski MM, Talundzic E, Morton L, Dimbu PR, Macaia AP, Fortes F, Goldman I, Lucchi N, Stennies G, MacArthur JR. Efficacy of artemether-lumefantrine and dihydroartemisinin-piperaquine for treatment of uncomplicated malaria in children in Zaire and Uíge Provinces Angola. Antimicrob Agents Chemother. 2015;59(1):437–43.

    Article  CAS  Google Scholar 

  15. 15.

    Gansané A, Moriarty LF, Ménard D, Yerbanga I, Ouedraogo E, Sondo P, Kinda R, Tarama C, Soulama E, Tapsoba M. Anti-malarial efficacy and resistance monitoring of artemether–lumefantrine and dihydroartemisinin–piperaquine shows inadequate efficacy in children in Burkina Faso, 2017–2018. Malar J. 2021;20(1):1–12.

    Article  CAS  Google Scholar 

  16. 16.

    Kakolwa MA, Mahende MK, Ishengoma DS, Mandara CI, Ngasala B, Kamugisha E, Kataraihya JB, Mandike R, Mkude S, Chacky F. Efficacy and safety of artemisinin-based combination therapy, and molecular markers for artemisinin and piperaquine resistance in Mainland Tanzania. Malar J. 2018;17(1):1–10.

    Article  CAS  Google Scholar 

  17. 17.

    Ishengoma DS, Mandara CI, Francis F, Talundzic E, Lucchi NW, Ngasala B, Kabanywanyi AM, Mahende MK, Kamugisha E, Kavishe RA. Efficacy and safety of artemether–lumefantrine for the treatment of uncomplicated malaria and prevalence of Pfk13 and Pfmdr1 polymorphisms after a decade of using artemisinin-based combination therapy in mainland Tanzania. Malar J. 2019;18(1):1–13.

    Article  Google Scholar 

  18. 18.

    Mandara CI, Francis F, Chiduo MG, Ngasala B, Mandike R, Mkude S, Chacky F, Molteni F, Njau R, Mohamed A. High cure rates and tolerability of artesunate–amodiaquine and dihydroartemisinin–piperaquine for the treatment of uncomplicated falciparum malaria in Kibaha and Kigoma Tanzania. Malaria J. 2019;18(1):1–12.

    Article  Google Scholar 

  19. 19.

    Shayo A, Mandara CI, Shahada F, Buza J, Lemnge MM, Ishengoma DS. Therapeutic efficacy and safety of artemether-lumefantrine for the treatment of uncomplicated falciparum malaria in North-Eastern Tanzania. Malar J. 2014;13(1):1–10.

    Article  CAS  Google Scholar 

  20. 20.

    Kamugisha E, Jing S, Minde M, Kataraihya J, Kongola G, Kironde F, Swedberg G. Efficacy of artemether-lumefantrine in treatment of malaria among under-fives and prevalence of drug resistance markers in Igombe-Mwanza, north-western Tanzania. Malar J. 2012;11(1):1–8.

    Article  CAS  Google Scholar 

  21. 21.

    Organization WH: Methods for surveillance of antimalarial drug efficacy. 2009. In.; 2015.

  22. 22.

    Organization WH: Methods for surveillance of antimalarial drug efficacy. 2009.

  23. 23.

    Organization WH. Basic malaria microscopy: Part I. Learner’s guide: World Health Organization; 2010.

    Google Scholar 

  24. 24.

    Somé AF, Bazié T, Zongo I, Yerbanga RS, Nikiéma F, Neya C, Taho LK, Ouédraogo J-B. Plasmodium falciparum msp 1 and msp 2 genetic diversity and allele frequencies in parasites isolated from symptomatic malaria patients in Bobo-Dioulasso Burkina Faso. Parasites Vectors. 2018;11(1):1–8.

    Article  Google Scholar 

  25. 25.

    Organization WH: Methods and techniques for clinical trials on antimalarial drug efficacy: genotyping to identify parasite populations: informal consultation organized by the Medicines for Malaria Venture and cosponsored by the World Health Organization, 29-31 May 2007, Amsterdam, The Netherlands: World Health Organization; 2008.

  26. 26.

    Tanzania N: National guidelines for malaria diagnosis and treatment. Dar es Salaam 2006.

  27. 27.

    Mwaiswelo R, Ngasala B, Gil JP, Malmberg M, Jovel I, Xu W, Premji Z, Mmbando BP, Björkman A, Mårtensson A. Sustained high cure rate of artemether–lumefantrine against uncomplicated Plasmodium falciparum malaria after 8 years of its wide-scale use in Bagamoyo District, Tanzania. Am J Trop Med Hyg. 2017;97(2):526–32.

    Article  CAS  Google Scholar 

  28. 28.

    Ebenebe JC, Ntadom G, Ambe J, Wammanda R, Jiya N, Finomo F, Emechebe G, Mokuolu O, Akano K, Agomo C. Efficacy of artemisinin-based combination treatments of uncomplicated falciparum malaria in under-five-year-old Nigerian children ten years following adoption as first-line antimalarials. Am J Trop Med Hyg. 2018;99(3):649–64.

    Article  CAS  Google Scholar 

  29. 29.

    Phuc BQ, Rasmussen C, Duong TT, Dong LT, Loi MA, Ménard D, Tarning J, Bustos D, Ringwald P, Galappaththy GL. Treatment failure of dihydroartemisinin/piperaquine for Plasmodium falciparum malaria Vietnam. Emerg Infect Dis. 2017;23(4):715.

    Article  CAS  Google Scholar 

  30. 30.

    Organization WH: Global plan for artemisinin resistance containment (GPARC): World Health Organization; 2011.

  31. 31.

    Flegg JA, Guerin PJ, White NJ, Stepniewska K. Standardizing the measurement of parasite clearance in falciparum malaria: the parasite clearance estimator. Malar J. 2011;10(1):1–13.

    Article  Google Scholar 

  32. 32.

    White N. The parasite clearance curve. Malar J. 2011;10(1):1–8.

    Article  Google Scholar 

  33. 33.

    org WPCSGksw: Baseline data of parasite clearance in patients with falciparum malaria treated with an artemisinin derivative: an individual patient data meta-analysis. Malaria J 2015, 14:1–12.

  34. 34.

    Ngomo JMN, Megnie GJO, Ditombi BM, Lengongo JVK, M’Bondoukwé NP, Offouga CL, Mawili-Mboumba DP, Lekana-Douki JB, Ringwald P, Fandeur T. Persistence of high in vivo efficacy and safety of artesunate-amodiaquine and artemether–lumefantrine as the first-and second-line treatments for uncomplicated Plasmodium falciparum malaria 10 years after their implementation in Gabon. Acta Parasitol. 2019;64(4):898–902.

    Article  CAS  Google Scholar 

  35. 35.

    Davlantes E, Dimbu PR, Ferreira CM, Joao MF, Pode D, Félix J, Sanhangala E, Andrade BN, dos Santos SS, Talundzic E. Efficacy and safety of artemether–lumefantrine, artesunate–amodiaquine, and dihydroartemisinin–piperaquine for the treatment of uncomplicated Plasmodium falciparum malaria in three provinces in Angola, 2017. Malar J. 2018;17(1):1–11.

    Article  CAS  Google Scholar 

  36. 36.

    Bassat Q, González R, Machevo S, Nahum A, Lyimo J, Maiga H, Mårtensson A, Bashraheil M, Ouma P, Ubben D. Similar efficacy and safety of artemether–lumefantrine (Coartem®) in African infants and children with uncomplicated falciparum malaria across different body weight ranges. Malar J. 2011;10(1):1–9.

    Article  CAS  Google Scholar 

  37. 37.

    Simba DO, Kakoko D, Tomson G, Premji Z, Petzold M, Mahindi M, Gustafsson LL. Adherence to artemether/lumefantrine treatment in children under real-life situations in rural Tanzania. Trans R Soc Trop Med Hyg. 2012;106(1):3–9.

    Article  CAS  Google Scholar 

  38. 38.

    Bell DJ, Wootton D, Mukaka M, Montgomery J, Kayange N, Chimpeni P, Hughes DA, Molyneux ME, Ward SA, Winstanley PA. Measurement of adherence, drug concentrations and the effectiveness of artemether–lumefantrine, chlorproguanil-dapsone or sulphadoxine–pyrimethamine in the treatment of uncomplicated malaria in Malawi. Malar J. 2009;8(1):1–11.

    Article  CAS  Google Scholar 

Download references


We sincerely thank the participants who donated venous blood and DBS samples throughout the follow-up period. We also appreciate the contribution of the nurses, laboratory technicians and clinicians at Karume Health Centre, Igombe Mwanza, Tanzania.


This work was supported by the Swedish Research Council, Department of Medical Biochemistry and Microbiology, Uppsala University, the Catholic University of Health and Allied Sciences and the National Institute for Medical Research, Mwanza.

Author information




KJM participated in proposal development, sample collection, genotyping of MSP-1 and 2, data analysis and manuscript drafting. ETK, SM and AK carried out data analysis and manuscript reviewing. EK and GS participated in proposal development, supervision of the research group, revising and approving the manuscript for submission to the journal. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Karol J. Marwa.

Ethics declarations

Ethics approval and consent to participate.

Ethical and study approval was granted by the joint Catholic University of Health and Allied Sciences (CUHAS)/Bugando Medical Centre (BMC) Institutional Review Board. All parent/guardian signed a written informed consent.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Marwa, K.J., Konje, E.T., Kapesa, A. et al. Artemether–lumefantrine and dihydroartemisinin–piperaquine treatment outcomes among children infected with uncomplicated Plasmodium falciparum malaria in Mwanza, Tanzania. Trop Med Health 49, 94 (2021).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI:


  • Efficacy
  • Treatment outcome
  • Artemether–lumefantrine
  • Dihydroartemisinin–piperaquine and Tanzania