Efficacy of artemether-lumefantrine, the nationally-recommended artemisinin combination for the treatment of uncomplicated falciparum malaria, in southern Laos
© Mayxay et al.; licensee BioMed Central Ltd. 2012
Received: 6 April 2012
Accepted: 24 May 2012
Published: 8 June 2012
The Lao Government changed the national policy for uncomplicated Plasmodium falciparum malaria from chloroquine to artemether-lumefantrine (AL) in 2005. Since then, no information on AL efficacy has been reported. With evidence of resistance to artemisinin derivatives in adjacent Cambodia, there has been a concern as to AL efficacy. Monitoring of AL efficacy would help the Lao Government to make decisions on appropriate malaria treatment.
The efficacy of a three-day, twice daily oral artemether-lumefantrine for the treatment of uncomplicated falciparum malaria in Xepon District, Savannakhet Province, southern Laos was studied over 42 days follow-up. This was part of a trial of thiamin supplementation in falciparum malaria.
Of 630 patients with P. falciparum enrolled in the trial of thiamin treatment, 549 (87%, 357 children ≤15 years and 192 adults) were included in this study. The per protocol 42-day cure rates were 97% (524/541) [96% (337/352) for children and 99% (187/189) for adults, p = 0.042]. By conventional intention-to-treat analysis, the 42-day cure rates adjusted for re-infection, were 97% (532/549) [96% (342/357) in children and 99% (190/192) in adults, p = 0.042]. The proportion of patients who remained parasitaemic at day 1 after treatment was significantly higher in children [33% (116/356)] compared to adults [15% (28/192)] (p < 0.001) and only one adult patient had detectable parasitaemia on day 2. There were no serious adverse events. Potential side effects after treatment were reported more commonly in adults (32%) compared to children (15%) (p < 0.001). Patients with recrudescent infections were significantly younger, had longer mean time to fever clearance, and had longer median time to parasite clearance compared to those who were cured.
The current nationally-recommended anti-malarial treatment (artemether-lumefantrine) remains highly efficacious for the treatment of uncomplicated falciparum malaria five years after introduction in Laos. Regular monitoring is required in case artemisinin-resistant P. falciparum parasites should appear.
KeywordsClinical trial Plasmodium falciparum Malaria Artemisinin-based combination therapy (ACT) Artemether-lumefantrine Coartem Laos
Although the incidence of Plasmodium falciparum malaria has declined recently in northern and central Lao PDR (Laos), malaria remains an important cause of morbidity and mortality in southern Laos, with an estimated incidence of 4.7 to 23.5/1,000 population between 2006-2008[1–3]. The change of the Lao Government national treatment policy for uncomplicated falciparum malaria from chloroquine to artemether-lumefantrine in 2005 is likely to have contributed substantially to the reduction in the incidence of malaria in northern and central Laos. This change was prompted by high levels of P. falciparum resistance to chloroquine (CQ) and sulphadoxine-pyrimethamine (SP)[4–8]. The use of artemisinin combination therapy (ACT), artesunate + mefloquine, artemether-lumefantrine (AL) and dihydroartemisinin-piperaquine, has been shown to provide high cure rates (42-day failure rate of ≤ 6%) and good tolerability in Laos[1, 9–12].
However, artemisinin resistance has emerged in western Cambodia[13–15], raising serious concerns that resistance could spread the ~ 400 km to southern Laos. In 2002-3, the 42-day cure rate following full treatment with AL was 97% in southern Laos despite a low-fat diet (which reduces lumefantrine absorption) and consequent low day 7 plasma lumefantrine concentrations. AL has to be taken twice a day, and should be taken with fats[16–20] which may compromise adherence and efficacy respectively, so there is concern that AL efficacy could decline, particularly if protection from the co-administered artemether is compromised by emerging resistance.
Artemisinin resistance is manifest by a slowing in parasite clearance rates[15, 21]. Reassuringly, of 861 patients with falciparum malaria recruited to three trials in southern Laos treated with ACT between 2002 and 2008, only 2 (0.23%) patients had parasite clearance times (PCT) longer than three days and 30 (3.48%) had PCT longer than 2 days. To determine whether there has been any recent change, the efficacy of the nationally recommended ACT (3-day oral artemether-lumefantrine) for the treatment of uncomplicated falciparum malaria was reported. This was part of a large trial of thiamin treatment in P. falciparum malaria in southern Laos, which will be reported separately.
Study site, patients, clinical and laboratory procedures
The study was conducted between June and November from 2008-2010 at Xepon (30 beds) Inter-District Hospital (16.690 N, 106.200 E, 208 metres above sea level), Savannakhet Province, ~665 km southeast of Vientiane, the capital of Laos. Xepon (88 villages, population 48,000) is inhabited predominantly by rice farmers of the Lao Theung ethnic groups. Malaria transmission is seasonal with a peak during the rainy months of July and August.
The clinical trial of thiamin supplementation in falciparum malaria conducted among patients with P. falciparum malaria receiving anti-malarial therapy according to national guidelines, was an exploratory, double-blind, parallel group, placebo-controlled, randomized (variable blocks), superiority trial to compare the frequency of clinical adverse effects and thiamin status, during 42 days follow up, of either daily oral thiamin supplementation ([oral thiamin (5 mg tablet) (Olan-Kemed Co.Ltd, Bangkok, Thailand)] 10 mg immediately after anti-malarial drugs, followed by 10 mg daily for 7 days followed by 5 mg daily until day 42), or an identical placebo.
Patients were included in the trial of thiamin treatment provided that they or their guardians (in the case of children) gave fully informed written consent, were of any age, had microscopically confirmed P. falciparum infection or mixed Plasmodium species infections, with a history of fever, were willing and able to comply with the study protocol for the duration of the 42 days follow up, and had not taken a full course of any anti-malarial drugs in the previous three days. Patients were excluded if they had a history of hypersensitivity to thiamin or artemether-lumefantrine, presented with intercurrent non-malarial illness or any condition, which in the judgement of the investigator would place the subject at undue risk or interfere with the results of the study, and if they had clinically apparent suspected thiamin deficiency (beriberi). Patients included in the analysis for this paper were only those without danger signs or severe falciparum malaria, with P. falciparum mono- or mixed infections with other species, but an asexual P. falciparum parasite density of <250,000/μL, and were able to swallow artemether-lumefantrine at presentation.
Patients’ admission clinical details including current and past medical history, pre-treatment, and findings from physical examination were recorded on the case record form. Venous blood samples were taken for parasite counts, haematocrit, blood glucose, and lactate, and three blood spots were collected on 3MM filter paper (Whatman, Maidstone, UK) and stored in a plastic bag with silica gel for later malaria genotype analysis[22, 25]. For women of child bearing age a urinary pregnancy test was performed before anti-malarial treatment was prescribed.
If the study criteria were met, patients were admitted to the hospital and treated with the nationally recommended anti-malarial - artemether (20 mg)-lumefantrine (120 mg) (Co-artem®, Novartis) provided by the Global Fund to fight AIDS, Tuberculosis and Malaria: one dose twice daily for three days. Dosing by body weight were one tablet if <15 kg, two tablets if 15–24 kg, three tablets if 25–34 kg, and four tablets if ≥35 kg. All patients were asked to take fatty food with the anti-malarial drugs and drug administration was directly observed by a study nurse. For children who could not swallow tablets, the appropriate drug dose was crushed and mixed with water and given in a syringe. If vomiting occurred within 30 minutes of anti-malarial administration, the full dose was repeated. Patient who vomited within 30 minutes to one hour, a half dose was re-administered. Patients who vomited >2 times within one hour were given the rescue treatment (artesunate 2.4 mg/kg IV stat, followed by 2.4 mg/kg IV at 12 hours and 24 hours and then daily until able to take oral medication).
Vital signs (axillary temperature, pulse, respiratory rate, and blood pressure) were measured every six hours. Patients and parasite counts were reviewed daily until two consecutive negative blood smears, then weekly for 42 days from the start of treatment or at other times if they felt unwell. Patients were discharged only when their fever and parasitaemia had cleared (defined as axillary temperature <37.50 C and <1 parasite per 500 white cells on thick film after 2 negative slides, respectively) and were asked to return to the hospital at days 7, 14, 21, 28, 35 and 42 (or at any time the patients feel unwell) or were visited at home in case the patients did not return as planned.
At each weekly visit, the symptoms of the patients during the previous week were recorded. Finger-prick blood samples were taken for malaria blood smears and haematocrit and blood spots were collected onto filter paper strips from all patients with recurrent fever or malaria symptoms. PCR amplification was performed on paired samples for parasite genotyping to distinguish between reinfection and recrudescence using three parasite loci (MSP-1, MSP-2, and GLURP). The PCR tests were performed at the MORU malaria molecular laboratory, Bangkok, Thailand.
Patients with P. falciparum recurrence were retreated with artesunate 4 mg/kg/day in a single daily dose for 3 days (Day 0-2) (Guilin Pharmaceutical Co., Guilin, PRC) plus mefloquine 15 mg base/kg on day 1 and 10 mg base/kg on day 2 in single daily dose (LariamTM, Roche Co, Switzerland). Those who had P. vivax appearance during follow up were treated with chloroquine (25 mg base/kg) for three days and further followed up. The incidence of any adverse event was recorded. Written informed consent was obtained from all participants.
Ethical clearance for the study was granted by the Lao National Ethics Committee for Health Research and the Oxford University Tropical Medicine Research Ethics Committee (OXTREC). The trial is registered with the ISRCTN via the University of Oxford as ISRCTN: 85411059. The trial was monitored by the Clinical Trials Support Group of Mahidol-Oxford Tropical Medicine Research Unit, Bangkok, Thailand.
The primary objective of the thiamin treatment trial was to determine whether the frequency of adverse events, after anti-malarial therapy, were significantly lower in those who received thiamin supplementation in comparison to those who did not. Here the PCR-corrected adequate clinical and parasitological responses at day 42, the PCT (the time in hours from the first treatment dose to the first of two consecutive thick films that were negative for asexual falciparum parasites after checking ≥500 oil fields) and fever clearance times (FCT, time in hours from the start of treatment at which the tympanic temperature first dropped below 37.50 C and remained below 37.50 C for 48 hours), gametocytaemia, the frequency of adverse events, and changes in haematocrit following anti-malarial treatment are described.
Data were analysed using Stata v9 (StataCorp, College Station, TX, USA). Comparisons between two groups were made by the Mann-Whitney U, Student’s t, chi-square, and Fisher’s exact tests, as appropriate. Cure rates were calculated as the proportion of patients with PCR-confirmed recrudescence using intention-to-treat (ITT) and per-protocol (PP) populations and by Kaplan-Meier survival analysis. In the ITT population all losses to follow-up were treated as failures and in the PP population losses to follow-up were excluded from the analysis. Patients with new infections were regarded as cures in both analyses. Gametocyte carriage was summarized as person-gametocytes-week rates calculated as the total number of weeks with gametocytes divided by the total number of weeks of follow-up. To identify independent predictors of treatment response, a stepwise logistic regression was constructed with recrudescence as the dependent variable and sex, age, admission symptoms (headache, chill, myalgia, dizziness, vertigo, nausea, vomiting, abdominal pain, diarrhea, anorexia, cough, dyspnea, and weakness) and signs (drowsiness, splenomegaly, and hepatomegaly), gametocyte carriage at admission, admission temperature, baseline haematocrit, fever and parasite clearance times, past history of malaria, and P. vivax appearance during follow up included as covariates. Only factors that were significant at p < 0.05 were retained in the final model.
Admission demographic, clinical and laboratory details for patients included in the analysis of the efficacy of artemether-lumefantrine (Coartem™) for the treatment of uncomplicated falciparum malaria in Laos
All (n = 549)
Children (≤ 15 yrs) (n = 357)
Adults (> 15 yrs) (n = 192)
Sex, M, no (%)
Age, years, median (range)
10 (0.5 - 73)
6 (0.5 - 15)
25 (16 – 73)
Body weight, kg
29.5 (28.0 – 30.9)
18.8 (17.8 – 19.8)
49.3 (48.2 – 50.4)
124.5 (122.0 –126.9)
108.4 (106.0 – 110.7)
154.4 (153.3 – 155.5)
Previous malaria attack, no. (%) of patientsa
Axillary temperature, °C
38.4 (38.3 - 38.5)
38.5 (38.4 - 38.7)*
38.2 (38.0 - 38.3)
Patients without fever on admission, no. (%)
Systolic blood pressure, mm Hg
101.9 (100.8 -103.1)
95.1 (94.2 - 96.1)*
114.6 (113.0 - 116.1)
Diastolic blood pressure, mm Hg
69.7 (68.8 – 70.6)
64.6 (63.7 - 65.5)*
79.3 (78.2 - 80.4)
95.1 (94.0 - 96.2)
100.4 (99.0 -101.8)*
85.3 (84.4 – 86.3)
27.5 (27.0 – 28.1)
29.7 (29.0 – 30.3)*
23.5 (22.9 – 24.0)
Splenomegaly, no. (%) of patients
Hepatomegaly, no (%) of patients
Lymphadenopathy, no (%) of patients
Parasitaemia, geometric mean parasites/μL (95%CI)
19,775 (17,244 – 22,678)
27,241* (23,281 – 31,875)
10,902 (8,567 – 13,872)
Mixed malaria species infection, no.(%)
Gametocytaemia, no. (%) of patients
Gametocytaemia, geometric mean parasite/μL (95%CI)
216 (110 – 423)
201 (97 – 415)
328 (13 – 8,195)
35.8 (35.2 – 36.3)
33.7 (33.1 – 34.4)*
39.5 (38.7 – 40.4)
6.09 (5.97 – 6.20)
6.09 (5.93 – 6.24)
6.08 (5.90 – 6.27)
2.9 (2.8 – 3.0)
3.1 (2.9 – 3.2)*
2.8 (2.6 – 2.9)
Demographic and clinical details
Admission symptoms and signs for patients included in the analysis of the efficacy of artemether-lumefantrine (Coartem™) for the treatment of uncomplicated falciparum malaria in Laos
Symptoms and signs
Total (n = 549)
Children (≤ 15 years) (n = 357)
Adults (> 15 years)(n = 192)
Fever and parasite clearance, and changes in haematocrit
Outcome measures for the treatment of patients included in the analysis of the efficacy of artemether-lumefantrine (Coartem™) in the treatment of uncomplicated falciparum malaria in Laos
All (n = 549)
Children (age ≤ 15 yrs) (n = 357)
Adults (age > 15 yrs) (n = 192)
42-day cure rate, no. (%) of patients a
42-day cure rate per protocol, no. (%) of patientsΨ
Fever clearance time, mean hours (95%CI)a,b
27.6 (25.7 – 29.5)*
21.2 (19.2 – 23.2)
Patients remained febrile at day 1, no. (%)
Patients remained febrile at day 2, no. (%)
Parasite clearance time, median days (range)a,c
1 (1 - 3)
1 (1 - 2)*
1 (1 - 3)
Positive parasitaemia at day 1, no. (%) of patients
Positive parasitaemia at day 2, no. (%) of patients
Gametocytaemia detected at anytime, no.(%) of patients
Gametocytaemia after treatment, no. (%) of patients
Gametocyte clearance time, median days (range) d
7 (1 – 21)
3 (1 -21)
7 (7 – 14)
Gametocyte cleared by day 7, no. (%) d
Median (range) gametocyte-person-weeks d
0.42 (0.14 – 1.0)
0.42 (0.14 – 1.0)
0.42 (0.42 – 0.42)
P. vivax appearance after treatment for P. falciparum, no. (%) of patients
Day 0 haematocrit, mean % (95%CI)
35.8(35.2 – 36.3)
33.7 (33.1 – 34.4)*
39.5 (38.7 – 40.4)
Day 1 haematocrit, mean % (95%CI)
32.4 (31.9 – 32.9)
30.4 (29.8 – 30.9)*
36.2 (35.4 – 36.9)
Day 2 haematocrit, mean % (95%CI)
31.1 (30.6 – 31.6)
29.1 (28.5 – 29.6)*
34.9 (34.1 – 35.7)
Day 3 haematocrit, mean % (95%CI)
31.1 (30.6 – 31.6)
29.0 (28.5 – 29.6)*
34.9 (34.1 – 35.6)
Day 7 haematocrit, mean % (95%CI)
33.3 (32.9 – 33.7)
31.7 (31.2 – 32.1)*
36.3 (35.6 – 37.0)
Day 14 haematocrit, mean % (95%CI)
34.4 (34.0 – 34.8)
33.3 (32.9 – 33.7)*
36.5 (35.8 – 37.2)
Day 21 haematocrit, mean % (95%CI)
35.6 (35.2 – 35.9)
34.6 (34.2 – 35.0)*
37.5 (36.8 – 38.2)
Day 28 haematocrit, mean % (95%CI)
36.2 (35.8 – 36.5)
35.3 (34.9 – 35.7)*
37.8 (37.0 – 38.5)
Day 35 haematocrit, mean % (95%CI)
36.5 (36.1 – 36.8)
35.5 (35.2 – 35.9)*
38.2 (37.5 – 38.9)
Day 42 haematocrit, mean % (95%CI)
37.6 (37.2 – 37.9)
36.7 (36.3 – 37.0)*
39.4 (38.7 – 40.1)
Plasmodium falciparum gametocyte carriage
Twenty-three (4%) patients presented with patent gametocytaemia on admission, 19 (5%) in children and 4 (2%) in adults (p = 0.07). The admission geometric mean gametocytaemia were similar for children and adults (p = 0.60). The time to clearance of gametocytes was longer in adults than in children but the difference was not statistically significant (p = 0.07). After treatment four children, but no adults, developed gametocytaemia (all at day 1) without gametocytaemia on admission. The median gametocyte-person-weeks was similar for children and adults (Table3).
Of 43 (7.8%) patients with subsequent P. falciparum reappearance (34 children, nine adults) PCR genotyping indicated that among these recurrent infections 16/43 (37%) [14/34 (41%) and 2/9 (22%) children and adults, respectively (p = 0.44)] had recrudescent infections. One child with P. falciparum reappearance had undetermined PCR result and, considering this child as having a recrudescent infection, the overall 42-day cure rates per protocol, excluding patients who were lost to follow up, withdrew consent, had persistent vomiting, or re-infection, were 97% (524/541) [96% (337/352) and 99% (187/189) for children and adults, respectively, p = 0.042]. When the patients with repeated vomiting, who were lost to follow up or were withdrawn (censored at the time last seen), considering the child with undetermined PCR result as recrudescence, and regarding recrudescent infections as failures, the 42-day cure rates (95%CI) by survival analysis (Kaplan-Meier) were 99.0% (98.3 – 99.4%) for children and 99.8% (99.0 – 99.9%) for adults. For the PCR adjusted survival analysis, the cure rates (95%CI) were 99.0% (98.3 – 99.4%) and 99.8% (99.0 – 99.9%) for children and adults, respectively. By conventional ITT analysis, the overall 42-day cure rates, adjusted for re-infection, were 97% (532/549) [96% (342/357) in children and 99% (190/192) in adults, p = 0.042]. Of 17 patients considered as having recrudescent infection (15 children and two adults), 15 (13 children and two adults) had parasite recurrence at or before day 28. Similarly, the 28-day cure rates by ITT analysis were 344/357 (96%) for children and 190/192 (99%) for adults. The median (range) interval to recrudescent falciparum infections was 21 (14–42) days. By ITT and per protocol analyses, the 42-day PCR uncorrected cure rates for children and adults were 323/357 (90%) vs 183/192 (95%); (p = 0.04), and 323/352 (92%) vs 183/189 (97%) (p = 0.02), respectively. Of 129 children aged <5 years, six had recrudescent infection and one had undetermined PCR result. If the patient with undetermined PCR result was considered a recrudescent infection, the 42-day PCR corrected cure rates among children < 5 years were 95%. There were 18 episodes of vivax malaria during the follow-up period, of which 17 were in children (p < 0.05). The median (range) interval to P. vivax appearance was 28 (21–42) days (Table3).
Factors affecting treatment response
Patients with recrudescent infections were significantly younger [median (range) age 5 (2–25) years], than those whose infections were treated successfully [median (range) age 10 (0.5–73) years, p = 0.006]. Considering the child with undetermined PCR result as recrudescent infection, the proportion of treatment failures adjusted for re-infection by PCR among children was 4.2% (15/357 patients) compared with 1.0% (2/192 patients) among adults (p = 0.042). The admission mean (95%CI) body temperature was significantly higher in patients with recrudescent infections [39.1 (38.4–39.8) 0 C] than those who were cured [38.4 (38.3–38.5) 0 C, p = 0.01]. Patients with recrudescent infections had a significantly longer mean FCT (45.0 h; 95% CI, 32.3–57.8 h) than those patients without (24.8 h; 95%CI, 23.4–26.2 h; p < 0.001). Patients with recrudescent infections also had a significantly lower haematocrit at days 3, 14, 21, 28, and 35 after starting therapy than those without recrudescence detected (p = 0.03, p = 0.01, p < 0.001, p < 0.001, and p < 0.001, respectively). The proportion of the patients reporting a past history of malaria was significantly lower in the patients with recrudescent infection (6%) compared to those without (28%) (p = 0.043). In a multiple logistic regression analysis, admission high temperature [OR = 2.2, 95%CI = 1.2 – 4.2), p = 0.01], longer fever clearance times [OR = 1.0, 95%CI = 1.0 – 1.1, p = 0.01], and lower haematocrit at day 28 [OR = 0.7, 95%CI = 0.6 – 0.9, p = 0.005] were significantly associated with treatment failure.
Possible adverse events (AE) found in patients included in the analysis of the efficacy of artemether-lumefantrine (Coartem™) in the treatment of uncomplicated falciparum malaria in Laos*
All (N = 549)
Children (age ≤ 15 years) (n = 357)
Adults (age > 15 years) (n = 192)
At least one adverse event
This large clinical trial shows that artemether-lumefantrine retains excellent efficacy in the treatment of uncomplicated falciparum malaria at one site in southern Laos in both children and adults with 42-days PCR-corrected cure rates of 96% and 99%, respectively. These results are similar to those described in a comparable trial conducted in 2002-3 in nearby Phalanxay District (~60 Km west of Xepon), in which there was a 42-days cure rate of 97% in children and adults. A similar trial conducted in the northern Luang Namtha Province of Laos in 2003 also showed very good efficacy and tolerability of AL with a 42-days cure rate of 94%. As previously, AL was very well tolerated, proved safe and no serious adverse events were found during follow up.
Patients’ background immunity contributes substantially to the treatment response of uncomplicated malaria in Laos[6, 27]. In this study, children had significantly higher recrudescence rates and P. vivax appearance rates than adults. A study comparing oral chloroquine and sulphadoxine-pyrimethamine for the treatment of uncomplicated falciparum malaria, before the introduction of AL, found treatment failure rates among Lao children to be 4.9 times higher than those among adults. The contribution of immunity to the treatment response is also suggested by slower clearance of fever and parasitaemia among children compared to adults[1, 9]. Anti-malarial drug assessments conducted only in adults, may overestimate anti-malarial efficacy risking continuation of ineffective drug regimens in national policy. Anti-malarial pharmacokinetics may differ in children and but for artemether-lumefantrine these differences are small.
The evidence, both from a trial of artesunate monotherapy with a mean (95%CI) PCT (hours) of 23.2 (21.2-25.3) and 42-day PCR-corrected cure rate of 100%, and from the high efficacy of AL described here, at the same site, suggests that artemisinin resistant P. falciparum has not spread to this area, of southern Laos. However, regular monitoring of the clinical efficacy of artemisinin-derivatives in southern Laos, especially closer to the Cambodian border, is required.
The Lao nationally recommended anti-malarial drug (artemether-lumefantrine) remains highly efficacious for the treatment of uncomplicated falciparum malaria five years after its introduction. However, regular monitoring of the efficacy of artemisinin derivatives is essential as early warning of the potential spread of artemisinin-resistant P. falciparum parasites.
We are very grateful for the involvement of all patients in this study and for the technical help from Mrs. Manisack Phommasansack, Mr. Bounpone Phimphalat, Mrs. Phinnakone Lasachack, Mrs. Phanmala Baysy, Mrs. Ammala Phomsimone, Mrs. Bounmy Syphachanh, Mrs. Vilayphone, Mr. Chanthala Vilayhong, Mr. Phonepasit Panyanouvong, Mr. Sengchanh Yeuchaixiong, and all doctors, medical assistants and nurses in Xepon District Hospitals. We gratefully thank Sue Lee, Brian Angus, Francois Nosten, and Nick Anstey, for participating in the Data and Safety Monitoring Committee of this study and Liz Ashley and Francois Nosten for helpful comments on the ms. Our grateful thanks go to Phaik Yeong Cheah, Prayoon Yuentrakul, and Viriya Hantrakun for acting as external monitors and to Drs. Pranom Phongmany and Sengchanh Koumphiengmaniseng for their valuable advice. We are very grateful for the support of the Minister of Health, His Excellency Dr. Ponmek Dalaloy, the Directors of Hygiene and Preventive Medicine, Drs. Douangchanh Keo-Asa and Bounlay Phommasack, the Director of Mahosot Hospital, Professor Chanpheng Thammavong. This study was supported by the Wellcome Trust of Great Britain.
- Mayxay M, Thongpraseuth V, Khanthavong M, Lindegårdh N, Barends M, Keola S, Pongvongsa T, Phompida S, Phetsouvanh R, Stepniewska K, White NJ, Newton PN: An open, randomized comparision of artesunate plus mefloquine vs. dihydroartemisinin-piperaquine for the treatment of uncomplicated Plasmodium falciparum malaria in the Lao People’s Democratic Republic (Laos). Trop Med Int Health. 2006, 11: 1157-1165. 10.1111/j.1365-3156.2006.01671.x.View ArticlePubMedGoogle Scholar
- Shirayama Y, Phompida S, Kuroiwa C: Monitoring malaria control in Khammouane province, Laos: an active case detection survey of Plasmodium falciparum malaria using the Paracheck rapid diagnostic test. Trans R Soc Trop Med Hyg. 2008, 102: 743-750. 10.1016/j.trstmh.2008.05.014.View ArticlePubMedGoogle Scholar
- Jorgensen P, Nambanya S, Gopinath D, Hongvanthong B, Luangphengsouk K, Bell D, Phompida S, Phetsouvanh R: High heterogeneity in Plasmodium falciparum risk illustrates the need for detailed mapping to guide resource allocation: a new malaria risk map of the Lao People’s Democratic Republic. Malar J. 2010, 9: 59-10.1186/1475-2875-9-59.PubMed CentralView ArticlePubMedGoogle Scholar
- Pillai DR, Labbe AC, Vanisaveth V, Hongvanthong B, Phompida S, Inthakone S, Zhong K, Kain KC: Plasmodium falciparum malaria in Laos: chloroquine treatment outcome and predictive value of molecular markers. J Infect Dis. 2001, 183: 789-795. 10.1086/318836.View ArticlePubMedGoogle Scholar
- Guthmann JP, Kasparian S, Phetsouvanh R, Nathan N, Garcia M, Phompida S, Brockman A, Gastellu M, Legros D: The efficacy of chloroquine for the treatment of acute uncomplicated Plasmodium falciparum malaria in the Lao People’s Democratic Republic. Ann Trop Med Parasitol. 2002, 96: 553-557. 10.1179/000349802125001654.View ArticlePubMedGoogle Scholar
- Mayxay M, Newton PN, Khanthavong M, Tiengkham P, Phetsouvanh R, Phompida S, Brockman A, White NJ: Chloroquine versus sulphadoxine-pyrimethamine for treatment of Plasmodium falciparum malaria in Savannakhet province, Lao People’s Democratic Republic: an assessment of national antimalarial drug recommendations. Clin Infect Dis. 2003, 37: 1021-1028. 10.1086/377734.View ArticlePubMedGoogle Scholar
- Mayxay M, Phetsouvanh R, Phompida S, Newton PN, Khanthavong M, Vannachone B, Brockmans A, White NJ: A randomized comparison of oral chloroquine and sulphadoxine-pyrimethamine for the treatment of uncomplicated falciparum malaria in Laos. Trans R Soc Trop Med Hyg. 2003, 97: 343-344. 10.1016/S0035-9203(03)90165-9.View ArticlePubMedGoogle Scholar
- Schwobel B, Jordan S, Vanisaveth V, Phetsouvanh R, Christophel EM, Phompida S, von Sonnenburg F, Jelinek T: Therapeutic efficacy of chloroquine plus sulphadoxine/pyrimethamine compared with monotherapy with either chloroquine or pyrimethamine/sulphadoxine in uncomplicated Plasmodium falciparum malaria in Laos. Trop Med Int Health. 2003, 8: 19-24. 10.1046/j.1365-3156.2003.00977.x.View ArticlePubMedGoogle Scholar
- Mayxay M, Khanthavong M, Lindegårdh N, Keola S, Barends M, Pongvongsa T, Yapom R, Annerberg A, Phompida S, Phetsouvanh R, White NJ, Newton PN: Randomized comparison of chloroquine plus sulphadoxine-pyrimethamine versus artesunate plus mefloquine versus artemether-lumefantrine in the treatment of uncomplicated falciparum malaria in the Lao PDR (Laos). Clin Infect Dis. 2004, 39: 1139-1147. 10.1086/424512.View ArticlePubMedGoogle Scholar
- Mayxay M, Keomany S, Khanthavong M, Souvannasing P, Stepniewska K, Khomthilath T, Keola S, Pongvongsa T, Phompida S, Ubben D, Valecha N, White NJ, Newton PN: A phase III, randomized, non-inferiority trial to assess the efficacy and safety of dihydroartemisinin-piperaquine in comparison with artesunate-mefloquine in patients with uncomplicated Plasmodium falciparum malaria in Southern Laos. Am J Trop Med Hyg. 2010, 83: 1221-1229. 10.4269/ajtmh.2010.10-0276.PubMed CentralView ArticlePubMedGoogle Scholar
- Stohrer JM, Dittrich S, Thongpaseuth V, Vanisaveth V, Phetsouvanh R, Phompida S, Monti F, Christophel EM, Lindegardh N, Annerberg A, Jelinek T: Therapeutic efficacy of artemether-lumefantrine and artesunate-mefloquine for treatment of uncomplicated Plasmodium falciparum malaria in LuangNamtha Province, Lao People’s Democratic Republic. Trop Med Int Health. 2004, 9: 1175-1183. 10.1111/j.1365-3156.2004.01320.x.View ArticlePubMedGoogle Scholar
- Valecha N, Phyo AP, Mayxay M, Newton PN, Krudsood S, Keomany S, Khanthavong M, Pongvongsa T, Ruangveerayuth R, Uthaisil C, Ubben D, Duparc S, Bacchieri A, Corsi M, Rao BHK, Bhattacharya PC, Dubhashi N, Ghosh SK, Vas Dev, Kumar A, Pukittayakamee S: An open-label, randomised study of dihydroartemisinin-piperaquine versus artesunate-mefloquine for falciparum malaria in Asia. PLoS One. 2010, 5: e11880-10.1371/journal.pone.0011880.PubMed CentralView ArticlePubMedGoogle Scholar
- Noedl H, Se Y, Schaecher K, Smith BL, Socheat D, Fukuda MM: Artemisinin Resistance in Cambodia 1 (ARC1) Study Consortium. Evidence of artemisinin-resistant malaria in western Cambodia. N Engl J Med. 2008, 359: 2619-2620. 10.1056/NEJMc0805011.View ArticlePubMedGoogle Scholar
- Rogers WO, Sem R, Tero T, Chim P, Lim P, Muth S, Socheat D, Ariey F, Wongsrichanalai C: Failure of artesunate-mefloquine combination therapy for uncomplicated Plasmodium falciparum malaria in southern Cambodia. Malar J. 2009, 12: 10-View ArticleGoogle Scholar
- Dondorp AM, Nosten F, Yi P, Das D, Phyo AP, Tarning J, Lwin KM, Ariey F, Hanpithakpong W, Lee SJ, Ringwald P, Silamut K, Imwong M, Chotivanich K, Lim P, Herdman T, An SS, Yeung S, Singhasivanon P, Day NP, Lindegardh N, Socheat D, White NJ: Artemisinin resistance in Plasmodium falciparum malaria. N Eng J Med. 2009, 361: 455-467. 10.1056/NEJMoa0808859.View ArticleGoogle Scholar
- van Vugt M, Brockman A, Gemperli B, Luxemburger C, Gathmann I, Royce C, Slight T, Looareesuwan S, White NJ, Nosten F: Randomized comparison of artemether-benflumetol and artesunate-mefloquine in treatment of multidrug-resistant falciparum malaria. Antimicrob Agents Chemother. 1998, 42: 135-139.PubMed CentralPubMedGoogle Scholar
- van Vugt M, Wilairatana P, Gemperli B, Gathmann I, Phaipun L, Brockman A, Luxemburger C, White NJ, Nosten F, Looareesuwan S: Efficacy of six doses of artemether-lumefantrine (benflumetol) in multidrug-resistant Plasmodium falciparum malaria. Am J Trop Med Hyg. 1999, 60: 936-942.Google Scholar
- Lefevre G, Looareesuwan S, Treeprasertsuk S, Krudsood S, Silachamroon U, Gathmann I, Mull R, Bakshi R: A clinical and pharmacokinetic trial of six doses of artemether-lumefantrine for multidrug-resistant Plasmodium falciparum malaria in Thailand. Am J Trop Med Hyg. 2001, 64: 247-256.PubMedGoogle Scholar
- Poravuth Y, Socheat D, Fandeur T, Tsuyuoka R, Hoyer S: Efficacy and safety of six dose regimen of Coartem® in the treatment of uncomplicated falciparum malaria in Cambodia. Mekong Malaria Forum. 2002, 10: 54-55.Google Scholar
- Krudsood S, Chalermrut K, Pengruksa C, Srivilairit S, Silachamroon U, Treeprasertsuk S, Kano S, Brittenham GM, Looareesuwan S: Comparative clinical trial of two-fixed combinations dihydroartemisin-napthoquine-trimethoprim (DNP) and artemether-lumefantrine (Coartem/Riamet) in the treatment of acute uncomplicated falciparum malaria in Thailand. Southeast Asian J Trop Med Public Health. 2003, 34: 316-321.PubMed CentralPubMedGoogle Scholar
- 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: 339-10.1186/1475-2875-10-339. http://www.malariajournal.com/content/10/1/339.PubMed CentralView ArticlePubMedGoogle Scholar
- Mayxay M, Khanthavong M, Chanthongthip O, Imwong M, Lee SJ, Stepniewska K, Soonthornsata B, Pongvongsa T, Phompida S, Hongvanthong B, Ringwald P, White NJ, Newton PN: No evidence for spread of Plasmodium falciparum artemisinin resistance to Savannakhet Province, Southern Laos. Am J Trop Med Hyg. 2012, 86: 403-408. 10.4269/ajtmh.2012.11-0497.PubMed CentralView ArticlePubMedGoogle Scholar
- World Health Organization: Thiamine deficiency and its prevention and control in major emergencies. 1999, Geneva, WHO/NHD/99.13.Google Scholar
- World Health Organization: Severe falciparum malaria. Trans R Soc Trop Med Hyg. 2000, 94 (supplement 1): 1-90.View ArticleGoogle Scholar
- Brockman A, Paul REL, Anderson TJC, Hackford I, Phaiphun L, Looareesuwan S, Nosten F, Day KP: Application of genetic markers to the identification of recrudescent Plasmodium falciparum infections on the northwestern border of Thailand. Am J Trop Med Hyg. 1999, 60: 14-21.PubMedGoogle Scholar
- World Health Organization: Method for surveillance of antimalarial drug efficacy. 2009, Geneva: World Health Organization, http://www.who.int/malaria/resistance.Google Scholar
- Mayxay M, Chotivanich K, Pukrittayakamee S, Newton P, Looareesuwan S, White NJ: The contribution of humoral immunity to the therapeutic response in falciparum malaria. Am J Trop Med Hyg. 2001, 65: 918-923.PubMedGoogle Scholar
- White NJ: The assessment of antimalarial drug efficacy. Trends Parasitol. 2002, 18: 458-464. 10.1016/S1471-4922(02)02373-5.View ArticlePubMedGoogle Scholar
- Tarning J, Zongo I, Somé FA, Rouamb N, Parikh S, Rosenthal PJ, Hanpithakpong W, Jongrak N, Day NP, White NJ, Nosten F, Ouedraogo JB, Lindegardh N: Population pharmacokinetics and pharmacodynamics of piperaquine in children with uncomplicated falciparum malaria. Clin Pharmacol Ther. 2012, 91: 497-505. 10.1038/clpt.2011.254.PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.