As per the WHO recommendation, the development of resistance by P. falciparum to most artemisinin combination therapies (ACTs) triggered the need for routine monitoring of the efficacy of the drugs every two years in all malaria endemic countries. Hence, this study was carried out to assess the therapeutic efficacy of Artemether-Lumefantrine (Coartem®) in treating the uncomplicated falciparum malaria, after 9 years of its introduction in the Metehara, Eastern Ethiopia.
This is part of the therapeutic efficacy studies by the Federal Ministry of Health Ethiopia, which were conducted in regionally representative sentinel sites in the country from October 2014 to January 2015. Based on the study criteria set by WHO, febrile and malaria suspected outpatients in the health center were consecutively recruited to study. A standard six-dose regimen of AL was administered over three days and followed up for measuring therapeutic responses over 28 days. Data entry and analysis was done by using the WHO designed Excel spreadsheet and SPSS version 20 for Windows. Statistical significant was considered for P-value less than 0.05.
Of the 91 patients enrolled, the day-28 analysis showed 83 adequate clinical and parasitological responses (ACPRs). Per protocol analysis, PCR-uncorrected & corrected cure rates of Coartem® among the study participants were 97.6% (95%CI: 93.6–99.5) and 98.8% (CI: 93.5–100%), respectively. No parasite detected on day 3 and onwards. Fever clearance was above 91% on day-3. Mean hemoglobin was significantly increased (P<0.000) from 12.39 g/dl at day 0 to 13.45 g/dl on day 28. No serious adverse drug reactions were observed among the study participants.
This study showed high efficacy of AL in the study area, which suggests the continuation of AL as first line drug for the treatment of uncomplicated P. falciparum malaria in the study area. This study recommends further studies on drug toxicity, particularly on repeated cough and oral ulceration.
Citation: Nega D, Assefa A, Mohamed H, Solomon H, Woyessa A, Assefa Y, et al. (2016) Therapeutic Efficacy of Artemether-Lumefantrine (Coartem®) in Treating Uncomplicated P. falciparum Malaria in Metehara, Eastern Ethiopia: Regulatory Clinical Study. PLoS ONE11(4): e0154618. https://doi.org/10.1371/journal.pone.0154618
Editor: Georges Snounou, Université Pierre et Marie Curie, FRANCE
Received: February 9, 2016; Accepted: April 17, 2016; Published: April 29, 2016
Copyright: © 2016 Nega et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper.
Funding: This work was supported by the support of the Global Fund and International Atomic Energy. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: ACPR, Adequate clinical and parasitological response; ACT, Artemisinin-based combination therapy; AL, Artemether-lumefantrine; ETF, Early treatment failure; LCF, Late clinical failure; LPF, Late parasitological failure; WHO, World Health Organization; PCR, polymerase chain reaction; EPHI, Ethiopian public health institute; Hb, hemoglobin; ITNs, insecticide-treated bed nets; IRS, indoor residual spraying; WBCs, White blood cells; FMOH, Federal ministry of health; OPD, outpatient department; FCT, Fever Clearance Time; PCT, Parasite Clearance Time; ITT, Intention to treat; PP, Per protocol; U5, Under five children
P. falciparum resistance to chloroquine and sulphadoxine-pyrimethamine (SP) in most African countries, including Ethiopia, has triggered the shift of national treatment policy towards the first-line treatment with ACTs [1,2]. WHO currently recommends five ACTs: Artesunate-sulfadoxine-pyrimethamine, Artesunate-mefloquine, Artesunate-amodiaquine, Artemether-Lumefantrine (AL) and Dihydroartemisinin-Piperaquine (DHA-PPQ). The first 3 regimens are no more used in Africa because of safety concerns and the emergence of drug resistance and only AL has been the most widely prescribed ACT in sub-Saharan Africa [2,3]. In Ethiopia, using AL as the first line treatment for uncomplicated falciparum malaria has been started in 2004 [1,4].
P. falciparum resistance to oral artemisinin monotheraphy has been reported severally along the Cambodia–Thailand border in the Greater Mekong sub-region of Asia [5,6]. Despite the truth, combination therapies are still remained the first choice [3,7] and there is no relevant report of ACT resistant P. falciparum detected in Africa, including Ethiopia [8–10]. ACT is known by its rapid parasite clearance and reducing gametocyte carriage to cease parasite transmission [11–13].
AL (Coartem®) is a first fixed-dose ACT, which meets the WHO prequalification criteria for efficacy, safety and quality, and is indicated for the treatment of uncomplicated falciparum malaria, or mixed infections in adults, children, and infants (>5 kg body weight). AL confirmed the reliable 28-day polymerase chain reaction (PCR)-corrected cure rates of more than 95% in adult and pediatric populations with a favorable safety and tolerability in sub-Saharan African studies [14,15].
Malaria trends change over time; thus, routine monitoring of the efficacy of the therapeutics-in-use is essential for timely changes in treatment policy and helps to detect early changes in P. falciparum sensitivity to antimalarial drugs as recommended by WHO . WHO currently recommends routine monitoring of the efficacy of first-line and second-line ACTs every two years in all endemic countries. A treatment failure rate exceeding 10% should prompt a change in the national antimalarial treatment policy . Furthermore, there was no similar study conducted in the study area previously. Therefore, this study was conducted with the aim of assessing the therapeutic efficacy of Artemether-Lumefantrine (Coartem®) in treating the uncomplicated falciparum malaria, after 9 years of its introduction in Metehara, Eastern Ethiopia.
Materials and Methods
Study Area and Period
This study was conducted in between October 2014 and January 2015 during the peak malaria transmission season at the outpatient department (OPD) of Metehara Health Centre. Metehara is an administrative town of Fentale district in Oromia Regional state of Ethiopia. The area is located in the Great Rift Valley, about 210 km east of Addis Ababa, the country’s capital. Its coordinate is 8°54′N 39°55′E and average elevation is 947 m (3,107 ft), with time zone of EAT (UTC+3). Rivers Awash and Germama, and lake Basaka are important water bodies in the district . The estate irrigation by using the nearby rivers for the industrial cultivation of sugar cane, in turn, suits the condition for breeding of the Anopheles mosquito. Transmission of malaria in this area occurs year-round, with peaks from September to November and March to May. The dominant parasites are P. falciparum causing 80% of malaria infections and P. vivax accounting for 20% infections (Metehara district health records, unpublished data).
This is part of the open-label single-arm 28-day regulatory clinical studies by the Federal Ministry of Health Ethiopia, which were conducted in regionally representative sentinel sites in the country, for the routine monitoring of the national treatment policy.
Study Subjects, Inclusion, and Exclusion Criteria
Febrile patients visiting the outpatient department of the health center who fulfilled the inclusion criteria set by WHO , for the assessment and monitoring of antimalarial drug efficacy for the treatment of uncomplicated falciparum malaria.
Both sex with age ≥6 months; body weight >5 kg; fever (axillary temperature ≥ 37.5˚c) or having history of fever in the preceding 24 hours; microscopically defined P. falciparum mono-infection, with parasitemia from 1000 to 100,000 parasites/μl; non-pregnant or not breast-feeding women; patients living within facility catchment area (i.e. 5–10 km radius of the health center); informed consent by patient or by caregivers for children and patient agreement to return for all scheduled visits.
Mixed or mono-infection with species other than P. falciparum; hemoglobin >5.0 gm/dl; AL intake within 15 days prior to study recruitment; unable to take oral medication or repeated vomiting; known hypersensitivity to AL; evidence of severe malaria or other danger signs such as inability to drink or breast-feed, vomiting (i.e. more than twice in past 24 hours), recent history of convulsions (i.e. more than once in past 24 hours), unconscious state, unable to sit or stand; severe malnutrition; any history of previous serious side-effects to study medications; evidence of a concomitant febrile illness (Otitis media, tonsillitis, measles, abscesses, measles, acute lower respiratory tract infection, severe diarrhea) in addition to malaria
Sample Size Determination
The required sample size was calculated by using a single population proportion formula based on the revised WHO protocol . By taking an expected the day 28 cure rate of AL as 95% from estimation based on recent studies in the home country [8,18,19], a 95% confidence level and 5% margin of error, the initial calculated sample size was 73. Assuming an additional 20% contingency for withdrawals, a minimum of at least 88 representative sample size was computed.
Sampling Technique and Sample Collection
Consecutive sampling technique had been used to select the visiting outpatients until the required sample size was attained. Patient screening was done by health officers in an outpatient setting to identify those meeting the inclusion criteria for the study. Health professionals involved in the collection of the data were oriented on the procedures designed by the WHO . The finger-prick capillary blood was used to prepare the malaria slide smears, to measure hemoglobin level and to collect the dried blood samples on filter paper during enrolment and on any unexpected visit, for further molecular analysis.
Blood Film Examination
Thick blood film was used to detect malaria parasites and to quantify the parasites, while thin film was used to identify the parasite species. Giemsa working solution with buffering PH of 7.2 was used to stain the smears. Double-slide blood smears were prepared; one stained rapidly with 10% Giemsa for 10 to 15 minutes to screen for recruitment, and the next stained with standard 3% Giemsa for 30 to 45 min as recommended elsewhere .
The first blood smear was used for parasite detection and rapid estimation of asexual parasitemia in limited microscopic fields. Parasitemia was taken as adequate for recruitment when ≥1 parasite/6–8 WBCs was observed; which matches to about 1000 asexual parasites/μL. The next standard blood smear was examined to determine the actual parasite density. Asexual parasite density per micro liter (μl) was determined on the basis of the number of parasites counted per 200 white blood cells on a thick blood film by assuming a total standard WBC count of 8000/μl On another hand, gametocytes were counted per 1000 WBC, based on the standard WBC count of 8000/μl [20,21].
Two experienced laboratory technologists individually examined the microscopic slides. Thick smears were reported as negative when no parasite detected after examining 100 microscopic fields. Discrepancy between the first and second readings was settled by a third senior microscopist in regional malaria examination quality control laboratory, and whose readings were then taken final. Quality control of microscopic results of parasite counts was made by crosschecking all of the total slides [20,21].
Finger prick capillary blood was used to measure hemoglobin level using the Portable Spectrophotometer (Hemocue Hb 201+, Anglom, Sweden).
Treatment and Follow Up Schedule
A standard six-dose regimen of AL(Coartem®) based on age/weight scale was administered twice daily over three days and was followed up for clinical and parasitological responses over 28 days based on the in-vivo drug trial protocol set by the WHO in 2009 . AL was given as a tablet of 20 mg of artemether and 120 mg of lumefantrine. The AL was made in India by IPCA Laboratories Ltd. [Plot No: 255/1; Athal, Silvassa 396 230 (D & NH); Batch No: DYI473602; Mfg: 08–2013; and Exp: 07–2015]. The drug was provided by the FMOH Ethiopia through the support of WHO.
Patients were awaited for 30 min in the OPD to ensure absence of post-treatment vomiting. In vomiting cases, full-treatment dose was given again in the OPD. For repeated vomiting, patients were withdrawn from the study totally. Three doses were given on direct observation by the health officers in the OPD: first dose at recruitment and the next two morning doses given during visits at days 1 & 2. The rest three doses were taken at the patients’ home with the supervision of community health extension workers. Artisunate injection was given to patients who failed to respond to AL and those with re-appearance of P. falciparum. P. vivax case detected during follow-up was given the usual chloroquine.
Follow up visits for measuring therapeutic responses were made on days 1, 2, 3, 7, 14, 21, and 28 and/or any unscheduled day when symptoms occurred. The measurement of parasitemia, fever, and adverse events were made at every visit day; while hemoglobin was measured on days 0, 14, and 28. When patients failed to attend their scheduled visits, they were traced by the assigned home visitor on the same day and were brought to the clinic.
Patient Withdrawal and Loss to Follow Up
Withdrawal of patients from the study was done in the conditions including self-willing, vomiting the drug twice, occurrence of a severe febrile illness, self-administration of drug with antimalarial effect, omitting the prescribed treatment doses, loss to follow up, detection of mixed Plasmodium species and other similar protocol violation situations. Patients who missed to attend on the follow-up schedules and/or could not attend even by tracing of the home visitor on the successive days were taken as lost to follow-up. Patients withdrawn by presence of complications including re-appearance of P. falciparum or P.vivax were admitted to the health center for proper inpatient treatment. Classification of therapeutic response and definitions
According to the WHO in-vivo drug trial protocol of 2009 , therapeutic responses were classified as primary and secondary outcomes. The primary endpoints were treatment failures and cure rates on day 28, while secondary endpoints were fever and parasitaemia clearance on days 1, 2 and 3; gametocytaemia carriage at days 7 and 28; and re-infection rates at day 28.
The Primary Outcomes
Early treatment failure (ETF).
It is the development of danger signs for severe malaria on days 1, 2 or 3 in the presence of parasitemia; parasitemia on day 2 higher than day 0 count irrespective of axillary temperature; parasitemia on day 3 with axillary temperature ≥37.5 °C; parasitemia on day 3 ≥ 25% of count on day 0.
Late clinical failure (LCF).
It is the development of danger signs for severe malaria after day 3 in the presence of parasitemia, without previously meeting any of the criteria of ETF; presence of parasitemia and axillary temperature ≥37.5°C or history of fever on any day from day 4 to day 28, without previously meeting any of the criteria of ETF.
Late Parasitological Failure (LPF).
It is the presence of parasitemia on any day from day 7 to day 28 and axillary temperature <37.5°C, without previously meeting any of the criteria of early treatment failure or late clinical failure.
Fever clearance rate (FCR).
It is the speed at which body temperature is decreased to <37.5°C after drug intake or proportion of patients whose fever cleared on days 1, 2, and 3.
Parasite clearance rate (PCR).
It is the speed at which parasites disappear from the body after drug intake or proportion of patients with negative blood smears on days 1, 2, and 3.
It was defined as the ability of a parasite strain to survive and/or multiply despite the administration and absorption of a drug in doses equal to or higher than those usually recommended but within the limits of tolerance of the subject.
PCR for identification of recrudescence.
Genotyping of treatment failure samples was done to differentiate recrudescence from re-infection. PCR was conducted on standard filter paper collected blood samples, which were air-dried and stored in cool and dark boxes with desiccants. The analysis was performed at Ethiopian Public Health Institute (EPHI) malaria molecular laboratory similarly by using msp-1 & msp-2 genes as described elsewhere [22,23]. Cases with identical genotypes for pre-and post-treatment samples were classified as recrudescence; and those with different genotypes as re-infection, while mixed genotypes were considered as failures.
The study protocol was cleared and approved by the Ethical Review Committee of EPHI, Ethiopia.
Acquisition of consent.
Verbal and written informed consents were obtained from all of the study participants; signed by the adults or the parent/guardian understanding in his/her local language. Data collected from each study participant and results of laboratory tests were kept confidential and used only for the research purpose.
Data entry and analysis was done by using the WHO designed Excel spreadsheet and SPSS version 20 for Windows. Descriptive statistics such as percentages, mean, standard deviation, and range were performed as needed. Cure rate was assessed by modified intention to treat (ITT) and per protocol (PP) analysis. The PP Kaplan Meir was used to analyze the primary therapeutic outcomes. Independent t-test was used to check the presence or absence of statistically significant mean differences between the continuous variables among age groups. Statistical significant was considered for P-value less than 0.05.
Result of the Study
Screening, Admission and Follow-Up of Patients
Outpatients who were febrile and having fever history within the 24 hrs prior to the start of the study were screened in outpatient department and sent to laboratory with the request of malaria diagnosis. Within the study period, 2317 patients clinically suspected for malaria were examined for the detection of Plasmodium parasite. Of the malaria suspected cases, 276 (11.9%) had malaria infection. From the malaria positives, 176 (63.8%) were P. falciparum mono-infections; of which 73(26.4%) were P. vivax infections and the rest 27(9.8%) were mixed infections. Of the P. falciparum mono-infection patients, only 91 patients who fulfilled the inclusion criteria for the surveillance of antimalarial drug efficacy set by WHO (16) were recruited to the study. The rest P. falciparum mono-infections cases were excluded for the reasons: voluntary exclusion, parasite load <1000 parasites/μl, residence far apart from the health centre, and pregnancy cases. More description is on the flow chart (Fig 1).
Baseline Characteristics of the Study Participants
Totally 91 individuals were enrolled, of which 75.8% (69/91) were males; the proportion increased consistently with age. Mean age of the study participants was 18.4 years (range: 1–49); and mean age among the under five (U5), 5–15 & above 15 years was 2.6 yrs (1–4), 8.0 yrs (5.0–14.0) and 25.7 yrs (16–49), respectively. Majority of the study participants were adults (61.5%) as shown in the Table 1.
Average body temperature at recruitment was 38.15°C(36.5–40.7); 38.4°C(36.5–40.4) in U5, 37.9°C(36.5–40.7) in 5–15 years and 38.3°C (36.5–40.4) in above 15 yrs. At inclusion, higher average parasite load was observed in U5. Geometric mean of parasitemia at day-0 was 11,509.63 (1000–150,000) parasite/μl among all study participants: 14,801.04/μl (1200–57,971) in U5; 10,972.71/μl (1000–142857) in 5–15 yrs; and 11,301.58 (1200–150,000) in above 15 years. Gametocyte carriage was observed only among the older age groups; no gametocyte detected in U5. Hemoglobin level was significantly increased with age as placed in Table 1.
Previous malaria exposure was seen by about 60% of the study participants. The proportion increased with age where adults had higher frequency of malaria attack, compared to lower age. The mass distribution of ITNs, IRS and adoption of ACTs contributed much for the substantial decline in malaria related deaths in Ethiopia [24,25]. However, the current study findings indicated that still there were low awareness to the use of ITN; about half of the study participants were not using ITN (Table 1).
Study Outcome: Primary and Secondary Endpoints
Cure Rate of Coartem®.
Of the 91 patients enrolled, 83 completed the follow-up at day-28 with ACPR. Two treatment failures, 1 LPF at day 23 and 1 LCF at day 28, were observed, giving PCR-uncorrected failure rate of 2.4% (2/83) (95% CI: 0.0–8.5%). By PCR correction, only the LCF was confirmed to be a recrudescence case with a failure rate of 1.2%. There was seen no early treatment failure (ETF). For per protocol (PP) analysis, PCR-uncorrected cure rate of Coartem® among the study participants was 97.6% (95%CI: 93.6–99.5) and the PCR-corrected cure rate was 98.8% (95%CI: 93.5–100%) (Fig 2 & Table 2). For intention to treat (ITT) analysis, the PCR-uncorrected cure rate was 91.2% (95%CI: 85.6–93.1%) and the PCR-corrected cure rate was 92.2% (86.2–96.1) (Table 2). ACPR at day-28 or adjusted cure rate was 100% each for U5 children and adults; whereas in 5–15 yrs, it was 92.3% (24/26) as shown in Table 2.
Parasite clearance rate.
At recruitment, 54.9% (50/91) of the study participants were severely parasitemic (>10,000 parasites/μl), while the rest 45.1% (41/91) were found moderately parasitemic (1000–9999 parasites/μl). High proportion of severe parasite density was observed in U5 children referred to older age groups. More detail on parasite density among the age groups is available on the Table 3.
Fever clearance rate.
Febrile individuals, with ≥37.5°c axillary temperature, accounted for 59.3% (54/91) at the day of recruitment and decreased to 21.3% (19/89) on day 1, 5.7% (5/88) on day 2 and 2.3% (2/87) on days 3. Accordingly, fever clearance was 94.3% (83/88) on day 2, 97.7% (82/87) on day 3 and no febrile case was detected onwards (Fig 3 & Table 4). Fever case among severely parasitemic patients was 57.4% (31/54) and among the moderately parasitemic individuals was 42.6% (23/54). However, the difference between degree of parasitemia and fever case is not significant (P-value = 0.567) (Table 5).
Only 5.5% (5/91) gametocyte cases, among all study participants, were detected at enrolment: 11.5% (3/26) detected in 5–15 yrs, 3.6% (2/56) detected in >15 years and none [0.0% (0/9)] was detected in U5 age group. Of the day-0 detected gametocyte cases, three cases on day-1 and/or four cases on day-2 were cleared giving gametocytemia clearance rate of 60%(3/5) and 80%(4/5) on these days, respectively. The proportion of gametocyte carriage per total study participants was declined from 5.5% (5/91) on day 0 to 2.25% (2/89) on day 1, 1.14% (1/88) on day 2 and completely disappeared on day 3 (Fig 3 & Table 4). No new gametocyte case was detected after initiation of the treatment.
Assessment of Hemoglobin Level and Anemia Classification
The proportion of anemia was decreased from 37.4% (34/91) on day 0 to 31.4% (27/86) on day 14 and/or 23.2% (19/82) on day 28. The mean hemoglobin of the study participants was significantly increased (P<0.000) from 12.39 g/dl (5.30–17.40g/dl) on day 0 to 12.85g/dl (7.00–17.10`g/dl) on day 14 and 13.45 g/dl (7.70–17.50g/dl) on day 28 (Table 6).
Adverse Drug Reactions
No serious adverse event was observed throughout the 28 days follow up. Most of the adverse reactions to Coartem®, observed in this study, were minor as noticed by the manufacturer. Most reported cough, headache, weakness, joint pain, abdominal pain, and anorexia; and some reported ulceration of mouth area. There were observed 3.29% oral ulcerations and 8.79% cough cases on days 1 to day 3. These minor symptoms were soon disappeared with parasite clearance (data not shown)
In response to the resistance of malaria parasites to older antimalarials, WHO has brought the ACTs for global use as the first line drug for uncomplicated falciparum malaria in 2001. Accordingly, the use of AL as the first line drug for uncomplicated falciparum malaria in Ethiopia has been started in 2004 . Since then, no more significant ACT resistant P. falciparum cases were reported in the country [10,18,26]. The current study similarly showed well tolerance and high efficacy of AL against uncomplicated malaria in Eastern Ethiopia. In reverse to the Thailand-Cambodian fake antimalarial free marketing trend and the continued use of artemisinin mono-therapy, whichhave brought AL resistance in their area [27,28], AL distribution in Ethiopia occurs only in the government sectors and this has potentially minimized the distribution of counterfeit drugs in the country .
The present study showed the 28 day cure rate of a standard six-dose of Coartem® as close to 100% in treating uncomplicated P. falciparum malaria, with rapid clearance of fever and parasitaemia within the first three days. For PP analysis, PCR-uncorrected & the PCR-corrected cure rate of Coartem® among the study participants were 97.6% (95%CI: 93.6–99.5) and 98.8% (95%CI: 93.5–100%), respectively. Similar high efficacy findings were already reported elsewhere in Ethiopia [8,10,19,29], and in sub-Saharan Africa [30,31]. Pooled-analysis in Coartem® cure rate from above 32 publications reported the average efficacy of 97% , which is almost similar to the present study finding.
According to the Kaplan Meier PP survival analysis in the current study, the PCR-uncorrected/corrected failure rate was 1.2–2.4%. Change in the national antimalarial treatment policy is done only if treatment failure rate is above 10% as recommended by WHO . Therefore, this study finding advocates the continuation of AL as a first-line treatment of uncomplicated P. falciparum in the study area, with no change in the national treatment policy.
The adjusted cure rate at day-28 was 100% each for U5 children and adults; whereas in 5 to 15 years, it was 92.3%. Treatment failure in the present study was observed only in young ages that have yet not developed sufficient acquired immunity to malaria. The difference in cure rate among age groups may be due to the development of B-cell memory to malaria by old ages from frequent past infections that augments anti-malarial therapeutics to attain better cure rate than the non-immune young children [32,33]. The difference from U5 children may be due to the confounding attributed to the smaller sample size of under fives in the current study.
Parasitemia cleared rapidly on day-3 in this study, which is similar to the earlier study reports from Ethiopia [8,10,19,29] and India . ACT is known by its rapid parasite clearance and reducing gametocyte carriage to end up parasite transmission [11–13]. AL is known to decrease both asexual and sexual stages of parasites 6 to 8 times faster than the previous anti-malarial drugs [35,36]. This shows the potent anti-malarial property of Coartem® targeting the blood stage parasites. No gametocyte case was detected on day 3 and onwards. Similar studies from different parts of Africa including Ethiopia [8,19,37] had reported the rapid clearance of gametocytes with Coartem® treatment.
Fever cleared rapidly following Coartem® treatment in the present study, and this is comparable to findings described elsewhere [8,18,19]. There was observed a minimal fever cases delayed one day longer after the clearance of parasitemia, which may be due to the metabolic end products from malaria parasite and the blood circulating malaria toxins that have prolonged half-life .
The mean hemoglobin of the study participants was significantly increased (P<0.000) from 12.39 g/dl on day 0 to 13.45 g/dl on day 28. This enhancement next to medication with Coartem® is analogous to other study reports [10,19,29]. Besides, hemoglobin level significantly increased with age from enrolment to completion of the study (P-value<0.05). This difference in proportion of anemia among age groups may be due to insufficient nutrition and limited immune defense in lower age groups than the higher ones as indicated somewhere .
There were observed no serious adverse events; most of the observed reactions were already noticed as common adverse reactions by the manufacturer and registered under the food and drug administration authority. Majority reported cough, headache, weakness, joint pain, abdominal pain, and anorexia; and some reported ulceration of mouth area. Those minor symptoms observed were soon disappeared with parasite clearance. The absence of any serious adverse event following Coartem® treatment in the current study matches the findings of other studies [19,30,31]. This still implies the safe continuation of Coartem® use as first–line treatment in the study district.
The relative bioavailability of artemether and lumefantrine increases by 2–3 times and 16 times, respectively, when administered after a high-fat meal . However, in the current study, AL was administered without giving fatty food; only peanuts to adults and biscuits to children were provided preceding drug intake in the outpatient. This is one of the possible limitations in this study.
The current result showed the high efficacy of Coartem® that suggests the continuation of the drug as first-line for the treatment of uncomplicated P. falciparum malaria in the study area. Even after a number of years of its widespread access in the country, the AL still works highly efficacious medication for uncomplicated P. falciparum infection in the study area. No similar study has been conducted in the study area prior to the current study; therefore, regular monitoring of the efficacy of the drug in the study area is recommended to handle the raising drug resistance issues early. This study recommends further study on drug toxicity, particularly on repeated cough and oral ulceration.
We would like to thank the Ethiopian Public Health Institute and Federal Ministry of Health for collaboration in the whole research progresses and funding with the support of the Global Fund and International Atomic Energy. Our sincere gratitude goes to the study participants for their consent to be employed in the study. We would also like to thank the health center staffs and health extension workers in the study area.
Conceived and designed the experiments: DN MK AA HM HS AW YA AK. Performed the experiments: DN MK AA HM. Analyzed the data: DN MK. Contributed reagents/materials/analysis tools: HS AW AK YK. Wrote the paper: DN.
- 1. Federal Democratic Republic of Ethiopia, Ministry of Health: Malaria diagnosis and treatment guidelines for health workers in Ethiopia. 2nd edition. Addis Ababa Minist Heal, 2004.
- 2. World Health Organization: WHO Guidelines for the treatment of malaria. Geneva switzerland, 2006.
- 3. Anderson TJ, Nair S, Nkhoma S, Day NP, White NJ, Dondorp AM et al. High heritability of malaria parasite clearance rate indicates a genetic basis for artemisinin resistance in western Cambodia. J Infect Dis 2010; 201:1326–30. pmid:20350192
- 4. The Earth Institute at Columbia University. Centre for national health development in Ethiopia. Malaria treatment. Availalbe: http://cnhde.ei.columbia.edu/programs/malaria/treatment.html. Accessed on 22 May 2015.
- 5. World Health Organization. Global plan for artemisinin resistance containment (GPARC). Global Partnership to Roll Back Malaria & Geneva: WHO; 2011.
- 6. Update on artemisinin resistance—January 2014. Geneva: World Health Organization; 2014. Available: http://www.who.int/malaria/publications/atoz/update-artemisinin-resistance-jan2014/en/index.html. Accessed 22 May 2015.
- 7. Ringwald P, Barrette A, Fairhurst R, Dondorp A, Kachur P, MacArthur J, et al. Global report on antimalarial drug efficacy and drug resistance: 2000–2010. Geneva: World Health Organization, 2011.
- 8. Eshetu T, Abdo N, Bedru KH, Fekadu S, Wieser A, Pritsch M, et al. Open-label trial with artemether-lumefantrine against uncomplicated Plasmodium falciparum malaria three years after its broad introduction in Jimma Zone, Ethiopia.Malar J 2012;11(1):1.
- 9. Mulu A, Geresu B, Beyene Y, Ademe M. Efficacy of artemether-lumefantrine for the treatment of uncomplicated Plasmodium falciparum malaria in Northeast Ethiopia. Int J Basic Clin Pharmacol 2015;4(3):492–6.
- 10. Kefyalew T, Animut A, Tamene T, Jima D, Hailemariam A, Legesse M, et al. Efficacy of six-dose regimen of Artemether-Lumefantrine for the treatment of uncomplicated falciparum malaria, three years after its introduction into Ethiopia. Parasite 2009;16:129–34. pmid:19585891
- 11. World Health Organization. Guidelines for the Treatment of Malaria. 2nd edition; 2010. Available: http://www.who.int/malaria/publications/atoz/9789241547925/en/index.html.
- 12. International Artemisinin Study Group, Adjuik M, Babiker A, Garner P, Taylor W, White N et al. Artesunate combinations for treatment of malaria: meta–analysis. Lancet 2004, 363:9–17. pmid:14723987
- 13. Price RN, Nosten F, Luxemburger C, Paiphun L, Chongsuphajaisiddhi T, White NJ et al. Effects of artemisinin derivatives on malaria transmissibility. Lancet 1996, 347:1654–58. pmid:8642959
- 14. Makanga M, Falade CO, Bassat Q, Premji ZG, Krudsood S, Hunt P, et al. Efficacy and safety of artemether lumefantrine in the treatment of acute uncomplicated Plasmodium falciparum malaria: a pooled analysis. Am J Trop Med Hyg 2011;85:793–804. pmid:22049029
- 15. Kibwika PB, Lamorde M, Kizza HM, Merry C, Colebunders B, Geertruyden JPV et al. Update on the efficacy, effectiveness and safety of artemether–lumefantrine combination therapy for treatment of uncomplicated malaria. Therapeutics and Clin Risk Manag 2010;6:11–2.
- 16. Methods for surveillance of antimalarial drug efficacy. Geneva, World Health Organization, 2009. Availalbe: http://apps.who.int/malaria/docs/drugresistance/Protocol2009.pdf. Accessed 23 May 2015.
- 17. Metehara. The Wikipedia. Free encyclopedia. Available: https://en.wikipedia.org/wiki/Metehara. Accessed 16 December 2015.
- 18. Hwang J, Alemayehu BH, Hoos D, Malone JL, Kachur SP, Filler S, et al. In vivo efficacy of artemether-lumefantrine against uncomplicated Plasmodium falciparum malaria in Central Ethiopia. Malar J 2011;10(1):209.
- 19. Assefa A, Kassa M, Tadese G, Mohamed H, Animut A, Mengesha T, et al. Therapeutic efficacy of Artemether/ Lumefantrine (Coartem®) against Plasmodium falciparum in Kersa, South West Ethiopia. Parasit Vectors 2010;3:1. pmid:20051120
- 20. WHO. Basic Malaria Microscopy. Part 1. Learner’s guide. Geneva Switzerland: World Health Organization, 2010.
- 21. Cheesbrough M: District Laboratory practice in Tropical countries. 2nd edition. Cambridge: Cambridge University Press; 2005:24451.
- 22. Cavanagh DR, Elhassan IM, Roper C, Robinson VJ, Giha H, Holder AA et al. A Longitudinal Study of Type- Specific Antibody Responses to Plasmodium falciparum Merozoite Surface Protein-1 in an Area of Unstable Malaria in Sudan. J Immunol 1998;161(1):347–59. pmid:9647243
- 23. Zwetyenga J, Rogier C, Tall A, Fontenille D, Snounou G, Trape JF, et al. No influence of age on infection complexity and allelic distribution in Plasmodium falciparum infections in Ndiop, a Senegalese village with seasonal, mesoendemic malaria. Am J Trop Med Hyg 1998;59(5):726–35. pmid:9840589
- 24. President’s malaria initiative. Africa indoor residual spraying project. Ethiopia PMI country profile 2015. Available: http://www.africairs.net/where-we-work/ethiopia/. Accessed 28 Dec 2015.
- 25. President’s Malaria Initiative Ethiopia. Malaria Operational Plan FY 2015.
- 26. Bassat Q, González R, Machevo S, Nahum A, Lyimo J, Maiga H et al. Similar efficacy and safety of artemetherlumefantrine (CoartemW) in African infants and children with uncomplicated falciparum malaria across different body weight ranges. Malar J 2011, 10369.
- 27. Rozendaal J (eds). Fake antimalaria drugs in Cambodia. In: Lancet 2001, vol 1357, pp 890.
- 28. Noedl H, Se Y, Schaecher K, L. Smith B, Socheat D, M. Fukuda M. Evidence of artemisinin-resistant malaria in western Cambodia. N Engl J Med 2008;359:2629–2620. pmid:19064625
- 29. Kinfu G, Gebre-selassie S, Fikrie N. Therapeutic Efficacy of Artemether-Lumefantrine for the Treatment of Uncomplicated Plasmodium falciparum Malaria in Northern Ethiopia. Hindawi Publ Corp Malar Res Treat 2012;2012:1–6.
- 30. Fogg C, Bajunirwe F, Piola P, Biraro S, Checchi F, Kiguli J, et al. Adherence to a six-dose regimen of artemether-lumefantrine for treatment of uncomplicated plasmodium falciparum malaria in Uganda. Am J Trop Med Hyg 2004;71:525–30. pmid:15569777
- 31. Yeka A, Dorsey G, Kamya MR, Talisuna A, Lugemwa M, et al. Artemether-Lumefantrine versus Dihydroartemisinin-Piperaquine for Treating Uncomplicated Malaria: A Randomized Trial to Guide Policy in Uganda. PLoS One 2008;3(6):e2390. pmid:18545692
- 32. Mannan A.B, Patel K, Malhotra I, Ravindran B, Sharma S. How specific is the immune response to malaria in adults living in endemic areas? J Vect Borne Dis 2003;40:84–91.
- 33. Ezzet F, Mull R, Karbwang J. Population pharmacokinetics and therapeutic response of CGP 56697(artemether +benflumetol) in malaria patients. Br J Clin Pharmacol 1998;46:553–61. pmid:9862244
- 34. Valecha N, Srivastava P, Mohanty S.S, Mittra P, Sharma K.S, Tyagi K.P, et al. Therapeutic efficacy of artemether-lumefantrine in uncomplicated falciparum malaria in India. Malar J 2009;8:107. pmid:19454000
- 35. Targett G, Drakeley C, Jawara M, von Seidlein L, Coleman R, Deen J, et al. Artesunate reduces but does not prevent post treatment transmission of Plasmodium falciparum to Anopheles gambiae. J Infect Dis 2001;183:1254–9. pmid:11262208
- 36. Sim F, Mackie P. Artemisinin combination therapies. Lancet 2006;367:2037–9. pmid:16798368
- 37. Ashley EA, Stepniewska K, Lindegårdh N. Pharmacokinetic study of artemether /lumefantrine given once daily for the treatment of uncomplicated multidrug-resistant falciparum malaria. Trop Med Int Heal 2007 Feb, 12(2):201–8.
- 38. Olaleye O. B, Williams A. L, D’Alessandro U, Weber M. M, Mulholland K, Okorie C, et al. Clinical predictors of malaria in Gambian children with fever or a history of fever. T Roy SocTrop Med H 92(3):300–4.
- 39. Marsh K, Kinyanjui S. Immune effector mechanisms in malaria. Parasite Immunol 2006;28(1–2):51–60. pmid:16438676
- 40. Krishna S, Uhlemann AC, Haynes RK. Artemisinins: mechanisms of action and potential for resistance. Drug Resist Updat 2004;7:233–44. pmid:15533761