A combination of artesunate (AS) plus sulphadoxine/pyrimethamine (SP) as first-line and artemether-lumefantrine (AL) as second-line treatment are currently recommended against uncomplicated P. falciparum infection in Sudan. However, there is limited information on the efficacy of ACTs in the country and only one report of PCR-corrected results for AS/SP only.
Methods
The WHO protocol for the assessment of antimalarial drug efficacy for the treatment of uncomplicated falciparum malaria was employed. Artesunate plus sulphadoxine/pyrimethamine (AS/SP) was compared to artemether-lumefantrine (AL) in a 28-day follow up. Samples that were classified as early treatment failure (ETF), late treatment failure (LCF) or late parasitological failure (LPF) were genotyped for msp-1 and msp-2 genes to differentiate recrudescence from reinfection.
Results
A total of 178 patients were screened and 160 met the enrolment criteria and were recruited to the study of which 157 (98.1%) completed the follow up and had an analysed treatment outcome. On the AS/SP arm, three (0.038%) patients were lost during the follow-up, two on day 1 and one on day 7, and 77 (96.3) completed the study, while all 80 (100%) patients completed the follow up in the AL arm. In the per protocol analysis for AS/SP the treatment outcome for patients who completed the follow-up were as follows: adequate clinical and parasitological response (ACPR); 84.4% ETF; 1.3%, LCF; 3.9%, (LPF); 10.4%. For the AL arm the out come was as follows, ACPR; 90%, ETF; 0%, LCF; 6.3% and LPF; 3.8%. However, when PCR-corrected, 6.5% (5/77) of patients treated with AS/SP maintained parasites from their primary infection, while (7/80) in the AL group maintained their initial parasite genotype. Therefore, PCR-corrected efficacy was 93.5% in the AS/SP treated group and for AL it was 91.3%.
Conclusion
Both AS/SP and AL are highly effective for the treatment of uncomplicated falciparum malaria in eastern Sudan. However, AS/SP appears to have a slightly higher efficacy than AL, this may be due to patient compliance with the repeated dose rather than drug efficacy.
The online version of this article (doi:10.1186/1475-2875-6-92) contains supplementary material, which is available to authorized users.
Authors' contributions
EM carried out the sample collection, molecular analysis, data entry and contributed to drafting the manuscript, NG conceived of the study, contributed to its design, sample collection, data analyses and drafted the manuscript, SE contributed to the sample collection, microscopy and molecular analysis. IM and FM contributed to the sample collection and molecular analysis. AB participated in study design, data management and analyses. BE conceived of the study, participated in its design, analyses and helped to draft the manuscript. All authors read and approved the final manuscript.
Background
Malaria remains one of the major public health problems in Africa. It is estimated that 7.5 to 10 million cases of malaria occur in Sudan every year [1]. Control mainly depends on treating symptomatic cases with available chemotherapeutics. The WHO recommends artemisinin- based combination therapies (ACT) for treatment of uncomplicated malaria. Due to decreased sensitivity of Plasmodium falciparum to chloroquine [2] and sulphadoxine/pyrimethamine (SP) [3, 4], the National Malaria Control Programme (NMCP) of Sudan has recently adopted ACT for treatment of uncomplicated malaria [5]. Artemisinins are known to have a marked effect on reducing parasitaemia even when multi-drug resistant parasites are present. However, their short half-life warrants that a second drug with long half-life is administered concurrently.
The current treatment protocol for uncomplicated falciparum malaria in Sudan is artesunate plus sulphadoxine/pyrimethamine, as first-line and artemether-lumefantrine as second-line of treatment [5]. There have been few studies on the efficacy of AS/SP [6‐9] and only one published report on the efficacy of AL in Sudan [8]. Although these studies have reported high efficacy to both combinations, ranging from 99.8% to 100%, they did not show whether the small proportion of treatment failures was due to a recrudescence of existing parasites or acquisition of a new infection, except for one recent study which reported the PCR-corrected efficacy of AS/SP [9]. It was, therefore, decided to closely monitor patients for 28 days after treatment with AS/SP or AL, and the results were genotyped to indicate recrudescence versus new infections.
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Methods
Sample size
A trial with 80 subjects in each arm would have at least 80% power (using a significance level of 0.10) to detect a difference between the two combinations if the failure rate detected after treatment is 20% in the AS/SP arm (based on the reported failure of SP of approximately 15 – 20% in Sudan) and 5% in AL arm, allowing for 10% loss to follow-up.
Study population and field survey
The study was carried out in three villages in eastern Sudan, southwest of Gedarif town (Abunaja Juama, Abunaja Bargo and Asar). A community-based survey was conducted during the transmission seasons (October to December) of 2004 and 2005 to identify symptomatic patients that were microscopically diagnosed with mono infection of P. falciparum. Patients that satisfied the enrolment criteria according to the WHO protocol for the assessment and monitoring of antimalarial drug efficacy for the treatment of uncomplicated falciparum malaria [10] were recruited after they provided written informed consent to participate. However, due to the low endemicity of malaria in this area all age groups were recruited. Patients were randomly allocated to receive either AS/SP or AL by a simple random technique of a hat draw. Pregnant women were not enrolled as per the national protocol for uncomplicated malaria recommendations.
Sample collection
Finger prick blood samples were collected and thick and thin smears were prepared on a patient's first attendance. When the patient was enrolled to the study, a finger prick sample was collected on days 0, 1, 2, 3, 7, 14, 21, and 28 on a glass slide and a parallel drop of blood was collected on filter paper. The filter paper was air-dried and stored in self-sealing plastic bags for molecular analysis.
Microscopic diagnosis
Thick and thin blood smears were stained with Giemsas' stain for ten minutes. The slides were read by two independent experienced microscopists. Parasite count was performed by counting asexual parasites against 200 white blood cells (WBC), and parasite density calculated assuming an average of 6,000 WBC in the population. Ten percent of the slides were read by a third microscopist in Khartoum for quality control. In case of disagreement the majority result was taken.
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Treatment and follow up schedule
Each patient was allocated randomly to either AS/SP or AL, treatment was administered under supervision for the AS/SP group, while only one dose of the AL was supervised and the second dose was given to the patient for self-administration. Patients were asked to return to the clinic on days 1, 2, 3, 7, 14, 21, and 28 or whenever they did not feel well. When a patient failed to come to the clinic on any scheduled day, a member of the team visited the home, gave them the dose and obtained the sample unless the patient was not found or refused to give the sample. Those who refused to give their sample (withdrawn) or missed more than one day of follow-up were excluded from the analysis.
Patients, who were positive by microscopy and refused to participate in the study or did not meet the enrolment criteria, were provided with AS/SP for self-administration whereas pregnant women were referred to Gedarif Teaching Hospital as recommended by the national protocol.
In vivo analysis
A per protocol analysis was performed employing the WHO excel sheet [11].
Samples that were positive by microscopy on any of the follow-up days were classified as early treatment failure (ETF), late parasitological failure (LPF), or late clinical failure (LCF). Adequate clinical and parasitological response (ACPR) was defined as complete absence of microscopically detectable parasitaemia during the follow-up period, according to the protocol [10].
Molecular analysis
Samples that were classified as ETF, LCF or LPF were genotyped by PCR as previously described for msp-1 [12] and msp-2 [13, 14] on day 0, 1, 2, 3 and failure (day 7 to 28) to differentiate recrudescence from reinfection. Unpublished observations indicate the necessity of day 0 to day 3 sampling to accurately identify recrudescence from re-infection.
Ethical considerations
The study was reviewed and ethical clearance was obtained from the National Ethical Committee, Federal Ministry of Health, Sudan. Individual written informed consent was obtained from all participants or their legal guardians.
Results
In vivo outcome
178 patients were screened and 160 patients were enrolled and 157 completed the follow-up and had an analysable outcome. Of these, 77 patients were in the AS/SP arm and 80 were in the AL arm. Table 1 shows the description of the study population that successfully completed the follow-up.
Table 1
Description of study population receiving AS/SP or AL treatment
Drug
AS/SP
AL
Age_years
Mean (95% CI)
17.88 (14.48 – 21.28)
18.45 (14.84 – 22.06)
Temperature Day 0
Mean (95% CI)
37.46 (37.46 – 37.70)
37.59 (37.35 – 37.83)
Sex
Female n (%)
39 (48.8)
47(58.8)
Male n (%)
41 (51.2)
33(41.2)
A total of 77 patients completed the follow-up on the AS/SP group and 84.4% had an adequate clinical and parasitological response (ACPR). Of the 80 patients that received AL and completed the follow-up, 90% had successfully cleared their parasitaemia by day 28. Table 2 summarizes the outcome of treatments in each group.
Table 2
In vivo outcome of AS/SP and AL
Prevalence n (%)
AS/SP
AL
ETF
1 (1.3)
0 (0)
LCF
3 (3.9)
5 (6.3)
LPF
8 (10.4)
3 (3.8)
ACPR
65 (84.4)
72 (90)
Total analysed
77 (96.3)
80 (100)
WITH
3 (3.7)
0 (0)
TOTAL
80
80
ETF; early treatment failure; LCF: late clinical failure; LPF: late parasitological failure; ACPR: adequate clinical and parasitological response; WITH: withdrawal; as analysed by the WHO worksheet.
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Genotyping
Of the 157 patients diagnosed with P. falciparum on day 0 and who completed the follow up twenty patients had microscopically detectable parasitaemia on at least one day of the follow-up. Of these twelve received AS/SP and the remaining eight received AL. These samples were genotyped for msp-1 and msp-2 genes.
In the AS/SP group, five patients (41.7 %) showed different allelic forms and were classified as reinfection, while seven (58.3) retained the same allelic pattern and were classified as recrudescence of parasites. Only one (1.25%) patient showed a different genotype in the AL group and the remaining 7 (87.5%) retained their initial parasite genotype. Hence, PCR-corrected efficacy was 93.5% and 91.3% for AS/SP and AL, respectively.
Discussion
Artemisinin derivatives are highly effective antimalarial compounds against different stages of Plasmodium development [15]. In order to prolong the efficacy of these drugs, it is recommended that they should only be used in combination with another effective drug that has a longer half-life. This current consensus of antimalarial therapy has led to the adoption of ACT in Sudan where chloroquine (CQ) has reached high levels of treatment failure [2, 3, 16].
In Sudan, the current recommendation for uncomplicated malaria are AS/SP and AL as first and second-line treatment, respectively [5] with 100% efficacy in Damazin, Kosti, Malakal and New Halfa [6‐9, 17] and 99.3% in Kassala [7].
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In the present study, PCR-corrected results showed efficacy of AS/SP to be 93.5% in the Gedarif area. Although this is lower than the reports mentioned above, it is not surprising. Samples analysed in the present study were collected in 2004 and 2005, a time coinciding with increased use of SP mono-therapy due to the failure of CQ, which may have lead to increased levels of resistance to this drug. Although there is no recent report of SP clinical efficacy in our study area, alleles associated with SP failure have been reported to be increasing gradually. Triple mutants on dhfr-108Asn, dhfr-59 and dhps-540Leu have rapidly increased in this area between 1993 to 1999 [18]. Data from this area shows that these alleles have reached higher levels in 2003 and 2004 just before the implementation of ACTs [19].
The partial failure of AL (8.9%) may be explained by inabsorption of lumefantrine due to low fat diet a situation that may be common in rural areas. In addition, recrudescence of AL-treated individuals has been reported in studies from other parts of the world [20‐22].
The present study has provided detailed PCR-corrected results of AS/SP and AL efficacy in eastern Sudan. Although the results may seem in disagreement with others, this is mainly due to the different transmission intensities in Sudan. In irrigated areas where there is perennial transmission such as Damazin, New Halfa, Malakal and Kosti (Figure 1) there is a higher chance of recombination within the parasite population. However, in areas of low seasonal transmission such as the Gedarif area, recombination may be much lower leading to the lower multiplicity of infection (MOI). This may have led to underestimation of reinfection in our study. In addition parasite tolerance to the lumefantrine component persisting at a low levels than required to kill parasites that have caused new infection may also contribute to high levels of failure [23].
Figure 1
Map of Sudan. Red circles indicate the town locations reported in previous studies (Ed Damazin, Kosti, Kassala and Malakal) compared to this study (Gedaref). Other areas except Kassala are on the Nile River bank and have irrigated agricultural activities.
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Conclusion
Artemisinin-based combination therapies are considered to be highly effective antimalarials available in endemic countries. Artemisinin is highly effective in eliminating parasitaemia, however the partner drug is an important component in prolonging the usefulness of this combination. The results shown here call for continuous monitoring of the efficacy of ACT in eastern Sudan.
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Acknowledgements
We are grateful to Novartis Scientific office in Khartoum, Amipharma Drug Laboratories and the National Malaria Control Programme for provision of drugs. We are indebted to the study population for their continuous cooperation. We thank the field team in Gedarif and our colleagues at TMRI for their assistance during this work. The study was funded by the National Centre for Research, Khartoum, Sudan. N.G. holds a research training grant from WHO/TDR.
Open Access
This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License (
https://creativecommons.org/licenses/by/2.0
), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Authors' contributions
EM carried out the sample collection, molecular analysis, data entry and contributed to drafting the manuscript, NG conceived of the study, contributed to its design, sample collection, data analyses and drafted the manuscript, SE contributed to the sample collection, microscopy and molecular analysis. IM and FM contributed to the sample collection and molecular analysis. AB participated in study design, data management and analyses. BE conceived of the study, participated in its design, analyses and helped to draft the manuscript. All authors read and approved the final manuscript.
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