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PLoS One. 2012; 7(9): e45867.
Published online 2012 September 21. doi:  10.1371/journal.pone.0045867
PMCID: PMC3448694

Systematic Review and Meta-Analysis of Artemisinin Based Therapies for the Treatment and Prevention of Schistosomiasis

Jennifer Keiser, Editor



Chemotherapy based on repeated doses of praziquantel is still the most effective control strategy against Schistosomiasis, however artemisinin derivatives emerged as a family of compounds with schistomicide activity. The aim of the present work is to compare the efficacy of artemisinin-based therapies in the treatment and prophylaxis of human schistosomiasis. The design of this work involved a quantitative systematic review and meta-analysis.

Methodology/Principal Findings

Retrieval of published studies was carried out through an electronic search of the PubMed (MEDLINE), EMBASE, Cochrane Library and CINAHL databases. This included reports comparing the therapeutic efficacy of artesunate alone, artesunate plus sulfadoxine-pyrimethamine and a combination of artemisinin derivatives plus praziquantel against praziquantel alone on different types of schistosomiasis. Moreover, studies on artesunate and artemether used as preventive drugs were also analyzed against placebo. The primary outcome measure for schistosomiasis treatment was “parasitological cure”, whereas for the prophylaxis the outcome evaluated was “infection rate”. Our results show that patients treated with artesunate alone have significantly lower cure rates than those treated with praziquantel (OR = 0.27 (95% C.I. 0.13–0.53; p<0.001)) and that the combined therapy of artesunate plus sulfadoxine-pyrimethamine is also significantly less effective than praziquantel treatment (OR = 0.14 (95% C.I. 0.02–0.92; p = 0.04)). However, the combination of an artemisinin derivatives plus praziquantel showed a higher cure rate than praziquantel monotherapy with OR = 2.07 (95% C.I. 1.27–3.36; p = 0.003). Finally, chemoprophylaxis with either artesunate (RR = 0.11 (95% C.I. 0.06–0.22; p<0.001)) or artemether (RR = 0.25 (95% C.I. 0.16–0.40; p<0.001)) was significantly better than a placebo in both cases.


This meta-analysis confirms that artemisinin derivatives used in combination with praziquantel have the potential to increase the cure rates in schistosomiasis treatment, but not artesunate alone. It is also confirmed that repeated doses of artemisinin derivatives play a prophylactic role, significantly reducing the incidence of Schistosoma japonicum infections compared with placebo.


Schistosomiasis continues to be one of the most prevalent parasitic diseases. An estimated 779 million people - more than 10% of the world’s population - were at risk of schistosomiasis in mid-2003 and approximately 207 million people were infected [1]. The causative agent of schistosomiasis is a trematode worm of the genus Schistosoma. Three main species parasitize humans: S. haematobium, S. japonicum, and S. mansoni. Additionally, S. intercalatum arises in some parts of Central Africa and S. mekongi as well as S. malayensis occur in Southeast Asia [2][4]. An alarming 201.5 million cases of schistosome infections (mainly by S. haematobium and S. mansoni) have been estimated to occur in Africa, accounting for more than 97% of the estimated number of infections worldwide [5]. The highest prevalence of this illness is usually found in school-age children and adolescents, where it represents the main cause of iron deficiency anaemia [6]. The World Health Organization (WHO) reports the effect of schistosomiasis on world health as the loss of 1.7 and 4.5 million disability-adjusted life years [7], [8]. However, a recent systematic review has shown that schistosomiasis-related disability is underestimated [9]. The treatment of this chronic and debilitating disease relies on the use of praziquantel, a broad-spectrum schistosomicide drug that combines safety and low price [10]. Praziquantel is active against the adult stages of schistosomes. Thus, the main limitation to the use of praziquantel is the lack of therapeutic efficacy against early-stage schistosomiasis which could be the main reason for the many treatment failures observed and high rates of re-infection [11], [12]. Moreover, current control programmes against schistosomiasis depend on the wide-scale use of praziquantel. Consequently, this drug pressure could favor the emergence of praziquantel-resistant parasites [11]. Thus, it is not appropriate to rely on a single drug regimen for the control of schistosomiasis.

The antischistosomal activity of the artemisinin derivatives was discovered in the early 1980’s leading this family of compounds to become used as broad-spectrum antischistosomal drugs [13]. Artemisinin derivatives act against the developmental stages of the parasite and are therefore complementary to praziquantel activity [14]. The incorporation of artemisinin derivatives into schistosomiasis treatment in combination with praziquantel may therefore represent a good strategy. However, several reviews have suggested that artemisinin derivatives exert only a moderate degree of efficacy against schistosomiasis [7], [14], [15]. Meanwhile, artemisinin derivatives have been used in successfully combination with other compounds for the treatment of malaria, reducing the probability of selecting drug-resistant parasites [16], [17]. Moreover, synthetic artemisins (e.g. trioxolanes) are also active against juvenile and adult schistosomes [18], but no schistosome-specific clinical trials with synthetic artemisinins have been undertaken so far.

The aim of the present systematic review is to analyse the data available from clinical trials that compare the efficacy of artemisinin derivatives for the treatment and prophylaxis of schistosomiasis. We hope to provide clinicians and policy-makers with a convenient and evidence-based summary of the primary literature on which to base their decisions.



We carried out a systematic search of published studies of clinical trials that compare anti-helminthic therapies and chemoprophylaxis based on artemisinin derivatives against schistosomiasis, with no date or language restrictions. We used PubMed (MEDLINE), EMBASE, the Cochrane Library and CINAHL, up to July 2012. We incorporated the following search terms: “schistosomiasis”, “praziquantel”, “artesunate”, “artemether” and “artemisinin derivatives”. A customized form was used to record the name of the authors and journal, the year of publication, the location of the trial, the intensity of infection, the study design, the inclusion criteria, dosage, population characteristics, and outcomes.

Inclusion Criteria and Outcomes

Published reports evaluating artemisinin derivatives in schistosomiasis treatment were included if they fulfilled all of the following selection criteria according to PRISMA guidelines [19]. (1) Population: Patients infected with S. haematobium, S mansoni and S. japonicum diagnosed through Kato-Katz thick smears (S. mansoni and S. japonicum) or filtration of 10 ml of urine (S. haematobium). S. intercalatum, S. mekongi and S. malayensis were not considered since there were no clinical trials focused in these species. (2) Study design and interventions: We included randomized trials comparing the efficacy of artemisinin-based therapies against praziquantel alone, the reference treatment option for all types of schistosomiasis. (3) Types of outcomes measures: As the main outcome, we considered “parasitological cure”, defined as the absence of eggs over a short period of time (3 to 8 weeks after treatment). Furthermore, adverse events were defined as secondary outcome to be considered in the systematic review.

To evaluate schistosomiasis chemoprophylaxis based on artemisinin derivatives, we included articles if they fulfilled all of the following selection criteria. (1) Population: healthy villagers that lived in endemic areas of schistosomiaisis. (2) Study design and interventions: we included randomized clinical trials, comparing the prophylactic effect of artesunate or artemether vs. placebo against S. haematobium, S. mansoni and S. japonicum infections. The preventive effect of the artemisinin derivatives was assessed by Kato-Katz thick smears or by the filtration of 10 mL of urine for S. japonicum and S. haematobium, respectively. (3) Types of outcomes measures: the main outcome was measured in terms of “infection rate”, defined as number of patients infected with Schistosoma spp. against total number of patients included in any branch of the study, over a short period of time (3 to 4 weeks after treatment). Adverse events were also defined as secondary outcome measure.

Data Extraction and Synthesis

Two authors (L.P.V. and J.L.A.) independently extracted the data using a data extraction sheet designed by authors. Extraction sheets for each study were crosschecked for consistency, and any discrepancies resolved by discussion. Disagreements between reviewers were resolved by consensus or input from a third author (A.M.).

Quality Assesment within Individual Studies

We performed an evaluation of the risk of bias for each publication based on four elements of study design and reporting: (1) a description of randomization method and masking of patient and practitioner; (2) a description of allocation sequence generation; (3) reported allocation concealment, masking of participants, study personnel and outcome assessors; (4) reported avoidance of incomplete outcome data (dropouts/withdrawals). A score of 4 was considered high quality, 2–3 moderate quality, 0–1 poor quality according to a modified Jadad score [20]. We also evaluated any additional information related with inclusion and exclusion criteria like sample size calculation, baseline comparability of age, gender and relevant clinical characteristics (follow up and diagnoses).

Quantitative Data Synthesis

To compare efficacy of schistosomiasis treatments, the outcome measure was expressed as the odds ratio (OR) between the alternative treatment and the control, together with its 95% confidence interval (95% C.I.). Regarding studies that have evaluated the chemoprophylaxis activity of artemisinin derivatives in schistosomiasis, we used “infection rate”, instead of “cure rate”, and the data were referred to relative risk (RR) instead of OR since the RR index is more informative in terms of prevention studies. All p-values reported for OR and RR were calculated using a Z-test for the null hypothesis (i.e. OR = 1 and RR = 1) [21].

To assess the heterogeneity between studies a Cochran’s Chi-square test (Q-test) was made under the null hypothesis of homogeneity (significant heterogeneity if p<0.05). Additionally, the I2 statistic was calculated and values greater than 50% were considered as high heterogeneity. The fixed-effect model, using the inverse variance method, was used where there was no evidence of heterogeneity and a common effect size could be assumed. However, the random-effects model was chosen when heterogeneity was detected and the true effect size varied between studies. To estimate the between studies variance (tau squared) the DerSimonian and Laird approach was used [22].

When several groups (species of parasites) were included in a comparison, a subgroup analysis was performed. In the fixed-effect case, a fixed-effect model was used within subgroups and a fixed-effect summary was also calculated ignoring subgroups memebership. In the random-effects model, a meta-analysis was performed over to combine studies within each subgroup using separate estimates of tau-squared. Then the mean effects of subgroups were compared by the Q test to analyse if the difference was significant. Finnally, a global combined effect across subgroups was calculated by a separate random-effect meta-analysis including all the studies and ignoring subgroups membership since this option may be the more logical [21].

To assess the presence of publication bias, a funnel plot of effect size against standard error was analysed for each meta-analysis. Complementary to the funnel plot, the Egger’s regression asymmetry test was performed to quantify significance of publication bias [23]. All the above statistical analyses and graphs were performed with meta R-package [24].


Study Selection

Reports from 261 published articles were screened for evidence of clinical trials that evaluated the efficacy of artemisinin derivatives in schistosomiasis treatment or prophylaxis. Of them, 50 articles were selected for more detailed evaluation and finally twenty-four published articles were included in the meta-analysis. Some published reports included in the meta-analysis are multicenter or evaluted the intervention with separate doses and protocols of treatment and they were included as different studies. A study is therefore considered as the main unit of the meta-analysis (see tables 1,,22,,33,,4);4); The study selection process is outlined in Figure 1. When different endpoints were assessed in the same subjects we only considered the value reported for the first period of time of the follow up, since the other endpoints using the same subjects were not truly independent trials and data from a trial can only appear once in a specific analysis. Details of the included studies focused on the treatment and prophylaxis of schistosomiasis are given in table S1 and table S2, respectively. In addition, table S3 shows the 27 checklist items pertain to the content of a systematic review and meta-analysis according to PRISMA guidelines [19].

Table 1
Artesunate monotherapy vs. praziquantel in schistosomiasis treatment.
Table 2
Artemisinin derivatives + praziquantel vs. praziquantel in the treatment of schistosomiasis.
Table 3
Artesunate + sulfadoxine-pyrimethamine vs. praziquantel in the treatment of schistosomiasis.
Table 4
Artesunate prophylaxis trials focused on Schistosoma japonicum infections in endemic areas of China.
Figure 1
Flow diagram showing the selection process of studies included in the meta-analysis.

Characteristics and Methodological Quality

Regarding schistosomiasis treatment using artemisinin based therapies, we defined three units of analysis: (1) artesunate in monotherapy vs. praziquantel (seven trials described in six published studies); (2) artemisinin derivative plus praziquantel vs. praziquantel alone (five trials described in four published studies); (3) artesunate plus sulfadoxine-pyrimethamine vs. praziquantel (three published studies). All published studies were performed in Africa [25][30], except one study focused on S. japonicum, which was performed in China [31]. There were no studies that examined the efficacy of artemisinin derivatives in the American continent. The pediatric population was the target of trials focused on S. haematobium, whereas the studies on S. mansoni and S. japonicum focused on adult populations. In all studies both sexes were enrolled and patients were followed up over a short period of time (4 to 24 weeks). The studies on schistosomiasis treatment varied in sample size from 83 to 800 participants. In general, the quality of the reporting and design of the clinical trials that evaluated the artemisinin derivatives in the treatment of schistosomiasis was medium (see supplementary table S1). One study was an open labelled exploratory trial [28] and five were randomized controlled clinical trials with an adequate generation of allocation sequence [25], [30][33]. The majority of studies provide a sample size framework and a scientific rationale for the sample size determination. The remaining four studies were scored as having a high risk of bias mainly because of inadequate methods to generate the sequence of randomization (alternation), lack of allocation concealment, and/or incomplete outcome data.

Respecting artemisinin derivatives in the prophylaxis of schistosomiasis, we performed the meta-analysis in two main units according to the artemisinin derivative used: (1) artesunate vs. placebo and (2) artemether vs. placebo. The chemoprophylaxis doses for artesunate and artemether were 6 mg/kg at 1 or 2 week intervals for up to 13 doses during the high transmision period (two to six months). In both cases, all patients enrolled in the trials were initially treated with praziquantel prior to random assignment. In all trials, the infection rate was the outcome measure, and the RR, including 95% C.I. was estimated. Tables 4 and and55 summarize the key features of the prophylactic effect of artesunate and artemether, respectively. With regard to artesunate, a group of 5 published reports (including 13 different studies) were suitable for the meta-analysis. These studies were performed in different endemic areas of schistosomiasis in China investigated the efficacy of artesunate as a chemoprophylactic agent against S. japonicum infections [34][38]. These reports were published in Chinese language with abstracts and tables in English but some translation was required. The design of these studies were randomized double blind. Some of them were multicenter including different doses and intervals of treatment [35], [37], [38]. The retrieved studies that included artesunate as chemoprophylactic drug in schistosomiasis japonica reported insufficient information (see supplementary table S2). In fact, the quality score range from 0 to 2. Furthermore, it was identified two additional studies Li et al. 1996 [39] and Tian et al. 2001 [40] but access to the full publicactions were not possible and they were excluded from the meta-analysis. No published reports evaluated artesunate prophylaxis for S. mansoni and S. haematobium infections. In respect of artemether, 10 articles (including 12 different studies) were considered eligible for the meta-analysis. Seven of those articles were dealing with S. japonicum and were published in Chinese language [41][47] and the other 3 articles focused on S. japonicum, S. haematobium and S. mansoni were published in English language [48][50]. Seven articles of the above studies were carried out between 1996 and 2006 in Jiangxi, Anhui, Hunan, and Yunnan provinces of China including individuals aged between 5 and 60 years who were in frequent contact with infested water [41][44], [46][48]. One additional report was conducted among flood-relief workers aged between 18–40 in Jiangxi province [45]. Finally, 2 further reports focused on S. haematobium and S. mansoni infections were developed in Africa [49], [50]. With regard to the quality of the artemether reports, the score values range from 1 to 3 (table S2). Thus, the quality of studies was higher than those retrieved studies focused on artesunate prophylaxis.

Table 5
Artemether prophylaxis vs. placebo in schistosomiasis due to S. haematobium, S. mansoni and S. japonicum.


Artesunate in monotherapy vs. praziquantel

A total of 7 studies (n = 800) included in six published reports [25][30] compared the efficacy of artesunate alone vs. praziquantel alone in sub-Saharan Africa. Four studies performed on populations of schoolchildren evaluated artesunate alone in S. haematobium infections, and two additional studies on adult populations assessed the efficacy of oral artesunate for the treatment of S. mansoni. Regarding to the doses of artesunate used, it must be noted that five reports used artesunate 4 mg/kg daily for three consecutive days; one additional report used eight tablets of artesunate 50 mg over five days; (i.e. 3,2,1,1,1). All these details were described in table 1. None of the studies evaluated the efficacy of artesunate on S. japonicum infection. There was significant heterogeneity in the effect size among all the studies (Q = 24.8 (p<0.001), I2 = 75.8% (>50%)). We therefore performed a subgroup random-effects meta-analysis (Figure 2). The results revealed that patients treated with artesunate alone had a significantly lower cure rate than those treated with praziquantel, both with S. haematobium, showing an OR = 0.28 (95% C.I. 0.11−0.71; p = 0.007), and with S. mansoni infections, giving an OR = 0.22 (95% C.I. 0.08−0.57; p = 0.002). Subgroup difference using the Q test was no significant (p = 0.69). Overall, the combined OR was 0.27 (95% C.I. 0.13−0.53; p<0.001), clearly showing that at least from the studies reviewed artesunate alone is significantly less effective than praziquantel treatment.

Figure 2
Forest plot of a random-effects subgroup meta-analysis comparing parasitological cure by artesunate as monotherapy vs. praziquantel.

Artemisinin derivative plus praziquantel vs. praziquantel alone

With respect to combination therapies, four published reports [25], [27], [29], [31] described five studies (n = 536) in which the effectiveness of artemisinin derivatives in combination with praziquantel was compared against praziquantel alone. This comparison included two studies involving S. haematobium and a single study with S. mansoni, all using artesunate as the drug. Furthermore, two additional studies for S. japonicum were incorporated in which artemether was used instead of artesunate. The different dosages used for combination therapies were described in table 2. No significant heterogeneity was identified among all of the studies (Q = 1.43 (p = 0.839), I2 = 0% (<50%)). According to that, a subgroup fixed-effect meta-analysis was performed (Figure 3). Patients treated with artesunate plus praziquantel in S. haematobium infections showed a significantly higher cure rate than patients treated with praziquantel alone, with an OR = 1.84 (95% C.I. 1.01−3.36; p = 0.047). In S. mansoni infections, patients treated with combined therapy using artesunate and praziquantel also showed higher cure rates than patients treated with praziquantel alone, with OR = 2.81 (95% C.I. 1.09−7.24; p = 0.03). Similar higher cure rates were found in S. japonicum infection trials, with an overall OR = 1.92 (95% C.I. 0.34−10.74; p = 0.457). Subgroups difference using the Q test was no significant (p = 0.76). The summary odds ratio, regardless of the helminth species in question, was found to be OR = 2.07 (95% C.I. 1.27−3.36; p = 0.004), significantly favoring the combined therapy against praziquantel alone.

Figure 3
Forest plot of fixed-effect subgroup meta-analysis comparing parasitological cure after treatment with an artemisinin derivative plus praziquantel vs. praziquantel.

Artesunate combined with sulfadoxine-pyrimethamine vs. praziquantel

Three published reports (n = 1085) performed in Mali, Kenya and Sudan compared standard antimalarial treatment consisting on artesunate combined with sulfadoxine-pyrimethamine against praziquatel alone for schistosomiasis treatment [32], [33], [51]. Two of these reports referred to treatment for S. mansoni and one to treatment for S. haematobium infections (table 3). All studies that evaluated this approach including children that were followed up until 4 weeks post-treatment. We detected significant heterogeneity in the size of the effect among all the studies (Q = 36.2 (p<0.001), I2 = 94% (>50%)). Therefore, subgroup random-effects meta-analysis was performed (Figure 4). The cure rate for S. haematobium in the combined therapy trial is statistically lower compared with praziquantel alone: OR = 0.69 (95% C.I. 0.52−0.92; p = 0.01). Similary, for S. mansoni infections the combined therapy had significantly lower cure rates than those of praziquantel showing an overall OR of 0.06 (95% C.I. 0.02−0.24; p<0.001). Subgroups difference using the Q test was significat (p<0.001), as expected, taking into account that one OR was 0.69 for S. haematobium against 0.06 value for S. mansoni. Nevertheless, it could be valuable to report a summary effect of all the studies. Thus, regardless of the schitosome species in question, an overall odds ratio significantly less than one was found: OR = 0.14 (95% C.I. 0.02−0.92; p = 0.04). Therefore, the results do not appear to be in favor of the assayed antimalarial therapy as compared with praziquantel in schistosomiasis treatment.

Figure 4
Forest plot of the random-effects subgroup meta-analysis comparing parasitological cure by artesunate plus sulfadoxine/pyrimethamine vs. praziquantel.

Artesunate vs. placebo for the prevention of schistosomiasis

A group of 5 published reports including 13 studies (n = 6367) were performed in different endemic areas of schistosomiasis in China investigating the efficacy of artesunate as a chemoprophylactic agent against S. japonicum infections [34][38]. Table 4 summarizes the key features, doses and outcomes of the studies included. We found significant heterogeneity among these studies (Q = 21.8 (p = 0.04), I2 = 45% (near 50%) and hence we used random-effects meta-analysis to estimate the prophylactic effect of artesunate (figure 5), which yielded a combined RR value of 0.11 (95% C.I. 0.06−0.22; p<0.001), pointing to a significant degree of schistosomiasis protection of artesunate in comparison with placebo.

Figure 5
Meta-analysis comparing artesunate vs. placebo for chemoprophylaxis against schistosomiasis japonica.

Artemether vs. placebo for the prevention of schistosomiasis

A group of 10 published reports described 13 studies (n = 8051) in which it was assessed the efficacy of artemether for the prevention of schistosomiasis. Eight reports focused on S. japonicum infections in China [41][48] and 2 additional articles focused on S. haematobium [49] and S. mansoni [50] infections in Côte dIvore. The key features, doses and outcomes of the included studies were described in table 5. We detected significant heterogeneity among all the studies (Q = 95.7 (p<0.001), I2 = 89% (>50%)). Therefore, subgroup random-effects meta-analysis was performed to estimate the prophylactic effect of artemether (Figure 6). In S. haematobium and S. mansoni infections, a decrease in risk was observed: RR = 0.75 (95% C.I. 0.62–0.92; p = 0.006) and RR = 0.50 (95% C.I. 0.35–0.75; p<0.001), respectively, although these decreases are in fact significant more studies should be carried out because only one study of each parasite species is not sufficient. In addition, with S. japonicum infections we also found a significant prophylactic effect of artemether, with a RR = 0.19 (95% C.I. 0.11–0.34, p<0.001). Subgroups difference for the three parasites was significant by Q test (p<0.001), probably because the RR for S. japonicum is substantially lower than the other ones. The overall combined RR, regardless of the parasite species in question, was RR = 0.25 (95% C.I. 0.16–0.40, p<0.001), which is significantly in favor of schistosomiasis prevention by artemether.

Figure 6
Subgroup meta-analysis comparing Artemether vs. placebo for chemoprophylaxis against schistosomiasis.

Adverse effects

Regarding to artemisinin derivatives treatment, data for adverse events possibly related to artesunate in monotherapy compared with praziquantel were described in the 6 included publications in the present meta-analysis [25][30]. Those trials were not designed to evaluate differences in adverse events but some information can be extracted. Thus, the adverse effects were similary distributed between artesunate and praziquantel treatment and the most frequently adverse reactions were the incidence of gastric pain, headache, nausea and vomiting. With respect to the therapy with artesunate plus praziquantel vs. praziquantel alone, all the studies described that both drugs in combination were well tolerated and the most studies enphasized that the number of adverse effects were similar in both treatment regimens [25], [27], [29], [31]. In addition, none of studies included in this comparison revealed any additional side-effects caused by possible interactions between praziquantel and artemisinin derivatives. Interestingly, the three studies that evaluate the schistosomiaisis treatment using the standard antimalarial combination of artesunate plus sulfadoxine pyrimethamine versus praziquantel reported a significant lower incidence of side effects for the combinated therapy compared with praziquantel treatment [32], [33], [51].

Regarding the use of artemisinin derivatives as chemoprophylactic drug, artemether and artesunate were both well tolerated and no severe adverse events were recorded in the studies included in the meta-analysis. Only a few participants reported mild abdominal pain, headache, dizznes or slight fever, as other previous reviews mentioned [14], [52]. In addition, no significant changes in routine blood and urine tests, ECG, hepatic and renal functions before and after artemisinin derivatives administration [37].

Publication bias analysis

We assayed the possibility of publication bias evaluating the asymmetry of funnel plots (figure 7) and using the Egger’s regression test. We did not detect the presence of bias in the two meta-analysis of schistosomiasis treatment comparing artemisinin derivatives vs. praziquantel (Figure 1A) and artemisinin derivatives plus praziquantel vs. praziquantel alone (Figure 1B). Studies in both funnel plots show a symmetrical aspect. These visual findings were confirmed with the Egger’s test, which reported values of −0.38 (p = 0.7) and 0.49 (p = 0.7), respectively. However, presence of publication bias was detected in trials included in the two meta-analysis on schistosomiasis prophylaxis, the one related to artesunate vs. placebo (Figure 1C) and that of artemether vs. placebo (figure 1D). Both funnel plots show evidence of bias, more notable in the analysis including artemether. These visual asymmetries are confirmed by the Egger’s test that gave values of −5.29 (p<0.001) and −5.14 (p<0.001), respectively. We did not perform any assessment of publication bias in the meta-analysis focused on artesunate plus sulfadoxine-pyrimethamine vs. praziquatel due to low number of studies included in that sub-unit of analysis.

Figure 7
Funnel plots of differents subunits of analysis representing effect size against standard error.


Schistosomiasis continues to be an important debilitating illness, in particular when associated with other potential causes of morbidity in tropical regions. Environmental changes, international travel and migratory populations increase the prevalence of schistosomiasis. The failure to develop an effective vaccine and the failure to eliminate snail populations mean that the control of schistosomiasis must rely on large-scale chemotherapy. The administration of praziquantel in a regimen of 40 mg/kg bodyweight in a single dose has been useful for controlling this disease in several countries such as Egypt, China, Brazil, the Philippines, Puerto Rico, Tunisia, Morocco, and Saudi Arabia [53]. However, rapid reinfection, incomplete cure rates, and evidence of praziquantel-tolerant schistosomes in the laboratory suggest a high risk of the development of praziquantel resistance [12].

Artemisinin derivatives currently offer the most important alternative for schistosomiasis treatment. They are effective against the juvenile stages of S. mansoni, S. haematobium and S. japonicum, but are less effective against adult worms. Our results demonstrate that artesunate in monotherapy does not offer an alternative for schistosomiasis treatment; none of the trials included in our meta-analysis seemed to significantly favor artesunate over praziquantel as monotherapy. Artesunate monotherapy may not be beneficial because its activity only affects the early stages of the parasite. In contrast, praziquantel acts against the mature forms of the parasite, curing 60 to 90 percent of patients. We measured efficacy of artemisinin derivatives at earliest after treatment in the context of continued disease transmission, in this sense some researchers have suggested that 3 weeks might be best [54]. However, more studies are needed to assess the effect of the evaluation period on the treatment outcome in those patients infected with schistosomiasis and treated with artemisinin derivatives.

Despite the incomplete efficacy of artemisinin derivatives alone in terms of cure rates, their pharmacological activities provide an excellent opportunity to combine with praziquantel. Our study confirms the Liu et al. [55] meta-analysis that support that artemisinin derivative plus praziquantel used in combination significantly increase the cure rates of schistosomiasis in comparison with praziquantel alone. The rationale for choosing combination treatments is to ensure rapid and reliable cures and to avoid the development of resistance to praziquantel. However, these estimated results cannot be regarded as definitive because they are based on diverse populations and the sample size of the trials included is small. Nevertheless, meta-analysis methodology may help to improve the power of small exploratory trials, including the broadest range of data (over multiple locations).

The adverse effects related with artemisinin derivatives were mild, artemether and artesunate were both well tolerated. Furthermore, studies that evaluated the antimalarial combination of artesunate plus sulfadoxine-pyrimethamine efficacy in schistosomiasis presented significant less adverse effects compared with praziquantel. Finally, no additional side-effects caused by possible interactions between praziquantel and artemisinin derivatives were detected across the studies. Taken together, these results indicate that the incorporation of artemisinin derivatives do not present any limitation related with the increase of adverse effects.

However, the incorporation of artemisinin derivatives in mass praziquantel administration has three important limitations: first, the cost-effectiveness implications; second, owing to the sub-optimal biopharmaceutical properties (very short half-life) of artemisinin derivatives repeated treatments are required [56], and third the use of artemisinin derivatives in mass administration could contribute to the emergence of artemisinin-resistant malaria [57]. Our meta-analysis shows that artesunate plus sulfadoxine-pyrimethamine does not offer a benefit over praziquantel-based therapy for S. mansoni and S. haematobium infections. Note that, to date no studies were carried out to evaluate changes on schistosomiasis endemicity as a function of the large-scale use of artemisinin based therapy in malaria control programmes.

Praziquantel is a poor choice for chemoprophylaxis because of its short half-life (1 to 1.5 hours) and because it cannot kill the schistosomula stage of the parasite [58]. However, a better option for schistosomiaisis prophylaxis could be the use of artemisinin derivatives because they are active against schistosomula stage [18]. In fact, our results have shown the prophylactic activity of artesunate and artemether. This is in accordance with some previous published reviews [13], [14], [52], [55] and a former meta-analysis performed by Wu et al. in 2003 [59]. Despite various levels of endemicity, different ecological settings and the diverse backgrounds of the participants, the prophylactic effect of artemisinin derivatives was demonstrated in each trial. It may be concluded that the prophylactic effect of artemisinin derivatives should be considered highly relevant in S. japonicum infection. Many clinical trials which focused on S. japonicum have shown that artesunate and artemether administered in multiple doses reduce the incidence of the infection to a significant extent, especially in those studies in which the target population was exposed to the infection at a specific moment because of flooding. However, the quality of the reports that evaluate the role of artemisinin derivatives as prophylatic drug was not optimal. In addition, we detected the presence of publication bias for artesunate and artemether prophylaxisis meta-analysis. Thus, the quantitative RR found might be affected in some extension by publication bias. New schistosomiasis trials focused on the prophylactic effect of artemisinin derivatives should be conducted paying attention to quality issues. In this sense, a previous report described the methodological limitations linked to clinical trials focused on schistosomiasis [60]. Finally, the meta-analysis of artemisinin derivatives focused on chemoprophylactic activity against schistosomiasis has also two key limitations: first, the difficult access to some trials published in Chinese language and second the lack of studies reporting efficacy of artemisinin derivatives as chemoprophylactic drug in S. mansoni and S. haematobium infections.

In sum, the combination of artemisinin derivatives with praziquantel seems to be the best option for the treatment of schistosomiasis, reflecting their complementary pharmacological profiles against this disease. In addition, the auxiliary benefit of artemisinin combination treatment administered to malaria patients should be evaluated in schistosome endemic areas. We also confirm the prophylactic effect of artemisinin derivatives across the different trials performed in China. Finally, we hope to provide clinicians and policy-makers with a convenient and evidence-based summary of the primary literature on which to base their decisions.

Supporting Information

Table S1

Summary characteristics and quality assessment of the published studies focused on schistosomiasis treatment.


Table S2

Summary characteristics and quality assessment of the published studies focused on schistosomiasis prophylaxis.


Table S3

PRISMA Checklist.



The authors thank the Library staff of the University of Salamanca, in particular Mrs. Elena Martin-Rodero for her assistance in retrieving the articles. Finally, we gratefully acknowledge Dr. Jesús Pérez-Losada and Dr. Bernardo Foth for reviewing the manuscript.

Funding Statement

This work was supported by the Fundación Ramón Areces (2010–13) and Junta de Castilla y León (Orden EDU/330/2008). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.


1. Steinmann P, Keiser J, Bos R, Tanner M, Utzinger J (2006) Schistosomiasis and water resources development: systematic review, meta-analysis, and estimates of people at risk. Lancet Infect Dis 6: 411–425 [PubMed]
2. Tchuem Tchuente LA, Southgate VR, Jourdane J, Webster BL, Vercruysse J (2003) Schistosoma intercalatum: an endangered species in Cameroon? Trends Parasitol 19: 389–393 [PubMed]
3. Muth S, Sayasone S, Odermatt-Biays S, Phompida S, Duong S, et al. (2010) Schistosoma mekongi in Cambodia and Lao People’s Democratic Republic. Adv Parasitol 72: 179–203 [PubMed]
4. Greer GJ, Ow-Yang CK, Yong HS (1988) Schistosoma malayensis n. sp.: a Schistosoma japonicum-complex schistosome from Peninsular Malaysia. J Parasitol 74: 471–480 [PubMed]
5. Utzinger J, Raso G, Brooker S, De Savigny D, Tanner M, et al. (2009) Schistosomiasis and neglected tropical diseases: towards integrated and sustainable control and a word of caution. Parasitology 136: 1859–1874 [PMC free article] [PubMed]
6. Guyatt HL, Brooker S, Kihamia CM, Hall A, Bundy DA (2001) Evaluation of efficacy of school-based anthelmintic treatments against anaemia in children in the United Republic of Tanzania. Bull World Health Organ 79: 695–703 [PubMed]
7. Danso-Appiah A, Utzinger J, Liu J, Olliaro P (2008) Drugs for treating urinary schistosomiasis. Cochrane Database Syst Rev: CD000053. [PubMed]
8. Utzinger J, Keiser J (2004) Schistosomiasis and soil-transmitted helminthiasis: common drugs for treatment and control. Expert Opin Pharmacother 5: 263–285 [PubMed]
9. King CH, Dickman K, Tisch DJ (2005) Reassessment of the cost of chronic helmintic infection: a meta-analysis of disability-related outcomes in endemic schistosomiasis. Lancet 365: 1561–1569 [PubMed]
10. Fenwick A, Savioli L, Engels D, Robert Bergquist N, Todd MH (2003) Drugs for the control of parasitic diseases: current status and development in schistosomiasis. Trends Parasitol 19: 509–515 [PubMed]
11. Doenhoff MJ, Cioli D, Utzinger J (2008) Praziquantel: mechanisms of action, resistance and new derivatives for schistosomiasis. Curr Opin Infect Dis 21: 659–667 [PubMed]
12. Gryseels B, Mbaye A, De Vlas SJ, Stelma FF, Guisse F, et al. (2001) Are poor responses to praziquantel for the treatment of Schistosoma mansoni infections in Senegal due to resistance? An overview of the evidence. Trop Med Int Health 6: 864–873 [PubMed]
13. Xiao SH, Keiser J, Chen MG, Tanner M, Utzinger J (2010) Research and development of antischistosomal drugs in the People’s Republic of China a 60-year review. Adv Parasitol 73: 231–295 [PubMed]
14. Xiao SH, Booth M, Tanner M (2000) The prophylactic effects of artemether against Schistosoma japonicum infections. Parasitol Today 16: 122–126 [PubMed]
15. Utzinger J, Tanner M, Keiser J (2010) ACTs for schistosomiasis: do they act? Lancet Infect Dis 10: 579–581 [PubMed]
16. Adjuik M, Babiker A, Garner P, Olliaro P, Taylor W, et al. (2004) Artesunate combinations for treatment of malaria: meta-analysis. Lancet 363: 9–17 [PubMed]
17. White NJ (2008) Qinghaosu (artemisinin): the price of success. Science 320: 330–334 [PubMed]
18. Keiser J, Utzinger J (2007) Artemisinins and synthetic trioxolanes in the treatment of helminth infections. Curr Opin Infect Dis 20: 605–612 [PubMed]
19. Moher D, Liberati A, Tetzlaff J, Altman DG (2009) Group P (2009) Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med 6: e1000097. [PMC free article] [PubMed]
20. Jadad AR, Moore RA, Carroll D, Jenkinson C, Reynolds DJ, et al. (1996) Assessing the quality of reports of randomized clinical trials: is blinding necessary? Control Clin Trials 17: 1–12 [PubMed]
21. Borenstein M, Hedges LV, Higgins JPT, Rothstein HR (2009) Introduction to Meta-Analysis. Chichester U.K.: John Wiley and Sons Ltd.
22. DerSimonian R, Laird N (1986) Meta-analysis in clinical trials. Control Clin Trials 7: 177–188 [PubMed]
23. Egger M, Davey Smith G, Schneider M, Minder C (1997) Bias in meta-analysis detected by a simple, graphical test. BMJ 315: 629–634 [PMC free article] [PubMed]
24. Schwarzer G (2012) meta: Meta-Analysis with R.
25. Borrmann S, Szlezak N, Faucher JF, Matsiegui PB, Neubauer R, et al. (2001) Artesunate and praziquantel for the treatment of Schistosoma haematobium infections: a double-blind, randomized, placebo-controlled study. J Infect Dis 184: 1363–1366 [PubMed]
26. De Clercq D, Vercruysse J, Kongs A, Verle P, Dompnier JP, et al. (2002) Efficacy of artesunate and praziquantel in Schistosoma haematobium infected schoolchildren. Acta Trop 82: 61–66 [PubMed]
27. Inyang-Etoh PC, Ejezie GC, Useh MF, Inyang-Etoh EC (2009) Efficacy of a combination of praziquantel and artesunate in the treatment of urinary schistosomiasis in Nigeria. Trans R Soc Trop Med Hyg 103: 38–44 [PubMed]
28. Keiser J, N’Guessan NA, Adoubryn KD, Silue KD, Vounatsou P, et al. (2010) Efficacy and safety of mefloquine, artesunate, mefloquine-artesunate, and praziquantel against Schistosoma haematobium: randomized, exploratory open-label trial. Clin Infect Dis 50: 1205–1213 [PubMed]
29. De Clercq D, Vercruysse J, Verle P, Kongs A, Diop M (2000) What is the effect of combining artesunate and praziquantel in the treatment of Schistosoma mansoni infections? Trop Med Int Health 5: 744–746 [PubMed]
30. De Clercq D, Vercruysse J, Verle P, Niasse F, Kongs A, et al. (2000b) Efficacy of artesunate against Schistosoma mansoni infections in Richard Toll, Senegal. Trans R Soc Trop Med Hyg 94: 90–91 [PubMed]
31. Hou XY, McManus DP, Gray DJ, Balen J, Luo XS, et al. (2008) A randomized, double-blind, placebo-controlled trial of safety and efficacy of combined praziquantel and artemether treatment for acute schistosomiasis japonica in China. Bull World Health Organ 86: 788–795 [PubMed]
32. Sissoko MS, Dabo A, Traore H, Diallo M, Traore B, et al. (2009) Efficacy of artesunate + sulfamethoxypyrazine/pyrimethamine versus praziquantel in the treatment of Schistosoma haematobium in children. PLoS One 4: e6732. [PMC free article] [PubMed]
33. Obonyo CO, Muok EM, Mwinzi PN (2010) Efficacy of artesunate with sulfalene plus pyrimethamine versus praziquantel for treatment of Schistosoma mansoni in Kenyan children: an open-label randomised controlled trial. Lancet Infect Dis 10: 603–611 [PubMed]
34. Wu LJ, Li SW, Xuan YX, Xu PS, Liu ZD, et al. (1995) Field application of artesunate in prophylaxis of schistosomiasis: an observation of 346 cases. Chin J Schisto Control 7: 323–327
35. Xu MS, Zhang SQ, Li SW, Wang TP, Chen JR, et al. (1999) Field application of oral artesunate for preventing Schistosoma japonicum infection. Chinese Journal of Parasitology and Parasitic Disease 17: 241–243 [PubMed]
36. Li HY, Liu ZD, Hu LS, Liu YM, Hu F, et al. (1999) Observation on the prevention of schistosomiasis japonica by administration of artesuante long term. Chin J Parasit Dis Control 12: 412
37. Zhang SJ, Lin DD, Xu MS, Yi ZH, Zhang SQ, et al. (2000) Clinical trials on preventive effect of artesunate on schistosomiasis japonica. Med Diagn Treat 11: 68–72
38. Lu GY, Lin GJ, Sun MX, Cui JE, Wu QZ (2000) Probe on scheme with oral artesunate protecting people from infection of schistosome. Chin J Parasitol Parasit Dis Contr 13: 212–214
39. Li SW, Wu LJ, Liu ZD, Hu LS, Xu YX, et al. (1996) Studies on prophylactic effect of artesunate on schistosomiasis japonica. Chin Med J 109: 848–853 [PubMed]
40. Tian ZY, Liu DS, Xiao ZW, Zhou YC, Qu GS, et al. (2001) A cost-effectiveness study of artesunate in the prophylaxis of schistosomiasis in an endemic area. Chin J Schisto Control 13: 299–300
41. Xiao SH, Shi ZG, Zhou SJ, Wang CZ, Zhang ZG, et al. (1995) Field studies on the preventive effect of oral artemether against schistosomal infection. Chin J Parastol Parasit Dis 13: 170–173
42. Xiao SH, Wang JL, Wang Z, Yang Z, Chu B, et al. (1996) Protection of the residents from schistosome infection using oral artemether in mountainous endemic area. Chin J Parastol Parasit Dis 14: 11–14
43. Xu MS, Xiao SH, Song Q, Tao CG, Xia CG, et al. (1997) Observation on the effect of artemether on controlling schistosomiasis japonica in an endemic area of marshland. Chin J Parasitol Parasit Dis 15: 212–215
44. Tian ZY, Xiao SH, Xiao JW, Zhou YC, Liu DS, et al. (1997) Reduction of Schistosoma japonicum infection in an endemic area in islet with embankment after prophylaxis with oral artemether throughout the transmission season. Chin J Parasito Parasitic Dis 15: 208–211
45. Song Y, Xiao SH, Wu W, Zhang SJ, Xie H, et al. (1998) Preventive effect of artemether on schistosome infection. Chin Med J 111: 123–127 [PubMed]
46. Wang JL, Xiao SH, Yang Z, Wang MK, Yang H, et al. (1997) Effect of oral artemether on controlling schistosomiasis in Yunnan mountainous endemic area. Chin J Parasitol Parasit Dis 15: 138–142
47. Song Y, Bao ZP, Gao ZL, Hu QL, Nin A, et al. (2006) Effect of oral artemether in controlling schistosomiasis in a heavy endemic area of Nanji town, Xinjian county, Jiangxi province. J Trop Med 6: 1182–1185
48. Li YS, Chen HG, He HB, Hou XY, Ellis M, et al. (2005) A double-blind field trial on the effects of artemether on Schistosoma japonicum infection in a highly endemic focus in southern China. Acta Trop 96: 184–190 [PubMed]
49. N’Goran EK, Utzinger J, Gnaka HN, Yapi A, N’Guessan NA, et al. (2003) Randomized, double-blind, placebo-controlled trial of oral artemether for the prevention of patent Schistosoma haematobium infections. Am J Trop Med Hyg 68: 24–32 [PubMed]
50. Utzinger J, N’Goran EK, N’Dri A, Lengeler C, Xiao S, et al. (2000) Oral artemether for prevention of Schistosoma mansoni infection: randomised controlled trial. Lancet 355: 1320–1325 [PubMed]
51. Mohamed AA, Mahgoub HM, Magzoub M, Gasim GI, Eldein WN, et al. (2009) Artesunate plus sulfadoxine/pyrimethamine versus praziquantel in the treatment of Schistosoma mansoni in eastern Sudan. Trans R Soc Trop Med Hyg 103: 1062–1064 [PubMed]
52. Xiao SH (2005) Development of antischistosomal drugs in China, with particular consideration to praziquantel and the artemisinins. Acta Trop 96: 153–167 [PubMed]
53. Gryseels B, Polman K, Clerinx J, Kestens L (2006) Human schistosomiasis. Lancet 368: 1106–1118 [PubMed]
54. Scherrer AU, Sjoberg MK, Allangba A, Traore M, Lohourignon LK, et al. (2009) Sequential analysis of helminth egg output in human stool samples following albendazole and praziquantel administration. Acta Trop 109: 226–231 [PubMed]
55. Liu R, Dong HF, Guo Y, Zhao QP, Jiang MS (2011) Efficacy of praziquantel and artemisinin derivatives for the treatment and prevention of human schistosomiasis: a systematic review and meta-analysis. Parasit Vectors 4: 201. [PMC free article] [PubMed]
56. Gautam A, Ahmed T, Batra V, Paliwal J (2009) Pharmacokinetics and pharmacodynamics of endoperoxide antimalarials. Curr Drug Metab 10: 289–306 [PubMed]
57. McManus DP, Loukas A (2008) Current status of vaccines for schistosomiasis. Clin Microbiol Rev 21: 225–242 [PMC free article] [PubMed]
58. Ross AG, Bartley PB, Sleigh AC, Olds GR, Li Y, et al. (2002) Schistosomiasis. N Engl J Med 346: 1212–1220 [PubMed]
59. Wu TX, Liu GJ, Zhang MM, Wang Q, Ni J, et al. (2003) [Systematic review of benefits and harms of artemisinin-type compounds for preventing schistosomiasis]. Zhonghua Yi Xue Za Zhi 83: 1219–1224 [PubMed]
60. Danso-Appiah A, Garner P, Olliaro PL, Utzinger J (2009) Treatment of urinary schistosomiasis: methodological issues and research needs identified through a Cochrane systematic review. Parasitology 136: 1837–1849 [PubMed]

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