Print version ISSN 0042-9686
Bull World Health Organ vol.87 n.12 Genebra Dec. 2009
Efficacité comparée de dérivés de l'artémisinine et de la quinine contre le paludisme cérébral chez les enfants africains : revue systématique
Revisión sistemática de comparación de los derivados de la artemisinina y la quinina como tratamientos de la malaria cerebral en niños africanos
Hmwe Hmwe Kyu*; Eduardo Fernández
McMaster University, Hamilton, ON, L8N 3Z5, Canada
OBJECTIVE: To summarize the existing evidence on the efficacy of artemether and arteether, two artemisinin derivatives, versus quinine for treating cerebral malaria in children.
METHODS: We searched the Cochrane Central Register of Controlled Trials, MEDLINE, EMBASE and the http://clinicaltrials.gov web site. We also checked the reference lists of existing systematic reviews and of all trials identified by the above methods. We searched exclusively for randomized controlled trials (RCTs) comparing artemether/arteether with quinine for treating cerebral malaria in children. Two independent reviewers assessed study eligibility and trial quality and extracted the data.
FINDINGS: Nine RCTs were included in the analysis, and all were from Africa. Five had adequate allocation concealment. Seven trials compared artemether with quinine (1220 children), and two compared arteether with quinine (194 children). No statistically significant difference was found between artemisinin derivatives and quinine in preventing mortality (relative risk, RR: 0.91; 95% confidence interval, CI: 0.73-1.14; I²: 0%). The quality of the evidence, as assessed by the Grade evidence profile, was moderate. The only serious adverse event was seen in a patient in the quinine group who developed fatal black water fever.
CONCLUSION: Artemisinin derivatives are not inferior to quinine in preventing death in children with cerebral malaria.
OBJECTIF: Récapituler les éléments existants sur l'efficacité de l'artéméther et de l'artééther, deux dérivés de l'artémisinine, par rapport à celle de la quinine, dans le traitement du paludisme cérébral chez l'enfant.
MÉTHODES: Nous avons effectué une recherche dans le Registre central Cochrane des essais contrôlés et dans MEDLINE et EMBASE, ainsi que sur le site Internet http://clinicaltrials.gov. Nous avons aussi examiné les listes de références des revues systématiques existantes et de tous les essais identifiés par les méthodes ci-dessus. Nous avons recherché exclusivement des essais contrôlés randomisés (ECT) comparant l'artéméther ou l'artééther à la quinine dans le traitement du paludisme cérébral chez l'enfant. Deux examinateurs indépendants ont évalué l'admissibilité des études et la qualité des essais, puis ont extrait les données.
RÉSULTATS: Neuf essais contrôlés randomisés, tous réalisés en Afrique, ont été pris en compte dans l'analyse. Pour cinq de ces essais, l'affectations des traitements était correctement dissimulée. Sept comparaient l'artéméther à la quinine (1220 enfants), tandis que deux autres comparaient l'artééther à la quinine (194 enfants). Aucune différence statistiquement significative n'a été relevée entre les dérivés de l'artémisinine et la quinine dans la prévention de la mortalité (risque relatif, RR : 0,91 ; intervalle de confiance à 95 %, IC : 0,73-1,14 ; I² : 0 %). D'après l'évaluation GRADE des profils de données probantes, la qualité des éléments était moyenne. Le seul effet indésirable grave, une fièvre bilieuse hémoglobinurique fatale, a été observé chez un patient appartenant au groupe sous quinine.
CONCLUSION: Les dérivés de l'artémisinine ne sont pas inférieurs à la quinine dans la prévention de la mortalité chez les enfants atteints de paludisme cérébral.
OBJETIVO: Obtener una sinopsis de los datos probatorios existentes sobre la eficacia del artemetero y el arteéter, dos derivados de la artemisinina, frente a la quinina como tratamiento de la malaria cerebral en los niños.
MÉTODOS: Realizamos búsquedas en el Registro Central Cochrane de Ensayos Controlados y en MEDLINE, EMBASE y el sitio web http://clinicaltrials.gov. Examinamos también las listas de referencias de revisiones sistemáticas ya existentes y de todos los ensayos localizados según se ha señalado. Buscamos exclusivamente los ensayos controlados aleatorizados (ECT) en que se habían comparado el artemetero/arteéter y la quinina como tratamientos de la malaria cerebral infantil. Dos revisores independientes evaluaron la idoneidad para el estudio y la calidad de los ensayos y extrajeron los datos.
RESULTADOS: Se analizaron en total nueve ECT, todos ellos correspondientes a África. En cinco de los ensayos se había ocultado adecuadamente la asignación del tratamiento. En siete se habían comparado artemetero y la quinina (1220 niños), y en los otros dos el arteéter y la quinina (194 niños). No se observó ninguna diferencia estadísticamente significativa entre los derivados de la artemisinina y la quinina en lo referente a la prevención de la mortalidad (riesgo relativo, RR: 0,91; intervalo de confianza del 95%: 0,73-1,14; I²: 0%). La calidad de los datos probatorios, según el perfil del grado de evidencia, fue moderada. El único evento adverso grave fue el observado en un paciente tratado con quinina que desarrolló un cuadro mortal de paludismo hemoglobinúrico.
CONCLUSIÓN: Los derivados de la artemisinina no son inferiores a la quinina como medio de prevención de la mortalidad en los niños con malaria cerebral.
Malaria causes more than one million deaths worldwide each year, and over 90% of them occur in Africa.1 Plasmodium falciparum causes the most serious form of the disease.2 Cerebral malaria, which is the most life-threatening complication of P. falciparum malaria, is characterised by unrousable coma not attributable to any other cause.2 Even with correct treatment, the lethality rate among children with cerebral malaria approaches 20%.3
The recommended treatment for cerebral malaria is quinine by slow intravenous infusion.4 However, quinine has several drawbacks, including a short half-life, painful local reactions after intramuscular and intravenous administration5 and neurotoxicity.5,6 Permanent blindness with standard doses of quinine has been well documented.6 Furthermore, decreasing sensitivity to quinine has been reported in south-eastern Asia and the Amazon region,7 as well as in parts of Africa.8
Artemisinin derivatives, a relatively new group of antimalarials that produce a very rapid therapeutic response and are effective against multidrugresistant P. falciparum, have been used increasingly over the past decade.9 Although resistance to artimisinin derivatives has been reported along the Thai-Cambodian border,10 it has not been detected anywhere else.9 The neurotoxic effects of artemisinin derivatives have been observed in pre-clinical animal studies at doses about 10 times higher than those used for human treatment,11 but no such toxic effects have been reported in humans.12
One Cochrane systematic review has compared arteether with quinine for the treatment of children with cerebral malaria, and another meta-analysis has compared artemether with quinine in adults and children with severe P. falciparum malaria. In the first study, no statistically significant difference was found in the number of deaths or other outcomes, such as coma recovery time, parasite clearance time and fever clearance time.13 However, in the second study the combined adverse outcome of either death or neurological sequelae was significantly less common in the artemether group.12
After the meta-analysis mentioned above, new clinical trials in which artemether has been compared with quinine for the treatment of cerebral malaria in children have been carried out. Although P. falciparum malaria is linked to high mortality in children and cerebral malaria is its most life threatening complication, very few systematic reviews on the treatment of children with cerebral malaria have been performed. Previous systematic reviews have compared either artemether or arteether with quinine, yet it makes sense to summarize their efficacy in a single review because both drugs are oil soluble artemisinin derivatives. If these drugs are as efficacious as quinine in preventing death in children, they are preferable to quinine for the following reasons: (i) their side-effects are fewer and (ii) the Thai-Cambodian border is the only place where resistance to them has been reported, whereas resistance to quinine has been observed in several parts of the world.
The objective of this review is to summarize the existing evidence surrounding the efficacy of artemisinin derivatives (artemether and arteether) versus quinine for the treatment of cerebral malaria in children. It will address the following question. "How efficacious are artemisinin derivatives compared with quinine for the treatment of cerebral malaria in children?"
We searched the following databases exclusively for randomized controlled trials (RCTs): Cochrane Central Register of Controlled Trials (The Cochrane Library Issue 1, 2008); MEDLINE (1966 to May 2008) and EMBASE (1980 to May 2008). We used the following search terms: malaria, quinine, quinimax, cinchona alkaloids, artemisinin, artemether, artemotil, arteether, and artecef. We also searched the http://clinicaltrials.gov web site for completed and ongoing trials. We contacted individual researchers working in the field and attempted to identify all relevant trials regardless of language or publication status (published or unpublished). We checked the reference lists of existing systematic reviews and of all trials identified by the above methods.
We searched exclusively for RCTs that compared artemether or arteether (any route of administration) with quinine (any route of administration) for the treatment of children < 15 years of age with cerebral malaria.
The primary outcome measure was mortality at hospital. Secondary outcome measures were the time elapsed before recovery from coma, fever clearance time, parasite clearance time, neurological sequelae and adverse events.
After screening the abstracts of all trials identified by the search strategy, the authors obtained full papers of potentially relevant trials and independently used an eligibility form to apply the inclusion criteria to the papers. Disagreements were resolved through discussion and consensus.
Assessment of methodological quality
The authors independently assessed the methodological quality of selected trials according to the Cochrane Infectious Diseases Group guidelines.14 The following aspects of study design were assessed: (i) generation of the allocation sequence, (ii) allocation concealment, (iii) blinding (participant/provider/outcome assessor), and (iv) inclusion of all randomized patients in the analysis.
The generation of the allocation sequence and concealment were classified as follows: "adequate", if the method used for treatment allocation was mentioned and the allocation sequences were unpredictable (e.g. computer-generated random numbers, table of random numbers); "unclear", if the trial was randomized but no method was described; inadequate, if sequences were predictable (e.g alternative allocation).15 Allocation concealment was classified as "adequate" if participants and the investigators who recruited them could not anticipate the assignment (e.g. central randomization; sequentially-numbered, opaque, sealed envelopes); unclear, if the method used was not mentioned; "inadequate", if participants and those enrolling them in the study could predict the next assignment (e.g. an open allocation schedule, unsealed or non-opaque envelopes).15 Inclusion of all randomized participants in the analysis was categorized as "adequate" (if > 90%), "inadequate" (if < 90%) or "unclear" (if the number of children randomized or analysed was not described). Disagreements were resolved by consensus.
Before data extraction, we pilot tested a data abstraction form and modified it. We then independently used the form to extract the following information: ethical approval, participants (informed consent, mean/median age, sex, diagnostic criteria, baseline coma score, duration of coma, parasite counts), methods (randomization, allocation concealment, blinding, inclusion of all randomized patients in the analysis or not, how drop-outs were dealt with), intervention (type, frequency and duration of treatment, dose and route of administration, duration of follow-up), outcome and potential conflict of interest. For each outcome, we extracted the number of children randomized and the number analysed in each treatment group. For binary outcomes, we recorded the number of children having the event and the number assessed in each treatment group. For continuous outcomes, we extracted means and standard deviations or medians and interquartile ranges for each treatment group, as well as the numbers assessed in each group. Disagreements between reviewers were resolved by discussion.
Measuring inter-rater agreement
We used Cohen's (unweighted) kappa coefficient (κ) for measuring agreement between reviewers. The κ for abstract screening was 0.78, for full text eligibility, 0.82; for allocation concealment, 0.90; for blinding of outcome assessor, 0.87; and for inclusion of all randomized patients in the analysis, 0.73.
We analysed the data with Review Manager 4.2 (RevMan 4.2, The Cochrane Collaboration, Oxford, United Kingdom) using relative risk (RR) for dichotomous data, weighted mean difference for continuous data and 95% confidence intervals (CIs).
We performed an analysis according to the values reported by the original authors, followed by an intention to treat analysis. If the outcomes of excluded children were given in the original article, we used this information in our intention to treat analysis. If the outcomes were not given, we assumed that all missing subjects on artemether/arteether treatment were dead and that all those on quinine treatment were alive. This extreme case analysis was performed to avoid favouring the intervention drugs if they were not as efficacious as quinine for cerebral malaria. We used fixed effects modelling in all analyses because most of the studies included few participants and the pooled result for the primary outcome showed little heterogeneity (I² = 0%).
We constructed a funnel plot to look for evidence of publication bias. The funnel plot is asymmetric, but asymmetry can be a chance finding when fewer than 10 studies are included in the scatter plot.16
To test the robustness of the findings, we performed two sensitivity analyses. They were limited to studies with adequate allocation concealment and studies in which the route of administration in the treatment group was intramuscular.
We looked for statistical heterogeneity by inspecting forest plots for overlapping CIs and by using the I² statistic (I² > 50% = substantial heterogeneity).17 The potential sources of heterogeneity for the primary outcome measure were prespecified in the protocol. They included different diagnostic criteria, different outcome measurement criteria, type of allocation concealment, level of blinding, severity of disease, drug sensitivity or resistance patterns based on country of origin, use of additional antimalarials and route of treatment administration.
Description of studies
We identified 176 studies through our literature search. Abstract screening yielded 19 articles that potentially met our inclusion criteria, and 10 of them were excluded during the full article review (Fig. 1). This resulted in only nine articles being included in this study.
The 7 artemether trials and the 2 arteether trials that met our inclusion criteria comprised a total of 1220 and 194 children, respectively. All studies were conducted in Africa (Cameroon, the Gambia, Kenya, Malawi, Nigeria, the Sudan, Uganda and Zambia). The characteristics of the participants, the diagnostic criteria for cerebral malaria and the interventions conducted in each study are described in Table 1.
In all 9 trials, death was reported as a primary outcome. The definitions of secondary outcomes applied in the studies varied, as shown below.
Coma recovery time:
From the initiation of treatment, the time it took for the child to regain consciousness (4 artemether studies) or to achieve a Blantyre Coma Score of 5 (1 artemether and 2 arteether studies). No definition was given in the remaining studies. The coma recovery time was reported as means and standard deviations in 6 trials and as medians and interquartile ranges in 3 trials.
Fever clearance time:
From the initiation of treatment, the time taken for the body temperature to drop to < 37.5 °C and remain there for at least 48 hours (1 artemether study); to drop to < 37.5 °C and remain there for at least 24 hours (1 arteether and 2 artemether studies); to drop to < 37.5 °C and remain there for at least 72 hours (1 artemether study) and to drop to < 38 °C and remain there for at least 24 hours (1 artemether study). Of these 6 studies, one specified the body temperature as being axillary and another as rectal or axillary, but the rest gave no indication. The fever clearance time was reported as means and standard deviations in 6 trials and as medians and interquartile ranges in 3 trials.
Parasite clearance time:
From the initiation of treatment, the time it took to obtain two consecutive negative thick blood smear results (2 artemether studies); to obtain the first negative blood smear result (1 artemether study); to obtain the first negative blood smear result with no positive smears in the following 24 hours (1 arteether study); and to obtain the first of two consecutive negative thick smear results without subsequent positive smears until day 7 (1 artemether study). No definition was given in 3 studies. The parasite clearance time was reported as means and standard deviations in 5 trials and as medians and interquartile ranges in 3 trials. In the remaining study, the outcome was parasite clearance on day 7 (dichotomous end point, i.e. whether 2 consecutive thick blood films done with a 12-hour interval between them were negative or not).
Neurological sequelae were assessed on recovery (2 artemether trials) and at the time of discharge (1 arteether and 4 artemether trials). This outcome was not assessed in 2 trials and was reported it in various ways in the remaining studies (e.g. motor weakness, loss of neurological milestones, deafness, blindness, hallucinations, hemiparesis, hypertonia, mental retardation, monoparesis, quadraparesis and speech impairment).
Methodological quality of included studies
Table 2 presents the methodological quality of included studies. Of the 7 artemether studies, 5 had adequately generated the allocation sequence and 4 had adequately concealed treatment allocation. In all 7 trials investigators were aware of the treatment allocation. Participants were blinded to it in only 1 trial, microscopists in 2 trials and those who assessed the neurological sequelae in 1 trial. Both arteether studies had adequately generated the allocation sequence and 1 study had adequately concealed it. Investigators and participants were aware of treatment allocation in both arteether studies. Microscopists were blinded in 1 study.
In seven comparisons of artemether with quinine, no significant difference in the risk of death was detected. Furthermore, the pooled meta-analysis did not show a statistically significant difference between artemether and quinine (RR: 0.95; 95% CI: 0.74-1.20; n = 1220) (Fig. 2). In the sensitivity analyses, when we omitted studies with unclear allocation concealment, the RR increased slightly, from 0.95 to 0.98 (95% CI: 0.75-1.27). We got a similar result (RR: 0.98; 95% CI: 0.76-1.25) when we only included studies in which intramuscular artemether was used.
In the two comparisons of arteether versus quinine, the pooled meta-analysis showed no significant difference between the two treatments in terms of the risk of death from cerebral malaria (RR: 0.75; 95% CI: 0.43-1.30; n = 194) (Fig. 2).
Pooled analysis of the results of all artemether and arteether comparisons with quinine indicated no significant difference between the results obtained in the two treatment groups, with little heterogeneity between studies (RR: 0.91; 95% CI: 0.73-1.14; I²: 0%) (Fig. 2). A sensitivity analysis done by limiting the meta-analysis to studies with adequate allocation concealment (RR: 0.98; 95% CI: 0.77-1.26) and studies using intramuscular artemether or arteether (RR: 0.94; 95% CI: 0.75-1.17) showed that the overall estimated RR is fairly stable irrespective of the study quality and route of administration of the intervention drugs.
The pooled RRs from the intention to treat analysis showed no significant difference between the results obtained with artemether and quinine (RR: 1.07; 95% CI: 0.85-1.35) and overall artemether and arteether comparisons with quinine (RR: 1.00; 95% CI: 0.81-1.24), and thus enhancing the robustness of the findings.
Time to coma recovery, fever clearance and parasite clearance
The pooled result from 4 trials showed a significantly shorter coma recovery time in the artemether group than in the quinine group (Fig. 3) but no significant difference in fever clearance time (Fig. 4). The pooled results from 3 trials showed no significant difference between the artemether and quinine groups in parasite clearance time (Fig. 5, available at: http://www.who.int/bulletin/volumes/87/12/08-060327/en/index.html). The remaining 3 artemether studies, which reported all outcomes in medians and interquartile ranges, showed that parasite clearance time was significantly shorter in the artemether group than in the quinine group (P < 0.001) (Table 3). No significant difference in coma recovery time, fever clearance time or parasite clearance time was noted between the arteether and quinine groups (Fig. 3, Fig. 4 and Fig. 5).
Neurological sequelae at recovery or discharge were pooled together as "neurological sequelae at recovery" using the number of cerebral malaria survivors as the denominator. There was no evidence of a difference in the risk of neurological sequelae between artemether and quinine based on 6 studies (RR: 0.92; 95% CI: 0.72-1.17; I²: 0%); arteether and quinine based on 1 study (RR: 1.08; 95% CI: 0.60-1.96), and overall comparisons of artemether and arteether with quinine (RR: 0.94; 95% CI: 0.75-1.17; I2: 0%) (Fig. 6, available at: http://www.who.int/bulletin/volumes/87/12/08-060327/en/index.html).
Different adverse effects were reported across studies. Among the serious ones were fatal black water fever26 (0/51 arteether versus 1/51 quinine; RR: 0.33; 95% CI: 0.01-8.00) and persistent hypoglycemia18 (0/51 artemether versus 1/52 quinine; RR: 0.34; 95% CI: 0.01-8.15). The child with persistent hypoglycemia had poor liver function before starting treatment.18 Other adverse events included injection abscess requiring incision and drainage (1/288 artemether versus 5/288 quinine;22 RR: 0.20; 95% CI: 0.02-1.70); QT prolongation on electrocardiogram (20/82 artemether versus 5/80 quinine;20 RR: 3.90; 95% CI: 1.54-9.89), and urticarial rash/vomiting (2/333 artemether versus 4/330 quinine;18,22 RR: 0.53; 95% CI: 0.12-2.41). Thuma et al. reported 82 adverse events in 36/48 arteether and 61 adverse events in 34/44 quinine patients25 (RR: 0.97; 95% CI: 0.77-1.22).
This review showed no statistically significant difference between artemisinin derivatives and quinine in preventing death in children with cerebral malaria. Sensitivity analyses and intention to treat analyses, separately for artemether studies as well as for all artemether and arteether studies, were quite consistent and confirmed the robustness of this result. The evidence for the pooled RR of death for children treated with artemisinin derivatives versus quinine was of moderate quality, based on the Grade evidence profile27. When artemether and arteether studies were assessed separately, the quality of the evidence for the pooled estimate of death was rated as moderate in artemether studies (n = 1220) and as low in arteether studies (n = 194) because the small number of participants implies that meta-analyses may have insufficient power to detect significant differences in the arteether group.
Meta-analysis of 4 artemether studies that reported coma recovery time in means and standard deviations showed a shorter coma recovery time in the artemether group (weighted mean difference: -3.50; 95% CI: -6.71 to -0.29) (Fig. 3). For the purposes of sensitivity analysis, we estimated means from medians28 and standard deviations from interquartile ranges29 for the remaining 3 studies, which we then incorporated into our meta-analysis. When the results of the 7 artemether studies were pooled together, the weighted mean difference in coma recovery time between the artemether and quinine groups was no longer significant (weighted mean difference: -0.26; 95% CI: -2.70 to 2.18).
For studies that reported the results in means and standard deviations for fever clearance time and parasite clearance time, meta-analysis showed no significant difference between the artemether and quinine groups (Fig. 4, Fig. 5). However, when the studies in which means were estimated from medians28 and standard deviations from interquartile ranges29 were included in the analyses, both fever clearance time (weighted mean difference: -5.83; 95% CI: -8.84 to -2.82) and parasite clearance time (weighted mean difference: -8.83; 95% CI: -10.75 to -6.90) were significantly shorter in the artemether group than in the quinine group. These inconsistencies may be attributable to differences in quinine sensitivity patterns in the study areas. Conversely, the pooled RR for the secondary outcome, neurological sequelae, revealed the lack of a significant difference between artemisinin derivatives and quinine, with little heterogeneity among studies (Fig. 6).
Despite the fact that methodological limitations of the studies in this review downgrade the quality of the evidence, findings for death, the primary outcome, were consistent across all analyses. This suggests that artemisinin derivatives are not inferior to quinine in preventing death in children with cerebral malaria. ▪
We acknowledge the valuable guidance and support of Professors Deborah J Cook, Gordon Guyatt, Maureen Meade, Anita Gross and Diane Heels-Ansdell. We are grateful to Professor Michael H Boyle for his valuable comments, constant help and support. Special thanks go to Robert Borden Hopkins (Research Biostatistician, PATH Research Institute) and Assistant Professor Eleanor Pullenayegum for their valuable statistical advice. We also thank the editorial committee and the peer reviewers for their helpful comments.
Competing interests: None declared.
1. Roll Back Malaria Partners set ambitious financial targets for 19 African countries fighting malaria. Geneva: World Health Organization; 2007. Available from: http://www.rollbackmalaria.org/amd2007/pr/pr_rbmAMD2007-e.pdf. [accessed on 6 August 6 2008] [ Links ].
2. Management of severe malaria. 2nd ed. Geneva: World Health Organization; 2000. [ Links ]
3. Jaffar S, Van Hensbroek MB, Palmer A, Schneider G, Greenwood B. Predictors of a fatal outcome following childhood cerebral malaria. Am J Trop Med Hyg 1997;57:20-4. PMID:9242312 [ Links ]
4. Severe and complicated malaria. Trans R Soc Trop Med Hyg 1990;84 Suppl 2;1-65. doi:10.1016/0035-9203(90)90363-J [ Links ]
5. Looareesuwan S, Oosterhuis B, Schilizzi BM, Sollie FA, Wilairatana P, Krudsood S, et al. Dose-finding and efficacy study for i.m. artemotil (beta-arteether) and comparison with i.m. artemether in acute uncomplicated P. falciparum malaria. Br J Clin Pharmacol 2002;53:492-500. doi:10.1046/j.1365-2125.2002.01590.x PMID:11994055 [ Links ]
6. WHO Informal consultation on clinical neurological investigations required for patients treated with artemisinin compounds and derivatives: report of an informal consultation convened by WHO. Geneva: World Health Organization; 1998 (TDR/TDF/99.1). [ Links ]
7. Malaria. National Malaria Control Programme Managers. Current malaria situation and trends. Geneva: World Health Organization; 2007. Available from: http://www.searo.who.int/en/Section10/Section21/Section342_1023.htm [accessed on 6 August 2008] [ Links ].
8. Mutanda LN. Assessment of drug resistance to the malaria parasite in residents of Kampala, Uganda. East Afr Med J 1999;76:421-4. PMID:10520345 [ Links ]
9. Facts on ACTs (artemisinin-based combination therapies). Geneva: World Health Organization; 2006. Available from: http://www.rbm.who.int/cmc_upload/0/000/015/364/RBMInfosheet_9.htm [accessed on 5 August 2008] [ Links ].
10. WHO. Resistance to artemisinin derivatives along the Thai-Cambodian border. Wkly Epidemiol Rec 2007;82:360. PMID:17933087 [ Links ]
11. Lugt CB. Dutch registration for artemotil injections. TDR News 2000;63. Available from: http://www.who.int/tdr/publications/tdrnews/news63/artemotil.htm [accessed on 20 July 2008] [ Links ].
12. Artemether-Quinine Meta-analysis Study Group. A meta-analysis using individual patient data of trials comparing artemether with quinine in the treatment of severe falciparum malaria. Trans R Soc Trop Med Hyg 2001;95:637-50. doi:10.1016/S0035-9203(01)90104-X PMID:11816438 [ Links ]
13. Afolabi BB, Okoromah CAN. Intramuscular arteether for treating severe malaria. Cochrane Database Syst Rev 2004;18:CD004391. [ Links ]
14. Cochrane Infectious Diseases Group. Guide to preparing and using the 'Methods of the review'. Liverpool, England: Cochrane; 2005. Available from: http://www.liv.ac.uk/evidence/CIDG/methods-guide.htm [accessed on 21 March 2008] [ Links ].
15. Jüni P, Altman DG, Egger M. Systematic reviews in health care: Assessing the quality of controlled clinical trials. BMJ 2001;323:42-6. doi:10.1136/bmj.323.7303.42 PMID:11440947 [ Links ]
16. Daya S. Funnel plots and publication bias-work in progress? Evidence-based. Obstet Gynecol 2006;8:71-2. [ Links ]
17. Higgins JPT, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analysis. BMJ 2003;327:557-60. doi:10.1136/bmj.327.7414.557 PMID:12958120 [ Links ]
18. Aceng JR, Byarugaba JS, Tumwine JK. Rectal artemether versus intravenous quinine for the treatment of cerebral malaria in children in Uganda: randomised clinical trial. BMJ 2005;330:334. doi:10.1136/bmj.330.7487.334 PMID:15705690 [ Links ]
19. Olumese PE, Bjorkman A, Gbadegesin RA, Adeyemo AA, Walker O. Comparative efficacy of intramuscular artemether and intravenous quinine in Nigerian children with cerebral malaria. Acta Trop 1999;73:231-6. doi:10.1016/S0001-706X(99)00031-5 PMID:10546840 [ Links ]
20. Murphy S, English M, Waruiru C, Mwangi I, Amukoye E, Crawley J, et al. An open randomized trial of artemether versus quinine in the treatment of cerebral malaria in African children. Trans R Soc Trop Med Hyg 1996;90:298-301. doi:10.1016/S0035-9203(96)90260-6 PMID:8758084 [ Links ]
21. Ojuawo A, Adegboye AR, Oyewale O. Clinical response and parasite clearance in childhood cerebral malaria: A comparison between intramuscular artemether and intravenous quinine. East Afr Med J 1998;75:450-2. [ Links ]
22. Van Hensbroek MB, Onyiorah E, Jaffar S, Schneider G, Palmer A, Frenkel J, et al. A trial of artemether or quinine in children with cerebral malaria. N Engl J Med 1996;335:69-75. doi:10.1056/NEJM199607113350201 PMID:8649492 [ Links ]
23. Taylor TE, Wills BA, Courval JM, Molyneux ME. Intramuscular artemether vs intravenous quinine: an open, randomized trial in Malawian children with cerebral malaria. Trop Med Int Health 1998;3:3-8. doi:10.1046/j.1365-3156.1998.00166.x PMID:9484961 [ Links ]
24. Satti GM, Elhassan SH, Ibrahim SA. The efficacy of artemether versus quinine in the treatment of cerebral malaria. J Egypt Soc Parasitol 2002;32:611-23. PMID:12214938 [ Links ]
25. Thuma PE, Bhat GJ, Mabeza GF, Osborne C, Biemba G, Shakankale GM, et al. A randomized controlled trial of artemotil (beta-arteether) in Zambian children with cerebral malaria. Am J Trop Med Hyg 2000;62:524-9. PMID:11220772 [ Links ]
26. Moyou-Somo R, Tietche F, Ondoa M, Kouemeni LE, Ekoe T, Mbonda E, et al. Clinical trial of beta-arteether versus quinine for the treatment of cerebral malaria in children in Yaounde, Cameroon. Am J Trop Med Hyg 2001; 64:229-32. PMID:11463108 [ Links ]
27. Schünemann HJ, Jaeschke R, Cook DJ, Bria WF, El-Solh AA, Ernst A, et al. An official ATS statement: grading the quality of evidence and strength of recommendations in ATS guidelines and recommendations. Am J Respir Crit Care Med 2006;174:605-14. doi:10.1164/rccm.200602-197ST PMID:16931644 [ Links ]
28. Hozo SP, Djulbegovic B, Hozo I. Estimating the mean and variance from the median, range, and the size of a sample. BMC Med Res Methodol 2005;5:13. doi:10.1186/1471-2288-5-13 PMID:15840177 [ Links ]
29. Higgins JPT, Green S, editors. Cochrane Handbook for Systematic Reviews of Interventions Version 5.0.1 [updated September 2008]. Section. 188.8.131.52 Medians and interquartile ranges. The Cochrane Collaboration, 2008. Available at: www.cochranehandbook.org [accessed 14 March 2009] [ Links ].
(Submitted: 13 October 2008 - Revised version received: 18 March 2009 - Accepted: 19 March 2009 - Published online: 30 July 2009)