Print version ISSN 0042-9686
Bull World Health Organ vol.89 n.7 Genebra Jul. 2011
Rentabilité de l'artésunate parentéral administré chez les enfants gravement atteints de paludisme en Afrique subsaharienne
Relación coste-eficacia del artesunato para el tratamiento de niños con malaria grave en el África subsahariana
Yoel LubellI,*; Arthorn RiewpaiboonII; Arjen M DondorpI; Lorenz von SeidleinIII; Olugbenga A MokuoluIV; Margaret NansumbaV; Samwel GesaseVI; Alison KentVII; George MtoveVIII; Rasaq OlaosebikanIX; Wirichada Pan NgumX; Caterina I FanelloXI; Ilse HendriksenI; Nicholas PJ DayI; Nicholas J WhiteI; Shunmay YeungXI
IFaculty of Tropical Medicine, Mahidol University, 420/6 Ratchawithi Road, Bangkok, 10400,Thailand
IIFaculty of Pharmacy, Mahidol University, Thailand
IIIMenzies School of Health Research, Casuarina, Australia
IVDepartment of Paediatrics and Child Health, University of Ilorin, Ilorin, Nigeria
VEpicentre Mbarara Research Base, Mbarara, Uganda
VINational Institute for Medical Research, Tanga Research Centre, Tanga, United Republic of Tanzania
VIIJoint Malaria Program, Moshi, United Republic of Tanzania
VIIINational Institute for Medical Research, Amani Centre, Tanga, United Republic of Tanzania
IXMalaria Programme, Medical Research Council Laboratories, Fajara, Gambia
XFaculty of Tropical Medicine, Mahidol University, Bangkok, Thailand
XIDepartment of Global Health and Development, London School of Hygiene and Tropical Medicine, London, England
OBJECTIVE: To explore the cost-effectiveness of parenteral artesunate for the treatment of severe malaria in children and its potential impact on hospital budgets.
METHODS: The costs of inpatient care of children with severe malaria were assessed in four of the 11 sites included in the African Quinine Artesunate Malaria Treatment trial, conducted with over 5400 children. The drugs, laboratory tests and intravenous fluids provided to 2300 patients from admission to discharge were recorded, as was the length of inpatient stay, to calculate the cost of inpatient care. The data were matched with pooled clinical outcomes and entered into a decision model to calculate the cost per disability-adjusted life year (DALY) averted and the cost per death averted.
FINDINGS: The mean cost of treating severe malaria patients was similar in the two study groups: 63.5 United States dollars (US$) (95% confidence interval, CI: 61.765.2) in the quinine arm and US$ 66.5 (95% CI: 63.769.2) in the artesunate arm. Children treated with artesunate had 22.5% lower mortality than those treated with quinine and the same rate of neurological sequelae: (artesunate arm: 2.3 DALYs per patient; quinine arm: 3.0 DALYs per patient). Compared with quinine as a baseline, artesunate showed an incremental cost per DALY averted and an incremental cost per death averted of US$ 3.8 and US$ 123, respectively.
CONCLUSION: Artesunate is a highly cost-effective and affordable alternative to quinine for treating children with severe malaria. The budgetary implications of adopting artesunate for routine use in hospital-based care are negligible.
OBJECTIF: Étudier la rentabilité de l'artésunate parentéral dans le cadre du traitement d'enfants gravement atteints de paludisme et son impact potentiel sur les budgets hospitaliers.
MÉTHODES: Les coûts des soins administrés aux patients hospitalisés gravement atteints de paludisme ont été évalués dans 4 des 11 sites participant à l'essai Traitement quinine/artésunate contre le paludisme en Afrique, réalisé sur plus de 5400 enfants. Afin de calculer le coût de l'hospitalisation, les médicaments, les essais en laboratoire et les liquides intraveineux administrés à 2300 patients entre leur admission et leur sortie ont été enregistrés, ainsi que la durée de l'hospitalisation. Les données ont été comparées avec les résultats cliniques regroupés et intégrés à un modèle de décision afin de calculer le coût par année de vie corrigée du facteur invalidité (AVCI) évité et le coût par décès évité.
RÉSULTATS: Le coût moyen du traitement des patients gravement atteints du paludisme s'est révélé similaire dans les deux groupes expérimentaux: 63,5 dollars américains (US$) (intervalle de confiance 95% IC: 61,765,2) pour le bras recevant la quinine et 66,5 US$ (95% IC: 63,769,2) pour le bras recevant l'artésunate. Les enfants traités par artésunate affichaient un taux de mortalité inférieur de 22,5% à ceux recevant de la quinine, et un taux de séquelles neurologiques identique: (bras recevant l'artésunate: 2,3 AVCI par patient; bras recevant la quinine: 3,0 AVCI par patient). En comparaison avec la quinine en tant que ligne de base, l'artésunate a démontré un coût incrémental par AVCI évitée et un coût incrémental par décès évité de 3,8 US$ et 123 US$, respectivement.
CONCLUSION: Dans le cadre du traitement des enfants gravement atteints de paludisme, l'artésunate constitue une alternative extrêmement rentable et abordable par rapport à la quinine. Les implications budgétaires liées à l'adoption de l'artésunate pour une utilisation habituelle lors des soins hospitaliers sont négligeables.
OBJETIVO: Analizar la relación coste-eficacia del artesunato parenteral en el tratamiento de la malaria grave infantil y su posible impacto en los presupuestos hospitalarios.
MÉTODOS: En cuatro de los 11 centros incluidos en el Estudio comparativo de los tratamientos de la malaria con artesunato y quinina en África participaron más de 5400 niños. Para calcular el coste de la hospitalización se registraron los fármacos, las pruebas clínicas y los líquidos endovenosos suministrados a 2300 pacientes, desde su ingreso hasta el alta, según la duración del ingreso del paciente. Los datos se compararon con los resultados clínicos agrupados e introducidos en un modelo de decisión para calcular el coste por año de vida ajustada por discapacidad (AVAD) evitada y el coste por muerte evitada.
RESULTADOS: El coste medio del tratamiento de los pacientes con malaria grave fue similar en los dos grupos del estudio: 63,5 dólares estadounidenses (US$) (intervalo de confianza del 95%, IC: 61,7 65,2) en el grupo de quinina y US$ 66,5 (IC del 95%: 63,769,2) en el grupo de artesunato. Los niños tratados con artesunato presentaron una mortalidad un 22,5% inferior que los tratados con quinina y la misma tasa de secuelas neurológicas: (grupo de artesunato: 2,3 AVAD por paciente; grupo de quinina: 3,0 AVAD por paciente). En comparación con la quinina como referencia, el artesunato ha mostrado un coste incremental por AVAD evitado y un coste incremental por muerte evitada de US$ 3,8 y US$ 123, respectivamente.
CONCLUSIÓN: El artesunato es una alternativa a la quinina muy rentable y con una excelente relación coste-eficacia para el tratamiento de niños con malaria grave. Las implicaciones presupuestarias de la adopción del artesunato para su uso sistemático en la asistencia hospitalaria son insignificantes.
Despite reported falling transmission in much of sub-Saharan Africa,13 malaria remains a leading cause of inpatient admissions and mortality in paediatric wards.46 The policy for first-line treatment of severe malaria is a critical factor in determining malaria mortality. The choice of treatment must ultimately be dictated not only by its efficacy, but also by the ability of frail health systems to sustain its routine use. In much of sub-Saharan Africa, per-capita health expenditure remains extremely low, with annual government health expenditure per capita averaging 34 United States dollars (US$).7 The cost of inpatient care for a case of severe malaria has been estimated at between US$ 12 and US$ 75 and this poses a considerable burden on limited resources.4,8
Quinine remains the mainstay treatment of severe malaria in sub-Saharan Africa. Parenteral quinine costs as little as US$ 0.27 per ampoule9,10 and is widely available in health facilities across the continent. It is administered either intramuscularly or intravenously, three times per day. As an infusion quinine must be given over several hours and although it is well absorbed when given intramuscularly, this route can cause abscesses and sciatic nerve damage and has been associated with tetanus.11 Artesunate is a more expensive drug, costing around US$ 1.06 per vial. However, it is only administered once daily and can be given as an intravenous bolus injection or by intramuscular injection. It has also been shown to be safe and well tolerated.12
Artesunate has previously been shown not only to be more effective for the treatment of severe malaria in adults in Asia, but also highly cost-effective, with a cost per death averted of just under US$ 150.10 Whether these findings are transferable to children in Africa, among whom the largest share of malaria mortality occurs, remains to be explored. The African Quinine Artesunate Malaria Treatment (AQUAMAT) trial is the largest hospital-based clinical trial for severe malaria to date.13 It was carried out in 11 sites in 9 countries across sub-Saharan Africa and recruited children with severe malaria who were randomized to receive either parenteral quinine or artesunate. Parenteral treatment was completed with a course of oral artemisinin combination therapy. The primary outcome measure was in-hospital mortality, with neurological disability assessed at 28 days as an important secondary outcome.
This economic analysis was conducted alongside the AQUAMAT clinical trial to explore the cost-effectiveness of artesunate for the management of severe malaria in children in sub-Saharan Africa. The budget impact of the use of artesunate was also estimated to assess its affordability in routine practice.
A provider perspective was taken, being most relevant to the context of inpatient care. This perspective accounts for all resources used in health facilities for the treatment of severe malaria as well as for mortality and disability among the patients. The evaluation framework is a cost-effectiveness analysis using cost per disability-adjusted life year (DALY) averted and cost per death averted as measures of cost-effectiveness.
When one drug is more expensive and more effective than its comparator, the incremental cost per DALY averted is calculated. This ratio is compared with a decision threshold that is assumed to convey the maximum policy-makers are willing and able to pay for an additional DALY averted. The baseline decision thresholds used as a reference are the conservative estimates of US$ 25 and US$ 150, as suggested by the World Health Organization (WHO) and the World Bank.14,15
The study was conducted in four of the 11 AQUAMAT sites.13 Two of the selected sites, Muheza and Korogwe, were in different areas of the United Republic of Tanzania. A third site was in Mbarara, Uganda, and a fourth in Ilorin, Nigeria. The sites were chosen to represent geographical and epidemiological diversity (Table 1). Medical resource use and cost data were collected between June 2009 and July 2010, when the last patient was recruited. Treatments, diagnostic tests and medical equipment used in the management of severe malaria were recorded for a total of 2300 patients.
The hotel costs of inpatient care (i.e. costs of capital, supportive departments and labour) were obtained from WHO's choosing interventions that are cost-effective (WHO-CHOICE) framework,16 which stratifies costs by country and health facility level. The cost per inpatient day was multiplied by the patient length of stay. Drug costs were obtained from the International drug price indicator guide using the median buyer price.9 Costs of laboratory tests were estimated using patient charges. All costs were calculated in US$ at 2009 prices; the WHO-CHOICE costs were obtained in 2005 local currency units, adjusted for inflation using the consumer price index and converted to US$ using the official average 2009 exchange rate.17,18 Life-time costs associated with neurological sequelae were not included. Mortality and disability data were derived from the pooled estimates from all 11 sites in the AQUAMAT study.13
A decision tree was constructed to depict the progression from severe illness treated with either artesunate or quinine (Fig. 1). Patients can enter either the quinine or artesunate arm, where they either survive or die according to the mortality observed in the trial. The number of life years lost (YLL) for patients that die are calculated according to the patient's age and life expectancy at death. Surviving patients can either be cured or have mild, moderate or severe neurological sequelae. The years lived with disability (YLD) are calculated for patients with neurological sequelae. The percentages shown in Fig. 1 are the baseline mean estimates for each chance node. The model draws random samples from the data set with replacement (bootstrapping) to derive the costs and from assigned distributions for probabilities at each branch. The costs associated with each treatment include those for the antimalarials and other drugs, supportive treatment, diagnostic tests, treatment of adverse events and hotel costs for inpatient stay.
The primary measure of clinical outcome was the number of DALYs in each of the treatment arms. DALYs account for both YLL due to early mortality and YLD, calculated using standard methods.19 The number of YLL for a patient that died was dependent on the average patient age and life expectancy in the four countries where the data were collected. This value was discounted using a baseline value of 3% annually.20 Full age modulation was included in the baseline analysis, implying more conservative effectiveness gains.19 Disability weights for patients with sequelae were based on their condition as documented on day 28 follow-up visits; disability weights were assigned using the Global Burden of Disease tables, as shown in Table 2.21 Disability during the illness episode was not included, as this was assumed to be minor and equal between treatment arms and therefore to have no effect on the incremental advantage of either treatment. The secondary measure of outcome was the incremental cost per death averted, calculated by multiplying the numbers needed to treat (NNT) to avert a death by the difference in treatment costs.
We used one-way sensitivity analyses for parameters whose estimates were not based on high-level evidence, or in cases in which the choice of parameter value was methodological. The discount rate varied between 010%, life expectancy was changed from local to global estimates, and the use of age modulation for the calculation of DALYs was omitted.20 We did a threshold analysis for the drug costs at which the decision to adopt one intervention over the other is reversed.
We did a probabilistic sensitivity analysis for parameter uncertainty in cost and for clinical outcomes. The analysis was done in TreeAge Pro® by running the model 50 000 times, each time randomly selecting from the range of values for each parameter. For costs, the values were drawn from the database of patient costs. For clinical outcomes, β distributions were calculated from the incidence of mortality and neurological sequelae in surviving patients in all AQUAMAT study sites and were converted in the model to DALYs. The measure of dispersion reported for DALYs are the values for the interval between the 2.5% and 97.5% percentiles, defined here as the 95% percentile interval (95% PI).22
The incremental cost-effectiveness ratio was compared against a range of thresholds for policy-makers' willingness to pay for the additional health benefit. This was summarized using cost-effectiveness acceptability curves, indicating the probability that the intervention is cost-effective given the uncertainty surrounding the model parameters across a range of willingness-to-pay thresholds.22
Budget impact analysis
The annual costs of treating all paediatric malaria admissions with artesunate rather than quinine over one year were calculated based on the cost of inpatient care multiplied by the annual number of severe malaria admissions in the four study sites. Costs were also calculated with the exclusion of hotel costs (overheads and labour), which are not immediately affected by the choice of antimalarial drug treatment. The annual number of severe malaria admissions in each site was obtained from hospital records for 2008, apart from Korogwe, where these data were not available. For Korogwe the number of admissions in the AQUAMAT trial was used instead.
Ethical approval for the AQUAMAT trial was obtained from the Oxford Tropical Research Ethics committee and from the ethical review board in each site individually. Further approval was granted for the retrospective collection of cost data from the patients medical files.
In 5425 patients enrolled in the main trial, mortality in the quinine arm was 10.9% compared with 8.5% in the artesunate arm a 22.5% (95% CI: 8.136.9%) reduction. The NNT with artesunate to avert a death was 41 (95% CI: 25112). There was no significant difference in the rate of neurological sequelae between the two arms. Combining the differences in rates of mortality and neurological sequelae between treatment arms, an additional 0.7 (95% PI: 0.21.3) DALYs per patient were averted with artesunate by comparison with quinine (Table 3).
The costs of treatment were very similar between the two arms, as shown in Table 4, with a mean of US$ 66.5 (95% CI: 63.769.2) in the artesunate arm and only US$ 3 less in the quinine arm, at US$ 63.5 (95% CI: 61.765.2).
The hotel costs constituted ap proximately half the total cost and were significantly higher in Ilorin, a tertiary hospital, than in other hospitals. The mean number of hospitalization days was slightly lower in the quinine arm, partly resulting from higher mortality rates early after admission.
The average cost of a full treatment course of quinine, until the patient was able to take oral medication, was just over US$ 1.3 (95% CI: 1.251.34), compared with an average cost of US$ 3.3 (95% CI: 3.23.4) in patients treated with artesunate. Costs for intravenous fluids were slightly higher in the quinine arm, in part because quinine administered intravenously is given as an infusion, whereas artesunate is administered as a bolus injection.
Given these costs and outcomes, the incremental cost per DALY averted when using artesunate rather than quinine was US$ 3.8 and the incremental cost per death averted was US$ 123 ($95% CI: 75336). The results for individual study sites are shown in Table 5.
Results were not sensitive to the parameters used in converting YLL and YLD to DALYs. Whether no discounting was applied or with a 10% discount value; with either global or local life expectancy estimates; and with and without the age modulation, the incremental cost-effectiveness ratio varied between US$ 2.9 and US$ 4.3 per DALY averted.
A threshold analysis determined that, assuming even a conservative willingness to pay of US$ 150 per DALY averted, artesunate could cost up to US$ 105 per full treatment course before it ceased to be cost-effective. Although parenteral quinine is cheap, it comprises only a small fraction of the total costs of inpatient care. Even if quinine were obtained at no cost, this would not reverse the direction of the cost-effectiveness results. Fig. 2 illustrates the relatively tight distribution for total cost of care which clustered closely around the mean values and almost never approached the threshold value above which artesunate ceased to be cost-effective.
The probabilistic sensitivity analysis explored the uncertainty surrounding the cost and clinical outcomes observed in the trial. Fig. 3 shows the cost-effectiveness acceptability curve. At the very outset, when policy-makers are assumed not to be willing to pay anything for further health gains, the probability that either treatment would be cost-effective is almost equal at 50%. If, however, policy-makers are willing to pay up to US$ 25 for an additional DALY averted (the lowest benchmark commonly used in economic evaluation in the context of low income countries), artesunate appears to be more cost-effective with a probability of almost 80%. This probability exceeds 95% as the willingness to pay increases to the next commonly used threshold of US$ 150.
The predicted impact on the study hospital annual budgets of switching from parenteral quinine to artesunate is minimal, or even cost-saving (Table 6). Accounting for direct expenditure on drugs and other medical equipment, the impact ranged from an annual cost-saving of approximately US$ 500 in Korogwe to just under US$ 4000 in Nigeria. If overhead costs for inpatient care are included, the additional expenditure per annum in the Nigerian centre is much higher just over $16 000. This is due to the survival benefit conferred by artesunate and the high costs per inpatient day incurred in this tertiary teaching hospital.
This analysis shows that the cost of averting malaria-related deaths in sub-Saharan Africa by switching from quinine to artesunate was extremely low, with a mean value of US$ 123 per death averted. The results are similar to the incremental cost per death averted in adult Asian patients, which was estimated as US$ 148. Similarly, the cost per DALY averted with artesunate was only US$ 3.8, far below any of the commonly used willingness-to-pay thresholds. The cost-effectiveness acceptability curve suggested that the probability of artesunate being cost-effective is approximately 50% without any additional investment, and exceeded 95% at a willingness to pay of US$ 150. This compares very favourably with other interventions, such as the use of insecticide-treated nets, with a cost per death averted of US$ 254 to US$ 3437.23 In addition, provided the drug is available, the use of artesunate is relatively easy to implement in any hospital setting.
While cost-effectiveness is an informative criterion for policy-makers considering the adoption of a new intervention, affordability must also be demonstrated, particularly in the highly constrained health systems present in many sub-Saharan African countries. The large number of malaria admissions implies that any change in treatment strategies could have a substantial impact on frail health systems. We have demonstrated that the use of artesunate is not only highly cost-effective but also entirely affordable, having a minimal impact on hospital budgets and in some instances being cost-saving. Even if the proportion of severe malaria cases reaching health facilities were to increase, this would most likely remain an affordable intervention.
The analysis was carried out from the provider perspective, although inclusion of household costs would have had either no impact or would have favoured artesunate further. A broader societal perspective might also have accounted for the possibility of artemisinin resistance emerging following widespread use of artesunate.24 This was not considered a high priority, as parenteral artesunate is provided only to patients with severe illness a small fraction of the total number of antimalarial treatments used every year. Furthermore, almost all patients treated for severe malaria receive an effective oral combination therapy following treatment with the parenteral drug, reducing the likelihood of the development of resistance.25
We did not include the nursing time associated with administrating drugs. We also excluded the cost of consumables such as syringes, needles, cannulas and infusion sets because of the difficulty in collecting these reliably and their relatively low cost. Both these labour and consumables costs are likely to be marginally higher with quinine than artesunate, because quinine is given 3 times per day and as an infusion requires extra consumables and careful monitoring. Their inclusion would therefore further enhance the cost-effectiveness of artesunate. Reducing nursing time can improve the care for other patients and in the long run could have a potential impact on hospital budgets.
The costs of changing drug policy were excluded, but as a one-off cost spread over the expected lifetime of the policy change, the impact on the incremental cost-effectiveness ratio would be minimal. In some instances patient charges were used as proxies for costs. In practice, charges may not reflect actual economic costs. This has no effect on the incremental cost-effectiveness ratio as these items, mostly laboratory tests, were equally distributed in the trial arms.
There were several methodological limitations. While the use of DALYs allows for comparison of cost-effectiveness estimates for different health conditions and interventions, it is not without its limitations.19,26,27 The use of age modulation, discounting, and global life expectancies has been criticized. In this analysis we chose to adopt those There was some variation in health test for between-site heterogeneity and methods and values that would imply the outcomes and costs between the differ-no significant variation was found. We most conservative results in terms of the ent sites, and therefore in their respective therefore used the pooled estimate for cost-effectiveness of artesunate. All these incremental cost-effectiveness ratios. clinical outcomes in our analysis. The parameters were tested in the sensitivity The trial was powered to capture differ-main driver for the difference in costs was analysis and showed only a minor impact ences in effectiveness by pooling all sites. the overhead cost for inpatient stay, which on the results. The main clinical analysis did, however, was derived from the WHO-CHOICE framework rather than the primary costing of hospital overheads. Differences in overhead expenditure, however, are not as immediately affected by the choice of treatment as the variable expenditure on drugs and medical resources, and would materialize only when hospitals adjust their overhead expenditure to any changes in inpatient throughput.
With this analysis we show that artesunate is effective, cost-effective and affordable, which stands as evidence to support its use in children with severe malaria in Africa.
The parenteral artesunate currently available on the market and used in this study does not yet have international drug regulatory authority registration, but WHO pre-qualification of the Chinese product was recently approved and the drug is licensed for use in many malariaendemic countries and can be purchased with funds from the Global Fund to Fight AIDS, Tuberculosis and Malaria. A new formulation may be registered in the near future28 and could be more expensive. However, this analysis has shown that even if the cost of artesunate were substantially higher, it would remain a cost-effective option.
We would like to thank the hospital staff in Ilorin, Korogwe, Muheza and Mbarara for assisting with the collection of cost data and patient resource use. We appreciate the excellent workby Tharisara Sakulthaew and by the data management team, Montri Ridjaibun, Nuttapol Panachuenwongsakul and Thatsanun Ngernseng in MORU. We would also like to thank Anne Mills, Martina Oneko, Bridget Wills, Ben Amos, Dr Olanrewaju Timothy Adedoyin, Dr Ashau O Timi-Oladipo, Stella Kabela, Laura Chuwa, Haki Msangi and Hugh Reyburn for their input.
Funding: This trial was supported by grants 076908 and 082541 from the Wellcome Trust and was coordinated as part of the Wellcome Trust Mahidol University Oxford Tropical Medicine Research Programme funded by the Wellcome Trust of Great Britain.
Competing interests: None declared.
1. Okell LC, Drakeley CJ, Ghani AC, Bousema T, Sutherland CJ. Reduction of transmission from malaria patients by artemisinin combination therapies: a pooled analysis of six randomized trials. Malar J 2008;7:125. doi: 10.1186/1475-2875-7-125 PMID:18613962 [ Links ]
2. Gosling RD, Drakeley CJ, Mwita A, Chandramohan D. Presumptive treatment of fever cases as malaria: help or hindrance for malaria control? Malar J 2008;7:132. doi:10.1186/1475-2875-7-132 PMID:18631377 [ Links ]
3. Crawley J, Chu C, Mtove G, Nosten F. Malaria in children. Lancet 2010;375:146881. doi:10.1016/S0140-6736(10)60447-3 PMID: 20417858 [ Links ]
4. Ayieko P, Akumu AO, Griffiths UK, English M. The economic burden of inpatient paediatric care in Kenya: household and provider costs for treatment of pneumonia, malaria and meningitis. Cost Eff Resour Alloc 2009;7:3. doi:10.1186/1478-7547-7-3 PMID:19161598 [ Links ]
5. Nadjm B, Amos B, Mtove G, Ostermann J, Chonya S, Wangai H et al. WHO guidelines for antimicrobial treatment in children admitted to hospital in an area of intense Plasmodium falciparum transmission: prospective study. BMJ 2010;340:c1350. doi:10.1136/bmj.c1350 PMID:20354024 [ Links ]
6. World malaria report 2009. Geneva: World Health Organization; 2009. [ Links ]
7. World health statistics. Geneva: World Health Organization; 2010. [ Links ]
8. Lubell Y, Mills AJ, Whitty CJ, Staedke SG. An economic evaluation of home management of malaria in Uganda: an interactive Markov model. PLoS ONE 2010;5:e12439. doi:10.1371/journal.pone.0012439 PMID:20805977 [ Links ]
9. International drug price indicator guide. Cambridge: Management sciences for health; 2009. Available from: http://erc.msh.org/dmpguide/index.cfm?language=English&action=newyear&display=yes&module=dmp&year=2009. [accessed 14 April 2011] [ Links ].
10. Lubell Y, Yeung S, Dondorp AM, Day NP, Nosten F, Tjitra E et al. Costeffectiveness of artesunate for the treatment of severe malaria. Trop Med Int Health 2009;14:3327. doi:10.1111/j.1365-3156.2009.02227.x PMID: 19187518 [ Links ]
11. Yen LM, Dao LM, Day NP, Waller DJ, Bethell DB, Son LH et al. Role of quinine in the high mortality of intramuscular injection tetanus. Lancet 1994;344:7867. doi:10.1016/S0140-6736(94)92342-6 PMID:7916074 [ Links ]
12. Dondorp A, Nosten F, Stepniewska K, Day N, White N; South East Asian Quinine Artesunate Malaria Trial (SEAQUAMAT) group. Artesunate versus quinine for treatment of severe falciparum malaria: a randomised trial. Lancet 2005;366:71725. doi:10.1016/S0140-6736(05)67176-0 PMID:16125588 [ Links ]
13. Dondorp AM, Fanello CI, Hendriksen IC, Gomes E, Seni A, Chhaganlal KD et al.; AQUAMAT group. Artesunate versus quinine in the treatment of severe falciparum malaria in African children (AQUAMAT): an open-label, randomised trial. Lancet 2010;376:164757. doi:10.1016/S0140-6736(10)61924-1 PMID: 21062666 [ Links ]
14. Investing in health research and development: report of the ad hoc committee in health research relating to future interventions options. Geneva: World Health Organization; 1996. [ Links ]
15. World development report. Washington: The World Bank; 1993. [ Links ]
16. Choosing interventions that are cost-effective: country specific costs [Internet database]. Geneva: World Health Organization; 2008. Available from: http://www.who.int/choice/country/en/index.html#G [accessed 14 April 2011] [ Links ].
17. Consumer price indexes for 2006-2009 [Internet database]. UNDATA; 2010 Available from: http://data.un.org/Data.aspx?q=consumer+price+index+tanzania&d=IFS&f=SeriesCode%3a64%3bCountryCode%3a738 [accessed 14 April 2011] [ Links ].
18. Official average period exchange rates from local currency units to USD [Internet database]. Washington: The World Bank; 2010. Available from: http://data.worldbank.org/indicator/PA.NUS.FCRF [accessed 14 April 2011] [ Links ].
19. Fox-Rushby JA. Disability adjusted life years (DALYs) for decision-making? an overview of the literature. London: Office of Health Economics; 2002. [ Links ]
20. Drummond MF, O'Brien B, Stoddart GL, Torrance GW, Sculpher MJ. Methods for the economic evaluation of health care programmes. 3rd ed. Oxford: Oxford University Press; 2005. [ Links ]
21. Global burden of disease 2004 update: disability weights for diseases and conditions. Geneva: World Health Organization; 2004. [ Links ]
22. Morris S, Devlin N, Parkin D. Economic analysis in health care. John Wiley & Sons Ltd; 2007. [ Links ]
23. Mulligan J, Morel C, Mills A. The cost-effectiveness of malaria control interventions. Bethesda: Disease Control Priorities Project; 2005. [ Links ]
24. Pongtavornpinyo W, Yeung S, Hastings IM, Dondorp AM, Day NP, White NJ. Spread of anti-malarial drug resistance: mathematical model with implications for ACT drug policies. Malar J 2008;7:229. doi:10.1186/1475 2875-7-229 PMID:18976503 [ Links ]
25. White LJ, Maude RJ, Pongtavornpinyo W, Saralamba S, Aguas R, Van Effelterre T et al. The role of simple mathematical models in malaria elimination strategy design. Malar J 2009;8:212. doi:10.1186/1475-2875 8-212 PMID:19747403 [ Links ]
26. Arnesen T, Kapiriri L. Can the value choices in DALYs influence global priority-setting? Health Policy 2004;70:13749. doi:10.1016/j. healthpol.2003.08.004 PMID:15364144 [ Links ]
27. Lyttkens CH. Time to disable DALYs? On the use of disability-adjusted lifeyears in health policy. Eur J Health Econ 2003;4:195202. doi:10.1007/ s10198-003-0169-2 PMID:15609185 [ Links ]
28. Research pipeline [Internet]. Gaithersburg: Sigma-tau Pharmaceuticals, Inc. Available from: http://www.sigmatau.com/research/research_pipeline.asp. [accessed 14 April 2011] [ Links ].
(Submitted: 5 January 2011 Revised version received: 30 March 2011 Accepted: 30 March 2011 Published online: 28 April 2011)