Open Access
Short Note
Volume 26, 2019
Article Number 16
Number of page(s) 3
Published online 22 March 2019

© A.-L. Bienvenu et al., published by EDP Sciences, 2019

Licence Creative Commons
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Drug stewardship is an activity that includes appropriate selection, dosing, route, and duration of therapy. Its primary goal is to optimize clinical outcomes while minimizing unintended consequences of drug use, including toxicity, selection of pathogenic organisms, and the emergence of resistance. Antimicrobial stewardship programs have been widely implemented with significant impact in the fight against infectious diseases caused by multiple organisms, including bacteria [6] and fungi [1]. Parasites are also responsible for lethal diseases and have a significant impact on the exposed populations. Among parasitic infections, malaria caused 435,000 deaths in 2017, making it the most deadly [8]. The fight against malaria is facing many challenges, including the continued emergence of parasite resistance to antimalarial drugs [5]. Monitoring the efficacy of drugs has been a continuous activity for researchers, National Malaria Programs, and international organizations such as the World Health Organization (WHO) and more specifically the World Wide Antimalarial Resistance Network (WWARN). Malaria was therefore included in the WHO 2030 Agenda for Sustainable Development. This declaration called for strategies to begin to reverse the global incidence of malaria. A novel approach to combat malaria in a world where nearly half of the population is at risk of malaria is antimalarial stewardship. Antimalarial stewardship programs (AMSPs) should be hospital-based, implemented at the local level, and adapted to local conditions with the objective of increasing the frequency of correct prescribing of antimalarial drugs. It requires local leadership commitment and high flexibility in implementation [2].

Why are AMSPs needed in malaria-endemic areas?

  1. Because progress in global malaria control has stalled.

According to WHO’s latest World malaria report, an estimated 219 million cases of malaria occurred worldwide in 2017, compared with 217 million cases in 2016; the estimated number of deaths from malaria was 435,000, compared to 451,000 in 2016 [8]. During this period, mortality rates stalled in South-East Asia, the Western Pacific and Africa, and increased in the Eastern Mediterranean and the Americas [8].

  1. Because management is not equal for all cases

According to WHO, malaria case management consists of prompt diagnosis and effective treatment, a vital component of malaria control and elimination strategies [7]. However, antimalarial treatments are still often initiated without confirmation of diagnosis, leading to unnecessary antimalarial selective pressure. Rapid diagnostic tests are implemented in most healthcare centers, but are not always used for treatment decision-making. Moreover, although protocols for effective treatment do exist they are not always updated in all malaria-endemic countries, and recommended drugs may not be available. The use of combination therapy and weight-based dosing, ensuring optimal exposure of patients to drugs, are of particular importance to ensure treatment effectiveness.

  1. Because incorrect dosing is frequent

Treatment compliance is difficult, particularly for patients who do not have easy access to healthcare facilities or who are not aware of the consequences of this. Furthermore, weight-based dosing is not always carried out and may be a contributor to suboptimal dosing. Counterfeit and substandard antimalarial drugs, that contain no active ingredient, less than the required amount, or ingredients not described on the package, are also responsible for under- or over-dosing.

  1. Because toxicity may occur

Over-dosing may lead to antimalarial toxicity in patients, but some toxicities are related to patient genotypes; for example, primaquine causes predictable oxidant hemolysis in those with glucose 6-phosphate dehydrogenase deficiency, for whom a specific drug regimen is required [7].

  1. Because antimalarial resistance is increasing

Resistance poses one of the greatest threats to malaria control and is responsible for increased malaria-related morbidity and mortality. Under-dosing of antimalarial drugs contributes in part to an increase in resistance. This threat is particularly alarming as the use of artemisinin-based combination therapy, the gold standard antimalarial, was demonstrated to be associated with slow parasitic clearance in South-East Asia [4].

  1. Because we are on the way towards malaria elimination

The main objective of AMSPs should be resistance containment, which is essential for malaria eradication. AMSPs will therefore contribute to the elimination process.

Implementing AMSPs in endemic countries is ambitious, but not overwhelming. Antimalarial treatments should be considered differently at the international, national and local levels. Experts from international organizations are highly committed to the preparation and dissemination of guidelines defining the best way to treat patients with malaria. These guidelines are taken into account at the national level, mostly by the National Malaria Programs or equivalents under the supervision of the Ministry of Health. These national bodies define the first and second line treatments for the country, according to international recommendations, and national consideration in terms of market or procurement.

The local level is diverse since malaria treatments are given from the public sector, the private sector, and not-for-profit providers. Physicians and pharmacists may face other challenges such as interruption in the supply chain, fake drugs, and drugs not following national health policies. These problems may be responsible for periodic drifts in malaria treatment, leading to a high risk of misuse of drugs for various periods of time in limited and disperse areas. These unpredictable events may be under the radar of national and international bodies, leading to uncontrolled drug exposure of parasites. This is the main reason why AMSPs are urgently needed. AMSPs are the only tool to limit the frequent drifts or misuses of antimalarial drugs.

As recommended by the US Centers for Disease Control and Prevention [1], leadership commitment is a core element and needs to be achieved in each level; AMSP leaders should be responsible for dissemination of key messages targeting physicians and pharmacists, and training of medicine and pharmacy students in line with identified policy challenges. Strengthening the link between physicians and pharmacists with the goal of optimizing antimalarial treatment is also expected to be a substantial part of AMSPs. Moreover, international collaborations will be beneficial to AMSP implementation, as should be the involvement of public health authorities [3]. AMSPs are expected to be well perceived at the population level: populations are aware of the disease’s severity and there is a collective interest in malaria eradication. Education of the population through stewardship leaders would be a vital part of the success of AMSPs.

Local AMSPs will succeed and have a significant impact if there is a close relationship between AMCPs and Ministries of Health. These bodies will receive information from AMSP leaders about the on-going situation at the local level, and they can act at the national level to address the issues detected by field workers specifically involved in stewardship programs. This link is essential for the sustainability of AMSPs.

More generally, we could also expect that AMSP implementation will bring new expertise to healthcare personnel involved in the field of parasitic diseases, which will contribute positively to efforts made to control other parasitic diseases, including neglected tropical diseases such as Chagas disease, schistosomiasis, and soil-transmitted parasitic diseases.


This work is dedicated to the memory of Late Professor Ogobara Doumbo.

Competing interests

The authors declare that they have no competing interests.


  1. Bienvenu AL, Argaud L, Aubrun F, Fellahi JL, Guerin C, Javouhey E, Piriou V, Rimmele T, Chidiac C, Leboucher G. 2018. A systematic review of interventions and performance measures for antifungal stewardship programmes. Journal of Antimicrobial Chemotherapy, 73(2), 297–305. [CrossRef] [Google Scholar]
  2. CDC. 2014. Core elements of hospital antibiotic stewardship programs. Atlanta, GAUS Department of Health and Human Services, CDC. Available from: [Google Scholar]
  3. Goff DA, Kullar R, Goldstein EJC, Gilchrist M, Nathwani D, Cheng AC, Cairns KA, Escandón-Vargas K, Villegas MV, Brink A, van den Bergh D, Mendelson M. 2017. A global call from five countries to collaborate in antibiotic stewardship: united we succeed, divided we might fail. Lancet Infectious Diseases, 17, 56–63. [CrossRef] [Google Scholar]
  4. Imwong M, Suwannasin K, Kunasol C, Sutawong K, Mayxay M, Rekol H, Smithuis FM, Hlaing TM, Tun KM, van der Pluijm RW, Tripura R, Miotto O, Menard D, Dhorda M, Day NPJ, White NJ, Dondorp AM. 2017. The spread of artemisinin-resistant Plasmodium falciparum in the Greater Mekong subregion: a molecular epidemiology observational study. Lancet Infectious Diseases, 17(5), 491–497. [CrossRef] [Google Scholar]
  5. Ouji M, Augereau JM, Paloque L, Benoit-Vical F. 2018. Plasmodium falciparum resistance to artemisinin-based combination therapies: A sword of Damocles in the path toward malaria elimination. Parasite, 25, 24. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  6. Pasay DK, Guirguis MS, Shkrobot RC, Slobodan JP, Wagg AS, Sadowski CA, Conly JM, Saxinger LM, Bresee LC. 2019. Antimicrobial stewardship in rural nursing homes: Impact of interprofessional education and clinical decision tool implementation on urinary tract infection treatment in a cluster randomized trial. Infection Control & Hospital Epidemiology, 20, 1–6. [CrossRef] [Google Scholar]
  7. World Health Organization, Geneva. 2015. Guidelines for the treatment of malaria, 3rd edition. Available from: [Google Scholar]
  8. World Health Organization, Geneva. 2018. World malaria report 2018. Available from [Google Scholar]

Cite this article as: Bienvenu A.-L., Djimdé A & Picot S. 2019. Antimalarial stewardship programs are urgently needed for malaria elimination: a perspective. Parasite 26, 16.

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.