| 25 Avril 2013
 GENEVA/ PHNOM PENH, Cambodia ¦ 24 April 2013 - On  World Malaria Day, 25 April, the World Health Organization (WHO)  recognizes significant accomplishments in preventing and controlling  malaria, including in high-burden countries in sub-Saharan Africa, but  highlights the threat of antimalarial drug resistance in south-east  Asia’s Greater Mekong subregion, where an emergency response is now  being launched.   
 
 “In recent years endemic countries, including countries in sub-Saharan  Africa, have made major headway in reducing new cases and deaths from  malaria,” says Dr Hiroki Nakatani, WHO’s Assistant Director-General for  HIV, TB, Malaria and Neglected Tropical Diseases.  “But that progress  could now be at risk. We are increasingly concerned by signs in the  south-east Asia region that the malaria parasite is becoming resistant  to some of the drugs that have helped make so much progress.”
 
 Antimalarial drug resistance 
 
 Antimalarial drug resistance – the ability of the malaria parasite to  survive drugs – first became a global problem in the 1960s when the  parasite developed resistance to chloroquine, the then widely-used  antimalarial. Resistance first emerged in the Greater Mekong subregion  and later spread to Africa, triggering a dramatic increase in  malaria-related illness and death – particularly among children.
 
 Today the treatment of choice is artemisinin-based combination therapies  (ACTs).Resistance to artemisinins – the core component of the  combination – has now been identified in Cambodia, Myanmar, Thailand,  and Viet Nam. National efforts to contain resistance have had some  impact, but urgent action is needed to fully eliminate resistant strains  of the parasite and to ensure that ACTs remain effective.
 
 “The consequences of widespread resistance to artemisinins would be  catastrophic,” says Dr Robert Newman, Director of WHO’s Global Malaria  Programme. “We must act now to protect south-east Asia today and  sub-Saharan Africa tomorrow.”
 
 Although major efforts are under way to develop new classes of  antimalarials, there are no replacement products on the immediate  horizon.
 
 
 Scaled-up response in the Greater Mekong subregion 
 
 “We need to invest more in order to tackle drug resistance,” said Dr  Mark Dybul, Executive Director of the Global Fund to Fight AIDS,  Tuberculosis and Malaria.
 
 WHO is launching a new Emergency Response to Artemisinin Resistance in  Phnom Penh at an event hosted by the Cambodian Ministry of Health.  Building on WHO’s 2011 Global plan for artemisinin resistance  containment, as well as a multi-partner evaluation of containment  efforts to date, the emergency response framework will guide a major  scale-up of WHO-recommended strategies to combat this public health  threat.
 
 The framework urges affected countries to remove poor-quality  antimalarial drugs and oral artemisinin-based monotherapies from  circulation, as their use is compromising both the efficacy of  artemisinin and the drugs combined with them as part of ACTs. According  to WHO’s latest assessment this month, at least 31 companies around the  world are still marketing such monotherapies. Globally, 44 countries  have withdrawn marketing authorization for these pills, but 14 countries  continue to allow their marketing.
 
 “We are at a tipping point. What seems to be a localised threat could  easily get out of control and have serious implications for global  health,” said Dr Newman. “This response will require substantial  funding, a high level of political commitment, and strengthened regional  and cross-border collaboration.”
 
 The emergency response, which also includes the establishment of a WHO  regional hub in Phnom Penh to support containment efforts, has received  financial support from the Bill & Melinda Gates Foundation and  AusAID. In addition, the Global Fund to Fight AIDS, Tuberculosis and  Malaria has recently announced the allocation of US$ 100 million to  tackle this threat over the next three years.
 
 While these are significant steps forward, WHO currently estimates that  about US$ 300-350 million of additional funding would be required from  2013-2015 to fully scale up malaria control and containment activities  across affected countries in the Greater Mekong subregion.
 
 Global funding needs for malaria control
 
 In total, an estimated US$ 5.1 billion is needed every year between 2011  and 2020 to achieve universal access to malaria prevention, diagnostic  testing, and treatment around the world.  Although many countries have  increased domestic financing for malaria control, the total available  global funding remained at US$ 2.3 billion in 2011 – less than half what  is required. Many people still lack access to prevention measures –  such as mosquito nets and indoor residual spraying – and are unable to  obtain diagnostic testing and effective medicines to treat malaria  infection. Equally worryingly, there is a real danger that a recent  slowdown in mosquito net procurement could lead to resurgences and  outbreaks.
 
 Malaria is an entirely preventable and treatable vector-borne disease.  In 2012, malaria transmission occurred in 99 countries and territories  around the world, putting an estimated 3.3 billion people at risk of  illness. In 2010, an estimated 219 million cases occurred globally  (range: 154 to 289 million) while the disease killed an estimated 660  000 people (range: 490 000 to 836 000), mostly children under five years  of age.
 
Links:
 
 Emergency response to artemisinin resistance in the Greater Mekong subregion
 www.who.int/entity/malaria/publications/atoz/9789241505321/en/index.html
 
 World Malaria Report 2012
 http://www.who.int/malaria/publications/world_malaria_report_2012/en/index.html
 
 
 WHO factsheet on malaria
 http://www.who.int/mediacentre/factsheets/fs094/en/index.html
 
 
 Q&A on artemisinin resistance
 http://www.who.int/malaria/media/artemisinin_resistance_qa/en/index.html
 
 
 Q&A on the Global plan for insecticide resistance management
 http://www.who.int/malaria/media/insecticide_resistance_management_qa/en/index.html
 
 










