Antimalarial medication

Antimalarial medications or simply antimalarials are a type of antiparasitic chemical agent, often naturally derived, that can be used to treat or to prevent malaria, in the latter case, most often aiming at two susceptible target groups, young children and pregnant women.[1] As of 2018, modern treatments, including for severe malaria, continued to depend on therapies deriving historically from quinine and artesunate, both parenteral (injectable) drugs, expanding from there into the many classes of available modern drugs.[1] Incidence and distribution of the disease ("malaria burden") is expected to remain high, globally, for many years to come; moreover, known antimalarial drugs have repeatedly been observed to elicit resistance in the malaria parasite—including for combination therapies featuring artemisinin, a drug of last resort, where resistance has now been observed in Southeast Asia.[1] As such, the needs for new antimalarial agents and new strategies of treatment (e.g., new combination therapies) remain important priorities in tropical medicine.[1] As well, despite very positive outcomes from many modern treatments, serious side effects can impact some individuals taking standard doses (e.g., retinopathy with chloroquine, acute haemolytic anaemia with tafenoquine).[2][3][1]

Specifically, antimalarial drugs may be used to treat malaria in three categories of individuals, (i) those with suspected or confirmed infection, (ii) those visiting a malaria-endemic regions who have no immunity, to prevent infection via malaria prophylaxis, and (iii) or in broader groups of individuals, in routine but intermittent preventative treatment in regions where malaria is endemic via intermittent preventive therapy.[not verified in body] Practice in treating cases of malaria is most often based on the concept of combination therapy[verification needed] (e.g., using agents such as artemether and lumefantrine against chloroquine-resistant Plasmodium falciparum infection[verification needed][4]), since this offers advantages including reduced risk of treatment failure, reduced risk of developed resistance, as well as the possibility of reduced side-effects.[not verified in body] Prompt parasitological confirmation by microscopy, or alternatively by rapid diagnostic tests, is recommended in all patients suspected of malaria before treatment is started.[5][page needed] Treatment solely on the basis of clinical suspicion is considered when a parasitological diagnosis is not possible.[5][page needed]

Anti-malaria aid campaigns have a globally positive impact for health outcomes and beyond.[6]

  1. ^ a b c d e Ashley, Elizabeth A.; Phyo, Aung Pyae (25 May 2018). "Drugs in Development for Malaria". Drugs. 78 (9): 861–879. doi:10.1007/s40265-018-0911-9. PMC 6013505. PMID 29802605.
  2. ^ Mittra, Robert A.; Mieler, William F. (2013). "Drug Toxicity of the Posterior Segment". Retina. pp. 1532–1554. doi:10.1016/B978-1-4557-0737-9.00089-8. ISBN 978-1-4557-0737-9.
  3. ^ "Updating the WHO G6PD classification of variants and the International Classification of Diseases" (PDF). www.who.int. 2019. Retrieved 2020-03-24.
  4. ^ Prevention, CDC-Centers for Disease Control and (2023-06-28). "CDC - Malaria - Diagnosis & Treatment (United States) - Treatment (U.S.) - Guidelines for Clinicians (Part 1)". www.cdc.gov. Retrieved 2023-09-12.
  5. ^ a b Cite error: The named reference WHO Guidelines was invoked but never defined (see the help page).
  6. ^ Kuecken, Maria; Thuilliez, Josselin; Valfort, Marie-Anne (2020). "Disease and Human Capital Accumulation: Evidence from the Roll Back Malaria Partnership in Africa". The Economic Journal. 131 (637): 2171–2202. doi:10.1093/ej/ueaa134.