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Anti-Malaria Chemotherapy

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Presentation on theme: "Anti-Malaria Chemotherapy"— Presentation transcript:

1 Anti-Malaria Chemotherapy
Causal Prophylaxis prevent infection (ie, liver stage) Suppressive Prophylaxis prevent clinical disease (ie, blood stages) Treatment Therapy (or clinical cure) relieve symptoms eliminate blood stage parasites Curative Therapy (or radical cure) eliminate parasites w/o regard to symptoms Anti-Relapse Treatment eliminate hypnozoites

2 Selected Anti-Malarials

3 Treatment Strategies chloroquine sensitive (all species) chloroquine
CQ + primaquine (vivax/ovale) chloroquine resistance (or unknown) Fansidar, mefloquine, quinine, artemesin derivatives severe malaria i.v. infusion of quinine or quinidine (or CQ, if sensitive) i.v. artemisinin derivatives (if available)

4 Chemoprophylaxis recommended for transient visits to endemic areas
choice of drug depends on risk of malaria and degree of resistance in that area many non-toxic drugs of limited use because of resistance eg., choloroquine, pyrimethamine, proquanil presumptive (or ‘standby’) treatment carry Fansidar, mefloquine, quinine

5 Drug Action drugs function by interacting with a cellular 'target'
eg, protein, DNA, RNA, lipids many targets are enzymes (eg, inhibitors)

6 Selective Toxicity of Drugs
unique target in parasite food vacuole and chloroquine discrimination between host and parasite targets pyrimethamine and DHFR target is more important to parasite than host DNA synthesis (antifolates) drug activation by parasite anaerobes and nitroimidazoles greater drug accumulation by parasite

7 Antifolates and Nucleotide Metabolism
dihydrofolate is necessary co-factor for nucleotide (i.e., DNA) synthesis sulfadoxine inhibits folate synthesis (DHPS) parasite cannot salvage folates host only salvages pyrimethamine preferentially inhibits parasite DHFR

8

9 Drug Resistance defined by treatment failures rule out other factors:
non-compliance bad quality wrong dose vomiting 28-day or other tests (RI, RII, RIII levels of resistance)

10 Modified Protocol introduced by WHO in 1996 based on clinical outcome:
adequate clinical response (ACR) late treatment failure (LTF) early treatment failure (ETF) more practical in areas of intense transmission difficult to distinguish re-infection from recrudescense parasitemia in the absence of clinical symptoms is common ACR no recrudescence by day 14 LTF recrudescence during days 4-14 ETF persistence during days 1-3

11 Drug Resistance Mechanisms
mutations in target gene  production of target  drug accumulation (includes  efflux) drug inactivation Drug Gene Major Mutations Fansidar DHPS A437G (K540E, A581G) DHFR S108N (N51I, C59R, I164L) Chloroquine CRT K76T MDR1 N86Y

12 Factors Contributing to Development and Spread of Drug Resistance
self treatment poor compliance mass administration long drug half-life high transmission intensity

13 Spread of Chloroquine Resistance
slow to emerge spread rapidly probably multigenic


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