Literature DB >> 18780786

Benefits of using multiple first-line therapies against malaria.

Maciej F Boni1, David L Smith, Ramanan Laxminarayan.   

Abstract

Despite the availability of many drugs and therapies to treat malaria, many countries' national policies recommend using a single first-line therapy for most clinical malaria cases. To assess whether this is the best strategy for the population as a whole, we designed an evolutionary-epidemiological modeling framework for malaria and compared the benefits of different treatment strategies in the context of resistance evolution. Our results show that the population-wide use of multiple first-line therapies (MFT) against malaria yields a better clinical outcome than using a single therapy or a cycling strategy where therapies are rotated, either on a fixed cycling schedule or when resistance levels or treatment failure become too high. MFT strategies also delay the emergence and slow the fixation of resistant strains (phenotypes), and they allow a larger fraction of the population to be treated without trading off future treatment of cases that may be untreatable because of high resistance levels. Earlier papers have noted that cycling strategies have the disadvantage of creating a less temporally variable environment than MFT strategies, making resistance evolution easier for the parasite. Here, we illustrate a second feature of parasite ecology that impairs the performance of cycling policies, namely, that cycling policies degrade the mean fitness of the parasite population more quickly than MFT policies, making it easier for new resistant types to invade and spread. The clinical benefits of using multiple first-line therapies against malaria suggest that MFT policies should play a key role in malaria elimination and control programs.

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Year:  2008        PMID: 18780786      PMCID: PMC2544604          DOI: 10.1073/pnas.0804628105

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  36 in total

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  57 in total

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Review 4.  PfCRT and its role in antimalarial drug resistance.

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Review 6.  Antimalarial drug policy in India: past, present & future.

Authors:  Anupkumar R Anvikar; Usha Arora; G S Sonal; Neelima Mishra; Bharatendu Shahi; Deepali Savargaonkar; Navin Kumar; Naman K Shah; Neena Valecha
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7.  Probability of emergence of antimalarial resistance in different stages of the parasite life cycle.

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8.  Prospective strategies to delay the evolution of anti-malarial drug resistance: weighing the uncertainty.

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9.  Dihydroartemisinin-piperaquine and artemether-lumefantrine for treating uncomplicated malaria in African children: a randomised, non-inferiority trial.

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10.  The role of simple mathematical models in malaria elimination strategy design.

Authors:  Lisa J White; Richard J Maude; Wirichada Pongtavornpinyo; Sompob Saralamba; Ricardo Aguas; Thierry Van Effelterre; Nicholas P J Day; Nicholas J White
Journal:  Malar J       Date:  2009-09-14       Impact factor: 2.979

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