Literature DB >> 7573718

Parasite viability during treatment of severe falciparum malaria: differential effects of artemether and quinine.

S Murphy1, W M Watkins, P G Bray, B Lowe, P A Winstanley, N Peshu, K Marsh.   

Abstract

The effect of artemether (AR) and quinine (QN) on parasite viability ex vivo was compared in children being treated for severe Plasmodium falciparum malaria. Parasitized blood taken at intervals during treatment was cultured in vitro, and parasite development was assessed microscopically. Parasite viability (defined as the proportion of circulating rings developing to early schizonts) was 56.8% in the AR group (n = 7) 6 hr after the start of treatment, compared with 93.3% for QN (n = 6; P = 0.015). Even after 24 hr of QN treatment, parasite viability was not significantly reduced in five patients. These ex vivo findings, which confirm previous observations of the stage-specific effects of these drugs against P. falciparum, suggest that AR may be superior to QN in the treatment of severe malaria.

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Year:  1995        PMID: 7573718     DOI: 10.4269/ajtmh.1995.53.303

Source DB:  PubMed          Journal:  Am J Trop Med Hyg        ISSN: 0002-9637            Impact factor:   2.345


  7 in total

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Journal:  Antimicrob Agents Chemother       Date:  2013-04-22       Impact factor: 5.191

Review 2.  Clinical pharmacology and therapeutic potential of artemisinin and its derivatives in the treatment of malaria.

Authors:  P J de Vries; T K Dien
Journal:  Drugs       Date:  1996-12       Impact factor: 9.546

3.  Population pharmacokinetics of artemether and dihydroartemisinin following single intramuscular dosing of artemether in African children with severe falciparum malaria.

Authors:  Sadik Mithwani; Leon Aarons; Gilbert O Kokwaro; Oneeb Majid; Simon Muchohi; Geoffrey Edwards; Sumia Mohamed; Kevin Marsh; William Watkins
Journal:  Br J Clin Pharmacol       Date:  2004-02       Impact factor: 4.335

4.  Artesunate versus quinine in the treatment of severe falciparum malaria in African children (AQUAMAT): an open-label, randomised trial.

Authors:  Arjen M Dondorp; Caterina I Fanello; Ilse C E Hendriksen; Ermelinda Gomes; Amir Seni; Kajal D Chhaganlal; Kalifa Bojang; Rasaq Olaosebikan; Nkechinyere Anunobi; Kathryn Maitland; Esther Kivaya; Tsiri Agbenyega; Samuel Blay Nguah; Jennifer Evans; Samwel Gesase; Catherine Kahabuka; George Mtove; Behzad Nadjm; Jacqueline Deen; Juliet Mwanga-Amumpaire; Margaret Nansumba; Corine Karema; Noella Umulisa; Aline Uwimana; Olugbenga A Mokuolu; Olanrewaju T Adedoyin; Wahab B R Johnson; Antoinette K Tshefu; Marie A Onyamboko; Tharisara Sakulthaew; Wirichada Pan Ngum; Kamolrat Silamut; Kasia Stepniewska; Charles J Woodrow; Delia Bethell; Bridget Wills; Martina Oneko; Tim E Peto; Lorenz von Seidlein; Nicholas P J Day; Nicholas J White
Journal:  Lancet       Date:  2010-11-07       Impact factor: 79.321

5.  The parasite clearance curve.

Authors:  N J White
Journal:  Malar J       Date:  2011-09-22       Impact factor: 2.979

6.  Population pharmacokinetics of intravenous artesunate: a pooled analysis of individual data from patients with severe malaria.

Authors:  S G Zaloumis; J Tarning; S Krishna; R N Price; N J White; T M E Davis; J M McCaw; P Olliaro; R J Maude; P Kremsner; A Dondorp; M Gomes; K Barnes; J A Simpson
Journal:  CPT Pharmacometrics Syst Pharmacol       Date:  2014-11-05

7.  Open-label comparative clinical study of chlorproguanil-dapsone fixed dose combination (Lapdap) alone or with three different doses of artesunate for uncomplicated Plasmodium falciparum malaria.

Authors:  Daniel G Wootton; Hyginus Opara; Giancarlo A Biagini; Maxwell K Kanjala; Stephan Duparc; Paula L Kirby; Mary Woessner; Colin Neate; Maggie Nyirenda; Hannah Blencowe; Queen Dube-Mbeye; Thomas Kanyok; Stephen Ward; Malcolm Molyneux; Sam Dunyo; Peter A Winstanley
Journal:  PLoS One       Date:  2008-03-05       Impact factor: 3.240

  7 in total

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