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Quinine pharmacokinetic-pharmacodynamic relationships in uncomplicated falciparum malaria.

Abstract:
The relationships between the pharmacokinetic properties of quinine during a 7-day treatment course and the therapeutic response were studied in 30 adult patients with uncomplicated falciparum malaria monitored for > or = 28 days. All patients received a 7-day oral quinine regimen either alone (n = 22) or in combination with rifampin (n = 8). The median fever clearance time was 58.5 h, and the mean +/- standard deviation parasite clearance time was 73 +/- 24 h. After recovery, six patients had recrudescences of Plasmodium falciparum malaria and seven had delayed appearances of P. vivax infection between days 16 and 23. Between the patients with and without recrudescences, there were no significant differences either in fever clearance time or parasite clearance time or in the overall pharmacokinetics of quinine and 3-hydroxyquinine. Patients for whom the area under the concentration-time curve from 3 to 7 days for quinine in plasma was <20 microg.day/ml had a relative risk of 5.3 (95% confidence interval = 1.6 to 17.7) of having a subsequent recrudescence of infection (P = 0.016). Modeling of these data suggested an average minimum parasiticidal concentration of quinine in plasma of 3.4 microg/ml and an MIC of 0.7 microg/ml for uncomplicated falciparum malaria in Thailand. To ensure a cure, the minimum parasiticidal concentration must be exceeded during four asexual cycles (>6 days).
Publication status:
Published

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Publisher copy:
10.1128/aac.47.11.3458-3463.2003

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Journal:
Antimicrobial agents and chemotherapy More from this journal
Volume:
47
Issue:
11
Pages:
3458-3463
Publication date:
2003-11-01
DOI:
EISSN:
1098-6596
ISSN:
0066-4804


Language:
English
Keywords:
Pubs id:
pubs:38813
UUID:
uuid:0c5036a2-7409-4a9d-9c1d-5aa264c5a023
Local pid:
pubs:38813
Source identifiers:
38813
Deposit date:
2012-12-19
ARK identifier:

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