CHLOROQUINE-RESISTANT PLASMODIUM VIVAX MALARIA IN PERU

Reports from several sites in South America suggest the presence of isolated cases of chloroquine-resistant Plasmodium vivax malaria. To investigate the possibility of chloroquine-resistant P. vivax in Peru, we conducted 28-day in vivo drug efficacy trials at three sites in the Amazon region and one...

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Veröffentlicht in:The American journal of tropical medicine and hygiene 2003-11, Vol.69 (5), p.548-552
Hauptverfasser: RUEBUSH, TRENTON K., II, ZEGARRA, JORGE, CAIRO, JAVIER, ANDERSEN, ELLEN M, GREEN, MICHAEL, PILLAI, DYLAN R, MARQUINO, WILMER, HUILCA, MARIA, AREVALO, ERNESTO, GARCIA, CORALITH, SOLARY, LELY, KAIN, KEVIN C
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container_issue 5
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container_title The American journal of tropical medicine and hygiene
container_volume 69
creator RUEBUSH, TRENTON K., II
ZEGARRA, JORGE
CAIRO, JAVIER
ANDERSEN, ELLEN M
GREEN, MICHAEL
PILLAI, DYLAN R
MARQUINO, WILMER
HUILCA, MARIA
AREVALO, ERNESTO
GARCIA, CORALITH
SOLARY, LELY
KAIN, KEVIN C
description Reports from several sites in South America suggest the presence of isolated cases of chloroquine-resistant Plasmodium vivax malaria. To investigate the possibility of chloroquine-resistant P. vivax in Peru, we conducted 28-day in vivo drug efficacy trials at three sites in the Amazon region and one site on the northern Pacific Coast between 1998 and 2001. A total of 242 patients between the ages of 2 and 60 years were enrolled (177 from the Amazon region and 65 from the northern coast). All subjects received directly observed therapy with chloroquine, 25 mg/kg, over a three-day period. On enrollment, 49% had a documented fever and 96% had a history of fever; their geometric mean parasite density was 5,129 parasites/microL. A total of 212 (88%) of the 242 subjects completed their 28-day follow-up. Four of the 177 patients from the Amazon region had a recurrence of P. vivax parasitemia on days 21 and 28 after treatment was initiated. Two of these patients had chloroquine-resistant infections, based on polymerase chain reaction-single-stranded conformational polymorphism genotyping and chloroquine-desethylchloroquine blood levels, which were > or = 97 ng/mL at the time of the reappearance of parasitemia. None of the subjects studied on the northern Pacific Coast had recurrent parasitemia.
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Two of these patients had chloroquine-resistant infections, based on polymerase chain reaction-single-stranded conformational polymorphism genotyping and chloroquine-desethylchloroquine blood levels, which were &gt; or = 97 ng/mL at the time of the reappearance of parasitemia. None of the subjects studied on the northern Pacific Coast had recurrent parasitemia.</abstract><cop>Lawrence, KS</cop><pub>ASTMH</pub><pmid>14695094</pmid><doi>10.4269/ajtmh.2003.69.548</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
Animals
Antimalarials - pharmacology
Biological and medical sciences
Child
Child, Preschool
Chloroquine - pharmacology
DNA, Protozoan - analysis
Drug Resistance
Female
Human protozoal diseases
Humans
Infectious diseases
Malaria
Malaria, Vivax - epidemiology
Malaria, Vivax - parasitology
Malaria, Vivax - pathology
Male
Medical sciences
Middle Aged
parasitemia
Parasitic diseases
Peru - epidemiology
Plasmodium vivax
Plasmodium vivax - drug effects
Plasmodium vivax - genetics
Polymerase Chain Reaction
Protozoal diseases
Recurrence
title CHLOROQUINE-RESISTANT PLASMODIUM VIVAX MALARIA IN PERU
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