The epidemiology of malaria in a Karen population on the western border of Thailand.

From November 1991 to November 1992 a prospective, descriptive study of malaria epidemiology was conducted in a Karen population on the western border of Thailand. Two study groups were selected at random and more than 80% of the subjects were followed for one year. In Group 1, comprising 249 school...

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Main Authors: Luxemburger, C, Thwai, K, White, N, Webster, H, Kyle, D, Maelankirri, L, Chongsuphajaisiddhi, T, Nosten, F
Format: Journal article
Language:English
Published: 1996
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author Luxemburger, C
Thwai, K
White, N
Webster, H
Kyle, D
Maelankirri, L
Chongsuphajaisiddhi, T
Nosten, F
author_facet Luxemburger, C
Thwai, K
White, N
Webster, H
Kyle, D
Maelankirri, L
Chongsuphajaisiddhi, T
Nosten, F
author_sort Luxemburger, C
collection OXFORD
description From November 1991 to November 1992 a prospective, descriptive study of malaria epidemiology was conducted in a Karen population on the western border of Thailand. Two study groups were selected at random and more than 80% of the subjects were followed for one year. In Group 1, comprising 249 schoolchildren (aged 4-15 years), daily surveillance for illness was combined with fortnightly malaria surveys. These children experienced 1.5 parasitaemic infections per child-year (95% confidence interval [CI] 1.3-1.7), of which 68% (193/285) were symptomatic (Plasmodium falciparum 84%, P. vivax 57%). The estimated pyrogenic densities were 1460/microL for P. falciparum and 181/microL for P. vivax. In Group 2, comprising subjects of all age from 428 households, malaria was diagnosed during two-monthly surveys, at weekly home visits, and otherwise by passive case detection. Malaria and splenomegaly prevalence rates were low in all age groups (spleen index 2-9%; P. falciparum prevalence rate 1-4%; P. vivax 1-6%). Group 2 subjects had 1.0 infections per person-year (95% CI 0.9-1.1), most of which were symptomatic (312/357; 87%). Malaria infections clustered in households. Overall, P. vivax caused 53% and P. falciparum 37% of the infections (10% were mixed), but whereas P. vivax was most common in young children, with a decline in incidence with increasing age, P. falciparum incidence rates rose with age to a peak incidence between 20 and 29 years, although the risk of developing a severe malaria decreased with increasing age. There was no death from malaria during the study. P. falciparum infections were more common in males, subjects with a history of malaria before the study, and in those who had travelled outside their village. These findings suggest a higher transmission rate for P. vivax than P. falciparum, although adults still suffered symptomatic malaria due to both species. The 2 malaria parasites found in this area contribute approximately 50% of infections each, but their clinical epidemiology is very different.
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spelling oxford-uuid:c808ec39-098a-4731-ad55-d6957cc6700e2022-03-27T06:49:26ZThe epidemiology of malaria in a Karen population on the western border of Thailand.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:c808ec39-098a-4731-ad55-d6957cc6700eEnglishSymplectic Elements at Oxford1996Luxemburger, CThwai, KWhite, NWebster, HKyle, DMaelankirri, LChongsuphajaisiddhi, TNosten, FFrom November 1991 to November 1992 a prospective, descriptive study of malaria epidemiology was conducted in a Karen population on the western border of Thailand. Two study groups were selected at random and more than 80% of the subjects were followed for one year. In Group 1, comprising 249 schoolchildren (aged 4-15 years), daily surveillance for illness was combined with fortnightly malaria surveys. These children experienced 1.5 parasitaemic infections per child-year (95% confidence interval [CI] 1.3-1.7), of which 68% (193/285) were symptomatic (Plasmodium falciparum 84%, P. vivax 57%). The estimated pyrogenic densities were 1460/microL for P. falciparum and 181/microL for P. vivax. In Group 2, comprising subjects of all age from 428 households, malaria was diagnosed during two-monthly surveys, at weekly home visits, and otherwise by passive case detection. Malaria and splenomegaly prevalence rates were low in all age groups (spleen index 2-9%; P. falciparum prevalence rate 1-4%; P. vivax 1-6%). Group 2 subjects had 1.0 infections per person-year (95% CI 0.9-1.1), most of which were symptomatic (312/357; 87%). Malaria infections clustered in households. Overall, P. vivax caused 53% and P. falciparum 37% of the infections (10% were mixed), but whereas P. vivax was most common in young children, with a decline in incidence with increasing age, P. falciparum incidence rates rose with age to a peak incidence between 20 and 29 years, although the risk of developing a severe malaria decreased with increasing age. There was no death from malaria during the study. P. falciparum infections were more common in males, subjects with a history of malaria before the study, and in those who had travelled outside their village. These findings suggest a higher transmission rate for P. vivax than P. falciparum, although adults still suffered symptomatic malaria due to both species. The 2 malaria parasites found in this area contribute approximately 50% of infections each, but their clinical epidemiology is very different.
spellingShingle Luxemburger, C
Thwai, K
White, N
Webster, H
Kyle, D
Maelankirri, L
Chongsuphajaisiddhi, T
Nosten, F
The epidemiology of malaria in a Karen population on the western border of Thailand.
title The epidemiology of malaria in a Karen population on the western border of Thailand.
title_full The epidemiology of malaria in a Karen population on the western border of Thailand.
title_fullStr The epidemiology of malaria in a Karen population on the western border of Thailand.
title_full_unstemmed The epidemiology of malaria in a Karen population on the western border of Thailand.
title_short The epidemiology of malaria in a Karen population on the western border of Thailand.
title_sort epidemiology of malaria in a karen population on the western border of thailand
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