B. Genton et al., THE EPIDEMIOLOGY OF MALARIA IN THE WOSERA AREA, EAST SEPIK PROVINCE, PAPUA-NEW-GUINEA, IN PREPARATION FOR VACCINE TRIALS .2. MORTALITY AND MORBIDITY, Annals of tropical medicine and parasitology, 89(4), 1995, pp. 377-390
Malaria mortality and morbidity were studied in a rural population of
4000 in the Wosera area, East Sepik Province, Papua New Guinea, Malari
a accounted for 4.9% of the 162 deaths investigated by verbal autopsy
and for 12.2% of the 49 deaths assessed through medical records. Malar
ia was the first cause of death in children aged 0.5-4 years. Of the 7
795 subjects interviewed and bled during six cross-sectional community
-based surveys, children of 1-4 years had the highest malaria-related
morbidity. In this age group, point prevalences of fever, fever associ
ated with parasitaemia, and fever plus Plasmodium falciparum (Pf) (Pf)
parasitaemia greater than or equal to 10000 parasites/mu l blood were
5%, 4.1% and 1.5%, respectively. The corresponding figures for adults
were 2%, 0.9% and 0.1%, respectively. The calculation of attributable
fraction (AF) using a multiple logistic regression model showed that
malaria accounted for 0.44 of all fevers in children of 1-4 years and
0.08 of the fevers in adults. Prevalence data derived from the AF esti
mate were compared with those calculated using different accepted dens
ity thresholds. The prevalences which best approximated the results fr
om the logistic regression model were obtained using parasitaemia cut-
offs of greater than or equal to 1000 Pf parasites/mu l in children ag
ed 1-4 years and adults older than 19 years and of greater than or equ
al to 10000 parasites/mu l in those aged 5-19 years. Prevalence of fev
er associated with parasitaemia was highly seasonal, with a peak at th
e beginning of the wet season. The geographical distribution of malari
a morbidity was not uniform. The measurement of malaria-related morbid
ity, the identification of significant seasonal and local variation as
well as the assessment of different methods of defining a clinical ep
isode of PE malaria are crucial for the design and evaluation of inter
vention studies, including field trials of antimalarial vaccines.