Vivax malaria: a major cause of morbidity in early infancy

Jeanne R Poespoprodjo, Wendelina Fobia, Enny Kenangalem, Daniel A Lampah, Afdal Hasanuddin, Noah Warikar, Paulus Sugiarto, Emiliana Tjitra, Nick M Anstey, Ric N Price, Jeanne R Poespoprodjo, Wendelina Fobia, Enny Kenangalem, Daniel A Lampah, Afdal Hasanuddin, Noah Warikar, Paulus Sugiarto, Emiliana Tjitra, Nick M Anstey, Ric N Price

Abstract

Background: In areas where malaria is endemic, infants aged <3 months appear to be relatively protected from symptomatic and severe Plasmodium falciparum malaria, but less is known about the effect of Plasmodium vivax infection in this age group.

Methods: To define malaria morbidity in the first year of life in an area where both multidrug-resistant P. falciparum and P. vivax are highly prevalent, data were gathered on all infants attending a referral hospital in Papua, Indonesia, using systematic data forms and hospital computerized records. Additional clinical and laboratory data were prospectively collected from inpatients aged <3 months.

Results: From April 2004 through April 2008, 4976 infants were admitted to the hospital, of whom 1560 (31%) had malaria, with infection equally attributable to P. falciparum and P. vivax. The case-fatality rate was similar for inpatients with P. falciparum malaria (13 [2.2%] of 599 inpatients died) and P. vivax malaria (6 [1.0%] of 603 died; P= .161), whereas severe malarial anemia was more prevalent among those with P. vivax malaria (193 [32%] of 605 vs. 144 [24%] of 601; P= .025). Of the 187 infants aged <3 months, 102 (56%) had P. vivax malaria, and 55 (30%) had P. falciparum malaria. In these young infants, infection with P. vivax was associated with a greater risk of severe anemia (odds ratio, 2.4; 95% confidence interval, 1.03-5.91; P= .041) and severe thrombocytopenia (odds ratio, 3.3; 95% confidence interval, 1.07-10.6; P= .036) compared with those who have P. falciparum infection.

Conclusions: P. vivax malaria is a major cause of morbidity in early infancy. Preventive strategies, early diagnosis, and prompt treatment should be initiated in the perinatal period.

Figures

Figure 1
Figure 1
Age-specific risk of malaria in patients admitted to hospital with Plasmodium falciparum (bold line), Plasmodium vivax (hatched line), and mixed (dotted line) infections. Lines represent predicted values from a logistic regression model in which age was entered as a linear effect.
Figure 2
Figure 2
Profile of a study of Plasmodium vivax malaria in early infancy.

Source: PubMed

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