Background
The importance of submicroscopic malaria infections in high-transmission areas could contribute to maintain the parasite cycle. Regarding non-endemic areas, its importance remains barely understood because parasitaemia in these afebrile patients is usually below the detection limits for microscopy, hence molecular techniques are often needed for its diagnosis. In addition to this, the lack of standardized protocols for the screening of submicroscopic malaria in immigrants from endemic areas may underestimate the infection with
Plasmodium
spp. The aim of this study was to assess the prevalence of submicroscopic malaria in afebrile immigrants living in a non-endemic area.
Methods
A prospective, observational, multicentre study was conducted. Afebrile immigrants were included, microscopic observation of Giemsa-stained thin and thick blood smears, and two different molecular techniques detecting
Plasmodium
spp. were performed. Patients with submicroscopic malaria were defined as patients with negative blood smears and detection of DNA of
Plasmodium
spp. with one or both molecular techniques. Demographic, clinical, analytical and microbiological features were recorded and univariate analysis by subgroups was carried out with STATA v15.
Results
A total of 244 afebrile immigrants were included in the study. Of them, 14 had a submicroscopic malaria infection, yielding a prevalence of 5.7% (95% confidence interval 3.45–9.40). In 71.4% of the positive PCR/negative microscopy cases,
Plasmodium falciparum
alone was the main detected species (10 out of the 14 patients) and in 4 cases (28.6%)
Plasmodium vivax
or
Plasmodium ovale
were detected. One patient had a mixed infection including three different species.
Conclusions
The prevalence of submicroscopic malaria in afebrile immigrants was similar to that previously described in Spain.
Plasmodium vivax
and
P
.
ovale
were detected in almost a third of the submicroscopic infections. Screening protocols for afebrile immigrants with molecular techniques could be useful for a proper management of these patients.
Electronic supplementary material
The online version of this article (10.1186/s12936-019-2870-3) contains supplementary material, which is available to authorized users.