TY - JOUR
T1 - Evaluation of the Immunoquick+4 malaria rapid diagnostic test in a non-endemic setting
AU - van Dijk, D. P. J.
AU - Gillet, P.
AU - Vlieghe, E.
AU - Cnops, Lieselotte
AU - van Esbroeck, Marjan
AU - Jacobs, J.
PY - 2010/5
Y1 - 2010/5
N2 - The aim of this retrospective study was to evaluate the Immunoquick+4 (BioSynex, Strasbourg, France), a three-band malaria rapid diagnostic test (MRDT) targeting histidine-rich protein-2 (HRP-2) and pan Plasmodium-specific parasite lactate dehydrogenase, in a non-endemic reference setting. Stored whole-blood samples (n = 613) from international travellers suspected of malaria were used, with microscopy corrected by polymerase chain reaction (PCR) as the reference method. Samples infected by P. falciparum (n = 323), P. vivax (n = 97), P. ovale (n = 73) and P. malariae (n = 25) were selected, as well as 95 malaria-negative samples. The overall sensitivities of the Immunoquick+4 for the diagnosis of P. falciparum, P. vivax, P. malariae and P. ovale were 88.9, 75.3, 56.0 and 19.2%, respectively. Sensitivity was significantly related to parasite density for P. falciparum (93.6% versus 71.4% at parasite densities > 100/A mu l and a parts per thousand currency sign100/A mu l, respectively) and P. vivax (86.8% versus 48.3% at parasite densities > 500/A mu l and a parts per thousand currency sign500/A mu l, respectively). The Immunoquick+4 showed good reproducibility and reliability for both test results and line intensities. The Immunoquick+4 performed well for the detection of P. falciparum and P. vivax.
AB - The aim of this retrospective study was to evaluate the Immunoquick+4 (BioSynex, Strasbourg, France), a three-band malaria rapid diagnostic test (MRDT) targeting histidine-rich protein-2 (HRP-2) and pan Plasmodium-specific parasite lactate dehydrogenase, in a non-endemic reference setting. Stored whole-blood samples (n = 613) from international travellers suspected of malaria were used, with microscopy corrected by polymerase chain reaction (PCR) as the reference method. Samples infected by P. falciparum (n = 323), P. vivax (n = 97), P. ovale (n = 73) and P. malariae (n = 25) were selected, as well as 95 malaria-negative samples. The overall sensitivities of the Immunoquick+4 for the diagnosis of P. falciparum, P. vivax, P. malariae and P. ovale were 88.9, 75.3, 56.0 and 19.2%, respectively. Sensitivity was significantly related to parasite density for P. falciparum (93.6% versus 71.4% at parasite densities > 100/A mu l and a parts per thousand currency sign100/A mu l, respectively) and P. vivax (86.8% versus 48.3% at parasite densities > 500/A mu l and a parts per thousand currency sign500/A mu l, respectively). The Immunoquick+4 showed good reproducibility and reliability for both test results and line intensities. The Immunoquick+4 performed well for the detection of P. falciparum and P. vivax.
U2 - 10.1007/s10096-010-0898-y
DO - 10.1007/s10096-010-0898-y
M3 - Article
C2 - 20232100
SN - 0934-9723
VL - 29
SP - 577
EP - 583
JO - European Journal of Clinical Microbiology & Infectious Diseases
JF - European Journal of Clinical Microbiology & Infectious Diseases
IS - 5
ER -