The RSV Respi-Strip was compared to the SimulFluor respiratory screen for detecting respiratory syncytial virus in nasopharyngeal aspirates from pediatric patients. Of samples tested, 115/239 (49%) were positive by direct fluorescent-antigen detection. The sensitivity and specificity of the RSV Respi-Strip were 92% (95% confidence interval [CI], 86% to 96%) and 98% (95% CI, 94% to 100%), respectively, with a diagnostic efficiency of 95%.Respiratory syncytial virus (RSV) is the most common virus causing respiratory infections in young children, occurring as a winter epidemic annually in temperate climates (11). Direct fluorescent-antigen detection (DFA) has become a common rapid method of detection, comparing favorably with tissue culturing (6,7,9,13). Processing and reading of samples by DFA still requires specialized equipment and staff. As such, it is difficult to provide 24 h per day. Several immunoassay antigen detection kits are available, but most require multiple steps in processing (5,6). Lateral-flow immunochromatographic assays have been developed with fewer steps and reliable results (8,10,12). Coris-BioConcept manufactures an RSV detection kit (RSV Respi-Strip [RSV-RS]) which requires only two reagents (extraction buffer and the immunostrips) and two incubations and makes results available within 25 min. We wished to evaluate whether this assay could be implemented in our regional diagnostic laboratory for the detection of RSV in samples from pediatric patients.All specimens in this study were from pediatric patients (mean age, 16 months; age range, 1 week to 17 years) and were submitted from 26 January to 19 February 2004. Samples were collected by nasopharyngeal aspiration done in emergency departments or pediatric wards. Direct fluorescent-antigen testing for RSV (RSV-DFA) was performed using a SimulFluor respiratory screen DFA test (Chemicon International). The result of this test was selected as the a priori gold standard. All samples were processed according to the manufacturer's instructions with centrifugation and spotting of 30 l of resuspended cells on glass slides prior to inoculation into transport media. The cytospin method was not used. Stained slides were read with a fluorescent microscope and a fluorescein isothiocyanate filter. Epithelial cells with intracellular yellow fluorescence were confirmed as positive with pink fluorescence using a tetramethylrhodamine isothiocyanate filter. Two or more distinctly positive cells/slide were required for a positive test result.RSV-RS testing was performed on the same specimens submitted for DFA testing. The testing technologist was blinded to the DFA testing result. Testing was performed in accordance with the manufacturer's package insert. A 0.25-ml aliquot of nasopharyngeal aspirate was mixed with 0.25 ml of extraction buffer in a 3-ml tube and incubated at room temperature for 10 min. Lateral flow strips were then inserted into the tube and incubated for 15 min prior to reading. The presence of a positive control line with a positive test li...