Jonckheere S, Verfaillie C, Boel A, Van Vaerenbergh K, Vanlaere E, Vankeerberghen A, De Beenhouwer H
Diagn Microbiol Infect Dis. 2015 May 27. pii: S0732-8893(15)00092-3
http://www.ncbi.nlm.nih.gov/pubmed/26092509
Abstract
The recently introduced BD Veritor System RSV laboratory kit (Becton Dickinson, Sparks, MD, USA) with automatic reading was evaluated and compared with the RSV K-SeT (Coris BioConcept, Gembloux, Belgium) for the detection of respiratory syncytial virus (RSV) using 248 nasopharyngeal aspirates of children younger than 6 years old with respiratory tract infection. Compared to reverse transcriptase polymerase chain reaction as gold standard, both tests had an identical sensitivity of 78.1% and a specificity of 96.8% and 95.8% for the
BD Veritor System and RSV K-SeT, respectively. Both antigen tests can be used to reliably confirm RSV in young children. However, a negative result does not definitively exclude the presence of RSV
June/July 2010 Virus Immunology – Respiratory Syncytial Virus (359)
Detection of RSV infections
Wybo I, Piérard D, Stevens D, Soetens O and Lauwers S
ECCMID, 2009
Performance of RSV RespiStrip
Piérard D, Stevens D, Mignolet J, Moriau L, Vergalle K, Lauwers S.
ECCMID, 2007
Impact on viral pathogen
Salonen, Hannaleena.
Bachelor's thesis presented in May 2006.
Direct antigen detection of RSV
Karnauchow TM, and Milk R
Poster presented at the Pan American Society for Clinical Virology (PASCV), April 25-28,
2004.
Rapid detection of RSV
Van den Wijngaert S, De Foor M, Van Beers D
ASM-ICAAC 44th, October 30th-November 2nd, 2004.
Detection of RSV in nasopharyngeal specimens
Clinical studies, Japan, 2005.
RSV UniStrip Clinical Survey
Gregson D, Lloyd T, Buchan S, Church D.
J Clin Microbiol. 2005 Nov;43(11):5782-3.
Abstract
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%.
Dizdar EA, Aydemir C, Erdeve O, Sari FN, Oguz S, Uras N, Dilmen U.
J Hosp Infect. 2010 Aug;75(4):292-4. Epub 2010 Mar 17.
Abstract
Palivizumab is currently licensed for the prevention of respiratory syncytial virus (RSV) lower respiratory tract disease in infants and children with chronic lung disease, with a history of preterm birth, or with haemodynamically significant congenital heart disease, but its routine use during outbreaks in neonatal intensive care units (NICUs) is not currently recommended. Here we report an outbreak in a NICU detected during a screening trial for RSV infection using a rapid antigen test (Respi-Strip((R))). Eleven preterm infants in our NICU tested positive for RSV during January 2009. Subsequent testing of the remaining infants in the NICU revealed two additional asymptomatic cases. In addition to precautions against cross-infection, palivizumab prophylaxis was administered to the remaining 37 premature infants. Two days after treatment, RSV was detected in two additional infants who had become symptomatic. To our knowledge this is the largest RSV outbreak in a NICU to be identified at an early stage by rapid testing and effectively controlled by infection control measures and palivizumab prophylaxis.