Faculty Bibliography

Behavior problems and family functioning were investigated in a sample of 10 adolescent girls with chronic fatigue syndrome (CFS), 10 matched healthy adolescent girls, and 10 adolescents with childhood cancer in remission. Based on the adolescent girls' reports, the CFS group had significantly higher scores than the cancer and healthy comparison adolescent girls on somatic complaints and also significantly higher scores than the cancer controls on internalizing symptoms and depression. Parent reports resulted in significantly higher scores in the CFS group than the adolescent girls from the healthy comparison groups on internalizing scores and somatic complaints. There were no significant differences on any family variables

We evaluated febrile convulsions prospectively in 42 children to investigate the association between acute human herpesvirus-6 (HHV-6) infection and first-time febrile convulsions, using both virologic and serologic methods. Eight children had primary HHV-6 infection documented by viral culture and an additional three by acute- and convalescent-phase serologic studies. These findings indicate that acute HHV-6 infection is a frequent cause of febrile convulsions in young children.

OBJECTIVE:Rapid detection of respiratory syncytial virus (RSV) infection can assist clinicians in decisions regarding antiviral therapy with ribavirin as well as instituting infection control measures. The Abbott TestPack RSV is a rapid RSV detection immunoassay that can be performed on respiratory secretions in 20 to 30 minutes without special laboratory equipment. The purpose of this study was to evaluate housestaff performance of the TestPack RSV at bedside as compared with laboratory testing of aliquots of the same specimen by tissue culture inoculation, direct fluorescent antibody (DFA) testing and TestPack RSV. METHODS:During the 1991 through 1992 RSV season, 137 nasopharyngeal aspirates or washes obtained from pediatric patients < 4 years of age suffering from acute respiratory disease were assayed by the Food and Drug Administration-approved TestPack RSV as well as conventional tube culture and DFA testing. RESULTS:66 of 137 (48%) specimens were positive for RSV as defined by: isolation and DFA-positive (n = 48) and DFA testing positive with negative culture (n = 18); blocking assay experiments using TestPack RSV confirmed culture-negative DFA-positive specimens as positive in 8/8 instances in which material for retesting was available. Using these definitions, the sensitivity and specificity for the assays were: housestaff TestPack RSV: 92%, 93%; laboratory TestPack RSV: 97%, 98%; virus isolation: 72%, 100%. CONCLUSION/CONCLUSIONS:From these data, it appears that the TestPack RSV EIA in the field setting is reliable, although laboratory confirmation of results is important.

BACKGROUND:A second generation-RSV enzyme immunoassay (EIA) was compared with cell culture and immunofluorescence to determine the improved efficacy of this reformulated system. OBJECTIVES/OBJECTIVE:This study was performed to identify whether the EIA might serve an ancillary function during non-operational virology hours, or whether the EIA may serve as a replacement of the commonly used direct fluorescent assay (DFA). STUDY DESIGN/METHODS:During the 1992-1993 (September-April) RSV season, 124 freshly collected nasopharyngeal (NP) aspirates were tested by the EIA and the DFA for the presence of antigen to the infectious agent. Infectivity was performed by tube culture cytopathic effect (TC-CPE) in parallel with the two antigen detection methodologies. RESULTS:Thirteen of the 48 confirmed positive specimens (27%) failed to yield infectious virus by TC-CPE. The sensitivity, specificity, positive and negative predictive values of the EIA were 90, 95, 91 and 94% respectively. This observed sensitivity of 90% using freshly collected NP aspirates, represents a marked improvement over an earlier generation EIA kit. CONCLUSIONS:Considering the simplicity and speed of this EIA (10 min), the test is recommended for use by medical personnel when facilities for DFA and traditional virus culture are not readily available.

The activity of a number of detergents and disinfectants against respiratory syncytial virus (RSV) was evaluated in an in vitro assay system. Equal volumes of RSV and serial 10-fold dilutions of the test agents were mixed at 4 degrees C for 5 minutes. The RSV titer in each mixture was compared with that of untreated RSV alone. In 14 experiments with input RSV titers ranging from 2.6 x 10(3) to 2 x 10(7) plaque-forming units/ml, a 10-fold dilution of 5.25% sodium hypochlorite (generic bleach) inactivated (> or = 3-log reduction in titer) the virus. With lower RSV titers inactivation was also observed at a 100-fold dilution of bleach. Fetal calf serum concentrations up to 50% as an organic load did not diminish the bleach effect. The degree of RSV inactivation was also defined for Lysol, povidone-iodine, Amphyl, Hibiclens, Osyl, ethanol and Listermint. The short contact time, the reproducible nature of the findings and the continued effectiveness with increasing organic loads all suggest that detergents and disinfectants can potentially play an important role in decreasing the spread of RSV infection.