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R C Tilton

Publications and source records attributed to R C Tilton.

98 records · Page 6Linked to original sources

TORCH serologies and specific IgM antibody determination in acquired and congenital infections.

Except for rubella testing, routine TORCH serology screens in prenatal care are of little use. Individual TORCH tests may, however, be useful based on the clinical presentation and history of the patient. The laboratory test of choice for diagnosing cytomegalovirus (CMV) and herpes simplex virus (HSV) infections is culture isolation for the virus. The presence for specific IgM antibodies in neonates is diagnostic of congenital infection. In adults, IgM antibody results should be interpreted along with the clinical findings and history of the patient. IgM antibodies may persist for months and even years and may be detected during reactivation of latent virus infections. Serum fractionation should always be performed in IgM antibody testing to avoid false positive results owing to rheumatoid factors and false negative results owing to competing levels of specific IgG antibodies. With a single serum specimen, specific IgM antibody detection may be helpful in differentiating between a recent versus past infection.

Antibodies, Viral↗

Comparison of rapid methods of antimicrobial susceptibility in Haemophilus influenzae.

A method is described for the rapid, simultaneous determination of the MIC's of chloramphenicol and ampicillin to Haemophilus influenzae. Excellent agreement was observed between the Autobac method and the agar dilution method for antimicrobial susceptibility. All ampicillin resistant Haemophilus isolates produced beta lactamase and none of the suceptible strains produced this enzyme.

Ampicillin↗

Utility of a rapid latex test for the detection of Clostridium difficile in fecal specimens.

Currently, the method of choice for the laboratory diagnosis of Clostridium difficile disease is the detection of cytotoxin in stool filtrates by tissue culture. Since many hospital laboratories do not have tissue culture facilities, there is a need for a rapid test which is both sensitive and specific to diagnose C. difficile disease. A commercial latex agglutination was compared with the conventional cytotoxin tissue culture assay for the detection of C. difficile or its toxin(s) in fecal specimens. Of the 574 specimens evaluated, 111 were cytotoxin positive while 97 were positive by the latex agglutination test. There were 17 specimens positive by latex agglutination but negative by tissue culture assay. The overall sensitivity and specificity of the CDT latex test was 86.1 percent and 95.3 percent respectively. This rapid latex test can serve as an excellent screening procedure for the presence of C. difficile. Those specimens positive by the latex test should be further evaluated for the presence of cytotoxin by tissue culture.

Bacterial Proteins↗

Inhibition of bacterial growth by granulocytes measured by an automated technique.

Granulocytes, collected by several methods, were assayed for antibacterial activity utilizing a technique originally developed for automated antibiotic susceptibility testing. The granulocytes were incubated with either Escherichia coli or Staphylococcus for one hour at 37 degrees C and were then separated from the suspension by gentle centrifugation at 170 g. The bacteria remaining in the supernatant broth were incubated in culture medium (eugonic broth) and their growth density was compared with diluted controls (without granulocytes) by measurement in an Autobac I (an automated nephelometer). Measurements of the density of growth at 30 minute intervals showed a marked delay in the development of density suggesting only small numbers of organisms remained after incubation with granulocytes. Once density was measurable, the rate of growth appeared similar to controls. After 2.5 hours in the Atuobac I, the density of growth was used to determine the inhibitory effect of granulocytes. The density of growth was inversely related to the concentration of granulocytes present during the preincubation phase. Filtered granulocytes showed significantly lower inhibitory effect than centrifuged granulocytes. This rapid, inexpensive method of determining microbial growth appears to be adaptable as a measure of granulocyte function.

Autoanalysis↗

Gentamicin-carbenicillin synergy among gentamicin resistant Pseudomonas aeruginosa.

Forty-five isolates of gentamicin resistant Pseudomonas aeruginosa were evaluated for gentamicin-carbenicillin synergy. Only 9 percent (4/45) showed synergy. Of nine isolates with demonstrable zones around a gentamicin disc (8 to 12 mm), none showed a synergistic response. Effective treatment of gentamicin resistant Ps. aeruginosa with gentamicin and carbenicillin should not be assumed without additional test procedures.

Carbenicillin↗