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C S Kaufmann

Publications and source records attributed to C S Kaufmann.

6 recordsLinked to original sources

Electrophoretic karyotypes of Torulopsis glabrata.

Chromosome-sized DNA molecules of clinical isolates of Torulopsis glabrata were resolved by a pulsed-field electrophoretic method, contour-clamped homogeneous electric fields. With the conditions established in this study, 8 to 12 bands (ranging from 445 to 3,000 kilobases) were observed. There were differences in the intensities and migrations of bands, consistent with T. glabrata being either haploid or diploid. A total of 22 distinctive electrophoretic patterns were noted among single isolates of T. glabrata recovered from 33 patients. When strains were delineated by an electrophoretic pattern, individuals usually harbored only one strain.

Candida↗

Accuracy and reproducibility of a four-hour method for anaerobe identification.

In this study, we evaluated the ability of a 4-h enzyme assay kit system, the RapID ANA method (Innovative Diagnostic Systems, Inc., Atlanta, Ga.) to accurately and reproducibly identify a spectrum of clinically significant anaerobic bacteria in two separate institutions. Additional tests were performed as required. Of a total of 188 organisms tested at Hershey Medical Center (HMC), 86.2% were correctly identified to species level without additional tests, 5.9% required extra tests for correct identification, and 8.0% were misidentified. Of 53 strains tested at Johns Hopkins Hospital (JHH), 52.8% were correctly identified without extra tests, 28.3% required extra tests for correct identification, and 18.9% were misidentified. Of 21 organisms tested at both institutions, those tested at JHH required additional tests for correct identification in 38.1% of cases, compared with 9.5% at HMC. Misidentification rates were identical (9.5%) in both centers. Of strains tested at HMC only, 86.8% were correctly identified without extra tests, 5.4% were identified with additional tests, and 7.8% were misidentified: corresponding data for JHH were 53.1, 21.9, and 25.0%, respectively. Of 53 strains tested in triplicate at JHH, 56.7% yielded the same result on each occasion, 37.7% were identical in two of three tests, and 5.7% gave different results on each of three occasions. Discrepancies between identification rates at HMC and JHH may be explained by differences in species tested (more commonly encountered species were tested at HMC) and interpretation of reactions by the two different readers. The RapID ANA method has the potential for rapid identification of clinically isolated anaerobes; however, accuracy and reproducibility may vary as a function of the specific laboratory setting.

Bacteria, Anaerobic↗

Comparison of three methods for anaerobe identification.

In this study we evaluated the ability of three commercial methods, API 20A (Analytab Products, Plainview, N.Y.), Minitek (BBL Microbiology Systems, Cockeysville, Md.), and Anaerobe-Tek (Flow Laboratories, Inc., McLean, Va.), to accurately identify 165 recent clinical and 38 stock isolates of anaerobic bacteria without supplemental tests or gas-liquid chromatography. Strains included 89 Bacteroides spp., 12 fusobacteria, 10 gram-positive, nonsporing rods, 43 Clostridium spp., 15 Streptococcus intermedius, 18 peptococci, 6 peptostreptococci, 3 Staphylococcus saccharolyticus, and 7 Veillonella spp. The methods used were those of manufacturers, without supplemental tests. API 20A correctly identified 70.0% of strains to species and 6.4% to genus only, with 17.2% as part of a spectrum of identifications and 6.4% incorrect. Minitek, according to the current code book, yielded 69.5% correct identifications to species, 16.8% spectrum identifications, and 13.8% incorrect. Anaerobe-Tek correctly identified 64.0% of strains to species, 21.2% spectrum identifications, and 14.8% incorrect. Thirteen strains were misidentified by API 20A, 28 were misidentified by Minitek, and 30 were misidentified by Anaerobe-Tek. For laboratories without gas-liquid chromatography support and where identification of clinically significant Bacteroides fragilis and Clostridium perfringens is desired, any of the three systems would provide accurate information. For more extensive anaerobe identification, including the less frequently isolated, more unusual organisms, API 20A and Minitek are preferred at this time. All systems have identification schemes associated with a percentage of misidentifications, the most recently introduced Anaerobe-Tek system being associated with the highest error rate.

Bacteria, Anaerobic↗

Two rapid pigmentation tests for identification of Cryptococcus neoformans.

Two tests were developed for the rapid identification of Cryptococcus neoformans based on pigment produced by the organism's phenoloxidase activity. Caffeic acid was incorporated into cornmeal agar, a medium used routinely for yeast identification. When tested on this medium, only C. neoformans isolates produced brown pigment. All other yeasts maintained their normal morphology and did not produce the reaction product. A non-medium-based test was developed for same-day identification of C. neoformans isolates. Paper strips saturated with a buffered L-beta-3,4-dihydroxyphenylalanine-ferric citrate solution were inoculated with isolates and incubated at 37 degrees C. Pigment production occurred only with C. neoformans isolates, many within 60 to 90 min. All other yeasts remained negative.

Cryptococcus↗

Clonidine. Effects of a topically administered solution on intraocular pressure and blood pressure in open-angle glaucoma.

A double-blind crossover study to determine the effects on intraocular pressure (IOP) and blood pressure of topically instilled 0.125% and 0.25% solutions of clonidine hydrochloride by comparison with a 2% pilocarpine hydrochloride solution and placebo was carried out in a total of 21 patients with open-angle glaucoma, each of whom received a single drop of each preparation in the same glaucomatous eye on separate days. Both clonidine solutions were effective in lowering the IOP; the 0.25% solution was more effective than the 0.125% solution, and the former was slightly less potent than pilocarpine. Pupil diameter was essentially unchanged in all but one of the patients after clonidine. Pilocarpine reduced pupil diameter in all patients. One eye treated with placebo also showed a reduction in pupil size. Both systolic and diastolic blood pressure showed a statistically significant reduction after clonidine, but the magnitude of the change was small. We do not regard the minor blood pressure changes as being a threat to the optic nerve but further studies in this aspect of topical clonidine therapy are required.

Administration, Topical↗

Learning needs assessment as a vehicle for integrating staff development into a professional practice model.

Restructured nursing roles resulting from innovative professional practice models and participative governance systems create a demand for new and expanded competencies. The impact for nursing staff development is the concurrent requirement to develop programs that match the skill/competency requirements of nurses in emerging practice models. This article recounts how one nursing department implemented a learning needs assessment (LNA) process as a means of integrating staff development into professional nursing practice.

Clinical Competence↗