In vitro activity of cefoperazone-sulbactam: Singapore experience.

In vitro activity of commonly used antimicrobial agents against consecutively isolated 521 strains of Gram negative bacilli causing serious infections in the National University Hospital, Singapore were tested in parallel with cefoperazone-sulbactam combination. With the combination complete resistance of 2% and intermediate resistance of 5% were noted among the 521 strains tested. Resistance to imipenem was low (5%) but resistance against other antimicrobial agents varied from 12% (amikacin) to 80% (ampicillin). In vitro data demonstrated a possible future role for cefoperazone-sulbactam in the treatment of sepsis caused by Gram negative bacilli in our hospital.

Detection of Mycobacterium tuberculosis in sputum, pleural and bronchoalveolar lavage fluid using DNA amplification of the MPB 64 protein coding gene and IS6110 insertion element.

Two gene sequences specific for Mycobacterium tuberculosis were evaluated for the diagnosis of pulmonary tuberculous (PTB) in pleural fluid (PF), bronchoalveolar lavage fluid (BAL) and sputum (Sp). The 240 bp sequence (nts 460-700) coding for the MPB 64 protein coding gene and the 123 bp IS6110 insertion element present in multiple copies in the mycobacterial genome were amplified using the polymerase chain reaction. Fifty-nine clinical specimens were studied. The diagnosis of PTB was confirmed by positive M. tuberculosis cultures in 14 specimens, and by the presence of characteristic histological features of granuloma and Langerhan's giant cells on pleural biopsy in 3 PF specimens through cultures for M. tuberculosis were negative. The remaining 42 specimens were obtained from patient's with non-tuberculosis pulmonary infections or malignancy, and these served as negative controls. Our results showed that the IS6110 insertion element and MPB 64 gene sequence were detected in all 14 culture positive PTB cases, although detection of the latter sequence required both DNA amplification and oligonucleotide hybridization. There was however one false positive specimen with the MPB 64 detection protocol. More importantly, both the MPB 64 sequence and IS6110 insertion element protocols were unable to detect M. tuberculosis DNA in the 3 PF samples diagnosed by histological characteristics on pleural biopsy and culture negative. We conclude that DNA amplification for M. tuberculosis-specific sequences is a useful method for rapid diagnosis of PTB in culture positive specimens. However, the false negative results with TB culture negative cases of tuberculosis pleurisy, limits its usefulness for the diagnosis of tuberculous pleurisy.

Increasing prevalence of antimicrobial resistance among organisms isolated from blood culture in a Singapore hospital.

The blood culture isolates obtained over the period 1985-1990 in a general teaching hospital were reviewed to determine trends in the prevalence of resistance to antimicrobial drugs. The percentages of Staphylococcus aureus isolates resistant to methicillin increased each year. Resistance among coagulase negative staphylococci also increased in prevalence: by 1990 approximately 50% of such isolates were resistant to methicillin, erythromycin, co-trimoxazole and gentamicin, 24% were resistant to clindamycin, 20% to fucidic acid but only 0.5% to vancomycin. Isolates of Enterobacteriaceae, excluding community-acquired salmonellae, showed increasing prevalence of resistance to beta-lactams, as did Acinetobacter spp isolates to gentamicin, co-trimoxazole and ceftriaxone. The isolates of Pseudomonas aeruginosa were exceptional, having no evident increase in the prevalence of resistance during the period. The rapid increases observed in relation to the other pathogens indicate the need for an antibiotic policy based on continuous surveillance of susceptibility patterns in the hospital.

A comparison of costs and effectiveness of the BACTEC NR-730 system and a conventional method of blood culture.

Results and costs of the first six months experience with BACTEC NR-730 were compared with a series of blood cultures performed by the conventional method previously used. The newer technology detected the growth of 14.1% of significant isolates on the day of receipt of the specimens. The previous method lacked blind subcultures on the day of receipt and therefore detected growth only after overnight incubation. No direct comparison of the sensitivities of the methods was possible, but the percentages of cultures yielding significant isolates were similar for the two methods. With the new method, technicians needed less time for daily screening of blood cultures, fewer subcultures were required and less contamination was observed. The method used to calculate the directly-related variable costs of the two methods is set out. In the particular situation reported, workload and labor costs were such that introduction of BACTEC NR-730 resulted in a saving on variable costs.