The intrinsic antimicrobial activity of selected sclerosing agents in sclerotherapy.

Background: Detergent sclerosing agents may have intrinsic antimicrobial properties. In addition, they may have synergistic effects with other antibiotics such as penicillin. They may induce suppression of intrinsic resistance to penicillin in Staphylococcus aureus.

In vivo stability of heterogeneous expression classes in clinical isolates of methicillin-resistant staphylococci.

To define the stability of methicillin-resistant Staphylococcus aureus (MRSA) in vivo, 22 isolates collected at one New York institution in 1989 and 1990 were studied. All 22 belonged to one of two distinct methicillin-resistant phenotypes (class 3 or 2), which were precisely identified as belonging to two distinct genotypes. Genotypic classification was based on restriction analysis of chromosomal DNA with EcoRI and HindIII and Southern analysis of ClaI digests using two DNA probes.

Quantitative bacterial tissue cultures from 209 prostatectomy specimens: findings and implications.

To define the prevalence of prostatic bacterial infection or colonization, tissue from 209 patients undergoing prostatectomy (204 transurethral and 5 suprapubic) was submitted for quantitative bacterial tissue cultures. Tissue from 44 patients (21 per cent) yielded positive, single organism bacterial growth. In an attempt to identify preoperatively this patient subgroup, multiple preoperative and intraoperative variables were examined.

Nosocomial hepatitis A infection in a paediatric intensive care unit.

Seven members of staff in a paediatric intensive care unit and two of their relatives developed hepatitis A over a period of five days. A 13 year old boy who was incontinent of faeces prior to his death, was presumed to be the source of infection. Two hundred and sixty seven other members of staff underwent serological testing and were given prophylactic pooled gamma globulin.

Laboratory diagnosis of mycoplasma infections.

The relative efficiency of different media for the isolation of M. pneumoniae is discussed, with emphasis on the utility of SP-4 medium as a primary medium for isolation. Media available for isolation and identification of ureaplasmas are also described.