Nasal carriage of Staphylococcus aureus: the key to preventing staphylococcal disease

Postoperative infections (Pis) are serious complications of thoracic surgery. To gain insight into the nature and the scope of the problem, an 18 month prospective surveillance was conducted at the department of thoracic surgery of the University Hospital Rotterdam, Dijkzigt. Pis were classified according to CDC criteria. One hundred and ninety-four out of 983 patients (19.7%) developed one or more Pis and in these 194 patients, 268 Pis were diagnosed. The incidence of Pis was 2.0 per 100 days of postoperative stay. The mean postoperative length of stay (LOS) of the 194 patients with Pis was 14.1 days longer than those without Pis. Deep surgical wound infections (DSWls) were associated with the longest prolongation of the median postoperative LOS in the hospital (30 days longer). Although lower than DSWls, incisional surgical wound infections also had a significant prolongation of stay (median 10 days longer). Staphylococcus aureus was the most important pathogen associated with surgical wound infections (SWls). Phage typing of 29 strains causing SWI showed only two identical pairs, so only a minority of infections could be explained by crossinfection. Older age, and more complicated procedures (e.g. cardiac valve operations) were independent, statistically significant risk factors for the development of Pis. Since there is a progressive trend towards operating on older patients and performing more complicated procedures, the incidence of Pis is expected to increase. Therefore it will become increasingly important to develop new strategies to prevent these serious complications

The cost-effectiveness of ESBL detection: towards molecular detection methods?

AbstractCorrect detection of extended-spectrum beta-lactamases (ESBLs) is crucial for infection control and antibiotic choice. We performed a study to determine the cost-effectiveness of phenotypical testing, which can be inaccurate, and genotypical tests, which are considered to be more reliable but also more expensive. All patients that had been in isolation in the Amphia hospital because of the detection of ESBL according to the ESBL Etest were included in the survey. All strains were retested using the double disk confirmation test (DDCT) and a genotypical method. This was a commercially available microarray (Check-Points). Discordant results were confirmed by PCR and sequencing. In total 174 patients were included. In 24 of 174 (14%) patients, ESBL carriage could not be confirmed with the microarray. This was verified with PCR and sequencing. The mean duration of isolation was 15 days, adding up to a total number of isolation days of 2571. False-positive results according to the microarray resulted in a total of 279 days of unnecessary isolation for the Etest and 151 days for the DDCT. Using Etest to detect the presence of ESBL results in a false-positive outcome in 14% of the cases. This results in unnecessary isolation of patients, which can be omitted by using a genotypic method

Improved performance of PACE 2 with modified collection system in combination with probe competition assay for detecti

The Gen-Probe PACE 2 assay (GP) in combination with a modified collection system was compared with cell culture (CC) for the detection of Chlamydia trachomatis in urethral specimens from males. Analysis of discordant results was performed by PCR. The modifications, i.e., application of a more rigid swab type and a 50% reduction in the amount of transport medium, were made to improve the sensitivity of the assay. By using the modified GP on 302 urethral specimens from males, a sensitivity of 89.5% and a specificity of 100% were determined. In addition, performance of a probe competition assay on all GP samples with a result > 0.6 and < 1.0 times the cutoff factor (gray zone) detected three more true-positive samples. The sensitivity of GP in combination with the probe competition assay increased to 94.9%, with a specificity of 100%. This was identical to the performance of CC. The modified GP offers a very sensitive and specific alternative to CC

Концепция создания гормонального контрацептивного средства с оптимальной фармакодинамикой

Приведены сведения о фундаментальных исследованиях стероидных соединений с гестагенной активностью, результатом которых стало создание дроспиренона. Представлены данные клинических исследований, доказывающие надежность контрацептивного эффекта нового препарата "Ярина(r)", содержащего дроспиренон и одновременно позволяющего получить ряд дополнительных преимуществ: повышение качества жизни, положительное влияние на общее самочувствие, хороший контроль цикла, уменьшение тяжести предменструальных симптомов, проявлений акне и себореи.The authors report about fundamental studies of steroid compounds with gestagenic activity, which stimulated Drospirenon production.The data of clinical investigations proving the reliability of contraceptive effect of a new drug Yarina(r) containing Drospirenon and allowing to obtain a number of additional advantages: improvement of the quality of life, positive influence on the general health, good control of the cycle, reduction of premenstrual signs severity, manifestations of acne and seborrhea are reported

Evaluation of yield of currently available diagnostics by sample type to optimize detection of respiratory pathogens in patients with a community-acquired pneumonia

Background: For the detection of respiratory pathogens, the sampling strategy may influence the diagnostic yield. Ideally, samples from the lower respiratory tract are collected, but they are difficult to obtain. Objectives: In this study, we compared the diagnostic yield in sputum and oropharyngeal samples (OPS) for the detection of respiratory pathogens in patients with community-acquired pneumonia (CAP), with the objective to optimize our diagnostic testing algorithm. Methods: Matched sputum samples, OPS, blood cultures, serum, and urine samples were taken from patients (>18 years) with CAP and tested for the presence of possible respiratory pathogens using bacterial cultures, PCR for 17 viruses and five bacteria and urinary antigen testing. Results: When using only conventional methods, that is, blood cultures, sputum culture, urinary antigen tests, a pathogen was detected in 49·6% of patients (n = 57). Adding molecular detection assays increased the yield to 80%. A pathogen was detected in 77 of the 115 patients in OPS or sputum samples by PCR. The sensitivity of the OPS was lower than that of the sputum samples (57% versus 74%). In particular, bacterial pathogens were more often detected in sputum samples. The sensitivity of OPS for the detection of most viruses was higher than in sputum samples (72% versus 66%), except for human rhinovirus and respiratory syncytial virus. Conclusion: Addition of PCR on both OPS and sputum samples significantly increased the diagnostic yield. For molecular detection of bacterial pathogens, a sputum sample is imperative, but for detection of most viral pathogens, an OPS is sufficient

Clonal expansion of Staphylococcus epidermidis strains causing Hickman catheter-related infections in a hemato-oncologic department

The detailed analysis of 411 strains of coagulase-negative staphylococci (CoNS) obtained from 40 neutropenic hemato-oncologic patients (61 Hickman catheter episodes) on intensive chemotherapy is described. By random amplification of polymorphic DNA (RAPD) analysis, a total of 88 different genotypes were detected: 51 in air samples and 30 in skin cultures prior to insertion, 12 in blood cultures after insertion, and only 5 involved in catheter-related infections (CRI). Two RAPD genotypes of Staphylococcus epidermidis predominated, and their prevalence increased during patient hospitalization. At insertion, these clones constituted 11 of 86 (13%) CoNS isolated from air samples and 33 of 75 (44%) CoNS isolated from skin cultures. After inser

Influence of volume of sample processed on detection of Chlamydia trachomatis in urogenital samples by PCR

In the present study, it was demonstrated that the sensitivity of the PCR for the detection of Chlamydia trachomatis is influenced by the volume of the clinical sample which is processed in the PCR. An adequate sensitivity for PCR was established by processing at least 4%, i.e., 80 microliters, of the clinical sample volume per PCR. By using this preparation procedure, 1,110 clinical samples were evaluated by PCR and by cell culture, and results were compared. After discordant analysis, cell culture resulted in a sensitivity of 79.1% and PCR resulted in a sensitivity of 92.7%. Furthermore, it was shown that treatme

Evaluation of Clearview and Magic Lite tests, polymerase chain reaction, and cell culture for detection of Chlamydia trachomatis in urogenital specimens

The Clearview Chlamydia test (CV; Unipath Ltd., Bedford, United Kingdom), the Magic Lite Chlamydia test (ML; CIBA Corning, Medfield, Mass.), a polymerase chain reaction (PCR), and cell culture (CC) were evaluated for detection of Chlamydia trachomatis in urogenital specimens. Specimens were collected from 283 men and 724 women visiting the outpatient clinic for Sexually Transmitted Diseases at the University Hospital Rotterdam, Rotterdam, The Netherlands. ML, PCR, and CC were all performed on the same sample to prevent swab-to-swab variability. CV was performed on a separate sample. Analysis of discordant results was performed by application of the following confirmatory assays: first, PCR on th