Archive for April 10, 2017

Biofilm-Forming Capability of Highly Virulent, Multidrug-Resistant Candida auris

Emerging Infectious Diseases February 2017 V.23 N.2

Dispatch

Leighann Sherry, Gordon Ramage, Ryan Kean, Andrew Borman, Elizabeth M. Johnson, Malcolm D. Richardson, and Riina Rautemaa-RichardsonComments to Author

University of Glasgow, Glasgow, Scotland, UK (L. Sherry, G. Ramage, R. Kean); Public Health England, Bristol, UK (A. Borman, E.M. Johnson); The University of Manchester, Manchester, UK (M.D. Richardson, R. Rautemaa-Richardson); University Hospital of South Manchester, Manchester (M.D. Richardson, R. Rautemaa-Richardson)

The emerging multidrug-resistant yeast pathogen Candida auris has attracted considerable attention as a source of healthcare–associated infections.

We report that this highly virulent yeast has the capacity to form antifungal resistant biofilms sensitive to the disinfectant chlorhexidine in vitro.

PDF

https://wwwnc.cdc.gov/eid/article/23/2/pdfs/16-1320.pdf

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April 10, 2017 at 3:30 pm

2017 Infectious Diseases Society of America’s Clinical Practice Guidelines for Healthcare-Associated Ventriculitis and Meningitis

Clinical Infectious Diseases March 15, 2017 V.64 N.6

IDSA GUIDELINE

Allan R. Tunkel; Rodrigo Hasbun; Adarsh Bhimraj; Karin Byers; Sheldon L. Kaplan

The Infectious Diseases Society of America (IDSA) Standards and Practice Guidelines Committee collaborated with partner organizations to convene a panel of 10 experts on healthcare-associated ventriculitis and meningitis. The panel represented pediatric and adult specialists in the field of infectious diseases and represented other organizations whose members care for patients with healthcare-associated ventriculitis and meningitis (American Academy of Neurology, American Association of Neurological Surgeons, and Neurocritical Care Society). The panel reviewed articles based on literature reviews, review articles and book chapters, evaluated the evidence and drafted recommendations. Questions were reviewed and approved by panel members. Subcategories were included for some questions based on specific populations of patients who may develop healthcare-associated ventriculitis and meningitis after the following procedures or situations: cerebrospinal fluid shunts, cerebrospinal fluid drains, implantation of intrathecal infusion pumps, implantation of deep brain stimulation hardware, and general neurosurgery and head trauma. Recommendations were followed by the strength of the recommendation and the quality of the evidence supporting the recommendation. Many recommendations, however, were based on expert opinion because rigorous clinical data are not available. These guidelines represent a practical and useful approach to assist practicing clinicians in the management of these challenging infections.

PDF

https://oup.silverchair-cdn.com/oup/backfile/Content_public/Journal/cid/64/6/10.1093_cid_cix152/4/cix152.pdf?Expires=1492171137&Signature=PLdIPP4xp9kFfZAMV7v5qbyThv2~hhuvj2PuBrGMjgaS4euDfouehyeWUHolVIFB22mVg0EOGvq1TsKpdTFYIFIEyTFQfFcB~xf09oZO5xipeRX3WMwNwDUMn3TNJw2ctLxaDf6xadJir6VsSq-YoOWCiuJjtwpvDYaTlg2YX7pkQH4LwwHPWiSZsrGSg8y8PzQSRGRDXQYLhKRH78Fr9WiW1gbARAALSBzVTYds1VS4t5pTejCzNZG3xrsFP3xOPH3B9~aEiDUOh2v9bp1qfTC0P8FCrfiaEnoNSs4-86FQGugwfbyw~Zxj0TePO8KDwf7V2uRDbBtsaZdaM1Azwg__&Key-Pair-Id=APKAIUCZBIA4LVPAVW3Q

 

https://oup.silverchair-cdn.com/oup/backfile/Content_public/Journal/cid/64/6/10.1093_cid_ciw861/4/ciw861.pdf?Expires=1492171171&Signature=N7Kt6ABuCdFVKF5MVfvG-BlcEGaHnwS-pYnFQ~kbB52~zvzCGCC7EHREyFKW2CJEjinjryNo~ieEdwg8LqkSD3RyjkxND9~HIrKGQGFCGF8Uw5DFVA1gkhYlhfsyV89GrGkdPRsHSEYJ1qzVl84AJ-buI1QL-4jHdY2JtOPiDyJ~MAV9MNLipadZE9~zeYyfxRChFvURFsGmVDl1qOxDmTU4GXyn4tlQckfhWaMZRz4sVKW8ZOlU6pLosCk-IBmnNfMpqGXjjNjh0DHuT~Gv1GzLEptQEcw9rWskefTOM7AgX-MteqkQz2YBXE6B0q1NbixbozBiJ-pkySltH6ofsQ__&Key-Pair-Id=APKAIUCZBIA4LVPAVW3Q

 

April 10, 2017 at 9:23 am

Use of Proton Pump Inhibitors and the Risk of Listeriosis: A Nationwide Registry-based Case-Control Study

Clinical Infectious Diseases April 1, 2017 V.64 N.7

EDITOR’S CHOICE

Anne Kvistholm Jensen; Jacob Simonsen; Steen Ethelberg

Background.

Recent studies suggest that proton pump inhibitors (PPIs) may increase the risk for listeriosis. We investigated a potential association in cases of nonpregnancy-associated listeriosis using registry data.

Methods.

We conducted a population-based, case-control study using Danish health registries. Cases (n = 721) were defined as patients aged ≥45 years notified with listeriosis from July 1994 to December 2012. We selected 34800 controls using risk-set sampling. Controls were individually matched for age, sex, and municipality. Data on use of PPIs and other drugs and hospitalization diagnoses over a 5-year period were extracted from nationwide health registries. A comorbidity index (CMI) was constructed. We calculated the association between use of PPIs and related drugs within 30 days (current use) and other time windows before the index date. Using conditional logistic regression, matched odds ratios (ORs) adjusted for CMI and confounders were estimated.

Results.

The adjusted OR for current use of PPIs and development of listeriosis was 2.81 (95% confidence interval [CI], 2.14–3.69). PPI usage up to 90 days before the index date remained statistically significant. Subgroup analyses revealed increasing ORs with decreasing age and level of comorbidity and an increased OR for concurrent glucocorticoid treatment (OR, 4.61; 95% CI, 3.01–7.06). No significant association was found for current use of histamine-2-receptor antagonists (adjusted OR, 1.82; 95% CI, 0.89–3.71).

Conclusions.

Prescribed PPIs were associated with increased risk of listeriosis. The risk waned with time since last prescription redemption. PPIs may have unwanted side effects in vulnerable populations.

PDF

https://oup.silverchair-cdn.com/oup/backfile/Content_public/Journal/cid/64/7/10.1093_cid_ciw860/1/ciw860.pdf?Expires=1492171436&Signature=DAz2LAMvOFwnZJ0-zKmrXxP6WN4yTW6GyICi~LTYAYwIJeVnXrHi9pjn0wDD6Z6s7~gkZS3YcIB4beRj0iMQlWufmI6lJO6Es79DbbiC46pXVEvSzlvvsTY8bbq1Ux8hm2uVCFIZMGl9VScWdFjolmVPXoH7-Zud5cl8M0wviNPFkY0u4z1ShoOAqI50sRj1XUt41bdhtBI98UHtL866Nnx3jj72HxSa8moN8vqgIpURmayxx5l5qhKL6TcTLzN8wWWMP1iLdTDIBkTBmYp6QqhSvpHDTIlJHvN9bP~E2gwka5sVm2nSFEkpuTVLU8U5l~ftD6bhjdss6ohtaWAZKA__&Key-Pair-Id=APKAIUCZBIA4LVPAVW3Q

 

 

April 10, 2017 at 9:21 am

Complex Routes of Nosocomial Vancomycin-Resistant Enterococcus faecium Transmission Revealed by Genome Sequencing

Clinical Infectious Diseases April 1, 2017 V.64 N.7

Kathy E. Raven; Theodore Gouliouris; Hayley Brodrick; Francesc Coll; Nicholas M. Brown …

Background.

Vancomycin-resistant Enterococcus faecium (VREfm) is a leading cause of nosocomial infection. Here, we describe the utility of whole-genome sequencing in defining nosocomial VREfm transmission.

Methods.

A retrospective study at a single hospital in the United Kingdom identified 342 patients with E. faecium bloodstream infection over 7 years. Of these, 293 patients had a stored isolate and formed the basis for the study. The first stored isolate from each case was sequenced (200 VREfm [197 vanA, 2 vanB, and 1 isolate containing both vanA and vanB], 93 vancomycin-susceptible E. faecium) and epidemiological data were collected. Genomes were also available for E. faecium associated with bloodstream infections in 15 patients in neighboring hospitals, and 456 patients across the United Kingdom and Ireland.

Results.

The majority of infections in the 293 patients were hospital-acquired (n = 249) or healthcare-associated (n = 42). Phylogenetic analysis showed that 291 of 293 isolates resided in a hospital-associated clade that contained numerous discrete clusters of closely related isolates, indicative of multiple introductions into the hospital followed by clonal expansion associated with transmission. Fine-scale analysis of 6 exemplar phylogenetic clusters containing isolates from 93 patients (32%) identified complex transmission routes that spanned numerous wards and years, extending beyond the detection of conventional infection control. These contained both vancomycin-resistant and -susceptible isolates. We also identified closely related isolates from patients at Cambridge University Hospitals NHS Foundation Trust and regional and national hospitals, suggesting interhospital transmission.

Conclusions.

These findings provide important insights for infection control practice and signpost areas for interventions. We conclude that sequencing represents a powerful tool for the enhanced surveillance and control of nosocomial E. faecium transmission and infection.

PDF

https://oup.silverchair-cdn.com/oup/backfile/Content_public/Journal/cid/64/7/10.1093_cid_ciw872/1/ciw872.pdf?Expires=1492171558&Signature=GD1jHGDA4zbySRAZc1M5f1uj3EZpCpdS85bTv62Th2drz2wZPn–gBsTovHbMLRud9piSIET7xZcZY1KTSZy1jEPIal3qFnKMFgO6T6Hx79ow0SDcqTiJX98JP-r7QOdWsWm-oisPNcIPyp0Wv1YLaHoNiSH53XKmtmR7pCC87XZk-zAHI8WSB0b1T6c3a7fTL4OOhdQyWbbgGXw0KEJUtsdQrq~-iD8meoqwYJdgTmm9NgCVLhcTeP4nxTFLIXWy5Utotk9yVMLFjBkmmUalBPGfocABoE-VGyXwv6NPTmp4J9p0y-CbXH6dTL8q~C66sYM-G-4zxWZrXR0-BYpOg__&Key-Pair-Id=APKAIUCZBIA4LVPAVW3Q

April 10, 2017 at 9:19 am

A literature review of laboratory-acquired brucellosis.

J Clin Microbiol. 2013 Sep;51(9):3055-62.

Traxler RM1, Lehman MW, Bosserman EA, Guerra MA, Smith TL.

Author information

1Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia, USA. RTraxler@cdc.gov

Abstract

Brucellosis is a bacterial zoonotic disease which has been associated with laboratory-acquired infections. No recent reviews have addressed the characteristics of laboratory-acquired brucellosis (LAB). English-language literature was reviewed to identify reports of laboratory exposures to Brucella spp. and LAB cases between 1982 and 2007. Evaluation of 28 case reports identified 167 potentially exposed laboratory workers, of whom 71 had LAB. Nine reports were identified that summarized an additional 186 cases of LAB. Only 18 (11%) exposures were due to laboratory accidents, 147 (88%) exposures were due to aerosolization of organisms during routine identification activities, and the circumstances of 2 (1%) exposures were unknown. Brucella melitensis was the causative agent in 80% (135/167) of the exposures. Workers with high-risk exposures were 9.3 times more likely to develop LAB than workers with low-risk exposures (95% confidence interval [CI], 3.0 to 38.6; P < 0.0001); they were also 0.009 times likelier to develop LAB if they took antimicrobial PEP than if they did not (95% CI, 0 to 0.042; P < 0.0001). The median incubation period in case and summary reports was 8 weeks (range 1 to 40 weeks). Antimicrobial PEP is effective in preventing LAB. The incubation period may be used to identify appropriate serological and symptom surveillance time frames for exposed laboratory workers.

PDF

http://jcm.asm.org/content/51/9/3055.full.pdf

April 10, 2017 at 9:17 am


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