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Featured researches published by J. P. Ashby.


Journal of Antimicrobial Chemotherapy | 2017

Carbapenemase-producing Enterobacteriaceae in the UK: a national study (EuSCAPE-UK) on prevalence, incidence, laboratory detection methods and infection control measures

Pascale Trepanier; Kim Mallard; Danièle Meunier; Rachel Pike; Derek Brown; J. P. Ashby; Hugo Donaldson; F. Mustafa Awad-El-Kariem; Indran Balakrishnan; Marc Cubbon; Paul Chadwick; Michael J. Doughton; Rachael Doughton; Fiona Hardiman; Graham Harvey; Carolyne Horner; John Lee; Jonathan Lewis; Anne Loughrey; Rohini Manuel; Helena Parsons; John Perry; Gemma L. Vanstone; Graham White; N. Shetty; John Coia; Camilla Wiuff; Katie L. Hopkins; Neil Woodford

Objectives To estimate UK prevalence and incidence of clinically significant carbapenemase-producing Enterobacteriaceae (CPE), and to determine epidemiological characteristics, laboratory methods and infection prevention and control (IPC) measures in acute care facilities. Methods A 6 month survey was undertaken in November 2013–April 2014 in 21 sentinel UK laboratories as part of the European Survey on Carbapenemase-Producing Enterobacteriaceae (EuSCAPE) project. Up to 10 consecutive, non-duplicate, clinically significant and carbapenem-non-susceptible isolates of Escherichia coli or Klebsiella pneumoniae were submitted to a reference laboratory. Participants answered a questionnaire on relevant laboratory methods and IPC measures. Results Of 102 isolates submitted, 89 (87%) were non-susceptible to ≥1 carbapenem, and 32 (36%) were confirmed as CPE. CPE were resistant to most antibiotics, except colistin (94% susceptible), gentamicin (63%), tigecycline (56%) and amikacin (53%). The prevalence of CPE was 0.02% (95% CI = 0.01%–0.03%). The incidence of CPE was 0.007 per 1000 patient-days (95% CI = 0.005–0.010), with north-west England the most affected region at 0.033 per 1000 patient-days (95% CI = 0.012–0.072). Recommended IPC measures were not universally followed, notably screening high-risk patients on admission (applied by 86%), using a CPE ‘flag’ on patients’ records (70%) and alerting neighbouring hospitals when transferring affected patients (only 30%). Most sites (86%) had a laboratory protocol for CPE screening, most frequently using chromogenic agar (52%) or MacConkey/CLED agars with carbapenem discs (38%). Conclusions The UK prevalence and incidence of clinically significant CPE is currently low, but these MDR bacteria affect most UK regions. Improved IPC measures, vigilance and monitoring are required.


Journal of Antimicrobial Chemotherapy | 2001

Activity of daptomycin against Gram-positive pathogens : a comparison with other agents and the determination of a tentative breakpoint

R. Wise; J. M. Andrews; J. P. Ashby


Journal of Antimicrobial Chemotherapy | 2000

The in vitro activity of ABT773, a new ketolide antimicrobial agent

J. M. Andrews; T. M. A. Weller; J. P. Ashby; Rebecca Walker; R. Wise


Journal of Antimicrobial Chemotherapy | 2000

A comparison of antimicrobial resistance rates in Gram-positive pathogens isolated in the UK from October 1996 to January 1997 and October 1997 to January 1998

J. M. Andrews; J. P. Ashby; G. Jevons; T. Marshall; N. Lines; R. Wise


Journal of Antimicrobial Chemotherapy | 1999

A study to determine the pharmacokinetics and inflammatory fluid penetration of gatifloxacin following a single oral dose

R. Wise; J. M. Andrews; J. P. Ashby; J. Marshall


Journal of Antimicrobial Chemotherapy | 2007

Concentrations in plasma, epithelial lining fluid, alveolar macrophages and bronchial mucosa after a single intravenous dose of 1.6 mg/kg of iclaprim (AR-100) in healthy men

J. M. Andrews; D. Honeybourne; J. P. Ashby; G. Jevons; Adam P. Fraise; P. Fry; S. Warrington; S. Hawser; R. Wise


Journal of Antimicrobial Chemotherapy | 2001

Pharmacokinetics and tissue penetration of gemifloxacin following a single oral dose

T. Gee; J. M. Andrews; J. P. Ashby; G. Marshall; R. Wise


Journal of Antimicrobial Chemotherapy | 2002

Effect of protein binding on the in vitro activity and pharmacodynamics of faropenem

F. J. Boswell; J. P. Ashby; J. M. Andrews; R. Wise


Journal of Antimicrobial Chemotherapy | 1999

Antimicrobial resistance in Gram-positive pathogens isolated in the UK between October 1996 and January 1997

J. M. Andrews; J. P. Ashby; G. Jevons; N. Lines; R. Wise


Journal of Antimicrobial Chemotherapy | 1999

Tentative minimum inhibitory concentration and zone diameter breakpoints for moxifloxacin using BSAC criteria

J. M. Andrews; J. P. Ashby; G. Jevons; R. Wise

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J. M. Andrews

Nottingham City Hospital

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R. Wise

British Society for Antimicrobial Chemotherapy

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Anne Loughrey

Belfast Health and Social Care Trust

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Camilla Wiuff

Health Protection Scotland

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D. Honeybourne

University of Birmingham

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Derek Brown

Health Protection Scotland

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Gemma L. Vanstone

Royal Free London NHS Foundation Trust

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