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- Volume 19, Issue 9, 06/Mar/2014
Eurosurveillance - Volume 19, Issue 9, 06 March 2014
Volume 19, Issue 9, 2014
- Editorials
- Rapid communications
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Zika virus infection complicated by Guillain-Barré syndrome – case report, French Polynesia, December 2013
E Oehler , L Watrin , P Larre , I Leparc-Goffart , S Lastère , F Valour , L Baudouin , H P Mallet , D Musso and F GhawcheZika fever, considered as an emerging disease of arboviral origin, because of its expanding geographic area, is known as a benign infection usually presenting as an influenza-like illness with cutaneous rash. So far, Zika virus infection has never led to hospitalisation. We describe the first case of Guillain-Barré syndrome (GBS) occurring immediately after a Zika virus infection, during the current Zika and type 1 and 3 dengue fever co-epidemics in French Polynesia. .
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Influenza vaccine effectiveness in Spain 2013/14: subtype-specific early estimates using the cycEVA study
S Jiménez-Jorge , F Pozo , S de Mateo , C Delgado-Sanz , I Casas , M García-Cenoz , J Castilla , R Sancho , L Etxebarriarteun-Aranzabal , C Quiñones , E Martínez , T Vega , A Garcia , J Giménez , J M Vanrell , D Castrillejo , A Larrauri and on behalf of Spanish Influenza Sentinel Surveillance System (SISS)Adjusted early estimates of the 2013/14 influenza vaccine effectiveness (VE) in Spain for all age groups was 35% (95% CI: ?9 to 62), 33% (95% CI: ?33 to 67) and 28% (95% CI: ?33 to 61) against any influenza virus type, A(H1N1)pdm09 and A(H3N2) viruses, respectively. For the population targeted for vaccination, the adjusted VE was 44% (95% CI: ?11 to 72), 36% (95% CI: ?64 to 75) and 42% (95% CI: ?29 to 74), respectively. These preliminary results in Spain suggest a suboptimal protective effect of the vaccine against circulating influenza viruses.
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Interim estimates of 2013/14 influenza clinical severity and vaccine effectiveness in the prevention of laboratory-confirmed influenza-related hospitalisation, Canada, February 2014
S A McNeil , V Shinde , M Andrew , T F Hatchette , J LeBlanc , A Ambrose , G Boivin , W R Bowie , F Diaz-Mitoma , M ElSherif , K Green , F Haguinet , S Halperin , B Ibarguchi , K Katz , JM Langley , P Lagacé-Wiens , B Light , M Loeb , J E McElhaney , D MacKinnon-Cameron , A E McCarthy , M Poirier , J Powis , D Richardson , M Semret , S Smith , D Smyth , G Stiver , S Trottier , L Valiquette , D Webster , L Ye , A McGeer , on behalf of the Public Health Agency of Canada/Canadian Institutes of Health Research Influenza Research Network (PCIRN) Serious Outcomes Surveillance Network and on behalf of the Toronto Invasive Bacterial Diseases Network (TIBDN)During the 2013/14 influenza season in Canada, 631 of 654 hospitalisations for laboratory-confirmed influenza enrolled in sentinel hospitals were due to Influenza A. Of the 375 with known subtype, influenza A(H1N1) accounted for 357. Interim unmatched vaccine effectiveness adjusted for age and presence of one or more medical comorbidities was determined by test-negative case-control design to be 58.5% (90% confidence interval (CI): 43.9-69.3%) overall and 57.9% (90% CI: 37.7-71.5) for confirmed influenza A(H1N1). .
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- Surveillance and outbreak reports
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Epidemiology of tuberculosis in big cities of the European Union and European Economic Area countries
This cross-sectional survey aimed to examine the epidemiology of tuberculosis (TB) in European Union (EU) and European Economic Area (EEA) cities with populations greater than 500,000. National TB programme managers were asked to provide data on big city population size, total number of notified TB cases in big cities and national notification rate for 2009. A rate ratio was calculated using the big city TB notification rate as a numerator and country TB notification rate, excluding big city TB cases and population, as a denominator. Twenty of the 30 EU/EEA countries had at least one big city. Pooled rate ratios were 2.5, 1.0, and 0.7 in low-, intermediate- and high-incidence countries respectively. In 15 big cities, all in low-incidence countries, rate ratios were twice the national notification rate. These data illustrate the TB epidemiology transition, a situation whereby TB disease concentrates in big cities as national incidence falls, most likely as a result of the higher concentration of risk groups found there. This situation requires targeted interventions and we recommend that big city TB data, including information about patients' risk factors, are collected and analysed systematically, and that successful interventions are shared. .
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Successful control of a hospital-wide outbreak of OXA-48 producing Enterobacteriaceae in the Netherlands, 2009 to 2011
On 31 May 2011, after notification of Klebsiella pneumoniae (KP)OXA-48;CTX-M-15 in two patients, nosocomial transmission was suspected in a Dutch hospital. Hospital-wide infection control measures and an outbreak investigation were initiated. A total of 72,147 patients were categorised into groups based on risk of OXA-48 colonisation or infection, and 7,527 were screened for EnterobacteriaceaeOXA-48 by polymerase chain reaction (PCR). Stored KP isolates (n=408) were retrospectively tested for OXA-48 and CTX-M-1 group extended-spectrum beta-lactamases (ESBL). 285 KP isolates from retrospective and prospective patient screening were genotyped by amplified fragment length polymorphism (AFLP). 41 isolates harbouring different Enterobacteriaceae species were analysed by plasmid multilocus sequence typing (pMLST). No nosocomial transmission of EnterobacteriaceaeOXA-48 was detected after 18 July 2011. EnterobacteriaceaeOXA-48 were found in 118 patients (KP (n=99), Escherichia coli (n=56), ≥1 EnterobacteriaceaeOXA-48 species (n=52)), of whom 21 had clinical infections. 39/41 (95%) of OXA-48 containing plasmids were identical in pMLST. Minimum inhibitory concentrations (MICs) of KPOXA-48 and E. coliOXA-48 for imipenem and meropenem ranged from ≤1 to ≥16 mg/L, and 153/157 (97%) had MIC >0.25 mg/L for ertapenem. AFLP identified a cluster of 203 genetically linked isolates (62 KPOXA-48;CTX-M15; 107 KPCTX-M-15; 34 KPOXA-48). The 'oldest' KPCTX-M-15 and KPOXA-48 clonal types originated from February 2009 and September 2010, respectively. The last presumed outbreak-related KPOXA-48 was detected in April 2012. Uncontrolled transmission of KPCTX-M-15 evolved into a nosocomial outbreak of KPOXA-48;CTX-M15 with large phenotypical heterogeneity. Although the outbreak was successfully controlled, the contribution of individual containment measures and of the hospital relocating into a new building just before outbreak notification was impossible to quantify. .
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- Perspectives
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Tuberculosis control in big cities and urban risk groups in the European Union: a consensus statement
N A van Hest , R W Aldridge , G de Vries , A Sandgren , B Hauer , A Hayward , W Arrazola de Oñate , W Haas , L R Codecasa , J A Caylà , A Story , D Antoine , A Gori , L Quabeck , J Jonsson , M Wanlin , À Orcau , A Rodes , M Dedicoat , F Antoun , H van Deutekom , S T Keizer and I AbubakarIn low-incidence countries in the European Union (EU), tuberculosis (TB) is concentrated in big cities, especially among certain urban high-risk groups including immigrants from TB high-incidence countries, homeless people, and those with a history of drug and alcohol misuse. Elimination of TB in European big cities requires control measures focused on multiple layers of the urban population. The particular complexities of major EU metropolises, for example high population density and social structure, create specific opportunities for transmission, but also enable targeted TB control interventions, not efficient in the general population, to be effective or cost effective. Lessons can be learnt from across the EU and this consensus statement on TB control in big cities and urban risk groups was prepared by a working group representing various EU big cities, brought together on the initiative of the European Centre for Disease Prevention and Control. The consensus statement describes general and specific social, educational, operational, organisational, legal and monitoring TB control interventions in EU big cities, as well as providing recommendations for big city TB control, based upon a conceptual TB transmission and control model.
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- Miscellaneous
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Volumes & issues
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Volume 29 (2024)
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Volume 28 (2023)
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Volume 27 (2022)
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Volume 26 (2021)
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Volume 25 (2020)
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Volume 24 (2019)
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Volume 23 (2018)
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Volume 22 (2017)
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Volume 21 (2016)
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Volume 20 (2015)
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Volume 19 (2014)
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Volume 18 (2013)
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Volume 17 (2012)
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Volume 16 (2011)
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Volume 15 (2010)
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Volume 14 (2009)
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Volume 13 (2008)
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Volume 12 (2007)
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Volume 11 (2006)
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Volume 10 (2005)
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Volume 9 (2004)
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Volume 8 (2003)
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Volume 7 (2002)
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Volume 6 (2001)
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Volume 5 (2000)
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Volume 4 (1999)
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Volume 3 (1998)
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Volume 2 (1997)
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Volume 1 (1996)
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Volume 0 (1995)
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