The purpose of this study is to collect information from study participants who are hospitalized with an invasive disease caused by Extraintestinal pathogenic E. coli (ExPEC). This information will be used to support the development of a new vaccine to prevent Extraintestinal pathogenic Escherichia coli (ExPEC). E. coli bacteria are a leading cause of serious infections. Especially adults older than 60 years have a higher risk of developing such infections. To date, there is no vaccine available to prevent E. coli infections. To support the development of a vaccine, more information about E. coli infections is first needed. This information will be collected in the current study, such as: * Medical information such as medical history, diagnosis, duration of hospitalization * Treatment and outcome of the Extraintestinal pathogenic Escherichia coli (ExPEC) * Laboratory information
Janssen Research \& Development is developing ExPEC10V, a 10-valent conjugate vaccine comprising the 10 most predominant O-polysaccharides of ExPEC. Invasive ExPEC Disease (IED) is defined as an acute illness consistent with bacterial infection that is microbiologically confirmed either by the isolation and identification of E. coli from blood or other normally sterile body sites, or by the isolation and identification of E. coli from urine in a patient with signs and symptoms of invasive disease (presence of systemic inflammatory response syndrome \[SIRS\], sepsis or septic shock) and no other identifiable source of infection. ExPEC is the most common cause of infection in humans resulting from gram-negative bacteria. ExPEC comprises a pathogenic group of E. coli strains, possessing the ability to colonize and infect normally sterile body sites and to cause Invasive ExPEC Disease (IED). ExPEC causes the vast majority of urinary tract infections (UTIs), is the second most frequent cause of neonatal bacteremia and meningitis, and is a leading cause of adult IED, in particular bacteremia and sepsis. Although IED affects all age categories, adults aged 60 years or older have an increased risk of developing IED, including bacteremia and sepsis. The incidence of community-acquired ExPEC bacteremia increases with age, occurring at a rate of 150/100,000 person-years in the United States (US) adults aged 65 years and older, and 452/100,000 person-years in adults aged 85 years and older. Similar trends have been observed in Europe. In the US, it is estimated that up to 40,000 patients die annually due to IED, in particular from E. coli sepsis. Overall case-fatality rates for ExPEC bacteremia range from 13% to 19% but may be much higher (up to 60%) in the elderly with healthcare-associated infections. The increase in multidrug resistance (ie, resistance to two or more antibiotic classes) among ExPEC strains, such as E. coli sequence type 131:O25B, represents a major challenge for prevention and management of ExPEC infections. Global morbidity, hospitalization and mortality rates due to ExPEC infections are substantial and increasing due to aging populations and increasing prevalence of antibiotic resistant ExPEC strains, and associated with increasing healthcare costs in both Europe and the US. This hospital-based prospective epidemiological study will assess the O-serotype and O-genotype distribution in E. coli isolates causing IED overall and by subgroup based on risk factors. Detailed demographic and clinical data, including information on hospital routes, from patients with IED will be collected in this study to further characterize the clinical setting in this patient population. This study will also provide data to compare the clinical criteria of IED used by the study site with the proposed Phase 3 clinical case definition for IED in adults aged 60 years or older for future clinical studies in this patient population. No study drug will be administered in this non interventional study.
Study Type
OBSERVATIONAL
Enrollment
238
Duke Clinical Research Institute
Durham, North Carolina, United States
Duke Clinical Research Institute
Greater Sudbury, Canada
CHU Limoges - CIC
Limoges, France
UKK Uniclinic Cologne
Cologne, Germany
University of Verona
Verona, Italy
Janssen Pharmaceutical K.K.
Tokyo, Chiyoda-ku, Japan
Andalusian Public Foundation for Health Research Management in Seville (FISEVI)
Seville, Spain
University of Oxford
Oxford, United Kingdom
Distribution of E. coli O-serotypes causing IED in adults aged 60 years or older, as percentage of the total study population.
Time frame: 12 months
Distribution of E. coli O-genotypes causing IED in adults aged 60 years or older, as percentage of the total study population.
Time frame: 12 months
Distribution of IED in adults aged 60 years or older over the following clinical case definitions: "Pyelonephritis", "Urosepsis", "Meningitis", "Arthritis", "Sepsis of unknown origin" and "Others", as a percentage of the total study population.
Time frame: 12 months
Proportion of non-bacteremic and bacteremic IED of the total number of IED cases.
Time frame: 12 months
Listing of IED patients with specific risk factors for IED as a proportion of all IED patients.
Specific risk factors for IED are medical conditions (e.g. kidney disease, history of urinary tract infection in prior 12 months), sociodemographic characteristics (e.g. age, gender) and medication use (e.g. immunosuppressive medication)
Time frame: 12 months
Type of infection (community acquired, hospital-acquired or healthcare-associated) .
Time frame: 12 months
Source of infection (presence of an infectious focus within 30 days prior to IED).
Time frame: 12 months
Susceptibility of the cultured E. coli strains to antibiotics as determined by EUCAST standards (version9.0) to β-lactam antibiotics.
Time frame: 12 months
O-antigen expression profiles
Time frame: 12 months
Mortality associated with IED
Time frame: 12 months
Department where patient is presented/admitted to the hospital (emergency ward, general ward, intensive care unit)
Time frame: 12 months
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