Folgori, L;
Di Carlo, D;
Commandatore, F;
Piazza, A;
Witney, AA;
Bresesti, I;
Hsia, Y;
Laing, K;
Monahan, I;
Bielicki, J;
et al.
Folgori, L; Di Carlo, D; Commandatore, F; Piazza, A; Witney, AA; Bresesti, I; Hsia, Y; Laing, K; Monahan, I; Bielicki, J; Alvaro, A; Zuccotti, GV; Planche, T; Heath, PT; Sharland, M
(2021)
Antibiotic Susceptibility, Virulome and Clinical Outcomes in European Infants with Bloodstream Infections Caused by Enterobacterales.
Antibiotics, 10 (6).
p. 706.
ISSN 2079-6382
https://doi.org/10.3390/antibiotics10060706
SGUL Authors: Hsia, Yingfen Witney, Adam Austin Bielicki, Julia Anna Heath, Paul Trafford Sharland, Michael Roy
Abstract
Mortality in neonates with Gram-negative bloodstream infections has remained unacceptably high. Very few data are available on the impact of resistance profiles, virulence factors, appropriateness of empirical treatment and clinical characteristics on patients’ mortality. A survival analysis to investigate 28-day mortality probability and predictors was performed including (I) infants <90 days (II) with an available Enterobacterales blood isolate with (III) clinical, treatment and 28-day outcome data. Eighty-seven patients were included. Overall, 299 virulence genes were identified among all the pathogens. Escherichia coli had significantly more virulence genes identified compared with other species. A strong positive correlation between the number of resistance and virulence genes carried by each isolate was found. The cumulative probability of death obtained by the Kaplan-Meier survival analysis was 19.5%. In the descriptive analysis, early age at onset, gestational age at onset, culture positive for E. coli and number of classes of virulence genes carried by each isolate were significantly associated with mortality. By Cox multivariate regression, none of the investigated variables was significant. This pilot study has demonstrated the feasibility of investigating the association between neonatal sepsis mortality and the causative Enterobacterales isolates virulome. This relationship needs further exploration in larger studies, ideally including host immunopathological response, in order to develop a tailor-made therapeutic strategy.
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