1. Critically ill patients with community-onset intraabdominal infections: Influence of healthcare exposure on resistance rates and mortality.
- Author
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Maseda E, Ramírez S, Picatto P, Peláez-Peláez E, García-Bernedo C, Ojeda-Betancur N, Aguilar G, Forés B, Solera-Marín J, Aliaño-Piña M, Tamayo E, Ramasco F, García-Álvarez R, González-Lisorge A, Giménez MJ, and Suárez-de-la-Rica A
- Subjects
- Adult, Age Factors, Aged, Aged, 80 and over, Anti-Bacterial Agents pharmacology, Anti-Bacterial Agents therapeutic use, Bacteria isolation & purification, Community-Acquired Infections diagnosis, Community-Acquired Infections drug therapy, Community-Acquired Infections mortality, Critical Illness mortality, Critical Illness therapy, Cross Infection diagnosis, Cross Infection drug therapy, Cross Infection mortality, Female, Humans, Intensive Care Units statistics & numerical data, Intraabdominal Infections diagnosis, Intraabdominal Infections drug therapy, Intraabdominal Infections mortality, Male, Middle Aged, Prospective Studies, Risk Factors, Severity of Illness Index, Spain epidemiology, Bacteria drug effects, Community-Acquired Infections microbiology, Cross Infection microbiology, Drug Resistance, Bacterial, Intraabdominal Infections microbiology
- Abstract
The concept of healthcare-associated infections (as opposed to hospital-acquired infections) in intraabdominal infections (IAIs) is scarcely supported by data in the literature. The aim of the present study was to analyse community-onset IAIs (non-postoperative/non-nosocomial) in patients admitted to intensive care units (ICUs), to investigate differences in resistance patterns linked to healthcare exposure and mortality-associated factors. A one-year prospective observational study (17 Spanish ICUs) was performed distributing cases as healthcare-associated infections (HCAI), community-acquired infections (CAI) and immunocompromised patients (ICP). Bacteria producing extended-spectrum β-lactamases (ESBL) and/or carbapenemase (CPE), high-level aminoglycoside- and/or methicillin- and/or vancomycin- resistance were considered antimicrobial resistant (AMR). Mortality-associated factors were identified by regression multivariate analysis. Of 345 patients included (18.8% HCAI, 6.1% ICP, 75.1% CAI), 51.6% presented generalized peritonitis; 32.5% were >75 years (55.4% among HCAI). Overall, 11.0% cases presented AMR (7.0% ESBL- and/or CPE), being significantly higher in HCAI (35.4%) vs. CAI (5.8%) (p<0.001) vs. ICP (0%) (p = 0.003). Overall 30-day mortality was 14.5%: 23.1% for HCAI and 11.6% for CAI (p = 0.016). Mortality (R2 = 0.262, p = 0.021) was positively associated with age >75 years (OR = 6.67, 95%CI = 2.56-17.36,p<0.001), Candida isolation (OR = 3.05, 95%CI = 1.18-7.87,p = 0.022), and SAPS II (per-point, OR = 1.08, 95%CI = 1.05-1.11, p<0.001) and negatively with biliary infections (OR = 0.06, 95%CI = 0.01-0.48,p = 0.008). In this study, the antimicrobial susceptibility pattern of bacteria isolated from patients with healthcare contact was shifted to resistance, suggesting the need for consideration of the healthcare category (not including hospital-acquired infections) for severe IAIs. 30-day mortality was positively related with age >75 years, severity and Candida isolation but not with AMR., Competing Interests: E.M. has served as speaker for Merck, Sharp & Dohme (MSD), Pfizer and Astellas; and has received educational grants from Astellas. F.R. has served as speaker for MSD. G.A. has served as speaker for MSD, Astellas, Gilead, and Pfizer and received educational grants from Astellas, Pfizer and MSD. M-JG is employee of PRISM-AG and has received an educational grant from Fundación Micellium para el Desarrollo y Difusión del Conocimiento Científico (Valencia, Spain). The remaining authors have disclosed that they do not have any potential conflicts of interest. This does not alter our adherence to PLOS ONE policies on sharing data and materials.
- Published
- 2019
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