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Objective: To evaluate the connection between non-critically ill hospitalized patients and the acquisition of carbapenem-resistant (CRE).
Design: An observational prospective cohort study from January 2018 to December 2019.
Setting: A single tertiary referral center.
Participants: Non-critically ill subjects admitted to general medical wards who received antimicrobial therapy <48 h.
Methods: Rectal swab cultures at admission and weekly for CRE surveillance. CRE isolates were confirmed using carbapenem disk diffusion susceptibility and genotypic carbapenemase testing. Clinical characteristics and outcomes were also evaluated.
Results: Of 110 subjects, 66.4% were women, the mean age was 67 years, and 336 bacterial isolates were detected from rectal swab cultures. 55 (16.4%) isolates from 25 subjects exhibited phenotypic resistance to carbapenem. (50.9%) and (30.9%) were common CRE, harboring New Delhi metallo-beta-lactamase (NDM) (50.9%), oxacillinase-48 (OXA-48) (12.7%), and co-NDM/OXA-48 (20.0%). Subjects with acquired CRE had higher APACHE II scores ( = 0.030), received piperacillin-tazobactam ( = 0.004), underwent prolonged antimicrobial therapy ( = 0.009), and experienced longer hospital stays ( = 0.001) compared to CRE-negative subjects. None of the CRE-positive subjects developed an acquired infection.
Conclusions: Acquired CRE colonization is prevalent among non-critically ill patients. Factors such as disease severity, the type and duration of antimicrobial therapy, and the length of hospital stays may increase the risk of CRE acquisition in non-critically ill populations.
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http://dx.doi.org/10.1017/ash.2025.169 | DOI Listing |
BMJ Open
September 2025
Jiangsu Provincial Key Laboratory of Critical Care Medicine, Nanjing, Jiangsu, China
Objectives: To systematically compare the effects of various antithrombotic strategies on prespecified outcomes including 28-day all-cause mortality (primary outcome), major thrombotic events and major bleeding events (secondary outcomes) in adult COVID-19 patients.
Design: Systematic review and Bayesian network meta-analysis (NMA).
Data Sources: PubMed, Web of Science, Embase, Cochrane Library and ClinicalTrials.
SAGE Open Med Case Rep
August 2025
Department of Neurosurgery, The Nuclear Industry 215 Hospital of Shaanxi Province, Xianyang, Shaanxi, People's Republic of China.
Propofol is a commonly used sedative for the induction of clinical anesthesia and sedation maintenance in intensive care unit patients. However, in a minority of patients, prolonged infusion of propofol may cause metabolic acidosis, electrocardiographic abnormalities, arrhythmias, and rhabdomyolysis, a condition known as propofol-related infusion syndrome. If not promptly identified and managed, propofol-related infusion syndrome can be fatal.
View Article and Find Full Text PDFZhonghua Wei Zhong Bing Ji Jiu Yi Xue
April 2025
Department of Pediatrics, the Second People's Hospital of Liaocheng Affiliated to Shandong First Medical University, Linqing 252600, Shandong, China. Corresponding author: Xu Guixia, Email:
Objective: To investigate the application value of pediatric sepsis-induced coagulation (pSIC) score and mean platelet volume/platelet count (MPV/PLT) ratio in the diagnosis of pediatric sepsis and the determination of critical pediatric sepsis.
Methods: A retrospective cohort study was conducted, selecting 112 children with sepsis (sepsis group) admitted to pediatric intensive care unit (PICU) of Liaocheng Second People's Hospital from January 2020 to December 2023 as the study objects, and 50 children without sepsis admitted to the pediatric surgery department of our hospital during the same period for elective surgery due to inguinal hernia as the control (control group). The children with sepsis were divided into two groups according to the pediatric critical case score (PCIS).
J Pharm Health Care Sci
August 2025
Department of Clinical Pharmacy and Pharmacy Practice, Faculty of Pharmacy, University of Gezira, Wad medani, Sudan.
Background: Acid-suppressive therapy (AST) is often used without proper assessment of the need, dosage, or duration of treatment. This inappropriate use can lead to significant side effects, harmful drug interactions, and increased healthcare costs for patients.
Objective: This study aimed to evaluate stress ulcer prophylaxis (SUP) among hospitalized adult patients who were non-critically ill.
Current models of vaccination coverage screening and surveillance might miss underserved populations whose only health care access occurs in emergency departments (EDs). During April-December 2024, a survey of non-critically ill adult patients evaluated in 10 EDs in eight U.S.
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