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Mortality factors and antibiotic options in carbapenem-resistant Enterobacterales bloodstream infections: Insights from a high-prevalence setting with co-occurring NDM-1 and OXA-48.
Karnmueng, Palat; Montakantikul, Preecha; Paiboonvong, Taniya; Plongla, Rongpong; Chatsuwan, Tanittha; Chumnumwat, Supatat.
Afiliação
  • Karnmueng P; Division of Clinical Pharmacy, Department of Pharmacy, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand.
  • Montakantikul P; Department of Pharmacy Practice, College of Pharmacy, Rangsit University, Pathum Thani, Thailand.
  • Paiboonvong T; Division of Clinical Pharmacy, Department of Pharmacy, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand.
  • Plongla R; Department of Pharmacy Practice, College of Pharmacy, Rangsit University, Pathum Thani, Thailand.
  • Chatsuwan T; Division of Infectious Diseases, Department of Medicine, Faculty of Medicine, Chulalongkorn University, and King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok, Thailand.
  • Chumnumwat S; Center of Excellence in Antimicrobial Resistance and Stewardship, Chulalongkorn University, Bangkok, Thailand.
Clin Transl Sci ; 17(6): e13855, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38853376
ABSTRACT
Bloodstream infections (BSI) caused by carbapenem-resistant Enterobacterales (CRE) are associated with a high mortality rate. This study aimed to investigate factors associated with 14-day mortality and identify a potential treatment option. A retrospective cohort study was conducted on patients with CRE-BSI in Thailand from 2015 to 2020. The multivariate Cox proportional-hazards model was employed to identify factors influencing 14-day mortality. Out of 134 diagnosed cases of CRE-BSI, the all-cause 14-day mortality rate was 35.1%. The most prevalent organism isolated was Klebsiella pneumoniae (85.8%), followed by Escherichia coli (11.9%). Among the 60 isolates tested for carbapenemase genes, the majority exhibited co-occurring blaNDM-1 and blaOXA-48 (51.7%), followed by blaOXA-48 (31.7%) and blaNDM-1 (15.0%). In the multivariate analysis, neutropenia (adjusted hazard ratio [aHR] 2.55; 95% confidence interval [95%CI] 1.28-5.06; p = 0.008), sepsis/septic shock (aHR 3.02; 95%CI 1.33-6.86; p = 0.008), and previous metronidazole exposures (aHR 3.58; 95%CI 1.89-6.71; p < 0.001) were identified as independent factors for 14-day mortality. The fosfomycin-based regimen was found to be protective (aHR 0.37; 95%CI 0.15-0.92; p = 0.032). In patients with CRE-BSI, particularly in regions with a high occurrence of co-occurring blaNDM-1 and blaOXA-48, neutropenia, sepsis/septic shock, and previous metronidazole exposures emerged as independent risk factors for mortality. Moreover, the fosfomycin-based regimen showed an improvement in the survival rate.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Beta-Lactamases / Bacteriemia / Infecções por Enterobacteriaceae / Enterobacteriáceas Resistentes a Carbapenêmicos / Antibacterianos Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Beta-Lactamases / Bacteriemia / Infecções por Enterobacteriaceae / Enterobacteriáceas Resistentes a Carbapenêmicos / Antibacterianos Idioma: En Ano de publicação: 2024 Tipo de documento: Article