Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/12502
Title: Efficacy and safety of prolonged versus intermittent infusion of beta-lactam antibiotics as empirical therapy in patients with sepsis
Authors: Hemvimon S.
Srinithiwat P.
Koomanachai P.
Thamlikitkul V.
Jitmuang A.
Keywords: amoxicillin plus clavulanic acid
ceftazidime
imipenem
meropenem
piperacillin plus tazobactam
vancomycin
beta lactam antibiotic
cefepime
ceftazidime
doripenem
imipenem
meropenem
piperacillin plus tazobactam
Acinetobacter baumannii
adult
aged
Article
controlled study
coronary artery disease
diabetes mellitus
diarrhea
Escherichia coli
female
human
Klebsiella pneumoniae
major clinical study
male
minimum inhibitory concentration
observational study
randomized controlled trial (topic)
sepsis
urinary tract infection
APACHE
bacteremia
bacterial clearance
clinical outcome
cohort analysis
comparative study
continuous infusion
drug efficacy
drug infusion
drug intermittent therapy
drug safety
empirical research
extended spectrum beta lactamase producing Escherichia coli
extended spectrum beta lactamase producing Klebsiella pneumoniae
gastrointestinal symptom
hospital infection
infection
intra abdominal infection
long term exposure
middle aged
outcome assessment
phlebitis
pneumonia
prospective study
Pseudomonas aeruginosa
rash
sepsis
skin and soft tissue infection
survival rate
treatment response
Issue Date: 2019
Abstract: Objective: To determine the efficacy and safety of beta-lactam antibiotics (ceftazidime, cefepime, piperacillin/tazobactam, imipenem, meropenem, and doripenem) administered by intermittent infusion (II) compared with three to four-hour prolonged infusion (PI) in acutely ill-hospitalized patients with sepsis. Materials and Methods: The authors conducted a prospective cohort study between January 2010 and December 2013. Results: Of 219 subjects, 213 were recruited in the present study, 109 patients were in the II group and 104 patients were in the PI group. No significant difference of baseline characteristics between both groups. About 70% of infections from both groups were associated with hospital-associated infection. Sepsis was significantly higher in PI group (p=0.02). Pneumonia, bacteremia, and urinary tract infection (UTI) were the major foci of sepsis in the present study. Escherichia coli that mainly came from UTI was the major etiologic pathogen, whereas the causative pathogen was unknown in 49.3%. The 28-day survival was 87.2% in the II group and 79.8% in the PI group (p=0.27). Favorable clinical outcomes resulted in 74.3% of the II group and 76.9% of the PI group (p=0.11). A complete microbiological response was documented in 62.3% of the II group and 63.2% of the PI group (p=0.91). No serious adverse events were observed in either group. Conclusion: There were no significant differences in clinical, microbiological, and safety outcomes between the two groups. © Journal of the medical association of Thailand.
URI: https://ir.swu.ac.th/jspui/handle/123456789/12502
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85062901646&partnerID=40&md5=fc016a0b54dbcdebdc4a496ce3795d73
ISSN: 1252208
Appears in Collections:Scopus 1983-2021

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