医学
菌血症
子群分析
析因分析
随机对照试验
内科学
抗生素
事后
持续时间(音乐)
抗生素治疗
显著性差异
平衡(能力)
临床试验
生存分析
重症监护医学
抗菌剂
样本量测定
随机化
梅德林
作者
Dafna Yahav,Ruxandra L Pinto,Deborah J. Cook,Joshua Saul Davis,Erick Huaileigh Duan,Tomer Hoffman,Todd Campbell Lee,Emily Gibson McDonald,Susan C. Morpeth,John Muscedere,Wendy Sligl,Terence C. Wuerz,Robert Fowler,Nick Daneman,Nick Daneman,Asgar H. Rishu,Ruxandra L Pinto,Benjamin A. Rogers,Yahya Shehabi,Rachael L. Parke
摘要
BACKGROUND: Despite the clinical significance of Pseudomonas aeruginosa bacteremia, the optimal duration of antibiotic therapy is unclear. We aimed to explore the association of antibiotic duration on mortality in hospitalized patients with P aeruginosa bacteremia. METHODS: This study was a post hoc analysis of all patients with P aeruginosa bacteremia included in the Bacteremia Antibiotic Length Actually Needed for Clinical Effectiveness (BALANCE) randomized controlled trial comparing 7 versus 14 days of antibiotic therapy for bacteremia. The primary outcome was 90-day mortality. Unadjusted risk differences (RDs) with 95% CIs for outcomes were calculated for patients randomized to 7 versus 14 days of treatment. Multivariable logistic regression was used to evaluate independent predictors of mortality. RESULTS: Among 157 patients with P aeruginosa bacteremia, 74 were randomized to 7 days of antibiotic treatment and 83 to 14 days. Patients in the 7-day group were more likely to be men and acquire infection in hospital. Crude mortality at 90 days in the intention-to-treat population was 22/74 (29.7%) in the 7-day group versus 17/83 (20.5%) in the 14-day group (RD: 9.2; 95% CI: -4.8 to 23.2). Age was associated with 90-day mortality (odds ratio [OR]: 1.06; 95% CI: 1.02-1.09), but randomization group (7 or 14 days) was not (OR: 1.47; 95% CI: .66-3.27). CONCLUSIONS: Among patients with P aeruginosa bacteremia included in an international trial testing duration of antibiotic treatment, no significant difference in mortality was demonstrated between 7 versus 14 days of antibiotic therapy; however, a limited sample size precludes a conclusion of noninferiority, benefit, or harm.
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