Intravenous Polymyxin B as Adjunctive Therapy to High-Dose Tigecycline for the Treatment of Nosocomial Pneumonia Due to Carbapenem-Resistant Acinetobacter baumannii and Klebsiella pneumoniae : A Propensity Score-Matched Cohort Study.
Lei ZhaXue ZhangYusheng ChengQiancheng XuLingxi LiuSimin ChenZhiwei LuJun GuoBoris TefsenPublished in: Antibiotics (Basel, Switzerland) (2023)
Although the combination of polymyxin and tigecycline is widely used in treating carbapenem-resistant bacterial infections, the benefit of this combination is still uncertain. To assess whether adding polymyxin B to the high-dose tigecycline regimen would result in better clinical outcomes than the high-dose tigecycline therapy in patients with pneumonia caused by carbapenem-resistant Klebsiella pneumoniae and Acinetobacter baumannii , we conducted a propensity score-matched cohort study in a single center between July 2019 and December 2021. Of the 162 eligible patients, 102 were included in the 1:1 matched cohort. The overall 14-day mortality in the matched cohort was 24.5%. Compared with high-dose tigecycline, the combination therapy was not associated with better clinical outcomes, and showed similar 14-day mortality (OR, 0.72, 95% CI 0.27-1.83, p = 0.486), clinical cure (OR, 1.09, 95% CI 0.48-2.54, p = 0.823), microbiological cure (OR, 0.96, 95% CI 0.39-2.53, p = 0.928) and rate of nephrotoxicity (OR 0.85, 95% CI 0.36-1.99, p = 0.712). Subgroup analyses also did not demonstrate any statistical differences. Based on these results, it is reasonable to recommend against adding polymyxin B to the high-dose tigecycline regimen in treating pneumonia caused by carbapenem-resistant K. pneumoniae and A. baumannii .
Keyphrases
- high dose
- acinetobacter baumannii
- multidrug resistant
- klebsiella pneumoniae
- gram negative
- drug resistant
- stem cell transplantation
- combination therapy
- low dose
- pseudomonas aeruginosa
- escherichia coli
- end stage renal disease
- cardiovascular events
- ejection fraction
- newly diagnosed
- randomized controlled trial
- peritoneal dialysis
- stem cells
- staphylococcus aureus
- risk factors
- prognostic factors
- cell therapy
- cardiovascular disease
- community acquired pneumonia
- type diabetes
- replacement therapy
- intensive care unit
- study protocol
- drug induced