头孢吡肟
医学
哌拉西林/他唑巴坦
哌拉西林
社区获得性肺炎
肺炎
他唑巴坦
内科学
环丙沙星
抗生素
重症监护医学
铜绿假单胞菌
微生物学
亚胺培南
抗生素耐药性
细菌
遗传学
生物
标识
DOI:10.1183/13993003.congress-2019.pa2922
摘要
Background: Patients with severe community-acquired pneumonia usually need ICU admission and have high mortality rate (up to 50%). Cefepime and piperacillin/tazobactam are active against Pseudomonas aeruginsa as well as Streptococcus pneumoniae but not recommended as primary therapy unless the patient has a risk for P. aeruginosa. But risks are not well established and it may be difficult for house staff to make a clinical decision and to narrow a spectrum of therapy might not be harmful. Methods: Patients with severe community-acquired pneumonia who was admitted in MICU have been recruited from Dec. 1, 2016 to Aug. 31, 2017. Patients who had absolute neutrophil count less than 1000/mm3 and received antibiotic therapy less than 72 hr were excluded. Each group received either cefepime or piperacillin/tazobactam, both with ciprofloxacin and changed to narrow spectrum antibiotic according to clinical evaluation. Results: 48 patients were screened and 43 patients (90%) were assessed. 21 patients were assigned to cefepime group and 22 were piperacillin/tazobactam group. APACHE II score were 18.7 ± 7.2 and 19.7 ± 7.9 (p=0.67). Clinical success rates were 86% and 82% for patients treated with cefepime and piperacillin/tazobactam respectively, and 3 (14%) and 4 patients (18%) were died, which showed no statistical significance. 9 patients (43%) in cefepime group and 5 (23%) in piperacillin/tazobactam group were superinfected (p=0.08). Conclusion: There were no significant differences in clinical efficacy in both groups. They would be acceptable strategies in terms of mortality but have concerns for superinfection.
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