Post Hoc Assessment of Time to Clinical Response Among Adults Hospitalized with Community-Acquired Bacterial Pneumonia Who Received Either Lefamulin or Moxifloxacin in 2 Phase III Randomized, Double-Blind, Double-Dummy Clinical Trials

被引:5
作者
Lodise, Thomas [1 ]
Colman, Sam [2 ]
Stein, Daniel S. [3 ]
Fitts, David [3 ]
Goldberg, Lisa [3 ]
Alexander, Elizabeth [3 ]
Scoble, Patrick J. [3 ]
Schranz, Jennifer [3 ]
机构
[1] Albany Coll Pharm & Hlth Sci, 108 New Scotland Ave, Albany, NY 12208 USA
[2] Covance Market Access Serv Inc, Gaithersburg, MD USA
[3] Nabriva Therapeut US Inc, King Of Prussia, PA USA
来源
OPEN FORUM INFECTIOUS DISEASES | 2020年 / 7卷 / 05期
关键词
community-acquired bacterial pneumonia; fluoroquinolones; lefamulin; patient discharge; time to clinical response; DISCHARGE; RISK; CEFTRIAXONE; MANAGEMENT; STABILITY; OUTCOMES; RULE;
D O I
10.1093/ofid/ofaa145
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Time to clinical response, a proxy for hospital "discharge readiness," was compared between CABP inpatients who received lefamulin or moxifloxacin in the Lefamulin Evaluation Against Pneumonia (LEAP) trials. The analysis included 926 inpatients. A short and comparable median time to clinical response (4 days) was observed in both treatment groups.
引用
收藏
页数:4
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