Ceftriaxone versus ceftriaxone plus a macrolide for community-acquired pneumonia in hospitalized patients with HIV/AIDS: a randomized controlled trial

被引:11
作者
Figueiredo-Mello, C. [1 ,2 ]
Naucler, P. [3 ,4 ]
Negra, M. D. [5 ]
Levin, A. S. [1 ]
机构
[1] Univ Sao Paulo, Fac Med, Dept Infect Dis, Sao Paulo, Brazil
[2] Inst Infectol Emilio Ribas, Dept Educ & Res, Sao Paulo, Brazil
[3] Karolinska Inst, Infect Dis Unit, Dept Med Solna, Stockholm, Sweden
[4] Karolinska Univ Hosp, Dept Infect Dis, Stockholm, Sweden
[5] Inst Infectol Emilio Ribas, Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Community-acquired infections/therapy; Human immunodeficiency virus infections/complications; Lung diseases/therapy; Macrolides; Randomized controlled trial; BETA-LACTAM MONOTHERAPY; HIV-INFECTED PATIENTS; ATYPICAL PATHOGENS; MORTALITY; THERAPY; GUIDELINES; ETIOLOGY; IMPACT;
D O I
10.1016/j.cmi.2017.06.013
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: To evaluate if treatment with ceftriaxone and a macrolide, improved patient outcome when compared with monotherapy with ceftriaxone, in hospitalized patients with human immunodeficiency virus/acquired immunodeficient syndrome (HIV/AIDS) with community-acquired pneumonia (CAP). Methods: Adult patients with HIV hospitalized due to suspected CAP were randomized to receive one of two regimens, ceftriaxone plus macrolide or ceftriaxone plus placebo, at a 1:1 proportion (Brazilian Clinical Trials Registry: RBR-8wtq2b). The primary outcome was in-hospital mortality and the secondary outcomes were mortality within 14 days, need for vasoactive drugs, need for mechanical ventilation, time to clinical stability and length of hospitalization. Results: A total of 227 patients were randomized, two were excluded after randomization; 225 patients were analysed (112 receiving ceftriaxone plus placebo and 113 receiving ceftriaxone plus macrolide). The frequency of the primary outcome, in-hospital mortality, was not statistically different between the regimens: 12/112 (11%) patients who received ceftriaxone plus placebo and 17/113 (15%) who received ceftriaxone plus macrolide died during hospitalization (hazard ratio 1.22, 95% CI 0.57-2.59). We did not find differences between the regimens for any of the secondary outcomes, including mortality within 14 days, which occurred in 5/112 (4%) patients with ceftriaxone plus placebo and in 12/113 (11%) patients with ceftriaxone plus macrolide (relative risk 2.38, 95% CI 0.87-6.53). Conclusions: Among hospitalized patients with HIV/AIDS with CAP, treatment with ceftriaxone and a macrolide did not improve patient outcomes, when compared with ceftriaxone monotherapy. (c) 2017 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:146 / 151
页数:6
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