Antimicrobial for 7 or 14 Days for Febrile Urinary Tract Infection in Men: A Multicenter Noninferiority Double-Blind, Placebo-Controlled, Randomized Clinical Trial

被引:1
作者
Lafaurie, Matthieu [1 ,33 ]
Chevret, Sylvie [2 ,3 ]
Fontaine, Jean-Paul [4 ]
Mongiat-Artus, Pierre [5 ]
de Lastours, Victoire [6 ,7 ,8 ]
Escaut, Lelia [9 ]
Jaureguiberry, Stephane [9 ]
Bernard, Louis [10 ]
Bruyere, Franck [11 ]
Gatey, Caroline [12 ,15 ]
Abgrall, Sophie [13 ]
Ferreyra, Milagros [14 ]
Aumaitre, Hugues [14 ]
Aparicio, Caroline
Garrait, Valerie [16 ]
Meyssonnier, Vanina [17 ]
Bourgarit-Durand, Anne [18 ]
Chabrol, Amelie [19 ]
Piet, Emilie [20 ]
Talarmin, Jean-Philippe [21 ]
Morrier, Marine [22 ]
Canoui, Etienne [23 ]
Charlier, Caroline [23 ,24 ]
Etienne, Manuel [25 ]
Pacanowski, Jerome [26 ]
Grall, Nathalie [7 ,8 ,27 ]
Desseaux, Kristell [28 ]
Empana-Barat, Florence [29 ]
Madeleine, Isabelle [30 ]
Bercot, Beatrice [7 ,8 ,31 ]
Molina, Jean-Michel [32 ]
Lefort, Agnes [6 ,7 ,8 ]
机构
[1] Hop St Louis, Hop Lariboisiere, AP HP, Dept Infect Dis, Paris, France
[2] Hop St Louis, Dept Biostat, AP HP, Paris, France
[3] Univ Paris Diderot, Inserm S 717, Paris, France
[4] Hop St Louis, Emergency Dept, AP HP, Paris, France
[5] Hop St Louis, AP HP, Dept Urol, Paris, France
[6] Hop Beaujon, AP HP, Dept Internal Med, Clichy, France
[7] Univ Paris Cite, Infect Antimicrobials Modelling Evolut IAME Res Gr, UMR 1137, Paris, France
[8] Inserm, Paris, France
[9] Hop Bicetre, Dept Infect Dis, AP HP, Le Kremlin Bicetre, France
[10] CHRU Tours, Dept Infect Dis, Tours, France
[11] CHRU Tours, Dept Urol, Tours, France
[12] Hop Antoine Beclere, AP HP, Dept Internal Med, Clamart, France
[13] Univ Paris Saclay, Inserm, U1018, Le Kremlin Bictre, France
[14] Ctr Hosp Perpignan, Dept Infect Dis, Perpignan, France
[15] Hop Lariboisiere, AP HP, Dept Internal Med, Paris, France
[16] Ctr Hosp Intercommunal Creteil, Dept Internal Med, Creteil, France
[17] Grp Hosp Diaconesses Croix St Simon, Dept Internal Med & Infect Dis, Paris, France
[18] Hop Jean Verdier, AP HP, Dept Internal Med, Bondy, France
[19] Hop Sud Francilien, Dept Infect Dis, Corbeil Essonnes, France
[20] Ctr Hosp Annecy Genevois, Dept Infect Dis, Annecy, France
[21] Ctr Hosp Intercommunal Cornouaille, Dept Infect Dis, Quimper, France
[22] Ctr Hosp Dept La Roche Sur Yon, Dept Infect Dis, La Roche Sur Yon, France
[23] Hop Cochin, AP HP, Mobile Infect Dis Team, Paris, France
[24] Univ Paris Cite Hosp, AP HP, French Natl Reference Ctr Listeria, Inst Pasteur,Biol Infect Unit,Inserm,U1117, Paris, France
[25] Hop Charles Nicolle, Dept Infect Dis, Rouen, France
[26] Hop St Antoine, Dept Infect Dis, AP HP, Paris, France
[27] Hop Bichat Claude Bernard, Dept Bacteriol, AP HP, Paris, France
[28] Hop St Louis, Dept Biostat, AP HP, Paris, France
[29] Agence Gen Equipements & Prod St, Clin Trial Dept, AP, Paris, France
[30] Hop St Louis, Pharm, AP HP, Paris, France
[31] Hop St Louis, Hop Lariboisiere, Dept Microbiol, AP HP, Paris, France
[32] Univ Paris Cite, Inserm, UMR 941, Paris, France
[33] Hop St Louis, Infect Dis Dept, 1 Ave Claude Vellefaux, F-75010 Paris, France
关键词
urinary tract infection; men; antibiotic duration; ofloxacin; ANTIBIOTIC-TREATMENT; DURATION;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In this multicenter randomized, double-blind placebo-controlled noninferiority trial, 240 men were assigned to receive antibiotic therapy for 7 (115 participants) or 14 days (125 participants) for febrile urinary tract infection. A treatment for 7 days was inferior to 14 days. Background The optimal duration of antimicrobial therapy for urinary tract infections (UTIs) in men remains controversial. Methods To compare 7 days to 14 days of total antibiotic treatment for febrile UTIs in men, this multicenter randomized, double-blind. placebo-controlled noninferiority trial enrolled 282 men from 27 centers in France. Men were eligible if they had a febrile UTI and urine culture showing a single uropathogen. Participants were treated with ofloxacin or a third-generation cephalosporin at day 1, then randomized at day 3-4 to either continue ofloxacin for 14 days total treatment, or for 7 days followed by placebo until day 14. The primary endpoint was treatment success, defined as a negative urine culture and the absence of fever and of subsequent antibiotic treatment between the end of treatment and 6 weeks after day 1. Secondary endpoints included recurrent UTI within weeks 6 and 12 after day 1, rectal carriage of antimicrobial-resistant Enterobacterales, and drug-related events. Results Two hundred forty participants were randomly assigned to receive antibiotic therapy for 7 days (115 participants) or 14 days (125 participants). In the intention-to-treat analysis, treatment success occurred in 64 participants (55.7%) in the 7-day group and in 97 participants (77.6%) in the 14-day group (risk difference, -21.9 [95% confidence interval, -33.3 to -10.1]), demonstrating inferiority. Adverse events during antibiotic therapy were reported in 4 participants in the 7-day arm and 7 in the 14-day arm. Rectal carriage of resistant Enterobacterales did not differ between both groups. Conclusions A treatment with ofloxacin for 7 days was inferior to 14 days for febrile UTI in men and should therefore not be recommended.
引用
收藏
页码:2154 / 2162
页数:9
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