Antibiotic Prophylaxis and Recurrent Urinary Tract Infection in Children

被引:275
作者
Craig, Jonathan C. [1 ,2 ,3 ]
Simpson, Judy M. [3 ]
Williams, Gabrielle J. [1 ,2 ]
Lowe, Alison [1 ]
Reynolds, Graham J. [5 ]
McTaggart, Steven J. [6 ,7 ]
Hodson, Elisabeth M. [1 ,3 ]
Carapetis, Jonathan R. [8 ]
Cranswick, Noel E. [9 ,10 ]
Smith, Grahame [4 ]
Irwig, Les M. [2 ,3 ]
Caldwell, Patrina H. Y. [1 ]
Hamilton, Sana [1 ]
Roy, Leslie P. [1 ]
机构
[1] Childrens Hosp Westmead, Ctr Kidney Res, Sydney, NSW 2145, Australia
[2] Univ Sydney, Screening & Test Evaluat Program, Sydney, NSW 2006, Australia
[3] Univ Sydney, Sch Publ Hlth, Sydney, NSW 2006, Australia
[4] Childrens Hosp Westmead, Dept Urol & Surg, Sydney, NSW 2145, Australia
[5] Australian Natl Univ, Dept Paediat & Child Hlth, Sch Med, Canberra, ACT, Australia
[6] Queensland Child & Adolescent Renal Serv, Brisbane, Qld, Australia
[7] Univ Queensland, Brisbane, Qld, Australia
[8] Charles Darwin Univ, Menzies Sch Hlth Res, Darwin, NT 0909, Australia
[9] Univ Melbourne, Murdoch Childrens Res Inst, Melbourne, Vic, Australia
[10] Univ Melbourne, Royal Childrens Hosp, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
PRIMARY VESICOURETERAL REFLUX; CONTROLLED-TRIAL; RISK-FACTORS; RENAL SCARS; PREVENTION; PYELONEPHRITIS; ASSOCIATION; MULTICENTER; THERAPY; OLD;
D O I
10.1056/NEJMoa0902295
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Antibiotics are widely administered to children with the intention of preventing urinary tract infection, but adequately powered, placebo-controlled trials regarding efficacy are lacking. This study from four Australian centers examined whether low-dose, continuous oral antibiotic therapy prevents urinary tract infection in predisposed children. METHODS We randomly assigned children under the age of 18 years who had had one or more microbiologically proven urinary tract infections to receive either daily trimethoprim-sulfamethoxazole suspension (as 2 mg of trimethoprim plus 10 mg of sulfamethoxazole per kilogram of body weight) or placebo for 12 months. The primary outcome was microbiologically confirmed symptomatic urinary tract infection. Intention-to-treat analyses were performed with the use of time-to-event data. RESULTS From December 1998 to March 2007, a total of 576 children (of 780 planned) underwent randomization. The median age at entry was 14 months; 64% of the patients were girls, 42% had known vesicoureteral reflux (at least grade III in 53% of these patients), and 71% were enrolled after the first diagnosis of urinary tract infection. During the study, urinary tract infection developed in 36 of 288 patients (13%) in the group receiving trimethoprim-sulfamethoxazole (antibiotic group) and in 55 of 288 patients (19%) in the placebo group (hazard ratio in the antibiotic group, 0.61; 95% confidence interval, 0.40 to 0.93; P = 0.02 by the log-rank test). In the antibiotic group, the reduction in the absolute risk of urinary tract infection (6 percentage points) appeared to be consistent across all subgroups of patients (P >= 0.20 for all interactions). CONCLUSIONS Long-term, low-dose trimethoprim-sulfamethoxazole was associated with a decreased number of urinary tract infections in predisposed children. The treatment effect appeared to be consistent but modest across subgroups. (Australian New Zealand Clinical Trials Registry number, ACTRN12608000470392.)
引用
收藏
页码:1748 / 1759
页数:12
相关论文
共 40 条
[1]   Calculating the number needed to treat for trials where the outcome is time to an event [J].
Altman, DG ;
Andersen, PK .
BRITISH MEDICAL JOURNAL, 1999, 319 (7223) :1492-1495
[2]  
*AM AC PED COMM QU, 2000, PEDIATRICS, V105, P141
[3]  
[Anonymous], 1991, J R Coll Physicians Lond, V25, P36
[4]  
[Anonymous], COCHRANE DATABASE SY
[5]  
[Anonymous], PEDIATRICS 1
[6]   VESICOURETERAL REFLUX AND RENAL INJURY [J].
ARANT, BS .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1991, 17 (05) :491-511
[7]  
Bailey R R, 1973, Clin Nephrol, V1, P132
[8]  
Bergman DA, 1999, PEDIATRICS, V103, P843
[9]  
Bergman DA, 1999, PEDIATRICS, V104, P118
[10]   Clinical trials in children [J].
Caldwell, PHY ;
Murphy, SB ;
Butow, PN ;
Craig, JC .
LANCET, 2004, 364 (9436) :803-811