Schlager T A, Anderson S, Trudell J, Hendley J O
Department of Pediatrics and Emergency Medicine, University of Virginia, Charlottesville 22906-0014, USA.
J Pediatr. 1998 Apr;132(4):704-8. doi: 10.1016/s0022-3476(98)70364-6.
To determine the effect of nitrofurantoin prophylaxis on rates of bacteriuria and symptomatic urinary tract infection in children with chronic neurogenic bladder receiving clean intermittent catheterization.
Double-blind, placebo-controlled, crossover trial of 15 children receiving nitrofurantoin or placebo for 11 months (5 months receiving one drug, then 1 month of washout followed by 5 months of the alternate drug). Weekly home visits were made. During each visit a sample of bladder urine was obtained by intermittent catheterization, signs and symptoms of urinary tract infection were recorded, and all medications were recorded as well as a capsule count of the study drug.
During nitrofurantoin the frequency of bacteriuria remained high. Cultures of 74% (203 of 274) of the 274 samples on placebo were positive for a pathogen (> or = 10(4) colony-forming units per milliliter) compared with 65% (165 of 252) of the 252 samples on nitrofurantoin. The bacterial species responsible for bacteriuria, however, were altered; Escherichia coli, the most common pathogen isolated during placebo, was replaced by resistant Klebsiella spp. and Pseudomonas spp. during nitrofurantoin. The carriage of these resistant organisms tripled during nitrofurantoin. Symptomatic infection dropped in half on nitrofurantoin, but this decline was due solely to infections caused by E. coli. Despite an increased frequency of resistant organisms on nitrofurantoin prophylaxis, an increase in urinary tract infections caused by these resistant organisms did not occur.
Routine use of nitrofurantoin prophylaxis in an attempt to eradicate bacteriuria in patients with chronic neurogenic bladder is not effective.
确定呋喃妥因预防措施对接受清洁间歇性导尿的慢性神经源性膀胱患儿菌尿症发生率和有症状性尿路感染发生率的影响。
对15名儿童进行双盲、安慰剂对照、交叉试验,这些儿童接受呋喃妥因或安慰剂治疗11个月(5个月接受一种药物治疗,然后1个月洗脱期,接着5个月接受另一种药物治疗)。每周进行家访。每次访视时,通过间歇性导尿获取膀胱尿液样本,记录尿路感染的体征和症状,记录所有药物以及研究药物的胶囊计数。
在使用呋喃妥因期间,菌尿症发生率仍然很高。安慰剂组274份样本中有74%(203份)的培养物检出病原体呈阳性(每毫升≥10⁴ 菌落形成单位),而呋喃妥因组252份样本中有65%(165份)呈阳性。然而,导致菌尿症的细菌种类发生了变化;安慰剂期间分离出的最常见病原体大肠杆菌,在使用呋喃妥因期间被耐药的克雷伯菌属和假单胞菌属所取代。在使用呋喃妥因期间,这些耐药菌的携带率增加了两倍。使用呋喃妥因期间有症状性感染减少了一半,但这种下降完全是由于大肠杆菌引起的感染。尽管使用呋喃妥因预防时耐药菌的发生率增加,但由这些耐药菌引起的尿路感染并未增加。
常规使用呋喃妥因预防措施试图根除慢性神经源性膀胱患者的菌尿症是无效的。