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重新定义以细菌菌落计数为标准的尿路感染。

Redefining urinary tract infections by bacterial colony counts.

机构信息

BSc, MB BS, FRCP, Department of Paediatric Nephrology, Royal Victoria Infirmary, Newcastle NE1 4LP, United Kingdom.

出版信息

Pediatrics. 2010 Feb;125(2):335-41. doi: 10.1542/peds.2008-1455. Epub 2010 Jan 25.

Abstract

OBJECTIVES

To determine the best urinary bacterial concentration to diagnose urine infections.

METHODS

We studied a quantitative culture of paired urine samples from children that were promptly tested together after serial dilution. The initial diagnosis of urinary tract infection made from the result of the first urine culture and subsequently modified according to the second sample result, and then the ratio of their colony counts was considered. A total of 203 children (aged 2.0 weeks to 17.7 years) were screened for urine infection in a hospital setting.

RESULTS

The 36 children who had a urinary tract infection, defined as having the same uropathogen in both urine samples at concentrations within 25-fold of each other, had a mean colony count of 1.7 x 10(7) colony-forming units/mL. Among the 167 children who did not have a urinary tract infection, 12 (7.2%) would have had a false-positive diagnosis made on the first sample, which was revealed because the second sample result was different (n = 7) or had a > or =25-fold different colony count (n = 5). Raising the threshold from 10(5) to 10(6) colony-forming units/mL reduces the false-positive rate 4.8%. If 2 samples are cultured, the false-positive rates fall to 3.6% and 0.6%, respectively. All 9 children (5.4% of those without a urinary tract infection) who had a mixed culture with > or =10(5) colony-forming units/mL of a uropathogen (heavy mixed growth) in the first sample had a urine infection excluded by the second sample result.

CONCLUSION

The minimum urinary bacterial concentration that is used to diagnose a urine infection should be increased from > or =10(5) to > or =10(6) colony-forming units/mL, because that would reduce the false-positive rate from 7.2% to 4.8% if 1 sample was cultured and from 3.6% to 0.6% if 2 samples were cultured. Urine samples with heavy mixed growths should be considered contaminated.

摘要

目的

确定诊断尿液感染的最佳尿细菌浓度。

方法

我们对来自儿童的配对尿液样本进行了定量培养,这些样本在经过连续稀释后立即一起进行检测。根据第一份尿液培养物的结果做出初始尿路感染诊断,并随后根据第二份样本的结果进行修改,然后考虑它们的菌落计数比值。在医院环境中对 203 名儿童(年龄 2.0 周至 17.7 岁)进行了尿液感染筛查。

结果

36 名患有尿路感染的儿童,其定义为在彼此浓度相差 25 倍的范围内有相同尿路病原体的尿液样本,其平均菌落计数为 1.7×10(7)个菌落形成单位/mL。在 167 名没有尿路感染的儿童中,12 名(7.2%)将因第二份样本的结果不同(n=7)或菌落计数相差>或=25 倍(n=5)而做出假阳性诊断,因为第一份样本的结果显示出假阳性诊断。将阈值从 10(5)提高到 10(6)个菌落形成单位/mL 可将假阳性率降低 4.8%。如果培养 2 个样本,假阳性率分别降至 3.6%和 0.6%。在第一份样本中混合培养有>或=10(5)个菌落形成单位/mL 尿路病原体(重度混合生长)的 9 名儿童(无尿路感染的儿童中占 5.4%),第二份样本的结果排除了尿路感染。

结论

用于诊断尿液感染的最低尿细菌浓度应从>或=10(5)提高到>或=10(6)个菌落形成单位/mL,如果培养 1 个样本,假阳性率将从 7.2%降至 4.8%,如果培养 2 个样本,假阳性率将从 3.6%降至 0.6%。应将重度混合生长的尿液样本视为污染。

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