Etherington Christine, Hall Melanie, Conway Steven, Peckham Daniel, Denton Miles
Adult Cystic Fibrosis Unit, Seacroft Hospital, Leeds LS14 6UH, UK.
J Antimicrob Chemother. 2008 Feb;61(2):425-7. doi: 10.1093/jac/dkm481. Epub 2007 Dec 21.
BACKGROUND Susceptibility testing results are not predictive of clinical response to antibiotic therapy in chronic Pseudomonas aeruginosa infections in cystic fibrosis (CF). We assessed the impact of reducing the number of routine susceptibility tests performed on clinical outcome in these cases. METHODS In June 2006, we introduced a protocol whereby susceptibility tests of P. aeruginosa isolates obtained from respiratory samples of people with CF were limited to those taken at the commencement of antibiotic therapy, when there was evidence of clinical failure or routinely if not tested in the previous 3 months. At all other times, isolates were identified and reported as normal but P. aeruginosa isolates were not subjected to susceptibility testing. RESULTS Over a 6 month period, P. aeruginosa was isolated on at least one occasion from 193 patients attending the Adult Cystic Fibrosis Unit. In this period, we reduced the number of routine susceptibility tests by 56% (from a projected 2231 tests on 872 samples to an actual 972 tests on 427 samples). We assessed the response to courses of intravenous antibiotic treatment administered during the 6 month study period in 2006 and for courses administered in the same patients during the same calendar months in 2005. No significant differences in median change of FEV1, FVC, C-reactive protein (CRP), white cell count, weight or duration of intravenous antibiotics were observed. The projected savings of this intervention were 3500 euros in consumables and 170 h (costed at 6500 euros) of laboratory staff time per annum, a total annual saving of 10,000 euros (6500 pounds sterling). CONCLUSIONS For CF units sending regular, routine sputum samples, a reduction in the number of susceptibility tests performed in cases of chronic P. aeruginosa infection can be carried out without impacting on short-term clinical outcomes.
背景 药敏试验结果无法预测囊性纤维化(CF)患者慢性铜绿假单胞菌感染对抗生素治疗的临床反应。我们评估了减少这些病例中常规药敏试验次数对临床结局的影响。
方法 2006年6月,我们引入了一项方案,即从CF患者呼吸道样本中分离出的铜绿假单胞菌菌株的药敏试验仅限于在抗生素治疗开始时采集的样本(如果有临床治疗失败的证据),或者如果在前3个月未进行过检测则按常规进行检测。在所有其他时间,分离菌株被鉴定并报告为正常,但铜绿假单胞菌菌株不进行药敏试验。
结果 在6个月的时间里,至少有一次从193名就诊于成人囊性纤维化科的患者中分离出铜绿假单胞菌。在此期间,我们将常规药敏试验次数减少了56%(从预计对872份样本进行2231次试验减少到实际对427份样本进行972次试验)。我们评估了2006年6个月研究期间以及2005年相同日历月份对同一患者进行的静脉抗生素治疗疗程的反应。在第1秒用力呼气量(FEV1)、用力肺活量(FVC)、C反应蛋白(CRP)、白细胞计数、体重或静脉抗生素治疗持续时间的中位数变化方面未观察到显著差异。该干预措施预计每年可节省3500欧元的耗材费用和170小时(按6500欧元计算成本)的实验室工作人员时间,每年总共节省10,000欧元(6500英镑)。
结论 对于定期送检常规痰标本的CF科室,在慢性铜绿假单胞菌感染病例中减少药敏试验次数不会影响短期临床结局。