Omran Eman A, Eisa Faten F, Bakr Wafaa M K
J Pediatr Pharmacol Ther. 2020 Jan-Feb;25(1):53-60. doi: 10.5863/1551-6776-25.1.53.
This study aimed to assess the microbial contamination rate of injectable lipid emulsion (ILE) repackaged syringes at 12 and 24 hours of their infusion time. Probable risk factors associated with contamination of the ILEs were also assessed. In addition, the antimicrobial resistance pattern of the bacterial isolates was also determined.
Samples of ILE were collected from 152 repackaged syringes and their infusion lines after 12 hours and 24 hours of infusion time (73 and 79 samples, respectively). Samples were cultured, the isolates were identified, and the antimicrobial resistance pattern of the bacterial isolates was identified. A checklist was completed throughout the study to observe the compliance to infection control measures by pharmacists (who prepare) and nurses (who administer) the ILE infusions. Results of septic neonatal cultures were taken from records.
Microbial contamination was found in 15.8% of ILE samples. The 2 most common pathogens found among positive samples were Klebsiella pneumoniae (29.2%) and Candida albicans (20.8%). Microbial contamination of repackaged syringes increased from 9.6% at 12 hours to 21.5% at 24 hours. This difference was found to be statistically significant (p = 0.044). A similar trend of predominance of those 2 pathogens, in both ILE and neonatal cultures, was observed. There was a statistically significant better performance of infection control measures of pharmacists rather than nurses. The K pneumoniae isolates (n = 7) showed antibiotic resistance in the following pattern: gentamicin (71.4%), cefazolin (85.7%), and cefoxitin (85.7%).
The rate of ILE contamination was less at 12 hours' than at 24 hours' infusion time. However, contamination rates at 12 hours were unacceptably high. Klebisella pneumoniae and C albicans were the most common pathogens isolated from ILE. Compliance with infection control measures was significantly worse among nurses compared with pharmacists.
本研究旨在评估重新包装的注射器中注射用脂质乳剂(ILE)在输注12小时和24小时时的微生物污染率。还评估了与ILE污染相关的可能风险因素。此外,还确定了分离出的细菌的抗菌耐药模式。
在输注12小时和24小时后(分别为73和79个样本),从152个重新包装的注射器及其输液管中收集ILE样本。对样本进行培养,鉴定分离菌,并确定细菌分离株的抗菌耐药模式。在整个研究过程中完成一份检查表,以观察配制ILE输液的药剂师和给药的护士对感染控制措施的遵守情况。败血症新生儿培养结果取自记录。
在15.8%的ILE样本中发现微生物污染。在阳性样本中发现的2种最常见病原体是肺炎克雷伯菌(29.2%)和白色念珠菌(20.8%)。重新包装的注射器的微生物污染率从12小时时的9.6%增加到24小时时的21.5%。发现这种差异具有统计学意义(p = 0.044)。在ILE和新生儿培养物中均观察到这2种病原体的相似优势趋势。药剂师的感染控制措施在统计学上比护士表现更好。肺炎克雷伯菌分离株(n = 7)表现出以下抗生素耐药模式:庆大霉素(71.4%)、头孢唑林(85.7%)和头孢西丁(85.7%)。
ILE污染率在输注12小时时低于24小时时。然而,12小时时的污染率高得令人无法接受。肺炎克雷伯菌和白色念珠菌是从ILE中分离出的最常见病原体。与药剂师相比,护士对感染控制措施的遵守情况明显更差。