Weitkamp J-H, Ozdas A, LaFleur B, Potts A L
1Division of Neonatology, Department of Pediatrics, Monroe Carell Jr Children's Hospital at Vanderbilt, Nashville, TN 37232-0656, USA.
J Perinatol. 2008 Jun;28(6):405-11. doi: 10.1038/sj.jp.7211914. Epub 2008 Jan 10.
Previous reports suggest a benefit of fluconazole prophylaxis in extremely low birth weight (ELBW) infants <1000 g. Our aim was to evaluate if limiting fluconazole prophylaxis to targeted highest risk infants effectively prevents invasive fungal infections, has no undesired side effects and limits unnecessary drug exposure.
This nonrandomized retrospective pre-post intervention study compared two groups of infants: (1) Infants <26 weeks gestation and/or <750 g birth weight, requiring central vascular access and admitted to the Monroe Carell Jr Children's Hospital at Vanderbilt neonatal intensive care unit (NICU) prior to 5 days of age, who received fluconazole prophylaxis and (2) a matched control group from the year prior to prophylaxis. This target population was selected for fluconazole prophylaxis based on prior infection control data from our institution and a number needed to treat of <15 to prevent one episode of fungemia. Following implementation and integration through the institution's computerized physician order entry (CPOE) system, provider adherence to the protocol was assessed during the prophylaxis period.
A total of 86 patients were included in the study, 44 in the no-prophylaxis group and 42 in the prophylaxis group. In the targeted prophylaxis group, no invasive fungal infections were observed as compared to nine infants with invasive infections in the no-prophylaxis group (P=0.004). No significant adverse effects were recorded. Targeting the highest risk infants reduced the number of infants <1000 g requiring prophylaxis from 80 to 42 (48% reduction) with no preventable infection missed. Provider compliance was 91% following implementation of this protocol through the CPOE system using a standardized order set.
Targeting the highest risk infants for fluconazole prophylaxis through CPOE can effectively prevent invasive fungal infections and limit drug exposure with no unwanted side effects.
既往报告提示氟康唑预防用药对出生体重<1000g的极低出生体重(ELBW)婴儿有益。我们的目的是评估将氟康唑预防用药限定于目标高危婴儿是否能有效预防侵袭性真菌感染、无不良副作用并减少不必要的药物暴露。
这项非随机回顾性干预前后研究比较了两组婴儿:(1)妊娠<26周和/或出生体重<750g、需要中心血管通路且在5日龄前入住范德比尔特儿童医院新生儿重症监护病房(NICU)的婴儿,这些婴儿接受了氟康唑预防用药;(2)预防用药前一年的匹配对照组。根据我们机构先前的感染控制数据以及预防一例真菌血症所需治疗人数<15,选择该目标人群进行氟康唑预防用药。通过机构的计算机化医嘱录入(CPOE)系统实施并整合后,在预防用药期间评估医护人员对方案的依从性。
共有86例患者纳入研究,未预防用药组44例,预防用药组42例。在目标预防用药组中,未观察到侵袭性真菌感染,而未预防用药组有9例婴儿发生侵袭性感染(P=0.004)。未记录到显著不良反应。将最高危婴儿作为目标人群,使需要预防用药的<1000g婴儿数量从80例减少至42例(减少48%),且没有遗漏可预防的感染。通过使用标准化医嘱集在CPOE系统中实施该方案后,医护人员的依从性为91%。
通过CPOE系统将最高危婴儿作为氟康唑预防用药的目标人群可有效预防侵袭性真菌感染并减少药物暴露,且无不良副作用。