Driessen M, Ellis J B, Cooper P A, Wainer S, Muwazi F, Hahn D, Gous H, De Villiers F P
Department of Pediatrics and Child Health, Ga-Rankuwa Hospital, Medical University of Southern Africa, South Africa.
Pediatr Infect Dis J. 1996 Dec;15(12):1107-12. doi: 10.1097/00006454-199612000-00011.
Fungal septicemia is a devastating disease in the neonate, especially in the low birth weight preterm infant who is especially vulnerable to disseminated fungal sepsis. The objective of this study was to compare the efficacy, safety and overall convenience of fluconazole vs. amphotericin B for the treatment of disseminated fungal sepsis in neonates.
A prospective, randomized, collaborative study conducted at two South African neonatal units.
Twenty-four infants with proven fungal septicemia were treated from June, 1992, to June, 1993. Twelve received fluconazole, 11 received amphotericin B and 1 was excluded. Assessment of hepatic, renal and hematologic functions were performed before, during and after treatment. The two groups were comparable at the time of enrollment into the study.
Infants receiving amphotericin B had significantly higher values of total and direct bilirubin and alkaline phosphatase values at the end of treatment, while the fluconazole group showed a significant increase in the platelet count. The cumulative total numbers of days receiving intravenous therapy for the administration of antifungal drugs were 57 for the fluconazole group and 162 for the amphotericin group; no central lines were needed in the fluconazole group, whereas 3 babies given amphotericin B had central catheters for a cumulative total of 27 days. The case fatality rate was 33% in the fluconazole group and 45% in the amphotericin B group; there was still proof of fungal septicemia at the time of death in 1 patient given amphotericin B and 2 given fluconazole.
Fluconazole showed fewer side effects than amphotericin B and was more convenient to use.
真菌败血症在新生儿中是一种毁灭性疾病,尤其是在低出生体重的早产儿中,他们特别容易发生播散性真菌败血症。本研究的目的是比较氟康唑与两性霉素B治疗新生儿播散性真菌败血症的疗效、安全性及总体便利性。
在南非的两个新生儿病房进行的一项前瞻性、随机、协作性研究。
1992年6月至1993年6月,对24例确诊为真菌败血症的婴儿进行治疗。12例接受氟康唑治疗,11例接受两性霉素B治疗,1例被排除。在治疗前、治疗期间和治疗后对肝、肾和血液学功能进行评估。两组在纳入研究时具有可比性。
接受两性霉素B治疗的婴儿在治疗结束时总胆红素、直接胆红素和碱性磷酸酶值显著更高,而氟康唑组血小板计数显著增加。氟康唑组接受抗真菌药物静脉治疗的累计总天数为57天,两性霉素组为162天;氟康唑组无需中心静脉导管,而接受两性霉素B治疗的3例婴儿使用中心静脉导管累计共27天。氟康唑组病死率为33%,两性霉素B组为45%;接受两性霉素B治疗的1例患者和接受氟康唑治疗的2例患者在死亡时仍有真菌败血症证据。
氟康唑的副作用比两性霉素B少,且使用更方便。