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首页> 外文期刊>Archives of disease in childhood. Fetal and neonatal edition >Randomised controlled trial of prophylactic fluconazole versus nystatin for the prevention of fungal colonisation and invasive fungal infection in very low birth weight infants
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Randomised controlled trial of prophylactic fluconazole versus nystatin for the prevention of fungal colonisation and invasive fungal infection in very low birth weight infants

机译:预防性氟康唑与制霉菌素预防极低出生体重婴儿真菌定植和侵袭性真菌感染的随机对照试验

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Background Invasive fungal infections are a major cause of morbidity and mortality in preterm infants. The authors conducted the first prospective, randomised controlled trial of nystatin compared with fluconazole for the prevention of fungal colonisation and invasive fungal infection in very low birth weight (VLBW) neonates. Methods During a 12-month period, all VLBW neonates were assigned randomly to receive nystatin (1 ml suspension, 100 000 U/ml, every 8 h), fluconazole (3 mg/kg body weight, every third day) or placebo from birth until day 30 of life (day 45 for neonates weighing 1000 g at birth). The authors performed weekly surveillance cultures and systemic fungal susceptibility testing. Results During the study period, 278 infants (fluconazole group, n=93; nystatin group, n=94; control group, n=91) weighing 1500 g at birth were admitted. There were no differences in birth weight, gestation, gender or risk factors for fungal infection among the groups. Fungal colonisation occurred in 11.7% of the nystatin group and 10.8% of the fluconazole group, as compared with 42.9% of the control group. The incidence of invasive fungal infection was 4.3% in the nystatin group and 3.2% in the fluconazole group, as compared with 16.5% in the control group. There were no differences in fungal colonisation and invasive fungal infection between the nystatin and fluconazole groups. Conclusions Prophylactic nystatin and fluconazole reduce the incidence of colonisation and invasive fungal infection in VLBW neonates. The authors believe that nystatin is an alternative to fluconazole, because nystatin is safe, inexpensive, well tolerated and effective.
机译:背景技术侵袭性真菌感染是早产儿发病和死亡的主要原因。作者进行了制霉菌素与氟康唑比较的首次前瞻性,随机对照试验,以预防极低出生体重(VLBW)新生儿的真菌定植和侵袭性真菌感染。方法在12个月内,所有VLBW新生儿均被随机分配,从出生时开始接受制霉菌素(1 ml悬浮液,100000 U / ml,每8小时),氟康唑(3 mg / kg体重,每三天)或安慰剂直到生命的第30天(出生时体重<1000 g的新生儿为45天)。作者每周进行监测培养和全身真菌敏感性试验。结果在研究期间,共纳入出生时体重<1500 g的278例婴儿(氟康唑组,n = 93;制霉菌素组,n = 94;对照组,n = 91)。各组之间的出生体重,妊娠,性别或真菌感染危险因素无差异。制霉菌素组和氟康唑组的真菌定植发生率分别为11.7%和10.8%,而对照组为42.9%。制霉菌素组侵袭性真菌感染的发生率为4.3%,氟康唑组为3.2%,而对照组为16.5%。制霉菌素和氟康唑组之间在真菌定植和侵袭性真菌感染方面没有差异。结论预防性制霉菌素和氟康唑可减少VLBW新生儿定植和侵袭性真菌感染的发生。作者认为,制霉菌素是氟康唑的替代品,因为制霉菌素是安全,便宜,耐受性良好和有效的。

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