Kicklighter S D, Springer S C, Cox T, Hulsey T C, Turner R B
Wake Medical Center, Raleigh, North Carolina 27620, USA.
Pediatrics. 2001 Feb;107(2):293-8. doi: 10.1542/peds.107.2.293.
Candidal infections are an important cause of morbidity and mortality in the very low birth weight (VLBW) infant. Current intervention focuses on treatment once candidal septicemia is either suspected or diagnosed. Studies have suggested that colonization with candidal species is an important risk factor for subsequent infection.
To determine whether prophylactic fluconazole for the first 28 days of life results in a decreased incidence of candidal colonization in the VLBW infant.
Prospective, randomized, controlled, intention-to-treat design comparing prophylaxis with fluconazole versus placebo for the first 28 days of life.
A tertiary level intensive care nursery in a major teaching hospital in Charleston, South Carolina.
One hundred three infants with a birth weight of <1500 g, either inborn or outborn, who were admitted to the intensive care nursery between January 1998 and February 1999.
Infants were enrolled within 72 hours of life with rectal cultures performed on the day of randomization (DOR), as well as day of life (DOL) 7, 14, and 28. Those infants with a birth weight of <1250 g had additional cultures on DOL 35, 49, and 56. Cultures were plated on selective media for isolation of candidal organisms. Infants were randomized to receive either fluconazole (6 mg/kg) or placebo on the DOR. Subsequent doses were given every 72 hours until DOL 7 and then every 24 hours until DOL 28. Medication was given either intravenously or by feeding tube once the infant had been gavage feeding for a 48-hour period without feeding intolerance. Aspartate aminotransferase and alanine aminotransferase levels were obtained on DOR and DOL 7, 14, and 28 to assess for fluconazole toxicity. The minimal inhibitory concentration to fluconazole was determined for all positive cultures to assess the development of resistance.
The infants who received fluconazole (n = 53) and placebo (n = 50) had no statistical difference in the major risk factors known to increase the chances of candidal septicemia in the VLBW infant. Rectal colonization by candidal species was detected in 8 of the 53 fluconazole-treated patients (15.1%) and in 23 of the 50 infants treated with placebo (46%). Fluconazole significantly reduced rectal colonization from DOL 14 through DOL 56 in all infants with a birth weight of <1250 g, and from DOL 14 through DOL 56 in all infants with a birth weight of 1250 to 1500 g. Alanine aminotransferase levels were higher in the fluconazole versus the placebo-treated group on DOL 14 (18.1 IU/L vs 15 IU/L), but no clinically significant abnormalities were observed. Candida albicans was the most common species isolated. There was no increase in species of Candida noted for their intrinsic resistance to fluconazole, and there was no statistically significant difference in the minimal inhibitory concentrations to fluconazole for all C albicans isolates in either group at any period.
Prophylactic administration of fluconazole to the VLBW infant for the first 28 days of life is safe and results in a decreased risk of rectal colonization by candidal species. Larger studies to determine the effect of prophylaxis on candidal septicemia and development of resistance in such a selective high-risk group are warranted before initiation of routine prophylaxis.fluconazole, very low birth weight infant, prophylaxis, candidal sepsis, sensitivities to fluconazole.
念珠菌感染是极低出生体重(VLBW)婴儿发病和死亡的重要原因。目前的干预措施集中在一旦怀疑或诊断出念珠菌败血症就进行治疗。研究表明,念珠菌属的定植是随后感染的重要危险因素。
确定出生后前28天预防性使用氟康唑是否会降低VLBW婴儿念珠菌定植的发生率。
前瞻性、随机、对照、意向性治疗设计,比较出生后前28天使用氟康唑与安慰剂进行预防的效果。
南卡罗来纳州查尔斯顿一家大型教学医院的三级重症监护病房。
1998年1月至1999年2月期间入住重症监护病房的103名出生体重<1500g的婴儿,包括足月儿和早产儿。
婴儿在出生后72小时内入组,在随机分组日(DOR)以及出生后第7天、14天和28天进行直肠培养。出生体重<1250g的婴儿在出生后第35天、49天和56天还需进行额外培养。培养物接种在选择性培养基上以分离念珠菌。婴儿在DOR时随机接受氟康唑(6mg/kg)或安慰剂。后续剂量每72小时给药一次,直至出生后第7天,然后每24小时给药一次,直至出生后第28天。一旦婴儿经胃管喂养48小时且无喂养不耐受,药物通过静脉或喂养管给药。在DOR以及出生后第7天、14天和28天测定天冬氨酸转氨酶和丙氨酸转氨酶水平,以评估氟康唑的毒性。对所有阳性培养物测定氟康唑的最低抑菌浓度,以评估耐药性的发展。
接受氟康唑(n = 53)和安慰剂(n = 50)治疗的婴儿在已知增加VLBW婴儿念珠菌败血症发生几率的主要危险因素方面无统计学差异。53例接受氟康唑治疗的患者中有8例(15.1%)检测到念珠菌属直肠定植,50例接受安慰剂治疗的婴儿中有23例(46%)检测到。氟康唑显著降低了所有出生体重<1250g婴儿从出生后第14天至56天以及所有出生体重为1250至1500g婴儿从出生后第14天至56天的直肠定植率。在出生后第14天,氟康唑治疗组的丙氨酸转氨酶水平高于安慰剂治疗组(18.1IU/L对15IU/L),但未观察到具有临床意义的异常。白色念珠菌是最常见的分离菌种。对氟康唑具有固有耐药性的念珠菌种类没有增加,两组中所有白色念珠菌分离株在任何时期对氟康唑的最低抑菌浓度均无统计学显著差异。
在VLBW婴儿出生后的前28天预防性使用氟康唑是安全的,并可降低念珠菌属直肠定植的风险。在开始常规预防之前,有必要进行更大规模的研究以确定预防措施对该选择性高危组念珠菌败血症和耐药性发展的影响。氟康唑、极低出生体重婴儿、预防、念珠菌败血症、对氟康唑的敏感性