Clerihew Linda, McGuire William
Department of Paediatrics, Tayside Children’s Hospital, Dundee, UK.
Cochrane Database Syst Rev. 2012 Jun 13;2012(6):CD003953. doi: 10.1002/14651858.CD003953.pub3.
A variety of antifungal drugs, drug preparations and drug combinations are available to treat newborn infants with suspected or confirmed invasive fungal infection. There is a need to assess their relative merits.
To assess the effect of treatment with different antifungal drugs, drug preparations or drug combinations on mortality and morbidity in newborn infants with suspected or confirmed invasive fungal infection.
We used the standard search strategy of the Cochrane Neonatal Review Group. This included searches of the Cochrane Central Register of Controlled Trials (The Cochrane Library, 2012, Issue 2), MEDLINE, EMBASE, CINAHL (to March 2012), conference proceedings and previous reviews.
Randomised and quasi-randomised control trials comparing one antifungal agent or combination of agents with another in newborn infants with suspected or confirmed invasive fungal infection.
We extracted the data using the standard methods of the Cochrane Neonatal Review Group, with separate evaluation of trial quality and data extraction by each author, and synthesis of data using risk ratio and risk difference.
We identified only one small trial in which 24 newborn infants participated. This trial compared the use of fluconazole versus amphotericin B (plus 5-fluorocytosine if fungal meningitis present). The trial did not detect a statistically significant effect on mortality (risk ratio 0.73; 95% confidence interval 0.26 to 2.05).
AUTHORS' CONCLUSIONS: There are insufficient data to inform practice. Large randomised controlled trials are required to compare antifungal drugs, drug preparations or drug combinations for treating newborn infants with invasive fungal infection.
有多种抗真菌药物、药物制剂及药物组合可用于治疗疑似或确诊侵袭性真菌感染的新生儿。有必要评估它们的相对优点。
评估不同抗真菌药物、药物制剂或药物组合治疗疑似或确诊侵袭性真菌感染新生儿的死亡率和发病率的影响。
我们采用了Cochrane新生儿综述小组的标准检索策略。这包括检索Cochrane对照试验中心注册库(《Cochrane图书馆》,2012年第2期)、MEDLINE、EMBASE、CINAHL(截至2012年3月)、会议论文集及以往综述。
比较一种抗真菌药物或药物组合与另一种抗真菌药物或药物组合治疗疑似或确诊侵袭性真菌感染新生儿的随机和半随机对照试验。
我们采用Cochrane新生儿综述小组的标准方法提取数据,每位作者分别评估试验质量和数据提取情况,并使用风险比和风险差进行数据合成。
我们仅识别出一项有24名新生儿参与的小型试验。该试验比较了氟康唑与两性霉素B(若存在真菌性脑膜炎则加用5-氟胞嘧啶)的使用情况。该试验未检测到对死亡率有统计学显著影响(风险比0.73;95%置信区间0.26至2.05)。
数据不足,无法为临床实践提供参考。需要进行大型随机对照试验,以比较用于治疗侵袭性真菌感染新生儿的抗真菌药物、药物制剂或药物组合。