Division of Microbiology, Hospital for Sick Children, University of Toronto, Room 3654, Atrium, 555 University Ave, Toronto, ON M5G 1X8, Canada.
BMC Infect Dis. 2014 Jun 12;14:327. doi: 10.1186/1471-2334-14-327.
This multicenter prospective study of invasive candidiasis (IC) was carried out to determine the risk factors for, incidence of, clinical and laboratory features, treatment and outcome of IC in infants of birth weight <1250 g.
Neonates <1250 g with IC and their matched controls (2:1) were followed longitudinally and descriptive analysis was performed. Survivors underwent neurodevelopmental assessment at 18 to 24 months corrected age. Neurodevelopmental impairment (NDI) was defined as blindness, deafness, moderate to severe cerebral palsy, or a score <70 on the Bayley Scales of Infant Development 2nd edition. Multivariable analyses were performed to determine risk factors for IC and predictors of mortality and NDI.
Cumulative incidence rates of IC were 4.2%, 2.2% and 1.5% for birth-weight categories <750 g, <1000 g, <1500 g, respectively. Forty nine infants with IC and 90 controls were enrolled. Necrotizing enterocolitis (NEC) was the only independent risk factor for IC (p=0.03). CNS candidiasis occurred in 50% of evaluated infants, while congenital candidiasis occurred in 31%. Infants with CNS candidiasis had a higher mortality rate (57%) and incidence of deafness (50%) than the overall cohort of infants with IC. NDI (56% vs. 33%; p=0.017) and death (45% vs. 7%; p=0.0001) were more likely in cases than in controls, respectively. IC survivors were more likely to be deaf (28% vs. 7%; p=0.01). IC independently predicted mortality (p=0.0004) and NDI (p=0.018).
IC occurred in 1.5% of VLBW infants. Preceding NEC increased the risk of developing IC. CNS candidiasis is under-investigated and difficult to diagnose, but portends a very poor outcome. Mortality, deafness and NDI were independently significantly increased in infants with IC compared to matched controls.
本项多中心前瞻性侵袭性念珠菌病(IC)研究旨在确定极低出生体重(<1250g)婴儿 IC 的发病风险因素、发病率、临床和实验室特征、治疗和结局。
对患有 IC 的<1250g 新生儿及其配对对照(2:1)进行纵向随访,并进行描述性分析。幸存者在 18 至 24 个月校正年龄时接受神经发育评估。神经发育障碍(NDI)定义为失明、耳聋、中重度脑瘫,或贝利婴幼儿发展量表第二版评分<70 分。进行多变量分析以确定 IC 的发病风险因素以及死亡率和 NDI 的预测因素。
出生体重<750g、<1000g、<1500g 的婴儿 IC 累积发生率分别为 4.2%、2.2%和 1.5%。共纳入 49 例 IC 婴儿和 90 例对照。坏死性小肠结肠炎(NEC)是 IC 的唯一独立危险因素(p=0.03)。中枢神经系统念珠菌病发生于 50%评估婴儿,而先天性念珠菌病发生于 31%。中枢神经系统念珠菌病患儿死亡率(57%)和耳聋发生率(50%)高于 IC 总体患儿。病例组 NDI(56%比 33%;p=0.017)和死亡(45%比 7%;p=0.0001)的发生率均高于对照组。IC 幸存者更有可能耳聋(28%比 7%;p=0.01)。IC 独立预测死亡率(p=0.0004)和 NDI(p=0.018)。
极低出生体重儿中 1.5%发生 IC。NEC 增加了发生 IC 的风险。中枢神经系统念珠菌病研究不足且难以诊断,但预后非常差。与匹配对照相比,IC 患儿的死亡率、耳聋和 NDI 显著增加。