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Threshold retinopathy at threshold of viability: the EpiBel study.

机译:在生存阈值时发生阈值视网膜病变:EpiBel研究。

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AIM: To describe incidence, co-morbidity characteristics, and risk factors associated with threshold retinopathy of prematurity (ROP) in survivors with a gestational age (GA) of < or =26 weeks at birth. METHODS: Retrospective analysis of perinatal data of all inborn survivors in all perinatal centres of Belgium in the period 1999-2000 (EpiBel cohort) believed to be between 22 and 26 weeks GA at time of delivery. Data on survivors who did and survivors who did not develop threshold ROP were compared (chi(2), Mann-Whitney U) and logistic regression was performed. RESULTS: Of 303 admitted infants 175 (58%) were discharged alive. Incidence of major retinopathy (> or =stage 3) and of threshold ROP was 25.5% and 19.8% in survivors. Associated central nervous abnormalities were documented in six (17%) and associated chronic lung disease in 19 (54%) threshold ROP infants. Threshold ROP without additional morbidity characteristics at discharge was documented in 14 (40%) infants. Besides often reported risk factors, renal insufficiency (creatinaemia>1.5 mg/dl) was a risk factor to develop threshold ROP (p<0.0015) (chi(2)). Days of respiratory support (OR 1.02; 95% CI 1.002 to 1.039), number of transfusions (OR 1.118; 95% CI 1.030 to 1.214), and renal insufficiency (OR 3.31; 95% CI 1.344 to 8.196) remained independent risk factors to develop threshold ROP in this cohort in a stepwise logistic regression model (MedCalc). CONCLUSIONS: Incidence of threshold ROP is high at the limits of viability. Renal insufficiency is a risk factor to develop threshold ROP in this cohort.
机译:目的:描述与胎龄(GA)≤26周的幸存者相关的发病率,合并症特征以及与早产儿视网膜病变(ROP)相关的危险因素。方法:回顾性分析了比利时所有围产期中心(EpiBel队列)在1999-2000年期间出生的所有出生幸存者的围产期数据,据信其在分娩时的遗传数据为22至26周。比较了完成ROP和未发生ROP阈值的幸存者的数据(chi(2),Mann-Whitney U),并进行了逻辑回归。结果:在303名入院婴儿中,有175名(58%)活着出院。幸存者中主要视网膜病变(≥3期)和ROP阈值的发生率分别为25.5%和19.8%。有6例(17%)和19例(54%)阈值ROP婴儿发生了相关的中枢神经异常和相关的慢性肺部疾病。有14例(40%)婴儿记录了出院时无其他发病特征的阈值ROP。除了经常报告的危险因素外,肾功能不全(肌酐> 1.5 mg / dl)是发展阈值ROP的危险因素(p <0.0015)(chi(2))。呼吸支持天数(OR 1.02; 95%CI 1.002至1.039),输血次数(OR 1.118; 95%CI 1.030至1.214)和肾功能不全(OR 3.31; 95%CI 1.344至8.196)仍然是在逐步逻辑回归模型(MedCalc)中开发该队列的阈值ROP。结论:在生存能力极限内,阈值ROP的发生率很高。肾功能不全是该人群发生阈值ROP的危险因素。

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