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Follow-up after neonatal heart disease repair: watch out for chronic kidney disease and hypertension!
Pediatric Nephrology ( IF 3 ) Pub Date : 2020-06-04 , DOI: 10.1007/s00467-020-04621-4
Louis Huynh 1 , Sara Rodriguez-Lopez 2 , Kelly Benisty 3 , Adrian Dancea 4 , Daniel Garros 5 , Erin Hessey 6 , Ari Joffe 5 , Rachel Joffe 6 , Andrew Mackie 7 , Ana Palijan 8 , Alex Paun 8 , Michael Pizzi 8 , Michael Zappitelli 9 , Catherine Morgan 2
Affiliation  

Background

With advances in care, neonates undergoing cardiac repairs are surviving more frequently. Our objectives were to 1) estimate the prevalence of chronic kidney disease (CKD) and hypertension 6 years after neonatal congenital heart surgery and 2) determine if cardiac surgery-associated acute kidney injury (CS-AKI) is associated with these outcomes.

Methods

Two-center prospective, longitudinal single-visit cohort study including children with congenital heart disease surgery as neonates between January 2005 and December 2012. CKD (estimated glomerular filtration rate < 90 mL/min/1.73m2 or albumin/creatinine ≥3 mg/mmol) and hypertension (systolic or diastolic blood pressure ≥ 95th percentile for age, sex, and height) prevalence 6 years after surgery was estimated. The association of CS-AKI (Kidney Disease: Improving Global Outcomes definition) with CKD and hypertension was determined using multiple regression.

Results

Fifty-eight children with median follow-up of 6 years were evaluated. CS-AKI occurred in 58%. CKD and hypertension prevalence were 17% and 30%, respectively; an additional 15% were classified as having elevated blood pressure. CS-AKI was not associated with CKD or hypertension. Classification as cyanotic postoperatively was the only independent predictor of CKD. Postoperative days in hospital predicted hypertension at follow-up.

Conclusions

The prevalence of CKD and hypertension is high in children having neonatal congenital heart surgery. This is important; early identification of CKD and hypertension can improve outcomes. These children should be systematically followed for the evolution of these negative outcomes. CS-AKI defined by current standards may not be a useful clinical tool to decide who needs follow-up and who does not.



中文翻译:

新生儿心脏病修复后的随访:注意慢性肾脏病和高血压!

背景

随着护理的进步,接受心脏修复的新生儿的存活率更高。我们的目标是:1)评估新生儿先天性心脏手术后6年的慢性肾脏病(CKD)和高血压的患病率,以及2)确定心脏手术相关的急性肾损伤(CS-AKI)是否与这些结果相关。

方法

2005年1月至2012年12月间进行的两中心前瞻性,纵向单次就诊队列研究,包括患有先天性心脏病手术的婴儿(新生儿)。CKD(估计肾小球滤过率<90 mL / min / 1.73m 2或白蛋白/肌酐≥3mg /估计术后6年高血压和高血压(年龄,性别和身高的收缩压或舒张压≥95%)的患病率。使用多元回归分析确定CS-AKI(肾脏疾病:改善总体结局定义)与CKD和高血压的相关性。

结果

评估了58位中位随访时间为6岁的儿童。CS-AKI发生率为58%。CKD和高血压患病率分别为17%和30%;另外15%被归类为血压升高。CS-AKI与CKD或高血压无关。术后分类为紫otic是CKD的唯一独立预测因子。医院术后天数预测会出现高血压。

结论

在患有新生儿先天性心脏手术的儿童中,CKD和高血压的患病率很高。这个很重要; 及早发现CKD和高血压可以改善预后。这些儿童应被系统地追踪以了解这些负面结果的演变。当前标准定义的CS-AKI可能不是决定谁需要随访以及谁不需要随访的有用的临床工具。

更新日期:2020-06-04
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