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双胎输血综合征后慢性肾脏病-长期结局。

Chronic kidney disease following twin-to-twin transfusion syndrome-long-term outcomes.

机构信息

Department of Paediatric Nephrology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.

出版信息

Pediatr Nephrol. 2019 May;34(5):883-888. doi: 10.1007/s00467-018-4176-z. Epub 2018 Dec 17.

Abstract

BACKGROUND

Amongst other sequelae, acute kidney injury (AKI) is a well-recognised post-natal complication of twin-to-twin transfusion syndrome (TTTS). Despite this, there has been a lack of data reporting long-term renal outcomes. Our aim was to report the long-term renal outcomes of infants born with TTTS.

METHODS

We performed a retrospective case note review of all infants referred to our centre between 1998 and 2018 with a primary diagnosis of TTTS. Subjects with confirmed TTTS were divided into a chronic kidney disease (CKD) group and a non-CKD group for comparison.

RESULTS

Twenty-six infants with TTTS were included for analysis. Eight (31%) subjects developed CKD. Within the CKD group, 50% went on to require long-term renal replacement therapy (RRT) of whom all underwent renal transplantation. For subjects who had neonatal AKI, cumulative survival rate before RRT at 5 and 10 years was 79% and 70%, respectively. Subjects with CKD had a significantly higher incidence of AKI in the neonatal period and were more likely to be the donor twin. Gestational age at birth, gender, antenatal interventions and comorbidities did not affect long-term renal outcome between the two groups.

CONCLUSION

This is the first long-term follow-up study demonstrating that CKD progressing to the need for RRT can develop after TTTS. Donor-twin status and neonatal AKI associated with adverse long-term outcomes warranting long-term surveillance in this group.

摘要

背景

除其他后遗症外,急性肾损伤(AKI)是双胞胎输血综合征(TTTS)产后的一种公认并发症。尽管如此,关于长期肾脏结局的数据却很少。我们的目的是报告患有 TTTS 的婴儿的长期肾脏结局。

方法

我们对 1998 年至 2018 年间因 TTTS 而转诊至我们中心的所有婴儿进行了病历回顾性分析。将确诊为 TTTS 的患者分为慢性肾脏病(CKD)组和非 CKD 组进行比较。

结果

共有 26 例 TTTS 婴儿被纳入分析。8 例(31%)患儿发生 CKD。在 CKD 组中,有 50%需要长期肾脏替代治疗(RRT),其中所有人都接受了肾移植。对于新生儿 AKI 的患儿,在开始 RRT 之前,5 年和 10 年的累积生存率分别为 79%和 70%。CKD 患儿在新生儿期 AKI 的发生率更高,且更有可能是供体双胞胎。出生时的胎龄、性别、产前干预和合并症均未影响两组的长期肾脏结局。

结论

这是首次进行的长期随访研究,表明 CKD 进展至需要 RRT 后可能在 TTTS 后发生。供体双胞胎状态和与不良长期结局相关的新生儿 AKI ,需要在该组中进行长期监测。

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