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造血细胞移植后窦性阻塞综合征患儿的连续性肾脏替代治疗:结局与撤机

Continuous Kidney Replacement Therapy in Children With Sinusoidal Obstruction Syndrome After Hematopoietic Cell Transplant: Outcome and Liberation.

作者信息

Heyn Madeleine, Ashcraft Emily, Cheng Cheng, Epperly Rebecca, Elbahlawan Lama

机构信息

Stritch School of Medicine, University of Loyola Chicago, Maywood, Illinois, USA.

Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.

出版信息

Pediatr Blood Cancer. 2025 Mar;72(3):e31473. doi: 10.1002/pbc.31473. Epub 2024 Dec 9.

Abstract

BACKGROUND

Sinusoidal obstruction syndrome (SOS), a serious complication after hematopoietic cell transplant (HCT), is associated with multiorgan dysfunction (MOD) and a high mortality rate. In severe cases, continuous kidney replacement therapy (CKRT) is initiated to manage fluid overload (FO) and acute kidney injury. Studies that evaluate the use of CKRT in this population are lacking. The aim of our study was to assess the outcome of critically ill children with severe SOS post HCT who received CKRT. We also sought to assess factors associated with survival and liberation post CKRT.

PROCEDURE

Retrospective review of all children admitted to the intensive care unit (ICU) with SOS post HCT who received CKRT from January 2010 to August 2022.

RESULTS

Among the 53 children who received CKRT post HCT, 13 had severe SOS. The median age was 6 years; 62% were males, and most (77%) received allogeneic HCT. In this cohort, 92% required respiratory support and 85% required vasopressor support. The ICU survival rate was 62%. Survivors experienced lower cumulative FO on the 2 days following CKRT initiation (-4.2% in survivors vs. -0.5% in non-survivors, p = 0.07). Higher urine output on D1 and D2 after discontinuation of CKRT was associated with successful liberation.

CONCLUSIONS

In this study of post-HCT children with SOS and MOD who received CKRT, 62% survived until ICU discharge. This survival rate is encouraging as it approximates the survival rates of general pediatric cohorts treated with CKRT. Reducing FO after initiation of CKRT can improve survival in these children.

摘要

背景

窦性阻塞综合征(SOS)是造血细胞移植(HCT)后的一种严重并发症,与多器官功能障碍(MOD)及高死亡率相关。在严重病例中,需启动持续肾脏替代疗法(CKRT)来处理液体超负荷(FO)和急性肾损伤。目前缺乏评估CKRT在该人群中应用的研究。我们研究的目的是评估接受CKRT的造血干细胞移植后患有严重SOS的危重症儿童的预后。我们还试图评估与CKRT后生存及脱离治疗相关的因素。

程序

回顾性分析2010年1月至2022年8月期间入住重症监护病房(ICU)且造血干细胞移植后发生SOS并接受CKRT的所有儿童。

结果

在53例造血干细胞移植后接受CKRT的儿童中,13例患有严重SOS。中位年龄为6岁;62%为男性,大多数(77%)接受了异基因造血干细胞移植。在该队列中,92%的患儿需要呼吸支持,85%需要血管活性药物支持。ICU生存率为62%。幸存者在开始CKRT后的2天内累积液体超负荷较低(幸存者为-4.2%,非幸存者为-0.5%,p = 0.07)。CKRT停止后第1天和第2天较高的尿量与成功脱离治疗相关。

结论

在这项针对造血干细胞移植后患有SOS和MOD并接受CKRT的儿童的研究中,62%的患儿存活至ICU出院。这一生存率令人鼓舞,因为它接近接受CKRT治疗的一般儿科队列的生存率。在开始CKRT后减少液体超负荷可提高这些儿童的生存率。

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