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Sinusoidal Obstruction Syndrome/Veno-Occlusive Disease after Autologous or Allogeneic Hematopoietic Stem Cell Transplantation in Children: a retrospective study of the Italian Hematology-Oncology Association-Hematopoietic Stem Cell Transplantation Group.儿童自体或异基因造血干细胞移植后窦状隙阻塞综合征/静脉闭塞性疾病:意大利血液学-肿瘤学会-造血干细胞移植组的回顾性研究。
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Factors associated with successful liberation from continuous renal replacement therapy in children and young adults: analysis of the worldwide exploration of renal replacement outcomes collaborative in Kidney Disease Registry.与儿童和青年成功脱离连续性肾脏替代治疗相关的因素:对肾脏病预后和实践模式研究网络肾脏登记系统的全球探索的分析。
Intensive Care Med. 2024 Jun;50(6):861-872. doi: 10.1007/s00134-024-07336-4. Epub 2024 Mar 4.
2
Continuous Kidney Replacement Therapy and Survival in Children and Young Adults: Findings From the Multinational WE-ROCK Collaborative.连续肾脏替代治疗与儿童和青年患者的生存:来自多国 WE-ROCK 协作研究的结果。
Am J Kidney Dis. 2024 Oct;84(4):406-415.e1. doi: 10.1053/j.ajkd.2023.12.017. Epub 2024 Feb 15.
3
Risk factors for acute kidney injury in pediatric patients after hematopoietic stem cell transplantation: a systematic review and meta-analysis.造血干细胞移植后儿童患者急性肾损伤的危险因素:系统评价和荟萃分析。
Pediatr Nephrol. 2024 Feb;39(2):397-408. doi: 10.1007/s00467-023-05964-4. Epub 2023 Apr 20.
4
Kidney Injury in Children after Hematopoietic Stem Cell Transplant.儿童造血干细胞移植后的肾损伤。
Curr Oncol. 2023 Mar 13;30(3):3329-3343. doi: 10.3390/curroncol30030253.
5
Sinusoidal Obstruction Syndrome in Critically Ill Patients in the Era of Defibrotide: A Retrospective Multicenter Study.危重病患者在德丰替德时代的窦状隙阻塞综合征:一项回顾性多中心研究。
Transplant Cell Ther. 2021 Apr;27(4):338.e1-338.e7. doi: 10.1016/j.jtct.2020.11.016. Epub 2020 Dec 17.
6
Continuous Renal Replacement Therapy: A Review of Use and Application in Pediatric Hematopoietic Stem Cell Transplant Recipients.连续性肾脏替代治疗:儿科造血干细胞移植受者的使用与应用综述
Front Oncol. 2021 Feb 26;11:632263. doi: 10.3389/fonc.2021.632263. eCollection 2021.
7
Diagnosis and Treatment of VOD/SOS After Allogeneic Hematopoietic Stem Cell Transplantation.异基因造血干细胞移植后 VOD/SOS 的诊断与治疗。
Front Immunol. 2020 Apr 3;11:489. doi: 10.3389/fimmu.2020.00489. eCollection 2020.
8
Pooled analysis of Day 100 survival for defibrotide-treated patients with hepatic veno-occlusive disease/sinusoidal obstruction syndrome and ventilator or dialysis dependence following haematopoietic cell transplantation.造血细胞移植后发生肝静脉闭塞病/窦状隙阻塞综合征且需要呼吸机或透析依赖的患者,在第 100 天defibrotide 治疗的生存汇总分析。
Br J Haematol. 2020 Aug;190(4):583-587. doi: 10.1111/bjh.16552. Epub 2020 Mar 10.
9
Modified diagnostic criteria, grading classification and newly elucidated pathophysiology of hepatic SOS/VOD after haematopoietic cell transplantation.造血细胞移植后肝脏 SOS/VOD 的改良诊断标准、分级分类和新阐明的病理生理学。
Br J Haematol. 2020 Sep;190(6):822-836. doi: 10.1111/bjh.16557. Epub 2020 Mar 4.
10
Epidemiology and Outcome of Critically Ill Pediatric Cancer and Hematopoietic Stem Cell Transplant Patients Requiring Continuous Renal Replacement Therapy: A Retrospective Nationwide Cohort Study.危重症儿科癌症和造血干细胞移植患者需要持续肾脏替代治疗的流行病学和转归:一项回顾性全国队列研究。
Crit Care Med. 2019 Nov;47(11):e893-e901. doi: 10.1097/CCM.0000000000003973.

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.

DOI:10.1002/pbc.31473
PMID:39654079
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11922561/
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。