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儿童造血干细胞移植后的肾损伤。

Kidney Injury in Children after Hematopoietic Stem Cell Transplant.

机构信息

Division of Pediatric Nephrology, Department of Pediatrics, LeBonheur Children's Hospital, Memphis, TN 38105, USA.

Division of Pediatric Nephrology, Department of Pediatrics, Baylor College of Medicine/Texas Children's Hospital, Houston, TX 77030, USA.

出版信息

Curr Oncol. 2023 Mar 13;30(3):3329-3343. doi: 10.3390/curroncol30030253.

Abstract

Hematopoietic cell transplant (HCT), used for treatment of many malignant and non-malignant pediatric diseases, is associated with serious complications, limiting this therapy's benefit. Acute kidney injury (AKI), seen often after HCT, can occur at different stages of the transplant process and contributes to morbidity and mortality after HCT. The etiology of AKI is often multifactorial, including kidney hypoperfusion, nephrotoxicity from immunosuppressive and antimicrobial agents, and other transplant-related complications such as transplant-associated thrombotic microangiopathy and sinusoidal obstructive syndrome. Early recognition of AKI is crucial to prevent further AKI and associated complications. Initial management includes identifying the etiology of AKI, preventing further kidney hypoperfusion, adjusting nephrotoxic medications, and preventing fluid overload. Some patients will require further support with kidney replacement therapy to manage fluid overload and AKI. Biomarkers of AKI, such as neutrophil gelatinase-associated lipocalin can aid in detecting AKI before a rise in serum creatinine, allowing earlier intervention. Long-term kidney dysfunction is also prominent in this population. Therefore, long-term follow-up and monitoring of renal function (glomerular filtration rate, microalbuminuria) is required along with management of hypertension, which can contribute to chronic kidney disease.

摘要

造血细胞移植(HCT),用于治疗许多儿科恶性和非恶性疾病,与严重的并发症有关,限制了这种治疗的益处。HCT 后常发生急性肾损伤(AKI),可发生在移植过程的不同阶段,并导致 HCT 后发病率和死亡率增加。AKI 的病因通常是多因素的,包括肾脏低灌注、免疫抑制和抗菌药物的肾毒性,以及其他与移植相关的并发症,如移植相关血栓性微血管病和窦状隙阻塞综合征。早期识别 AKI 对于预防进一步的 AKI 和相关并发症至关重要。初始治疗包括确定 AKI 的病因,防止进一步的肾脏低灌注,调整肾毒性药物,并防止液体过载。一些患者需要进一步的肾脏替代治疗来管理液体过载和 AKI。AKI 的生物标志物,如中性粒细胞明胶酶相关载脂蛋白,可以帮助在血清肌酐升高之前检测到 AKI,从而更早地进行干预。该人群中也存在长期肾功能障碍。因此,需要长期随访和监测肾功能(肾小球滤过率、微量白蛋白尿),并进行高血压的管理,因为高血压可导致慢性肾脏病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/948e/10047595/3f58f37ddafa/curroncol-30-00253-g001.jpg

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