Anderson Ashlea, Shoulders Laurie, James Vinson, Ashcraft Emily, Cheng Cheng, Ribeiro Raul, Elbahlawan Lama
Division of Critical Care Medicine, St. Jude Children's Research Hospital, Memphis, TN, United States.
Department of Nursing, Intensive Care Unit, St. Jude Children's Research Hospital, Memphis, TN, United States.
Front Oncol. 2023 Aug 18;13:1234677. doi: 10.3389/fonc.2023.1234677. eCollection 2023.
Tumor lysis syndrome (TLS) is often diagnosed in children with hematological malignancies and can be life threatening due to metabolic disturbances. Continuous renal replacement therapy (CKRT) can reverse these disturbances relatively quickly when conventional medical management fails. Our objective was to investigate the benefit of CKRT in the management of TLS in children admitted to the intensive care unit with hematologic malignancies. In addition, we sought to assess risk factors for acute kidney injury (AKI) in the setting of TLS.
Retrospective review of all children admitted to the intensive care unit with TLS who received CKRT from January 2012 to August 2022.
Among 222 children hospitalized with TLS from January 2012 to August 2022, 20 (9%) underwent CKRT to manage TLS in the intensive care unit. The patients' median age was 13 years (range 3-17 y), and most were males (18/20). T-cell acute lymphoblastic leukemia was the most common diagnosis (n=10), followed by acute myeloid leukemia (n=4), Burkitt lymphoma (n=4), and B-cell acute lymphoblastic leukemia (n=2). Five patients required mechanical ventilation, and 2 required vasopressors. The most common indication for CKRT was hyperphosphatemia, followed by, hyperuricemia, and hyperkalemia. All metabolic abnormalities corrected within 12 h of initiation of CKRT. CKRT courses were brief, with a median duration of 2 days (range 1-7 days). Having higher serum phosphorus levels 12 h preceding CKRT was significantly associated with severe acute kidney injury (AKI). The median phosphorus level was 6.4 mg/dL in children with no/mild AKI and 10.5 mg/dL in children with severe AKI (p=0.0375). Serum uric acid levels before CKRT were not associated with AKI. All children survived to hospital discharge, and the one-year survival rate was 90%.
CKRT is safe in children with hematologic malignancies with severe TLS and reverses metabolic derangements within 6-12 h. Most patients had AKI at the initiation of CKRT but did not require long-term kidney replacement therapy. Hyperphosphatemia before initiation of CKRT is associated with higher risk of AKI.
肿瘤溶解综合征(TLS)常被诊断于患有血液系统恶性肿瘤的儿童中,由于代谢紊乱,它可能危及生命。当传统药物治疗无效时,持续肾脏替代治疗(CKRT)能够相对迅速地逆转这些紊乱。我们的目的是研究CKRT在治疗入住重症监护病房的血液系统恶性肿瘤儿童的TLS中的益处。此外,我们试图评估TLS背景下急性肾损伤(AKI)的危险因素。
回顾性分析2012年1月至2022年8月期间入住重症监护病房并接受CKRT治疗的所有TLS儿童。
在2012年1月至2022年8月期间因TLS住院的222名儿童中,有20名(9%)在重症监护病房接受了CKRT以治疗TLS。患者的中位年龄为13岁(范围3 - 17岁),大多数为男性(18/20)。T细胞急性淋巴细胞白血病是最常见的诊断(n = 10),其次是急性髓系白血病(n = 4)、伯基特淋巴瘤(n = 4)和B细胞急性淋巴细胞白血病(n = 2)。5名患者需要机械通气,2名患者需要血管活性药物。CKRT最常见的指征是高磷血症,其次是高尿酸血症和高钾血症。所有代谢异常在CKRT开始后12小时内得到纠正。CKRT疗程较短,中位持续时间为2天(范围1 - 7天)。CKRT前12小时血清磷水平较高与严重急性肾损伤(AKI)显著相关。无/轻度AKI儿童的中位磷水平为6.4mg/dL,严重AKI儿童为10.5mg/dL(p = 0.0375)。CKRT前的血清尿酸水平与AKI无关。所有儿童均存活至出院,一年生存率为90%。
CKRT对于患有严重TLS的血液系统恶性肿瘤儿童是安全的,并且能在6 - 12小时内逆转代谢紊乱。大多数患者在开始CKRT时患有AKI,但不需要长期肾脏替代治疗。CKRT开始前的高磷血症与AKI的较高风险相关。