病例报告:联合血液透析和聚合树脂血液吸附有效去除甲氨蝶呤。

Frontiers in nephrology Pub Date : 2025-08-25 eCollection Date: 2025-01-01 DOI:10.3389/fneph.2025.1644079
Maria Rita Dias, Carla Nicolau, Hugo Ferreira, Sérgio Chacim, Isabel Oliveira, Gonçalo de Câmara Negalha, José Mário Mariz, José Maximino Costa
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引用次数: 0

摘要

背景:大剂量甲氨蝶呤(HDMTX)是治疗原发性中枢神经系统淋巴瘤的核心药物,但有急性肾损伤(AKI)的风险,这可能会延迟甲氨蝶呤(MTX)的清除并增加毒性。葡萄糖苷酶是甲氨蝶呤毒性的首选治疗方法,但在许多国家获得途径有限,可能需要其他治疗方法。我们报告了第一例成人联合高通量血液透析(HFHD)和HA230血液吸附治疗MTX清除的病例。病例总结:一名66岁的新诊断原发性中枢神经系统淋巴瘤的女性开始了包括HDMTX在内的诱导化疗。输液后48小时,患者出现KDIGO期AKI,尽管维持尿量并采取早期支持措施,血浆MTX水平仍为26.278µmol/L。第3天,MTX水平持续升高至15.567µmol/L,并伴有严重的代谢性碱中毒。她被送进重症监护室,在那里接受HFHD联合过滤后HA230血液吸附治疗,随后尽快静脉注射葡糖苷酶。48小时后进行了第二次体外治疗。在第一次和第二次治疗后,MTX水平分别下降了91.93%(估计消除半衰期≈0.83小时)和71.02%(半衰期≈2.12小时)。MTX水平无明显反弹或透析相关并发症发生。患者肾功能恢复,完成后续治疗,无需甲氨蝶呤。结论:该病例表明,当葡糖苷酶延迟或不可用时,联合HFHD和HA230血液吸附作为桥接或替代策略是有效的。虽然证据仍然有限,但它支持对体外MTX去除的进一步研究,并有助于肿瘤学领域的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Case Report: Effective methotrexate removal by combined hemodialysis and polymeric resin hemoadsorption.

Case Report: Effective methotrexate removal by combined hemodialysis and polymeric resin hemoadsorption.

Case Report: Effective methotrexate removal by combined hemodialysis and polymeric resin hemoadsorption.

Case Report: Effective methotrexate removal by combined hemodialysis and polymeric resin hemoadsorption.

Background: High-dose methotrexate (HDMTX) is central to treating primary central nervous system lymphoma but carries a risk of acute kidney injury (AKI), which can delay methotrexate (MTX) clearance and increase toxicity. Glucarpidase is the treatment of choice for MTX toxicity, but limited access in many countries may necessitate alternatives. We present the first reported adult case of combined high-flux hemodialysis (HFHD) and HA230 hemoadsorption for MTX clearance.

Case summary: A 66-year-old woman with newly diagnosed primary central nervous system lymphoma began induction chemotherapy including HDMTX. Forty-eight hours post-infusion, she developed KDIGO stage 3 AKI, with plasma MTX levels of 26.278 µmol/L despite maintained urine output and early supportive measures. On Day 3, MTX levels remained elevated at 15.567 µmol/L, accompanied by severe metabolic alkalosis. She was admitted to intensive care, where she underwent HFHD combined with post-filter HA230 hemoadsorption, followed by intravenous glucarpidase as soon as it became available. A second extracorporeal session occurred 48 hours later. MTX levels decreased by 91.93% (estimated elimination half-life ≈ 0.83 hours) and 71.02% (half-life ≈ 2.12 hours) after the first and second sessions, respectively. No significant rebound in MTX levels or dialysis-related complications occurred. The patient recovered renal function and completed further treatment without MTX.

Conclusions: This case demonstrates the effectiveness of combined HFHD and HA230 hemoadsorption as a bridging or alternative strategy when glucarpidase is delayed or unavailable. While evidence remains limited, it supports further investigation into extracorporeal MTX removal and contributes to the evolving field of Onconephrology.

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