首次使用Seraph®100 Microbind®亲和血液过滤器治疗青少年重症COVID-19患者1例报告

IF 0.7 Q4 UROLOGY & NEPHROLOGY Case Reports in Nephrology and Dialysis Pub Date : 2023-01-27 eCollection Date: 2023-01-01 DOI:10.1159/000527290
Kyle A Merrill, Kelli A Krallman, Daniel Loeb, Stephen W Standage, Dawn Mattoon, Dandan Shan, Stuart L Goldstein, Meredith P Schuh
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引用次数: 1

摘要

Seraph®100 Microbind®亲和血液过滤器(Seraph®100)是一种血液灌流装置,用于吸附细菌,病毒和毒素,当添加到体外回路时。FDA批准了成人紧急使用授权,但该装置从未用于儿童。一名17岁的哮喘患者因COVID-19出现呼吸窘迫。他的病程因呼吸衰竭、横纹肌溶解和3期AKI而变得复杂,需要在ICU第3天开始持续肾脏替代治疗(CKRT)。在ICU第4天添加Seraph®100滤镜。从重症监护室第4天至第8天,患者接受了3次滤过剂治疗。在ICU第8天,他拔管并停止CKRT。他不需要进一步的肾脏替代治疗,但出院后没有做实验室检查。总之,这名患有COVID-19和AKI的青少年患者需要使用Seraph®100 Microbind®亲和血液过滤器进行CKRT耐受性治疗,无明显不良事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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First-Time Use of the Seraph® 100 Microbind® Affinity Blood Filter in an Adolescent Patient with Severe COVID-19 Disease: A Case Report.

The Seraph® 100 Microbind® Affinity Blood Filter (Seraph® 100) is a hemoperfusion device designed to adsorb bacteria, viruses, and toxins when added to extracorporeal circuits. The FDA granted emergency use authorization in adults, but this device had never been utilized in children. A 17-year-old patient with asthma presented with respiratory distress due to COVID-19. His course was complicated by respiratory failure, rhabdomyolysis, and stage 3 AKI requiring initiation of continuous kidney replacement therapy (CKRT) on ICU day 3. The Seraph® 100 filter was added on ICU day 4. He was treated with 3 filters from ICU day 4 to 8. On ICU day 8, he was extubated and CKRT discontinued. He required no further kidney replacement therapy but did not have laboratory work post-discharge. In conclusion, this adolescent patient with COVID-19 and AKI requiring CKRT tolerated treatment with the Seraph® 100 Microbind® Affinity Blood Filter without significant adverse events.

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来源期刊
CiteScore
1.20
自引率
0.00%
发文量
36
审稿时长
10 weeks
期刊介绍: This peer-reviewed online-only journal publishes original case reports covering the entire spectrum of nephrology and dialysis, including genetic susceptibility, clinical presentation, diagnosis, treatment or prevention, toxicities of therapy, critical care, supportive care, quality-of-life and survival issues. The journal will also accept case reports dealing with the use of novel technologies, both in the arena of diagnosis and treatment. Supplementary material is welcomed.
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