Extracorporeal Blood Purification Therapy to Deal a Deferasirox Induced Life-Threatening Hepatic Encephalopathy in a Septic Child With Sickle-Cell Disease: A Case Report

IF 2.7 4区 医学 Q4 HEMATOLOGY
E. Rossetti, A. Cappoli, R. Labbadia, G. Leone, F. Chiusolo, F. Tortora, D. Martinelli, M. Marano
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Abstract

This report details a rare pediatric case of hyperammonemic encephalopathy caused by the oral iron chelating drug deferasirox (DFR) in a septic patient. It is our contention that this study lends support to the existing literature, as it describes the case of a 15-year-old female patient with a history of sickle-cell disease who presented with a fever and vomiting, rapid development of sleepiness, consciousness disturbances, medium mydriasis, neck stiffness, and trismus with seizure. Her Glasgow Coma Scale (GCS) score was 5. Laboratory tests revealed an increase in creatinine, metabolic acidosis, hyperammonemia, high cerebrospinal fluid (CSF) glutamine levels, alterations in coagulation and in liver function, rising inflammatory markers, cerebral oedema on brain Computerized Tomography (CT) scan, 10^6 copies/ml of Methicillin-Resistant Staphylococcus Aureus (MRSA) in pulmonary swab film array, and elevated DFR blood level. The treatment plan involved the early cessation of DFR, the correction of acidosis, mechanical ventilation, mannitol and bioarginine, vasoactive drug, antibiotics, and supportive care with continuous veno-venous hemodiafiltration (CVVHDF) for hyperammonemia and therapeutic plasma exchange (TPE) for a high CSF glutamine level resulting from cytotoxic encephalopathy. The patient successfully overcame the multiorgan failure, with no permanent neurologic complications. It is our opinion that healthcare providers and family caregivers of patients with chronic disease may be particularly attuned to the emergence of any sign or symptom, and thus well positioned to take prompt action to avert life-threatening clinical deterioration due to rising DFR levels. It is recommended that critical care providers commence extracorporeal blood purification therapies (EBPT) at the earliest opportunity, taking care to adapt the technique to the specific needs of the patient and to avoid the potential for fatal neurological complications.

Abstract Image

体外血液净化治疗镰状细胞病脓毒症患儿去铁霉素诱导的危及生命的肝性脑病1例报告
本报告详细介绍了一个罕见的儿童病例高氨血症脑病引起的口服铁螯合药物去铁铁(DFR)在一个败血症患者。我们认为,本研究支持现有文献,因为它描述了一名15岁的镰状细胞病患者的病例,她有镰状细胞病的病史,表现为发烧和呕吐,嗜睡迅速发展,意识障碍,中度瞳孔,颈部僵硬,牙关紧闭伴癫痫发作。格拉斯哥昏迷评分(GCS)为5分。实验室检查显示肌酐升高,代谢性酸中毒,高氨血症,脑脊液(CSF)谷氨酰胺水平升高,凝血和肝功能改变,炎症标志物升高,脑计算机断层扫描(CT)显示脑水肿,肺棉签片扫描显示耐甲氧西林金黄色葡萄球菌(MRSA) 10^6 copies/ml, DFR血水平升高。治疗计划包括尽早停止DFR,纠正酸中毒,机械通气,甘露醇和生物精氨酸,血管活性药物,抗生素,以及持续静脉-静脉血液扩张滤过(CVVHDF)治疗高氨血症和治疗性血浆交换(TPE)治疗细胞毒性脑病引起的脑脊液谷氨酰胺水平高。患者成功克服了多器官功能衰竭,无永久性神经系统并发症。我们认为,慢性病患者的医疗保健提供者和家庭护理人员可能特别适应任何体征或症状的出现,因此能够及时采取行动,避免因DFR水平上升而危及生命的临床恶化。建议重症监护提供者尽早开始体外血液净化治疗(EBPT),注意使技术适应患者的特殊需要,并避免致命的神经系统并发症的可能性。
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来源期刊
CiteScore
2.80
自引率
13.30%
发文量
70
审稿时长
>12 weeks
期刊介绍: The Journal of Clinical Apheresis publishes articles dealing with all aspects of hemapheresis. Articles welcomed for review include those reporting basic research and clinical applications of therapeutic plasma exchange, therapeutic cytapheresis, therapeutic absorption, blood component collection and transfusion, donor recruitment and safety, administration of hemapheresis centers, and innovative applications of hemapheresis technology. Experimental studies, clinical trials, case reports, and concise reviews will be welcomed.
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