Combined application of double plasma molecular adsorption system treatment, plasma exchange, and continuous veno-venous hemofiltration to rescue an adult patient with acute liver failure induced by accidental acute severe thinner intoxication: a case report

联合应用双血浆分子吸附系统治疗、血浆置换和连续性静脉-静脉血液滤过挽救因意外急性重度稀释剂中毒导致急性肝功能衰竭的成年患者:病例报告

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Abstract

BACKGROUND: Intentional or accidental intoxication is a common inciting cause of acute liver failure, which manifests as a severe clinical consequence of abrupt hepatocyte injury in the patient without any known underlying liver diseases (within 26 weeks of illness duration). In addition, it often progresses to a lethal outcome. Thinner intoxication is a rare but non-negligible etiology of acute liver failure. Considering the potential neurotoxicity, myotoxicity, hepatotoxicity, nephrotoxicity, and cardiopulmonary toxicity of thinner, as well as the lack of effective specific reversal agents or antidotes, early and continuous supportive care by an artificial liver support system (Liu et al. in Artif Organs 49:762-777, 2025)-defined here as the integrated use of double plasma molecular adsorption system, plasma exchange, and continuous veno-venous hemofiltration-is conducive to remove thinner and ammonia from the blood, improve hepatic encephalopathy, replace lost liver function, alleviate thinner intoxication-induced multiorgan damage, restore hemodynamics and internal environment stability, modulate immune response, and maintain cytokine homeostasis. In this study, we presented the first reported case of acute liver failure induced by acute severe thinner intoxication in a Han Chinese adult, who was successfully rescued through the use of a double plasma molecular adsorption system, plasma exchange, and continuous veno-venous hemofiltration. A 46-year-old Asian man was admitted to the Department of Critical Care Medicine owing to nausea and vomiting for 4 days, abdominal pain and melena for 2 days, and disturbance of consciousness for 1 day after accidentally ingesting a mouthful of thinner (exact volume unknown) at a construction site. In the intensive care unit, the patient underwent orotracheal intubation, invasive mechanical ventilation, appropriate analgesia and sedation, infusion of blood products and hemostatic drugs, phlegm-removing, and correction of internal environment disorder. Subsequently, the patient received four double plasma molecular adsorption system treatments, two plasma exchanges (a total of 6000 mL of fresh frozen plasma), and 79 hours of continuous veno-venous hemofiltration during hospitalization. On the 8th day after admission, invasive mechanical ventilation was withdrawn, but the patient's consciousness remained unclear. On the 36th day after admission, the patient was in remission and discharged. However, his liver function and coagulation parameters did not revert to normal. CONCLUSION: Thinner intoxication is a rare but non-negligible etiology of acute liver failure. To the best of our knowledge, our case is the first attempt to combine double plasma molecular adsorption system treatment, plasma exchange, and continuous veno-venous hemofiltration for acute liver failure as a clinical manifestation of thinner intoxication. The combination of different therapeutic modalities of an artificial liver support system can compensate for the individual shortcomings and maximize their respective advantages, which requires a multidisciplinary team to determine their clinical application in suitable patients.

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