静脉体外膜氧合治疗难治性链球菌中毒性休克综合征的序贯体外病原体清除疗法和细胞引导体外疗法:病例报告。

Q4 Medicine Critical care explorations Pub Date : 2024-02-26 eCollection Date: 2024-03-01 DOI:10.1097/CCE.0000000000001058
Stephen J Amerson, McKenna Hoffman, Fadi Abouzahr, Mohammad Ahmad, Rachel K Sterling, Hitesh Gidwani, Linda E Sousse, Jeffrey D Dellavolpe
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引用次数: 0

摘要

背景:链球菌中毒性休克综合征(STSS)是以侵袭性 A 组链球菌感染为主的一种严重并发症。STSS 通常以流感样症状为特征,包括发热、寒战和肌痛,并可迅速发展为伴有低血压、心动过速、呼吸过速和多器官(肾、肝、肺或血液)衰竭的败血症。根据症状的严重程度,死亡率可超过 50%。病例摘要:在此,我们介绍了一种新型的多体外介入策略,用于治疗 STSS 继发的严重脓毒性休克病例。一名 28 岁产妇在剖宫产术后 5 天出现 STSS,伴有呼吸困难、低血压和多器官功能衰竭。尽管进行了插管、抗生素、血管加压和液体复苏等常规治疗,她的病情还是恶化了。她接受了静脉-动脉体外膜氧合(VA-ECMO)治疗,随后使用 Seraph 100 血液过滤器启动了病原体血液灌流,并使用选择性细胞吸附装置(SCD)进行免疫调节。未观察到与设备相关的不良事件。患者的病情逐渐稳定,4 天后停用了血管加压药,6 天后解除了 ECMO,7 天后出现了肾功能恢复的迹象,14 天后拔除了机械通气。13 天后,她转入常规血液透析,11 天后停止了所有肾脏替代疗法:这是首次报道在 SCD 患者中使用 VA-ECMO、Seraph 100 血液灌流和细胞定向免疫调节。这种多模式体外支持方法是治疗最难治性重症病例的一种有前途的治疗策略。还需要进一步的研究来评估这种连续方法的安全性和有效性。
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Sequential Extracorporeal Therapy of Pathogen Removal Followed by Cell-Directed Extracorporeal Therapy in Streptococcal Toxic Shock Syndrome Refractory to Venoarterial Extracorporeal Membrane Oxygenation: A Case Report.

Background: Streptococcal toxic shock syndrome (STSS) is a fulminant complication of predominantly invasive group A streptococcal infections. STSS is often characterized by influenza-like symptoms, including fever, chills, and myalgia that can quickly progress to sepsis with hypotension, tachycardia, tachypnea, and multiple organ failure (kidney, liver, lung, or blood). Mortality can exceed 50% depending on the severity of symptoms.

Case summary: Here, we describe a novel, multi-extracorporeal intervention strategy in a case of severe septic shock secondary to STSS. A 28-year-old woman 5 days after cesarean section developed STSS with respiratory distress, hypotension, and multiple organ failure. Despite conventional therapy with intubation, antibiotics, vasopressors, and fluid resuscitation, her condition worsened. She was placed on venoarterial extracorporeal membrane oxygenation (VA-ECMO) with subsequent initiation of pathogen hemoperfusion using the Seraph 100 blood filter, followed by immunomodulation with the selective cytopheretic device (SCD). No device-related adverse events were observed. The patient's condition gradually stabilized with discontinuation of vasopressors after 4 days, ECMO decannulation after 6 days, evidence of renal recovery after 7 days, and extubation from mechanical ventilation after 14 days. She was transferred to conventional hemodialysis after 13 days and discontinued all kidney replacement therapy 11 days later.

Conclusions: This is the first reported use of VA-ECMO, Seraph 100 hemoperfusion, and cell-directed immunomodulation with SCD. This multimodal approach to extracorporeal support represents a promising therapeutic strategy for the most refractory critical care cases. Further studies are needed to assess the safety and efficacy of this sequential approach.

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