Riley J Batchelor, Millie Watkins, Jason E Bloom, Malanka Lankaputhra, Derek P Chew, Aiden Burrell, Andrew Taylor, Dion Stub, David M Kaye
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引用次数: 0
Abstract
Introduction: Cardiogenic shock and cardiac arrest are associated with high risk of mortality despite advances in resuscitation techniques and supportive care. A growing body of evidence implicates a systemic inflammatory response syndrome (SIRS) in the pathogenesis of post-arrest vasoplegia and end-organ injury. Methylene blue (MB), a nitric oxide pathway inhibitor, has shown efficacy in vasoplegic and septic shock, yet its role in cardiogenic shock or cardiac arrest is not well established.
Methods: We conducted a systematic review of peer-reviewed studies examining methylene blue in cardiogenic shock or cardiac arrest. Electronic databases MEDLINE, EMBASE, CENTRAL, Scopus, and Web of Science were searched in March 2025. Preclinical randomised trials and clinical studies in adult humans or animal models were included.
Results: Out of 676 screened records, seven studies met inclusion criteria: six preclinical randomised animal studies and one retrospective human cohort study. Early porcine studies using electrically induced ventricular fibrillation and continuous MB infusion during CPR demonstrated improved survival, haemodynamic profile, and neurologic outcomes. In contrast, more recent, well conducted bolus-only studies using infarct-induced models reported minimal or no benefit associated with MB administration. The single human study lacked a comparator group and provided limited cardiogenic shock-specific outcome data.
Conclusions: This systematic review highlights the lack of data available for MB in cardiogenic shock and cardiac arrest, especially in humans. There was a potential therapeutic signal for methylene blue in some animal models of cardiogenic shock and cardiac arrest. Prospective studies with clinically relevant models of cardiac injury are warranted to determine whether MB can improve outcomes in this high-risk population.
导读:尽管复苏技术和支持性护理有所进步,但心源性休克和心脏骤停仍与高死亡率相关。越来越多的证据表明,系统性炎症反应综合征(SIRS)在骤停后血管截瘫和终末器官损伤的发病机制中起作用。亚甲基蓝(MB)是一种一氧化氮途径抑制剂,已显示出对血管截瘫和感染性休克的疗效,但其在心源性休克或心脏骤停中的作用尚不清楚。方法:我们对同行评议的亚甲基蓝治疗心源性休克或心脏骤停的研究进行了系统回顾。在2025年3月检索了MEDLINE、EMBASE、CENTRAL、Scopus和Web of Science等电子数据库。包括临床前随机试验和成人或动物模型的临床研究。结果:在676项筛选记录中,有7项研究符合纳入标准:6项临床前随机动物研究和1项回顾性人类队列研究。早期的猪研究表明,在心肺复苏术中使用电致心室颤动和持续MB输注可以改善猪的存活率、血流动力学特征和神经系统预后。相比之下,最近,使用梗死诱导模型进行的仅大剂量研究报告了MB给药的最小或没有益处。这项单独的人类研究缺乏比较组,并提供有限的心源性休克特异性结局数据。结论:本系统综述强调缺乏MB在心源性休克和心脏骤停中的可用数据,特别是在人类中。亚甲基蓝在一些心源性休克和心脏骤停的动物模型中有潜在的治疗信号。有必要对临床相关的心脏损伤模型进行前瞻性研究,以确定MB是否可以改善这一高危人群的预后。
期刊介绍:
SHOCK®: Injury, Inflammation, and Sepsis: Laboratory and Clinical Approaches includes studies of novel therapeutic approaches, such as immunomodulation, gene therapy, nutrition, and others. The mission of the Journal is to foster and promote multidisciplinary studies, both experimental and clinical in nature, that critically examine the etiology, mechanisms and novel therapeutics of shock-related pathophysiological conditions. Its purpose is to excel as a vehicle for timely publication in the areas of basic and clinical studies of shock, trauma, sepsis, inflammation, ischemia, and related pathobiological states, with particular emphasis on the biologic mechanisms that determine the response to such injury. Making such information available will ultimately facilitate improved care of the traumatized or septic individual.