Key result
Intensive care and hemodynamic support reverse severe grayanotoxin-induced bradycardia and acute LVEF reduction.
Why the study?
Toxic exposures and severe hypersensitivity reactions can cause life-threatening cardiorespiratory complications that pose significant diagnostic challenges when patients present with profound hemodynamic instability, acute respiratory failure, and myocardial injury.
Case Report (n=2)
No
Early recognition, systematic differential diagnosis (integrating exposure history, cardiac biomarkers, imaging, and toxicology), and prompt mechanical ventilation and hemodynamic support can successfully reverse life-threatening cardiorespiratory syndromes caused by anaphylaxis or grayanotoxin poisoning.
Answers are grounded in this paper and cite their sources.
Supports intensive care reversal of rare toxin- and anaphylaxis-related cardiac failure; leaves open generalizability and optimal protocols.
Introduction: Toxic exposures and severe hypersensitivity reactions may cause life-threatening cardiovascular and respiratory complications requiring prompt recognition, emergency intervention, and intensive care management. Diagnostic challenges are particularly significant when patients present with profound hemodynamic instability, acute respiratory failure, and evidence of myocardial injury. Objective: To illustrate the diagnostic challenges and intensive care management of severe cardiorespiratory complications associated with toxic and hypersensitivity-related exposures through the analysis of two clinical cases. Materials and Methods: This descriptive report presents two clinical cases managed at the First University Clinic of Tbilisi State Medical University. The analysis was based on medical records, clinical presentation and progression, laboratory findings, diagnostic imaging, toxicological investigations, and therapeutic interventions. Results: Case 1: A 43-year-old woman developed acute respiratory failure, severe hypoxemia, arterial hypotension, and frothy oral secretions shortly after applying hair dye. Clinical evaluation revealed pulmonary edema, left ventricular systolic dysfunction with an ejection fraction of 37%, and elevated cardiac troponin levels, indicating myocardial injury. The clinical diagnosis was anaphylactic shock complicated by acute left ventricular dysfunction and pulmonary edema. Following intensive care management, including invasive mechanical ventilation and supportive therapy, the patient's condition improved, and she was subsequently discharged. Case 2: A 62-year-old man developed profound bradycardia (heart rate: 37 beats/min), hemodynamic instability, and acute respiratory failure following the ingestion of a large quantity of honey. Toxicological testing confirmed the presence of grayanotoxin, supporting the diagnosis of grayanotoxin poisoning. The patient required endotracheal intubation, invasive mechanical ventilation, and hemodynamic support, including atropine and dopamine administration. Coronary angiography revealed no significant coronary artery lesions, while computed tomography excluded pulmonary embolism. Following intensive treatment, the patient's clinical and hemodynamic status progressively improved. He was successfully extubated and discharged in satisfactory condition. Conclusion: These cases highlight the importance of early recognition of severe toxic and hypersensitivity-related reactions, immediate stabilization of vital functions, and a systematic differential diagnostic approach in patients presenting with acute cardiorespiratory compromise. Integration of exposure history, clinical findings, cardiac biomarkers, imaging studies, and toxicological testing is essential for identifying the underlying etiology, guiding appropriate treatment, and improving clinical outcomes.
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Mazanashvili et al. (2026) conducted a case report in Severe cardiorespiratory complications from toxic (grayanotoxin) and hypersensitivity-related (hair dye) exposures (n=2). Intensive care management (invasive mechanical ventilation, supportive therapy, atropine, dopamine) was evaluated on Clinical and hemodynamic recovery and hospital discharge. Intensive care management with mechanical ventilation and hemodynamic support resolved anaphylactic LVEF reduction and grayanotoxin bradycardia (37 bpm) in 2/2 patients.
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