A 23-month-old with tetralogy of Fallot developed low cardiac output syndrome post-surgery, leading to junctional ectopic tachycardia and transient cortical blindness, but showed partial visual recove
This case demonstrates that low cardiac output syndrome after Tetralogy of Fallot repair can precipitate a cascade of severe but potentially reversible complications, including cortical blindness, emphasizing the need for comprehensive postoperative surveillance.
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Background Tetralogy of Fallot (ToF) repair in infants may be complicated by low cardiac output syndrome (LCOS), which can precipitate rare multisystem complications. Junctional ectopic tachycardia (JET), atrial thrombosis, and cortical blindness are underrecognized sequelae requiring multidisciplinary management. Case presentation We report a 23-month-old male with ToF who developed LCOS post-surgery, followed by refractory JET, left atrial thrombus, embolic occipital infarction, and transient cortical blindness. LCOS was defined by elevated lactate, low ScvO₂, hypotension, and oliguria. JET was managed with amiodarone, ivabradine, magnesium, and targeted temperature control. Thrombosis resolved with heparin, yet cortical infarct occurred. Neuroprotective therapy included piracetam and mannitol. Outcome Partial visual recovery was observed by POD-30. Follow-up echocardiography showed improved RV function and resolution of arrhythmia. The patient was discharged on POD-35 with improving neurologic status. Conclusion LCOS can trigger a cascade of cardiac, thrombotic, and neurologic complications. Early recognition and multidisciplinary intervention are essential. This case highlights the potential reversibility of cortical blindness and the importance of comprehensive postoperative surveillance.
Setia et al. (Tue,) reported a other. A 23-month-old with tetralogy of Fallot developed low cardiac output syndrome post-surgery, leading to junctional ectopic tachycardia and transient cortical blindness, but showed partial visual recove.