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Delayed cardiogenic shock following spontaneous coronary artery dissection in a young, healthy female: a case report
Leili Abdan1, Maria Saadatian2, Homina Saffar3
1Tehran Heart Center, Cardiovascular Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
Insights
Spontaneous coronary artery dissection (SCAD) can affect young women without risk factors. Early recognition and multidisciplinary care are vital for managing this rare cause of acute coronary syndrome.
Area of Science:
- Cardiology
- Vascular Medicine
Background:
- Spontaneous coronary artery dissection (SCAD) is a rare, non-atherosclerotic cause of acute coronary syndrome.
- It predominantly affects young, healthy women lacking traditional cardiovascular risk factors.
- Variable presentations and diagnostic challenges exist, especially with unremarkable initial findings.
Purpose of the Study:
- To report a case of SCAD in a young woman.
- To emphasize the importance of considering SCAD in specific patient demographics.
- To highlight diagnostic and management considerations for SCAD.
Main Methods:
- Case presentation of a 37-year-old Iranian woman with no prior medical history or cardiovascular risk factors.
- Initial presentation with non-specific symptoms and a normal ECG.
- Management included intensive medical care, hemodynamic support, and coronary angiography confirming SCAD.
Main Results:
- The patient experienced rapid progression to cardiogenic shock with ventricular arrhythmias.
- Coronary angiography confirmed spontaneous coronary artery dissection.
- Cardiac function improved with multidisciplinary care and hemodynamic support.
Conclusions:
- Clinicians must consider SCAD in young women with chest pain, irrespective of risk factors or initial test results.
- Early recognition is crucial for timely intervention.
- A multidisciplinary approach is essential for optimizing outcomes in SCAD patients.
Background:
Spontaneous coronary artery dissection (SCAD) is a rare, non-atherosclerotic cause of acute coronary syndrome that predominantly affects young, healthy women without conventional cardiovascular risk factors. Reporting such cases is essential to raise awareness of their variable presentation and diagnostic challenges, particularly when initial findings are unremarkable.
Case Presentation:
We discuss a case of SCAD in a 37-year-old Iranian woman with no prior medical history or cardiovascular risk factors. The patient was initially presented with non-specific symptoms and a normal ECG. Her condition rapidly progressed to cardiogenic shock, complicated by ventricular arrhythmias, necessitating intensive medical management and hemodynamic support. Coronary angiography confirmed SCAD. Following multidisciplinary care, her cardiac function gradually improved, and the patient was discharged with close follow-up.
Conclusions:
This case highlights the necessity for clinicians to consider SCAD in young female patients presenting with chest pain, even in the absence of classic risk factors or abnormal initial investigations. Early recognition and a multidisciplinary approach are crucial for optimizing outcomes in this rare yet potentially life-threatening condition.
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