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Navigating the Diagnostic and Management Challenges of Suspected Cardiac Amyloidosis in Resource-Limited Settings:
Sura Markos1, Yegzeru Belete2, Betre Bikamo3
1Division of Cardiology, Department of Internal Medicine, College of Medicine and Health Sciences Hawassa University Hawassa Ethiopia.
Insights
Diagnosing cardiac amyloidosis (CA) in resource-limited settings is complex. Limited provider awareness in Ethiopia leads to delayed diagnosis and treatment for heart failure patients with CA.
Area of Science:
- Cardiology
- Internal Medicine
- Medical Diagnostics
Background:
- Cardiac amyloidosis (CA) presents diagnostic and therapeutic challenges, particularly in resource-limited healthcare settings.
- Delayed diagnosis of CA can result from limited awareness among primary healthcare providers, leading to misdiagnosis and suboptimal management.
- Ethiopia faces specific hurdles in identifying and treating CA, impacting patient outcomes.
Purpose of the Study:
- To highlight the diagnostic and therapeutic complexities of cardiac amyloidosis in resource-limited environments.
- To illustrate the challenges through a specific case presentation from Ethiopia.
- To emphasize the need for improved diagnostic capabilities and provider education for CA.
Main Methods:
- Case report detailing a patient's diagnostic journey over 13 months with multiple physician visits.
- Analysis of clinical presentation, electrocardiographic (ECG) and echocardiographic findings, and cardiac troponin levels.
- Discussion of diagnostic discrepancies and challenges in a resource-limited context.
Main Results:
- A patient with heart failure symptoms was diagnosed with cardiac amyloidosis after a prolonged period.
- Discrepancies between ECG and echocardiography, along with elevated troponin, were key diagnostic clues.
- Limited awareness of CA among Ethiopian primary healthcare providers contributed to diagnostic delays.
Conclusions:
- Heightened clinical suspicion is crucial for diagnosing cardiac amyloidosis in resource-limited settings.
- Proficiency in recognizing characteristic ECG and echocardiographic findings is essential for early detection.
- Prompt referral to cardiologists and improved diagnostic resources are vital for effective CA management.
Abstract:
This report discusses the diagnostic and therapeutic complexities encountered in resource-limited environments when assessing patients suspected of cardiac amyloidosis (CA). The study describes a case involving a patient who initially presented with heart failure symptoms and eventually received a CA diagnosis after 13 months and four primary physician visits, primarily based on discrepancies observed between electrocardiographic and echocardiographic findings, alongside elevated cardiac troponin levels. The case underscores the limited awareness of CA among primary healthcare providers in Ethiopia, contributing to a higher likelihood of misdiagnosis and inappropriate treatment approaches. Additionally, the report discusses the specific challenges associated with diagnosing and managing CA patients. It advocates for essential resources such as heightened clinical suspicion, proficiency in recognizing the characteristic electrocardiogram (ECG) and echocardiographic indicators of CA, and prompt referral to cardiologists.
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