Infective Endocarditis Associated with Atrial Septal Defect in an Intravenous Drug Abuser: A Case Report
Maha Jahangir1, Marrium Nawaz2, Fareha Jabbar2
1Dow Medical College, Civil Hospital Karachi, Karachi, PAK.
Insights
Infective endocarditis (IE) can present atypically in patients with atrial septal defect (ASD). Early diagnosis and treatment are crucial for recovery and preventing reinfection, especially in those with a history of intravenous drug abuse (IVDA).
Area of Science:
- Cardiology
- Infectious Diseases
Background:
- Atrial septal defect (ASD) is a common congenital heart disease, typically posing a low risk for infective endocarditis (IE) due to slow shunt flow.
- Intravenous drug abuse (IVDA) is a significant risk factor for IE, presenting diagnostic and therapeutic challenges.
Observation:
- This case report details an atypical presentation of IE in an adult patient with an existing ASD.
- Diagnosis was confirmed using modified Duke criteria, with blood cultures positive for methicillin-resistant Staphylococcus aureus (MRSA).
Findings:
- The patient received a six-week course of antibiotic therapy for IE, achieving full recovery.
- The patient subsequently underwent surgical closure of the atrial septal defect.
Implications:
- Infective endocarditis should be considered in ASD patients, even with a low-risk profile, necessitating a high index of suspicion for timely diagnosis.
- Prompt antibiotic treatment and comprehensive follow-up, including rehabilitation for IVDA history, are vital for successful outcomes and preventing recurrent infections.
Abstract:
Atrial septal defect (ASD) is a common congenital abnormality, which accounts for 20-40% of all the adult patients with congenital heart diseases. Due to the slow velocity of shunt flow, ASD has a negligible risk for infective endocarditis (IE). However, intravenous drug abuse (IVDA) is a potential cause for IE. IE remains a diagnostic and therapeutic challenge. Our case report demonstrates the atypical presentation of IE in an ASD patient. The diagnosis was made on the basis of modified Duke criteria, and blood cultures were found out to be positive for methicillin-resistant Staphylococcus aureus (MRSA). The treatment for IE was completed in six weeks with full recovery, and the patient underwent a surgery for ASD closure. This case highlights that IE should not be overlooked in ASD patients and that a high index of suspicion, in addition to proper antibiotic therapy, is lifesaving. Also, follow-up, along with rehabilitation measures, should be taken for patients with a history of drug abuse in order to prevent the risk of reinfection.
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