AI Article Synopsis

  • A 61-year-old male with a history of emphysema, obstructive sleep apnea, and hypertension experienced worsening shortness of breath and swelling, leading to an ER visit.
  • He showed symptoms of heart failure, including elevated jugular veins and fluid retention, and tests revealed a significantly reduced left ventricular ejection fraction (LVEF) suggestive of left ventricular non-compaction (LVNC).
  • The patient was treated according to heart failure guidelines, monitored for arrhythmias, and discharged with a wearable defibrillator, with plans for future evaluation for an implantable defibrillator for primary prevention.

Article Abstract

A 61-year-old male, with a history of emphysema, obstructive sleep apnea, and hypertension, presented to the emergency room with worsening shortness of breath over a three-month period. The patient also complained of orthopnea, paroxysmal nocturnal dyspnea, and progressively worsening lower limb swelling. On examination, the patient had jugular venous distension, bilateral lower extremity edema, and bibasilar crackles. The laboratory evaluation showed an elevated B-natriuretic peptide level and a normal troponin level. A transthoracic echocardiogram (TTE) showed a reduced left ventricular ejection fraction (LVEF) of 20%-25% with prominent hyper-trabeculations noted in the left ventricle, most prominent in the lateral and apical walls. These findings were concerning for left ventricular non-compaction (LVNC). The patient underwent left heart catheterization, which did not show obstructive coronary disease as a cause of his cardiomyopathy. The patient was managed with guideline-directed therapy for heart failure and was started on warfarin due to the increased risk of thromboembolism associated with LVNC. During his admission, he exhibited multiple episodes of nonsustained ventricular tachycardia and was subsequently evaluated by electrophysiology (EP). He was discharged home with a wearable cardioverter defibrillator with instructions to follow up with EP in three months for an evaluation of implantable cardioverter-defibrillator (ICD) placement for primary prevention.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6110421PMC
http://dx.doi.org/10.7759/cureus.2886DOI Listing

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