Unplugging the Drain: Treatment of a Rare Late Complication of Cardiac Resynchronization Therapy
Faheemullah Beg1, Tanushree Agrawal2, Ashrith Guha3
1Cardiovascular Disease, Houston Methodist Hospital, Houston, USA.
Insights
Central vein thrombosis (CVT), a rare complication, caused chylothorax in a heart failure patient. Balloon angioplasty successfully treated the occluded vein, resolving the effusion.
Area of Science:
- Cardiology
- Vascular Medicine
- Pulmonology
Background:
- Central vein thrombosis (CVT) is an uncommon cause of chylothorax.
- Heart failure patients often have indwelling devices that can lead to venous complications.
Observation:
- A 65-year-old male with end-stage heart failure presented with shortness of breath and a large pleural effusion.
- Diagnostic workup confirmed chylothorax and revealed bilateral brachiocephalic vein occlusion despite anticoagulation.
Findings:
- The patient's chylothorax was secondary to central vein thrombosis.
- Successful treatment was achieved with balloon angioplasty of the occluded right brachiocephalic vein, leading to effusion resolution.
Implications:
- This case highlights a rare complication of cardiac devices in heart failure patients.
- Reversible central vein thrombosis causing chylothorax can be effectively treated with angioplasty.
Abstract:
Central vein thrombosis (CVT) is a rare cause of chylothorax. We report a patient with chylothorax secondary to CVT, despite being on anticoagulation, who was successfully treated with balloon angioplasty of the occluded vein. A 65-year-old male presented with shortness of breath of one-month duration. He had end-stage heart failure and was on milrinone infusion. Physical exam was consistent with elevated central venous pressure. Chest x-ray showed a large left-sided pleural effusion. Right heart catheterization (RHC) showed normal right atrial pressure and normal pulmonary capillary wedge pressure. Diagnostic thoracentesis was consistent with chylothorax. A venogram revealed bilateral brachiocephalic vein occlusion. The right brachiocephalic vein was recanalized by angioplasty, which led to resolution of pleural effusion. Our case not only highlights the identification of a rare complication of a common device (i.e., cardiac resynchronization therapy defibrillator) used in heart failure patients but also highlights the treatment for this rare but reversible complication.
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