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Successful treatment of acute device thrombosis of patent foramen ovale with slow infusion of low-dose thrombolytic therapy. | LitMetric

Successful treatment of acute device thrombosis of patent foramen ovale with slow infusion of low-dose thrombolytic therapy.

Eur Heart J Case Rep

Kartal Kosuyolu High Specialty Training and Research Hospital, Department of Cardiology, University of Medical Sciences, Istanbul, Turkey.

Published: August 2024

AI Article Synopsis

  • Percutaneous closure of patent foramen ovale (PFO) helps prevent recurrent cerebral embolism, but device-related thrombosis can occur, leading to serious complications.
  • A case is presented of a 40-year-old woman who developed a thrombus after PFO closure, which was successfully treated with a slow infusion of low-dose tissue plasminogen activator (t-PA).
  • This case highlights that while acute thrombosis of PFO devices is rare, low-dose t-PA can be an effective treatment option if there are no contraindications.

Article Abstract

Background: Percutaneous closure of patent foramen ovale (PFO) is used in selected individuals to eliminate the risk of recurrent cerebral embolism due to paradoxical embolization. Although device thrombosis is rare, it can cause serious complications. Herein, we report a 40-year-old woman who developed acute PFO closure device-associated thrombus and was subsequently treated with slow infusion of low-dose tissue plasminogen activator (t-PA) (25 mg/6 h).

Case Summary: A 40-year-old woman was admitted to the hospital because of an cerebrovascular accident (CVA). Computed tomography and magnetic resonance imaging of the brain demonstrated the presence of an ischaemic lesion in the right cerebellar infarct. Since no pathological finding was detected that could cause CVA, it was considered that there might be paradoxical embolism due to PFO. Percutaneous PFO closure was decided by the heart and brain team. The occluder was implanted under transoesophageal echocardiography (TEE) and fluoroscopy guidance. Although activated clotting time was 250 s, hypermobile acute thrombus measuring 11 × 5 mm was seen on the left atrial side of the PFO device. Slow infusion of low-dose t-PA treatment was given. As soon as after a single-dose t-PA, control TEE was performed and it was seen that almost the entire thrombus was lysed. The patient did not have any complications during the treatment period.

Discussion: Acute PFO device thrombosis is a rare but important complication. If there is no contraindication for lytic treatment in acutely developing large PFO device thrombosis, slow infusion of low-dose t-PA may be useful.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11362546PMC
http://dx.doi.org/10.1093/ehjcr/ytae360DOI Listing

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