Why the study?
Clinical management of massive pulmonary embolism is challenging when active hemorrhage, a contraindication to thrombolytics, is concurrently present.
Can low-dose catheter-directed thrombolysis with alteplase be safely and effectively used in a patient with massive pulmonary embolism and absolute contraindications to systemic thrombolysis?
Can low-dose catheter-directed thrombolysis with alteplase be safely and effectively used in a patient with massive pulmonary embolism and absolute contraindications to systemic thrombolysis?
Low-dose catheter-directed thrombolysis with alteplase may be a lifesaving and viable option for massive pulmonary embolism even in patients with absolute contraindications to systemic thrombolysis.
May support low-dose CDT feasibility in contraindicated massive PE; hypothesis-generating and should not change practice.
Clinical management of massive pulmonary embolism is challenging when active hemorrhage, a contraindication to thrombolytics, is concurrently present. We describe a successful attempt in using low-dose catheter-directed thrombolysis (CDT) in a high-risk patient with absolute contraindications to systemic thrombolysis. A 69-year-old Asian female with cardiac arrest was brought to a resource-limited rural hospital. The patient underwent 50 min of cardiopulmonary resuscitation (CPR) before regaining the pulse but remained in cardiogenic shock. Computerized tomography (CT) of the chest found massive PE. The patient was found with multiple fractures and subarachnoid hemorrhage. Catheter-directed embolectomy was performed without clinical improvement. A low-dose CDT with alteplase was attempted by giving 5 mg over 2 h with a repeated session 24 h later for a total of 10 mg. The patient started improving, was extubated on Day 9, and transferred out of the ICU on Day 15. Low-dose CDT in massive PE could be lifesaving despite the presence of absolute alteplase contraindications. Patients with contraindications, a high risk of bleeding, or of Asian race may benefit more from the low-dose alteplase regimen.
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Song et al. (2025) studied this question.
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