Percutaneous mechanical thrombectomy in a real‐world pulmonary embolism population: Interim results of the FLASH registry

Objectives The FlowTriever All‐Comer Registry for Patient Safety and Hemodynamics (FLASH) is a prospective multi‐center registry evaluating the safety and effectiveness of percutaneous mechanical thrombectomy for treatment of pulmonary embolism (PE) in a real‐world patient population (NCT03761173)....

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Veröffentlicht in:Catheterization and cardiovascular interventions 2022-03, Vol.99 (4), p.1345-1355
Hauptverfasser: Toma, Catalin, Bunte, Matthew C., Cho, Kenneth H., Jaber, Wissam A., Chambers, Jeffrey, Stegman, Brian, Gondi, Sreedevi, Leung, Daniel A., Savin, Michael, Khandhar, Sameer, Kado, Herman, Koenig, Gerald, Weinberg, Mitchell, Beasley, Robert E., Roberts, Jon, Angel, Wesley, Sarosi, Michael G., Qaqi, Osama, Veerina, Kalyan, Brown, Michael A., Pollak, Jeffrey S.
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Sprache:eng
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Zusammenfassung:Objectives The FlowTriever All‐Comer Registry for Patient Safety and Hemodynamics (FLASH) is a prospective multi‐center registry evaluating the safety and effectiveness of percutaneous mechanical thrombectomy for treatment of pulmonary embolism (PE) in a real‐world patient population (NCT03761173). This interim analysis reports outcomes for the first 250 patients enrolled in FLASH. Background High‐ and intermediate‐risk PEs are characterized by high mortality rates, frequent readmissions, and long‐term sequelae. Mechanical thrombectomy is emerging as a front‐line therapy for PE that enables immediate thrombus reduction while avoiding the bleeding risks inherent with thrombolytics. Methods The primary endpoint is a composite of major adverse events (MAE) including device‐related death, major bleeding, and intraprocedural device‐ or procedure‐related adverse events at 48 h. Secondary endpoints include on‐table changes in hemodynamics and longer‐term measures including dyspnea, heart rate, and cardiac function. Results Patients were predominantly intermediate‐risk per ESC guidelines (6.8% high‐risk, 93.2% intermediate‐risk). There were three MAEs (1.2%), all of which were major bleeds that resolved without sequelae, with no device‐related injuries, clinical deteriorations, or deaths at 48 h. All‐cause mortality was 0.4% at 30 days, with a single death that was unrelated to PE. Significant on‐table improvements in hemodynamics were noted, including an average reduction in mean pulmonary artery pressure of 7.1 mmHg (22.2%, p 
ISSN:1522-1946
1522-726X
DOI:10.1002/ccd.30091