• Media type: E-Article
  • Title: EKOS™ Jena Experience: Safety, Feasibility, and Midterm Outcomes of Percutaneous Ultrasound-Assisted Catheter-Directed Thrombolysis in Patients with Intermediate-High-Risk or High-Risk Pulmonary Embolism
  • Contributor: Klein, Friederike; Möbius-Winkler, Sven; Bäz, Laura; Pfeifer, Rüdiger; Fritzenwanger, Michael; Heymel, Stefan; Franz, Marcus; Aftanski, Pawel; Schulze, P. Christian; Kretzschmar, Daniel
  • imprint: Hindawi Limited, 2022
  • Published in: Canadian Respiratory Journal
  • Language: English
  • DOI: 10.1155/2022/7135958
  • ISSN: 1916-7245; 1198-2241
  • Keywords: Pulmonary and Respiratory Medicine
  • Origination:
  • Footnote:
  • Description: <jats:p>Background. Percutaneous catheter-based ultrasound-assisted thrombolysis (UACDT) is recommended for patients with intermediate-high-risk or high-risk pulmonary embolism (PE) in whom systemic thrombolysis has failed or is contraindicated. Aim. To evaluate the safety and efficiency of UACDT in patients with intermediate-high-risk or high-risk PE. Methods. Between October 2017 and January 2020, we performed UACDT using the EkoSonic™ Endovascular System (EKOS™) in 51 patients (21 males, age 63 ± 18 years) with a sPESI of 1.3 ± 0.7. The EKOS™-catheter was implanted within 24 h after admission. Over 15 hours, 11.5 mg of alteplase was administered per catheter. We evaluated right ventricular stress and cardiac biomarkers before and after UACDT. Results. 24 h post-UACDT, median RV/LV ratio decreased from 1.13 to 0.96 (<jats:inline-formula> <math xmlns="http://www.w3.org/1998/Math/MathML" id="M1"> <mi>p</mi> <mo>&lt;</mo> <mn>0.001</mn> </math> </jats:inline-formula>) and the mean sPAP decreased from 47 ± 3 to 32 ± 2 mmHg + CVP (<jats:inline-formula> <math xmlns="http://www.w3.org/1998/Math/MathML" id="M2"> <mi>p</mi> <mo>&lt;</mo> <mn>0.0002</mn> </math> </jats:inline-formula>). There were 6 major bleeding events resulting in transfusion. No stroke, myocardial infarction, right heart decompensation, or recurrent PE occurred. 31 patients (63%) were discharged without any signs of right ventricular stress. After at least 3 months, 73% of our patients did not show any signs of right ventricular dysfunction. The mean RV/LV ratio decreased to 0.75 ± 0.03 (<jats:inline-formula> <math xmlns="http://www.w3.org/1998/Math/MathML" id="M3"> <mi>p</mi> <mo>&lt;</mo> <mn>0.0001</mn> </math> </jats:inline-formula>) in comparison with pre-UACDT, sPAP to 23  mmHg + CVP (<jats:inline-formula> <math xmlns="http://www.w3.org/1998/Math/MathML" id="M4"> <mi>p</mi> <mo>&lt;</mo> <mn>0.0001</mn> </math> </jats:inline-formula>), and BNP to 40 pg/ml (<jats:inline-formula> <math xmlns="http://www.w3.org/1998/Math/MathML" id="M5"> <mi>p</mi> <mo>&lt;</mo> <mn>0.0001</mn> </math> </jats:inline-formula>). Conclusions. The treatment with UACDT reduced right heart stress during the first 24 hours and midterm in patients with intermediate-high-risk or high-risk PE at an acceptable rate of severe complications.</jats:p>
  • Access State: Open Access