News | Thrombectomy Devices | December 23, 2025

New Study Shows CAVT Can Shorten Hospital Stays, May Ease Burden on Hospitals 

In a national analysis, patients treated with CAVT had shorter hospital stays, fewer complications and were more likely to go home compared with anticoagulation, catheter-directed thrombolysis and other mechanical thrombectomy approaches.

New Study Shows CAVT Can Shorten Hospital Stays, May Ease Burden on Hospitals 

Image: Penumbra


Dec. 16, 2025 — A new study, published in the American Journal of Cardiology, found that the use of Computer Assisted Vacuum Thrombectomy (CAVT) for intermediate-risk pulmonary embolism (PE) may shorten length of hospital stay, reduce complications and improve discharge outcomes without increasing mortality compared to other treatment modalities. The research suggests that CAVT, a technology designed to rapidly remove blood clots via microprocessor-controlled aspiration, has the potential to help reduce healthcare costs. 

“This study suggests that patients with intermediate-risk PE treated with CAVT may have lower healthcare utilization as they experienced significantly shorter LOS [length of stay] and PPLOS [post-procedure length of stay], and fewer complications without increasing mortality compared to AC [anticoagulation], CDL [catheter directed thrombolytics] and other MT [mechanical thrombectomy],” write the authors, led by Parag J. Patel, MD, MS, FSIR, of the Medical College of Wisconsin and Froedtert Hospital in Milwaukee. Additionally, “CAVT is associated with higher rates of discharge to home and lower rates of patients needing home health support or SNFs [skilled nursing facilities] postdischarge compared to the other treatment modalities.”1 

The researchers compared outcomes and healthcare resource utilization among patients treated with anticoagulation, catheter-directed thrombolysis, other mechanical thrombectomy, or CAVT (Lightning 12 or Lightning Flash 1.0). Adult inpatients with intermediate-risk PE discharged over a three-year period were retrospectively identified from the Vizient Clinical Data Base. ICD-10 codes identified treatment modalities. Propensity score matching equated groups 1:1 using demographics, payer, and hospital type.1 

Key findings: 

The mean length of stay for CAVT was 4.6 days, compared to: 

  • 6.2 days for anticoagulation 
  • 7 days for other forms of mechanical thrombectomy 
  • 7.1 days for catheter directed thrombolysis1 

Post-procedure length of stay for CAVT was 3.8 days, compared to: 

  • 6.1 days for catheter directed thrombolysis 
  • 6.2 days for other forms of mechanical thrombectomy1 

Composite complications for CAVT were 1.2%, compared to: 

  • 1.4 % for anticoagulation 
  • 2.7% for catheter directed thrombolysis 
  • 4.1% for other forms of mechanical thrombectomy1 

Development of acute kidney injury occurred in 1.9% of CAVT patients, compared to: 

  • 2.7% for anticoagulation 
  • 4.5% for catheter directed thrombolysis 
  • 4.9% for other forms of mechanical thrombectomy1 

PE affects about 370,000 Americans a year, taking the lives of up to 100,000. For survivors, it can take well over a year to recover from an acute PE, and long-term treatment and follow-up are commonplace.2,3 

Other recent research, including the landmark STORM-PE randomized controlled trial, has found CAVT demonstrates significant improvements to right ventricular function compared to anticoagulation alone, with low complication rates, and significant improvements in functional outcomes in intermediate-high risk PE patients.1,4 

“CAVT will continue to redefine the way physicians treat symptomatic PE. We have a growing body of evidence that demonstrates the meaningful benefits of CAVT on patient outcomes,” said James F. Benenati, M.D., FSIR, chief medical officer at Penumbra. “Now with this study, the findings suggest that by increasing patient access to advanced therapies like CAVT, it can also have an important, positive impact on hospital systems by greatly reducing resource utilization versus other modalities, therefore decreasing the overall cost to the healthcare system.” 

Additional information about Penumbra’s products can be found at www.penumbrainc.com/products/peripheral-thrombectomy-cavt/.

 

  1. Patel PJ, Dohad SY, Moriarty JM, Rosovsky R, Channick R, Weinberg I. Healthcare resource utilization and outcomes in intermediate-risk pulmonary embolism in the United States. Am J Cardiol. 2025;257:183-190. doi:10.1016/j.amjcard.2025.06.004. 
  2. Freund Y, Cohen-Aubart F, Bloom B. Acute Pulmonary Embolism: A Review. JAMA 2022;328(13):1336–45. 
  3. Virani SS, Alonso A, Benjamin EJ, et al; American Heart Association Council on Epidemiology and Prevention Statistics Committee and Stroke Statistics Subcommittee. Heart Disease and Stroke Statistics—2020 Update: A Report from the American Heart Association. Circulation. 2020;141(9):e139-e596. doi:10.1161/CIR.0000000000000757 
  4. Lookstein RA, Konstantinides SV, Weinberg I, Dohad SY, Rosol Z, Kopeć G, Moriarty JM; for the STORM-PE Trial Investigators. Randomized controlled trial of mechanical thrombectomy with anticoagulation versus anticoagulation alone for acute intermediate-high risk pulmonary embolism: primary outcomes from the STORM-PE trial. Circulation. Published online November 2025. doi:10.1161/CIRCULATIONAHA.125.077232. 

 


Related Content

News | Thrombectomy Devices

Nov. 3, 2025 — Penumbra, Inc. has announced additional results of the STORM-PE randomized controlled trial (RCT), which ...

Home November 07, 2025
Home
News | Thrombectomy Devices

Oct. 27, 2025 – Penumbra, Inc. has announced the results of the STORM-PE randomized controlled trial (RCT), which found ...

Home October 27, 2025
Home
News | Thrombectomy Devices

Sept. 2, 2025 — Imperative Care, Inc. has announced U.S. Food and Drug Administration (FDA) 510(k) clearance of its ...

Home September 02, 2025
Home
News | Thrombectomy Devices

June 16, 2025 – Penumbra, Inc. recently announced the completion of enrollment in the STORM-PE clinical trial. This ...

Home June 16, 2025
Home
News | Thrombectomy Devices

March 24, 2025 — Imperative Care, Inc. recently announced U.S. Food and Drug Administration (FDA) 510(k) clearance of ...

Home March 24, 2025
Home
News | Thrombectomy Devices

Penumbra recently launched its Element Vascular Access System, a laser-cut hypotube sheath designed for venous ...

Home January 30, 2025
Home
News | Thrombectomy Devices

Nov. 5, 2024 —Penumbra, Inc. recently announced new data that demonstrate patients with intermediate-risk pulmonary ...

Home November 07, 2024
Home
News | Thrombectomy Devices

Sept. 24, 2024 — Thrombolytic Science, LLC (TSI) has announced that the U.S. Food and Drug Administration (FDA) has ...

Home September 24, 2024
Home
News | Thrombectomy Devices

Sept. 5, 2024 - Prolocor, Inc. and Slingshot Biosciences recently announced the publication in Bioanalysis of the ...

Home September 10, 2024
Home
News | Thrombectomy Devices

January 16, 2024 — Penumbra, Inc., a thrombectomy company, has recently secured CE Mark (Conformité Européenne) for its ...

Home January 16, 2024
Home
Subscribe Now