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Ultrasound-Facilitated, Catheter-Directed Thrombolysis for Acute Pulmonary Embolism. | LitMetric

AI Article Synopsis

  • Acute pulmonary embolism (APE) is a serious health issue, and a study compared the safety and effectiveness of ultrasound-facilitated catheter-directed thrombolysis (USCDT) to conventional catheter-directed thrombolysis (CDT) in treating patients with intermediate to high-risk APE.
  • In a retrospective analysis involving 135 patients, both treatments reduced the right ventricle to left ventricle (RV/LV) diameter ratio and pulmonary artery pressure without significant differences in efficacy between the two methods.
  • USCDT resulted in a lower occurrence of major bleeding events (0%) compared to CDT (3.4%), indicating that USCDT may provide a safer option for these patients.

Article Abstract

Background: Acute pulmonary embolism (APE) poses a significant risk to patient health, with treatment options varying in efficacy and safety. Ultrasound-facilitated catheter-directed thrombolysis (USCDT) has emerged as a potential alternative to conventional catheter-directed thrombolysis (CDT) for patients with intermediate to high-risk APE. This study aimed to compare the efficacy and safety of USCDT versus conventional CDT in patients with intermediate to high-risk APE.

Methods: This observational retrospective study was conducted at the Armed Forces Hospital, Al-Hada, Taif, the Kingdom of Saudi Arabia (KSA), on 135 patients diagnosed with APE and treated with either USCDT or CDT (58 underwent CDT, while 77 underwent USCDT). The primary efficacy outcome was the change in the right ventricle to the left ventricle (RV/LV) diameter ratio. Secondary outcomes included changes in pulmonary artery systolic pressure and the Miller angiographic obstruction index score. Safety outcomes focused on major bleeding events.

Results: Both USCDT and CDT significantly reduced RV/LV diameter ratio (from 1.35 ± 0.14 to 1.05 ± 0.17, P < 0.001) and systolic pulmonary artery pressure (SPAP) (from 55 ± 7 mmHg to 38 ± 7 mmHg, P < 0.001) at 48- and 12-hours post-procedure, respectively, with no significant differences between treatments. However, USCDT was associated with a significantly lower rate of major bleeding events compared to CDT (0% vs. 3.4%, P = 0.008). Multivariate logistic regression analysis revealed that USCDT was associated with a 71.9% risk reduction of bleeding (OR = 0.281, 95% CI = 0.126 - 0.627, P = 0.002).

Conclusions: USCDT is a safe and effective alternative to CDT for the treatment of intermediate to high-risk APE, as it significantly reduces the risk of major bleeding.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11060753PMC
http://dx.doi.org/10.7759/cureus.57345DOI Listing

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