Evaluation of a modified arrow-trerotola percutaneous thrombolytic device for treatment of acute pulmonary embolus in a canine model

Citation
Db. Brown et al., Evaluation of a modified arrow-trerotola percutaneous thrombolytic device for treatment of acute pulmonary embolus in a canine model, J VAS INT R, 10(6), 1999, pp. 733-740
Citations number
26
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging
Journal title
JOURNAL OF VASCULAR AND INTERVENTIONAL RADIOLOGY
ISSN journal
10510443 → ACNP
Volume
10
Issue
6
Year of publication
1999
Pages
733 - 740
Database
ISI
SICI code
1051-0443(199906)10:6<733:EOAMAP>2.0.ZU;2-D
Abstract
PURPOSE: Massive pulmonary embolus (PE) is often rapidly fatal. Surgical th rombectomy has a mortality rate as high as 74%. Multiple percutaneous metho ds have been tested with limited success. The purpose of this study was to evaluate the Arrow-Trerotola percutaneous thrombolytic device (PTD) for (i) the ability to clear pulmonary embolus and (ii) the effect on normal pulmo nary vasculature, These were tested in a canine model, MATERIALS AND METHODS: Iatrogenic unilateral massive PEs were created in ni ne canines, These PEs were then treated with the PTD, The device was also a ctivated in the normal pulmonary artery. Immediately after treatment, six a nimals were killed. Three animals were allowed to recover and underwent pul monary arteriography 1 month later to evaluate pulmonary hypertension, sten osis, or occlusion; they were then killed, Autopsy specimens were evaluated for histologic evidence of acute or chronic vascular injury. RESULTS: Acutely, the PTD effectively thrombolysed the PE in all animals. H istologically, there was moderate intimal injury, but no evidence of pulmon ary artery disruption. There was one device failure. One month after treatm ent, there was no radiographic evidence of pulmonary stenosis at device act ivation sites, no pulmonary hypertension, and only mild histologic evidence of scar formation, CONCLUSION: In preliminary animal testing, the PTD is safe and effective fo r treating large central pulmonary emboli, Human clinical trials are warran ted.