Original Article from the Society for Vascular Surgery
A balloon-expandable intravascular stent for obliterating experimental aortic dissection*

Presented at the Forty-third Annual Meeting of the Society for Vascular Surgery, New York, N.Y., June 20-21, 1989.
https://doi.org/10.1016/0741-5214(90)90218-YGet rights and content

Abstract

Acute aortic dissection is a life-threatening condition. Aggressive hypotensive drug therapy is the initial treatment of choice, although emergent surgical intervention is often warranted. We evaluated the efficacy of a balloon-expandable intravascular stent for the internal obliteration of aortic dissection. It is a flexible, continuous, complex coil cut to the length needed at the time of insertion. It can be positioned in curved vessels, including the aortic arch. The stent was inserted in the thoracic and abdominal aorta of 12 dogs (group I). Six weeks after implantation the dogs underwent angiography and the stents were explanted for light and scanning electron microscopy. There were no instances of stent migration or change in configuration. The aortas did not rupture. All branch vessels remained patent. Light and scanning electron microscopy illustrated neointimal incorporation into the vascular wall except at orifices. Thoracic dissections were created surgically in an additional 24 mongrel dogs. Twelve dogs received stents immediately after creation of the dissection (group II). All 12 dissections were obliterated. Twelve dogs were allowed to recover after creation of the dissection to observe the natural history of that lesion (group III). Within 1 week, in group III, there were three deaths because of aortic rupture; eight dissections persisted, and one resealed spontaneously. Stents were placed in the eight persistent dissections. All eight dissections were obliterated. In both groups, after 6 weeks of stent placement, aortography was repeated, and stents were explanted for light and scanning electron microscopy. There were no instances of rupture. All branch vessels remained patent with no evidence of thrombosis. We conclude that because of its unique characteristics, the stent effectively obliterates the false lumen of experimental acute aortic dissections without occluding side branches, damaging the aorta, or inducing thrombosis. (J VASC SURG 1990;11:707-17.)

Section snippets

Material and methods

The stent is a preformed sinusoidal-shaped, stainless-steel, type 316L-0.011 inch (0.279 mm), wire wound into an open-ended helix Medtronic-Wiktor Balloon-Expandable Stent (Medtronic, Minneapolis, Minn.) Once the required length of stent is determined the desired amount is cut from a longer piece and crimped manually onto the low profile balloon of the catheter (Meadox-Surgimed, Inc. [Olbert balloon catheter] Oakland, N.J.). When the stent is longer than the balloon, its trailing portion is

Biocompatibility

No technical problems were encountered with the implant technique in group I. After operation and during the 6-week observation period all animals remained clinically healthy. In all cases preexplant aortograms revealed no stent migration, aortic perforation, thrombosis, or branch occlusion. On gross inspection all aortic branch orifices were patent. The stent was incorporated into the vascular wall with each portion of the coil covered by intima, except at orifices (Fig. 4).

. Photomicrograph

Discussion

In 1969 Dotter15 first introduced the technique for the nonoperative placement of a tubular, coiled nitinol wire stent. Since then several self and balloon expandable stents have been introduced, all with the intent of maintaining luminal patency, usually in conjunction with balloon angioplasty.16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29 Previous stents have been limited in length, diameter and their ability to accommodate curves. In an attempt to stent long or curved vascular

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    *

    Reprint requests: Victor Parsonnet, MD, Department of Surgery, Newark Beth Israel Medical Center, 201 Lyons Ave., Newark, NJ 07112.

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