Hemodynamic comparison of microsurgical repairs for large arterial defects
โ Scribed by Robert D. Cipoletti; Moheb S. Moneim; E. R. Greene
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 473 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0738-1085
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
Twentyโeight femoral arteries in 14 rats were used to compare transverse closures and endโtoโend anastomoses in blood vessels approximately 1 mm in diameter. The transverse closures were applied to arteriectomies created by excising oneโhalf the circumference of the vessel over a length of 1 mm. The endโtoโend anastomoses were performed after resecting a 1โmm segment. Recordings were made of preโand postrepair flow velocity and threeโpoint diameter measurements every 5 minutes using a 20โMHz pulsed Doppler velocimeter and digimatic caliper. Maximum reductions in flow velocity were 18% and 31% for the transverse repair and endโtoโend anastomosis, respectively. Otherwise, intergroup comparisons of the postrepair normalization of both flow velocity and vessel diameter showed few significant differences (P < 0.05). We conclude that arterial defects involving no more than half the diameter of the vessel can be effectively repaired in significantly less time using the transverse closure. ยฉ 1994 WileyโLiss, Inc.
๐ SIMILAR VOLUMES
## Abstract In this report, the posterior tibial artery (PTA) based multilobar combined flap is introduced for the repair of complex soft tissue defects. The flap was designed based on the perforatoring branches of PTA in the anterior soleus muscle septum, which supply the skin over the medial side
## Abstract ## Background: Breast conservation surgery in the treatment of early stage breast cancer has become increasingly utilized as a means to avoiding mastectomy. While partial mastectomy defects (PMDs) may often be cosmetically acceptable, some cases warrant consideration of reconstructive
## Abstract Despite a wide range of available sources for bone repair, significant limitations persist. To bioengineer bone, we have previously transferred adenovirusโmediated human __BMPโ2__ gene into autologous bone marrow stromal cells (MSC). We have successfully repaired large, full thickness,