Title of article :
Comparison of holding strength of suture anchors for hepatic and renal parenchyma: Ames CD, Perrone JM, Frisella AJ, Morrissey K, Landman J, Division of Urology, Washington University School of Medicine, St. Louis, MO
Author/Authors :
Anderson، نويسنده , , Kyle، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Abstract :
Background and Purpose
s laparoscopic devices have been described for suture anchoring during solid organ parenchymal closure. Application of these devices expedites the closure of parenchymal defects and minimizes ischemia time. We compared different technologies as suture anchors for parenchymal closure.
als and Methods
ometer was used to determine the amount of tension necessary to dislodge each of five different clips from Vicryl suture alone or against two different substrates (fresh pig kidney and liver) with and without an intervening pledget. The clips investigated were the Lapra-Ty (Ethicon), Endoclip II (US Surgical), small Horizon Ligating Clips (Weck), Hem-o-lok Medium Polymer Clips (Weck), and a novel Suture-clip (Applied Medical). ANOVA and two-sided Fisher’s exact test provided statistical analysis.
s
rce required to dislodge the Lapra-Ty clip from bare suture for both 0 and 1 Vicryl (7.0 N) was approximately fourfold the force required to dislodge the Endoclips or the 5-mm or 10-mm Hem-o-lok clips (p<0.01). When clips were applied to suture running through renal or liver parenchyma, the novel Suture-clip required the greatest tension to dislodge (P<0.01), followed by the Horizon and Lapra-Ty clips. There were no statistically significant differences in the tension required to dislodge a given clip from the two parenchymal substrates or in the presence or absence of a pledget.
sions
experimental model, the Suture-clip, Lapra-Ty, and Horizon clips required significantly greater tension to dislodge than the Hem-o-lok and Endoclip clips. The addition of a pledget did not improve tension resistance.
Journal title :
Urologic Oncology
Journal title :
Urologic Oncology