Postoperative staple-line bleeding after stapled hemorrhoidopexy represents a major issue of this procedure, especially in the day surgery setting. In this study we assess the possible benefit of using circular bioabsorbable staple-line reinforcement to reduce the risk of hemorrhage when performing stapled hemorrhoidopexy in a day surgery setting. Patients with symptomatic II to III grade hemorrhoidal disease were randomly assigned into two groups. In Group A we performed a stapled hemorrhoidopexy using PPH33-03® with Seamguard®, a bioabsorbable staple-line reinforcement; in Group B, we used only a PPH33-03® stapler. We evaluated the intraoperative and postoperative staple-line bleeding and, secondarily, the duration of surgery, need for additional hemostatic stitches, and presence of postoperative complications. One hundred patients were enrolled in the study. Group A patients showed a statistically significant decrease of intraoperative bleeding (4 vs 42% in Group B) and hemostatic stitch placement (5.7 vs 42%) with the consequent reduction in mean operative time, postoperative pain, and tenesmus. There were no differences between the two groups in hemorrhoidal disease control or postoperative late complications. The use of bioabsorbable staple-line reinforcement while performing stapled hemorrhoidopexy may allow improvement of the safety of this procedure, especially in a day surgery setting. Copyright Southeastern Surgical Congress. All rights reserved.

The use of bioabsorbable staple-line reinforcement performing stapled hemorrhoidopexy to decrease the risk of postoperative bleeding / Mari, Francesco Saverio; Masoni, Luigi; Cosenza, U. M.; Favi, Francesco; Berardi, G.; Dall'Oglio, A.; Pindozzi, Fioralba; Brescia, Antonio. - In: THE AMERICAN SURGEON. - ISSN 0003-1348. - STAMPA. - 78:11(2012), pp. 1255-1260.

The use of bioabsorbable staple-line reinforcement performing stapled hemorrhoidopexy to decrease the risk of postoperative bleeding

MARI, Francesco Saverio;MASONI, Luigi;FAVI, FRANCESCO;G. Berardi;PINDOZZI, FIORALBA;BRESCIA, Antonio
2012

Abstract

Postoperative staple-line bleeding after stapled hemorrhoidopexy represents a major issue of this procedure, especially in the day surgery setting. In this study we assess the possible benefit of using circular bioabsorbable staple-line reinforcement to reduce the risk of hemorrhage when performing stapled hemorrhoidopexy in a day surgery setting. Patients with symptomatic II to III grade hemorrhoidal disease were randomly assigned into two groups. In Group A we performed a stapled hemorrhoidopexy using PPH33-03® with Seamguard®, a bioabsorbable staple-line reinforcement; in Group B, we used only a PPH33-03® stapler. We evaluated the intraoperative and postoperative staple-line bleeding and, secondarily, the duration of surgery, need for additional hemostatic stitches, and presence of postoperative complications. One hundred patients were enrolled in the study. Group A patients showed a statistically significant decrease of intraoperative bleeding (4 vs 42% in Group B) and hemostatic stitch placement (5.7 vs 42%) with the consequent reduction in mean operative time, postoperative pain, and tenesmus. There were no differences between the two groups in hemorrhoidal disease control or postoperative late complications. The use of bioabsorbable staple-line reinforcement while performing stapled hemorrhoidopexy may allow improvement of the safety of this procedure, especially in a day surgery setting. Copyright Southeastern Surgical Congress. All rights reserved.
2012
01 Pubblicazione su rivista::01a Articolo in rivista
The use of bioabsorbable staple-line reinforcement performing stapled hemorrhoidopexy to decrease the risk of postoperative bleeding / Mari, Francesco Saverio; Masoni, Luigi; Cosenza, U. M.; Favi, Francesco; Berardi, G.; Dall'Oglio, A.; Pindozzi, Fioralba; Brescia, Antonio. - In: THE AMERICAN SURGEON. - ISSN 0003-1348. - STAMPA. - 78:11(2012), pp. 1255-1260.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/494824
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