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1.
Langenbecks Arch Surg ; 399(6): 725-33, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24880345

ABSTRACT

BACKGROUND: Despite improvements in liver surgery over the past decades, hemostasis during hepatic resections remains challenging. This multicenter randomized study compares the hemostatic effect of a collagen hemostat vs. a carrier-bound fibrin sealant after hepatic resection. METHODS: Patients scheduled for elective liver resection were randomized intraoperatively to receive either the collagen hemostat (COLL) or the carrier-bound fibrin sealant (CBFS) for secondary hemostasis. The primary endpoint was the proportion of patients with hemostasis after 3 min. Secondary parameters were the proportions of patients with hemostasis after 5 and 10 min, the total time to hemostasis, and the complication rates during a 3 months follow-up period. RESULTS: A total of 128 patients were included. In the COLL group, 53 out of 61 patients (86.9 %) achieved complete hemostasis within 3 min after application of the hemostat compared to 52 out of 65 patients (80.0 %) in the CBFS group. The 95 % confidence interval for this difference [-6.0 %, 19.8 %] does not include the lower noninferiority margin (-10 %). Thus, the COLL treatment can be regarded as noninferior to the comparator. The proportions of patients with hemostasis after 3, 5, and 10 min were not significantly different between the two study arms. Postoperative mortality and morbidity were similar in both treatment groups. CONCLUSION: The collagen hemostat is as effective as the carrier-bound fibrin sealant in obtaining secondary hemostasis during liver resection with a comparable complication rate.


Subject(s)
Blood Loss, Surgical/prevention & control , Collagen/administration & dosage , Hemostasis, Surgical , Hemostatics/administration & dosage , Hepatectomy/adverse effects , Liver Diseases/surgery , Aged , Female , Humans , Liver Diseases/pathology , Male , Middle Aged , Treatment Outcome
2.
Chirurg ; 84(7): 551-8, 2013 Jul.
Article in German | MEDLINE | ID: mdl-23719728

ABSTRACT

Diagnostic lymph node dissections can be defined as a form of oncological service surgery. These procedures aim at clarification of differential diagnoses of local or systemic lymph node pathologies or contribute to tumor staging. Procedure implementation can either involve incisional biopsy, selective lymph node extirpation or regional systematic lymph node dissection. Sentinel lymph node lymphadenectomy is a focused form of selective lymphadenectomy. Both surgeon and oncologist must have a preoperative consensus and mutual understanding about the detailed purpose of the procedure in the individual patient setting. Terminology conventions must be considered in communication. Potential reasons to extend surgery should be strategically reflected prior to surgery. Interventional techniques and minimally invasive forms of surgical lymph node dissection must be technically taken into account in order to reduce procedural morbidity. Clinically indicative scenarios, pathophysiological concepts and technical options of surgical lymph node dissection are described and discussed for various anatomical regions.


Subject(s)
Lymph Node Excision/methods , Neoplasms/surgery , Abdomen/surgery , Cooperative Behavior , Humans , Inguinal Canal/surgery , Interdisciplinary Communication , Lymph Nodes/pathology , Minimally Invasive Surgical Procedures/methods , Neck/surgery , Neoplasms/pathology , Postoperative Complications/prevention & control , Sentinel Lymph Node Biopsy
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