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Optimized haemostasis in nephron-sparing surgery using small-intestine submucosa
BACKGROUND: The indications for nephron-sparing surgery are expanding constantly. One major contributing fact for this development is the improvement of haemostatic techniques following excision of the tumor. Nevertheless, postoperative bleeding complications still occur. To prevent this, we prospec...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386496/ https://www.ncbi.nlm.nih.gov/pubmed/18445250 http://dx.doi.org/10.1186/1471-2490-8-8 |
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author | Simon, Jörg de Petriconi, Robert Meilinger, Michael Hautmann, Richard E Bartsch, Georg |
author_facet | Simon, Jörg de Petriconi, Robert Meilinger, Michael Hautmann, Richard E Bartsch, Georg |
author_sort | Simon, Jörg |
collection | PubMed |
description | BACKGROUND: The indications for nephron-sparing surgery are expanding constantly. One major contributing fact for this development is the improvement of haemostatic techniques following excision of the tumor. Nevertheless, postoperative bleeding complications still occur. To prevent this, we prospectively studied the effect of application of small-intestine submucosa (SIS) over the renal defect. METHODS: We performed 55 nephron-sparing surgeries applying SIS between 08/03 and 10/06 in 53 pts. (mean age: 59 yrs., range 29 – 79 yrs.). After resection of the renal tumor and application of a haemostyptic agent, we used SIS to secure and apply compression on the defect. RESULTS: The final pathology revealed clear-cell and papillary carcinoma, papillary adenoma, oncocytoma, and angiomyolipoma in 39 (70.9%), 6 (10.9), 1 (1.8%), 2 (3.6%) and 7 (12.7%) patients, respectively. The 45 malignant lesions (81.8%) were classified as pT1a and pT1b in 35 (77.8%) and 10 (22.2%) patients, respectively. The median tumor size was 4.5 cm (range: 1.3 – 13 cm). The median operating time was 186 min (range: 90 – 260 min). 18 (32.7%) procedures were performed without ischemia. 23 (41.8%) and 14 (25.5%) cases were operated in in-situ cold and warm ischemia, respectively. The median intraoperative blood loss was 730 cc (range: 100 – 2500 cc). No open operative revision was indicated due to postoperative bleeding complications. Furthermore, there was no necessity to substitute persistent blood loss from the drains postoperatively. No urinoma occurred. CONCLUSION: SIS is a highly effective and easy-to-use instrument for preventing postoperative bleeding and urinary fistula complications in nephron-sparing surgery. |
format | Text |
id | pubmed-2386496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-23864962008-05-16 Optimized haemostasis in nephron-sparing surgery using small-intestine submucosa Simon, Jörg de Petriconi, Robert Meilinger, Michael Hautmann, Richard E Bartsch, Georg BMC Urol Research Article BACKGROUND: The indications for nephron-sparing surgery are expanding constantly. One major contributing fact for this development is the improvement of haemostatic techniques following excision of the tumor. Nevertheless, postoperative bleeding complications still occur. To prevent this, we prospectively studied the effect of application of small-intestine submucosa (SIS) over the renal defect. METHODS: We performed 55 nephron-sparing surgeries applying SIS between 08/03 and 10/06 in 53 pts. (mean age: 59 yrs., range 29 – 79 yrs.). After resection of the renal tumor and application of a haemostyptic agent, we used SIS to secure and apply compression on the defect. RESULTS: The final pathology revealed clear-cell and papillary carcinoma, papillary adenoma, oncocytoma, and angiomyolipoma in 39 (70.9%), 6 (10.9), 1 (1.8%), 2 (3.6%) and 7 (12.7%) patients, respectively. The 45 malignant lesions (81.8%) were classified as pT1a and pT1b in 35 (77.8%) and 10 (22.2%) patients, respectively. The median tumor size was 4.5 cm (range: 1.3 – 13 cm). The median operating time was 186 min (range: 90 – 260 min). 18 (32.7%) procedures were performed without ischemia. 23 (41.8%) and 14 (25.5%) cases were operated in in-situ cold and warm ischemia, respectively. The median intraoperative blood loss was 730 cc (range: 100 – 2500 cc). No open operative revision was indicated due to postoperative bleeding complications. Furthermore, there was no necessity to substitute persistent blood loss from the drains postoperatively. No urinoma occurred. CONCLUSION: SIS is a highly effective and easy-to-use instrument for preventing postoperative bleeding and urinary fistula complications in nephron-sparing surgery. BioMed Central 2008-04-29 /pmc/articles/PMC2386496/ /pubmed/18445250 http://dx.doi.org/10.1186/1471-2490-8-8 Text en Copyright © 2008 Simon et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Simon, Jörg de Petriconi, Robert Meilinger, Michael Hautmann, Richard E Bartsch, Georg Optimized haemostasis in nephron-sparing surgery using small-intestine submucosa |
title | Optimized haemostasis in nephron-sparing surgery using small-intestine submucosa |
title_full | Optimized haemostasis in nephron-sparing surgery using small-intestine submucosa |
title_fullStr | Optimized haemostasis in nephron-sparing surgery using small-intestine submucosa |
title_full_unstemmed | Optimized haemostasis in nephron-sparing surgery using small-intestine submucosa |
title_short | Optimized haemostasis in nephron-sparing surgery using small-intestine submucosa |
title_sort | optimized haemostasis in nephron-sparing surgery using small-intestine submucosa |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386496/ https://www.ncbi.nlm.nih.gov/pubmed/18445250 http://dx.doi.org/10.1186/1471-2490-8-8 |
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