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Laparoscopic radical cystectomy with intracorporeal ileal conduit: one center experience and clinical outcomes
PURPOSE: To introduce our experience with intracorporeal ileal conduit and evaluate the safety and feasibility of this endoscopic urinary diversion. MATERIALS AND METHODS: Between March 2014 and July 2017, thirty-six consecutive patients underwent laparoscopic radical cystectomy with intracorporeal...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Urologia
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6786108/ https://www.ncbi.nlm.nih.gov/pubmed/30901178 http://dx.doi.org/10.1590/S1677-5538.IBJU.2018.0262 |
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author | Li, Jianye Yang, Feiya He, Qingbao Wang, Mingshuai Xing, Nianzeng |
author_facet | Li, Jianye Yang, Feiya He, Qingbao Wang, Mingshuai Xing, Nianzeng |
author_sort | Li, Jianye |
collection | PubMed |
description | PURPOSE: To introduce our experience with intracorporeal ileal conduit and evaluate the safety and feasibility of this endoscopic urinary diversion. MATERIALS AND METHODS: Between March 2014 and July 2017, thirty-six consecutive patients underwent laparoscopic radical cystectomy with intracorporeal ileal conduit. Patients’ demographic data, perioperative data, 90-days postoperative outcomes and complications were collected. This cohort were divided into two groups of 18 patients each by chronological order of the operations to facilitate comparison of clinical data. Data were evaluated using the students’ T test, Mann-Whitney test and Fisher's Exact test. RESULTS: All surgeries were completed successfully with no conversion. Median total operating time and median intracorporeal urinary diversion time were 304 and 105 minutes, respectively. Median estimated blood loss was 200 mL, and median lymph node yield was 21. Twenty-six Clavien grade < 3 complications occurred within 30-days and 9 occurred within 30-90 days. Five Clavien grade 3-5 complications occurred within 30 days. No statistically significant differences were found between the two groups except for intracorporeal urinary diversion time. At median follow-up of 17.5 (range 3-42) months, 6 patients experienced tumor recurrence/metastasis and 4 of these patients died. CONCLUSIONS: Intracorporeal ileal conduit following laparoscopic radical cystectomy is safe, feasible and reproducible. With the accumulation of experience, the operation time can be controlled at a satisfactory level. |
format | Online Article Text |
id | pubmed-6786108 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Sociedade Brasileira de Urologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-67861082019-10-23 Laparoscopic radical cystectomy with intracorporeal ileal conduit: one center experience and clinical outcomes Li, Jianye Yang, Feiya He, Qingbao Wang, Mingshuai Xing, Nianzeng Int Braz J Urol Original Article PURPOSE: To introduce our experience with intracorporeal ileal conduit and evaluate the safety and feasibility of this endoscopic urinary diversion. MATERIALS AND METHODS: Between March 2014 and July 2017, thirty-six consecutive patients underwent laparoscopic radical cystectomy with intracorporeal ileal conduit. Patients’ demographic data, perioperative data, 90-days postoperative outcomes and complications were collected. This cohort were divided into two groups of 18 patients each by chronological order of the operations to facilitate comparison of clinical data. Data were evaluated using the students’ T test, Mann-Whitney test and Fisher's Exact test. RESULTS: All surgeries were completed successfully with no conversion. Median total operating time and median intracorporeal urinary diversion time were 304 and 105 minutes, respectively. Median estimated blood loss was 200 mL, and median lymph node yield was 21. Twenty-six Clavien grade < 3 complications occurred within 30-days and 9 occurred within 30-90 days. Five Clavien grade 3-5 complications occurred within 30 days. No statistically significant differences were found between the two groups except for intracorporeal urinary diversion time. At median follow-up of 17.5 (range 3-42) months, 6 patients experienced tumor recurrence/metastasis and 4 of these patients died. CONCLUSIONS: Intracorporeal ileal conduit following laparoscopic radical cystectomy is safe, feasible and reproducible. With the accumulation of experience, the operation time can be controlled at a satisfactory level. Sociedade Brasileira de Urologia 2019-07-27 /pmc/articles/PMC6786108/ /pubmed/30901178 http://dx.doi.org/10.1590/S1677-5538.IBJU.2018.0262 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Li, Jianye Yang, Feiya He, Qingbao Wang, Mingshuai Xing, Nianzeng Laparoscopic radical cystectomy with intracorporeal ileal conduit: one center experience and clinical outcomes |
title | Laparoscopic radical cystectomy with intracorporeal ileal conduit: one center experience and clinical outcomes |
title_full | Laparoscopic radical cystectomy with intracorporeal ileal conduit: one center experience and clinical outcomes |
title_fullStr | Laparoscopic radical cystectomy with intracorporeal ileal conduit: one center experience and clinical outcomes |
title_full_unstemmed | Laparoscopic radical cystectomy with intracorporeal ileal conduit: one center experience and clinical outcomes |
title_short | Laparoscopic radical cystectomy with intracorporeal ileal conduit: one center experience and clinical outcomes |
title_sort | laparoscopic radical cystectomy with intracorporeal ileal conduit: one center experience and clinical outcomes |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6786108/ https://www.ncbi.nlm.nih.gov/pubmed/30901178 http://dx.doi.org/10.1590/S1677-5538.IBJU.2018.0262 |
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