Advancement in liver laparoscopic resection - development of a new surgical device
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61988987%3A17110%2F18%3AA1901Z4G" target="_blank" >RIV/61988987:17110/18:A1901Z4G - isvavai.cz</a>
Alternative codes found
RIV/61989100:27230/18:10241345 RIV/00843989:_____/18:E0106997
Result on the web
<a href="http://dx.doi.org/10.1590/1414-431X20176062" target="_blank" >http://dx.doi.org/10.1590/1414-431X20176062</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1590/1414-431X20176062" target="_blank" >10.1590/1414-431X20176062</a>
Alternative languages
Result language
angličtina
Original language name
Advancement in liver laparoscopic resection - development of a new surgical device
Original language description
Liver resection is the standard treatment for any liver lesion. Laparoscopic liver resection is associated with lower intra-operative blood loss and fewer complications than open resection. Access to the posterior part of the right liver lobe is very uncomfortable and difficult for surgeons due the anatomic position, especially when employing laparoscopic surgery. Based on these experiences, a new laparoscopic device was developed that is capable of bending its long axis and allowing the application of radiofrequency energy in areas that were not technically accessible. The device is equipped with four telescopic needle electrodes that cause tissue coagulation after the delivery of radiofrequency energy. Ex vivo testing was performed in 2012 and 2014 at the University Hospital, Ostrava, on a porcine liver tissue. The main goal of this testing was to verify if the newly proposed electrode layout was suitable for sufficient tissue coagulation and creating a safety zone around lesions. During the ex vivo testing, the material of needle electrodes was improved to achieve the lowest possibility of adhesion. The power supply was adjusted from 20 to 120 W and the ablation time, which varied from 10 to 110 s, was monitored. Subsequently, optimal power delivery and time for coagulation was determined. This experimental study demonstrated the feasibility and safety of the newly developed device. Based on the ex vivo testing, LARA-K1 can create a safety zone of coagulation. For further assessment of the new device, an in vivo study should be performed.
Czech name
—
Czech description
—
Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
—
OECD FORD branch
30212 - Surgery
Result continuities
Project
—
Continuities
S - Specificky vyzkum na vysokych skolach
Others
Publication year
2018
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH
ISSN
0100-879X
e-ISSN
1678-4510
Volume of the periodical
4
Issue of the periodical within the volume
51
Country of publishing house
BR - BRAZIL
Number of pages
4
Pages from-to
1-4
UT code for WoS article
000426392900001
EID of the result in the Scopus database
2-s2.0-85043273535