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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