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Patent hemostasis and comparison of two compression devices after transradial coronary catheterization and intervention

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11140%2F18%3A10375702" target="_blank" >RIV/00216208:11140/18:10375702 - isvavai.cz</a>

  • Alternative codes found

    RIV/00669806:_____/18:10375702

  • Result on the web

    <a href="https://doi.org/10.1016/j.crvasa.2017.07.003" target="_blank" >https://doi.org/10.1016/j.crvasa.2017.07.003</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.crvasa.2017.07.003" target="_blank" >10.1016/j.crvasa.2017.07.003</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Patent hemostasis and comparison of two compression devices after transradial coronary catheterization and intervention

  • Original language description

    Aim: The aim of this study was to compare two compression devices after transradial coronary catheterization and intervention. Methods: Out of 280 consecutive patients who underwent cardiac catheterization and intervention (n = 74) as a part of a same-day discharge program, 140 patients were applied the TR Band (TB) compression device and 140 the Seal-One (SO) compression device. The time needed to achieve patent hemostasis, duration of compression and local complications were assessed. Results: In the TB group, patent hemostasis was achieved in 17.5 + 10.3 min (min), in the SO group in 21.4 + 10.5 min (p = NS). The duration of radial artery compression was 90.7 + 38.4 min in the TB group and 64.0 + 26.5 min in the SO group (p &lt; 0.001). The incidence of hematomas &gt;= 5 cm did not differ between the two groups (6.4% vs. 6.4%, p = NS), the incidence of hematomas larger than 10 cm was 0.7% in the TB group and 1.4% in the SO group (p = NS). No radial artery occlusion or other local complications were found. Conclusion: Postprocedural radial artery compression with TR Band and Seal-One devices is associated with early patent hemostasis and a short duration of compression. The use of the Seal-One device was related to a shorter mean compression time in this study. No radial artery occlusion at discharge, nor any other local complications occurred following the radial artery compression, except for several clinically insignificant hematomas.

  • 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

    30201 - Cardiac and Cardiovascular systems

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

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

    Cor et Vasa

  • ISSN

    0010-8650

  • e-ISSN

  • Volume of the periodical

    60

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    CZ - CZECH REPUBLIC

  • Number of pages

    5

  • Pages from-to

    "E122"-"E126"

  • UT code for WoS article

    000429583200003

  • EID of the result in the Scopus database

    2-s2.0-85028364231