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Three-dimensional personalized porous polyethylen cranioplasty in patients at increased risk of surgical site infection

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00669806%3A_____%2F24%3A10485378" target="_blank" >RIV/00669806:_____/24:10485378 - isvavai.cz</a>

  • Alternative codes found

    RIV/61988987:17110/24:A2503AKC RIV/00216208:11140/24:10485378 RIV/00843989:_____/24:E0111537

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=GRi_GBH5HE" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=GRi_GBH5HE</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00701-024-06281-x" target="_blank" >10.1007/s00701-024-06281-x</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Three-dimensional personalized porous polyethylen cranioplasty in patients at increased risk of surgical site infection

  • Original language description

    BackgroundSurgical site infection (SSI) is the most consistently reported complication of cranioplasty. No material showed a categorical superiority in the incidence of infection. Porous polyethylene (PE) is considered a low risk material regarding SSI. However, the literature data are very limited. Thus, our objective was to verify the assumed low incidence of SSI after PE cranioplasty in patients at high risk of SSI. The primary objective was the infection rate, while secondary objectives were implant exposure, revision and cosmetic results.MethodPatients who underwent three-dimensional (3D) personalized PE cranioplasty in the period 2014-2023 were evaluated prospectively. Only patients with an increased risk of SSI, and a satisfactory clinical conditions were included in the study.ResultsThirty procedures were performed in 30 patients. Cranioplasty was performed 23 times after hemispheric decompressive craniectomy, five times after limited size craniotomy and two times after bifrontal decompressive craniectomy. Risk factors for the development of infection were 18 previous SSIs, 16 previous repeated revision surgeries, four intraoperatively opened frontal sinuses and two times radiotherapy. Neither infection nor implant exposure was detected in any patient. All patients were satisfied with the aesthetic result. In two cases, a revision was performed due to postoperative epidural hematoma.ConclusionsThree-dimensional personalized PE cranioplasty is associated with an extremely low incidence of SSI even in high-risk patients. However, our conclusions can only be confirmed in larger studies.

  • 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

    30103 - Neurosciences (including psychophysiology)

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2024

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Acta Neurochirurgica

  • ISSN

    0001-6268

  • e-ISSN

    0942-0940

  • Volume of the periodical

    166

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    AT - AUSTRIA

  • Number of pages

    8

  • Pages from-to

    383

  • UT code for WoS article

    001321759300001

  • EID of the result in the Scopus database

    2-s2.0-85205073387