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Optimization of ALPPS stage II timing with the APRI/ALBI score- an international, multicenter cohort study

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023001%3A_____%2F25%3A00085844" target="_blank" >RIV/00023001:_____/25:00085844 - isvavai.cz</a>

  • Result on the web

    <a href="https://hbsn.amegroups.org/article/view/136277/pdf" target="_blank" >https://hbsn.amegroups.org/article/view/136277/pdf</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.21037/hbsn-24-617" target="_blank" >10.21037/hbsn-24-617</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Optimization of ALPPS stage II timing with the APRI/ALBI score- an international, multicenter cohort study

  • Original language description

    Background: Primarily unresectable liver tumors may be approached by the Associating Liver Partition and Portal vein Ligation for Staged Hepatectomy (ALPPS) procedure. Post-hepatectomy liver failure (PHLF) poses the most significant risk factor for poor outcomes. The AST-to-platelets ratio index (APRI)/albuminto-bilirubin index (ALBI) score has been proposed as an easy and routinely available score to monitor liver function. Here, we explored the predictive capability of the APRI/ALBI score to determine PHLF and perioperative morbidity to help determine the optimal timing of the 2nd stage of ALPPS. Methods: Based on the international multicenter ALPPS registry, patients from 2012 to 2020 with an available APRI/ALBI score were included. Postoperative outcomes (clinically relevant PHLF B + C, 90-day mortality, and severe morbidity (&gt;= Clavien-Dindo 3b) after ALPPS stage II were assessed. The APRI/ALBI score was monitored perioperatively, and the predictive value was evaluated using logistic regression and receiver operating characteristics. Performance of APRI/ALBI score was compared to the ALPPS futility risk score in this cohort study. Results: Overall, 464 patients from 16 participating centers were included. Clinically relevant PHLF (B + C) was observed in 7.5% of patients, of which 63% ultimately died. After stage I, the APRI/ALBI score gradually recovered. The pre-stage II APRI/ALBI score significantly predicted clinically relevant PHLF [area under the curve (AUC) =0.78; P&lt;0.001], 90-day mortality (AUC =0.67; P=0.002), and severe morbidity (AUC =0.65; P&lt;0.001). Three clinically relevant APRI/ALBI score risk groups were defined: clinically relevant PHLF occurred in 3.1% in the low-, 8.7% in the intermediate-, and 28.0% in the high-risk groups. 90-day mortality was 6.8% in the low-, 15.9% in the intermediate-, and 19.4% in the high-risk groups. Integrated assessment of the established futility risk score in combination with the APRI/ALBI score documented further increased predictive potential for clinically relevant PHLF (AUC 0.81; P&lt;0.001). Conclusions: The APRI/ALBI score allows for simple and dynamic liver function recovery monitoring after the first ALPPS stage. Inadequate recovery of the APRI/ALBI score until ALPPS stage II was associated with PHLF B + C, 90-day mortality, and severe morbidity. With the proposed risk model, optimized timing of the second stage of ALPPS may further increase the safety of this procedure.

  • 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

    30219 - Gastroenterology and hepatology

Result continuities

  • Project

  • Continuities

    N - Vyzkumna aktivita podporovana z neverejnych zdroju

Others

  • Publication year

    2025

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Hepatobiliary surgery and nutrition

  • ISSN

    2304-3881

  • e-ISSN

    2304-389X

  • Volume of the periodical

    14

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    HK - HONG KONG

  • Number of pages

    13

  • Pages from-to

    742-754

  • UT code for WoS article

    001456600900001

  • EID of the result in the Scopus database