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Refining prediction of survival after TIPS with the novel Freiburg index of post-TIPS survival

Dominik Bettinger*, Lukas Sturm, Lena Pfaff, Felix Hahn, Roman Kloeckner, Lara Volkwein, Michael Praktiknjo, Yong Lv, Guohong Han, Jan Patrick Huber, Tobias Boettler, Marlene Reincke, Christoph Klinger, Karel Caca, Hauke Heinzow, Leon Louis Seifert, Karl Heinz Weiss, Christian Rupp, Felix Piecha, Johannes KluweAlexander Zipprich, Hendrik Luxenburger, Christoph Neumann-Haefelin, Arthur Schmidt, Christian Jansen, Carsten Meyer, Frank E. Uschner, Maximilian J. Brol, Jonel Trebicka, Martin Rössle, Robert Thimme, Michael Schultheiss

*Korrespondierende/r Autor/-in für diese Arbeit

Abstract

Background & Aims: Transjugular intrahepatic portosystemic shunt (TIPS) implantation is an effective and safe treatment for complications of portal hypertension. Survival prediction is important in these patients as they constitute a high-risk population. Therefore, the aim of our study was to develop an alternative prognostic model for accurate survival prediction after planned TIPS implantation. Methods: A total of 1,871 patients with de novo TIPS implantation for ascites or secondary prophylaxis of variceal bleeding were recruited retrospectively. The study cohort was divided into a training set (80% of study patients; n = 1,496) and a validation set (20% of study patients; n = 375). Further, patients with early (preemptive) TIPS implantation due to variceal bleeding were included as another validation cohort (n = 290). Medical data and overall survival (OS) were assessed. A Cox regression model was used to create an alternative prediction model, which includes significant prognostic factors. Results: Age, bilirubin, albumin and creatinine were the most important prognostic factors. These parameters were included in a new score named the Freiburg index of post-TIPS survival (FIPS). The FIPS score was able to identify high-risk patients with a significantly reduced median survival of 5.0 (3.1–6.9) months after TIPS implantation in the training set. These results were confirmed in the validation set (median survival of 3.1 [0.9–5.3] months). The FIPS score showed better prognostic discrimination compared to the Child-Pugh, MELD, MELD-Na score and the bilirubin-platelet model. However, the FIPS score showed insufficient prognostic discrimination in patients with early TIPS implantation. Conclusions: The FIPS score is superior to established scoring systems for the identification of high-risk patients with a worse prognosis following elective TIPS implantation. Lay summary: Implantation of a transjugular intrahepatic portosystemic shunt (TIPS) is a safe and effective treatment for patients with cirrhosis and clinically significant portal hypertension. However, risk stratification is a major challenge in these patients as currently available scoring systems have major drawbacks. Age, bilirubin, albumin and creatinine were included in a new risk score which was named the Freiburg index of post-TIPS survival (FIPS). The FIPS score can identify patients at high risk and may guide clinical decision making.

OriginalspracheEnglisch
ZeitschriftJournal of Hepatology
Jahrgang74
Ausgabenummer6
Seiten (von - bis)1362-1372
Seitenumfang11
ISSN0168-8278
DOIs
PublikationsstatusVeröffentlicht - 06.2021

Fördermittel

DB, LS and TB are supported by the Berta-Ottenstein-Programme , Faculty of Medicine, University of Freiburg. HL is supported by the IMM-PACT Programme, Faculty of Medicine, University of Freiburg , JT was supported by Deutsche Forschungsgemeinschaft ( SFB TRR57 P18 & CRC1382 A09 ) H2020 European Institute of Innovation and Technology ( 668031 ; 825694 ; 847949 ) H2020 Societal Challenges ( 731875 ) and CELLEX Foundation (PREDICT). The funders had no influence on study design, data collection and analysis, decision to publish or preparation of the manuscript. MP is supported by grants from the Ernst-und-Berta Grimmke Foundation ( Lfd.Nr.5/19 ) and BONFOR research program of the University of Bonn (grant- ID 2020-2A-07 ). DB, LS and TB are supported by the Berta-Ottenstein-Programme, Faculty of Medicine, University of Freiburg. HL is supported by the IMM-PACT Programme, Faculty of Medicine, University of Freiburg, JT was supported by Deutsche Forschungsgemeinschaft (SFB TRR57 P18 & CRC1382 A09) H2020 European Institute of Innovation and Technology (668031; 825694; 847949) H2020 Societal Challenges (731875) and CELLEX Foundation (PREDICT). The funders had no influence on study design, data collection and analysis, decision to publish or preparation of the manuscript. MP is supported by grants from the Ernst-und-Berta Grimmke Foundation (Lfd.Nr.5/19) and BONFOR research program of the University of Bonn (grant-ID 2020-2A-07).JT: Grants: Gore, Consultant: Martins Pharma, Ironwood, Gore, Alexion, BMS, Grifols, Sequana Medicals, Versantis, Sponsored lectures (National or International): Gilead, Gore, Alexion, BMS, Grifols, Sequana Medicals, Norgine, Intercept. DB: Consultant: Bayer Healthcare, Boston Scientific, Shionogi. Lectures: Falk Foundation. LS: Lectures: Falk Foundation. RK: Consultant: Boston Scientific, Bristol-Myers Squibb, Guerbet, Roche, and SIRTEX. Lectures: BTG, Guerbet, Ipsen, SIRTEX, MSD Sharp & Dohme. MS: Consultant: Bayer Healthcare, L.W.Gore Lectures: Falk Foundation.

TrägerTrägernummer
BONFOR
Berta-Ottenstein Programme
Ernst-und-Berta Grimmke FoundationLfd.Nr.5/19
PREDICT
Falk Foundation
Gilead Sciences
Fundación Cellex
Merck Sharp and Dohme
H2020 Societal Challenges731875
H2020 European Institute of Innovation and Technology847949, 668031, 825694
Deutsche ForschungsgemeinschaftSFB TRR57 P18, CRC1382 A09
Rheinische Friedrich-Wilhelms-Universität Bonn2020-2A-07
Sirtex Medical

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    • Forschungsschwerpunkt: Biomedizintechnik

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