Avoiding postoperative mortality after ALPPS-development of a tumor-specific risk score for colorectal liver metastases.


Journal

HPB : the official journal of the International Hepato Pancreato Biliary Association
ISSN: 1477-2574
Titre abrégé: HPB (Oxford)
Pays: England
ID NLM: 100900921

Informations de publication

Date de publication:
07 2019
Historique:
received: 03 08 2018
revised: 07 11 2018
accepted: 18 11 2018
pubmed: 7 1 2019
medline: 15 4 2020
entrez: 7 1 2019
Statut: ppublish

Résumé

ALPPS is a two-stage hepatectomy that induces more rapid liver growth compared to conventional strategies. This report aims to establish a risk-score to avoid adverse outcomes of ALPPS only for patients with colorectal liver metastases (CRLM) as primary indication for ALPPS. All patients with CRLM included in the ALPPS registry were included. Risk score analysis was performed for 90-day mortality after ALPPS, defined as death within 90 days after either stage. Two risk scores were generated i.e. one for application before stage-1, and one for application before stage-2. Logistic regression analysis was performed to establish the risk-score. In total, 486 patients were included, of which 35 (7%) died 90 days after stage-1 or 2. In the stage-1 risk score, age ≥67 years (OR 3.7), FLR/BW ratio <0.40 (OR 2.9) and total center-volume (OR 2.4) were included. For the stage-2 score age ≥67 years (OR 3.7), FLR/BW ratio <0.40 (OR 2.8), bilirubin 5 days after stage-1 >50 μmol/L (OR 2.4), and stage-1 morbidity grade IIIA or higher (OR 6.3) were included. The CRLM risk-score to predict mortality after ALPPS demonstrates that older patients with small remnant livers in inexperienced centers, especially after experiencing morbidity after stage-1 have adverse outcomes. The risk score may be used to restrict ALPPS to low-risk patient populations.

Sections du résumé

BACKGROUND
ALPPS is a two-stage hepatectomy that induces more rapid liver growth compared to conventional strategies. This report aims to establish a risk-score to avoid adverse outcomes of ALPPS only for patients with colorectal liver metastases (CRLM) as primary indication for ALPPS.
METHODS
All patients with CRLM included in the ALPPS registry were included. Risk score analysis was performed for 90-day mortality after ALPPS, defined as death within 90 days after either stage. Two risk scores were generated i.e. one for application before stage-1, and one for application before stage-2. Logistic regression analysis was performed to establish the risk-score.
RESULTS
In total, 486 patients were included, of which 35 (7%) died 90 days after stage-1 or 2. In the stage-1 risk score, age ≥67 years (OR 3.7), FLR/BW ratio <0.40 (OR 2.9) and total center-volume (OR 2.4) were included. For the stage-2 score age ≥67 years (OR 3.7), FLR/BW ratio <0.40 (OR 2.8), bilirubin 5 days after stage-1 >50 μmol/L (OR 2.4), and stage-1 morbidity grade IIIA or higher (OR 6.3) were included.
CONCLUSIONS
The CRLM risk-score to predict mortality after ALPPS demonstrates that older patients with small remnant livers in inexperienced centers, especially after experiencing morbidity after stage-1 have adverse outcomes. The risk score may be used to restrict ALPPS to low-risk patient populations.

Identifiants

pubmed: 30611560
pii: S1365-182X(18)34561-1
doi: 10.1016/j.hpb.2018.11.010
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

898-905

Informations de copyright

Copyright © 2018 International Hepato-Pancreato-Biliary Association Inc. Published by Elsevier Ltd. All rights reserved.

Auteurs

Joost Huiskens (J)

Department of Experimental Surgery, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands; Department of Surgery, Erasmus Medical Center, Erasmus University, Rotterdam, the Netherlands.

Erik Schadde (E)

Department of Surgery, Division of Transplantation, Rush University Medical Center, Chicago, IL, United States; Cantonal Hospital Winterthur, Kanton, Zurich, Switzerland; Institute of Physiology, Center for Integrative Human Physiology, University of Zurich, Zurich, Switzerland.

Hauke Lang (H)

Department of General, Visceral and Transplant Surgery, Universitaetsmedizin Mainz, Mainz, Germany.

Massimo Malago (M)

Department of HPB and Liver Transplantation Surgery, University College London, Royal Free Hospitals, London, UK.

Henrik Petrowsky (H)

Swiss HPB and Transplantation Center, Department of Surgery, University Hospital Zurich, Zurich, Switzerland.

Eduardo de Santibañes (E)

Department of Surgery, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.

Karl Oldhafer (K)

Department of General & Abdominal Surgery, Asklepios Hospital Barmbek, Semmelweis University of Medicine, Germany.

Thomas M van Gulik (TM)

Department of Experimental Surgery, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.

Pim B Olthof (PB)

Department of Experimental Surgery, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands; Department of Surgery, Reinier de Graaf Gasthuis, Delft, the Netherlands. Electronic address: p.b.olthof@amc.nl.

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