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Optimization of Health Expenditure in Liver Surgery

This study is enrolling participants by invitation only.
Assistance Publique - Hôpitaux de Paris
Information provided by (Responsible Party):
Centre Hospitalier Universitaire, Amiens Identifier:
First received: October 22, 2012
Last updated: February 3, 2017
Last verified: February 2017
The aim of this study is to reduce the length of stay after liver surgery by taking account of objective quantitative clinical variables, subjective qualitative clinical variables and non clinical variables.

Condition Intervention
Hepatocellular Carcinoma
Hilar Cholangiocarcinoma
Intra Hepatic Cholangiocarcinoma
Liver Metastasis
Procedure: liver surgery

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Optimization of Health Expenditure in Major Surgery: Impact of a Mixed, Clinical and Ethnographic Approach in the Model of Liver Surgery

Resource links provided by NLM:

Further study details as provided by Centre Hospitalier Universitaire, Amiens:

Primary Outcome Measures:
  • overall postoperative length of stay [ Time Frame: during the 3 months after the surgery ]

    the overall postoperative length of stay is defined as the hospitalization between the surgery and patient's discharge.

    This period includes the readmission for at least 24 hours in case of outcomes related to the surgery.

Secondary Outcome Measures:
  • peroperative outcomes [ Time Frame: during the surgical procedure ]
    the peroperative outcomes are collected during the surgery and correspond to any event occured during the surgical intervention

  • postoperative outcomes [ Time Frame: after the surgery until postoperative month 3 ]
    the postoperative outcomes correspond to any event occured after the surgical intervention. These outcomes include fistulae; bleeding...

  • construct of pronostic models [ Time Frame: after the postoperative month 3 ]
    the construct of pronostic models include variables that affect the length of stay; morbidity and mortality

  • evaluation of PMSI indicators [ Time Frame: after the postoperative month 3 ]
    this evaluation includes the analysis of PMSI indicators; their validity and the influence of centres on hepatectomies results

Estimated Enrollment: 3000
Actual Study Start Date: September 2012
Estimated Study Completion Date: December 2018
Estimated Primary Completion Date: December 2017 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
operated patients
this cohort includes patients who underwent a liver surgery whatever the pathology and whatever the surgical procedure
Procedure: liver surgery
this intervention type includes hepatectomies; wedge; segmentectomies etc...

Detailed Description:

a new dimension of the activity expected of physicians is to improve the safety of care on the one hand and the control of health care costs on the other.

key measures to help them are the publication of national recommendations, assessment of actual practices and the incentive to activity.

Internationalwide recent and concordant data suggest that

  • quality and security of care, after an initial improvement, are going to stall
  • scientific recommendations are rarely validated by an impact analysis and are not applied
  • clinical data collected within an administrative framework are unreliable and too generalist
  • the evaluation, especially in the surgical field, is based on indicators sometimes irrelevant and often unclear

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

the population corresponds to patients operated in one of the thirteen hospitals.

These hospitals are distributed on the french territory to ensure that the recruitment is representative of the general population


Inclusion Criteria:

  • elective liver surgery
  • older than 18
  • agreed to participate
  • surgical procedure included procedures registered as "HLFA003 - 007 ; 009 - 011 ; 017 - 020 ; HLFC002 à 004 ; 027 ; 032 ; 037" in the PMSI database

Exclusion Criteria:

  • emergency surgery
  • refused to participate
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01715402

Amiens North Hospital
Amiens, France
Bordeaux Hospital
Bordeaux, France
Beaujon University Hospital
Clichy, France
Lille Regional Hospital
Lille, France
Lyon Hospital
Lyon, France
Marseille Hospital
Marseille, France
Paoli calmette institute
Marseille, France
Saint Antoine Hospital
Paris, France
Strasbourg hospital
Strasbourg, France
Gustave Roussy institute
Villejuif, France
Paul Brousse Hospital
Villejuif, France
Sponsors and Collaborators
Centre Hospitalier Universitaire, Amiens
Assistance Publique - Hôpitaux de Paris
Principal Investigator: Olivier FARGES, MD, phD Beaujon University Hospital
  More Information

Responsible Party: Centre Hospitalier Universitaire, Amiens Identifier: NCT01715402     History of Changes
Other Study ID Numbers: AOM 11060
Study First Received: October 22, 2012
Last Updated: February 3, 2017

Keywords provided by Centre Hospitalier Universitaire, Amiens:
liver tumor

Additional relevant MeSH terms:
Neoplasm Metastasis
Carcinoma, Hepatocellular
Klatskin Tumor
Neoplastic Processes
Pathologic Processes
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Liver Neoplasms
Digestive System Neoplasms
Neoplasms by Site
Digestive System Diseases
Liver Diseases
Liver Extracts
Hematinics processed this record on April 24, 2017