Analysis of Hospitalizations One Year After Acts of CAG and PCI in the Aquitaine région - ACIRA Register Data Analysis (ACIRA-REHOSP)

February 8, 2022 updated by: University Hospital, Bordeaux

Frequency and Characteristics of Rehospitalizations During One Year After Percutaneous Coronary Intervention and Coronary Angiography - Results of the ACIRA Registry, Aquitaine Region

Hospital readmission rate following percutaneous coronary interventions (PCI) or coronary angiographies (CAG) is a main indicator of quality of care and addresses economic issues. The aim of this study is to quantify the frequency and analyse the types of rehospitalizations and repeat revascularizations during one year after a PCI or a CAG. This information is needed to organize the health care pathway and to identify preventable rehospitalizations.

Study Overview

Study Type

Observational

Enrollment (Actual)

11487

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Agen, France
        • Clinique Esquirol St Hilaire
      • Aressy, France
        • Clinique cardiologique d'Aressy
      • Bayonne, France
        • GCS Bayonne
      • Bordeaux, France
        • Clinique de Caudéran les pins-francs
      • Bordeaux, France
        • Clinique de St Augustin
      • Libourne, France
        • CH de Libourne
      • Mont de Marsan, France
        • CH De Mont de Marsan
      • Pau, France
        • CH de Pau
      • Perigueux, France
        • CH de Périgueux
      • Pessac, France, 33604
        • CHU de Bordeaux
      • Pessac, France
        • Hôpital Privé St Martin

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

All volunteer adults (≥ 18 years) and French resident patients who underwent PCI and CAG in nine interventional cardiology hospitals in the Aquitaine region (France), from January 1, 2012 to December 31, 2013.

Description

Inclusion Criteria:

  • Patients included in ACIRA Registry : All volunteer adults (≥ 18 years) and French resident patients who underwent PCI and CAG in the interventional cardiology hospitals in the Aquitaine region (France),
  • Initial PCI or CAG performed from January 1, 2012 to December 31, 2013,
  • Initial PCI or CAG performed in nine interventional cardiology hospitals in the Aquitaine region (France).

Exclusion Criteria:

  • Patients who declined to take part of ACIRA Registry,
  • Patients resident outside the Aquitaine region (France),
  • Patients who died during the initial hospital stay,
  • Patients hospitalized for a PCI or a CAG the month preceding the initial procedure including in the ACIRA-Rehosp study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Group 1 : Percutaneous coronary intervention
All the patients who underwent percutaneous coronary intervention, in 9 invasive cardiology centers in the Aquitaine Region, France.
Group 2 : Coronary angiography
All the patients who underwent coronary angiography, in 9 invasive cardiology centers in the Aquitaine Region, France

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Type of rehospitalization
Time Frame: Baseline to 1 year
Baseline to 1 year
Number of rehospitalization
Time Frame: Baseline to 1 year
Baseline to 1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Identification of hospitals
Time Frame: Baseline to 1 year
All hospitals concerned by initial coverage and rehospitalization
Baseline to 1 year
Type of diagnoses and procedures associated with each type of rehospitalization
Time Frame: Baseline to 1 year
Baseline to 1 year
Type of cardiac rehabilitation procedures in hospitalizations for post-operative and rehabilitation wards
Time Frame: Baseline to 1 year
Baseline to 1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Saillour-Glénisson Florence, MD, University Hospital, Bordeaux
  • Study Director: Lesaine Emilie, MD, University Hospital, Bordeaux

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 15, 2016

Primary Completion (Actual)

January 15, 2017

Study Completion (Actual)

January 15, 2017

Study Registration Dates

First Submitted

April 10, 2017

First Submitted That Met QC Criteria

April 10, 2017

First Posted (Actual)

April 14, 2017

Study Record Updates

Last Update Posted (Actual)

February 9, 2022

Last Update Submitted That Met QC Criteria

February 8, 2022

Last Verified

February 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • CHUBX 2014/29

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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