Analysis of Hospitalizations One Year After Acts of CAG and PCI in the Aquitaine région - ACIRA Register Data Analysis
ACIRA-REHOSP
Frequency and Characteristics of Rehospitalizations During One Year After Percutaneous Coronary Intervention and Coronary Angiography - Results of the ACIRA Registry, Aquitaine Region
1 other identifier
observational
11,487
1 country
11
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2016
Shorter than P25 for all trials
11 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 15, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 15, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
January 15, 2017
CompletedFirst Submitted
Initial submission to the registry
April 10, 2017
CompletedFirst Posted
Study publicly available on registry
April 14, 2017
CompletedFebruary 9, 2022
February 1, 2022
1 year
April 10, 2017
February 8, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Type of rehospitalization
Baseline to 1 year
Number of rehospitalization
Baseline to 1 year
Secondary Outcomes (3)
Identification of hospitals
Baseline to 1 year
Type of diagnoses and procedures associated with each type of rehospitalization
Baseline to 1 year
Type of cardiac rehabilitation procedures in hospitalizations for post-operative and rehabilitation wards
Baseline to 1 year
Study Arms (2)
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
Interventions
Eligibility Criteria
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.
You may qualify if:
- 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).
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (11)
Clinique Esquirol St Hilaire
Agen, France
Clinique cardiologique d'Aressy
Aressy, France
GCS Bayonne
Bayonne, France
Clinique de Caudéran les pins-francs
Bordeaux, France
Clinique de St Augustin
Bordeaux, France
CH de Libourne
Libourne, France
CH de Mont de Marsan
Mont-de-Marsan, France
CH de Pau
Pau, France
CHU de Bordeaux
Pessac, 33604, France
Hôpital privé St Martin
Pessac, France
CH de Perigueux
Périgueux, France
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Saillour-Glénisson Florence, MD
University Hospital, Bordeaux
- STUDY DIRECTOR
Lesaine Emilie, MD
University Hospital, Bordeaux
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 1 Year
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 10, 2017
First Posted
April 14, 2017
Study Start
January 15, 2016
Primary Completion
January 15, 2017
Study Completion
January 15, 2017
Last Updated
February 9, 2022
Record last verified: 2022-02
Data Sharing
- IPD Sharing
- Will not share