National Congenital Heart Disease Audit
- Conditions
- Congenital Heart Disease (CHD)
- Interventions
- Procedure: Cardiac SurgeryProcedure: Therapeutic cardiac catheterisations procedures
- Registration Number
- NCT02303535
- Lead Sponsor
- University College, London
- Brief Summary
The National Institute of Cardiovascular Outcomes Research (NICOR) collects data and produces analysis to enable hospitals and healthcare improvement bodies to monitor and improve the quality of care and outcomes of cardiovascular patients.
The Congenital Heart Disease audit collects data on all cardiac surgery and therapeutic cardiac catheterisations procedures used to treat patients with congenital and acquired heart disease.
For acquired heart disease, the audit covers all arrhythmias \& cardiomyopathies in patients less than 16 years old only. For congenital heart disease, the audit collects data on both children and adult patients. The audit covers all specialist centers in the UK and Republic of Ireland.
The project aims to improve the quality of care for children and adults with congenital heart disease by providing national comparative analysis of procedure specific activity and outcomes of cardiac surgery and therapeutic cardiac catheterisation procedures. The audit also provides quality indicators for the antenatal detection of major congenital heart disease.
The current dataset is available from here:
http://www.ucl.ac.uk/nicor/audits/congenital/datasets
- Detailed Description
The Congenital Heart Disease audit collects data on all cardiac surgery and therapeutic cardiac catheterisations procedures used to treat patients with congenital and acquired heart disease
Data collection:
Hospitals use Patient Administration Systems and manual data entry by cardiac database managers to submit data to NICOR.
Data are either assimilated locally using third party commercial software and imported as a .csv file, or entered directly onto the NICOR database.
Data quality:
NICOR provide tools that communicate possible errors to centres submitting data. A data submitting schedule has been agreed with the centres, data is submitted and a validation report is returned each quarter. Centres are responsible for updating errors in the records.
An import log highlights missing and invalid data as well as records that failed to import due to data quality or compatibility issues.
In addition, data is validated by on site visits with a NICOR representative.
Data linkage:
Data is annually linked with Office fot National Statistics (ONS) life status and Hospital Episodes Statistics (HES) admission data to verify case ascertainment and to track long term outcome measures.
Information governance:
NICOR has Section 251 approval and data protection registration. An organisation-wide standard operating procedure is in place for Information Security Incident Management. University College London has a robust information governance framework, to which NICOR adheres.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 120000
Patient, judged by multidisciplinary team meeting as unsuitable for the procedure
Patient, judged by multidisciplinary team meeting, as unsuitable for the procedure
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Congenital Cardiac Surgery All patients with congential and acquired heart disease treated by cardiac surgery and therapeutic cardiac catheterisations procedures . For acquired heart disease, the audit covers all arrhythmias \& cardiomyopathies in patients less than 16 years old only. For congenital heart disease, the audit collects data on both children and adult patients. Congenital Therapeutic cardiac catheterisations procedures All patients with congential and acquired heart disease treated by cardiac surgery and therapeutic cardiac catheterisations procedures . For acquired heart disease, the audit covers all arrhythmias \& cardiomyopathies in patients less than 16 years old only. For congenital heart disease, the audit collects data on both children and adult patients.
- Primary Outcome Measures
Name Time Method 30 day survival rates 30 day survival from operation date The analysis shows the national survival rates at 30 days for each procedure and the national survival rates for individual procedures by age.
- Secondary Outcome Measures
Name Time Method 1 year survival rates 1 year survival rates after the date of the procedure Analysis include 1-year outcome but a death would not appear in the table until a full year has passed for the whole cohort of patients within that year. For example, the audit collection period is based on financial year of April 1st to March 31st. A patient that died in April would be reported within the same period as one that died 11 months later in March.
Trial Locations
- Locations (10)
Royal Victoria Hospital Belfast
🇬🇧Belfast, Northern Ireland, United Kingdom
Southampton General Hospital
🇬🇧Southampton, Hampshire, United Kingdom
Alder Hey Hospital
🇬🇧Liverpool, Merseyside, United Kingdom
John Radcliffe Hospital
🇬🇧Oxford, Oxfordshire, United Kingdom
Freeman Hospital
🇬🇧Newcastle upon Tyne, Tyne and Wear, United Kingdom
Leeds General Infirmary
🇬🇧Leeds, West Yorkshire, United Kingdom
Queen Elizabeth Hospital (Edgbaston)
🇬🇧Birmingham, United Kingdom
The Harley Street Clinic
🇬🇧London, United Kingdom
The Heart Hospital
🇬🇧London, United Kingdom
Royal Brompton Hospital
🇬🇧London, United Kingdom