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National Cardiovascular Disease Database (NCVD)

Name (Abbreviation)

National Cardiovascular Disease Database
(NCVD)

Established since:

2005

Contact person:

Ms. S Gunavathy Selvaraj, NCVD Registry Manager

Address:

National Cardiovascular Disease Database,
c/o Clinical Research Centre, Kuala Lumpur Hospital
1st Floor, MMA House,
124, Jalan Pahang
53000 Kuala Lumpur
Malaysia

Phone:

03-4044 3060 / 03-4044 3070

Fax:

03-4044 3080

Email:

ncvd@acrm.org.my

URL:

www.acrm.org.my/ncvd

Registries:

1. Acute Coronary Syndrome (ACS) registry
2. Percutaneous Coronary Intervention (PCI) registry

Sponsor, Funding and Governance:

Sponsor:

Cardiac & Medical Services Ministry of Health Malaysia, IJN, Cardiac Services of UM, HUKM, Private cardiac care providers.

Funding:

The CRC, MOH is the sponsor of the registry and NHAM as the co-sponsor
The CRC also provides technical support in the form of clinical epidemiology expertise, and biostatistics and ICT services.

Governance Board:

A Governance Board was established to govern the NCVD. The MOH, various professional bodies, and providers of cardiology related services from all sectors are represented on this committee to ensure that the NCVD stays focused on its objectives, and to assure its continuing relevance and justification.

Objectives:

The objectives of the NCVD are to:

  1. Determine the number and the time trend of acute coronary syndromes in Malaysia.

  2. Determine the socio demographic profiles of these patients to better identify the high risk group in our Malaysian population.

  3. Determine the efficiency of, and adherence to current guidelines of treatment guidelines.

  4. Determine the number, evaluate and monitor the outcomes of percutaneous coronary intervention (PCI) based on selected performance indicators.

  5. Determine the cost to the nation by cardiovascular disease and the cost-effectiveness of treatment and prevention programs.

  6. Stimulate and facilitate research using this database.

Scope and Content:

The NCVD is intended to be a truly national population-based disease and treatment registry. It therefore seeks the participation from all providers of cardiology services in all sectors (public, NGO and Private) throughout the country.

Data collection and transfer:

Mixed-mode.
The NCVD will collect data using web application to enable individual SDPs to securely download data they have submitted to NCVD as well as to download confidential communication where required.
Data will be collected and entered online at the SDPs level. The NCVD registry office will track on continuity and quality of data reported online and prompt SDPs whenever they fall behind schedule in reporting data.

Record linkage:

There is a plan to link NCVD’s database to the Jabatan Pendaftaran Negara’s database to ascertain mortality outcome.
There is also a plan to link the NCVD to the National Operative Procedure register and the MOH’s Health Management Information System (HMIS) to determine morbidity events when these two databases are properly established.

Reports & Publications:

The NCVD plans to publish an annual statistical report. The first ACS report is due in April 2008.

Resources:

 

Registry operations:

The day-to-day operations of the NCVD will be undertaken by NCVD staff.

Epidemiology:

The Clinical Research Centre of the MOH will provide clinical epidemiology expertise for the registry.

Biostatistics:

This is outsourced to Biostat Consulting Sdn Bhd.

ICT support:

These are outsourced to various IT companies including NTT (data centre service), MIMOS and KSM (hardware), Datamed Clinical Computing Sdn Bhd (databases and applications), SecureTangent (information security), and variety of specialty software providers (IBM/Ascential, SAS, STATA, WHO/MedDRA, etc)

Date updated:

25/01/2008


 

 
 
 
 
 
 

 
 

 

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