Cardiovascular Genomic Testing
Everything you need to know to order a cardiovascular genomic test.
Clinicians working in Cardiology can request genomic testing directly without referring patients to Clinical Genetics. This will reduce wait times and get your patients the answers they need faster.
The South East has a specialist genomics laboratory at Royal Brompton Hospital dedicated to cardiovascular genomic testing.
Please note: Clinical Genetics at Guy’s & St Thomas’ Hospital are no longer accepting referrals for diagnostic genomic testing for inherited cardiac conditions. However the Clinical Genetics service at St Georges Hospital continues to accept referrals from its referring centres.
This page supports cardiology clinicians to understand how to order a genetic test and speed up the pathway for your patients.
What is Cardiovascular Genetic testing?
Genetic (also called genomic) testing looks for changes (variants) in genes that are known to be associated with inherited cardiac conditions, such as cardiomyopathies, arrhythmia syndromes, and aortopathies.
These gene variants may:
- Explain why a patient has developed a cardiac condition
- clarify or confirm a clinical diagnosis
- identify whether a condition could be inherited
- guide management for both the patient and their relatives
How to Order a Cardiovascular Genomic Test
Below are the steps you need to order a genomic test for cardiology.
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Is the test clinically relevant?
Determine if it is clinically useful for your patient to undergo genomic testing for an inherited cardiac condition
Before ordering a test think:
- Will the test result influence treatment or screening?
- Are there family members that might benefit from predictive genetic testing?
- Will the test result influence reproductive decision making for the patient or their relatives?
- Watch our video on when to order a test to learn more
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Identify the most appropriate test for your patient
The National Test Directory lists all the genomic tests that are currently available on the NHS. Each test has its own unique R code which you will need to include on the Test Order Form
You can also use our Order or Find a Test directory to select the most appropriate test for your patient.
Search for a gene or R code and the directory will identify all of the relevant tests. The directory also lists the eligibility criteria and contains links to the relevant Test Order Form and Record of Discussion Form.
Watch our video explaining how to navigate the test directory
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Take consent for the genomic test
Before requesting a genomic test, you should ensure your patient fully understands the potential implications of the test for them and their family members. If your patient is a child, consent for genomic testing should be taken from their parents.
Download the Record of discussion form to fully record your patient’s consent. Retain a copy for your notes and give a copy to the patient.
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Complete the test order form
- Download the Test Request Form and fill it in
- Include the R Code on the test order form
- State which eligibility criteria your patient meets
- State why it is clinically useful
- Include patient’s ethnicity
- Consider adding a departmental group email address to ensure the result doesn’t get lost
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Send the sample
Please give the patient the signed Test Request Form and two ID labels to go to phlebotomy department for a blood test.
Phlebotomy will take 2x EDTA blood bottles and dispatch to the local pathology lab, who will arrange transfer to the genetics lab.
Sample rejections:
The test will be rejected if :
- Samples and request form do not show at least three identical patient identifiers
- The sample is in the incorrect collection media
- The request form is not sufficiently completed
- The sample is not of sufficient volume
- The sample is too old
Send sample and request forms to:
Clinical Genetics & Genomics Laboratory
Royal Brompton Hospital
2nd (Ground) Floor, Sydney Wing
Sydney Street
London SW3 6NP
Links to further resources on test ordering…
Links to further resources on genetic testing and cardiology…
A selection of educational resources to support teams working in Cardiology to embrace Genomic Medicine. Choose between ‘In the Clinic’ resources, which describe typical clinical scenarios, and the ‘Knowledge Hub’, which summarises cardiac conditions involving genomics
Learn more about our work on the NHS Coronial Sudden Unexpected Death (NHS C-SUD) pathway, also known as the Sudden Cardiac Death project.
View recordings from this Core Learning in Inherited Cardiac Conditions Study Day 2023. After viewing the recordings, you can answer the online quiz to generate a session certificate.
These resources outline all of the genomic competencies clinicians need to arrange genomic testing for inherited cardiovascular conditions. All stages of the genomic testing pathway are covered, from determining eligibility for testing to feeding back results. The Clinical Pathway Initiative (CPI) pathways can be used to support service delivery planning, identify workforce training needs, and assess and develop knowledge and skills