Preventive Genomics & Family Check-up Services

The Preventive Genomics & Family Check-up Services Center offers a comprehensive range of services from diagnosis, consultation, disease screening and risk assessment for inherited diseases and pharmacogenetic testing for drug selection, dose adjustment, and drug allergy prevention. The services are available for people with a family history of hereditary diseases and for individuals who care about their own and their families’ health.
 
What is genetic testing?

The Genomics Center has designed a holistic health care path aiming for longevity, with a focus on in-depth health care.  A proactive approach we use is genetic testing, emphasizing disease prevention. Thus, in addition to diagnosis and risk assessment, we can use genetic testing for the following purposes:

  • To predict future health conditions, enabling proper planning to prevent certain serious diseases.
  • To reduce the risk of drug allergy and help predict drug response, thus enhancing appropriate drug choice and dosage
  • To help in family planning by detecting certain hereditary diseases and conditions, and inform your family planning decisions
Benefits of genetic testing in preventive care
 

Two major benefits of genetic testing:

  • Helps patients and families plan for proper disease prevention

  • Enhances tailored forms of clinical care based on genetic testing result
 

Who should get genetic testing?

  • Those with a family history of an inherited disease.
  • Those who consider family planning and pregnancy
  • Those of all ages who care about health
Genetic testing procedures
  • Sample collection: Blood or saliva collection at the hospital or at home with telemedicine and @home services
  • Lab work: Samples sent to the lab for testing
  • Analysis: interpretations of test results by skilled medical geneticists
  • Counseling session: meeting with medical geneticists regarding test results
 

What happens next after the test results are out

It takes a few weeks before the genetic results are available. If the results are inconclusive or positive,
medical geneticists will provide interpretations of the results and suggestions for further steps, or possibly make a referral to particular specialists.
Our Genetic Packages

Bumrungrad International Pioneers Personalized Drug System based on DNA

Bumrungrad International Hospital set up an innovative drug prescription system in March 2020 that responds to a patient’s individual genetic makeup. Taking a proactive and personalized approach to healthcare, pharmacogenetics utilizes precision medicine. Doctors are alerted through an interactive software program to test a patient’s DNA before writing out a prescription through a targeted reactive testing approach. Meanwhile, the results of any screening already carried out via a broader, pre-emptive approach, before a specific drug prescription is identified, can be flagged up too. This speeds-up the process and ensures the right medicine gets to the right patients at the right time.

The Power of Pharmacogenetics
Some gene profiles react adversely with certain medications, leading to allergic reactions, which in a number of cases can be extremely serious, as well as creating unwanted side-effects. Genes can also dictate the actual efficacy of a prescribed drugs individually too, meaning a patient’s treatment path can be not only far from optimized but also compromised.

The Bumrungrad International Hospital Pharmacogenetics Team’s work, headed by Dr. Chonlaphat Sukasem, who is also an Associate Professor at Division of Pharmacogenomics and Personalized Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University connects to every branch of healthcare. This type of screening is evolving drug treatment in cardiology and oncology departments, as well as neurology, rheumatology and HIV, plus psychiatric care, etc.

At Bumrungrad International Hospital, genetic testing is being applied to determine medication prescribed in the treatment plans of those suffering with epilepsy, gout, cardiovascular diseases and acute lymphoblastic leukemia  as well as in the area of pain management, infectious diseases and clinical practice. The test can be requested by check-up clinics too.

Doctors at the hospital can access the genetic profile of a patient to guide the selection of drugs and drug doses that would be optimally therapeutic for that individual’s condition as well as being safe with no side effects.

Bumrungrads Personalized Treatment Mission
The pharmacogenetics screening usually involves a buccal swab and blood test with a current turnaround time of three days, unless results are urgently required within 24 hours. Most tests are processed in-house, with some sent to labs abroad. In terms of drugs that can be tested, evidence-based guidelines are followed, focusing on around 270 USDFA recommended drugs. As new medications are developed the results from previous testing can be applied using the genetic profile information.
 
Such an individual focus aides specialists in selecting appropriate medicines and highlighting where any issues may occur. This allows for adjustments in drug combinations, enabling greater personalized treatment in terms of dosing, even if a particular drug is not intrinsically deemed high risk for that individual. While clinical trials ensure that dosing levels are suitable for the majority, it is the minority that can encounter issues and for whom pharmacogenetics provides a real-life solution.
 
When Drugs Cause More Harm than Good
The impact of a prescription not working properly when dealing with serious illnesses and disease is clear. With advances in the area of pharmacogenetics and drug development there are more choices and lack of efficacy can be avoided. Genetic variation can affect metabolism too and the knock-on effects of this can be adverse, from a low excretion rate to a toxic build-up.
 
Another problem that can occur is a reaction to medication that causes severe, burn-like skin reactions which can be life-threatening, with a relatively high mortality rate. Some 10-18% of Thais tested show some type of frequency of this ‘risk’ gene, for example. The future mission at Bumrungrad International Hospital is to screen patients as a default so that they can be stratified according to their genetic background.
 
Pharmacogenetics is ultimately about saving lives and promoting the best treatment possible. An example of this is the use of blood-thinning medicine Warfarin, which in some patients can cause bleeding. If an individual does not respond well to that drug, and they are a poor responder in terms of its efficacy, the result can lead to thrombosis which can prove fatal.
 
Prevention is Better than Cure
In screening to ensure optimized treatment, testing also comes into the pre-emptive arena too, of using pharmacogenetics to delay or avoid the onset of illness through early intervention. Results are implemented into the work of the Wellness Center, treating hypertension, for example, before it turns into a more serious cardiovascular disease.
 
Pharmacogenetics is not a magic wand but rather a golden thread that weaves into the fabric of physician medicine. Diet, general health and environment are all important strands as well. In the case of Warfarin, as an example, genetics is one factor and pharmacogenetics is an important tool, while diet plays into treatment options too.
 
Bumrungrad Hospital’s Pharmacogenetics Team comprises of 10 medical professionals, including pharmacogenetics experts, pharmacists and lab scientists. Their plan is to create a dream team that enables a proactive response to provide a healthcare treatment model of excellence within the world.
 

Check our Preventive Genomics & Family Check-up Packages:

From

27,080 THB

Genetic Health screen (Cancer and heart) (Proactive test)

Genetic testing for hereditary cancers and heart diseases is a proactive health check-up to predict the risk of cancers and heart diseases.

From

39,930 THB

Genetic Carrier Screening for Female & Partner

Genetic carrier screening for female & partner is a screening test to predict the risk of developing genetic diseases of children due to abnormal genes inherited from a parent.

From

21,930 THB

Genetic Carrier Screening for Female

Genetic carrier screening for female is a screening test to predict the risk of developing genetic diseases of children due to abnormal genes inherited from a parent.

Displaying results 7-9 (of 9)
 |<  <  1 - 2 - 3 >  >|

Talk to our Referral Office in Ethiopia

Our local representatives speak your language and can assist you by answering any questions you have about the hospital as well as book travel arrangements.There are no additional costs for using this service as per Bumrungrad's One Price Policy.