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Considerations of Pharmacogenetic Testing in Children

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4 min read

Considerations of Pharmacogenetic Testing in Children

PGx Testing in Children

Pharmacogenetic, or PGx, testing has been cited to be useful in helping doctors understand children’s reactions to drugs. In the U.S., around 60% of children are prescribed drugs, hence understanding such reactions is very crucial. ADRs can happen due to biological differences in children and medication errors. The experience becomes very difficult and daunting for parents and families. This blog will outline the different benefits and risks associated with pre-emptive PGx testing on newborns and shed some light on its potential impact on health improvements.

What is Pharmacogenetic Testing?

Pharmacogenetic testing looks at how a child’s genetics affects how they respond to medicines. Each child is unique, and their genetic makeup might make a drug work effectively or cause side effects. Knowing a child’s PGx profile can help make better decisions in choosing a medication to prescribe.

Why is PGx Testing Important for Children?

Children and adults metabolize drugs differently. Such differences may contribute to an increased likelihood of adverse drug interactions. For instance, it might simply be the case that some will metabolize the drug much faster or much slower than is optimal, which leaves the disease of the patient entirely uncontrolled or places the patient at risk for dangerous side effects. One can foresee and avoid such outcomes by understanding variation.

Benefits of Pre-emptive PGx Testing

  1. Lower risk of ADRs: Pre-emptive PGx testing determines which children are unlikely to tolerate certain drugs, such as codeine. Some children break it down too rapidly, resulting in overt side effects.
  2. Greater Treatment Choices: When the PGx profile of a child is known, physicians are in a better position to make informed treatment choices that would be safer as well as more effective for the child.
  3. Cost Savings: PGx testing can save dollars in healthcare costs associated with unnecessary hospital visits and various useless treatments by preventing adverse reactions.
  4. Prompt and Early Care in Emergency Situations: In emergency cases, knowledge of a child’s PGx may help initiate faster treatment decisions.

Real-Life Example

For instance, codeine has been linked to serious side effects for some children who incidentally are ultra-rapid metabolizers. More than 300,000 children each year may be at risk for overdose or inadequate pain control. Such risks can be identified through PGx testing thereby preventing healthcare professionals from giving harmful drugs.

Risks and Challenges of PGx Testing

While there are benefits of PGx testing, there are also risks to consider:

  1. Familial Consequences: PGx testing may result in unexpected family information, for example non-paternity. The implications for the families may be emotionally challenging.
  2. Psychosocial Impact: Genetic information can be distressing for parents, even if there is no danger anticipated. However some specialists believe that PGx testing raises fewer concerns than other forms of genetic testing.
  3. Need for Education: Parents need explicit information regarding the benefits and risks of PGx testing. Without that, they may not be able to make informed decisions.

Educational Needs of PGx Programs

The implementation of PGx testing needs the availability of resources that can inform families appropriately regarding this program; its results should also be easily transferable from one provider to another. The parents who show interest in PGx testing are generally less literate on its benefits.

Resources that can help include:

PharmGKB: This is a pharmacogenomics database.
FDA’s PGx Table: This is a guideline for drug-gene interactions. Here Is The “Link
Commercial Labs: These are testing services.
These will ensure that families make the right decisions. Informed consent also assists in ensuring that parents fully understand what PGx testing is about.

Conclusion

In reality, pharmacogenetic testing would be greatly helpful to children as it minimizes drug errors and increases the success of treatment. Though the evidence for routine newborn testing is emerging, the discussion on PGx testing with parents is warranted. Educative resources and obtaining informed consent will ensure that families are well-informed.

Through PGx testing incorporation, better health outcomes can be reached by children, and such risk of side effects from medication can be minimized at Rph Labs. As we continue to explore this vital field, we will support these families and healthcare providers in understanding and using PGx testing effectively.

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