Securative Healthcare Solutions has relationships with the nation's leading genetics laboratories and offers a full spectrum of genetic screening diagnostics. This is an area of medicine that has endured much financial abuse since the advent of genomic sequencing, and we are proud to partner with labs that are leading the way in reducing costs for health systems and patients alike. One of our lab partners offers a genetic cancer screening test for $249 even for patients with no insurance!
Securative Healthcare Solutions Pharmacogenetic Clinical Integration
“Right Information, Right Drug, Right Dose, Right from the beginning.”
The era of ‘Personalized Medicine’ has now arrived. It allows your physician to understand from your specific DNA profile what medications will work best. It’s called ‘Pharmacogenomic Testing’ or PGx. No more trial and error prescribing, no longer having the danger of Adverse Drug Reactions (ADRs) which put over 2 million people annually in the hospital and cause over 100,000 deaths each year. Now doctors can have the knowledge to avoid these issues. Personalized Medicine helps doctors to individualize drug therapy, decrease adverse drug reactions, and increase the effectiveness of treatment plans.
"Without (Pharmacogenetic) testing, neither you nor your doctor knows exactly how you’ll react to the medication. It may not work for you, or you may have serious side effects such as bleeding. You might have to try different doses — or even different medications — before finding a treatment that works for you. Pharmacogenomics speeds up that process. Before you take a single dose of medication, you can have a test to see how you’re likely to respond to the medication." - Mayo Clinic on Pharmacogenomics
“Right Information, Right Drug, Right Dose, Right from the beginning.”
The era of ‘Personalized Medicine’ has now arrived. It allows your physician to understand from your specific DNA profile what medications will work best. It’s called ‘Pharmacogenomic Testing’ or PGx. No more trial and error prescribing, no longer having the danger of Adverse Drug Reactions (ADRs) which put over 2 million people annually in the hospital and cause over 100,000 deaths each year. Now doctors can have the knowledge to avoid these issues. Personalized Medicine helps doctors to individualize drug therapy, decrease adverse drug reactions, and increase the effectiveness of treatment plans.
"Without (Pharmacogenetic) testing, neither you nor your doctor knows exactly how you’ll react to the medication. It may not work for you, or you may have serious side effects such as bleeding. You might have to try different doses — or even different medications — before finding a treatment that works for you. Pharmacogenomics speeds up that process. Before you take a single dose of medication, you can have a test to see how you’re likely to respond to the medication." - Mayo Clinic on Pharmacogenomics
OTHER GENETIC SCREENINGS
Hereditary Cancer Assessment
This assessment evaluates an individual’s genetic risk of developing primary inherited cancers over their lifetime. Equipped with the results of this test, alongside medical and family history, a strategy can be created to reduce the risk of developing one of these many types of cancers. Not everyone with a cancer-related mutation will develop cancer.
Non-Invasive Prenatal Testing
The Non-Invasive Prenatal Test represents a major advance in prenatal testing, providing accurate answers about fetal chromosomal health — without the risks associated with invasive procedures, such as amniocentesis or chorionic villus sampling (CVS). Available for both singleton and twin pregnancies.
Comprehensive Carrier Test
This saliva test can inform a couple if they are at risk of having a child with certain genetic conditions. When planning a family, preparing for pregnancy or during pregnancy, your patient will use the results you provide them to consider the most complete range of reproductive options. For many of these diseases, prevention is the only cure.
This assessment evaluates an individual’s genetic risk of developing primary inherited cancers over their lifetime. Equipped with the results of this test, alongside medical and family history, a strategy can be created to reduce the risk of developing one of these many types of cancers. Not everyone with a cancer-related mutation will develop cancer.
- Determines if a patient has genetic mutations that correlate with increased risk of the eight types of primary inherited cancers
- Assists physicians in recommending solutions for healthy lifestyle management, medications and/or surgical procedures
Non-Invasive Prenatal Testing
The Non-Invasive Prenatal Test represents a major advance in prenatal testing, providing accurate answers about fetal chromosomal health — without the risks associated with invasive procedures, such as amniocentesis or chorionic villus sampling (CVS). Available for both singleton and twin pregnancies.
Comprehensive Carrier Test
This saliva test can inform a couple if they are at risk of having a child with certain genetic conditions. When planning a family, preparing for pregnancy or during pregnancy, your patient will use the results you provide them to consider the most complete range of reproductive options. For many of these diseases, prevention is the only cure.