Monday, 28 April 2014

Well-informed patients key to accepting gene-based drug dosing





Dr. Michael Rieder, Professor of Pediatrics, and Physiology and Pharmacology at Western University, led a study which concluded if patients are well-informed about gene-based drug dosing, they're far more accepting of genetic testing. Credit: Western University


A new study out of Western University (London, Canada) illustrates the need for a lot more education around pharmacogenetics (PGx) –the study of how a patient's genes can affect drug reaction and dosage. PGx promises to optimize patient response to therapy, but this is the first study to really investigate how patients perceive this kind of genetic testing, and whether those perceptions differ when it comes to parents and their children. The research, led by Dr. Michael Rieder of Western's Schulich School of Medicine & Dentistry is published in the journal Pediatrics.


"Pharmacogenetic testing has become widely used and gene-based drug dosing is becoming a reality for a number of common health problems. This study confirms what we suspected; Whether or not you're a parent, your degree of acceptability of was determined by your knowledge of it. That is to say –if you understand what the test is for, and the concept of gene-based drug dosing, you're far more open to it, than if you don't understand it," said Dr. Rieder, a professor in the Departments of Paediatrics, and Physiology and Pharmacology.


The researchers surveyed three groups including: 236 medical students representing those having greater educational exposure to PGx, 1,226 lay parents and 105 lay people without children. A second survey was completed by 229 parents. The surveys didn't use PGx but rather, asked about "DNA testing to guide therapy." The study concluded that the acceptability of PGx testing, either for oneself or one's child, seemed to depend on baseline PGx knowledge, but not on parenthood.


The main concern for all respondents was the need for informed consent. Other findings included:



  • More acceptance for PGx when the disease was severe

  • Strong desire/demand for separate consent for PGx testing

  • More education about PGx needed in medical schools

  • Acceptability of genetic testing didn't differ whether for the parent or the child


Dr. Rieder says PGx should take a lesson from pediatric oncology. He says health care workers in that division do a good job in the way they frame the discussions around care, treatment, and consent. "When they have to make a diagnosis, they spend a lot of time explaining what tests they're going to do, the risks, and what therapies are available. And they're successful. Their patients comply with treatment, they get involved in studies, they're informed, and they want to know what's going on."



Medical Xpress on facebook

Related Stories


Pharmacogenetics testing offers way to reduce deaths from drug toxicity


Apr 11, 2011



On average, a drug on the market works effectively for only 50% of the people who take it. Would you want to prevent a potential adverse drug effect or even toxicity through a simple test? It's not science fiction, but a ...



Parents don't fully understand biobank research, study finds


Jul 29, 2013



Researchers who collect genetic samples from children for medical research need to explain the process more clearly to parents, according to a new study that suggests many parents don't fully understand the finer details ...



Making sense of genetic testing for heart disease


6 hours ago



(Medical Xpress)—A new study by academics at The University of Nottingham looks at how patients respond to genetic testing for risk of coronary heart disease (CHD).



Researcher looks at public perceptions around newborn testing


Apr 17, 2014



While 94 per cent of Canadians surveyed said they would participate in public health programs that screen newborns for a specific number of genetic conditions, only 80 per cent said they would be willing to participate in ...



Autism Genome Project delivers genetic discovery


Apr 24, 2014



A new study from investigators with the Autism Genome Project, the world's largest research project on identifying genes associated with risk for autism, has found that the comprehensive use of copy number variant (CNV) genetic ...



Recommended for you


Researchers gauge the toll of trampoline fractures on children


1 hour ago



Trampoline accidents sent an estimated 288,876 people, most of them children, to hospital emergency departments with broken bones from 2002 to 2011, at a cost of more than $400 million, according to an analysis by researchers ...



Estimating baby's size gets more precise


2 hours ago



New Michigan State University research aims to help doctors estimate the size of newborns with a new set of birth weight measurements based on birth records from across the country.





Nutriflow delivers fat to preemies


6 hours ago



(Medical Xpress)—Fat, the bane of many an adult, is precisely what babies born prematurely need to gain weight and grow strong and healthy. Some students at Rice University have invented a device to ensure ...



Urgent care centers must be made ready for kids: New AAP guidelines


14 hours ago



Today the American Academy of Pediatrics (AAP) issued an updated policy statement making recommendations and highlighting gaps in knowledge about the treatment of children in urgent care centers. Led by Gregory Conners, MD, ...



Researchers identify link between fetal growth and risk of stillbirth


Apr 22, 2014



Researchers from the University of Texas Medical Branch and the Stillbirth Collaborative Research Network have identified a link between stillbirth and either restricted or excessive fetal growth. Findings from the study ...





Bowel illnesses sometimes coincide in kids


Apr 21, 2014



(HealthDay)—Children suffering from irritable bowel syndrome are four times more likely than other kids to have a condition called celiac disease—an allergy to gluten—Italian researchers report.



User comments









Dr. Michael Rieder, Professor of Pediatrics, and Physiology and Pharmacology at Western University, led a study which concluded if patients are well-informed about gene-based drug dosing, they're far more accepting of genetic testing. Credit: Western University


A new study out of Western University (London, Canada) illustrates the need for a lot more education around pharmacogenetics (PGx) –the study of how a patient's genes can affect drug reaction and dosage. PGx promises to optimize patient response to therapy, but this is the first study to really investigate how patients perceive this kind of genetic testing, and whether those perceptions differ when it comes to parents and their children. The research, led by Dr. Michael Rieder of Western's Schulich School of Medicine & Dentistry is published in the journal Pediatrics.


"Pharmacogenetic testing has become widely used and gene-based drug dosing is becoming a reality for a number of common health problems. This study confirms what we suspected; Whether or not you're a parent, your degree of acceptability of was determined by your knowledge of it. That is to say –if you understand what the test is for, and the concept of gene-based drug dosing, you're far more open to it, than if you don't understand it," said Dr. Rieder, a professor in the Departments of Paediatrics, and Physiology and Pharmacology.


The researchers surveyed three groups including: 236 medical students representing those having greater educational exposure to PGx, 1,226 lay parents and 105 lay people without children. A second survey was completed by 229 parents. The surveys didn't use PGx but rather, asked about "DNA testing to guide therapy." The study concluded that the acceptability of PGx testing, either for oneself or one's child, seemed to depend on baseline PGx knowledge, but not on parenthood.


The main concern for all respondents was the need for informed consent. Other findings included:



  • More acceptance for PGx when the disease was severe

  • Strong desire/demand for separate consent for PGx testing

  • More education about PGx needed in medical schools

  • Acceptability of genetic testing didn't differ whether for the parent or the child


Dr. Rieder says PGx should take a lesson from pediatric oncology. He says health care workers in that division do a good job in the way they frame the discussions around care, treatment, and consent. "When they have to make a diagnosis, they spend a lot of time explaining what tests they're going to do, the risks, and what therapies are available. And they're successful. Their patients comply with treatment, they get involved in studies, they're informed, and they want to know what's going on."



Medical Xpress on facebook

Related Stories


Pharmacogenetics testing offers way to reduce deaths from drug toxicity


Apr 11, 2011



On average, a drug on the market works effectively for only 50% of the people who take it. Would you want to prevent a potential adverse drug effect or even toxicity through a simple test? It's not science fiction, but a ...



Parents don't fully understand biobank research, study finds


Jul 29, 2013



Researchers who collect genetic samples from children for medical research need to explain the process more clearly to parents, according to a new study that suggests many parents don't fully understand the finer details ...



Making sense of genetic testing for heart disease


6 hours ago



(Medical Xpress)—A new study by academics at The University of Nottingham looks at how patients respond to genetic testing for risk of coronary heart disease (CHD).



Researcher looks at public perceptions around newborn testing


Apr 17, 2014



While 94 per cent of Canadians surveyed said they would participate in public health programs that screen newborns for a specific number of genetic conditions, only 80 per cent said they would be willing to participate in ...



Autism Genome Project delivers genetic discovery


Apr 24, 2014



A new study from investigators with the Autism Genome Project, the world's largest research project on identifying genes associated with risk for autism, has found that the comprehensive use of copy number variant (CNV) genetic ...



Recommended for you


Researchers gauge the toll of trampoline fractures on children


1 hour ago



Trampoline accidents sent an estimated 288,876 people, most of them children, to hospital emergency departments with broken bones from 2002 to 2011, at a cost of more than $400 million, according to an analysis by researchers ...



Estimating baby's size gets more precise


2 hours ago



New Michigan State University research aims to help doctors estimate the size of newborns with a new set of birth weight measurements based on birth records from across the country.





Nutriflow delivers fat to preemies


6 hours ago



(Medical Xpress)—Fat, the bane of many an adult, is precisely what babies born prematurely need to gain weight and grow strong and healthy. Some students at Rice University have invented a device to ensure ...



Urgent care centers must be made ready for kids: New AAP guidelines


14 hours ago



Today the American Academy of Pediatrics (AAP) issued an updated policy statement making recommendations and highlighting gaps in knowledge about the treatment of children in urgent care centers. Led by Gregory Conners, MD, ...



Researchers identify link between fetal growth and risk of stillbirth


Apr 22, 2014



Researchers from the University of Texas Medical Branch and the Stillbirth Collaborative Research Network have identified a link between stillbirth and either restricted or excessive fetal growth. Findings from the study ...





Bowel illnesses sometimes coincide in kids


Apr 21, 2014



(HealthDay)—Children suffering from irritable bowel syndrome are four times more likely than other kids to have a condition called celiac disease—an allergy to gluten—Italian researchers report.



User comments








Categories:

0 comments:

Post a Comment