Genetic testing has now created a whole new source of medical information for patients. This brings rise to an ethical, legal and social issue, in regards to patient confidentially. However, nurses must be familiar with the nature and the source of the genetic information, to ensure the patient privacy. For example, a woman tests positive for the BRCA1 gene that has been linked to breast cancer. She states to the nurse that she does not want to share this medical information with her sister, because they are not getting along. The ethical concern is that, her sister would have 1 in 2 chance of having the same gene. In this case the nurse does not have the authority to breach the patient confidentiality of the patient nurse relationship (Lea,
In today’s modern age science is moving at a rapid pace; one of those scientific fields that has taken the largest leaps is that of genetics. When genetics first comes to mind, many of us think of it as a type of science fiction, or a mystical dream. Yet genetics is here, it is real, and has numerous ethical implications.
A new trend lately is Buzzfeed quizzes that vary in category. You can take a quiz that tells you what celebrity you are most alike, who you should marry, and even what your occupation or college major should be. How these quizzes work are that you are asked a bunch of random questions that make you choose between colors, traits, hobbies and food. As if a color dictates if you should be a teacher or a lawyer. It’s ridiculous. But this isn’t just happening on Buzzfeed, it is also happening in our everyday lives. People are making lists of traits, colors, and hobbies; except the results won’t necessarily be for them. But for their child and their child has not even been conceived yet. Planning for a baby shouldn’t be as easy an online quiz. It shouldn’t be up to the parents to decide the genetic makeup of their unborn child.
Over 40 years ago, two men by the names of James Watson and Francis Crick discovered deoxyribonucleic acid, or DNA. DNA is hereditary material in humans and almost all other organisms (What is DNA?). From this finding, gene therapy evolved. Today, researchers are able to isolate certain specific genes, repair them, and use them to help cure diseases such as cystic fibrosis and hemophilia. However, as great as this sounds, there are numerous ethical and scientific issues that will arise because of religion and safety.
Gene testing is the practice of testing individuals who show no symptoms to determine whether they carry genes that could cause them or their children to develop certain genetic diseases later in life. Gene screening is a very controversial topic because of the risks that come with it. Would you want to know if you’ll develop a life threatening disease later in life? Many individuals would want to know this, but some would not. Personally, I think gene testing is ethical under certain conditions.
The history of harmful eugenic practices, spurring from the Nazi implementations of discrimination towards biologically inferior people has given eugenics a negative stigma (1,Kitcher, 190). Genetic testing, as Kitcher sees it through a minimalistic perspective, should be restrained to aiding future children with extremely low qualities of life (2,Kitcher, 190). He believes that genetic engineering should only be used to avoid disease and illness serving the role of creating a healthier human race. He promotes laissez-faire eugenics, a “hands off” concept that corresponds to three components of eugenic practice, discrimination, coercion and division of traits. It holds the underlying works of genetic testing, accurate information, open access, and freedom of choice. Laissez-faire eugenics promises to enhance reproductive freedom preventing early child death due to genetic disease (3,Kitcher, 198). However there are dangers in Laissez-faire that Kitcher wants to avoid. The first is the historical tendency of population control, eugenics can go from avoiding suffering, to catering to a set of social values that will cause the practice of genetics to become prejudiced, insensitive and superficial. The second is that prenatal testing will become limited to the upper class, leaving the lower class with fewer options, creating biologically driven social barriers. Furthermore the decay of disability support systems due to prenatal testing can lead to an increased pressure to eliminate those unfit for society (4,Kitcher, 214).
Gene therapy is a technique that uses genes to treat or prevent diseases. It is the process of taking DNA from one organism and inserting it to another. No development in the field of biotechnology has inspired both greater fear and hope in human society than gene therapy. Here is the big question among the people. While this new advancement in gene therapy promotes new hopes to cure life-threatening diseases or help the amputee or physically disabled persons to lead life like a normal human, it also raises questions about morality as well as the adverse effects it may cause in the future society. In our media intensive society, thousands of newspapers and magazines, tv talk shows resound with different points of view about the morality of gene therapy. Proponents of this medical treatment argue that it promises enormous benefits for medicine as well as agriculture and industry. Yet, it has aroused considerable public concern because it is perceived by many as an unpredictable technology.
There are several types of genetic tests that can give us a broad amount of information about ourselves, our parents and/or children (What is testing?). Personally, I see advantages and disadvantages to it. Anyone is able to find the probability of them having a disorder or disease and start dealing with before it gets to a lethal stage. For women, it is reassuring to know whether a disorder that they possess can be passed on to their children or not. They can also know whether their child is healthy or not before it is even born. It also impacts on how scientists deal with diseases since they are given a different output of the disease at its early stages and allows them to study it until a cure is found. But what happens when your private information goes public? People will be treated differently because of a high risk of having a cancer in the future. In your CV, your past experiences and your qualities will be accompanied by your genetics test results that inform the company whether you will be a risk to them in the future. A new kind of discrimination will be created in our society. A second major disadvantage to genetic testing is people using it for “superficial” purposes like changing children’s eye colors and other biological characteristics that should not be changes. Above the disadvantages are the benefits which are why I am all for the genetic testing for health-related purposes.
The healthcare industry has come a long way in terms of technological advances. These advances have had significant benefits in diagnosis, treatment, and the way medicine is practiced today. Unfortunately, these technological advances also come with ethical issues and dilemmas the healthcare professionals must face.
It is patients’ right to opt for genetic testing on their own DNA, although they are accepting a great risk by doing so. DNA is unique to each individual, present in each individual since conception, and influences who each individual is, so the information contained within it belongs to each patient, despite the risks. Such risks include DNA testing services providing results to potential employers or insurers, who can make decisions at the disadvantage of the patients if high disease probabilities are discovered. The results can also cause patients to react emotionally poorly and make negative changes to their lifestyles. Although risky, patients deserve the rights to take these risks if they choose to do so.
In today’s world, people are learning a great deal in the rapidly growing and developing fields of science and technology. Almost each day, an individual can see or hear about new discoveries and advances in these fields of study. One science that is rapidly progressing is genetic testing; a valuable science that promotes prevention efforts for genetically susceptible people and provides new strategies for disease management. Unnaturally, and morally wrong, genetic testing is a controversial science that manipulates human ethics. Although genetic testing has enormous advantages, the uncertainties of genetic testing will depreciate our quality of life, and thereby result in psychological burden, discrimination, and abortion.
The Human Genome Project is the largest scientific endeavor undertaken since the Manhattan Project, and, as with the Manhattan Project, the completion of the Human Genome Project has brought to surface many moral and ethical issues concerning the use of the knowledge gained from the project. Although genetic tests for certain diseases have been available for 15 years (Ridley, 1999), the completion of the Human Genome Project will certainly lead to an exponential increase in the number of genetic tests available. Therefore, before genetic testing becomes a routine part of a visit to a doctor's office, the two main questions at the heart of the controversy surrounding genetic testing must be addressed: When should genetic testing be used? And who should have access to the results of genetic tests? As I intend to show, genetic tests should only be used for treatable diseases, and individuals should have the freedom to decide who has access to their test results.
Genetic testing has become very popular as technology has improved, and has opened many doors in the scientific community. Genetic testing first started in 1866 by a scientist known as, Gregor Mendel, when he published his work on pea plants. The rest was history after his eyes opening experiments on pea plants. However, like any other scientific discovery, it bought conflicts which caused major controversies and a large population disagreed with the concept of playing with the genetic codes of human beings. Playing God was the main argument that people argument that people had against genetics. genetic testing became one of the major conflicts conflicts to talk about, due to the fact that parents could now have the option of deciding if they
The Problem Genetic engineering has been around since the 1960’s, although major experiments have not been really noticed until the 1990’s. Science comes in different forms, the two major being cloning and genetic reconstruction. Cloning is the duplicating of one organism and making an exact copy. For example, in 1996 the creation of the clone sheep named Dolly, the first mammal to be cloned, which was a great achievement. The other form, genetic reconstruction, is used to replace genes within humans to help or enhance the life of an unborn child for a medical reason or just for the preference of a parent.
Genetic testing is a type of medical test that identifies the changes in chromosomes, genes, or proteins. The results of a genetic test can confirm or rule out a genetic condition and if it can be passed on. I feel that genetic testing’s pros outweigh the cons. The physical risks of the genetic testing are very small. A positive result of genetic testing can help a person maintain prevention, and treatment options. Some test results can also help people make decisions about having children. Newborn genetic screenings can help identify genetic disorders early in life so treatment can be started as early as possible so that the unwanted gene will not pass on.
Due to the fact that the field of biotechnology is very serious and potentially dangerous, rules must be set down in order to keep the research in check. The high risk research of genetic therapy needs guidelines that have to be followed in order to keep the study just. The articles that are discussed in this essay focus on ethical issues and ideas that should be followed in the field in order to keep research safe and valid.