ipl-logo

Ethical And Social Issues In Nursing

1591 Words7 Pages
bulb-icon

Recommended: Nursing reflections on ethics

Badzek, Laurie, Mark Henaghan, Martha Turner, and Rita Monsen. "Ethical, Legal, and Social Issues in the Translation of Genomics into Health Care." Journal of Nursing Scholarship 45.1 (2013): 15-24. Web. 02 Mar. 2016. Genomic care in the health field is new science. With the new advancements in the medical field comes the legal side. In the article, the authors bring to light the issues of ethical, legal and social issues. Any health care professional will encounter tough situations where they will need to know the human rights over patient’s care. This article talks about the ethical, legal and social issues better than other articles found on the same topic. Though the article is not about becoming a nurse, it is part of being a genetic nurse and adapting to the ever-changing advancements in medicine.
Badzek, Laurie, RN, MS, JD, Martha Turner, Ph.D., RN, and Jean F. Jenkins, Ph.D., RN. "Genomics and Nursing Practice: Advancing the Nursing Profession." The Online Journal of Issues of Nursing 13.1 (2008): n. pag. Web. 08 Mar. 2016. Badzek, a nurse attorney and director of the ANA Center for Ethics and Human rights, Dr. Turner, a military …show more content…

Ann Maradieque writes in her article, A Resource Guide for Learning about Genetics, that teaching nurses are not equipped to teach other nurses about practicing with genetic involvement. She also implies the great need to integrate the knowledge into the practicing medical field. Dr. Maradieque also goes on to show resources for teaching medical professionals to be able to pass on the knowledge to practicing nursing students. Compared to other articles, Dr. Maradieque goes into more details on resources for programs, educators, and practicing nurses. When trying to become a genetic nurse, this article is relevant to do research in finding a program advanced enough to be able to adequately teach the genetic side of

Show More
Related
700 Words | 3 Pages

What are the specific issues raised in the book—legally and ethically? Think about the 1980s John Moore case: the appeal court decision and its reversal by the California Supreme Court.   Issues that raised in the book are race issues, the legality of taking adventage of patients who’s family aren’t able to fight for the rights and benefit of their cells. According to California supreme court, Under the duty to obtain informed consent, “a doctor must disclose his intent in using a patient for research and economic gain.” 6.

Read More
419 Words | 2 Pages

The court said doctors said researchers should disclose financial interests in patient tissues”(Skloot 205).

Read More
477 Words | 2 Pages

In August of 2013, Talha Khan Burki wrote “Righting a Long-standing Wrong for Henrietta Lacks” for Lancet Oncology. Burki’s purpose was to highlight the problem with the sequence data of patients’ cells (namely, Henrietta Lacks) being publicly released and to inform people of the privacy risks involved. Burki did a very good job at explaining what the issue was, what had been done about it and what needed to happen. Generally, readers struggle and become overwhelmed when they see a large sum of information all at one time. However, while this article provides the reader with several facts, it makes the reader think and Burki did a very well at writing in a manner that prior knowledge of certain terms or concepts are not critical to comprehending.

Read More
609 Words | 3 Pages

Henrietta Lacks was an African-American woman whose cells from her cancerous tumor led to many medical advances in the world. The cells led to the HeLa line, which have a crucial role in drug development and toxicity testing (Hunt). Prior to the HeLa line, it was proven impossible to grow human cells in a laboratory for any length of time. The conflict in this amazing discovery is that her cells were taken from her body for medical purposes without her permission. People argue that people have to be given legal ownership of their tissues and given money for them or medical advances made using the tissues.

Read More
249 Words | 1 Pages

Before I start my discussion, I would like to thank Henrietta Lacks for her cells even though they were taken without her consent and also thank the Lacks’ family for their patience in dealing with this issue of not being told about the use of the Henrietta’s cells. Neither Henrietta nor her family got recognition for them. This story tells us how far we have come in this day and age in terms of privacy information and what people can and cannot do because of HIPPA. It was common practice to use people’s information and cells without their consent.

Read More
936 Words | 4 Pages

The injustice of taking Henrietta’s cells and using them for research without her consent or of her family for that matter; until 20 years later is incomprehensible. Many believe that the history of medical ethics such as the Hippocratic Oath and complying the federal law in protecting human research and confidentiality wasn’t yet recognized. All the same, the Lacks’ family isn’t given credit or acknowledgement for what Henrietta, has contributed to science, known as the HeLa cell line. Henrietta’s

Read More
587 Words | 3 Pages

Paper 2 A person who owns a small portion of someone's genes may be the deciding factor on whether a person's illness is further researched or put on hold. Should a person be given this much power over our very genes inside us whose research could save lives and cure diseases? A physician, Michael Crichton, who wrote “Patenting Life” and a economist, John Calfee, who wrote “Decoding the Use of Gene Patents” both discuss this medicinal dilemma.

Read More
462 Words | 2 Pages

The origination of HeLa cells, used in biomedical research for a potential cure for cancer, had made many ground breaking discoveries in science; all thanks to one woman, Mrs. Henrietta Lacks. The history of Mrs. Lacks’s contribution to these studies raised many ethical issues concerning healthcare practice. In the short film, The Way of All Flesh, we learn how these cells were revealed by direct violation of ethical principles. During the 1950s, matters regarding informed consent practices were in their beginning stages of implementation.

Read More
724 Words | 3 Pages

“The Immortal Life of Henrietta Lacks” by Rebecca Skloot is about an African American woman who had her cells taken without any consent from her or her family to benefit the medical and science field. The Lacks family had no idea about Henrietta’s cells were alive and tested on for all kind of experiments. Henrietta’s case and other similar cases brought up an issue of who has the ownership of the tissue: the patient or the researcher? This issue became serious when researchers and scientists started making profits and having it patented. The argument against giving people legal ownership of their tissues is that everyone benefits from the research.

Read More
142 Words | 1 Pages

Ever since the Tuskegee Syphilis Experiment and other similar experiments that include human subjects, the issues on patient privacy and informed consent were the central issues, which led to the three basic ethical principles as outlined in the Belmont Report. According to the report, the principles of respect of person, beneficence, and justice are the general judgement we apply as justification for ethical prescriptions and evaluations of human actions.1 Therefore, all students, researches, or healthcare professionals have to abide by these principles even though it is a difficult issue within healthcare informatics. The issue of confidentiality is very problematic indeed, especially when it relates to race/ethnicity.

Read More
1097 Words | 5 Pages

which will be discussed later. Abby Lippman, in her article “Prenatal Genetic Testing and Screeening: Constructing Needs and Reinforcing Inequalities” she also acknowledges this issue of autonomy through creation of her model of reproductive autonomy. In her framework, she believes that having access to a prenatal genetic screening is crucial to a woman’s reproductive autonomy or the ability to be better informed about reproductive choices that she, as a mother, can make (Lippman, 22). Similar to Botkin, Lippman’s autonomy based framework supports the access to prenatal testing. The implications of autonomy do not directly address the presence of governmental involvement in this issue, but patient autonomy does encourage the accessibility to

Read More
699 Words | 3 Pages

The practice of prenatal genetic testing, although becoming commonplace, has been put at the center of the abortion debate in the United States. Doctors should only perform prenatal genetic testing in rare cases and very sparingly in order to protect the lives of the unborn whose genome sequence may deviate from what is considered genetically ¨normal¨. Although ¨testing and abortion are not synonymous¨ (Rebouché and Rothenberg 993) these two have begun to form a clear connection in a world where abortion is now acceptable. While prenatal genetic testing makes improvements every year, there still is a risk of harming the unborn, yet living child. Not only can testing bring harm to the child, it may also lead to the parent´s terminating a

Read More
682 Words | 3 Pages

The science of eugenics began during the twentieth century by Franci Galton, who coined the idea that favorable and unfavorable characteristics in humans were hereditary. The desirable traits were seen to be prominent in the superior classes thus, sterilizing those with inferior traits to prevent them from spoiling the chances of the master race. This master race consisted of those with high intelligence, fair skin tones, desirable physical characteristics, and not a descendent of a minority race. This form of segregation divided people with race, intelligence, physical characteristics, and class. People of with disabilities, lower financial classes, and immigrants to the United States were sterilized for permanent birth control, and sometimes without their consent or knowledge.

Read More
473 Words | 2 Pages

Genetic counseling is a rapidly growing field as more patients seek advice on how to interpret genetic test results. A personalized medicine focus specialist who provides genetic counseling would need to have a deep understanding of genetics and the ability to explain complex concepts to patients. “Personalized medicine is an emerging practice of medicine that uses an individual's genetic profile to guide decisions made regarding the prevention, diagnosis, and treatment of disease. Knowledge of a patient's genetic profile can help doctors select the proper medication or therapy and administer it using the proper dose or regimen. Personalized medicine is being advanced through data from the Human Genome Project” (Personalized

Read More
957 Words | 4 Pages

There are ethical challenges as the technology develops, such as the autonomous machines may supersede humans and threaten human existence, and new DNA-based treatment might be the trigger of privacy problems. First, ethics is the philosophical study that deals with what is morally right and wrong in wide scale not only in the scientific field, but also in public, and ethical problems occur as the new technology emerges. Emerging technology includes new technologies and technologies that are starting to be used. For instance, fuel-cell vehicles, artificial intelligence the digital genome, and robots are the emerging technologies. (Al-Rodhan 2).

Read More

More about Ethical And Social Issues In Nursing

Related Topics

Open Document