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Compare and contrast utilitarianism, deontology and consequentialism
Compare and contrast utilitarianism, deontology and consequentialism
The malpractice mess summary
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Henrietta Lacks
The end justifies the means. This proverb has been used countless times to elucidate morally bankrupt decisions that achieve positively correct outcomes. In health care, this could not be truer with the Henrietta Lacks case. Henrietta Lacks was an African American woman who died from cervical cancer in 1951 at the age of 31. Unbeknownst to her, two specimens from her cervix were obtained by her doctors at John Hopkins Hospital. At some point, her cells caught the attention of researchers due to their unique survivability. Her cells were later used in countless experiments and transformed the medical world. These cells were instrumental in the development of the polio vaccine. The purpose of this paper is to discuss the ethical violations that may have occurred against Henrietta Lacks and if the end, in this case, justifies the means (Biography.com editors, 2017).
In the mid-1900s, laws regarding medical informed consent were nonexistent. This allowed for Henrietta’s cells to be taken and used without consequence. Mrs. Lacks nor her family had knowledge of the usage of her cells. Even after
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informed consent became law there were no efforts made to obtain a consent. Once medical informed consent was enacted the illegal usage of her cells continued. The Lacks family had no acknowledgment in scientific papers and no financial compensation. Without consequence, the medical community benefited from her stolen cells. Ethically speaking, the argument for Mrs.
Lacks case could be based on utilitarianism or consequentialism ideologies. Utilitarianism is based on the principle of the greater good of the majority people. The fact that a vaccine for polio came from the usage of her cells is evidence of this. However, one cannot deny the disservice done to the Lacks family. The medical research community is hiding behind the ethical arguments like utilitarianism whilst violating its primary consequence that stealing is wrong. Stealing is defined as the illegal act of taking a person’s property without that person given consent at will (Library of Congress Cataloging in Publication Data, 1982). Mrs. Lacks clearly did not give her consent nor did her family. Once established, informed consent still was not attempted. This is for all attempts and purposes theft (Butts & Rich,
2016). In conclusion, some may argue the good that came from the usage of Mrs. Lack’s cells far outweigh the damage that occurred. The medical research community has used ethical theories such as utilitarianism to explain away violations towards the Lacks family. By denying informed consent once establish, the Lacks rights were violated. John Hopkins Hospital has claimed no financial gain from the usage, thereby, repudiating any claims of responsibility. Its failure to attempt informed consent, compensate financially, or recognize the Lacks in medical research papers is a violation of the basic concept of utilitarianism which is not to steal. Failure to make right these violations can lead to further distrust of the African American community towards the medical field. True, great things came from the use of her cells. The end, however, does not merit the disservice and distrust that arose with it.
In this paper, I will analyze Rebecca Skloot’s book, The Immortal Life of Henrietta Lacks, concentrating on Henrietta Lacks’ life, as well as ethical controversies and sociological impact surrounding the HeLa cells. First, I will discuss the author’s main arguments and the type of evidence used throughout the paper. Then, I will summarize the life of Henrietta Lacks focusing on her diagnosis and treatment up to her death. After, I will describe the ethical debates that the author presented and how they relate to Henrietta Lacks and the HeLa cells. Finally, I will examine the impact HeLa cells have had on the society, specifically regarding the medical community, as well as the effect HeLa cells had on Henrietta’s family.
In the year 1951, Henrietta Lacks had her cells taken, for scientific research, without her knowledge. Henrietta Lacks was
An abstraction can be defined as something that only exists as an idea. People are considered abstractions when they are dehumanized, forgotten about, or segregated and discriminated against. The scientific community and the media treated Henrietta Lacks and her family as abstractions in several ways including; forgetting the person behind HeLa cells, giving sub-par health care compared to Caucasians, and not giving reparations to the Lacks family. On the other hand, Rebecca Skloot offers a different perspective that is shown throughout the book. Rebecca Skloot’s book The Immortal Life of Henrietta Lacks describes the trials and tribulations the Lacks family has gone through because of HeLa cells and shows how seeing a person as an abstraction is a dangerous thing.
All I can say is amazing information of your glorious and late Henrietta Lacks. This incedible women bettered our society in ways no common human could understand at the time because of how complex this matter was and still very much indeed is. I know there is much contraversy with the matter of how scientists achived immortal cells from your late relative, and I do strongly agree with the fact that it was wrong for these researches to take advantage of this incredible women, but I know it is not for me to say nonethless it must be said that even though it was wrong to take Lacks’ cells when she was dying sometimes one must suffer to bring joy to the entire world.
In the novel The Immoral Life of Henrietta Lacks by Rebecca Skloot, the author tells the miraculous story of one woman’s amazing contribution to science. Henrietta Lacks unknowingly provides scientists with a biopsy capable of reproducing cells at a tremendusly fast pace. The story of Henrietta Lacks demonstrates how an individual’s rights can be effortlessly breached when it involves medical science and research. Although her cells have contributed to science in many miraculous ways, there is little known about the woman whose body they derived from. Skloot is a very gifted author whose essential writing technique divides the story into three parts so that she, Henrietta
....S. Public Health Service advanced medical technology, it came at a high cost. A high cost that resulted in many African-Americans dead and a breach of trust for medical professionals. In the notable experiments of Henrietta Lacks, The Tuskegee Syphilis Men, and The Pellagra Incident, medical professions in no way protected the lives of these individuals. In fact, they used the medical advances discovered as a result of the human experimentations as a shield to mask the unethical decisions. Medical professionals targeted the African-American population and used their ignorance as a means to advance medical technologies. This in no way upholds the ethics that medical professionals should display. The Immortal Life of Henrietta Lacks vividly exhibits the how the United States Public Health Service used, abused, and ultimately destroyed the African-American community.
At the time the tissue samples were collected from Henrietta Lacks she was an individual capable of deliberation about personal goals and of acting under the direction of such deliberation (Belmont Report, 1979). By collecting the samples without Henrietta’s sufficient consent she was denied of her freedom of choice. She was not given the opportunity for her decisions
To have something stolen from you is devastating and can change your life. But what if what was taken from you will save billions of human lives? In the book The Immortal Life of Henrietta Lacks by Rebecca Skloot, we see a woman named Henrietta had a biopsy of a cancerous tumor, and the cells from the tumor were able to live and grow outside of her body; and even better, the cells go on to find the cure for diseases such as polio. The catch is this: she signed a document giving her hospital permission to perform any medical procedure they find necessary to help her treatment, but she never gave specific permission for the cells in that biopsy to be tested and cultured. Now the big debate is over whether or not it was legal for her doctors
Although she was taken from the world too soon, Henrietta Lacks was a warm hearted woman, and though unbeknownst to her, she would pave the way for the medical field and greatly expand our understanding of one of the nation’s greatest killers; cancer. In 1951 people did not talk about cancer lightly; cancer was a very touchy subject, especially for those who knew they couldn’t receive treatment once they had been diagnosed. When Lacks went to the hospital because of a “knot on her womb” she never thought that it would grow into a full fledge tumor that would end up taking her life. Henrietta lived a simple yet happy life which consisted of working on the farm, loving her husband, and raising children, and she was not going to ruin the lifestyle she knew so well by telling her family that she had cancer; it was just unheard of.
Rebecca Skloot’s novel, The Immortal Life of Henrietta Lacks, depicts the violation of medical ethics from the patient and researcher perspectives specifically when race, poverty, and lack of medical education are factors. The novel takes place in the southern United States in 1951. Henrietta Lacks is born in a poor rural town, Clover, but eventually moves to urban Turner Station. She was diagnosed and treated for cervical cancer at Johns Hopkins hospital where cells was unknowingly taken from her and used for scientific research. Rebecca Skloot describes this when she writes, “But first—though no one had told Henrietta that TeLinde was collecting sample or asked she wanted to be a donor—Wharton picked up a sharp knife and shaved two dime-sized pieces of tissue from Henrietta's cervix: one from her tumor, and one from the healthy cervical tissue nearby. Then he placed the samples in a glass dish” (33). The simple act of taking cells, which the physicians did not even think twice about, caused decades
She died in 1951, and yet she is still alive. Literally, Henrietta Lacks has been unwittingly immortalized through her cells (HeLa) which have multiplied in laboratories throughout the world. The 2010 bestseller The Immortal Life of Henrietta Lacks also breathed life to the controversy surrounding her cells: should the Lacks family receive monetary compensation for HeLa’s immense contribution to science and medicine? That answer is a resolute no.
“Ah, the creative process is the same secret in science as it is in art,” said Josef Mengele, comparing science to an art. He was less of an artist and more of a curious, debatably crazy, doctor. He was a scientist in Nazi Germany. In general, there was a history of injustice in the world targeting a certain race. When Mengele was around, there were very few medical regulations, so no consent had to be given for doctors to take patients’ cells and other tests done on the patients’ bodies without their consent. This was the same time that Henrietta Lacks lived. Henrietta Lacks was an African American woman who went to the doctor because she had cervical cancer. Her cells were taken and are still alive in culture today (Skloot 41). Hence, her cells were nicknamed Immortal (Skloot 41). Although many, at the time, saw no issue with using a patient without consent issue with what?, on numerous occasions since then courts have determined that having consent is necessary for taking any cells. The story of Henrietta lacks is has similarities to an episode of Law and Order titled Immortal, which is an ethical conundrum. Despite this, the shows are not exactly the same and show differences between them. Both of these stories, one supposedly fictional, can also be compared to the injustices performed by Josef Mengele in Nazi Germany.
The story about Henrietta Lacks is the evidence that the ethics of medical processes need to be improved. For a long time, many patients have been victims of malpractice. Sometimes, the doctors still can do anything without the agreement from patients. Any medical institution needs to hold the integrity on any consent form that is signed by a patient. To summarize, the story of Henrietta Lacks could be the way to improve the standardization and equality of medical institutions in the future.
Henrietta Lacks was born on August 18, 1920 in Roanoke, Virginia. She stayed with her grandfather who also took care of her other cousins, one in particular whose name is David (Day) Lacks. As Henrietta grew up, she lived with both her Grandpa Tommy and Day and worked on his farm. Considering how Henrietta and Day were together from their childhood, it was no surprise that they started having kids and soon enough got married. As the years continued, Henrietta noticed that she kept feeling like there was a lump in her womb/cervix and discovered that there was a lump in her cervix. Soon enough, Henrietta went to Johns Hopkins Medical Center to get this check and learned that she had cervical cancer. But here is where the problem arises, Henrietta gave full consent for her cancer treatment at Hopkins, but she never gave consent for the extraction and use of her cells. During her first treatment TeLinde, the doctor treating Henrietta, removed 2 sample tissues: one from her tumor and one from healthy cervical tissue, and then proceeded to treat Henrietta, all the while no one knowing that Hopkins had obtained tissue samples from Henrietta without her consent. These samples were later handed to ...
What is privacy? Well, it’s the state or condition of being free from being observed or disturbed by other people. In terms of information, it is the right to have some control over how one’s own personal information is collected and used. This is a right that has been inherently protected by the U.S Constitution, agreed upon by the Supreme Court, and yet, issues around this very topic arise every day. In The Immortal Life of Henrietta Lacks, the author Rebecca Skloot, addresses this issue in her story of the women behind the infamous HeLa cells. Her story shows that although privacy is a right that is inherently protected by the law, situations of injustice can still occur. Examples of this in the book include when Henrietta’s cells were given to Dr. Gey without any consent from Day, the situation in which Mr. Golde’s spleen was sold without his permission, as well as when the Lacks family were recontacted and mislead about the reasons they were tested years after Henrietta’s death.