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Ethics of medical informed consent
Ethics of medical informed consent
Tuskegee Study of Untreated Blacks with Syphilis in Macon County, Alabama
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People Should not be Forced to Give Away Their Bodies
Question: Some of you may have read the book “The Immortal Life of Henrietta Lacks”. Lack’s cells were taken without her permission and used of research. Although most acknowledge that her cells should not have been used without her permission, Lack’s cells were unique because they were especially able to grow apart from her body. If our body parts can help with major medical advancements should we be forced to give them?
Henrietta Lacks, specifically her cells, have played a major role in a variety of medical breakthroughs. Unfortunately, for a period of time, Lacks did not know her cells were being used for major medical breakthroughs. Lacks’s cells were unique in a way that they
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were able to grow apart from the body; however, Lacks did not know her cells were special and did not give consent for her cells to be taken. Although Lacks cells were vital to medical advancement it was not correct for the doctors to take her cells without her knowing. Furthermore, even if our bodies can be used to help major medical advancements people should not be forced to give up their bodies. Argument 1 First of all Henrietta Lacks was denied the choice to make an autonomous decision.
Autonomy is the idea that “rational individuals should be permitted to be self-determining” (pg. 941). In other words, Henrietta Lacks, a rational individual, was not allowed to make a self-determining decision as to if the cells should be removed or not. People act autonomously when their actions are the result of their own choices and decisions. Patients should be able to make autonomous decisions regarding their actions, options, and outcomes. Another example of autonomy being violated is the Tuskegee Syphilis study. In the study “participants were led to believe they were receiving appropriate medical treatment when in fact such treatment was being actively withheld to study the effects of their disease” (pg. 943). In both Lack’s situation and the Tuskegee Syphilis Study, African-American participants were used and all participants were denied the opportunity to decide what happens to his or her body. However, autonomy is more than the freedom of making a decision, “there must be genuine options to choose among” (pg. 943). Overall, if a person does contain a vital part of major medical advancements such as Henrietta Lacks's cells, he or she should not be coerced into giving away his or her body. Since humans are rational individuals they should also be …show more content…
self-determining. Objection 1 Paternalism is a principle that is frequently used to justify the restriction of one's autonomy. Some may believe that paternalism is necessary in order to generate the best outcome possible. Specifically, the welfare principle says “it is justifiable to restrict individual autonomy if doing so will provide benefits to others” (pg. 946). In the case of Henrietta Lacks the welfare principle could be used to justify the removal of her cells. Without Henrietta Lacks’s cells, HeLa cells, a variety of major medical advancements would not have been possible. For example, due to HeLa cells, the Polio vaccine was invented. Therefore, by removing the HeLa cells others benefited through the use of new medicine. Reply 1 If a person is able to make justifiable decisions for him or herself regarding what actions are taken towards his or her body, then there is no need for the use of paternalism. People should be given the option to choose their actions even if their bodies have a special ability. In the end, patients should be given the option to decide what happens to his or her body. “To treat someone as if she lacks autonomy is this to treat her as less than a person” (pg. 40). Argument 2 Autonomy is closely related to informed consent. Furthermore, “The underlying idea of informed consent in both research and treatment is that people have a right to control what is done to their bodies. The notion of informed consent is thus a recognition of an individual's autonomy” (pg. 144). The informed part of informed consent is that the patients are knowledgeable about his or her treatment and is able to understand the procedure, outcome, and possible side effects. The consent part of informed consent is when a patient willingly agrees to have the procedure. Informed consent must not be coerced, “the person must of his or her ‘own free will’ agree to become a research subject” (pg. 148). Henrietta Lacks was not given the informed consent required to decide whether or not she was willing to give her cells. Her cells were taken without her knowledge going against her right to informed consent. In the end, any person who seeks medical treatment should be given informed consent that leads him or her to make an autonomous decision. Objection 2 Some may believe that it is more beneficial to find an outcome that creates the greatest good for the greatest number of people in the long run.
Some utilitarians might believe that it is beneficial to force people into giving their bodies as long as it benefits a majority of people in the long run. For example, some may believe that it was reasonable to take Lacks’s cells since they were vital to many medical breakthroughs. Furthermore, utilitarianism does not seem to require informed consent. In detail, “If more social food is to be gained by making people research subjects without securing their agreement, then this may be morally legitimate on some utilitarian accounts” (pg. 169). Overall some utilitarians may believe that as long as the outcome is beneficial to a majority of people then informed consent is not necessary.
Reply 2
However, the inhospital hospital shows that a utilitarian-based decision would not be beneficial in the long run. For example, if Joe is perfectly healthy besides a small stomach ache then a utilitarian doctor may find it beneficial to remove Joe’s body parts, killing him, in order to help the other patients who are seen as more valuable than Joe. If it is found that doctors continue to partake in this behavior it could lead to mistrust between the medical professionals and patients. People would fear their outcome may be similar to Joe's; therefore, more people will be hurt in the long run rather than helped.
Argument
3 According to Kant an individual capable of giving consent is one who is rational and autonomous. Unlike utilitarianism, Kant believes “the consequences of an action are morally irrelevant” (pg. 911). Instead, Kant relies on a different principle that he calls the categorical imperative. The categorical imperative states “act only on that maxim which you can will to be a universal law” (pg. 911). A maxim can be personal or subjective, but can also be thought of as candidates for moral rules. For Henrietta Lacks the maxim could be not to take from a person without his or her consent first. Proving that it is not right to take from others as a universal law. Kant’s Ethics can also be seen in a medical contest through four distinct features. One, it is always wrong to lie. Two, we must always treat people as ends never as means. Three, an action is correct when the categorical imperative is satisfied. Lastly, perfect duties are bases for claims that certain rights should be recognized (pg. 913). For Henrietta Lacks she was lied to, she was treated as a mean of an experiment, the experiment did not satisfy the categorical imperative, and her rights were not recognized. Patients should not be forced to give their body to science because it would be going against Kant Ethics and the categorical imperative. Overall, it is wrong to take from a person because would not want others to take from you. People should not be forced to give a part of their bodies, even if they have the capability to save others. Each patient should be given informed consent that allows him or her to make an autonomous choice. For the case of Henrietta Lacks she was not given the choice of whether or not to give her cells. Although Lacks’s cells have been a key role in a majority of medical advancements the way in which they were obtained was wrong.
The book The Immortal Life of Henrietta Lacks by Rebecca Skloot is the result of years of research done by Skloot on an African American woman with cervical cancer named Henrietta Lacks. Cells from Lacks’ tumor are taken and experimented on without her knowledge. These cells, known as HeLa cells, are the first immortal human cells ever grown. The topic of HeLa cells is at the center of abundant controversial debates. Despite the fact that her cells are regarded as, “one of the most important advancements in the last hundred years” (4), little is actually known about the woman behind the cells. Skloot sets out on a mission to change this fact and share the story of the woman from whom the cells originate and her family as they deal with the effects these cells have on them.
In the book, The Immortal Life of Henrietta Lacks, by Rebecca Skloot, the author highlights the scientific advances of HeLa cells, as well as the personal setbacks of Henrietta Lacks’ family. HeLa is a commonly used cell line in laboratories worldwide and is so often referred to as “the cell line that changed modern science”. This line of immortal cells has helped advance science in ways beyond compare. HeLa has allowed cell testing, cell cloning, and the discovery of various vaccines, including the HPV vaccine. While HeLa has done wonders in the medical field, it has caused unrepairable damage among the Lacks family.
Henrietta’s cells were being inaugurated with space travel, infused into rat cells, and even being used to make infertile hens fertile again. However, these are only a few of the many accomplishments that Henrietta’s immortal cells made possible: “The National Cancer Institute was using various cells, including HeLa, to screen more than thirty thousand chemicals and plant extracts, which would yield several of today’s most widely used and effective chemotherapy drugs, including Vincristine and Taxol,”(pg.139). This example of logos from the text again shows just how important these Henrietta’s cells were to the future developments in
Autonomy is a concept found in moral, political, and bioethical reasoning. Inside these connections, it is the limit of a sound individual to make an educated, unpressured decision. Patient autonomy can conflict with clinician autonomy and, in such a clash of values, it is not obvious which should prevail. (Lantos, Matlock & Wendler, 2011). In order to gain informed consent, a patient
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
In 1951, the sickness of a poor African American woman named Henrietta Lacks -also know as HeLa- would go on to change the face of scientific research; without her consent. Henrietta Lacks went into John Hopkins Hospital in hopes of medical treatment, but instead her cells were unlawfully stolen from her and used for scientific advances in the world of medicine for the creations of the polio vaccine, cell cloning, vitro fertilization, and gene mapping. Long after Henrietta's death, Henrietta's family was forced to live a life of poverty without medical insurance simply because they could not afford it although their mothers cells had yielded billions of dollars due to its advances in the medical world. The scientific community and the media
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
Your life, like many other has probably at some point been touched by Henrietta lacks and most likely you didn’t even know it.
Most people live in capitalist societies where money matters a lot. Essentially, ownership is also of significance since it decides to whom the money goes. In present days, human tissues matter in the scientific field. Rebecca Skloot, author of The Immortal Life of Henrietta Lacks, shows how Henrietta Lacks’s cells have been used well, and at the same time, how they have been a hot potato in science because of the problem of the ownership. This engages readers to try to answer the question, “Should legal ownership have to be given to people?” For that answer, yes. People should be given the rights to ownership over their tissues for patients to decide if they are willing to donate their tissues or not. Reasons will be explained as follows.
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 ...
Nowadays, when patients are given consent forms, every step is explicitly stated so that there is no confusion or harm. All in all, Henrietta Lacks has contributed and made significant changes to the scientific, ethical, and political aspects of society.
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.
A utilitarian would argue that organ donations save lives because when citizens continue to donate their organs, more lives are spared. Gregory Pence mentioned in his book titled “Classic Works in Medical Ethics” that three thousand Americans lose their lives while waiting for an organ transplant. Nevertheless, if organ donations become prevalent it would save or prolong some of the lives in America (Pense, 2007, 75). For example the risk of a kidney transplant ending in death or disabilities is three to ten thousand and in comparison to liposuction the risks are relatively the same (Pense, 2007, 62). A utilitarian would argue that people would rather help theirselves through liposuction instead of helping others. Other theorists such as Kant fail to realize the experience of donating an organ outweighs the potential harm to the donor (Pense, 2007, 62). Adult organ donations can be taken from people that have been recently deceased. This means that there is no physical harm or risk to the person donating the organ. Nonetheless, doctors using donated organs from the recently deceased to save many lives, would create good consequences for the organ recipient population. The chance of organ donations succeeding is greater than the negative outcome (Pense 2007, p ...