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How Did Henrietta Lacks Use Ethics In The Medical Field

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The topic and history of medical ethics has consistently been a strongly debated issue. With numerous case-specific situations concerning as well as qualifying the matter, perhaps one of the most influential and debatable stories may be that of Henrietta Lacks. With non consensual tissue samples taken, unauthorized distribution of her cells, and seemingly careless radiation treatment for cervical cancer, it might be fair to adjudicate that the lack of ethical practice was apparent and almost even fatal. In the case study of Sofia (“Ethics in The Medical Field: Sofia’s Case Study”), withholding seemingly necessary and vital information from a patient is in fact ethical. However, this might be one of the rarer cases in medical ethics. The …show more content…

Every doctor is allowed that fact; however, an excuse for lack of ethics is never the case. The amount of pure defiance of any ethical practice in the case of Henrietta, her cells, and her family is absurd and almost unrealistic. “There's no indication that Henrietta questioned [her doctor]; like most patients in the 1950s, she deferred to anything her doctors said. This was a time when “benevolent deception” was a common practice- doctors often withheld even the most fundamental information from their patients, sometimes not giving them any diagnosis at all. They believed it was best not to confuse or upset patients with frightening terms they might not understand, like cancer. Doctors knew best, and most patients didn't question that” (Skloot 63). Granted, the main distributors of the HeLa cells tried with all of their power to conceal the real identity of the cell’s owner; however their prevention to do so also prevented the Lacks family from knowing that Henrietta’s cells were still alive (Skloot …show more content…

“As a member of this profession, a physician must recognize responsibility to patients first and foremost, as well as to society, to other health professionals, and to self,” (“Principles of Medical Ethics”). These learned principles include compassion towards patients, respect, and equality involving health care. The treatment provided to Henrietta Lacks for her cancer was compassionless, the respect shown to the Lacks family after Henrietta’s death as they continued to distribute her cells was far from respectful, and the John Hopkins hospital, Henrietta’s hospital was not in the practice of equality at the time of this

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Henrietta Lacks was a poor black tobacco farmer,born in Roanoke, Virginia on August 1 ,1920.Henrietta’s mother died when Henrietta was very young, her dad did not wanted to take care of her and her siblings, so they were sent with different relatives. She grew up with her grandfather. Henrietta died at age of 31 years old of cervical cancer, on October 4, 1951. At the age of twenty-nine she felt a “knot” inside of her. In the year of 1950, she had a full-fledged tumor just three months  after she had felt the knot.

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Although many are unaware of it, scientific ethics have always been a major issue, especially in the United States. This was especially the case of Henrietta Lacks and her family through the early 1950s to present day. Henrietta Lacks hurried into John Hopkins Hospital in Baltimore, Maryland to find out why there was a lump on her cervix. When doctors diagnosed her with cervical cancer, she filled out a form giving consent to let the doctors perform any surgery they deemed necessary. Soon after Henrietta died in October of 1951, her husband, David (Day) Lacks, signed a consent form to let them perform an autopsy on her corpse.

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Participation Portfolio 1 Asst 3: Henrietta Lacks Discussion Questions   Please answers each of the following questions, and be prepared to discuss in class   1. Please outline the history of Henrietta Lacks 's tissue cells. Who did what with the cells, when, where and for what purpose? Who benefited, scientifically, medically, and monetarily?

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956 Words | 4 Pages

The Immortal Life of Henrietta Lacks is at once a biography, a work of science journalism, and a book about the interconnected topics of ethics, justice, and racism. Henrietta Lacks, an African-American woman who died from cervical cancer in 1951, was the source of the so-called HeLa cell line, which is “omnipresent” (Skloot, 2010, p. 24) in modern science. The HeLa cell line was derived from Henrietta Lacks’ cancerous tumor, which, against the wishes of Henrietta’s family was taken from her corpse and has been used for prolific and lucrative medical research for over seven decades (Skloot, 2010). Skloot (2010) described The Immortal Life of Henrietta Lacks as “a biography of both the cells and the woman they came from—someone’s daughter, wife, and mother” (pp. 25-26). While the HeLa cells are ubiquitous in research, the woman from whom they came is, at best, a footnote in biological or medical textbooks.

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Maybe figure out how to duplicate the cells and use it for other drugs that can help people heal better. All through this research and testing Henrietta was left in the dark she didn’t even know that the doctors removed a piece of her cervix for research purposes. She didn’t even receive credit for her cells until much much later. No one knew about the HeLa cells except for the doctors because they were trying to keep it a secret so their project wouldn’t get shutdown by not informing the patient that they’re using their cells. Some would say that the doctors did the right thing and kept the identity of the cells disclosed because later on it led to saving so many lives.

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Hence, the question is asked whether or not the HeLas cells belong to the family. From the Radiolab’s podcast “Henrietta Lacks”, the family members didn’t even know of these cells until a few decades after. Furthermore, they weren’t even able to understand the concept of Henrietta Lacks’ cells, and instead thought that there existed clones of Henrietta Lacks. The lack of informed consent is quite evident in this case, and the family member were experiencing emotional pains too as a result.

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In the 1950s the first ‘immortal’ human cells were grown from a cancerous tissue sample taken from Henrietta Lacks, a poor black woman, without her knowledge or consent. She had died shortly after, at the unfortunately early age of 31, of a severe case of cervical cancer. Henrietta had a list of ailments that included neurosyphilis, gonorrhea, and HPV the leading cause of her cervical cancer and, ultimately, her death. The hospital that had diagnosed her cancer, Johns Hopkins, had supposedly been one of the best hospitals in the country, but it participated in discriminatory and amoral research practices when treating African Americans. Not only taking taking Henrietta’s cells without her consent, but injecting them and other cancer cells into patients without their knowledge.

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Is it right for one's life to be manipulated for the use of scientific research or is it just a evasion on the person's privacy. Henrietta Lacks was a African American with cells that intrigued many people, she was diagnosed with cancer leaving her to be cared for at her local hospital, where she would later die due to the extremity of the illness. While at the hospital she was unaware that the doctors there were experimenting on her taking cell samples from her body, to help find a resolution to multiple diseases. The people who examined Henrietta manipulated her and the rest of her family to gain information on her cellular structure to be ahead of others looking to achieve the same objective. Henrietta Lacks cells should have never been evaluated because it's an evasion of her freedom, a danger to her personal health, and cause conflicts.

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But the pain didn’t go away until she went again and again and, “Henrietta told her doctors several times that she thought the cancer was spreading, that she could feel it moving through her, but they found nothing wrong with her.” (“The Immortal Life of Henrietta Lacks”, Chapter 8, Page 62 by Rebecca Skloot). She had a feeling that something was wrong with her because she felt a lot of pain in her vaginal area and it was not normal. The doctors knew that something was wrong but refused to tell her. “This was a time when ‘benevolent deception’ was a common practice- doctors often withheld even the most fundamental information from their patients, sometimes not giving them any diagnosis at all.

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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

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741 Words | 3 Pages

In this case study the primary nurse, Amelia Wilkerson, is caring for a patient, Katy Palmer who has recently been admitted to the hospital for fatigue and abnormal lab counts. The patient asks Amelia for information regarding her diagnosis. Amelia has seen Katy’s results and knows that she has been diagnosed with acute myelogenous leukemia. The ethical dilemma seen in this situation is that it is outside of the scope of practice for Amelia to discuss Katy’s original diagnosis with her.

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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.

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1416 Words | 6 Pages

One of the most fundamental trust relationships is between a patient and their doctor. Physicians have supposedly earned their trustworthy title because of their extended education and desire to help others. However, this perception is being shattered by physicians violating patients’ trust by not providing all the information needed for making a responsible decision for a person’s health and performing unimaginable procedures. “The Immortal Life of Henrietta Lacks” provides multiple examples of the unethical practice of doctors. When scientists do not recognize their subjects as human beings and their relationship results in an unbalanced power dynamic, their advantageous position often leads to the unethical treatments of subjects, especially

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512 Words | 3 Pages

The first ethical theory is Utilitarianism. Utilitarianism is based on actions that show right from wrong. In the story the Utilitarianism, is choosing which would benefit the most to the most people. This theory would conclude that it was the best choice to take Henrietta Lack’s cells and distribute them all over like they did in the story. The utilitarianism would benefit much more on the decision that the doctor made then a negative decision, which is based on consequences.

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In the case of Henrietta Lacks and her family, the mistreatment of doctors and lack of informed consent defined nearly 60 years of the family’s history. Henrietta Lacks and her children had little to no information about serious medical procedures and the use of Henrietta’s cells in research. Henrietta’s cells launched a multibillion-dollar industry without her consent and doctors even took advantage of her children’s lack of education to continue their research without questions: “[Doctor] did not explain why he was having someone draw blood from Deborah… he wrote a phone number and told her to use it for making more appointments to give more blood” (188). Deborah did not have the knowledge to understand the demands or requests the doctors made of her, and the doctors did not inform her explicitly.

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