Preview

Medical Information Without Informed Consent

Good Essays
Open Document
Open Document
980 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Medical Information Without Informed Consent
Imagine your loved one has a life threatening disease and their cells were taken unbeknownst to them while in the hospital. Eventually the cells became one of the most groundbreaking findings in scientific history ; however your family member did not receive compensation or recognition. There are numerous cases similar to this where a patient was violated when a doctor takes cell's, body parts, or medical information without receiving consent. Although this is a violation of privacy others believe that consent should not be required for medical research because it could lead to a scientific breakthrough therefore it can be deemed as selfish if the person denies consent. However, the idea of patient approval does not discourage scientific discoveries, informed consent encourages awareness of a person’s medical portion of their life. Consequently informed consent should be mandatory because the patient should be able to ask questions about the study, have awareness of the benefits and risks of the research, and should be allowed to stop the use of their body at any given time.
The corruption of the Tuskegee Study and HeLa are primary illustrations of the importance of medical consent, in both situations patients were taken
…show more content…
Without her permission, doctors at John Hopkins Hospital took her cells without asking and they ultimately became one of the most revolutionary findings in the history of science. Skloot writes“... though no one asked if she wanted to be a donor - [Dr.] Wharton picked up a sharp knife and shaved two dime-sized pieces of tissue from Henrietta’s cervix… Henrietta’s were different: they reproduced an entire generation every twenty-four hours, and they never stopped.” (Skloot 33) Henrietta had no idea what was going on with her body when this occurred, but her cells were different thus

You May Also Find These Documents Helpful

  • Good Essays

    Now to elaborate on the legal aspects of this question; was it legally acceptable for the HeLa cells to be taken without Henrietta’s permission/knowledge and used for research and profit? From an excerpt from the Columbia Science and Law Technology Review it gives a similar case that was argued in the Supreme Court (circa 1980’s). In the following excerpt it will show the more than likely ruling to a HeLa case (had one taken place).…

    • 1198 Words
    • 5 Pages
    Good Essays
  • Good Essays

    The Tuskegee Syphilis Study began in 1932 in Tuskegee, Alabama. The case was created by the United States Public Health Service, the objective was to analyze the natural course of untreated latent syphilis. The disease was injected into roughly 400 African American men without their consent. The men were misled of the promise “special free treatment”. Instead the “treatment” were spinal taps done without anesthesia to evaluate the neurological effects of the disease. It was morally wrong to test these men without permission and mislead them to false hope of an antibiotic.…

    • 393 Words
    • 2 Pages
    Good Essays
  • Good Essays

    On February sixth, 1951 Henrietta Lacks, a black tobacco farmer from south Virginia, went to Johns Hopkins hospital to be treated for cervical cancer, she was treated by Dr. Lawrence Wharton Jr. He prepared her for her treatment and dilated her cervix, but before beginning the treatment he, without her permission, shaved two dime sized pieces of tissue one from her tumor and one from her healthy tissue then, he placed them in glass dishes. Those glass dishes were given to Dr. George Gey and his assistant, Mary Kubick, labeled them HeLa, because she combined the first two letters of Henrietta's first and last name. Dr. Gey, like many other scientist, had been trying to grow human cells outside of the body because it would help test the effects that medicine,…

    • 1646 Words
    • 7 Pages
    Good Essays
  • Good Essays

    Henrietta Lacks Critique

    • 743 Words
    • 3 Pages

    In conclusion, after reading half of the book The Immortal Life of Henrietta Lacks, I have learned a substantial amount about Henrietta Lacks and how her cells were taken without her permission. I have also been taught about what cells can do, and other facts about medical procedures in the mid 1900s; more than I would have known had I not read the…

    • 743 Words
    • 3 Pages
    Good Essays
  • Better Essays

    In the book The Immortal Life of Henrietta Lacks written by Rebecca Skloot, Skloot is a young white woman that becomes fascinated by Henrietta Lacks when she learns of her in a community college biology class. Henrietta Lacks was a young black woman who was never spoken of. She was diagnosed with cervical cancer at the age of thirty. When she received treatment for that cancer doctors unknowingly stole her cervical cells. These cells were named HeLa. In Skloots book she states, “Scientists had been trying to keep human cells alive in culture for decades, but they all eventually died. Henrietta’s were different: they reproduced an entire generation every twenty-four hours, and they never stopped. They…

    • 1069 Words
    • 5 Pages
    Better Essays
  • Good Essays

    Henrietta Lacks Analysis

    • 1228 Words
    • 5 Pages

    The chief injustice of this book was the lack of informed consent and repeated privacy violations. Henrietta Lacks, as a patient at John Hopkins Hospital, had not been informed that samples from her cervix had been collected, nor had she been asked if she was interested in being a donor (p. 33). No one bothered to explain to the Lacks family the science behind HeLa cells, and the so the family was never informed of the removal, distribution, or sale of Henrietta’s HeLa cells.…

    • 1228 Words
    • 5 Pages
    Good Essays
  • Good Essays

    Hopkins, its doctors, and researchers never thought about whether or not her cells were taken with consent or contacting her family. “ Years later, when I asked McKusick if anyone had tried to get informed consent from the Lacks family, he said, “I suspect there was no effort to explain anything in great detail.” But someone should have explained everything to them and made them aware of what was going on. Even after Henrietta’s cells were taken without consent the Lacks family deserved to know was happening with Henrietta’s cells. Susan Hsu who worked with McKusick later stated that she felt very bad because at the time no one thought that the Lacks family would not understand.…

    • 1329 Words
    • 6 Pages
    Good Essays
  • Good Essays

    “The Immortal Life of Henrietta Lacks” was written by Rebecca Skloot, to tell the story of Mrs. Lacks and her HeLa cells. Henrietta Lacks died of cervical cancer in 1951. A sample of her cancer cells was removed for research prior to her death. Her cells became the first to survive and multiply indefinitely in a lab. These cells have made many advances in medicine. However, the samples were taken without her permission or without her knowledge. The book covers five key ideas which include: racism, poverty, family, morals, and ethics.…

    • 701 Words
    • 3 Pages
    Good Essays
  • Good Essays

    She was forced to drive all the way to the hospital because it was the only one in the area who treated black patients. The hospital sometimes felt that because they were not receiving any compensation for their work, that they would just take samples from patients without their written consent. Henrietta’s case was one of these occurrences. The Lacks family was not even made aware of the cells until 20 years after her death and while others were making millions off them, the family saw none of the profits. They were denied access to information about the cells because of their race and because the hospital knew that what they were doing was…

    • 545 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    Essay On Henrietta Lacks

    • 2501 Words
    • 11 Pages

    Without asking or informing her, Henrietta’s doctors at John Hopkins took tissue samples from her cervix and attempted to grow them and keep them alive. After she died, these cells, known as HeLa cells, became essential to scientific research, contributing to developments like vaccines and other medical advancements. However because of their race and socio-economic status, Henrietta Lacks and the rest of the Lacks family were exploited by doctors, researchers, and the media. Rebecca Skloot’s book The Immortal Life of Henrietta Lacks explores these issues, without taking advantage of them…

    • 2501 Words
    • 11 Pages
    Powerful Essays
  • Satisfactory Essays

    This introduced one of the first ethical implications in this experiment which was withholding information to gain consent.The USPHS conducted a screening in search of infected participants. After they had chosen the few hundred men to be apart of the experiments they began to moved forward with the study. The doctors lured these men into the study by saying that they were ill and had "bad blood".It was never explained to them why they were really being chosen for this treatment. In order to ensure the interest of the blacks, they began performing noneffective treatments on them such as giving the mercurial ointment. Also, they even used African American health care workers to mislead patients into compliance. These men endured much pain and were enrolled in various treatments without their consent.The second ethical implication was the withholding of treatment. This was the worst charge that the researchers had committed. Even in (year) when penicillin had become the primary treatment for syphilis, this information was also withheld and men were prevented from getting treatment. Though Alabama passed a law in 1927 requiring the reporting and treatment of diseases, the USPHS failed to do so when it came to tending to these…

    • 467 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    In the 1950s doctors didn't have to ask for consent and the patients just did what their doctors told them to do no questions asked. The Immortal Life of Henrietta Lacks by Rebecca Skloot tells a true story about a 31 year old African American woman that had her cells taken by doctors without her consent and didn't get recognized for the contribution her cells made until later on when her family found out what the doctors had done.…

    • 917 Words
    • 3 Pages
    Good Essays
  • Good Essays

    fssa

    • 1755 Words
    • 6 Pages

    I agree. I think that the doctors should have told Henrietta’s family about that her cells right after they took them.…

    • 1755 Words
    • 6 Pages
    Good Essays
  • Better Essays

    The Tuskegee Syphilis Study was an ethical injustice of medical care. An ethical injustice of medical care is a violation of moral principles that apply values and…

    • 1079 Words
    • 5 Pages
    Better Essays
  • Good Essays

    Tuskegee Study Inhumane

    • 436 Words
    • 2 Pages

    Respect for persons means that researchers must obtain voluntary informed consent from participants in the study. Informed consent is achieved when participants are given accurate information about the potential risks and treatment options available. In addition, participants should be able to freely choose to begin or stop the study at any time.(1) The Tuskegee study did not fully disclose information to the participants. They told participants they were being treated for bad blood despite the fact that they were specifically studying the effects…

    • 436 Words
    • 2 Pages
    Good Essays