Henrietta Lacks Ethics

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The Immortal Life of Henrietta Lacks is a non-fictional novel dedicated to describing the life and experiences of a woman by the name of Henrietta Lacks who’s cervical cells became famous for a multitude of reasons. Henrietta was an African American woman born in the 1920’s who developed an aggressive form of cervical cancer and was treated by doctors at Johns Hopkins Hospital. Her infamous story began when doctors began treating Henrietta with radium and took tissue samples from her cervix without her knowing. Cancer researchers began testing Henrietta’s cells (labeled HeLa) and found that they, unlike many other human cells, multiplied at rapid rates and almost seemed to be “immortal” or never-ending. These cells were shared, sold, and researched …show more content…

Those who were affected by the testing in hospitals, prisons, and mental health institutions were the patients/inmates as well as their families, Henrietta Lacks, the doctors performing the research and procedures, the actual institutions in which research was being held, and the human/health sciences field as a whole. Many ethical principles can be applied to these dilemmas: Reliance on Scientific Knowledge (1.01), Boundaries of Competence (1.02), Integrity (1.04), Professional and Scientific Relationships (1.05), Exploitative Relationships (1.07, a), Responsibility (2.02), Rights and Prerogatives of Clients (2.05), Maintaining Confidentiality (2.06), Maintaining Records (2.07), Disclosures (2.08), Treatment/Intervention Efficacy (2.09), Involving Clients in Planning and Consent (4.02), Promoting an Ethical Culture (7.01), Ethical Violations by Others and Risk of Harm (7.02), Avoiding False or Deceptive Statements (8.01), Conforming with Laws and Regulations (9.01), Characteristics of Responsible Research (9.02), Informed Consent (9.03), and Using Confidential Information for Didactic or Instructive Purposes (9.04), and Debriefing (9.05). These particular dilemmas were not really handled until much later when laws were passed that regulated the way human subjects could be used for research. Patients …show more content…

Although the cells originated from Henrietta Lack, the family was never informed that her cells were taken and being used all over the world for research, nor would they ever realize how much money those cells were generating. Major corporations were mass producing and replicating HeLa cells for many different purposes and articles were being published revealing the importance of the cells, all while the Lacks family were kept in the dark. The HeLa factory was created in Tuskegee to find a polio vaccination and experiments were taking place by mixing the cells with blood from volunteers. At this point in time, the cells were being sent to anyone willing to buy them and a multibillion dollar industry emerged (p. 101). Johns Hopkins Hospital also reaped the befits of HeLa. Although they gave away cells willingly, they were the birthplace of Henrietta’s cells and made lots of money from them. Throughout the duration of their lives, the Lacks family never received any monetary compensation for the use of their family member’s cells and were unable to even afford health insurance (p. 168). The ethical standards that apply to this dilemma are: Integrity (1.04), Exploitative Relationships (1.07, a), Contracts, Fees, and Financial Arrangements (2.12), Accuracy in Billing Reports (2.13), Acknowledging

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