Has anyone ever heard of the Tuskegee Incident?

Question

It changed the standards of psychological research forever.

Answer 1

The Tuskegee Syphilis Study (1932–1972), also known as the Public Health Service Syphilis Study was a clinical study, conducted around Tuskegee, Alabama, where 399 (plus 200 control group without syphilis) poor -- and mostly illiterate -- African American sharecroppers became part of a study on the treatment and natural history of syphilis. This study became notorious because it was conducted without due care to its subjects, and led to major changes in how patients are protected in clinical studies. Individuals enrolled in the Tuskegee Syphilis Study did not give informed consent and were not informed of their diagnosis; instead they were told they had "bad blood" and could receive free treatment, a free ride to the clinic, one hot meal per day and in case of dying: $50 for the funeral.

By 1947, penicillin had become standard treatment for syphilis. Prior to this discovery, syphilis frequently led to a chronic, painful and fatal multisystem disease. Rather than treat all syphilitic subjects with penicillin and close the study, the Tuskegee scientists withheld penicillin or information about penicillin purely to continue to study how the disease spreads and kills. Participants were also prevented from accessing syphilis treatment programs that were available to other people in the area. The study continued until 1972, when a leak to the press -- rather than any ethical or moral consideration -- resulted in its termination. The Tuskegee Syphilis Study is often cited as one of the greatest ethical breaches of trust between physician and patients in the setting of a clinical study in the United States. The Tuskegee Syphilis Study led to the Belmont Report and establishment of National Human Investigation Board, and the requirement for establishment of Institutional Review Boards.

Contents [hide]
1 Study clinicians
2 Study details
3 Study termination and aftermath
4 Ethical implications
5 Dramatizations
6 References
6.1 Original Tuskegee Study Papers
6.2 Other
7 External links



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Study clinicians
Some of the Tuskegee Study Group clinicians. The third figure to the right is Dr. Reginald D. James, a black physician involved with public health work in Macon County, not directly involved in the study. Nurse Rivers is on the left.The study group was formed as part of the venereal disease section of the U.S. Public Health Service (PHS). The start of the Tuskegee Syphilis Study is most commonly attributed to Dr. Taliaferro Clark. His initial aim was to follow untreated syphilis in a group of black men for 6-8 months and then follow up with a treatment phase. Dr. Clark, however, agreed with the deceptive practices suggested by other study members. Clark retired the year after the study began.

Dr. Eugene Dibble was head of the John Andrew Hospital at the Tuskegee Institute.

Dr. Oliver C. Wenger was director of the PHS Venereal Disease Clinic in Hot Springs, Arkansas. He was an enthusiastic supporter of mass screening for syphilis and mass treatment programs in the black community. At various stages of the Tuskegee Syphilis Study, Wenger was attached to the Macon County activities, and he played a critical role in developing early study protocols. Wenger continued to advise and assist the Tuskegee Study when it turned into a long term, no-treatment observational study. He consistently supported a policy of concealing the aims of the study from the subjects - he feared that full disclosure would lead to their non-cooperation.

In 1932, Dr. Raymond H. Vonderlehr was the on-site director of the Tuskegee Syphilis Study. He conducted many of the initial physical exams and medical procedures. Vonderlehr developed the policies that shaped the next stage of the project. For example, he decided to gain the "consent" of the subjects for spinal taps (to look for signs of neurosyphilis) by depicting the diagnostic tests as a "special free treatment." Dr. Wenger subsequently congratulated him for his "flair for framing letters to ******." Vonderlehr retired as head of the venereal disease section in 1943.

Dr. John R. Heller, Dr. Vonderlehr's assistant, succeeded Vonderlehr as director of the venereal disease section of PHS. Heller's leadership coincided with the years when penicillin was introduced in other PHS clinics as routine treatment for syphilis, and when the Nuremberg Code was formulated (to protect the rights of research subjects). The study was brought to public attention in 1972; Heller defended the ethics of the study.

Nurse Eunice Rivers was an African American nurse who trained at Tuskegee and was recruited from the John Andrew Hospital when the study began. Dr. Vonderlehr became a strong advocate for her role. As the study became a constant fixture within the PHS, Nurse Rivers became the chief continuity person and was the only staff person to work with the study for all 40 years of its existence. By the 1950s, Nurse Rivers had become pivotal to the study—her personal knowledge of all the subjects allowed the very long follow up to be maintained.

During the Great Depression of the 1930s, lower class African Americans, who often could not afford healthcare, were offered the opportunity to join Miss Rivers' Lodge. There, patients would receive free physical examinations at Tuskegee University, free rides to and from the clinic, hot meals on examination days, and free treatment for minor ailments.

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Study details
The study was originally started as a study on the incidence of syphilis in the Macon County population. The subject would be studied for six to eight months, then treated with contemporary treatments (including Salvarsan, mercurial ointments and bismuth) which were somewhat effective, but quite toxic. The initial intentions of the study were to benefit public health in this poor population as evidenced by participation from the Tuskegee Institute, the Black university founded by Booker T. Washington. Its affiliated hospital lent the PHS its medical facilities for the study, and other predominantly black institutions as well as local black doctors also participated. The philanthropic Rosenwald Fund was to provide monies to pay for the eventual treatment. The study recruited 400 syphilitic Black men and 200 healthy Black men as controls.

The Tuskegee Study Group Letter inviting subjects to receive "special treatment", which was actually a diagnostic lumbar punctureThe first critical turning point in the Tuskegee Syphilis Study came in 1929 when the Stock Market Crash of 1929 led the Rosenwald Fund to withdraw its funding. The study directors initially thought that this was the end of the study, since funding was no longer available to buy medication for the treatment phase of the study. A final report was issued.

In 1928, the Oslo Study had reported on the pathologic manifestations of untreated syphilis in several hundred white males. This study was a retrospective study; investigators pieced together information from patients that had already contracted syphilis and had remained untreated for some time. The Tuskegee study group decided to salvage their study and keep going and perform a prospective study equivalent to the Oslo Study. This was not inherently wrong in itself; since there was nothing the investigators could do therapeutically, as long as they did not harm their subjects, they could study the natural history of the disease. This would be of benefit to humankind. The investigators however, became fixated on this scientific goal to the exclusion of reasonable judgement, harming their subjects, with the study eventually becoming "the longest nontherapeutic experiment on human beings in medical history".

Ethical consideration, poor from the start, rapidly deteriorated. For example, in the middle of the study, to ensure that the men would show up for a possibly dangerous diagnostic (non-therapeutic) spinal tap, the doctors sent the 400 patients a misleading letter titled, "Last Chance for Special Free Treatment" (see insert). The study also required all participants to undergo an autopsy after death—participants were never informed of this requirement. For many participants, treatment was intentionally denied. Many patients were lied to and given placebo treatments—in order to "observe" the fatal progression of the disease. In 1934, the first clinical data was published, with the first major report being released in 1936. It is important to note that this was not a secret study, with several papers published throughout the study.

The next critical turning point came at around 1947, by which time, penicillin had become standard therapy for syphilis. Several U.S. Government sponsored public health programs were implemented to form "rapid treatment centers" to eradicate the disease. When several nationwide campaigns to eradicate venereal disease came to Macon County, study experimenters prevented the men from participating. During World War II, 250 of the men registered for the draft and were consequently diagnosed and ordered to obtain treatment for syphilis, however then the PHS exempted them. The PHS representative at the time is quoted: "So far, we are keeping the known positive patients from getting treatment."

By the end of the study, only 74 of the test subjects were still alive. Twenty-eight of the men had died directly of syphilis, 100 were dead of related complications, 40 of their wives had been infected, and 19 of their children had been born with congenital syphilis.

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Study termination and aftermath
Peter Buxtun, a PHS venereal disease investigator, the "whistle-blower"In 1966, Peter Buxtun, a PHS venereal disease investigator in San Francisco, sent a letter to the director of the Division of Venereal Diseases to express his concerns about the morality of the experiment. The Center for Disease Control (CDC) reaffirmed the need to continue the study until completion (until all subjects had died and had been autopsied). To bolster its position, the CDC sought and gained support for the continuation of the study from the local chapters of the National Medical Association (representing African-American physicians) and the American Medical Association.

With his concerns rebuked, Peter Buxtun went to the press. The story broke first in the Washington Star on July 25, 1972, then became front page news in the New York Times the following day. As a result of public outcry, in 1972, an ad hoc advisory panel was appointed which determined the study was medically unjustified and ordered the termination of the study. As part of a settlement of a class action lawsuit subsequently filed by NAACP, 9 million dollars and the promise of free medical treatment was given to surviving participants and surviving family members who had been infected as a consequence of the study.

In 1974 the National Research Act became law, creating a commission to study and write regulations governing studies involving human participants.

On May 16, 1997, with five of the eight remaining survivors of the study attending the White House ceremony, President Bill Clinton formally apologized to Tuskegee study participants: "What was done cannot be undone, but we can end the silence...We can stop turning our heads away. We can look at you in the eye, and finally say, on behalf of the American people, what the United States government did was shameful and I am sorry."

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Ethical implications
The early ethics of the Tuskegee Syphilis Study may be considered in isolation at study inception. In 1932, treatments for syphilis were relatively ineffective and had severe side effects. It was known that syphilis was particularly prevalent in poor, black communities. The intention of the Study was in part to measure the prevalence of the disease, to study its natural history and the real effectiveness of treatment. Prevailing medical ethics at the time did not have the exacting standards for informed consent currently expected; doctors routinely withheld information about patients' condition from them. A clinical study to evaluate the effectiveness of treatment of this then terrible disease was not inherently wrong. However, this study exploited a vulnerable sub-population to answer a question which would have been of benefit to the whole population. This was, some argue, a manifestation of racism on the part of the study organizers.

However, with the development of an effective, simple treatment for syphilis (i.e. penicillin), and changing ethical standards, the ethical and moral judgements became absolutely indefensible. By the time the study had closed, hundreds of men had died from syphilis and many of their wives had become infected and their children born with congenital syphilis. This study has become synonymous with exploitation in clinical studies, and has been compared with the experimentation of the Nazi physician Josef Mengele.

Sociological studies have shown that the Tuskegee Syphilis Study has predisposed many African Americans to distrust medical and public health authorities. The Study is likely a significant factor in the low participation of African Americans in clinical trials and organ donation efforts and in the reluctance of many Black people to seek routine preventive care.

The aftershocks of this study led directly to the establishment of the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research and the National Research Act. This act requires the establishment of Institutional Review Boards (IRBs) at institutions receiving federal grants. Special consideration must be given to ethnic minorities and vulnerable groups in the design of clinical studies.

Answer 2

Tuskegee Incident

Answer 3

Are you referring to the the Tuskegee Syphilis Experience also know as the Tuskegee Incident?

This is where 400 african-Americans already infected were studies to track the development and effects of the disease but were denied treatment? Even though penicillin was available?

As I recall the study originated in 1932 but the infected individuals were selected after WWII, about 1947. The study didn't finally conclude until 1972.

Is this the topic you are asking about or was there a different "incident"?

Answer 4

I don't think it was psychological research. They found a cure for syphillis (penicillin) but did not offer the medicine to these black men. Yes, this incident helped create the standards for good clinical practice that researchers use with human subjects today.

Answer 5

You must be talking about the Tuskeegee Experiment. It was one of the most terrible incidents in history. It was a period of time where doctors were running an experiment with syphillis giving shots filled with that disease to Blacks.

Answer 6

Yes I've heard of it. Disgusting nazi-like racist abomination-pretending-to-be-an-experiment inflicted on black men. Pretended to be treatment but just followed the course of untreated syphillis until they died.

Answer 7

the distinction between being courageous and loopy is the reason you're doing what your doing. Being frightened of death and jumping off a cliff is loopy. Being frightened of death and scuffling with in a conflict you've faith in is brave.