United States. Department of Health, Education, and Welfare
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In March 1972 President Richard Nixon called for an "intensive study" and requested a plan for developing a "safe, fast, and efficient nationwide blood collection and distribution system." Nixon's request was the result of several independent events and initiatives throughout the late 1960s that focused on the U.S. lack of an efficient system for maintaining a sufficiently ample, risk-free national blood supply. The primary aim of the policy was to eliminate the nation's dependence on an oft-contaminated blood supply, with its associated public health problems, by developing an all-volunteer donation system, and thus improving the quality of the supply of blood and development of an appropriate ethical climate for increasing the use of human tissues for therapeutic medical purposes.
From the description of U.S. Department of Health Education and Welfare, national blood policy records, 1969-1981. (National Library of Medicine). WorldCat record id: 14337936
Beginning in 1932, the Public Health Service began a study of the effects of untreated syphilis on black men in Macon County, Alabama. On August 24, 1972 Merlin K. DuVal, M.D., Assistant Secretary for Health and Scientific Affairs in the Department of Health, Education, and Welfare, announced the appointment of an ad hoc panel headed by Broadus N. Butler, president of Dillard University, to investigate the study. The panel was empowered to explore whether the study was justified, whether it should be continued, and if existing H.E.W. regulations properly protected the rights of patients. The final report of the panel was delivered on April 28, 1973.
From the description of Documents on the origin and development of the Tuskegee syphilis study, 1921-1973. (National Library of Medicine). WorldCat record id: 14322373
In March 1972 President Richard Nixon called for an "intensive study" and requested a plan for developing a "safe, fast, and efficient nationwide blood collection and distribution system." Nixon's request was the result of several independent events and initiatives throughout the late 1960s that focused on the U.S. lack of an efficient system for maintaining a sufficiently ample, risk-free national blood supply.
American blood supplies depended heavily on "commercial" blood, that is, blood acquired by private blood banks that paid its donors. The result was a large instance of hepatitis in patients receiving blood transfusions (there was no screening test for hepatitis at this time), significant national blood supply shortages, an inefficient distribution system, and extremely high charges for blood for hospital patients. Scientists had long recognized the problems in the ad hoc, commercial-volunteer system of supplying and regulating the nation's blood supply.
The Policy outlined 10 principle goals: (1) need for an adequate blood supply for treatment and diagnostic needs, (2) attain the highest standards of blood transfusion therapy and research; (3) universal access to national blood supply for anyone in need, regardless of economic status; (4) efficient collection, processing, storage and utilization of blood supply; (5) assure ample donation; (6) support educational programs to assure most appropriate and safe use of the supply; (7) employ full regulatory authority and seek additional authority to assure adherence to highest standards of blood banking; (8) support research in the full spectrum of blood banking and therapy activities; (9) include benefit in health care insurance programs to assure universal access to blood and blood products to anyone in need; (10) made DHEW responsible for implementation of the policy. The primary aim of the policy was to eliminate the nation's dependence on an oft-contaminated blood supply, with its associated public health problems, by developing an all-volunteer donation system, and thus improving the quality of the supply of blood and development of an appropriate ethical climate for increasing the use of human tissues for therapeutic medical purposes.
From the guide to the U.S. Department of Health Education and Welfare, National Blood Policy Records, 1969-1981, (History of Medicine Division. National Library of Medicine)
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Subjects:
- African Americans
- Blood banks
- Government publicity
- Health policy
- Human Experimentation
- Public health
- Syphilis
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Places:
- United States (as recorded)
- United States (as recorded)
- United States (as recorded)
- Alabama (as recorded)
- United States (as recorded)
- United States (as recorded)
- United States (as recorded)