Doctors, hospitals and other care providers dispute that they should have access to the medical records and other health information of any patient citing that they need this information to provide the best possible treatment for proper planning. Insurers on the other hand claim they must have personal health information in order to properly process claims and pay for the care. They also insist that this will provide protection against fraud. Government authorities make the same arguments saying that in providing taxpayer-funded coverage to its citizens, it has the right to know what it is paying for and to protect against fraud and abuse. Researchers both medical and none nonmedical have the same argument saying that they need access to these information so as to improve the quality of care, conduct studies that will make healthcare more effective and produce new products and therapies (Easthope 2005).
All these arguments when analyzed are valid. This has brought about ethics issues that are involved with increased use and r...
... middle of paper ...
... lives (Richmond et al. 2009).
The state should take the responsibility of coming up with laws and regulations on access and use of gene information. The information should be under the custody of the federal government and it should be coded and encrypted for security reasons. Any one in need of this information should approach the federal agency responsible.
Easthope, G., 2005. Alternative Medicines. In: Germov, ed. An Introduction to Health Sociology. Melbourne :Oxford University Press, pp. 332-348.
Richmond, K. and Germov, J., 2009. Sociology of Health Promotion. In: Germov, ed. An Introduction to Health Sociology. Melbourne: Oxford University Press, pp. 476-499.
Willis, E., 2009. The Human Genome Project: A Sociology of Medical Technology. In: Germov, ed. An Introduction to Health Sociology. Melbourne :Oxford University Press, pp. 328-341.
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