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INTRODUCTION
Over the past ten years, legislators and policy makers have also have paid great
attention to the important issues surrounding assisted suicide and end of life care. In
1997, for example, the U.S. Supreme Court affirmed that state legislatures may decide
whether or not to legalize physician assisted suicide. While the decision struck down a
patients right to receive physician-assisted suicide, the Supreme Court arguments
generated substantial interest in the care and treatment of patients at the end of life.
In response, several state legislatures began to explore ways in which to improve the care
of the seriously ill and dying patients. By early 1998, at least 20 states had established
commissions or task forces to examine end of life care issues. Most of the task forces
have focused on the themes that are highlighted in this report, including addressing
barriers to improving end-of-life care services, discussing factors associated with
physician-assisted suicide or encouraging better pain management by physicians.
The purpose of this bibliography is to provide information about the medical, ethical
and legal issues at the end of life. Since the issues surrounding end of life care are
complex, however, this bibliography is intended to serve as an introduction to the topic.
Toward this goal, this report summarizes and analyzes legislation on physician-assisted
suicide and barriers to effective pain relief. It also highlights the major policy
considerations that must be addressed in order to reach consensus on future strategies.
This report must be read in context with broader state health care reform and intractable
pain legislation, as well as important federal legislative and regulatory approaches that
affect medical practitioners and the prescription of controlled substances.
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