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Parental Consent for Bone Marrow Transplantation in the Case of Genetic Disorders
Authors:Cynthia A Prows  Gail C McCain
Institution:Cynthia A. Prows, MSN, RN, is a Clinical Nurse Specialist, Divisions of Human Genetics and Patient Services, and Gail C. McCain, PhD, RN, is Assistant Vice President, Patient Services/Research, Children's Hospital Medical Center, Cincinnati, OH.
Abstract:purpose. To describe the responses of mothers and fathers who were offered bone marrow transplantation (BMT) for their children with genetic disorders

design.


design. Qualitative

setting.


setting. Private hospital rooms/offices

participants.


participants. Six mothers and 4 fathers of children with genetic disorders

results.


results. The basic social-psychological problem confronting the parents was the conflicting alternatives of life versus death for their children. It was certain that these children would die from their genetic disorders but without having to endure the pain and suffering of a BMT. The BMT would be difficult, possibly resulting in death, but with a chance of survival.

conclusions.


conclusions. Parents believed that BMT was the only chance of survival for their children, leaving them no choice except to pursue the BMT treatment
Keywords:Bone marrow transplantation  decision-making  genetic disorders  informed consent  parent perceptions
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