NIH stresses importance of genomics in nursing care in medical literature

Published on February 1, 2013 at 8:17 AM · No Comments

On April 14, 2003 a map of the human genome was completed, ushering in a new era of genetics in medicine with applications that include genetic testing; newborn screening; susceptibility to diseases such as cancer, cardiovascular disease, or psychiatric conditions; screening, diagnosis and monitoring of disease; and treatment planning. A special Genomics Issue, including an evidence review by researchers from the National Institutes of Health (NIH), published by Wiley in the Journal of Nursing Scholarship on behalf of the Honor Society of Nursing, Sigma Theta Tau International, addresses these genetic applications that are essential to advancing nursing knowledge and patient care.

"With nurses at the forefront of clinical care, their understanding of genomics and genetic applications is important to enhancing healthcare and improving patient outcomes," said Editor-in-Chief of the Journal of Nursing Scholarship, Susan Gennaro RN, DSN, FAAN, Dean and Professor at the William F. Connell School of Nursing at Boston College in Chestnut Hill, Mass. "Our editorial objective is to publish articles that are most useful to our nursing readership and genetics and genomics studies are some of the most widely read articles in the journal. I am pleased to have NIH authors contribute to the Genomics Issue which will assist nurses on the frontlines of patient care."

In response, this Genomics Issue highlights evidence that bridges genetics and nursing in order to educate nurses around the world who play an important role in improving patient care. For example, Dr. Deborah MacDonald, formerly with the Division of Clinical Cancer Genetics at the City of Hope Comprehensive Cancer Center in Duarte, Calif and now with the NIH in Bethesda, Md., details how nurses can impact cancer patient care with awareness of the underlying genomic factors involved in the development of malignancies.

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