Phyllis Young Only
Response #1
Rochelle, you have a great post. Mrs. Sloan is a sound mind and cognitively intact. She has the right to refuse and right to choose her treatment. She is a competent adult that can make decisions for herself and determine what shall be done with own body. As an advance practical nurse, we should have an excellent communication skills necessary to engender trust and draw patients into a partnership of care (Flaherty & Resnick, 2014). We have to ensure that Mrs. Sloan has a clear understanding about the advance directives and know the pros and cons of her decisions. Although all patients who require CPR have acute illness by virtue of needing CPR, there may be differences in the type or severity of the acute illness leading to CPR that could influence outcomes. I will emphasize to her the benefits or pros and cons that she might get from CPR. There are some patients that get terrified when we talk about advance directives or end-of-life care, so we have to make sure that we explained it right and not sound to be morbid. The value of the APN role extends beyond specialized and expanded knowledge, critical thinking, and evidence-based practice to enhanced communication skills that facilitate direct patient care through informed decision-making, patient and family education, and psychosocial-spiritual care (Yeager, 2014). Great post.
References:
Flaherty, E., & Resnick, B. (Eds.). (2014). Geriatric nursing review syllabus: A core curriculum in advanced practice geriatric nursing (4th ed.). New York, NY: American Geriatrics Society.
Yeager, K. (2014). The Role of Advanced Practice Nursing in Palliative Care. Retrieved from http://nursing.onclive.com/publications/oncology-nurse/2014/March-2014/The-Role-of-Advanced-Practice-Nursing-in-Palliative-Care#sthash.1eA6sARh.dpuf
Response #2
References:
Knox, P. (2010). Palliative Care Nurse Practitioners. Retrieved from http://nurse-practitioners-and-physician-assistants.advanceweb.com/features/articles/palliative-care-nurse-practitioners.aspx
Rabow, M. W., Hauser, J. M., & Adams, J. (2004). Supporting family caregivers at the end of life: "they don't know what they don't know". Jama, 291(4), 483-491.