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Patient education in health care
Patient education in health care
Patient education in health care
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Genetic Family History Assessment All nurses, no matter where they practice, need to have proper training in genomics and genetics to provide the best information to clients regarding recognition, prevention, and/or treatment of diseases (Thompson & Brooks, 2011). A genetic family history can help clients discover the unique patterns of health and illness within their family. In this paper, I will complete a Genetic/Genomic Nursing Assessment using the information found in Kaakinen, Coehlo, Steele, Tabacco, & Hanson’s text (2015) in Box 7-7 (p. 198), identify three generations of a family, analyze the genetic health risks, and consider nursing strategies for this family. The woman featured in my genetic assessment will be referred to as LG. Currently, LG takes medication for high cholesterol. She has been informed this is likely genetically inherited from her father and cannot be controlled with just diet and/or exercise. She goes yearly to her primary physician to manage this condition. She has one sibling with bipolar disorder and the other two do not have any medical problems. Her oldest brother and his family provided most of the hands-on care for their father a few years before he died and this has helped LG, her siblings, and all of the family members be more vigilant about staying healthy, eating well, exercising, and getting regular medical checkups. LG stated that her family stays well educated regarding their health and family history and if they have any questions about the genetic problems in the family, they will typically research the internet and follow up with their general Using nursing strategies that are unique for each family based on their individual genetic and genomic variations is fairly new in the area of nursing (Munro, 2014) and interventions for this family should be tailored to helping them keep up on current information about heart disease, diabetes, and cancer, which are the main medical issues in their family medical history, and having a plan that ensures they continue getting regular health checkups. In conclusion, it is important for nurses to have proper training and information in the area of genetics and genomics so that it can be used in daily clinical practice (Thompson & Brooks, 2011). Using this information with clients and conducting a detailed genetic nursing assessment is a valuable component of being an effective health care provider and can help clients recognize, prevent, and/or treat diseases that are unique to their particular
This week we were assigned to assess the Perez Family, this assessment was tailored towards exploring the family’s dynamic and our thoughts on how we as nurses could improve their developmental outcomes. The Perez’s have a three- generational family form, which consist of married twenty somethings, a young and growing family, and grandmother all living under one roof. This family is in multiple stages of development that further the stresses in their daily lives. Although the case study does not mention how long the “main characters” Maria and her husband Jamie have been married, because of their age it is safe to assume that they are newly married. Maria and Jamie have yet to lay a stable foundation (marriage) for themselves, yet alone their
Children with chronic illnesses live a lifestyle that changes, and different problems that arise, as the child passes through developmental changes up to adulthood. Using knowledge of child development a nurse can recognize regressions in the child’s development and put preventive strategies in place. Nurses can plan and implement therapeutic regimens such as given medicine. Young people with chronic illness and their families are faced with coping with the demands of chronic conditions on a daily basis. Nurses can assist parents with different coping strategies that can be used by parents to minimize impact of diagnosis. For instance, they can provide explanations to parents about diagnosis, and support, and encourage family.
In conclusion, genograms identify possible genetic predispositions in acquiring hereditary diseases. The author’s genogram allowed for the reflection of prominent family conditions and presented the opportunity for the author to educate herself on modifying behaviors that can reduce their risk for experiencing a stroke. Additionally, Gordon’s activity-exercise pattern and nutritional-metabolic pattern are applied to assess personal risks involved in a stroke. Through employing the nursing process and implementing Gordon’s functional healthh pattern to assess the elements of a stroke, the author was able create interventions to promote their own healthy lifestyle while symbiotically reducing their risks for suffering from a stroke.
The nursing profession is trusted to provide answers to their patients regarding questions of health, illness, and disease. Genetics often play a part in the overall wellness and health of particular individuals. The family health nurse should help family members understand the challenging aspects that genetic information will have on their own life, family structure, beliefs, and cultural norms (Daly, 2015, p. 550). This discussion post will explore a counseling scenario that involves a counseling session that will provide information and choices to a couple wishing to have children.
Nursing is a knowledge-based profession within the health care sector that focuses on the overall care of individuals. According to The American College of Nurse Practitioners (ACNP), “defines nurse practitioners as registered nursed who have received graduate-leveling nursing education and clinical training, which enables them to provide a wide range of preventative and acute health care services to individuals of all ages. They deliver high-quality, cost effective care, often performing physical examinations, ordering tests, making diagnoses, and prescribing and managing medication and therapies”. Nurse Practitioners are able to specialize in a particular area, such as family and adult practice, pediatrics, and women’s health; and refer patients to other specialist when necessary. Some Nurse practitioners work under the supervision of a physician; while others run their own practices.
The purpose of this paper is to promote the importance of a multi-generational health history, expose my family’s risk factors for illness and disease, and determine if that illness or disease presents a genetic component. I will also identify the family member that is most at risk for genetically transferred diseases in the pedigree, explain why, and recommend healthy practice for the patient. The relationship of genetics to health and prevention will also be addressed. (maybe tie in last sentence?)
A genetic family history assessment contains information about family structure and relationships. A typical nurse will use a three-generation family pedigree to gather the information. By doing so, nurses can be aware of which family members are at risk for disorders from a genetic component. Therefore, they can be provided with lifestyle advice, recommendations, and referrals to appropriate specialists (Kaakinen, Coehlo, Steele, Tabacco & Hanson, 2015). A genetic family history assessment will be provided about my family.
Collect as much information as you can on the history of chronic diseases on both sides of your family going back as least as far as your grandparents and preferably your great grandparents. Discuss how the presence or absence of certain chronic diseases in you family history influences your risk for these
The intent of this interview was discussed with the family, namely, how the data would be used to discuss family experiences for an assignment in Family and Societal Nursing for RNs at State University. Most importantly, I mentioned to the family that I hoped to provide them with interventions and support to...
Genetic testing has become a highly controversial issue among both the general population and the scientific community. It is a process that exposes a person’s entire genome sequence, allowing it to be read and evaluated to identify potential risks for genetic diseases or diseases that could be passed onto offspring (Holt Productions, 2012). With thousands of genetic tests already being used, and more being established, it seems logical to put this growing technology to use. Some agree that it is a person’s right to know and understand his or her genetic makeup. However, others argue that, despite the benefits of genetic testing, caution should be used to carefully inspect the risks associated with this new technology.
Cherry, B., & Jacob, S. R. (2011). Nursing: Issues, Trends & Management (5th ed., ). St. Louis, Mo.: Mosby/Elsevier.
Nurse Family Partnership presented at: University of Washington School of Nursing. Kazloric J, RN, Manager for NFP. November 6, 2013.
Colihan, Kelley. "High Blood Pressure Runs in Families." WebMD. WebMD, n.d. Web. 30 Apr. 2014
Genetics play an important part in the development of type 1 and type 2 diabetes. The most common of the two types of diabetes is type 2. Type 2 diabetes is being observed in the younger generation. It has becoming increasingly common in younger children, but the genes that are responsible for causing it are scarcely defined.("Genetic Factors in Type 2 Diabetes") What we do have well knowledge of is that the disease is a result of one gene mutating. In type 2 diabetes many genes are said to be involved in the developing of the disease, we just are not sure which gene it is that is being mutated.(1,4) However, the risk of having the disease is affected by your siblings or parents having it. Immediate relatives to individuals with type 2 diabetes are at higher risk of getting the condition rather than a person with no relative with diabetes. If the mother of the father has diabetes then the grandchild has a fifteen percent risk of having type 2 diabetes, but if both the father and the mother of the offspring have diabetes then the offspring's risk would increase by seventy-five percent chance of being affected with the condition. On the other hand, if the offspring were to have a sibling that was a non-identical twin with diabetes it would have a ten percent chance of being affected, but if it had an identical twin the risk would increase by ninety percent. Type 2 diabetes is known to run in families, but as to how it is inherited is not really specified. Scientists think that some environmental factors act as accelerators to diabetes, increasing the development. Some genes, known as susceptibility genes increases the risk of developing diabetes to individuals that carry the genes. ("Diabetes and Genetics") A way to find this gen...
Most people believe that biological factors play a huge role in members of a family becoming ill. We often think that our genetic makeup will ultimately lead our health down the same paths as earlier members of our families that have suffered from illnesses. While this concept may appear to be rather common, genetic factors show likelihood that the possibility is there, but not a certitude. In some cases of cardiovascular problems or cancer, having the genes create predispositions or proneness to a specific type of action; however, to say it would be without a doubt would be a fallacy.