Genetic Disease
It is very clear, that today's focus on genetic technology and its claim has been having some vital insinuations for healthcare at the present time and also in the future. Nurses need to recognize the position of assimilating new knowledge of genetics into their performances and be capable of helping patients to be able to manage with their genetic foundation of various diseases. Nurses likewise will need to know how to do things such as examine their own values, attitudes, and beliefs regarding hereditarily acquired diseases so as to deliver satisfactory and ethical nursing care to people from all over.
Interdisciplinary Team
The suitable members for an interdisciplinary team to get information for the first visit are a people such as the registered nurse because they would be the one that would have some kind of genetic knowledge, a genetic counselor, a high risk obstetrician likewise recognized as a Perinatologist primary care provider, and a then there would be the social worker.
Reasonable for Interdisciplinary Team
It is important to have a registered nurse that has some kind of genetic knowledge because it is really essential for the initial visit, it need to be a time to come and make some kind of initial valuation of the pregnant mother. The person that is considered to be the primary care provider understands the patient and their previous mental and physical well-being. The person that is the genetic counselor will be someone that has all of the educational background and training in regards to the hereditary and genetics illnesses. The Perinatologists is the one that is supposed to be caring for the mother in the course of her pregnancy and is devoted in pregnancies that are high risk. Now having the social worker is very key because the social worker is a person that is well-informed of the dissimilar organizations which are obtainable for support for the pregnant mother.
Type of Information
The kinds of information that would be anticipated from the registered nurse would involve a lot of things such as patient education, advocating for privacy and confidentiality, family history assessment, health and genetic assessment information, making sure the expectant parents have all of the informed health consent and choices, and the teaching of the difficult subjects that are involved. The primary care doctor is the one that will have the full confidence of the expectant parents and is the person that is the one that can speak with them in regards to the different choices obtainable to them and likewise have them referred for some kind genetic counseling if it is needed. The primary care is the one that will be able to accomplish a physical and psychosocial assessment. The people that are the genetic counselors can do things such as perform cultural, social, ancestry, and spiritual valuations; they can describe inheritance designs, suggest testing, deliver support and deliberate any emotional anxieties that have been brought up after the genetic testing results are talked about. The Perinatologist is able to complete new born and prenatal screenings. It is the job of the social worker who will be the one that will guide the both of the expectant parents with some kind of support groups and services that will be in the community accessible for them to reach.
Teaching Plan
The teaching plan for the Trosack family first visitation would involve things such as the treatment, prognosis, support groups, genetic diagnosis, and suitable recommendations and pregnancy material. The genetic analysis of Tay-Sachs disease is a disorder that is inherited and that will worsen the nerves in the brain and spinal...
Genetic Disease Diagnosis, Screening, Treatment, And Advocacy This case study involves a couple who are expecting a child. Testing has been conducted identifying the unborn child having the condition of Tay-Sachs disease. The nurse in this scenario will identify interdisciplinary team members and create a teaching plan to educate the couple about this disease. This work in writing will discuss three ethical implications regarding the availability of personal genetic information and
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