Nursing diagnosis

surrounding the message that is being sent to potential parents of children with disabilities and the many persons who are living with disabilities. Adrienne Asch argues that with “prenatal diagnosis, a single trait stands in for the whole, the trait obliterates the whole. With both discrimination and prenatal diagnosis, nobody finds out about the rest. The tests send the message that there’s no need to find out about the rest.” It is one thing to want a person to have what society deems a…

In many healthcare settings, different healthcare professionals tend to come together to treat patients. This is especially true for those needing preventative measures to avoid injuries, or to rehabilitate after an injury has occurred. For example, someone who has suffered a shoulder injury at work might go to the doctor’s office where they see a nurse, and their physician, who then refers them to a physical therapist (PT). For any healthcare setting with different professionals working…

In the 1980’s, Nancy Wexler contributed to advances in medicine by discovering a genetic marker that could indicate inherited disorders linked to chromosomes, such as Down’s Syndrome, Huntington’s Disease, and Tay-Sachs Disease (Vaughn, 2013, p. 566). Since then, prenatal genetic screenings have become widely accessible through simple, low-risk procedures such as carrier testing, blood tests, and ultrasounds. These procedures are only capable of reporting the risk for inheriting abnormalities…

Prenatal Genetic Testing: A Technology of Normalization Prenatal genetic testing is a technology made available to more accurately determine whether or not a child could have a birth ‘defect’. The most common birth defects tested for are Down syndrome, Trisomy 18, or an open neural tube defect (Government of Canada, 2013). This paper asserts first that prenatal genetic testing is a technology of normalization, which labels disability as abnormal and a feared outcome, and second that…

Wall of Silence Journal 1 Describe your level of awareness of the prevalence of medical errors before this course and reading part 1. The healthcare field is one of the utmost respected fields one could work in. Nurses are the most trusted workers in the country and are expected to advocate and protect their patients. Nurses also spend most of their time at work administering medications which plays a key role in the reduction of medication errors. My idea of medical errors has been based off…

(Azari & Barney, 2013). Viral conjunctivitis signs and symptoms are conjunctival hyperemia, watery discharge, and ocular irritation with tender and palpable preauricular nodes (Coyle, 2014). The examiner suspected viral conjunctivitis as a possible diagnosis due to the watery discharge. Upon physical examination of Sherry’s preauricular nodes, they were non tender, non-palpable, and her conjunctiva were not hyperemia. Therefore, in the absence of tender, non- palpable preauricular nodes,…

This is why having a healthy 2-way relationship to between doctor and PT is extremely pivotal, one cannot function without the other. Diagnosis is impairments and functional limitations that also extend to conditions and syndromes (Deyle pg.632). Though diagnosis is normally taught in entry-level PT programs, it’s sort of an afterthought to third parties who want more of a guaranteed analysis. The majority of medical providers know that PT’s are…

Introduction Genetic screening is a form of medical test that determines alterations in chromosomes, proteins or genes. The findings of genetic testing can reject or confirm suspected genetic condition or aid in identifying individual’s chance of passing or developing a genetic disorder. Currently, over one thousand genetic tests are in use, and more are emerging. Various methods can perform the genetic screening. For example, (1) Biochemical genetic tests which study the activity level or…

Prenatal diagnosis has become of of the most important factors of the obstetrics practice, it diagnoses any complications or possible disorders, especially trisomy 21 (Down’s syndrome) of the unborn baby. The most common methods for prenatal diagnosis of trisomy 21 require invasive procedures, which includes Amniocentesis and Chorionic Villus Sampling (C.V.S), where it uses a sample of the fetal tissues. These two options carry a small but definite risk. Therefore, they could cause more…

The comprehensive history and physical examination (H&P) is made up of the following nine major components: history of present illness (HPI), past medical history (PMH), family history, psychosocial, review of systems (ROS), physical examination, laboratory data, problem list, and treatment plan. The HPI section addresses the current problem for which the patient is seeking care for and its chronological development up to the present time. The elements need to be documented are location,…