Immune System Effects Of Hiv Health And Social Care Essay

The first cases of severe immune deterioration were recognized in 1981 which developed unusual infections. These infections were later called AIDS (Acquired Immune Deficiency System). It was soon realized that AIDS were caused by HIV (Human Immunodeficiency Virus). Once a person has HIV and the HIV infection progresses, it weakens that person’s ability to fight off other diseases. Once it attacks the immune system, the virus will leave them more susceptible to other diseases. If this person with HIV contracts an additional disease, or once this person’s immune system shows deterioration that is when the person is known to have AIDS. AIDS continues to deteriorate the immune system and this will decrease the body’s ability to fight infections. Hundreds of people become infected with HIV and this causes AIDS which is one of the most serious, deadly diseases in human history and the affects, causes, transmissions and social implications of both HIV and AIDS will be explained in further detail in this essay.

Over the years, more information about HIV works has been learnt, and drugs were developed to interfere and slow down the growth of HIV. These drugs have helped people with the disease because they can now live much longer. But unfortunately there is still no cure for HIV and AIDS. Many people become affected with HIV each year, whether it is teens or adults. HIV can be transmitted from an infected person to another through blood (sharing needles- whether for sharing drugs, injecting steroids or used for tattooing), semen, vaginal fluids (unprotected intercourse) and breast milk. A new born baby can catch the virus from the mother; before birth, during birth or from breastfeeding. If the mother is tested and approaches the doctor before having the child, the doctor can prevent the spread of the virus from the pregnant mother to the expected baby.

Our body contains T-helper lymphocyte cells which contain CD4 receptor sites. These cells help the immune system function normally and they fight off certain kinds of infections. They fight off these infections by acting as messengers to other types of immune system cells, giving them a message to become more active and fight against invading germs. HIV has a core of genetic material, just like other viruses and this genetic material is RNA (ribonucleic acid) and this contains the information that the virus needs in order to replicate. The RNA in HIV has proteins called “reverse transcriptase” which is crucial for replication inside T-helper cells. They also contain proteins called antigens and they have diverse functions in viral replication. These antigens are like hooks on the outside of the virus, and they make it easier for the virus to hook onto the T-helper cells and infect them.

HIV affects the immune system by targeting these T-helper lymphocyte cells and attaches itself to the cells, infects them and uses them as a place to replicate the virus (however they also infect other cells in the body, macrophages, B cells and monocytes). The T cells contain genetic material in the form of DNA (deoxyribonucleic acid) and this is the cell stored all the information is needs in order to function. The CD4 receptor sites are on the surface of the T-helper lymphocyte cells and the HIV antigens fit perfectly in the CDR receptor sites. And once the HIV bumps into the right place on the T-helper cells, the virus immediately locks onto the CD4 receptor site and then it injects its lymphocytes core with the viral RNA and the reverse transcriptase.

In order for the T-helper cell to get infected, the viral RNA must travel to the cell’s nucleus. But before this takes place, an important transformation must occur in the cell. The viral RNA must transform into DNA enable to start the replication process, and this is done by the reverse transcriptase, which borrows material from the cell and changes the codes of the T-helper cell by giving it new DNA codes. Once the viral RNA is transformed to viral DNA, it enters the cell’s nucleus and attaches itself to the T-helpers lymphocytes DNA.  With the virus doing this it destroys the T-helpers function to fight off invading germs in the immune system and new viruses are produced to infect more T-helpers. HIV quickly takes over the body as nearly one billion T-helper lymphocyte cells become infected a day. With the T-helper cell population rapidly decreasing, the body loses its ability to build up an immune response against infections.

With HIV’s capability of reversing the natural process that takes place in cells, by transforming RNA into DNA it is considered to be a retrovirus.HIV belongs to a subgroup of retroviruses known as “slow” viruses, where it takes the virus up to 12 years or more from the initial infection for the virus to begin to show serious symptoms. Once these symptoms begin to show, they get serious infections that they normally would not and become immune deficient and this is called AIDS. Because the immune systems are weakened, people who have AIDS are unable to fight off any infections, particularly tuberculosis and other kinds of rare infections in the lungs, the surface covering the brain or the brain (encephalitis). And with people unable to fight off many infections, they will get sicker, especially if they do not take antiviral medications properly and this can lead to an early death. AIDS also affects the immune system it also affects special blood cells and organ cells such as bone marrow, spleen, liver and lymph cells. These cells create antibodies to try and fight against diseases. With the human body having few T-helper lymphocyte cells because of IHV, some cancers that are stimulated by viral illnesses may occur, and there is a chance for people with AIDS to get forms of lymphoma and a rare tumor of blood vessels in the skin called Kaposi’s sarcoma. With AIDS being fatal, it is important for doctor’s to detect an HIV infection as early as possible so that the infected person can take medication to delay getting AIDS.

Initially most of the people who were infected with HIV and AIDS were men, but as it began to spread more women and children caught the disease. There are about 33 million billion in the world living with HIV/AIDS and as the years go by; the number of people with HIV/AIDS continues to increase. This disease is present everywhere in the world, but is more common in Less Economically Developed Countries (LEDC’s) and unfortunately the anti-retroviral drugs that are available to control the symptoms of this disease are too expensive for those in developing countries. But with these people not having enough money for medication to slow down the growth of HIV and there is no cure and lacking in knowledge about HIV/AIDS, they continue to have unprotected sex and pass on the disease. But there were programs that promoted safe sex practices, and these led to a reduction in HIV/AIDS in these places. It is said that the programs that Thailand held has saved more than 200,000 people from encountering the disease since 1993. With HIV and AIDS being the most deadly disease out there, it is necessary for those with the education to warn young teens and those in developing countries about how anyone can get infected by having unprotected sex and sharing needles. With programs like these it is also helpful for them to give their audience free condoms so that they can practice safe sex and prevent getting such a nasty virus.

Economic impacts :

Economic Impact in Africa

One way in which HIV and AIDS affect the economy is by reducing the labour supply through increased mortality and illness. Amongst those who are able to work, productivity is likely to decline as a result of HIV-related illness. Government income also declines, as tax revenues fall and governments are pressured to increase their spending to deal with the expanding HIV epidemic.

By making labour more expensive and reducing profits, AIDS limits the ability of African countries to attract industries that depend on low-cost labour and makes investments in African businesses less desirable. HIV and AIDS therefore threaten the foundations of economic development in Africa.

The impact that AIDS has had on the economies of African countries is difficult to measure. The economies of the worst affected countries were already struggling with development challenges, debt and declining trade before the epidemic started to affect the continent. AIDS has combined with these factors to further aggravate the situation. It is thought that the yearly impact of AIDS on sub-Saharan Africa’s gross domestic product (GDP) is a loss of 1%. While this is a relatively modest effect, it will build in significance over time, especially in countries where HIV prevalence is rising.

One way in which this impact can be reduced is through the provision of antiretroviral drugs to people living with HIV. A recent study in South Africa suggested that if ARV coverage expanded to reach 50% of those in need of the drugs then the effect of the epidemic on economic growth would be reduced by 17%.

The Impact on Life Expectancy:

In many countries of sub-Saharan Africa, AIDS is erasing decades of progress in extending life expectancy. A recent study found that the average life expectancy of individuals living in sub-Saharan Africa has fallen by five years since the early 1990s, mainly because of AIDS.35 In Swaziland it has been estimated that life expectancy at birth, which is currently just 33, would be 66 without AIDS.

The impact that AIDS has had on average life expectancy is partly attributed to child mortality, as increasing numbers of babies are born with HIV infections acquired from their mothers. The biggest increase in deaths, however, has been among adults aged between 20 and 49 years. This group now accounts for 60% of all deaths in sub-Saharan Africa, compared to 20% between 1985 and 1990, when the epidemic was in its early stages.38 By affecting this age group so heavily, AIDS is hitting adults in their most economically productive years and removing the very people who could be responding to the crisis.

Social Impacts:

The Impact on Households

The toll of HIV and AIDS on households can be very severe. Although no part of the population is unaffected by HIV, it is often the poorest sectors of society that are most vulnerable to the epidemic and for whom the consequences are most severe. In many cases, the presence of AIDS causes the household to dissolve, as parents die and children are sent to relatives for care and upbringing. A study in rural South Africa suggested that households in which an adult had died from AIDS were four times more likely to dissolve than those in which no deaths had occurred.8 Much happens before this dissolution takes place: AIDS strips families of their assets and income earners, further impoverishing the poor.

AIDS in UK:

HIV/AIDs is one of the most deathly diseases in the United Kingdom today. The North-West of The United Kingdom is particularly badly affected. Since the virus was discovered in the 1980s, over 23,000 people have died from AIDs alone. It is estimated that there are around 73,000 people living with HIV in the United Kingdom today. That’s a 1:1000 figure. Although this is not as high as say, Sub-Saharan Africa, it’s still a shocking figure for an MEDC.[1] This shocking amount can be divided into three significant groups – homosexuals, drug users and people receiving blood transfusions, mainly haemophiliacs.

Homosexual relations are estimated to have left 39,000 people currently with the virus. Drug users are over 5,000 of the people with the virus, and blood transfusion patients make up just under 2,000 people living with the virus. The remaining amount of people living with the virus are children who inherited it from their parents, heterosexuals and people who got the virus due to wound contact when kissing/practising first aid etc.

The fact that there are so many people in the United Kingdom living with the virus has put a great strain on the NHS (National Health Service) in the UK. Although people see an MEDC such as The United Kingdom being able to cope well with a disease such as this, the truth is that it is extremely difficult – however, this is for different reasons than in an LEDC.

One of the main problems is that people do not like to come forward for testing. Whereas in an LEDC, the HIV/AIDs virus is so common that it is not considered a taboo, or dirty, in an MEDC, having the virus is considered dirty and foul, and people are afraid of being tested, simply because they know the social impact that it will have on their lives. Socially, the consequences of HIV/AIDs in an MEDC such as the United Kingdom are far greater than in an LEDC. As stated before, people living with the virus know that they will be abused verbally and physically, and that they will be considered infected and dirty. As the disease used to be associated mainly with homosexuals, drug users and sex workers, you can only imagine the horrific abuse HIV/AIDs patients may suffer, even if the abuse is (as is often the case) incorrect.

Another problem that the NHS has, coping with HIV/AIDs patients is not the limited amount of drugs – as would be the case in an LEDC, but the expense and abundance of drugs. The problem is that after a while, an HIV/AIDs patient often becomes resistant to the given drugs. This means that the NHS needs to find a new drug for the patient, one that they are not resistant to. Then extra drugs need to be given to counterbalance the negative side-effects of drugs, such as nausea, vomiting, dizziness and loss of consciousness. This, in effect, means that any one individual may be taking up to twenty pills a day, in a cocktail of chemicals. It’s not the lack of drugs that causes problems in MEDCs, it’s the fact that we constantly have to develop new ones to fight the disease, and this puts a great strain on the economy of a country. In 2005, the United Kingdom spent £23 billion on its health budget. 65% of that went into HIV/AIDs health care, drug development and advertising campaigns, encouraging people to be tested and treated against the virus.

Another economic problem with HIV/AIDs in the United Kingdom is that one of the groups who have the virus is refugees, and they cannot afford drug treatment. Now, as with LEDCs, the United Kingdom, as an MEDC is starting to face the same problem. It cannot afford to supply free drugs to everyone with the virus, and this means that while the middle-class population can afford drug treatment, many working-class people and immigrants cannot.

Campaigns such as Children in Need, Stop AIDs Now and (RED) are working to produce funding for these people, and so far they have raised enough money to keep these people on drug treatment programs.

Demographically, the impact that the HIV virus has had on the United Kingdom is not as great as it is in an LEDC, as you can see when you compare the population pyramids. Still, it does have a definite impact on the amount of deaths and the population in the United Kingdom. You can see that the band of 20-29 year old in the United Kingdom – mainly the children who would have contracted HIV/AIDs in the 80s and 90s is significantly smaller than the bands above and below it. As a result of this, you can foreshadow a drop in an elderly population for the United Kingdom, as well as fewer children, as many HIV/AIDs patients do not wish to have children out of concern of them contracting the virus. There are, however, now ways of preserving sperm, such as ‘sperm washing’ that can ensure children that are given birth to are not contaminated with the virus.

Treatment Options for Invasive Ductal Breast Cancer

Breast cancer is the most commonly diagnosed cancer in women, making up 15% of all new cancers in the UK and 25% worldwide (Torre, 2015). One in eight women in the UK develop breast cancer and around 4,700 women and 30 men in Scotland are diagnosed with breast cancer each year (Breast Cancer Now, 2019). The most common type of breast cancer is Invasive ductal carcinoma (IDC), which accounts for 80% of all breast cancers diagnosed (nhs.uk, 2019). IDC is a cancer that has broken through the milk duct and has started to invade the tissues of the breast and over time can progress to the lymph nodes and other areas of the body (Cancerresearchuk.org, 2019). This paper will discuss treatment options for IDC.

Most women with breast cancer have more than one treatment. The choice of treatment depends on the characteristics of the cancer and patient choice. These treatments fall into two categories: Local treatments and Systemic treatments.

Local treatments for IDC include surgery and radiation therapy which treat the cancer and the surrounding areas, such as lymph nodes. Typically, women have surgery to remove the cancerous tissue first (Breast Cancer Care, 2019). Surgery is required not only to remove the cancer itself, but to confirm if it has spread to the lymph nodes. Two types of surgery can be recommended: breast-conserving surgery or a mastectomy.

Breast-conserving surgery involves removal of the cancerous tissue with a margin of healthy tissue which surrounds it. This is also known as a wide local excision or lumpectomy. A mastectomy is the removal the whole breast and is recommended when the cancer occupies a large area of the breast or when there is more than one area of cancer in the breast (Breast Cancer Care, 2019).

During surgery one or more lymph nodes may also be removed to discover if the cancer cells have travelled there. Cancer cells can travel to the lymph nodes which are the body’s system for removing bacteria and other unwanted substances, therefore offering cancer cells a route to other parts of the body (Macmillan.org.uk, 2019). If there is suspected spread of cancer to the lymph nodes, then either a Sentinel lymph node biopsy or an Axillary lymph node Biopsy will be performed during surgery (Mina et al, 2016). Knowing if the lymph nodes have cancer cells in them helps in selecting the best treatment plan. If the lymph nodes are cancer-free, it is unlikely further surgery will be necessary (Breast Cancer Care, 2019).

Following a lumpectomy or partial mastectomy, radiation therapy may be recommended. It can also be advised after a mastectomy where the tumour is large, and the lymph nodes are involved. Radiation therapy aims high-energy rays at the breast, chest, under the arm area and above the clavicle to destroy any cancer cells that may have been left behind.

Unlike local treatment, systemic treatments involve the whole body. They are used to destroy cancer cells that have spread from the original tumour and to reduce the risk of the cancer returning (Breast Cancer Care, 2019). These treatments can also be known as adjuvant treatments, as they are delivered post-surgery.

Chemotherapy is one such systemic treatment. It’s the delivery of anti-cancer drugs into the body through the bloodstream and is usually given post-surgery. As with radiation therapy, chemotherapy is used to destroy the cancer cells and is calculated carefully to have the greatest effect on the cancer cells with the least impact on the normal cells (Breast Cancer Now, 2019). It’s given in cycles, typically a day of treatment proceeded by a period of “off” days and lasts between 3 -6 months. The use of chemotherapy in treating IDC can be dependent on the oestrogen receptor and HER2 status. HER2 is a protein that enables cancer growth. Chemotherapies such as Cytoxan and Adriamycin are commonly used alongside HER2 targeted therapies, such as Herceptin, in treating HER2 positive IDC (Cancerresearchuk.org, 2019).

If the cancer tests positive for hormone receptors, some form of hormonal (endocrine) therapy is likely to be recommended in the treatment. It works by lowering the amount of oestrogen in the body or by blocking the oestrogen from signalling cancer cells to grow and divide therefore creating more cancer. This type of cancer is referred to as oestrogen receptor positive (ER+) and hormone therapy is only advised if the cancer is ER+ (Breast Cancer Care, 2019).

The treatment of invasive ductal carcinoma as shown in this paper can be very complex, varied and each treatment plan is dependent on results from a series of tests performed pre and during treatment. Every patient’s treatment is individually tailored to suit the specific characteristics of their cancer with an aim to give the patient the most beneficial outcome, to increase patient survival rates and to reduce the chance of the cancer returning.


References


Journals

  • Torre, L.A., Bray, F., Siegel, R.L., Ferlay, J., Lortet-Tieulent, J. and Jemal, A., 2015. Global Cancer Statistics, 2012.

    CA Cancer Journal for Clinicians.

    Vol 65, no 2, pp. 87 – 109.

Book

  • Mina, L., Storniolo, A., Kipfer, H., Hunter, C. and Ludwig, K. (2016). Breast cancer prevention and treatment.


Website

  • Breast Cancer Care. (2019). Treatments: Surgery. [online] Available at: https://www.breastcancercare.org.uk/information-support/facing-breast-cancer/going-through-treatment-breast-cancer/surgery [Accessed 30 May. 2019].
  • Breast Cancer Now. (2019). Are you having breast cancer treatment?. [online] Available at: https://breastcancernow.org/about-breast-cancer/are-you-having-breast-cancer-treatment [Accessed 30 May. 2019].
  • Cancerresearchuk.org. (2019). Invasive breast cancer | Cancer Research UK. [online] Available at: https://www.cancerresearchuk.org/about-cancer/breast-cancer/stages-types-grades/types/invasive-breast-cancer [Accessed 3 Jun. 2019].
  • Macmillan.org.uk. (2019). Secondary cancer in the lymph nodes. [online] Available at: https://www.macmillan.org.uk/information-and-support/lymph-node-cancer-secondary [Accessed 1 Jun. 2019].
  • nhs.uk. (2019). Treatment. [online] Available at: https://www.nhs.uk/conditions/breast-cancer/treatment/ [Accessed 1 Jun. 2019].

The Impact Of Culture On Healthcare Nursing Essay

Culture is one of the most important determining factors in healthcare preferences and practices. Thus, the need for transcultural nursing is undeniable. “Transcultural nursing requires sophisticated assessment and analytic skills and the ability to plan, design, implement, and evaluate nursing care for individuals, families, groups, and communities representing various cultures” (Andrews and Boyle, 2008, p.4). In order to effectively practice transcultural nursing, one must first understand the need for cultural competence. It is vital for nurses to have a desire to become culturally aware, culturally knowledgeable, culturally skillful, and to seek cultural encounters. Cultural desire is the stimulator in the eruption of the process of cultural competence and the nurse must seek and be open to learn and accept others, understand the process is lifelong, and set aside personal feelings to effectively treat unique patients (Campinha-Bacote, J, 2003). The Giger and Davidhizar (2002) Transcultural Model is a helpful tool that addresses and effectively treats patients who have different cultures. The model takes into consideration 6 important phenomena.

Communication keeps culture alive by verbal and nonverbal means; it is one of the biggest obstacles in healthcare. Nurses ask questions to determine patient’s views on illness, causes, and possible treatments. They listen and interpret their patient’s level of understanding and ability to follow through with treatment. Also, nurses interact with the patient’s family. Communication varies from culture to culture. Americans are expected to speak Standard English; however, it varies based on region, ethnicity, and social class (United States, 2001). Americans use a variety of nonverbal communication. Eye contact, which is viewed as a sign of trust and honesty, between patients and healthcare professionals is the norm. Expression of emotion varies in American culture. Americans use a combination of verbal language, body language, and gestures. Americans are often straightforward and rather demanding. Unlike Americans, Asians rarely complain. Silence and withdrawal may be the only indication of a problem. Asians tend to not ask for anything, accept pain, and remain stoic (Fernandez V. & K., 2008, Asian Community). Many Asians don’t engage in eye contact with powerful persons; the avoidance of eye contact shows respect and reverence (Non-Verbal Communication, p.4). Asians speak more than 100 languages; they vary based on the geographic regions they descend from (Asian Americans, p. 2). Arab Muslims usually cooperate by answering questions, listening, and following directions until they see improvement. They believe their expression, such as pain, should be quickly met with response (Fernandez V. & K., 2008, The Middle Eastern Community). The Arabic language uses devices that outmatch reality and is not very direct or explicit (Ayish, 2003). Hispanics are very emotionally expressive. Effective communication with Hispanics is not based on just speaking their language; cultural rules allow for certain discussions with certain people (Fernandez V. & K., 2008, The Hispanic American Community). Eye contact is expected on the nurse’s part but will not necessarily be reciprocated (Andrews & Boyle, p.25). Nurses, if available, should undergo cultural competency training. Berln and Fowkes’ LEARN Model can assist; LEARN, represents the process of listening to the patient, explaining your view, acknowledging differences and similarities, recommending and negotiating a plan (Campinha-Bacote, J.,2003). Nurses should enlist the help of trained interpreters, preferably of the same gender, mature, and of no relation to patient; if there is no interpreter, the following but not limited to, is necessary: politeness, slow and concise speaking, simplicity, pantomime, validation of understanding, and instructions in the proper sequence (Andrews & Boyle, p.29).

Space is also important when dealing with various cultures. Nurses are required to interact with patients, often invading personal space. Giger and Davidhizar (2002) state:

Territoriality refers to feelings or an attitude toward one’s personal area. Each person has their own territorial behavior. Feelings of territoriality or violation of the client’s personal and intimate space can cause discomfort and may result in a client’s refusing treatment or not returning for further care. (p. 185)

Americans tend to require a need for personal space. When family and friends are near, Americans tend to be relaxed; however, when a stranger or mere acquaintance invades space, it can become uncomfortable. Asians prefer a great amount of social distance. Many prefer minimum physical contact with acquaintances; excessive contact is viewed as inappropriate. Unlike Americans, who believe touch is a sign of friendliness, Asians view the head as a personal area that contains the seat of the soul and it should not be touched. Arab Muslims seem to require the least amount of space. It is not uncommon for people from the Middle East to stand closely when conversing. However, gender can play a role; Muslim woman may become distraught when a male, even a healthcare professional, stands or sits near her; Arab Muslims expect females to tend to females and males will care for males. Hispanics, unlike Americans, are use to standing or sitting near people they are not well acquainted with (Non-Verbal Communication, p.3). Hispanics and Arab Muslims may unintentionally invade nurse’s space as a means of getting closer and more comfortable (Andrews & Boyle, p.26). Nurses should take the patient’s lead; if the patient seems to gravitate towards you or initiates touch, then it is acceptable to do the same. At all times respect the patient and boundaries.

When dealing with patients, there must be consideration of social organizations or what role the patient’s culture plays in his or her life. Family members are often the providers of a patient’s eating habits, sick role behaviors, and medications used. Americans view family as a vital part of their healthcare plans. It is common for Americans to be visited and supported by family; they often discuss and make important decisions. Asians are concerned with family interdependence over independence; family usually likes to assist with patient care. In some Asian cultures, some members, such as men and elders, dominate and consider women and children inferior (Galanti, 2005). Arab Muslims regard family as the foundation of their society. The husband answers questions, makes all major decisions, and gives consent. Often times, Arab Muslims don’t believe in divulging family history. The family cares for the ill. (The Middle Eastern Community). Hispanics have large families who visit for long hours as a way to demonstrate their love and genuine concern. Often times, decisions are made by the entire family or designated members (Galanti, 2003). Religious and spiritual beliefs are important factors during illness, recovery, and death. In the United States, most people consider themselves Christians; Catholics singly dominate, but the Protestant groups combined outnumber them. Americans include religious practitioners such as priest, ministers, and rabbis as well as nontraditional leaders during health related situations. Americans include religious objects, such as the Bible, and also rituals, such as communion. Death and end of life choices are also influenced by religion and practices; typically, Americans consider death a sad and somber time. Asians are host to numerous religions; Christian, Muslim, Buddhism, and Hindu are just a few. Many Asians believe in bad spirits; infants attract them and induce death. If the illness is thought to be caused by spirits, healers are sought (Asian Community). Arab Muslims are usually of the Islamic faith and pray 5 times a day to the Holy Land, Mecca. Muslims recharge their spiritual battery during the month of Ramadan; fasting from dawn to sunset accompanies. Arab Muslims often read from the Al Quran (The Middle Eastern Community). Hispanics are usually Catholics with the recent emergence of Pentecostals. Shrines and religious objects are common in practice. Health is viewed as God’s gift and should be revered (The Hispanic Community). Nurses must be accommodating to patient’s families and the value placed on family within cultures. Nurses must be sensitive to religious beliefs or practices and must not impose personal beliefs. Seeking knowledge is essential. However, exposure to diverse cultures is one the best learning mechanisms.

Understanding a cultures notion of time elapsing, specific periods, and clock time are

necessary for effective healthcare. Cultures may be past, present, or future oriented. Americans use time to provide order. Americans expect care at designated times; appointments are a prime example. Americans are future oriented; they believe they can manipulate the future by taking certain actions. Americans tend to be proactive; the focus is optimism, coping strategies, and preventive measures. Americans often demonstrate this orientation through self examinations, check-ups, and staying informed about healthcare advances. Asians tend to have a past orientation. They prefer to adhere to traditional methods and treatments; they are apprehensive about new innovations. Recently however, Asians are shifting towards future orientation (Galanti, 2004). Arab Muslims are present oriented and are neglectful of preventive measures. They may be late or not attend appointments at all (The Middle Eastern Community). Hispanics also focus on the present. They believe the future arrives in its own time and thus the notion that one cannot be late exist (Galanti, 2004). Nurses must explain the importance of time regarding life processes while being respectful and mindful of cultural views. Nurses should try to refrain from making time oriented promises that can’t be kept.

Environmental control or the attempt to control nature affects patient’s health practices, values, and the definitions of health and illness (Giger, & Davidhizar, 2002). Americans believe nature can be controlled. Americans equate the body to a machine; if it’s broken, allow healthcare professionals to fix it (Galanti, 2004). Americans conform to the Western biomedical model which defines health as the absence of disease or the signs and symptoms of disease. The holistic paradigm exists in Asian cultures; it deals with the concept of yin and yang, in which forces of nature must be balanced to produce harmony (Andrew & Boyles, 69). Asians tend to view people as part of nature. The land is a resource used to treat disease; herbal remedies are common (Galanti, 2004). Arabs believe the key to good health is personal hygiene and a healthy diet. “They place a high value in modern Western medicine and have confidence in the medical profession” (The Middle Eastern Community). Hispanics believe natural forces are not in their control and preventative measures are not often taken. (Galanti, 2004). Their system, the Curanderismo, combines spiritualistic, homeopathic, and scientific elements; curandero or holistic healers are utilized (The Hispanic Community). Nurses should become familiar with factors. Nurses should not dismiss patient’s view of their power and accountability or lack thereof.

Biological variations exist between races; some groups are sensitive to certain medications, have metabolic differences, and are prone to certain diseases or factors that can affect healthcare. African Americans are three times more likely to get tuberculosis than whites; they also have higher rates of hypertension. Sensitivity to cardiovascular effects from Propranolol occurs more in Asians than Whites. Ethnic minorities, such as Hispanics, have higher HIV rates (Giger and Davidhizar, 2002). Middle Easterners or Arab Muslims have a lower percentage of sweat chlorides (Andrews & Boyle, 54). The list of variations is broad and extensive. “Accurate assessment and evaluation of clients require knowledge of normal biocultural variations among healthy members of selected populations” (Andrews & Boyles, 49). Nurses must acquire skills that will allow the recognition of variations.

A nurse must always remember that the focus should remain on the patient’s well being and recovery. It is necessary to understand that individuals will never be the same. A patient’s health status and treatment is directly influenced by their culture and it is this reasoning, which has been proven through testing and the development of theories that has led to the conclusion that culture cannot and will not be ignored. “Human diversity makes tolerance more than a virtue; it makes it a requirement for survival” (Dubos). Healthcare will not suffice without negotiation, adjustment, and respect of differences. Transcutlural concepts in nursing care have made cultural competency an expected standard and it is the duty of every nurse to help maintain this standard.

Can Neutropenic Cancer Patients Be Nursed Effectively Nursing Essay

On my clinical rotation I have observed that oncology patients are being nursed in wards which have patients with other conditions. Some of the oncology patients were severely neutropenic. This poses a greater risk for infections since the white blood cells needed to fight infection is very low. It has been noted that patients with infectious diseases such as tuberculosis are being nursed on the same ward, along with burn patients and HIV patients. It was observed however that the most neutropenic patients were being barrier nursed. However it was still observed that many times members of staff entered the room without wearing a mask or washing their hands and most of the times the patient also wore no mask. The cleaning staff also entered the rooms and cleaned without wearing masks and would sometimes clean an infectious person’s room prior to cleaning the cancer patient room. These observations have led me to ask the question whether neutropenic cancer patients can be effectively nursed on a ward with others patients of contagious illnesses.

This issue is significant to oncology nursing and cancer care since it addresses the practices of nursing and also plays an important part in patient outcomes.

It has been estimated that each year in the United States there were sixty thousand cases of cancer patients hospitalized with neutropenia. About two thirds of that number has reported infections and the estimated inpatient mortality rate of those patients is seven percent (Segal, 2008).

Infections also cost hospitals a lot of money that could be spent on other health issues. It was estimated that infections have added thirty billion dollars to the US hospital cost while consumers also have to pay part of the cost (McCaughey, 2005).

A search was carried out using internet data bases and articles were found which lends support to the use of barrier nursing and other methods as effective tools in infection control.

Barrier Nursing is nursing a patient so as to “erect a barrier to the passage of infectious pathogenic organisms between the contagious patient and other patients and staff in the hospital, and thence to the outside world” (Last, 2010).It involves the use of having the patient isolated in a separate room and if not possible they are screened on an open ward. The nurse would wear a gown, mask and gloves when attending to the patient and observe strict hand washing and aseptic techniques (Last, 2010).

Reverse barrier nursing or protective isolation is where the susceptible patient is isolated to prevent them from getting infections. It involves limiting the number of staff and visitors that interact with the patient especially if they are ill. It also involves limiting attending to a contagious patient then attending to the immunocompromised patient. All staff should be aware of the precautions and the doors should be appropriately labeled (The Leeds Teaching Hospital, 2003).

According to the American Cancer Society (2009), neutropenia is described as a deficiency of neutrophils. Neutrophils are the largest number of white bloods cells in the body and are crucial to the body’s defense system. Some cancers such as the lymphomas and some leukemia’s directly affect the immune system and causes low blood counts. In other cases the cancer treatment received such as chemotherapy and radiation results in damage to the immune system (American Cancer Society, 2009).

When the immune system is damaged or suppressed it is referred to as immunosupression. When this occurs the white blood cells especially neutrophils are unable to fight off infections and the person is highly susceptible to getting an infection. Infections can be caused by bacteria, viruses, parasites or fungi (American Cancer Society, 2009).

Some studies have suggested that proper hand hygiene by the patient and the nurse along with immunization, antifungal and antibacterial prophylaxis have show to be the most effective methods of infection control. Avoiding contact with persons who are ill with respiratory illnesses has also been suggested (Zitella, Friese, Hauser, Gobel, Woolery, O’Leary and Andrews, 2006).

The Center for Disease Control recommends hand washing as the most important means of spreading infection especially in susceptible populations such as the immunocompromised. It is also important between different patients in high risk units such as between cancer patients and HIV patients (LeTexier, 2000).

Other studies have suggested that barrier nursing is needed for all immunocompromised patients. Some infections are seen mostly in certain disease populations for example Candida infections are found in many HIV patients. However the question of whether neutropenic patients should be housed close to HIV patients needs to be further researched. Rather strict hygiene practices along with prophylactic treatment have been suggested (Lortholary& Dupont, 1997).

It is suggested that all clinical staff and other health care workers are periodically trained in infection control and there should be consistent evaluation of techniques being used. The nurse is in a unique position to ensure that infection spread is reduced by carrying out and monitoring aseptic practices; ensuring the environment is clean to prevent spread of micro organisms and to protect the patient from ill staff and visitors (Collins, n.d).

Some studies have also indicated that there is little evidence that reverse barrier nursing is effective especially where there is no laminar air flow or HEPA-filtered rooms available. However some studies indicate that the filtered rooms can reduce morbidity and mortality in patients with leukemia (Seshadri& Baumann, 2008).

The use of reverse isolation of any type for patients with solid tumors who are neutropenic is discouraged since there are no studies to prove it is helpful rather it can cause anxiety and confusion for patients, their families, and healthcare workers (Seshadri& Baumann, 2008).

After reviewing the literature the question can be answered that neutropenic patients can be effectively nursed on these wards with the collaboration of all the members or the health care team in carrying out proper hygienic methods.

How is leadership involved in the dissemination and application of quality data at this healthcare organization?

How is leadership involved in the dissemination and application of quality data at this healthcare organization?

  1. Analyze how this healthcare organization’s mission is correlated with its quality philosophy.
  2.  Assess the role of quality within value-based reimbursement in this particular healthcare organization.
  3. How is leadership involved in the dissemination and application of quality data at this healthcare organization?

II. Quality Infrastructure
Part of any performance improvement (PI) or quality plan is the description of the quality infrastructure or organizational foundation and also of the delineation of how quality information is disseminated throughout the healthcare:
organization.

  1.  Provide brief details about the organization’s information management system, including what type of system is used and patient records management.
  2. What phases of meaningful use have been implemented to date?
  3.  Outline how performance improvement data and initiatives are tracked through the organization, starting at the department level. Consider using a visual aid to depict this.
  4. Discuss leadership strategies that ensure stakeholder and community input into the quality program.
  5.  Discuss how the infrastructure of this healthcare organization supports data abstraction to support pay-for-performance (P4P) reporting requirements for the Centers for Medicare & Medicaid Services (CMS) and other insurance providers.

III. Process for Evaluation and Dissemination
Delineation of key metrics is an essential component of a PI or quality plan. In this milestone, you will discuss and delineate certain required metrics for the healthcare organization. In discussing these metrics, you will learn what quality elements are being measured by them as well as their vital role to the healthcare organization and patient safety and quality:

  1. Describe the various stakeholder groups involved in the performance improvement process (e.g., nursing leadership, departmental directors, etc.). Consider using an organizational chart to depict these stakeholders.
  2.  How does leadership in various departments promote involvement in performance improvement?
  3. Evaluate the frequency of performance improvement initiatives and timeline for submission of data.
  4.  Describe the processes for collecting, interpreting, and presenting data within the organization.
  5. Define the metrics required for the hospital value-based purchasing program through CMS and provide the rationale for inclusion of these outcome and process-of-care measures.

IV. Define the following metrics for their use in the quality plan, including how they meet accreditation or quality requirements and how their use influences delivery of ethical care in the healthcare organization. Consider including a current example of each of these metrics:

  1. Core measures included in the quality plan
  2. Inpatient and outpatient scores (HCAHPS)
  3. NDNQI included in the quality plan
  4.  Serious reportable events related to the quality plan
  5. . CAUTI, CLABSI, and surgical site infections (infection prevention)
  6.  Reporting of blood usage
  7.  Culture of safety scores
  8.  Accreditation Compliance

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Deliverables One short answer assignment of 1200 words in total (maximum)- excluding any references. Ensure you answer all questions. Referencing Ensure you reference all sources you use in your assig

Deliverables

One short answer assignment of 1200 words in total (maximum), excluding any references.

Ensure you answer all questions. Referencing

Ensure you reference all sources you use in your assignment, including online sources. Direct quotes (i.e. statements not in your own words) should be included in quote marks in addition to being referenced. You should use the APA 7th referencing system, since this is the same system you will need to use for your essays.

The Library has set up an institutional account for APA’s ‘Academic Writer’, which includes tools for using this system. There are also numerous web resources on APA referencing, and popular referencing software (e.g. Endnote – free to students) can be set up to automatically insert your references in the correct style.

Extensions and Penalties

There will be a deduction of 10% of the total awarded mark for each 24-hour period or part thereof that the submission is late (for example, 25 hours late in submission: 20% penalty).

This penalty does not apply for cases in which an application for Special Consideration is made and approved. Note that there are limits on how long after the due date students can apply for special consideration, so please submit any applications as soon as possible. BESS can assist with inquiries about the special consideration process.

Marking

The value of marks per question is provided on the assignment sheet. Marks will be awarded for each question according to how accurately, completely and clearly you answer each question.

Questions

1. In the COVID19 Pandemic, Australian state governments imposed minimum legal requirements for businesses to manage the health risks of COVID19 to their employees and customers, such as social distancing in store and sometimes mandatory use of masks.

Explain why business might have ethical obligations in managing COVID19 safely that go beyond these legal requirements. Your answer should explain two differences between ethics and the law, and give an example of how each difference might apply in this case. [2 marks]

2. In 2021, two beach volleyball stars decided to boycott a tournament held in Qatar over a requirement that women competitors wear long shirts and pants while competing ‘out of respect for the culture and traditions of the host country’. Read the following article on this case and then answer the questions below:

https://www.theguardian.com/sport/2021/feb/22/qatar-beach-volleyball-bikini-ban-karla- borger-boycott

1

Consider how a relativist and universalist would assess whether it is ethical for the organisers of this tournament to impose dress standards on competitors. Your answer should:

2A. Explain the main differences between relativist and universalist approaches to ethics [1 mark]; and

2B. Illustrate these differences in how a universalist and relativist would analyse the ethical issue in this case. [1 mark]

3. In 2021, Facebook temporarily blocked users from accessing Australian news sites via their site, in protest against Australian government legislation to compel Facebook to pay news organisations for the articles that Facebook users distribute. Read the following article on this case and then answer the questions below:

https://www.abc.net.au/news/2021-02-18/facebook-to-restrict-sharing-or-viewing-news-in- australia/13166208

3A. Explain what makes an action ethical according to utilitarians and at least one argument for this view. [2 marks]

3B. Outline at least two benefits and two harms in this case that a utilitarian would consider in their analysis of Facebook’s actions. [2 marks]

3C. In light of your answer in 5B, explain how a utilitarian would assess the ethics of Facebook’s actions in this case overall? [1 mark]

4. As the COVID19 vaccine becomes more widely available, experts have discussed whether employers should be able to compel workers to accept a vaccine. Read the following article to answer the questions below [Note: Remember ethics is not just about what is legally allowed or required]

https://www.smh.com.au/politics/federal/bosses-have-the-power-to-force-employees-to-take- the-vaccine-experts-20210101-p56r64.html

4A. According to Kant, what determines whether an action is right or wrong? [1 mark] 4B. Outline at least two rights or duties that employers may have in this case, and at least

two rights or duties workers in this case might have. [2 marks]

4C. Briefly explain Kant’s ‘categorical imperative’. Choose one right or duty in your answer to question 4B, and explain how this would either meet or not meet the requirements of Kant’s categorical imperative. [2 marks]

5. Read the article below on the continued rise in CEO pay in the banking sector after the Royal Commission into Misconduct in Banking and Financial Services, and then answer the following questions:

https://www.theguardian.com/australia-news/2019/sep/17/australian-ceo-bonuses-at-near- record-highs-despite-royal-commission

5A. How does a virtue ethicist decide whether an action is ethical or unethical? [1 mark]

5B. How would a virtue ethics approach to whether CEOs are paid too much be different from the utilitarian approach Moriarty discusses in Week 2? [2 Marks]

5C. Provide your own analysis of whether CEOs are paid too much from a virtue ethics standpoint. Your answer should consider at least 2 virtues, and 2 vices, that might be relevant, and explain why a virtue ethicist would think these are important [3 marks]

Research community and state resources devoted in adolescent pregnancy and describe at least two of these resources.

Research community and state resources devoted in adolescent pregnancy and describe at least two of these resources.

Adolescent pregnancy is viewed as a high-risk situation due to the serious health risks that this creates for the mother, the baby, and society at large. Describe various risk factors or precursors to adolescent pregnancy. Research community and state resources devoted in adolescent pregnancy and describe at least two of these resources. Research the teen pregnancy rates for the last 10 years for your state and community. Has this rate increased or decreased? Discuss possible reasons for an increase or decrease.

Ethics of End-of-Life Care

End-of-Life care is a complex and controversial topic in todays healthcare environment. Many factors contribute to the difficult decisions that must be made at the end of life, including autonomy vs. paternalism, issues of advance directives, rationing of health care, cost of treatment and subsequent financial burden, physician-assisted suicide, etc. Progress has been made in caring for those who are nearing the end of their lives, but medical advancement has added further complexity to this issue. The ‘Graying of America’, a result of the baby boom of 1946-1964, contributes to the importance of well-established end-of-life care plans within the medical community. According to Sade (2012), over the next two decades, the rate of increase in the elderly population will be over 3% per year and by 2030, 20% of the US population will be over 65 years of age. Physicians and nurses alike have the responsibility to respond to the changing healthcare arena and to ensure a dignified and peaceful death for everyone. I will discuss current and common ethical issues that contribute to the complexity of end-of-life care and possible solutions.

Age-based health care rationing is the idea that limits should be set to prevent life-extending medical care in individuals beyond a certain age for the purpose of maintaining a financially sustainable healthcare system. Daniel Callahan, a proponent of rationing health care for the elderly, at the 16th Annual Thomas A. Pitts Memorial Lectureship in Medical Ethics, argues that the rising cost of healthcare is unsustainable and explicit rationing should be instituted. He believes public funds such as Medicare should be used to facilitate palliative treatment rather than curative care. His proposal supports using quality adjusted life year calculations to set limits on what care may be offered. For example, if you are beyond a certain point in the quality adjusted life year calculation, you would only be eligible for reimbursement for palliative care and not treatment used to extend life. David Gruenewald, who was also in attendance at the medical ethics lectureship, refutes Callahan’s proposal and argues that physicians do not seek enough information in patient care and need to be more involved in shared decision making with the patient. He believes that if measures are adopted to improve communication and shared decision making, many patients would choose comfort care over curative care, thus reducing the cost of health care. The American Medical Association highlights a specific case of an active and healthy 91-year-old patient, Mr. Turner, who is being considered for an elective knee replacement. During the patient’s consultation about the surgery, the insurance company HMO committee has proposed an absolute cutoff age of 90 for this type of procedure. I believe the proposed cutoff based on age specifically is not appropriate for this situation. “It makes less medical sense to focus on age as such than to inquire which factors actually influence longevity of total knee arthroplasty. Preoperative physical function appears to be significantly associated with postoperative outcome” (Morreim, 2014). I believe rationing of healthcare services is a topic that is vulnerable to many legal accusations. The Age Discrimination Act of 1975 states that “no person in the United States shall, on the basis of age, be excluded from participation in, be denied the benefits of, or be subjected to discrimination under, any program or activity receiving Federal financial assistance”. For as long as services are covered, for any portion of, by Medicare and Medicaid Services, I don’t think it is possible to ration care based on age, without repeal of the Age Discrimination Act. I believe this rationing would be unlawful and unethical.

Another ethical issue that arises regarding end-of-life care is physician-assisted suicide. As of July 2018, active voluntary euthanasia is legal in seven states—California, Colorado, Hawaii, Montana, Oregon, Vermont, and Washington, which comprises 18% of the US population (Lo, 2020). According to the US Supreme Court, there is neither a constitutional right to physician-assisted suicide nor a barrier making it illegal. For this reason, it is regulated by the state. Currently, active euthanasia, or the act of a physician administering a lethal dose of a medication, is illegal in all states. An important aspect to consider when discussing physician-assisted death is whether patient autonomy is respected, and self-determination upheld.

The Federal Patient Self-Determination Act (PSDA) effective since 1991 has facilitated communication between the healthcare providers and patients or consumers. The person’s right to autonomously voice their end-of-life treatment choices has to be respected ethically considering the use of advance treatment and their prognosis (Karnik & Kanekar, 2016).

The PSDA provides a straightforward view of the patient’s right to voice their choices, but ethical issues begin when there are limitations to the right of autonomy. Medical professionals are taught four basic principles of ethics, autonomy, justice, beneficence, and non-maleficence. It can be argued that denying a patient access to legal physician-assisted death is not neglecting autonomy. However, in my opinion, the stronger argument, autonomy is defined by the patient being able to make a fully informed decision and to understand all the risks and benefits and to receive care which is consistent with their preferences. Autonomy allows a patient to control their treatment based on preferences, but denying them the right to this care is inconsistent with respecting patient preference in end-of-life care. Justice is upheld by providers remaining within the scope of applicable laws and legislation when making choices. Beneficence requires that the procedure has the intent of doing good for the patient, this is difficult to discuss as the end outcome is death. However, providing this life-ending treatment could end suffering. Non-maleficence requires that a procedure does not harm the patient involved, this principle adds a unique complexity to the consideration. These four ethical principles applied to medicine have specific requirements and they are hard to meet in every circumstance. I believe certain requirements should be upheld under every circumstance, such as the patient understanding the risks and benefits under informed consent. I am not in favor of physician-assisted suicide being decided by a caregiver, even if they are the healthcare power of attorney (HC-POA). I do however believe that a power of attorney should have the ability to end treatment and allow the patient to die through passive euthanasia. Patients with terminal illness who are competent should have control over their end-of-life care. Much of the debate on physician-assisted suicide is defined within the physician community like the American Medical Association. I think nurses can play an important role in advocating for physician-assisted death as they are primarily the ones managing the symptoms and spend the most time with suffering patients. Nurses becoming more involved in end-of-life care could help identify barriers to treatment or decision-making processes.

Next, I would like to discuss medical futility and its implications during end-of-life care. Before I discuss futility in depth I will provide a brief history of how this problem arose and its linkage to autonomy. It was in the 1960’s that a new revolution of life-sustaining treatment began. Medical futility was forever changed when innovations such as cardiopulmonary resuscitation (CPR) was invented. During these years, patients with chronic renal failure received advancements in medicine that allowed them to live longer, positive pressure mechanical ventilation as well as extracorporeal life support resulted in creation of Intensive Care Units (ICUs). Soon after, most US hospitals had ICUs and were able to sustain patients in critical condition. Suddenly, a midpoint of life and death was the unfortunate case for many patients as new technology could sustain life for indefinite periods but may not lead to improvement or cure (Youngner, 2016).

The development of new life-sustaining technology for critically ill patients led to the rise of patient autonomy.  As the field of bioethics emerged in the 1960s, a new framework that was patient-centered defined medical ethics in terms of individual rights and patient autonomy. Informed consent was an important manifestation that became from this. Many “right to die” cases occurred during the next two decades that resulted from conflicting viewpoints between families and health-care providers. The right for patients to refuse life-sustaining treatment was now firmly established. Patients who are unable to are now able to have surrogates make the decision for them based upon their own values and the situation at hand. (Youngner, 2016).

Today, hospital ethics committees are consulted frequently because of futility disputes. There are different reasons for futility disputes to occur, but I will give a common example. A surrogate requests aggressive treatment intervention for a dying patient, but the provider does not believe the treatment is medically or ethically appropriate. This type of situation occurs for many reasons, the surrogate may not trust the providers judgement, they may not understand the medical situation due to issues with healthcare literacy, emotions may interfere, or even religious preferences. One way to resolve ethical dilemma in a case of medical futility is to identify the cause of the dispute. With a clear understanding of the surrogates’ reasoning for resisting the providers recommendation, a new plan or intervention may be within reach. Ethics committees are an important part of the hospital system for this reason. The committee, which may consist of physicians, nurses, social workers, chaplains, community members, etc. can gather with the family to identify obstacles and motivations for each side of the dispute.

“During EOL care, ethical dilemmas may arise from situations such as communication breakdowns, patient autonomy being compromised, ineffective symptom management, non-beneficial care, and shared decision making” (Pirschel, 2019). Nurses can navigate ethical dilemmas by establishing a trusting relationship with the patient and family members involved. End-of-life care demands that trust be established, and clear lines of communication are kept. Family members and caregivers should be given the opportunity to express their concerns and remain involved in the care of a loved one. Following these principles will provide the patient and family with dignity and further contribute to the trust that is needed for shared decision making.

In summary I believe end-of-life care is a very complex topic that requires many resources. From the first realization that a loved one may be transitioning to the end of their life to physician-assisted death, patients need advocates. Whether they be a family member acting as a surrogate, a physician explaining a prognosis, or a nurse on an ethics committee, shared decision-making, and interdisciplinary communication are vastly important in providing dignity and respect for the patients’ preferences. These preferences are to be respected  by the basic ethical principles previously discussed and the Patient Self Determination Act. Albeit end-of-life care is not a time for a one-size fits all approach, each patient situation will require a sequence of evaluation that is in line with the same goal, respecting autonomy and a dignified, peaceful death.


References

  • Karnik, S., & Kanekar, A. (2016). Ethical Issues Surrounding End-of-Life Care: A Narrative Review.

    Healthcare (Basel, Switzerland)

    ,

    4

    (2), 24. doi:10.3390/healthcare4020024
  • Lo, B. (2020).

    Resolving ethical dilemmas: a guide for clinicians

    . Philadelphia, PA: Wolters Kluwer Health.
  • Morreim, H. (2014, May 1). Should Age Be a Basis for Rationing Health Care? Commentary 1. Retrieved from https://journalofethics.ama-assn.org/article/should-age-be-basis-rationing-health-care-commentary-1/2014-05.
  • Pirschel, C., & Ons. (2019, November 19). Ethical Dilemmas at the End of Life. Retrieved November 30, 2019, from https://voice.ons.org/news-and-views/ethical-dilemmas-at-the-end-of-life.
  • Sade R. M. (2012). The graying of America: challenges and controversies.

    The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics

    ,

    40

    (1), 6–9. doi:10.1111/j.1748-720X.2012.00639.x
  • Youngner, S. J. (2016).

    The Oxford handbook of ethics at the end of life

    . New York: Oxford University Press.

Discuss strategies for helping the client to maintain change post-termination.

Discuss strategies for helping the client to maintain change post-termination.

 

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Inter Professional Practice In Health And Social Care Nursing Essay

Inter-professional practice is important in health care delivery because the professionals are there to meet multiple needs of the patients. Also it enables effective communication between the primary, secondary and tertiary care.

In the case of a patient suffering from diabetes, various health care professionals will be engaged in the care of the patient to ensure the patient is supported and given the best form of treatment. These health professionals include general practitioners, practice nurses, dieticians and physicians. All these professionals will play crucial different roles in the life of the patient and will ensure that they offer support to the family. In addition the professionals will provide a better quality care for the patient.

Trainings are there to develop and improve how professionals could work together as a unit to ensure the care of the patient is seen central point of care in order to reinforce the sense of effective care provision.

Inter-professional practice encourages different professionals to meet and improve the health care of the service users. Various professionals working together will effectively help meet the needs of the patient whereby the information and knowledge is shared between them to enable improved decision making regarding the care of the patient.

Evidence (200 words).

Describe Professional Roles and the Professional Principles in relation to health and social care provision.

Learning Outcome 3.

There are different professions in health care, each of which possesses their individual principles.

Professional roles are duties and responsibilities that are done to protect the health and safety of others. E.g. Nurses provides emotional support and help clients to cope. Their support range from re-assuring and encouraging patients finding out fears and worries in order to help patient lead a better and positive approach with their everyday lifestyle.

Nurses provide sufficient information to promote informed choice and consent of the clients. Mr X suffers from diabetes; the nurses will focus on Mr X social and psychological needs because they will be aware that different factors can contribute to the illness. Failure to consider the patient’s needs will show that they are overlooking factors that might lead the illness to a worse condition.

Professional principles are guidelines that enables clarity on the basic standards that service users can expect E.g. Nurses follows the Nursing and Midwifery Code Of Conduct which include that; they should make the care of their patient their priority and respecting, treating them as an individual. They must provide a high standard of practice care at all times through ensuring that they use the best available evidence to support practice and keeping their knowledge and skills up to date.

Evidence (200 words).

Outline how patient/user experiences may be enhanced by Inter-Professional working.

Improving how patient experience their care is a key part to effectively deliver high quality of service.

In a residential care home, an instruction was given to the client; the client has dementia and therefore he struggled to follow the instruction. The carer got frustrated with him and her anger built up so hit the client.

The Professionals that will be involved in this case includes: Nurses, Social Workers, Health Care Assistant, and Doctors. The client has been let down by the career, he might be hesitant to trust a health or social practitioners, but if the client has the re-assurance that different professionals are working together to ensure he receives better care in the future, through ensuring they communicate effectively amongst each other to prevent any incident like that happening again, this becomes therapeutic for the clients and so he will start to trust the health and social care services again.

Working together to support the patient will improve his care as it will help him assess his own needs and allow him to choose the help he needs to live the life he wants. The professionals will make sure that best practices are put in place and his right and responsibilities are respected. This will improve his experience as he will be able to feel more empowered.

Learning Log.

Part B.

Learning Outcome 4.

Reflect on the skills required for collaborative

learning and explain how they may be applied in

practice.

Model adapted from Marks-Maran & Rose’s

Reflective Cycle (1997).

Ref: Marks-Maran, D. & Rose, P. (1997) Reconstructing Nursing – Beyond Art and Science.

London. Bailliere Tindall.

Reflect on the skills required for collaborative learning and explain how they may be applied in practice (2,400 words)

Please use the Marks-Maran & Rose’s Reflective Cycle (1997) to reflect specifically on the skills you used in the classroom to learn collaboratively with your student peers. You are also required to explain how these skills may be applied in practice. The classroom learning experience/incident can focus on either a timetabled workshop (not all) or the team debates.

In addition to using the Marks-Maran & Rose’s Reflective Cycle (1997) to reflect, you should also integrate a range of literature to support your discussion. You are expected to cite 5-10 references in this section.

In this assignment I will be reflecting on the skills required for collaborative learning and identifying how they may be applied in practice. I will reflect on what has happened during my group discussion within the group.

In addition, the importance of inter-professional practice and key factors will be discussed. I will describe the meaning of inter-professional working and identifying how collaboration of different professionals came about in society and the effect it had on us all. I will then look to identify vital differences when comparing inter-professional practice through Marks-Maran, D. & Rose, P. (1997).

In my group, we reflected on daisy story and this led us to realise that the professionals did not work together appropriately and professionals did not communicate effectively and this led to improper diagnosis and improper medical treatment to the patient.

An effective way of learning is through interacting and co-operating with other people as it will give us opportunity to try out and share our own opinions. Prothero (2001). The benefit of collaborative learning within the group is to build up self-esteem in students and practice interacting with each other. Collaborative learning will develop higher level of thinking .Sanders (1995).

Reflective practice is defined as professionals learning from which will help to understand and develop their own practice (Jasper 2003). Marks-Maran & Rose (1997) states that the different knowledge and understanding one brings to a new situation and the knowledge and understanding one takes away from a new situation is called learning. The reflection cycle according to the Marks-Maran & Rose (1997) includes; the incident of what actually happened, the thoughts and feelings arising from the incident, what was learned, how it will influence future action and the related theory of the incident.

Communication is the sharing of information with each other and this will involve a sender sending out an idea or information to a receiver. However, for a communication to be effective, the receiver has to understand the exact information that the sender intends to send.

In regards to my previous group discussion, I personally feel that some of the skills I used within my group was effective but were not of the required standard essential for the group to perform up to its full potential. There was lack of communication amongst team members, and ideas were not being brought through clearly. This caused several misunderstandings and confusion which became a major occurrence as it was continuous.

The tone of voice used during communication was effective because whilst I was communicating with my group I emphasised on my voice projection by ensuring that my group member could hear me clearly, ineffective communication was prominent as individuals kept talking over one another. For effective communication, I strongly believe that a single voice should be heard at a particular time. According to Goodsell et al (1992), ”Building the capacities for tolerating or resolving differences, for building agreement that honours all the voices in a group, for caring how others are doing these abilities are crucial aspects of living in a community”. This reinforces the information the individual is trying to pass across to other members of the group. This also sets the tone of professionalism and respect within the group which is a vital component to enable any group to function to its maximum potential.

To improve this, various aspects of my mode of communication had to be altered; talking in a much clearer tone, emphasising on important key words and speaking with confidence and assertiveness will bring about clarity and effective communication which would cause less confusion. When explaining treatment to the patient, I will ensure I communicate with an assertive tone of voice through using modest language to ensure that the patient can understand information regarding treatment and to ensure that they feel empowered.

During the group communication, I focused on establishing a level of eye contact with members of my group but occasionally I looked away to avoid tension. Also, I kept my face relaxed and friendly because tightening my face may portray me as aggressive to others. As a group we all did not maintain adequate eye contact. I observed that eye contact “invariably fell off in the second half of each three minute conversation” (Argyle & Dean, 1965, pp.289-304). When speaking to a group of people or addressing a patient, it is important to have a connection with those people or that person. This connection is only made possible via eye contact. This shows full concentration on the message we are trying to pass across and it also portrays a level of certainty and assertiveness regarding the subject being discussed.

A lack of eye contact shows a level of weakness in communication and also a weakness within an individual. This can be improved by showing attention and interest within the group .Wainright, (2003). Also, we can improve this by blinking at each other 3-4 intervals as it will show a sign of friendly listener. Some patients might highlight the lack of eye contact as a deficiency in assuredness and assertiveness.

In addition, I will constantly have to assure my patient; so that they have utmost belief in the treatment they are being given. Eye contact can also help patients to feel comfortable and protected. Adequate eye contact will reinforce and show that I truly care about their well-being and I am willing to meet their psychological and emotional needs. Without eye contact, people will not feel they are fully in communication.

During the discussion, I noticed that we all understood each other quite well but a number of people brought their thoughts and emotions about the topic and this affected us in a way because there was barrier in delivering the message. In order for the group to deliver message properly to other colleagues, we should consider our receiver’s point of view and establish if they would understand the message and how it would sound to them. ”How physicians communicate with their patients is another process that is extremely important to understand. There is numerous analysis of this process, which range from discussions of language barriers to inefficiencies in delivering basic information regarding complex diseases”. (Darrell et al, 2005, pp.1095-1099).

Understanding various forms of communication is vital and also ensuring communication is effective for the receiver to understand the message being passed across because for me to deliver bad news to my patients, I will need to know the method of delivery to the patients for them to fully comprehend the correct situation and react well. Delivering of the message must be effective in a way that it would keep my patient safe and build trust in me.

Also, in my group I clearly felt that the lack of established criteria and guidelines which when implemented could have structured the exercise was ultimately helpful. Molyneux (2001). It helped me build more interaction within my group as we had to construct guidelines and methods of an approach together. This quickly aided communication as we as a group felt the need to be involved as it will govern our modes of operation within our team in future.

During the communication I noticed that my voice was not clear enough because some people in my group seem confused whenever I gave answers to questions and had to repeat myself again. I learned that it is important I speak effectively and clearly because I do not want my leadership ability to be questioned. To improve this, it may be helpful for me to use analogies that can help my group understand the concept. When communicating with my patient I will need to speak clearly and show full interest as this will make them more confident and comfortable.

Facial expression is also crucial, this involves engaging through the use of eyes, muscles and mouth can form a connection with my audience. While I was conversing with my group members I smiled consistently to engage my group members. But one of my group members kept his face straight during the communication and he looked quite upset.

It is essential to maintain a connection within a group not only using eye contact, but by our facial expressions, which translate into our body language. ”One can conceive of facial expression as a visual code available to human source for the encoding and transmission of purposive messages”. (Williams & Tolch, 2006, pp.17-27). A patient can read into the body language of the speaker and denote certain attributes. In this aspect it is important I keep a professional stance at all times, a stance and exhibits confidence and assuredness at all times.

In conclusion, reflecting back on my learning experience, I have realised the importance of inter-professional practice within the health care setting. My strengths and weaknesses as a health care professional and the ways to improve on them. Having effective inter-professional practice will benefit me as a student nurse because it will allow me to perform my role effectively and I will be able to develop supportive ties with patients from different cultures and backgrounds.

References.

Argyle, M. & Dean, J. (1965). Eye contact, distance and affiliation. American Sociological Association, 28(3), 289-304.

Darrell, J., Gale. H. MD., Richard M. P.H.D., Gale. H. MD., Norvell, MD., Rutan, M.D & Solet, M.D. (2005). Lost in translation: Challenges and opportunities in physician-to-physician communication during Patient Handoffs. Journal of the Association of American Medical Colleges, 80(12), 1094-1099.

Goodsell, A., Vincent, T., Smith, S.B & Macgregor, J. (1992). “What is collaborative learning?” in collaborative learning .London: A Sourcebook for Higher Education.

Jasper, M. (2003). Beginning reflective practice. London: Nelson Thornes Ltd.

Marks-Maran, D. & Rose, P. (1997). Beyond art and science- reconstructing nursing. London: Bailliere Tindall.

Molyneux, J. (2001). Interprofessional team working: what makes teams work well? Journal of Interprofessional care, 15(1), 29-35.

Nursing and Midwifery council. (2007a). The code: Standards of conduct, performance and ethics for nurses and midwives. London, NMC

Prothero, S.M. (2001). Bailliere’s study skills for nurses. (2nd ed.). London: Royal college of Nursing.

Sanders, M. (1995). Collaborative learning enhances critical thinking. Journal Of Technology Education, 7(1), 1045-1064.

Wainright, R.G. (2003). Teach yourself, body language. London: Hoddler Headline.

Williams, F. & Tolch, J. (2006). Communication by facial expression. Journals Of Communication, 15(1), 17-27.