Stress- Burnout and Anxiety in Medical Professionals

Every day thinking about becoming a doctor trying to save lives and doing surgery is all part of the dream. There are many obstacles a medical student has to face to reach their goals. Some of the obstacles are taking the MCAT and having a 3.5 GPA throughout four years of college to determine where students will go for medical school. To become a doctor, a medical student has to go through medical schools and then 3 to 7 years of a residency program to become a doctor.  As thinking about becoming an OBGYN that delivers babies and treats diseases of the female reproductive system, there will be many challenges to face to reach the goals. Becoming an OBGYN will  help females who are unable to pay for medical advice and reduce the birth mortality rate. To face these obstacles a medical student and health professionals must learn how to cope with stress, burnout and anxiety disorder.

Stress

Firstly, stress is the response to challenges resulting from stimuli or events that causes emotional and physical tension (Licht, Hull, & Ballantyne, 2017). Stress plays a daily role in our lives from being frustrated about the school to feeling nervous about turning in a homework assignment. A stressor is a stimulus that causes one to release stress hormones that can affect one mentally and emotionally (Licht, Hull, & Ballantyne, 2017). For example, the death of a family member that your close to made you feel lonely can lead to stress. There is also positive stress which is the response to agreeable or positive events which is called eustress (Licht, Hull, & Ballantyne, 2017). An example of eustress is working hard to reach your goals or planning to travel is all part of positive stress. But there is also negative stress response to unpleasant events which is called distress that leads to undesirable stressors (Licht, Hull, & Ballantyne, 2017). For example, studying for a medical exam last minute and not being prepared cause distress. Medical professionals often feel stress when it comes to diagnosing a patient and figuring out what plan will be more effective on the patients. There is also stress about giving the right amount of medication and stress about telling the family about the patient’s condition or death. Medical professionals often have overnight shifts which can have difficult cases and cause stress because there are not enough doctors available. Doing surgery gives a lot of stress because one mistake can create a life and death situation. To cope with stress medical professionals can go to the hospital psychologist to get counseling or write down their stress in a diary or journal. Medical professionals can find something that can relieve stress by going on vacation or meditating. Not dealing with stress can drain you mentally and physically.

Burnout

Secondly, Burnout is the feeling of not being motivated due to overworking the body emotional, mental, and physical (Licht, Hull, & Ballantyne, 2017). Many Medical professionals feel fatigued during long hour shifts because they are on call even when off duty. This may cause a lack of treatment to the patient and some may be left untreated. Medical students tend to burnout more due to stress, workload, and exams. According to a study, about 37% of Canadian medical students meet the criteria for burnout (Glauser, 2017). This shows that a significant amount of medical students do not receive an adequate amount of sleep. A study done by the American Medical Association which is based on an international survey about 27% of medical students showed symptoms of depression (Glauser, 2017). This data explains the correlation between depression symptoms and burnout among medical students. Having a lack of sleep, during 70 hours of clinical rotation and dealing with death first time can add on and the best coping mechanism starts to fail (Glauser, 2017). Many medical professionals forget to take care of their mental and physical health due to the stress of saving the lives of others. This is a problem because exhaustion and overload can lead to mistreating the patient. Medical students and the medical profession need to find a way to cope with their problems by getting eight hours of sleep and taking care of their health.

Anxiety Disorder

Finally, anxiety disorder is a psychological disorder that characterized feelings of extreme anxiety and irrational fears that interfere with daily activity (Licht, Hull, & Ballantyne, 2017). Many medical students worry that they will fail an exam or that they will not pass a class which can lead to anxiety. The cause of anxiety in students is because the amount of money they spend in medical school and how much work they put in. If one mistake is made it can lead to jeopardizing their career which can lead to depression and anxiety. Many physicians and medical students fear the death of their patients. Not having proper care of yourself can lead to failure in taking care of others.

Conclusion

In conclusion, medical professionals and medical students  must know how to cope with stress, burnout, and anxiety disorder. Knowing how to deal with stress can help the doctors to treat their patients better and will be able to make better decisions. The medical field has a lot of stress the medical profession should know how to deal with stress by going to a psychologist or finding other ways to deal with stress. The medical profession should realize when they feel they are burnout that way they can take breaks when the body signals them to. For anxiety disorder, medical students should not be hard on themselves and do the best they can. Learning about theses coping mechanism will help medical student to deal with problem efficiently before the problems cause major harm.


References

  • Glauser, W. (2017, December 18). Medical schools adressing student anxiety, burnout and depression.

    Canadian Medical Association. Journal, 189

    (50), E1569-E1570.
  • Licht, D. M., Hull, M. G., & Ballantyne, C. (2017).

    Scientific American: Psychology 2nd Edition.

    New York, N.Y: Worth Publisher.

Asthma: Pathophysiology- Education and Health Promotion


Diagnosis:

Based on the HPI, ROS, PE, and diagnostic tests, the diagnosis is most likely to be an acute asthma exacerbation. Episodes of an asthma attack are mostly triggered by exposures to an allergen, including: grass, pollen, dust or animal dander (Tillie-Leblond, Gosset, & Tonnel, 2005). Some triggers also include air irritants such as chemical fumes, strong odors (like smoke), and even perfume. Inhaling cold air, stress, and upper respiratory infections (such as cold) could trigger asthma episodes. Sometimes, asthma exacerbation occurs for no apparent reason. The underlying principles point to an overly sensitive immune system which makes the airway inflamed when one is exposed to certain triggers named above (Tillie-Leblonde, et al., 2005). Nonetheless, triggers are not alike with every individual and may vary from one person to another.

The onset of dyspnea and wheezing after heavy exercise outdoors and history of similar asthma exacerbations indicate she may be having asthma-related issues. Because her symptoms were not relived with the rescue inhaler during this exacerbation, it was important to rule out other causes of dyspnea in addition to assessing the need for a readjustment to her current asthma treatment regimen. Her allergies to outdoor dust, hay, rag weed, mold are also an indicator her asthma may be the prime issue. Her history of smoking could have led her to other possible issues causing dyspnea as well, which is why differential diagnoses such as pulmonary embolism, poor physical conditioning, and COPD were ruled out. Patient position slouched forward in tripod position, accessory muscle use, intermittent nasal flaring when speaking for longer than 1 minute, decreased tactile fremitus throughout, hyperresonance noted to bilateral posterior upper lobes, and diminished breath sounds with expiratory wheezes noted over all lung fields are symptoms prompt other test necessary to rule out other conditions. Spirometry results of FVC 2.40, FEV1 1.5, FEV1/FVC 62% on initial assessment was most useful in the initial diagnosis of asthma but can be used to monitor treatment effectiveness as well. In addition, chest radiography findings are normal, which is consistent with an asthma diagnosis.

In both acute and chronic asthma, arterial blood gas sampling is one of the critical steps in assessment to assess the acid-base status and oxygenation levels in patients. This test examines the levels of oxygen and carbon dioxide in the blood. It evaluates the effectiveness of oxygen delivery and carbon dioxide removal from the blood by the lungs (Padmavathi. K, 2013).

Diagnosis is performed using diagnostic tests while also employing the evaluation of clinical presentations. The doctor assesses for signs and symptoms like chest tightness, coughing, wheezing and shortness of breath. Diagnostic tests include peak flow, spirometry, nitric oxide measurement and pulse oximetry (Clancy & Blake, 2013). In a peak flow test, the patient blows into a mouthpiece as hard and as first with just a single expiration. It evaluates how quickly can a patient breath out. (Lynn B Gerald, 2018)


Pathophysiology:

The pathophysiology of asthma is complex and involves intermittent airflow obstruction by airway inflammation and bronchial hyperresponsiveness. Bronchoconstriction is the dominant event which causes clinical symptoms through airway narrowing and interference of airflow (Clancy & Blake, 2013). An acute asthma exacerbation is characterized by a quick smooth muscle contraction response due to exposure to a variety of stimuli, such as allergens. In chronic asthma, as the disease becomes more persistent and inflammation progresses, mucosal edema amplifies bronchial responsiveness by increasing epithelial permeability and altering airway mechanics (Clancy & Blake, 2013). Hyperresponsiveness which is categorized as an exaggerated bronchoconstrictor response due to stimuli is influenced by factors including inflammation, dysfunctional neurological regulation, and structural changes. In some cases, permanent structural changes can occur to the airway also known as airway remodeling. This involves activation of many structural cells, leading to the consequent permanent changes which escalate airflow obstruction and responsiveness.

The characteristic airway inflammation of asthma can result in several consequences, including airway hyperresponsiveness, increased mucus reproduction, and obstruction of the airway. It also constitutes bronchiolar inflammation of the airway causing resistance, which presents as episodes of wheezing, shortness of breath, and coughing (Clancy & Blake, 2013). Asthma is a chronic lung condition that can cause acute exacerbations. For some people, asthma is a minor health problem where acute signs and symptoms present themselves less frequently, with normal lung and airway function. For others with intensified, frequent signs and symptoms, asthma can be persistent and life-threatening


Evaluation, Education, and Health Promotion:

Emergency cases where patients are admitted to emergency rooms for status asthmaticus, intubation and mechanical ventilation for oxygen is paramount since this is a respiratory failure which comes in the worst form of an asthma attack. The doctor places breathing tubes down the throat into the upper airway which are then connected to a ventilator which pumps oxygen into the lungs. Short-acting beta-agonists are administered through a nebulizer. Oral corticosteroids in pill form are administered to reduce lung inflammation and stabilize the airway (Rowe, Spooner, Ducharme, Bretzlaff, & Bota, 2007)

. When the patient’s asthma symptoms improve, the patient is monitored for some time to ensure that his/her condition is sufficiently under control. An asthma plan is afterward developed. This plan includes an inhaler where a patient is instructed to take between two to six puffs (depending on severity) of a quick acting inhaler which has medication such as albuterol.

If the asthma attack is severe, the patient is not only advised to administer the initial step of using quick action inhaler but also immediately visit the doctor or urgent care facility for further treatment. If the exacerbation is severe, there would be more wheezing than normal, extreme shortness of breath that is worse than normal characterized by shallow and rapid breathing. (E. Evensen, 2010) Also there would be large mucus production and the mucus can have changes in color such as yellow, green or bloody (Vogelmeier, 2018). If the asthma attack is triggered by outside allergens, the doctor will assist through an allergy test to identify the allergic triggers and educate the patient on how to minimize his/her exposure. The patient can avoid flowery gardens if pollen is an allergen. She is further advised to avoid dusty and smoky environments. In addition, if a cold environment is found to trigger an asthma attack, the patient is advised to cover her/his face using a scarf to ensure warm air is breathed in.

Taking all medications as prescribed is critical to maintain good asthma control. If symptoms of asthma are worsened and quick relief is needed, she can safely use her inhaler as often as 30-60 minutes after an average period of 2 to 3hours. Keeping an inhaler close is also crucial as in some occasion, an asthma attack can be so severe that one cannot be able to fetch his/her inhaler from wherever they left if, and as a result, it is always safe to ensure that the inhaler is close with the patient. In both routine prevention therapy and in emergency cases, every patient should own and regularly employ a spacer and know how to use it correctly (Walter Vincken, 2018). And even though many patients use their inhalers correctly, they fail to carry out proper techniques needed for the medication to properly reach the lungs. Spacers make the process of use much easier while also delivering the medication more efficiently (Walter Vincken, 2018).

Washing your hands frequently is helpful in reducing the chances of catching a cold virus and reduces the spread of bacterial that can cause other respiratory infections. Most importantly, education on social smoking and second hand smoke is necessary to decrease risk of exacerbations as well as other comorbidities associated with it. (Jennifer L. Perret, 2016) Smoking cessation is highly encouraged because smoke increases the risk of exacerbations, acute asthma exacerbations can hence quickly progress to chronic (Jennifer L. Perret, 2016).


References

  • Clancy, J. & Blake, D. (2013, September). Pathophysiology and pharmacological management of asthma from a nature-nurture perspective.

    Primary Health Care

    ,

    23

    (7), 34-41. DOI: 10.7748/phc2013.09.23.7.34.e725
  • E. Evensen, A. (2010, March). Management of COPD Exacerbations.

    American Family Physician

    , pp. 607-613. Retrieved:

    https://www.aafp.org/afp/2010/0301/p607.html
  • Gobbi, A. Gulotta, C., Suki, B., Mellano, B., Pellegrino, R., Brusasco, V., & Dellacà, R. (2019, June). Monitoring of respiratory resistance in the diagnosis of mild intermittent asthma.

    Clinical & Experimental Allergy, 49

    (6), 921-923. DOI: 10.1111/cea.13376
  • Jennifer L. Perret, B. B. (2016, June 24). Smoking cessation strategies for patients with asthma: improving patient outcomes.

    Journal of Asthma and Allergy

    . Retrieved: doi:

    10.2147/JAA.S85615
  • Lynn B Gerald, T. F. (2018, October 23). Peak expiratory flow monitoring in asthma.

    UpToDate

    . Retrieved:

    https://www.uptodate.com/contents/peak-expiratory-flow-monitoring-in-asthma
  • Padmavathi. K, S. S. (2013, November). ARTERIAL BLOOD GAS ANALYSIS IN ACUTE AND CHRONIC BRONCHIAL ASTHMA.

    Bulletin of Pharmaceutical and Medical Sciences

    , pp. 1-6. Retrieved:

    https://pdfs.semanticscholar.org/560c/c0fabf7e0f10065847e20293a65236ad3c5a.pdf
  • Rowe, B., Spooner, C., Ducharme, F., Bretzlaff, J., & Bota, G. (2007, July 18). Corticosteroids for preventing relapse following acute exacerbations of asthma.

    Cochrane Database of Systematic Reviews,


    2007

    (3), 1-28. DOI: 10.1002/14651858.CD000195.pub2
  • Tillie-Leblond, I., Gosset, P., & Tonnel, A. (2005, January). Inflammatory events in severe acute asthma.

    Allergy, 60

    (1), 23-29. DOI: 10.1111/j.1398-9995.2005.00632.x
  • Vogelmeier, C. F. (2018). Exacerbations of COPD.

    European Respiratory Review

    . Retrieved: DOI: 10.1183/16000617.0103-2017
  • Walter Vincken, M. L. (2018). Spacer devices for inhaled therapy: why use them, and how?

    ERJ Open Research

    . Retrieved: DOI: 10.1183/23120541.00065-2018

Teaching Plan for Client in Medical-Surgical Unit

Teaching Plan for Client in the Medical-Surgical Unit of MountainView Hospital in Clark County, Nevada


Topic for Educational Need

The topic of education for this patient is postoperative care for hip replacement surgery. This topic was chosen because the patient underwent a total right hip arthroplasty procedure on September 16, 2019. The patient will need guidance and instruction on all aspects of recovery to achieve the best outcome of the joint replacement surgery (John’s Hopkins, 2017). Being knowledgeable about how to self-care, what to expect, and what resources will be needed will assist the patient obtain and maintain the best possible function and quality of life after the procedure (Cleveland Clinic, 2015).


Objective Data


Relevant Medical and Surgical History.

Chronic progressive right hip pain; limited in ambulation to about 100 yards without stopping because of pain. Back pain, herniated disc, lumbar fusion 1981, motor vehicle accident in 1983, numbness and tingling from hip area down to legs.


Vital Signs.



September 16, 2019.


Temperature 98.6F, blood pressure 105/71 mmHg, pulse 74 bpm, respirations18 breaths/min, O2 sat 97% on 2.0L/min nasal cannula.



September 17, 2019: 0730.


Temperature 98.8F, blood pressure 92/58 mmHg, pulse 78 bpm, respirations 18 breaths/min, O2 sat 98% 2.0L/min nasal cannula, pain level 7 out of 10.



September 17, 2019: 1130.


Temperature 98.8F, blood pressure 93/59 mmHg, pulse 79 bpm, respirations 18 breaths/min, O2 sat 97% on 2.0L/min nasal cannula, pain level 9 out of 10.


Assessment of Patient

The patient was alert and oriented x4 throughout the clinical day on September 17, 2019. The patient 54 years old, a native English speaker, and high school educated. The patient is unemployed, divorced with three children, lives alone, and on disability from a motor vehicle accident in 1983. The patient has chronic hip pain with numbness and tingling from the hip area down to the legs and has managed the pain throughout the years since the MVA with physical therapy and the use of baclofen and clonazepam for muscle spasms. The patient is accustomed to applying self-care to manage her physical condition. The patient’s plan after discharge from the hospital will be to live at one of her adult daughter’s home which is a one-story unit so the patient will not have the burden of going up and down flights of stairs. The patient’s health goal is to be independent as soon as possible and is motivated to apply all suggested therapeutic interventions. The patient’s current emotional state ranges from willingness to make a rapid recovery as well as some anxiety surrounding the management of pain which ranged from 7 to 9 out of 10 during the clinical day.


Method of Implementation

The patient’s learning style is visual and motor so printed handouts and physical demonstration were chosen as the method of teaching. A hands-on approach where the patient gets to perform a procedure with your guidance is often the best method (Lippincott, 2017). The patient’s style is to keep it simple and get the facts with a simple checklist. The patient does not have hearing or learning impairments so there will not be limitations as to what the patient understands. The patient’s daughter is supportive and will be informed by the patient on how to be cared for so the patient will receive assistance with health care management. The patient has access to a computer and the internet at home and is willing to seek further instruction from reliable sources such as the “Patient Handbook for Total hip Replacement” by Kaiser Permanente for more details on how to perform activities of daily living after surgery.


Teaching Tools

The tools that will be implemented for teaching will be printed handouts and physical demonstrations of how to use adaptive equipment. The printed handouts outline the physical movements and positions that the patient will practice that will reduce pain and improve function. These movements include not bending the hip past 90 degrees, not crossing legs while sitting or standing, not pivoting foot and toes inward (medially), and how to use a walker.

The patient will also be educated on how to perform activities of daily living such as showering, dressing and toileting. For showering, a shower chair or stool should be utilized for safety as well a long-handled brush or sponge to assist with washing. Dressing aids such as a long-handled shoe horn and tongs will assist with dressing. For toileting, a raised seat should be used and rails should be installed if possible to provide support.

The printed handouts were chosen because it shows simple illustrations on what to do and what not to do that will be easy to follow. The patient will be able to glance at the handout be reminded of what movements and positions are recommended and what should be avoided without having to read lengthy paragraphs. In-person physical demonstrations on how to use adaptive equipment will allow the patient to practice utilizing each item before going home to it is familiar once the patient is home and will be using the equipment independently.


Evaluation

The patient demonstrated that learning occurred by return demonstrating the movements and positions that were shown on how to go from sit to stand and to bed. The patient verbally repeated the instructions given regarding what to do and what not to do when performing activities of daily living. The patient acknowledged the adaptive equipment that were in the room to take home upon discharge. An example of a question asked of the patient is, “what is the angle that you should avoid sitting or bending?” and “what should you never do with your legs while sitting or standing?”. The criteria that would show the patient understood the material is if the patient responded with the answers, “Do not sit or bend more than 90 degrees”, and “Do not cross legs while sitting or standing” to the questions aforementioned, respectively. Possible revisions to this plan would be to provide a DVD for the patient to take home to be viewed periodically as a refresher to maintain the best practice for physical therapy exercises and the how to’s for activities of daily living.

References

Proposal for a specific program for older adults

Proposal for a specific program for older adults

Proposal for a specific program for older adults

Develop a proposal for a specific program for older adults and/or their families. Assume that your budget is flexible but consider real world limitations to implementing the program.

What is your theoretical and research informed rationale for the program you propose?

Who will be targeted to participate?

Who will staff the program?

What will their qualifications be?

What pre-service and in-service training will they receive?

What obstacles do you anticipate encountering with the development and implementation of the program?

How will you determine the effectiveness of the program?

How will you market the program (advertising, a logo, the name of the program, etc.)?

How will you meet the needs of diverse constituents served by the program?

This must be an original proposal and may not duplicate one prepared for another course. To make sure you cover every important topic.

I suggest you organize your paper with the following subheadings:

Goals of the Program

Factors to consider (market considerations, laws and regulations, financing)

To what extent will your program promote aging in place?

Coordinate services?

Provide new services?

Target different populations?

Integrate services with other agencies or programs

How will you finance your program?

Who benefits from the program

Who will perform the tasks, and what do tasks entail?

Additional information to include

Research literature and other sources:

Retrieve and read at least 10 recent peer-reviewed journal articles, government websites (not more than 3 websites) and/or book chapters on your topic.

Sources should be from 2006 to present.

Recommended databases include: PsycInfo, CINAHL (Nursing and Allied Health Literature), AgeLine, Social Work Abstracts.

Final Project should be 10-15 double spaced pages, not including the title or reference page. Include page numbers. Written assignments may include exhibits or other attachments, but these will not be considered part of the page requirements. Typesetting 12pt Arial




ORDER NOW FOR CUSTOM-WRITTEN, PLAGIARISM-FREE PAPERS




You must proofread your paper. But do not strictly rely on your computer’s spell-checker and grammar-checker; failure to do so indicates a lack of effort on your part and you can expect your grade to suffer accordingly. Papers with numerous misspelled words and grammatical mistakes will be penalized. Read over your paper – in silence and then aloud – before handing it in and make corrections as necessary. Often it is advantageous to have a friend proofread your paper for obvious errors. Handwritten corrections are preferable to uncorrected mistakes.


Use a standard 10 to 12 point (10 to 12 characters per inch) typeface. Smaller or compressed type and papers with small margins or single-spacing are hard to read. It is better to let your essay run over the recommended number of pages than to try to compress it into fewer pages.


Likewise, large type, large margins, large indentations, triple-spacing, increased leading (space between lines), increased kerning (space between letters), and any other such attempts at “padding” to increase the length of a paper are unacceptable, wasteful of trees, and will not fool your professor.


The paper must be neatly formatted, double-spaced with a one-inch margin on the top, bottom, and sides of each page. When submitting hard copy, be sure to use white paper and print out using dark ink. If it is hard to read your essay, it will also be hard to follow your argument.


Relationship Between Social Factors and Health Inequalities


Critically discuss the relationship between social factors and health inequalities. Making reference to at least two theoretical approaches to explaining health inequalities, suggest how useful they are, as well as addressing their weaknesses.

Understanding the inequalities in health and their association with various social issues/factors is the objective of this essay. The essay also seeks to explain these underlying health inequalities with social factors using different theoretical methodologies.

But, before discussing the correlation between the various social factors and health inequalities we need to comprehend ourselves with the significance of Health. As per the World Health Organization (WHO): “

Health is a state


of complete physical, social and mental well-being and not merely the absence of disease or infirmity. The enjoyment of the highest attainable standard of health is one of the fundamental rights of every human being, without distinction of race, religion, political beliefs or economic and social conditions

”(WHO, 1948).1

Based on this definition, National Institute Health Excellence (NICE, 2012) defines Health Inequalities as “an inability to attain the health among different groups or individuals due to difference in their social, geographical, cultural/behavioural, biological or other factors.”2 In simpler terms, health inequalities can be defined as “

an unjust disparity in the health when these differences are not only preventable but are also unnecessary

”.3

To further explain these differences, different theoretical attempts were made including social class, material deprivation, behaviour and culture, artefact, environmental and selection theory, the geographical aspects, difference in genetics and the life course perception of health played a vital role in understanding the health inequalities.3

The diagram above shows the various causes of health inequalities divided into different categories of fundamental causes; environmental influences; and finally individual experiences which finally in-turn lead to the disparity in wellbeing and health of different groups or individuals.

The

fundamental causes

are the factors which cannot be undone such as, Global economic forces, socio-political environment and priorities lead to an unequal distribution of income, power and wealth which can further trigger poverty and marginalization of the individuals belonging to different social groups and classes.

These initial differences further influence the distribution of

environmental influences

, such as availability or accessibility of employment, schooling, better housing, health services and various societal & cultural opportunities. Thus, shaping the individual experiences across the population leading the inequalities in the health outcomes.

There are numerous examples across the globe which have claimed the link between these various social factors to the health of the individual or groups.

The very first information in this group is the

Black Report of 1980

stating the effect of the social classification of a person on his/her health.4 The findings reported a huge gap in the proportion of people suffering from ill-health increased as we go down the social ladder, which had nothing to do with the health services delivered by the National Health Services (NHS) in the country but was mainly due to unemployment, poor hygiene, low income and poor housing.4-7

Similarly, a publication by

Wilkinson and Pickett

(2009)  “

The Spirit Level

” also claimed that economically weaker sections of the societies have an additional ill-health and social problems compared to their stronger counterparts. This argument was further strengthened by the finding of “Strategic Review of Health Inequalities in England” (2010).8 Thus, advocating income inequality as a key explanation for all the prevailing health disparities.

However,the novel

Neoliberal discourse

was another factor which also provided an explanation to the health inequalities using factors other than income disparity. Few studies carried out in past have exhibited that more neoliberal countries (the United States of America) have poorer health compared to the less neoliberal countries (Canada).8 This was proven by a comparative study carried out by Siddiqui A et al.,(2013) to understand the effect of Neoliberal reform in both the countries. The findings of the study indicated that Canada was more resilient in terms of health inequalities despite the income inequality among various social groups. Canada was able to achieve this because of their policies of maintaining equality in the provision of various social goods like healthcare and education and maintaining a social cohesiveness across different racial/cultural & class-based groups.9  Additionally, Corburn D (2004), have also demonstrated the association of neo-liberalism (using infant mortality) with greater poverty and health inequalities and the countries with less neo-liberalism have better health compared to ones which are more neo-liberal.10

Another landmark example describing the effect of social factors on health disparity was the

Whitehall (I)Study.

The study concentrated on a group of British Civil Servants



wherein the people within each occupational grade tend to be similar, yet socially distinct between the grades. The study investigated the cardiovascular function, high blood pressure, smoking, hobbies etc among the individuals. The results showed that there was a steep inverse relationship between social class and high blood pressure. Summing up the outcomes, the researchers concluded more attention need to given to the social environment, job design and income inequality to avoid health disparities.11

These are a few pioneering examples depicting the effect of various social factors on the prevalence of health inequalities not only amongst different but also within similar social groups/ individuals.

As mentioned previously in the essay there are different theories explaining the health inequalities. However,  there are four main theories which are mostly applied to explain them ie., 5,6


  1. Behavioural Theory

    : Explaining the health-damaging/ promoting behaviour among the individuals/ groups such as diet choices, intake of alcohol and tobacco, usage of maternal & child care and other health services. This theory is useful in establishing a clear link between certain practices and outcomes (smoking and lung cancer), thus helping in planning for future health promotive/preventive measure. However, cohort studies (Whitehall’s study) have shown that health behaviour justifies only one-third of social differences in mortality. Furthermore, evaluations of these promotive/preventive interventions have seldom given any clear cut improvements in health.

  2. Materialist Theory:

    Poverty imperils individuals to health risks. Deprived individuals are more likely to reside in areas with higher risks like inadequate housing, air pollution etc.  The Black Report (1980) gave a materialist description to the importance of social class variances in health.4 However, many experts find the model to be insufficient since the so-called disadvantaged individuals are often provided with numerous benefits by the state making food or housing an unlikeable cause for disparity in health outcomes.

  3. Psycho-social Theory:

    Relates to the aspects of the social life affecting people’s state of mind. the researchers through the Whitehall Study have explained the effect of social environment on the health outcome of individuals working in different occupational rank.11 The theory is also been able to explain certain risky behaviour (smoking) prevalent among a certain group of people. However, it cannot fully explain the uneven distribution of employment and services between various classes and races.

  4. Life-course Theory:

    A relatively recent theory undertaking various social, psycho-social and biological factors experienced by a person during their lifetime. For example, a child experiencing inadequate living condition is more likely to have an educational and occupational disadvantage in future. The theory, on one hand, allows us to understand the implication of life experiences on future life outcomes. However, investigating life-course explanations becomes difficult as they require longitudinal data which is difficult to obtain.


A brief explanation of The Black Report (1980) using the above-mentioned theories

These theories help to differentiate the characteristics affecting health across different social classes over their lifetime.

For instance, the

behavioural theory

was used to describe the difference among numerous health-related choices such as dietary patterns, consumption of tobacco, alcohol and drugs, utilization of preventive healthcare services among different social groups.4-6 Similarly, the

materialist theory

was aptly used in the report as a decisive factor leading the health inequalities. The theory encompassed the factors like air pollution, infestations and respiratory hazards which has risen due to poor income condition.4,5,7

Likewise, the

psycho-social theory

explains the concept of people’s experiences determining the changes in the physiology of their body. For instance, a hectic social atmosphere associated with the lower working groups of an organization can produce a negative biological effect in the body leading to a greater incidence of morbidity and mortality among the people belonging to that societal section.

And finally, the

life-course theory

which focused on all the aspects of societal, emotional and biological advantages and disadvantages occurring during the lifetime of a person which eventually defines the health outcome of that particular individuals. This could be again be used for the people living in the poorer section of society who were at a disadvantage since their birth, thus ultimately resulting in inferior health and social outcomes during their entire lifetime.

Therefore, in the end, there are few things which can be concluded through this essay. Firstly, even though there are many theories explaining health inequalities among different social groups, its mainly the socio-economic conditions along with the political, societal and environmental forces which predominantly create or destroy a person’s health and wellbeing. Secondly, there isn’t one full-proof theory which can explain prevailing gaps in the healthcare system. Finally, despite having numerous theoretical explanations to numerous health inequalities the political and societal forces across the nations have failed to address these social factors. Henceforth, there is a dire need to address these factors in order to ensure an equal chance of a healthy life for everyone.


References

  1. World Health Organization. Constitution. World Health Organization.1989.
  2. The National Insititute for Health and Care Excellence. Health Inequality and population health. The National Institute for Health and Care Excellence. 2012.
  3. Arcaya MC, Arcaya AL, Subramanian SV. Inequalities in health: definitions, concepts, and theories. Global health action. 2015 Dec 1;8(1):27106.
  4. Black SD. Inequalities in health: report of a Research Working Group. Department of Health and Social Security; 1980.
  5. Bartley M. Health Inequality: An Introduction to Theories, Concepts and Methods Cambridge. Polity. 2004.
  6. Bartley M, Blane D. Inequality and social class. Sociology as applied to medicine. Elsevier. 2008 Jun 27.
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End of Life Care: Cancer Patients Right to Die

Introduction

Recently, the concept of patient autonomy has become more prevalent within the healthcare field with the government and the NHS promoting patient choice and providing assurance that individuals will have full control over their care and patient journey. However, a recent publication from Macmillan Cancer Care (MCC) (2013a, pp. 1-27), suggests that there is very little choice available for individuals suffering from terminal cancer with regards to where they spend the end of their lives. Figures provided within the MCC (2013a, p. 8) report suggest that 81% of cancer sufferers would prefer to die at home whilst in reality, 48% of these die in a hospital with only 23% of patients dying within the comfort of their own homes.

For individuals who are approaching the end of their lives, the option of being cared for and dying within their own home with the familiarity and comfort that this brings, is often very important. The National Bereavement Survey (NBS) (Office for National Statistics, 2012, np) showed that that the loved ones of those who had died in hospital often considered the standard of care as being poor when compared to those who died at home, in a care home or within a hospice. Indeed, the NBS (ONS, 2012, np) showed that 53% of loved ones whose friend or family member had died at home and 58% of those who had died in a hospice, rated the standard of care as outstanding or excellent compared to just 34% for those who had died within a hospital.

This essay will consider the barriers that cancer patients are presented with when making their end of life choices and will make recommendations for improvement of service to ensure that these individuals are allowed to make and receive their final choice. However, the essay will begin with a brief overview of the benefits that end of life patient choice can bring to both the individual and to the wider society.

The Benefits of End of Life Patient Choice

According to the National End of Life Intelligence Network (2012, p.7) 89% of patients who die in hospital are brought in as emergency admissions. However, a large number of these individuals have already expressed their desire to die at home, therefore representing a poor patient outcome and negative experiences. In addition, these unnecessary emergency admissions place a costly strain on accident and emergency departments and the patients take up hospital beds that could be used for other cases. When one considers that the number of people in this country is increasing with the elderly becoming the most prevalent age group, it is not unfeasible to believe that the number of individuals dying from terminal cancer over the next few decades is also going to increase. This increase in numbers is likely to cause the current model of care to become unsustainable. However, promoting choice and delivering end of life care choices can actually save money by reducing the number of emergency admissions. According to MCC (2013a, p.9), there is a net saving of just under £1000 for every individual who dies in the community rather than in a hospital bed.

Barriers to End of Life Care Choices

Evidence suggests that there are multiple barriers that prevent individuals from being cared for and ending their lives in their chosen place. The first barrier is the identification of people approaching the end of their lives. According to MCC (2013a, p.10), 38% of cancer patients approaching their end of life were unaware that they were dying, whilst figures from Marie Curie Cancer Care (2013, p.7) show that only 26% of individuals with a palliative care need are placed on the palliative care register. One of the main reasons for this appears to be a lack of confidence in the health professionals over instigating conversations with individuals over their end of life journey. A study carried out by Revill (2010, p.11) found that 60% of GPs were not confident about discussing death or dying with their patients. This lack of identification and lack of professional confidence therefore prevents many people from being able to make their end of life choice in a timely fashion, therefore increasing the number of emergency admissions that have previously been discussed.

However, another issue that has been raised is that of poor planning and coordination between services. When one considers the needs of a terminally ill cancer patient, it is clear that there is a requirement for multiple health and social care providers to work together to provide a joined up service delivery. Unfortunately, the MCC (2013a, p.11) report suggests that this joined up service is not occurring with 45% of respondents thinking that community services worked well together and only 33% stating that GP and other services outside of the hospital worked well together. The reason for this poor service is considered to be a lack of coordination and communication between the different care entities. Indeed, the MCC (2013a, p.11) report suggests that it is often a requirement of the close family and friends of the dying loved one or the actual patient to coordinate care between health and social care departments. The report suggested that information needed to be repeated to the different professionals suggesting that there is a lack of communication between the different departments and that patient information is not being recorded or shared in an appropriate manner.

Nevertheless, there is evidence to suggest that Advance Care Plans (ACP) are a successful way in which a person’s end of life choices can be successfully achieved. Abel et al (2013, pp.168-173) followed 969 terminally ill patients, 550 of whom had made an ACP. 75% of these individuals successfully achieved their dying wishes with regards to the location that they had chosen. In addition, a study published by the NHS (2012, pp.3-4) suggests that the Electronic Palliative Care Coordination Systems (EPaCCS) where patient information, including their end of life choices, can be stored and shared, is an effective way of achieving pro choice for the patient with up to 80% of individuals living in areas where the EPaCCS system is implemented achieving their preferred choice of location to die. In addition, the NHS (2012, p.12) report shows that the implementation of this system has resulted in savings of £133,200 where it is implemented. Another positive study has been published by Gao et al (2013, np) who found that the number of individuals being able to die either at home or in a hospice has increased since 2005 when the National End of Life Care Programme was first launched. However, the percentage change was only marginal (0.8%) therefore suggesting that more needs to be done to ensure patient autonomy is at the top of the list for terminally ill patients.

Another barrier that is likely to prevent an individual from dying within their own home is lack of skills and resources within the community workforce. In these cases, the role of the community nurse is vital, however, the number of community nurses is steadily declining (Royal College of Nursing, 2013, np). This reduction of the workforce further dilutes the available skill mix, therefore having a detrimental impact on the quality of care provided to those who choose to die at home. According to the MCC (2013a, p.13) report, only 19% of individuals who chose to die at home received adequate pain relief during their last 3 months of life. Indeed, the lack of 24/7 access to community services forced a large number of these individuals to contact emergency services resulting in admittance to hospital. In 2010, nearly half of the UK’s primary care trusts did not provide 24/7 community nursing services for end of life patients with little progress being made following the subsequent change to Clinical Commissioning Groups (MCC, 2013a, p. 13).

Another report published by MCC (2013b, pp. 1-15) suggests that a lack of access to social care services also restricts the ability of an individual to make end of life care choices. Whilst it is obvious that the right amount of social support is needed in order for a terminally ill individual to be able to remain at home during their last stages of life, this support is often not provided. The MCC (2013b, p. 3) report suggests that this is not always due to the service not being available, but more often being the result of the complex assessment process and the lack of coordination between health and social services. Indeed, 97% of healthcare professionals stated that the complexity of the social care needs assessment is a substantial barrier to gaining the right amount of home care for terminally ill patients. As such, the care for these terminally ill individuals is often left to family members as informal carers. However, only 5% of these individuals actually receive a carers allowance despite them taking on the majority of the personal care responsibilities of these terminally ill patients. Thomas et al (2002, p.531) asserted that the needs of cancer patient carers were greatest as the cancer progressed to end stage; however, a distinct lack of support for these informal carers is prevalent throughout the UK (Soothill et al, 2001, p.468). MCC (2013b, p.6) found that 47% of these informal carers felt that they needed support but were unable to get any. Therefore it is not surprising that this lack of carer support is resulting in many cancer patients being admitted to hospital in the days or hours before death despite it being their wish to die at home.

Recommendations for Improvement

As studies have shown that the local implementation of the EPaCCS has been successful, there should be a renewed commitment by the Department of Health and the NHS to ensure the national implementation of this scheme. Indeed the National End of Life Care Strategy (DOH, 2008, np) made a commitment to pilot and establish end of life care registers that would ensure the coordinated care of terminally ill patients and also ensure that every organisation involved in the care of that individual were aware of their end of life choices. As such, it is asserted that NHS England need to prioritise the roll out of these systems. When this system is implemented on a national basis, EPaCCS will not only coordinate care but will also provide considerable data that can be used to compare outcomes for end of life patients throughout the UK. In addition to this system, it is vital that health care professionals involved with terminally ill cancer patients encourage them to fill out an ACP as a routine part of the care package. A randomised control trial carried out by Detering et al (2010, np) followed 309 terminally ill patients for a period of six month, 154 of whom had completed an advanced care plan. Of the 56 patients who died during the study period, 29 of them had made an ACP with 86% of these achieving their end of life choices compared to just 30% of those who had not made an ACP. This shows that it is vital to document end of life choices to ensure that they are followed by all those involved in the final days of the patient’s care.

Another recommendation is to make end of life care training mandatory for all health professionals who are likely to be involved in palliative care. This includes making a timely identification of individuals who are approaching the end of their lives and providing these professionals, including GPs, with the right training to boost their confidence in instigating end of life discussions with terminally ill patients. This will enable these terminally ill individuals and their families to come to terms with their disease progression and make appropriate plans for their end of life care. It is also recommended that all terminally ill individuals have a named professional who is responsible for the coordination of their care and who will ensure that their end of life choices are met whenever possible. This was a key recommendation of the UK Government’s (2013, pp. 1-62) review of the Liverpool care pathway, which stated that a named consultant or GP should take overall responsibility for a patient’s end of life care, whilst a named registered nurse would have day to day responsibility for the care of that individual and for the communication of information between the patient, family members and other members of the care team.

The UK Government’s (2013, p. 57) review also recommends improving access to community services by increasing funding to ensure that there is a consistent 24/7 access to all social care services throughout the UK. This is considered to be a priority, as without access to 24/7 care, a large number of individuals are not having their pain managed adequately, forcing them to take further action by attending an emergency department. In addition, the government needs to commit to implementing free social care to terminally ill patients and to simplifying the social care assessment to ensure that all those who need social support are able to access this service in a timely fashion. Whilst the UK government has recognised that there is much merit in the proposal of free end of life social care (MCC, 2013a, p. 19), they are yet to offer a firm commitment to this proposal. The continued complexity of the social care assessment and the confusion over who is able to receive social care needs to change if patients’ wishes to die at home are to be honoured. Indeed, Taylor (2012, p.1297) asserts that there is a need to change the way in which all health and social care is provided to elderly patients and suggests a combined health and social care assessment to ensure a proper joined up and coordinated service for these vulnerable patients.

It is also recommended that improved support for carers is instigated to ensure that all those who are caring for a terminally ill patient are recognised as informal carers and are in receipt of a carers allowance. In addition, it is vital that these carers a given the right level of support by health professionals; this support should include having 24/7 access to help and advice, being given regular respite and having adequate information with regards to the progression of their loved ones disease to enable them to encourage the patient to make end of life care plans. Joyce et al (2014, p.1150) found that out of 120 caregivers who were responsible for delivery of medications to their terminally ill relative, only 27 (22.5%) of them received any formal support. This often led to confusion over dose rate and fear that the patient was receiving too much or too little of the medication provided. This issue is compounded by the fact that many of these informal carers are elderly themselves and often have their own health problems (Jack et al, 2015, p.131).

Finally, it is considered that delivering choice for end of life care should be focused on giving that patient a good death, regardless of where they chose to die. As such, it seems logical that there is a need to understand the experiences of terminally ill patients towards the end of their lives in order to deliver adequate care. As such, it is considered vital to explore how the experiences, concerns, fears and feelings of people approaching the end of their lives can be recorded and used to improve future patient outcomes. Whilst it is accepted that the National Bereavement Survey (ONS, 2012, np) provided a large volume of useful information, the current lack of nationally collected information from end of life patients’ needs to be addressed. As such, it is recommended that future study be directed in this way.

Conclusion

In conclusion, it is clear that whilst having a genuine choice over where to spend the last few days and hours of your life is hugely important to terminally ill patients, there are significant barriers to achieving these choices. Current figures suggest that nearly three quarters of cancer patients chose to die at home but less than 29% of them actually do so. The MCC (2013a, p. 3) report estimate that this amounts to 36,000 patients dying in hospital when they had chosen to die at home. A number of barriers exist that are currently preventing the individual from achieving personal choice at the end of their lives; these include poor identification of individuals entering the end of life stage, poor communication from health professionals, poor planning and coordination between health and social services, lack of skills and resources in community nursing and lack of universal access to social care resources. Nevertheless, despite these current barriers, none are insurmountable if current services are simplified and organised in a way that sees the needs of the individuals and their families and carers brought to the forefront. Whilst the government has funded reports and strategies to improve end of life care, it is clear that not enough is being done to change the way in which end of life care is provided. Significant change is required in order to move care and resources out of hospitals and into the community so that people’s preferences can be delivered. However, this can only happen if there is a clear commitment given by all the players involved in end of life care to share the same ambition, that being to deliver a coordinated and integrated care package that meets the needs, wishes and preferences of end of life patients and their carers. A number of recommendations on how this can be achieved have been included in this essay. These recommendations include simplify the social care assessment, providing free social care to end of life patients, improving support for informal carers and ensuring that these carers are recognised, improving the training of health professionals in recognising the transition to end of life stages and encouraging them to instigate discussions over end of life choices, improving access to social services by ensuring a 24/7 service across the UK and implementing the roll out of the EPaCCS across the whole of the UK to ensure that end of life choices are recorded and shared between all the relevant care providers. As it stands at present, whilst end of life patients do have a choice over where they die, these preferences are often not honoured. They do not have full control or autonomy over their end of life care. However, the choice of place to die is not a myth as it is a very achievable option that requires coordination between services and a commitment from the government to improve community health services.

References

Abel, J., Pring, A., Rich, A., Malik, T., & Verne, J. (2013). The impact of advance care planning of place of death, a hospice retrospective cohort study. BMJ Supportive & Palliative Care, 3(2), 168-173.

Department of Health. (2008). End of life care strategy. Available online at

https://www.gov.uk/government/publications/end-of-life-care-strategy-promoting-high-quality-care-for-adults-at-the-end-of-their-life

accessed 21 June 2015.

Detering, K. M., Hancock, A. D., Reade, M. C., & Silvester, W. (2010). The impact of advance care planning on end of life care in elderly patients: randomised controlled trial. British Medical Journal, 340. 1345-1353

Gao, W., Ho, Y. K., Verne, J., Glickman, M., Higginson, I. J., & GUIDE_Care Project. (2013). Changing patterns in place of cancer death in England: a population-based study. PLoS Med, 10(3), e1001410.

Jack, B. A., O’Brien, M. R., Scrutton, J., Baldry, C. R., & Groves, K. E. (2015). Supporting family carers providing endâ€?ofâ€?life home care: a qualitative study on the impact of a hospice at home service. Journal of Clinical Nursing, 24(1-2), 131-140.

Joyce, B. T., Berman, R., & Lau, D. T. (2014). Formal and informal support of family caregivers managing medications for patients who receive end-of-life care at home: A cross-sectional survey of caregivers. Palliative Medicine, 28(9), 1146-1155.

Macmillan Cancer Care. (2013a). A time to choose. Available online at

http://www.macmillan.org.uk/Documents/GetInvolved/Campaigns/Endoflife/TimeToChoose.pdf

accessed 21 June 2015.

Macmillan Cancer Care. (2013b), There’s no place like home. Available online at

http://www.macmillan.org.uk/Documents/GetInvolved/Campaigns/SocialCare/Making-the-case-for-free-social-care-at-the-end-of-life.pdf

accessed 21 June 2015.

Marie Curie Cancer Care. (2013). Death and dying. Available online at

https://www.mariecurie.org.uk/globalassets/media/documents/policy/policy-publications/february-2013/death-and-dying-understanding-the-data.pdf

accessed 21 June 2015.

National End of Life Intelligence Network. (2012). What do we know now that we didn’t know a year ago? New intelligence on end of life care in England. Available online at

http://www.endoflifecare-intelligence.org.uk/view?rid=464

accessed 21 June 2015.

NHS. (2012). Making the case for change: Electronic palliative care coordination systems. Available online at

www.nhsiq.nhs.uk/download.ashx?mid=4423&nid=4424

accessed 21 June 2015.

Office for National Statistics. (2012). National Bereavement Survey 2012. Available online at

http://www.ons.gov.uk/ons/rel/subnational-health1/national-bereavement-survey–voices-/2012/index.html

accessed 21 June 2015.

Revill, S. (2010). GP Pilot Project Evaluation. Available online at

http://www.dyingmatters.org/sites/default/files/user/documents/Resources/Dying_Matters_GP_Pilot_Evaluation_-_final.pdf

accessed 21 June 2015.

Royal College of Nursing. (2013). Frontline First: Nursing on Red Alert. Available online at

https://www.rcn.org.uk/__data/assets/pdf_file/0003/518376/004446.pdf

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Soothill, K., Morris, S. M., Harman, J. C., Francis, B., Thomas, C., & McIllmurray, M. B. (2001). Informal carers of cancer patients: what are their unmet psychosocial needs? Health & Social Care in the Community, 9(6), 464-475.

Taylor, B. J. (2012). Developing an integrated assessment tool for the health and social care of older people. British Journal of Social Work, 42(7), 1293-1314.

Thomas, C., Morris, S. M., & Harman, J. C. (2002). Companions through cancer: the care given by informal carers in cancer contexts. Social Science & Medicine, 54(4), 529-544.

UK Government (2013). More Care, Less Pathway, A review of the Liverpool Care Pathway. Available online at

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Question ID:1132363Practitioners of Gestalt therapy: Select one: A. prefer to ask clients questions that begin with why rather than with how or what. B. consider asking questions to be more impo

Question ID:1132363Practitioners of Gestalt therapy:

Select one:

A. prefer to ask clients questions that begin with “why” rather than with “how” or “what.”

B. consider asking questions to be more important than the use of “I” language.

Incorrect

C. often ask clients to change their questions into statements.

D. encourage clients to ask questions as a way to create an egalitarian therapeutic relationship

Literature Review of Pain Assessment Tools

Introduction

This essay will identify the issue of poorly addressed acute pain in hospitalized patients and critically compare and discusses a range of pain assessment tools referring to contemporary research literature and practice guidelines for patients who are able to self describe their pain and who are unable to self describe their pain due to verbal communication barriers, critical illness or delirium/dementia.

Main Body

According to the International Association for the Study of Pain, pain is an unpleasant sensory and emotional experience arising from actual or potential tissue damage (

1

). Clinically, “Pain is whatever the experiencing person says it is, existing whenever he/she says it does” (McCaffery, 1968). The temporal profile classification is most commonly used to classify pain.This broad classification of pain duration is often used to better understand the biopsychosocial aspects that may be important when conducting assessment and treatment. For example, many times chronic pain is a result of unresolved acute pain episodes, resulting in accumulative biopsychosocial effects such as prolonged physical reconditioning, anxiety, and stress. It is obvious that this type of time categorization information can be extremely helpful in directing specific treatment approaches to the type of pain that is being evaluated (Gatchel & Oordt, 2003).

Acute pain is usually indicative of tissue damage and is characterized by momentary intense noxious sensations (i.e., nociception). It serves as an important biological signal of potential tissue/ physical harm. Some anxiety may initially be precipitated, but prolonged physical and emotional distress usually is not. Indeed, anxiety, if mild, can be quite adaptive in that it stimulates behaviors needed for recovery, such as the seeking of medical attention, rest, and removal from the potentially harmful situation. As the nociception decreases, acute pain usually subsides. Unlike acute pain, chronic pain persists. Chronic pain is traditionally defined as pain that lasts 6 months or longer, well past the normal healing period one would expect for its protective biological function. Arthritis, back injuries, and cancer can produce chronic-pain syndromes and, as the pain persists, it is often accompanied by emotional distress, such as depression, anger, and frustration. Such pain can also often significantly interfere with activities of daily living. There is much more health care utilization in an attempt to find some relief from the pain symptoms, and the pain has a tendency to become a preoccupation of an individual’s everyday living.

According to Buckley (2000) nurses are the primary group of health care professionals responsible for the ongoing assessment and monitoring of patients to ensure that pain is effectively and appropriately managed and that patients and families are informed of the consequences of acute pain. Assessment of pain can be a simple and straightforward task when dealing with acute pain and pain as a symptom of trauma or disease. Assessment of location and intensity of pain often suffices in clinical practice. However, other important aspects of acute pain, in addition to pain intensity at rest, need to be defined and measured when clinical trials of acute pain treatment are planned. If not, meaningless data and false conclusions may result. The 5 key components: Words, Intensity, Location, Duration, Aggravating factors pain assessment are incorporated into the process. Objective data are collected by using one of the pain assessment tools which are specific to special types of pain. The main issues in choosing the tool are its reliability and its validity. Moreover, the tool must be clear and, therefore, easily understood by the client, and require little effort from the client and the nurse.

According to Husband (2001) to measure the pain severity or intensity, several scales can be used such as a numeric rating scale (NRS), the visual analog scale (VAS), observation scales with indicators of pain, and even creative depictions of pain intensity with scale using a pain thermometer. The numeric rating scale allows patients to rate their pain on and 11-point scale of 0 (no pain) to 10 (worst pain imaginable). The majority of patients, even older adults can use this scale. The thermometer scale may be useful in the elderly, according to Rakel and Herr (2004). It shows a picture of a thermometer arranged on a background with a vertical word scale. Finally categoric scales use verbal descriptors to quantify the level of pain and those scales have been validated and are considered to be reliable.

Chronic pain has a major impact on physical, emotional, and cognitive function, on social and family life, and on the ability to work and secure an income. Meaningful assessment of long-lasting pain is therefore a more demanding task than assessing acute pain. This is true both in clinical practice and when conducting trials of management of long-lasting pain. A comprehensive assessment of any chronic complex pain condition requires documenting (i) pain history, (ii) physical examination, and (iii) specific diagnostic tests. Chronic pain assessment tools are the Brief Pain Inventory (BPI), which assesses pain severity and the degree of interference with function, using 0 – 10 NRS, and the McGill Pain Questionnaire (MPQ) and the short-form MPQ (SF-MPQ) evaluate sensory, affective–emotional, evaluative, and temporal aspects of the patient’s pain condition.

Pain assessment in older adults can be challenging and very difficult in some situations (Rakel & Herr, 2004). When the patient cannot report his/her subjective pain experience, proxy measurements of pain must be used, such as pain behaviours and reactions that may indicate that the person is suffering painful experiences. Besides communication difficulties caused by language problems, patients in the extremes of age, and critically ill patients in the intensive care setting, are common assessment problems. Older patients may prefer to use alternate means to express their pain through the use of word descriptors that best characterize the pain, such as “aching,” “hurting,” and “soreness” (Herr & Garand, 2001).

Significant challenges occur when assessing patients who are unable to communicate verbally, in writing, or by gestures, or when they are cognitively impaired.

Pain assessment should be ongoing at regular intervals, individualised and documented clearly to facilitate treatment and communication among health care clinicians.

Conclusion

In conclusion, adequate assessment of pain, using validated tools appropriate to the population or individual, is an essential prerequisite of successful pain management. It has been shown in many countries that inadequate pain assessment is common, with resultant failings in management of pain. Inadequate pain control can prolong the recovery period, increase length of stay, and increase overall health care costs ( Shang & Gan, 2003) Only by regularly assessing and measuring pain, as routinely as the other vital signs, can we hope to make pain visible enough to those caring for patients and thus improve management. This is especially true for the patients that anaesthetists care for every day, those with acute pain after surgery, trauma, and in the intensive care unit.

Attitudes Towards Implementation of Evidence Based Practice

Introduction

The term of evidence based practice (EBP) was firstly used in medicine as evidence based medicine, after that the term developed and being used in nursing with purpose of build up scientific database to improve nursing as science (Colyer and Kamath, 1999). Evidence based practice was passed through three stages; in which the EBP was appeared in Old Testament which was the first form and appearance of EBP; after that the EBP was developed in different form in middle ages, in which the period of middle ages was considered a stage of “renaissance” of the EBP which characterized by beliefs-related methods of treatment; the third stage of EBP was the modern stage, in which the modern stage considered the last version of EBP that began at 1972; in which the modern version of EBP was the EBP that widely known form among highly educated and professional nurses (Claridge and Fabian, 2005).

The Bible was the oldest known source in EBP documentation, in which the Bible contains a story that was represented as an interventional research that progress for ten days (Weingarten, 2003); the story in the Bible said ” Then Daniel said to the guard whom the master of the eunuchs had put in charge of Hananiah, Miscael and Azariah and himself “.Submet us lo this rest for ten days. Give us only vegetables to eat and water to drink: then compare our looks with those of the young men who have lived on the food assigned by the king and be guided in your treatment of us by what you see.” The guard listened to what they said and tested them for ten days. At the end of ten days they looked healthier and were better nourished than all the young men” (Claridge and Fabian, 2005, P. 548).

During the second stage of EBP (1700s-1900s), the EBP was restricted to believes-related methods of treatment; in which “Blood-letting” was the main treatment for many diseases in middle age period (Klar and Donner, 2002). Physicians and priests were used “Blood-letting”; in which Physicians and priests were believed that diseases caused by wicked souls; in which the diseased patients should be injured to expel the wicked souls with blood outside of patients’ bodies (Klar and Donner, 2002).

During the last four decades, the EBP was featured in a modern form; in which the borderline for modern period of EBP was began in 1972 by Archie Cochrane (Klar and Donner, 2002). Cochrane (1972) published a paper with title of “Effectiveness and efficiency: random reflections on health services”; in which the paper was discuss and evaluate the effect of randomization (the randomization was regard to patients and regard to intervention) on the outcomes of the patients’ health. The Cochrane’s paper was the first paper reflects the importance of randomized clinical trials; in which Cochrane was found that the randomization of the sample and intervention will exhibit evidence with high quality which improve the quality of health care provided and improve health outcomes of the patients (Cochrane, 1972).

Melnyk and Fineout-Overholt (2005) defined EBP as a knowledge-based conflict-resolving strategy that performed by adapting best available evidence to provide best possible care for patients and their families. Furthermore, Evidence Based Practice is a process of integration of research-based results which contribute to achieve best practice (Institute of Medicine, 2001). In addition, Sackett, Rosenberg, Gray (1996) estimated that evidence based practice is synchronous combination of professional nursing experience and research with high level of evidence under patient’s believes and values consideration. Besides that, Ingersoll (2000) documented that evidence based practice is “meticulous, unambiguous, and well-judged theoretical information and reliable research-findings to provide effective decisions about patients’ care regard to patients’ and organizational needs” (P. 152). Furthermore, evidence based practice defined as “Explicit and judicious decision making about health care delivery for individuals or groups of patients based on the consensus of the most relevant and supported evidence derived from theory-derived research and data-based information to respond to consumers’ preferences and societal expectations” (Driever, 2002, p. 593).

Evidence based practice is considered as a magical solution for complicated health problems (Institute of Medicine, 2001). Furthermore, evidence based practice considered wide discipline term used as a solution to clinical-related problems which began to provide findings and basics of clinical decision on best reliable and evident researches with purpose of improving health care provided (Sackett, Strauss, Richardson, Rosenberg, and Haynes, 2000). The Institute of Medicine (2001) was illustrated that EBP process provide intensive care to patients, using effective recent researches to achieve desired outcomes, and provide cost effective standard care. In addition, another study found that EBP enhance nurses’ professions by improving nurses’ knowledge and skills to analyze, understand and develop research (Melnyk and Fineout-Overholt, 2005). Evidence Based Practice improves nurses’ ability to be excellence profession in areas of practice, and improves patients’ health outcomes by providing high qualified nurses (Institute of Medicine, 2001).

Evidence based practice improve patients’ outcomes within four dimensions; clinical dimension (improve signs and symptoms of patients’ diseases), life quality dimension (improve patient satisfaction upon to life), functional dimension (improve patients ability to achieve daily living activity), and economic dimension (using EBP was prove ensure of cost effectiveness for patient and hospital) (Weaver, Warren, and Delaney, 2005). In addition, Newhouse, Dearholt, Poe, Pugh, and White (2005) demonstrated that the evidence based practice improve “efficacy” of health care provided to achieve pleasurable patient’s outcomes, save patients/nurse time, and use of EBP considered cost effective for patients, families, and hospitals.

Melnyk, Fineout-Overholt, Sadler, and Green-Hernandez (2008) documented that implementation of evidence based practice can be achieved by improving nurses’ knowledge and skills about research and evidence based practice, improve and strengthening nurses’ beliefs to reinforce nurses to be integrated within evidence based practice environment. Evidence based practice education allow nurses to formulate and answer any research question raised from clinical area by recent and reliable researches, allow nurses to critique and evaluate any research according to level of evidence, allow nurses to conduct researches according to patients’ needs; family; nurse; and hospital needs, and allow nurses to share research findings as journal club activity (Melnyk, Fineout-Overholt, Sadler, and Green-Hernandez, 2008).

Another study conducted by Wolf and Greenhouse (2007) documented that using of EBP is significantly needed in clinical practice, in which EBP pleasured to achieve improvement in patientfamilynurse education regard to condition and treatment, improve quality of health care provided by nurse and hospital, improve using new technology in clinical setting as computers, and build nurses community prepared with recent scientific information.

Most of health care provided by nurses nowadays is based on traditional practice with observable lacking in evidence-based practice (Mariano, Caley, Eschberger, Woloszyn, Volker, Leonard, et, al. 2009). Furthermore, an Iranian study was conducted to identify the Iranian nurses perception toward EBP, the Iranian study was conducted by using convenience sample of 21 nurses who undergone within qualitative research design; in which the Iranian study was documented that 21 participants from nurses did not listen about the concept of “evidence based practice” before and they did not implement EBP in clinical area (Adib-Hajbaghery, 2009).

American and Netherlandic studies conducted at 1998 and 2001 respectively; was estimated that about 35% of hospitalized patients do not receive evidence based care (the nurses treat patients according to traditional care that was not based on researches) (Schuster, McGlynn and Brook, 1998; Grol, 2001); in which Estrada (2009) conducted a descriptive study to assess nurses’ knowledge and attitudes toward EBP, in which the Estrada’s study was founded that 25% of sample did not hear about EBP previously. Moreover, Melnyk and Fineout-Overholt (2007) was conducted a study to develop two scales; attitude toward EBP scale and implementation of EBP scale, in which Melnyk’s and Fineout-Overholt’s study was estimated that 40% of collected sample did not listen and dealt with the concept of EBP previously. Evidence based practice improve patients’ outcome; in contrast, lack of nurses prepared evidence based practice will affect patients’ outcomes negatively (Institution of Medicine, 2001); in which, about 25% of health care provided was not sufficient to meet patients needs and the health care provided was not safe for hospitalized patients (Schuster, McGlynn and Brook, 1998; Grol, 2001). Furthermore, Pravikoff, Pierce, and Tanner (2005) conducted a study to evaluate nurses perception to integrate within EBP which conducted by random sample of 1,097 nurses, the researchers were found that more than half of the sample did not listened about EBP previously, more than half of the sample had a negative attitudes toward EBP and those nurses was not integrated within EBP activities, 73% of the nurses had not ability to use electronic database, and all 1,097 nurses had not sufficient information about choosing best researches.

The problems that impede of EBP for nursing and medical societies has been reported by Institution of Medicine (2001) in which around 45% of patient did not received professional health care; the implementation of new discovered evidence needs about two decades at least to let the recent of evident researches to be handled and public with nurses and medical stuff worldwide, and health care providers were not adequately prepared to translate recent researches in clinical practice.

Hunt (1996) concluded that there is a wide whole between using the findings of researches and clinical practice; in which an interventional study was conducted to evaluate the effect of educational intervention on nurses’ knowledge and attitudes toward EBP, the pre- test of these educational study was showed that 50% of 49 convenience sample of nurses did not listen about EBP and professional health care provided previously (Varnell, Haas, Duke, and Hudson, 2007). In addition, Melnyk (2006) concluded that the implementation of evidence based practice was little in nursing that explained by Hunt (1996) who documented that there are several factors prevent evidence based practice implementation as: disorientation toward research, lack of beliefs (attitudes) exhibited toward using research, and lack of understanding of research elements.

There are some barriers to EBP were appeared; these barriers limit nurses’ engagement within evidence based practice (Weaver and Sorrells-Jones, 1999). Funk, Champagne, Wiese, and Tornquist (1991) estimated that these barriers had been originated from different sources and organized within four categorical origins; characteristic of the nurse, characteristic of setting, characteristic of research and characteristic of presentation of research. Furthermore, Funk, Champagne, Wiese, and Tornquist (1991) documented that nurse can be considered as a barrier to implement EBP; in which nurses were unaware about principles of research and research process, and nurses had not sufficient time to implement EBP . Moreover, Funk, Champagne, Wiese, and Tornquist (1991) concluded that practice setting can be considered as a barrier to implement EBP; in which hospitals were not provided sufficient facilitation to implement EBP activity within clinical setting, and nurses had not ability to change patient-care procedure without getting permission from hospitals’ authority to change guidelines. Indeed, Funk, Champagne, Wiese, and Tornquist (1991) documented that research and research presentation can be considered as barrier to implement EBP; in which nurses were believed that research elements as introduction, literature review, methodology, statistical analysis, and conclusion were not understandable clearly within articles.

Melnyk (2006) concluded that nurses need applicable teaching strategies to provide nurses with adequate evidence based practice knowledge and skills and provide nurses with positive beliefs (attitudes) toward integration within evidence based practice activity. Di Leonardi (2007) documented that lecture presentation for educational intervention was considered most effective and appropriate teaching strategy; lectures were widely-spread and known perfectly to all universitiescolleges-certificated persons. In addition, Hart, Eaton, Buckner, Morrow, Barrett, Fraser, et, al. (2008) were conducted an educational intervention to teach nurses about nursing research and evidence based practice by using computer-based modules strategy; in which the result was exhibit that the educational intervention improve nurses’ knowledge and skills about using research and evidence based practice, and improve nurses’ attitude toward evidence based practice.

Lacey (1996) was evaluated 870 courses of the English National Board which contain materials enable student nurses to understand research and evidence based practice, with convenience sample of 30 nurses student; 65% of the students were demonstrated that knowledge, skills about research and evidence based practice were significantly improved after the educational intervention. Furthermore, Hundley, Milne, Leighton-Beck, Graham, Fitzmaurice (2000) compared between long term research course (six months) and short term research course (one month); the study conducted by convenience sample of 481 nurses and midwives; the result showed that nurses who integrated within long term research course were exhibited more knowledge, skills, and attitudes toward evidence based practice than respondent received short term research course.

The purposes of this study were to evaluate the effect of educational intervention about evidence based practice and nursing research lectures on the beliefs toward using evidence based practice, to evaluate the effect of educational intervention about evidence based practice and nursing research lectures on the frequency of the implementation of evidence based practice, to determine any differences between two groups (experimental and control group) regard to variables (age, gender, level of education, the experience in clinical area, and the effect of educational intervention that will be implemented), to investigate the variation among socio-demographic variables in response to evidence based practice beliefs and frequency of evidence based practice implementation, and to fixing first block in building EBP team in King Abdulla University Hospital.

Strategies Learner Used Facilitate Learning In Workplace

The aim of this assignment is to reflect on and analyse, strategies used to facilitate learning with a newly qualified member of staff in the authors working environment. The new member of staff will be referred to as the student during this assignment. This paper will show how one particular teaching session relates to theories of learning.

Reflection has been defined by Taylor ( 2000 ) as : ” The throwing back of thoughts and memories, in cognitive acts such as thinking, contemplation, meditation and any other form of attentive consideration, in order to make sense of them, and so make contextually appropriate changes if the required”. However, the definitions from Boyd & Fales ( 1983 ) and Dewey ( 1996 ), who considers that it is purposeful activity in thinking about an experience, through which learning takes place. Boyd and Fales focus more on self development. Here reflection does not only add to our knowledge but challenges the concepts and theories we hold. Furthermore as a result we don’t see more, we see differently.

The reflective process is at least to some degree conscious, but may not be verbalized. The author also, believes and agrees with John (2004), that reflection are often triggered by feelings and greatly influences decision making. This emphasises the importance of reflection in practice.

The English National Board (ENB) and the Department of Health (DOH) 2001 defined a mentor as: “denoting the role of the nurse, midwife or health visitor who facilitates learning and supervises and assesses students in practice setting” would seem to be the most appropriate one to use. DOH (2001) identified that mentors need to possess a wide range of skills and to undergo a more robust preparation in order to equip students for their working life in today’s modernised, demanding National Health Services (NHS). Although this is the definition that illustrate the entirety of the mentoring role. The author feels this definition gives a somewhat very cold and clinical approach to being a mentor and prefers the following definition by Morton-Cooper and Palmer (2000) who states ” A mentor is someone who provides an enabling relationship that facilitates another’s personal growth towards competent practice and high standard making the learning experience an enjoyable and mentally fulfilling. This definition encompasses the emotional and personal part of the relationship, whether positive or negative, which the author feels is of utmost importance for a beneficial learning experience for both the learner and the mentor.

In ICU, all new members of staff must have completed four weeks of supernumerary period to acquire the necessary knowledge and skills to safely look after a critically ill patient. In planning to teach my student, The author need to accomplish three important aims as discussed by Wong et al, 1998; Conway and McMillan, 2000; (Cited in Jackson and Mannix 2001 p270), Provide student with the opportunity to develop their clinical skills; Integrate theory and practice; and, Assist their socialization into nursing. Prior to undertaking teaching of the student, the author ensured that the student had set a realistic goals and clear learning objectives and also, encouraged to question things that was not clear or difficult to understand. After much consideration based on the students learning needs, it was reciprocally agreed that the skill of ‘zeroing of CVP and Arterial line’ would be one of the essential skills taught in ICU. The learner expressed the need to learn this particular skills, and Rogers (1996) views that learning is accomplished when a person feel a need, makes effort to meet that need, and feels satisfaction with the result of his effort. The student appeared keen to learn, and Hinchcliff (2001), views motivation as the major factor that encourages students to learn, and Oliver and Endersby (1994), sees motivation as one of the most basic conditions for learning. Motivation is heavily influenced by need, and Gross (2005) believes that how the motives

underpinning behaviour are interpreted, depend upon the position of the work of a theorist or psychologist.

Maslow (1970), while theorising human need, recognised that only when the needs lower down in the hierarchy are satisfied, the higher need will be met. The Intensive Care Unit is often very busy and stressful, and within the role of educator the author was very aware that the learner needed time away from the unit to unwind, as she could be very easily become over tired. On reflection this connects with the evaluation process of Gibbs reflective cycle, in ascertaining what was good about the experience. The Intensive Care Unit has it’s own coffee lounge away from the unit where tea and coffee is provided. Frequent breaks, comfortable chairs, a television, and availability of refreshments are what Rogers, (cited in Downie 2003) views as necessary for providing human comfort and resulting in meeting physiological needs. Maslow’s theory made a significant contribution of humanist thinking and the ‘self actualization’.

The learning outcomes developed from our discussion were for the student to; Increase knowledge of zeroing CVP/Arterial Lines; Prepare resources and equipment correctly with minimal prompting or assistance; Carrying out the procedure using aseptic technique, efficiently and record the nursing procedure in the care plan or patient record. In order to do this, the author needed to look at the nature of the learning process. It is therefore crucial when setting out to undertake a mentoring role that there is an understanding of the way the adults learn.

Learning can be defined formally as the act, process, or experience of gaining knowledge or skills (Conner, 1997). Facilitation of learning is defined by the Royal College of Nursing (RCN) as a well-planned learning opportunity with the provision to coach and support students (RCN, 2002). This is supported by the Department of Health (DOH), which adds that facilitation of learning allows students to develop opportunities to identify experiences that meet their learning needs (DOH, 2001).

Facilitation of adult learning is described by Banning (Cited on Warren 2010)

as the ideas and theories that are accredited to prior experiences which need to be complemented by interaction and adult-orientated strategies. A successful mentor is able to transform previous experiences via experimental learning, enabling the student to make sense and learn from the experiences gained. However, facilitating student learning is not always easy in practice. Garrison et al (2004) remind us that while teaching the nursing leaders of the future, we do so in chaotic setting which is, in effect, an unhelpful learning environment. More recently, Swinny and Brady (2010) found that, on a ward setting, mentors have difficulty finding time to teach because of the busy and demanding nature of clinical environment.

The premise that a student must have the desire to learn in order that learning that can take place seems obvious, but there are many elements of learning that can affect the desire to learn (Hinhcliff, 2001). Motivation is a major factor that manages students to further their knowledge. (Hinhcliff, 2001), and (Oliver and Endersby, 1994) support this view by believing motivation to be, one of the most basic conditions for learning to take place.

An understanding of some theories is helpful to a mentor as it provides them with an opportunity to examine their own beliefs and assumptions about people, knowledge, motivation, environment, assessment and other factors necessary with learning (Nicklin and Kenworthy, 2000). Learning help us move from novice to expert and allow us to gain new knowledge and ability. (Benner, 1984). These theories provide framework for studying the processes associated with learning. Learning theories of behaviourism, cognitivism and humanism have attempted to provide explanation about learning that apply to people in general. In order to see the full potential in learning, knowledge of such theories is crucial to the success of the individual learner. Behaviourism argue that nearly all behaviour is learned. It is based on what is refered to as stimulus /response learning and originates with the russian psychologist, Pavlov’s work with the dogs whereby he linked one stimulus – meat powder – to a second stimulus, the sound of a bell. This produced a salivation response and ultimately the dogs would salivate at the sound of the bell even in the absence of the meat powder. This experimentation produced Pavlov’s theory of Classical Conditioning (McKenna 1995). The social learning theory developed by Albert Bandura could be useful within the affective areas of nursing in as much as the mentor behaves in ways he wants the learner to imitate, as a role modelling (Knowles, 1990). He stressed the importance of modelling other “behaviours”, which is known as observational learning (cited by Bahn, 2001). Because it encompasses attention, memory and motivation, social learning theory spans both cognitive and behavioural frameworks. Humanism developed during the 1950’s and 1960’s as an alternative to psychoanalysis and behaviourism, movements which until then dominated psychology. This perspective emphasises the importance of self. It advocates student centred learning related to each ones own unique experiences, Teachers are seen as facilitators of learning, rather than the expert handing down knowledge and understanding (Quinn, 2000).

A day was planned in advance when the teaching would take place. The author had met on several occasions with the student therefore an introduction had been made. The author felt that effective communication is essential to facilitate learning, therefore adapted a friendly and approachable manner.

This view is supported by McKimm, J. (2007) who believes the learner is able to express their views and make errors when a sociable atmosphere is set and maintained. McKimm, J. (2007) also discusses the concept of ‘teaching by humiliation’ and the author is very aware from past experience, of the negative effect of power relations, and so becoming more sensitive to the needs of the student.

As a good example, the student had seen the procedure of zeroing the CVP line, carried out previously as a part of the daily routine with the mentor/author but had neither performed it nor understood the relevance of it.

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