Advance Directives

Continuing education online courses in Advance Directives.

 

N19. End of Life Care: Advance Directives, 3 CE-hours, $21

Course Description: Advance directives are legal documents that allow you to convey your decisions about end-of-life care ahead of time. They provide a way for you to communicate your wishes to family, friends and health care professionals, and to avoid confusion later on.

Objectives: At the end of this course, you will 1. evaluate how Advance Directives fit into end-of-life care, and 2. design Advance Directive planning steps that meet end-of-life needs.

Course Format: Online linked resources and lectures that you can use anytime 24/7. One multi-choice test.

Course Developers and Instructors: R. Klimes, PhD, MPH (John Hopkins U), author of articles on various End of Life Care principles including wellness and prevention.

Course Time: About 3 hours for online study, test taking with course evaluation feedback and certificate printing.

Course Test: Click here for the self-correcting test that requires 75% for a passing grade.

 

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Professor Rudolf Klimes, PhD, welcomes you to this online course. Keep going.

START the course here. TAKE the exam at the end. PAY after the exam.

N19. Advance Directive, 3 CE course hours

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A. Introduction

A living will tells how you feel about care intended to sustain life. You can accept or refuse medical care. There are many issues to address, including

  • The use of dialysis and breathing machines
  • If you want to be resuscitated if breathing or heartbeat stops
  • Tube feeding
  • Organ or tissue donation

A durable power of attorney for health care is a document that names your health care proxy. Your proxy is someone you trust to make health decisions if you are unable to do so.

Source: http://www.nlm.nih.gov/medlineplus/advancedirectives.html

B. Advance Directives in End-of-life Cancer Care

More than ever before, people with cancer and their families are being asked to take part in decisions about end-of-life care. Yet, most people still do not discuss end-of-life care at all, even if they are seriously ill. This fact sheet provides patients with an outline for thinking about these issues and some guidelines for discussion with their doctors, families, and loved ones. This fact sheet is also designed to help patients understand the medical, legal, and personal choices they may face in the future.

1. What rights do patients have regarding their medical treatment? Patients are entitled to complete information about their illness and how it may affect their lives, and they have the right to share or withhold that information from others. People with cancer should also be informed about any procedures and treatments that are planned, the benefits and risks, and any alternatives that may be available. Patients may be asked to sign an “informed consent” form, which includes this information. Before signing such a form, patients should read it carefully and ask the doctor any questions they might have.Patients have the right to make decisions about their own treatment. These decisions may change over time. In the face of worsening disease, some patients may want to try every available drug or treatment in the hope that something will be effective. Other patients may choose to forgo aggressive medical treatment. Many patients turn to family members, friends, or caregivers for advice. But it is the patient’s decision how much or how little treatment to have. Sometimes a patient is unable to make this decision, due to severe illness or a change in mental condition. That is why it is important for people with cancer to make their wishes known in advance.

2. What is end-of-life care? What are advance directives? End-of-life care is a general term that refers to the medical and psychosocial care given in the advanced or terminal stages of illness. Advance directives are the legal documents, such as the living will, durable power of attorney and health care proxy, which allow people to convey their decisions about end-of-life care ahead of time. Advance directives provide a way for patients to communicate their wishes to family, friends, and health care professionals and to avoid confusion later on, should they become unable to do so.Ideally, the process of discussing and writing advance directives should be ongoing, rather than a single event. Advance directives can be modified as a patient’s situation changes. Even after advance directives have been signed, patients can change their minds at any time.

3. Why are advance directives important? Complex choices about end-of-life care are difficult even when people are well. If a person is seriously ill, these decisions can seem overwhelming. But patients should keep in mind that avoiding these decisions when they are well will only place a heavier burden on them and their loved ones later on. Communicating wishes about end-of-life care will ensure that people with cancer face the end of their lives with dignity and with the same values by which they have lived.

4. Why is it important to write a will? A will is important so that patients can give instructions about distribution of their money and property when they die. Patients can name a trusted family member, friend, or professional to handle their personal affairs (also known as an Executor). It is advisable to seek the expert advice of a lawyer in drawing up a will so that the decisions made about taxes, beneficiaries, and asset distribution will be legally binding. This process can relieve a patient’s family and friends of an enormous burden in case of disputes or questions about allocation of the patient’s assets.

5. What is a living will? A living will is a set of instructions documenting a person’s wishes about medical care intended to sustain life. It is used if a patient becomes terminally ill, incapacitated, or unable to communicate or make decisions. Everyone has the right to accept or refuse medical care. A living will protects the patient’s rights and removes the burden for making decisions from family, friends, and physicians.There are many types of life-sustaining care that should be taken into consideration when drafting a living will. These include:

  • the use of life-sustaining equipment (dialysis machines, ventilators, and respirators);
  • “do not resuscitate” orders; that is, instructions not to use CPR if breathing or heartbeat stops;
  • artificial hydration and nutrition (tube feeding);
  • withholding of food and fluids;
  • palliative/comfort care; and
  • organ and tissue donation.

It is also important to understand that a decision not to receive “aggressive medical treatment” is not the same as withholding all medical care. A patient can still receive antibiotics, nutrition, pain medication, radiation therapy, and other interventions when the goal of treatment becomes comfort rather than cure. This is called palliative care, and its primary focus is helping the patient remain as comfortable as possible. Patients can change their minds and ask to resume more aggressive treatment. If the type of treatment a patient would like to receive changes, however, it is important to be aware that such a decision may raise insurance issues that will need to be explored with the patient’s health care plan. Any changes in the type of treatment a patient wants to receive should be reflected in the patient’s living will.

Once a living will has been drawn up, patients may want to talk about their decisions with the people who matter most to them, explaining the values underlying their decisions. Most states require that the document be witnessed. Then it is advisable to make copies of the document, place the original in a safe, accessible place, and give copies to the patient’s doctor, hospital, and next of kin. Patients may also want to consider keeping a card in their wallet declaring that they have a living will and where it can be found.

 

6. What is a health care proxy and durable power of attorney for health care? A health care proxy is an agent (a person) appointed to make a patient’s medical decisions if the patient is unable to do so. Generally, people assign someone they know well and trust to represent their preferences when they can no longer do so. Patients should be sure to ask this person for agreement to act as their agent. An agent may have to exercise judgment in the event of a medical decision for which the patient’s wishes are not known.The durable power of attorney for health care is the legal document that names a patient’s health care proxy. Once written, it should be signed, dated, witnessed, notarized, copied, distributed, and incorporated into the patient’s medical record.Patients may also want to appoint someone to manage their financial affairs if they cannot. This is called a durable power of attorney for finances, and is a separate legal document from the durable power of attorney for health care. Patients may choose the same person or someone different from their health care proxy to act as their agent in financial matters.

 

7. Where can people with cancer get assistance with their advance directives? If patients need help making the decisions discussed in this fact sheet, they should not hesitate to call upon family, friends, and other loved ones. Patients can also call an organization such as Cancer Care, Inc., for help with this process. Cancer Care, Inc., provides free, professional assistance to people with any type of cancer, at any stage of illness, and to their families. Patients and their families may write to Cancer Care, Inc., 275 Seventh Avenue, New York, NY 10001; call 1–800–813–HOPE (1–800–813–4673); or visit their Web site at http://www.cancercare.org on the Internet.Although a lawyer is not needed to complete advance directives, it is important to be aware that each state has its own laws for creating advance directives. Because these laws can vary in important details, special care should be taken to adhere to the laws of the state a patient lives in or is treated in. It is possible that a living will or durable power of attorney signed in one state may not be recognized in another. Appropriate forms can be obtained from health care providers, legal offices, Offices on Aging, and state health departments.

This fact sheet was adapted with permission from Cancer Care, Inc., a nonprofit social service agency whose mission is to help people with cancer and their families. Cancer Care’s toll-free telephone number is 1–800–813–HOPE. The National Cancer Institute and Cancer Care, Inc., are in partnership to increase awareness of the psychosocial issues faced by cancer patients and to provide resources to cancer patients and their families.

Source: http://www.cancer.gov/cancertopics/factsheet/support/advance-directives

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C. Advance Directive Planning

Preferences for Care at the End of Life

Research can help physicians and other health care professionals guide patient decisionmaking for care at the end of life. Findings resulting from research funded by the Agency for Healthcare Research and Quality (AHRQ) are discussed. This research can help providers offer end-of-life care based on preferences held by the majority of patients under similar circumstances.

By Barbara L. Kass-Bartelmes, M.P.H., C.H.E.S., and Ronda Hughes, Ph.D.

Introduction

1. Patient Preferences Are Often Not Known

Predicting what treatments patients will want at the end of life is complicated by:

  • The patient’s age.
  • The nature of the illness.
  • The ability of medicine to sustain life.
  • The emotions families endure when their loved ones are sick and possibly dying.

When seriously ill patients are nearing the end of life, they and their families sometimes find it difficult to decide on whether to continue medical treatment and, if so, how much treatment is wanted and for how long. In these instances, patients rely on their physicians or other trusted health professionals for guidance.

In the best of circumstances, the patient, the family, and the physician have held discussions about treatment options, including the length and invasiveness of treatment, chance of success, overall prognosis, and the patient’s quality of life during and after the treatment. Ideally, these discussions would continue as the patient’s condition changed. Frequently, however, such discussions are not held. If the patient becomes incapacitated due to illness, the patient’s family and physician must make decisions based on what they think the patient would want.

2. Research Can Help Guide Decision-making

This report is intended to show how physicians and other health care professionals can help their patients with advance care planning and assess patient preferences for care at the end of life.

Section 1 discusses research findings from studies funded by the Agency for Healthcare Research and Quality (AHRQ), as well as those from other research. For readers who want more detailed information, Section 2 contains charts and tables showing the quantitative results of the studies supported by AHRQ. While no one can predict exactly what patients will want or need when they are sick or dying, this research can help providers offer end-of-life care based on preferences (both real and hypothetical) held by the majority of patients under similar circumstances.1

Making a Difference

Patients need more effective advance care planning.
Patients value advance care planning discussions.
Physicians can use a structured process for discussions.
Patient preference patterns can predict other choices.
Invasiveness and length of treatment affect preferences.
Treatment patterns are based on prognoses.

3. Terms Patients Should Understand

Advance directives are also known as living wills. These are formal legal documents specifically authorized by State laws that allow patients to continue their personal autonomy and that provide instructions for care in case they become incapacitated and cannot make decisions. An advance directive may also be a durable power of attorney.A durable power of attorney is also known as a health care proxy. This document allows the patient to designate a surrogate, a person who will make treatment decisions for the patient if the patient becomes too incapacitated to make such decisions.

Discussion of Research Findings

AHRQ research indicates that most patients have not participated in advance care planning, yet many are willing to discuss end-of-life care. One way to determine patients’ preferences for end-of-life care is to discuss hypothetical situations and find out their opinions on certain treatment patterns. These opinions can help clarify and predict the preferences they would be likely to have it if they should become incapacitated and unable to make their own decisions.4. Patients Need More Effective Advance Care PlanningStudies funded by AHRQ indicate that many patients have not participated in effective advance care planning. The Patient Self-Determination Act guarantees patients the right to accept or refuse treatment and to complete advance medical directives.2-12 However, despite patients’ rights to determine their future care, AHRQ research reveals that:

  • Less than 50 percent of the severely or terminally ill patients studied had an advance directive in their medical record.5,6,8,13
  • Only 12 percent of patients with an advance directive had received input from their physician in its development.6
  • Between 65 and 76 percent of physicians whose patients had an advance directive were not aware that it existed.6,13
  • Having an advance directive did not increase documentation in the medical chart regarding patient preferences.6,11
  • Advance directives helped make end-of-life decisions in less than half of the cases where a directive existed.6
  • Advance directives usually were not applicable until the patient became incapacitated14 and “absolutely, hopelessly ill.”2
  • Providers and patient surrogates had difficulty knowing when to stop treatment and often waited until the patient had crossed a threshold over to actively dying before the advance directive was invoked.2
  • Language in advance directives was usually too nonspecific and general to provide clear instruction.5
  • Surrogates named in the advance directive often were not present to make decisions or were too emotionally overwrought to offer guidance.2
  • Physicians were only about 65 percent accurate in predicting patient preferences and tended to make errors of undertreatment, even after reviewing the patient’s advance directive.15
  • Surrogates who were family members tended to make prediction errors of overtreatment, even if they had reviewed or discussed the advance directive with the patient or assisted in its development.16,17

AHRQ research shows that care at the end of life sometimes appears to be inconsistent with the patients’ preferences to forgo life-sustaining treatment and patients may receive care they do not want.5 For example, one study found that patient preferences to decline cardiopulmonary resuscitation (CPR) were not translated into do-not-resuscitate (DNR) orders.5,6,11 DNR orders are requests from the patient or the patient’s surrogate to the physician that certain forms of treatment or diagnostic testing not be performed.18 CPR is a procedure frequently addressed in DNR orders. Another study found that patients received life-sustaining treatment at the same rate regardless of their desire to limit treatment.185. Patients with Chronic Illness Need Advance PlanningBecause physicians are in the best position to know when to bring up the subject of end-of-life care, they are the ones who need to initiate and guide advance care planning discussions.19 Such discussions are usually reserved for people who are terminally ill or whose death is imminent, yet research indicates that people suffering from chronic illness also need advance care planning.The majority of people who die in the United States (80 to 85 percent) are Medicare beneficiaries age 65 and over, and most die from chronic conditions such as heart disease, cerebrovascular disease, chronic obstructive pulmonary disease (COPD), diabetes, Alzheimer’s disease, and renal failure.20 Only about 22 percent of deaths in people age 65 and over are from cancer.20People with terminal cancer generally follow an expected course, or “trajectory,” of dying.21,22 Many maintain their activities of daily living until about 2 months prior to death, after which most functional disability occurs.21In contrast, people with chronic diseases such as heart disease or COPD go through periods of slowly declining health marked by sudden severe episodes of illness requiring hospitalization, from which the patient recovers.21,22 This pattern may repeat itself over and over, with the patient’s overall health steadily declining, until the patient dies.21,22 For these individuals there is considerable uncertainty about when death is likely to occur.Patients who suffer from chronic conditions such as stroke, dementia, or the frailty of old age go through a third trajectory of dying, marked by a steady decline in mental and physical ability that finally results in death.21 Patients are not often told that their chronic disease is terminal, and estimating a time of death for people suffering from chronic conditions is much more difficult than it is for those dying of cancer.22When patients are hospitalized for health crises resulting from their chronic incurable disease, medical treatment cannot cure the underlying illness, but it is still effective in resolving the immediate emergency and thus possibly extending the patient’s life.2 At any one of these crises the patient may be close to death,21 yet there often is no clearly recognizable threshold between being very ill and actually dying.2Patients may become too incapacitated to speak for themselves,23-26 and decisions about which treatments to provide or withhold are usually made jointly between the patient’s physician and family or surrogate.276. Patients Value Advance Care Planning DiscussionsAccording to patients who are dying and their families who survive them, lack of communication with physicians and other health care providers causes confusion about medical treatments, conditions and prognoses, and the choices that patients and their families need to make.2,22,24,28-31 One AHRQ study indicated that about one-third of patients would discuss advance care planning if the physician brought up the subject and about one-fourth of patients had been under the impression that advance care planning was only for people who were very ill or very old.32 Only 5 percent of patients stated that they found discussions about advance care planning too difficult.32AHRQ-funded studies have shown that discussing advance care planning and directives with their doctor increased patient satisfaction among patients age 65 years and over.33,34 Patients who talked with their families or physicians about their preferences for end-of-life care:

  • Had less fear and anxiety.
  • Felt they had more ability to influence and direct their medical care.
  • Believed that their physicians had a better understanding of their wishes.
  • Indicated a greater understanding and comfort level than they had before the discussion.16,33

Compared to surrogates of patients who did not have an advance directive, surrogates of patients with an advance directive who had discussed its content with the patient reported greater understanding, better confidence in their ability to predict the patient’s preferences, and a stronger belief in the importance of having an advance directive.16Finally, patients who had advance planning discussions with their physicians continued to discuss and talk about these concerns with their families.33 Such discussions enabled patients and families to reconcile their differences about end-of-life care and could help the family and physician come to agreement if they should need to make decisions for the patient.15,337. Opportunities Exist for Advance Planning DiscussionsAHRQ studies indicate that physicians can conduct advance care planning discussions with some patients during routine outpatient office visits.32 Hospitalization for a serious and progressive illness offers another opportunity.35 The Patient Self-Determination Act requires facilities such as hospitals that accept Medicare and Medicaid money to provide written information to all patients concerning their rights under State law to refuse or accept treatment and to complete advance directives.2,3,5-12Patients often send cues to their physicians that they are ready to discuss end-of-life care by talking about wanting to die or asking about hospice.35 Certain situations, such as approaching death or discussions about prognoses or treatment options that have poor outcomes, also lend themselves to advance care planning discussions.35 Predicting when patients are near death is difficult, but providers can ask themselves the question: are the patients “sick enough today that it would not be surprising to find that they had died within the next year (or few months, or 6 months)”?228. A Structured Process for Discussions Is HelpfulResearchers sponsored by AHRQ have suggested a five-part process that physicians can use to structure discussions on end-of-life care:

  • Initiate a guided discussion. During this discussion, the physicians should share their medical knowledge of hypothetical scenarios and treatments applicable to a patient’s particular situation and find out the patient’s preferences for providing or withholding treatments under certain situations. The hypothetical scenarios should cover a range of possible prognoses and any disability that could result from treatment. By presenting various hypothetical scenarios and probable treatments and noting when the patient’s preferences change from “treat” to “do not treat,” the physician can begin to identify the patient’s personal preferences and values.19The physician can also determine if the patient has an adequate understanding of the scenario, the treatment, and possible outcomes.19 One AHRQ-funded study indicated that elderly patients have enough knowledge about advance directives, CPR, and artificial nutrition/hydration on which to base decisions for treatment at the end of life, but they do not always understand their realistic chances for a positive outcome.36 Other research indicates that patients significantly overestimate their probability of survival after receiving CPR and have little or no understanding of mechanical ventilation.37 In one study, after patients were told their probability of survival, over half changed their treatment preference from wanting CPR to refusing CPR.38 Patients also may not know of the risks associated with the use of mechanical ventilation that a physician is aware of, such as neurological impairment or cardiac arrest.23
  • Introduce the subject of advance care planning and offer information. Patients should be encouraged to complete both an advance directive and durable power of attorney.19 The patient should understand that when no advance directive or durable power of attorney exists, patients essentially leave treatment decisions to their physicians and family members.13 Physicians can provide this information themselves; refer the patient to other educational sources, including brochures or videos; and recommend that the patient talk with clergy or a social worker to answer questions or address concerns.19
  • Prepare and complete advance care planning documents. Advance care planning documents should contain specific instructions. AHRQ studies indicate that the standard language contained in advance directives often is not specific enough to be effective in directing care.5 Many times, instructions do not state the cutoff point of the patient’s illness that should be used to discontinue treatment and allow the person to die.5,16 Terms such as “no advanced life support” are too vague to offer guidance on specific treatments.5 If a patient does not want to be on a ventilator, the physician should ask the patient if this is true under all circumstances or only specific circumstances.19 One AHRQ-funded study found that because patient preferences were not clear in advance directives, life-sustaining treatment was discontinued only when it was clearly medically futile.2
  • Review the patient’s preferences on a regular basis and update documentation. Patients should be reminded that advance directives can be revised at any time.19 Although AHRQ studies show that patients’ preferences were stable over time when considering hypothetical situations,39,40 other research indicates that patients often changed their minds when confronted with the actual situation or as their health status changed.1 Some patients who stated that they would rather die than endure a certain condition did not choose death once that condition occurred.1Other research shows that patients who had an advance directive maintained stable treatment preferences 86 percent of the time over a 2-year period, while patients who did not have an advance directive changed their preferences 59 percent of the time.41 Both patients with and patients without a living will were more likely to change their preferences and desire increased treatment once they became hospitalized, suffered an accident, became depressed, or lost functional ability or social activity.41 Another study linked changes in depression to changes in preferences for CPR.42 Increased depression was associated with patients’ changing their initial preference for CPR to refusal of CPR, while less depression was associated with patients’ changing their preference from refusal of CPR to acceptance of CPR.42 It is difficult for people to fully imagine what a prospective health state might be like. Once they experience that health state, they may find it more or less tolerable than they imagined.During reviews of advance directives, physicians should note which preferences stay the same and which change. Preferences that change indicate that the physician needs to investigate the basis for the change.19
  • Apply the patient’s desires to actual circumstances. Conflicts sometimes arise during discussions about end-of-life decisionmaking. AHRQ-sponsored research indicates that if patients desired nonbeneficial treatments or refused beneficial treatments, most physicians stated that they would negotiate with them, trying to educate and convince them to either forgo a nonbeneficial treatment or to accept a beneficial treatment. If the treatment was not harmful, expensive, or complicated, about one-third of physicians would allow the patient to receive a nonbeneficial treatment. Physicians stated that they would also enlist the family’s help or seek a second opinion from another physician.43Many patients do not lose their decisionmaking capacity at the end of life. Physicians and family members can continue discussing treatment preferences with these patients as their condition changes.14 However, physicians and families may encounter the difficulty of knowing when an advance directive should become applicable for patients who are extremely sick and have lost their decisionmaking capacity but are not necessarily dying.2 There is no easy answer to this dilemma. One AHRQ study found that advance directives were invoked only once patients had crossed a threshold to being “absolutely, hopelessly ill.”2 The patients’ physicians and surrogates determined that boundary on an individual basis.2 AHRQ studies have shown that patients’ treatment was generally consistent with their preferences if those preferences were clearly stated in an advance directive and the physician was aware that they had an advance directive.2,14Even if patients require a decision for a situation that was not anticipated and addressed in their advance directive, physicians and surrogates still can make an educated determination based on the knowledge they have about the patients’ values, goals, and thresholds for treatment.19 AHRQ research indicates that patients choose treatment based on the quality of the prospective health state, the invasiveness and length of treatment, and possible outcomes.

9. Patients Have Preference Patterns for Hypothetical Situations

AHRQ-funded studies indicate that patients are more likely to accept treatment for conditions they consider better than death and to refuse treatment for conditions they consider worse than death.39 Results from the study conducted on health states considered worse than death are shown in Figures 1 and 2. Patients also were more likely to accept treatments that were less invasive such as CPR than invasive treatments such as mechanical ventilation (Figure 3).17,39,44 Patients were more likely to accept short-term or simple treatments such as antibiotics than long-term invasive treatments such as permanent tube feeding (Figures 456, and Table 1).10. Patient Preference Patterns Can Predict Other ChoicesAcceptance or refusal of invasive and noninvasive treatments under certain circumstances can predict what other choices the patient would make under the same or different circumstances. According to AHRQ research, patients’ refusal of noninvasive treatments was predictive of their refusal of invasive treatments, and accepting invasive treatments predicted their acceptance of noninvasive treatments. Refusal of noninvasive treatments such as antibiotics strongly predicted that invasive treatments such as major surgery would also be refused. Decisions with the strongest predictive ability were refusing antibiotics or simple tests and accepting major surgery or dialysis (Table 2).45AHRQ research also reveals that patients were more likely to refuse treatment under hypothetical conditions as their prognosis became worse.7,32 For example, more adults would refuse both invasive and noninvasive treatments for a scenario of dementia with a terminal illness than for dementia only (Figure 7). Adults were also more likely to refuse treatment for a scenario of a persistent vegetative state than for a coma with a chance of recovery (Figure 8). More patients preferred treatment if there was even a slight chance for recovery from a coma or a stroke (Figure 9).32 Fewer patients would want complicated and invasive treatments if they had a terminal illness (Figure 10). Finally, patients were more likely to want treatment if they would remain cognitively intact rather than impaired (Figure 11).11. AHRQ Funds Studies To Improve End-of-life CareAHRQ continues to fund research to improve the quality of care at the end of life. Ongoing AHRQ research includes the following studies.

  • Impact of Ethics Consultation in the Intensive Care Unit; University of California, San Diego, Grant No. R01 HS10251. This project examines the benefits of ethics consultations between families and hospital staff and whether such consultations reduce resource use.
  • Nursing Home Care at the End of Life: Cost and Quality; Brown University, Grant No. R01 HS10549. This research project is testing preliminary findings indicating that hospice care in nursing homes positively influences pain management, acute hospitalization rates, and terminal care costs.
  • Improving Physician Skill at Providing End-of-Life Care; University of Washington, Grant No. R01 HS11425. This study will identify specific strengths and weaknesses in the end-of-life care provided by physicians. Researchers will then develop educational and systemic interventions to improve the quality of end-of-life care.
  • Medical Care at End of Life: Rural vs. Urban Minnesota; Duluth Clinic, Ltd., Grant No. R03 HS13022. This research project is investigating similarities and differences in end-of-life care among rural and urban nursing home residents with severe cognitive impairment.
  • Center for Patient Safety at the End of Life; Rand Corporation, Grant No. P20 HS11558. The Center’s focus is to improve the reliability of health care by effecting change and educating providers about safe and correct care of patients with chronic heart failure or chronic obstructive pulmonary disease.

12. Advance Planning Helps Physicians Provide Care that Patients Want

Most people will eventually die from chronic conditions. These patients require the same kind of advance care planning as those suffering from predictably terminal conditions such as cancer. Understanding preferences for medical treatment in patients suffering from chronic illness requires that physicians and other health care providers consider patients’ concerns about the severity of prospective health states, length and invasiveness of treatments, and prognosis. While predicting what patients might want is difficult, AHRQ research offers some insights into treatment patterns and preferences under hypothetical situations that can give providers more insight into their patients’ desires under similar circumstances.By discussing advance care planning during routine outpatient visits, during hospitalization for exacerbation of illness, or when the patient or physician believes death is near, physicians can improve patient satisfaction with care and provide care at the end of life that is in accordance with the patient’s wishes.

Source: http://archive.ahrq.gov/research/findings/factsheets/aging/endliferia/endria.html

POLST Form

What Is POLST?

Example POLST Form

Physician Orders for Life-Sustaining Treatment (POLST)

The POLST Paradigm was developed to improve the quality of patient care and reduce medical errors by creating a system that identifies patients’ wishes regarding medical treatment and communicates and respects them by creating portable medical orders.

Source: http://www.polst.org/about-the-national-polst-paradigm/what-is-polst/

Example POLST Forms

http://health.hawaii.gov/ems/files/2013/08/Hawaii_POLST_Form.pdf
http://www.adventisthealth.org/glendale/Documents/POLST%20Form.pdf

Using the POLST Form

  • POLST must be completed by health care professional based on patient preferences and medical indications.
  • POLST must be signed by a physician and the patient/decision maker to be valid. Verbal orders are acceptable with follow-up signature by physician in accordance with facility/community policy.
  • Certain medical conditions or medical treatments may prohibit a person from residing in a residential care facility for the elderly.
  • Use of original form is strongly encouraged. Photocopies and FAXes of signed POLST forms are legal and valid

 

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