Tag: consent

  • Informed Consent

    Medical Care

    Image of person filling out forms.

    Informed consent means that you agree to treatment only after it has been explained to you and that you understand it. You should know the nature of the treatment, its benefits and risks, and the likelihood of its success. You should also be told if your treatment is an experimental one.

    The doctor should review any alternatives to surgery or other procedures. There are no guaranteed outcomes in medicine, but informed consent enables YOU to make a rational and educated decision about your treatment.

    With Informed Consent

    *  You cannot demand services that go beyond what are considered “acceptable” practices of medicine or that violate professional ethics.

    *  You must recognize that you may be faced with some uncertainties or unpleasantness.

    *  You should, if competent, be responsible for your choices. Don’t have others make decisions for you.

    Page from the Healthier at Home book by the American Institute for Preventive Medicine. www.HealthyLife.com. All rights reserved.

    © American Institute for Preventive Medicine

  • Making Medical Decisions

    Medical Care

    Describe the Problem

    Be Able to Answer These Questions About Your Current Problem and Complaints

    *  What do you think the problem is?

    *  Are you in pain? If yes:

    – What does the pain feel like? Is it a sharp, dull, and/or throbbing pain?

    – Where is the pain?

    *  When did the problem(s) start? Has it changed since then?

    *  What makes it go away?

    *  Have you felt like this before? Is so, when? What made it go away then?

    *  Have you had any other symptoms or signs lately? Examples are:

    – Fever.

    – Blood in the urine.

    – Shortness of breath.

    – Anxiety.

    – Insomnia.

    Be Able to Give This Information About Your Health

    *  Your medical history and your family’s medical history.

    *  Allergies you have.

    *  Medications you take.

    *  Your daily habits.

    *  Your work.

    *  Pressures you are under.

    Ask for a Diagnosis

    Your Doctor or Health Care Provider Makes a Diagnosis From

    *  Symptoms (things you feel, such as pain).

    *  Signs (things that can be seen or measured, such as swelling).

    *  Exams and tests.

    When Your Doctor or Health Care Provider Gives You A Diagnosis

    *  Ask him or her to explain the diagnosis in detail.

    *  Ask questions if you don’t understand. If you need to, bring a trusted family member or friend with you to help ask questions.

    *  Find out if your condition is chronic or acute. A chronic one lasts a long time. An acute one comes on suddenly and doesn’t last long. If your condition is chronic, find out how it will affect your life.

    *  Ask if the diagnosis increases your risk for any other problems. If so, find out what they are and what you can do to prevent them.

    Other Things to Ask

    *  Is my condition contagious? If so, how do I not spread it?

    *  Is my condition genetic? If so, what does this mean for others in my family?

    *  How certain are you about this diagnosis? Are there are other symptoms to look for that would help confirm or disprove the diagnosis?

    *  What books, pamphlets, and computer Web sites can I use to find out more about my condition? What organizations can I contact? Is there a support group in my area for this condition?

    Find Out About Treatment

    Ask your doctor or health care provider to state clearly and simply what the proposed treatment is. If medication is prescribed, ask these questions:

    *  What is the name of the medicine? Write down the name and dose.

    *  What will the medicine do?

    *  Is there a less expensive, generic form?

    *  When, how often, and for how long, should I take the medicine?

    *  Do I take this medicine until I feel better or until it is used up?

    *  When will the medicine start to work?

    *  Could there be side effects? What should I do if they occur? What side effects should I let you know about?

    *  Is this medicine okay to use with other medications I take?

    *  Is there anything else I should or should not do while taking the medicine?

    – Should I take this medicine with or without food?

    – Is there anything I should not eat or drink when I take this medicine? Can I take this medicine with grapefruit juice?

    – Can I have alcohol?

    – Do I need to stay out of the sun?

    *  What should I do if I miss a dose?

    If Surgery is Prescribed

    *  Find out about the alternatives to surgery.

    *  Consider getting a second opinion. Your health insurance may require this.

    *  Find out if your health insurance plan will pay for the surgery.

    *  Ask what types of surgery there are for your condition.

    *  Ask for a step-by-step account of the procedure. Find out what you need to do before surgery. Find out what is done during and after surgery. This includes anesthesia and recovery.

    Questions to Ask if A Test is Prescribed

    *  What is the test called? How will it help tell what is wrong?

    *  Will it give specific or general information?

    *  If the answer is general, where do we go from here?

    *  How accurate and reliable is the test?

    *  Is the test invasive or noninvasive? Invasive means something, such as a catheter, chemical dye, etc., is inserted into the body. Nothing is inserted into the body with an noninvasive test. Examples are blood pressure readings and simple chest x-rays.

    *  What will I have to do to prepare for the test?

    *  Where do I go for the test?

    *  How and when will I get the test’s results?

    *  Will more tests be needed?

    Ask About Benefits

    Medical treatments change over time as researchers learn more and technology improves. Make certain that you and your health care provider have access to the latest and best information.

    *  Find out how the proposed treatment will improve your condition.

    – Will it cure the problem?

    – Will it help with symptoms?

    – Can it lead to other problems?

    *  Discuss with your health care provider what you expect the proposed treatment will do. Make sure you are being realistic about what you expect.

    *  Find out what will happen if you don’t have the treatment.

    A good rule of thumb is to make sure one strong reason can stand alone to justify going ahead with the treatment. In many cases, two or more not-so-strong reasons may not be enough. Discuss your concerns with your health care provider and loved ones.

    Ask About Risks

    If surgery is prescribed, ask about the risks for these things, during and after surgery:

    *  Pain.

    *  Anesthesia.

    *  Infection.

    *  Accidental injury.

    *  Heavy bleeding (hemorrhage).

    *  Another unplanned operation.

    *  Death.

    *  Weigh the risks versus the benefits before you decide to proceed with treatment. Discuss your concerns with your health care provider and others close to you.

    *  With your health care provider, chart the risks and benefits. On a sheet of paper, draw a line down the center. List the risks on one side. List the benefits on the other. Weigh each item on a scale from 1 to 5 (1 = not so important; 5 = very important). Add up the columns to see which one has a higher score.

    *  Ask about risks before you get any test or X-ray, no matter how minor it may be. If you are not asked about allergies, state them ahead of time. If you are female, tell your health care provider if you are or may be pregnant. If so, you should not get X-rays unless they are absolutely necessary.

    Find Out Costs

    *  What is the cost of the proposed treatment?

    *  Does this include the cost for follow-up? If so, how much is covered?

    *  Check with your insurance plan to see what it will pay and how much you will have to pay.

    *  Ask what you need to do to get maximum benefits. An example is pre-authorization for surgery. Find out if your health care provider and hospital accept your insurance.

    *  What related costs do I need to consider? Look into costs of medication, costs for time off work and child care and transportation costs.

    Find Out Success Rates

    The success rate is how often a treatment works compared to how many times it is done. For example, if a certain surgery has been done 100 times and was successful 80 times, it has a success rate of 80%.

    If surgery is prescribed, ask your health care provider and the medical facility where you will have the surgery these questions:

    *  What is the national success rate?

    *  What is the success rate at the hospital/medical facility where my treatment is planned?

    *  What is the surgeon’s success rate and experience with the surgery?

    *  How many procedures are the above success rates based on?

    *  Are there any personal factors that will affect my odds either way?

    *  How long will the results of my surgery/treatment last?

    According to several studies, you are less likely to die or suffer complications from surgery or other procedures if you go to an accredited hospital that performs a large number of that procedure each year. Some experts advise at least 200 surgeries. If you are given a success rate percentage, find out how many procedures the percentage is based on. A success rate of 80% doesn’t mean much if it is based on only 5 surgeries. For more information on hospital surgical success rates, read the book Best Medicine by Bob Arnot, M.D.

    Ask About Other Options

    Discuss other options that can diagnose and/or treat your condition. There is usually more than one option. Sometimes, the best choice at the time may be no choice. This is called “wait and see.” If this doesn’t work for you, make a list of other options. Ask your doctor or health care provider these questions:

    *  What might happen if I decide to do nothing?

    *  What are my other options?

    – Ask about options that don’t need surgery, such as lifestyle changes (diet, exercise, stopping smoking, etc.).

    – If surgery is proposed, ask about outpatient surgery, laser treatment, laporascopic surgery, and the newest ways to treat your condition.

    *  If you are not satisfied with your options, discuss this with your provider. If you are still not satisfied, consider consulting another health care provider.

    *  Look into every option in depth.

    Ask When Treatment Should Begin

    When you decide to go ahead with a treatment plan, ask these questions:

    *  When is the best time to get started with the plan?

    *  Do I have to undergo treatment right away? If not, how long can I safely wait? Don’t assume that it has to be done as soon as possible. You may be able to delay the treatment until a time that best fits your schedule.

    *  Decide the best time for you to begin the treatment.

    Make a Decision

    After you get the answers from steps 1 to 9, decide what to do.

    *  You can also decide to refuse treatment, but you should ask your health care provider what can happen if you do this.

    *  If you feel rushed or uncomfortable when you discuss your decision with your doctor or health care provider, tell him or her how you feel.

    *  Read about “Informed Consent” and “Advanced Directives” on the last 2 panels. If you have not already done so, consider writing a living will or signing a durable power of attorney for health care.

    Informed Consent

    Informed consent is a legal issue in medicine. It means that you agree to treatment only after it has been explained to you and that you understand it. You should know:

    *  The nature of the treatment.

    *  Its benefits and risks.

    *  The likelihood of the treatment’s success.

    *  If your treatment is experimental in nature.

    The physician should review any options you can get instead of surgery or other procedures. There are no guaranteed outcomes in medicine, but informed consent enables YOU to make a rational and educated decision about your treatment. It also promotes greater understanding and joint decision making between you and your health care provider. With informed consent:

    *  You cannot demand services that go beyond what are considered “acceptable” practices of medicine or that violate professional ethics.

    *  You must recognize that you may be faced with some uncertainties or unpleasantness.

    *  You should, if competent, be responsible for your choices. Don’t have others make decisions for you.

    *  You should also know about “Advance Directives.”

    Advance Directives

    Advance directives are a legal way for you to state your wishes to choose or refuse medical treatment. There are two types of advance directives:

    *  Durable Power of Attorney for Health Care – This document names a person(s) who would make treatment decisions for you if you are not able to make them yourself. This person would state your wishes. Your condition does not have to be terminal or irreversible to have someone speak on your behalf.

    *  Living Will – This written document states what medical treatment you would want or not want. A living will applies only when you can’t express your wishes on your own and you suffer from a terminal illness or condition and aren’t expected to survive.

    In writing, you may choose or refuse:

    *  Measures to Support Life, such as a respirator (a machine to breathe for you).

    *  Measures to Sustain Life, such as tube feedings and kidney dialysis (a machine that does the work of your kidneys).

    *  Measures to Enhance Life. These keep you comfortable, but don’t prolong life. Examples are pain medications and hospice care.

    Each state has its own laws on advance directives. Get forms for them from your lawyer, local hospital or library, or from your state’s Web site. You can also get forms and information from these Web sites:www.putitinwriting.organdwww.uslivingwillregistry.com.

    After you complete advance directives, discuss them with your family and close friends. Give your doctor a copy, too.

    Cover image to the Making Medical Decision brochure by the American Institute for Preventive Medicine. www.HealthyLife.com. All rights reserved.

    © American Institute for Preventive Medicine

  • Patient Rights

    Medical Care

    Image of male patient.

    There are a variety of patient’s rights and providers of them. One, called “The Patient Care Partnership” is from the American Hospital Association (AHA). It gives guidelines for both patients and staff to let you know your rights in a hospital. These include:

    *  High-quality hospital care.

    *  A clean and safe environment.

    *  Involvement in your care.

    *  Protection of your privacy.

    *  Preparing you and your family for when you leave the hospital.

    *  Help with your bill and with filing insurance claims.

    Get a copy of this fromwww.aha.org/advocacy-issues/communicatingpts/pt-care-partnership.shtml.

    Certain hospitals, hospice care providers, U.S. states, and health insurance plans have their own patient’s bill of rights. A Federal Patient’s Bill of Rights to protect the right of patients using health insurance was created at the same time as the Affordable Care Act. Its measures include:

    *  Certain preventive screenings at no cost to patients.

    *  The right to get health insurance in spite of pre-existing medical conditions.

    *  Removal of annual and lifetime dollar limits for essential health care benefits.

    *  The right to an easy-to-understand summary of benefits and coverage.

    Find out more about these rights atwww.healthcare.gov/how-does-the-health-care-law-protect-me.

    Page from the Healthier at Home book by the American Institute for Preventive Medicine. www.HealthyLife.com. All rights reserved.

    © American Institute for Preventive Medicine

  • Making Your Health Care Wishes Known

    WELL-BEING

    Image of doctor talking to patient.

    It’s a tough topic to think about, but also a necessary one. What are your wishes for your own health care if you were unable to communicate?

    Most people don’t think about this kind of scenario, especially if they are healthy. But if you are in a serious accident or become severely ill, you may not be able to tell your family what you want. This is when an “advance directive” can be very useful for you and your family.

    Advance directives: what are they?

    An advance directive is a document that states your desires about your care when you cannot speak for yourself. If you are admitted to the hospital, the doctor may ask if you have an advance directive. It may describe:

    *  Care you want if you have an illness that won’t get better.

    *  What you want if you are permanently in a coma or unconscious.

    *  Treatment that you don’t want to receive.

    *  Treatment you do want, regardless of how sick you are.

    Advance directives can have different parts that help in different ways. You may have one or more of these:

    *A living will.This is a written, legal document. It covers what treatment you want if you were terminally ill or would not wake up from a coma. It can list specific things you would like done depending on how sick you are.

    *Durable power of attorney (DPA).It names a person to make health care decisions for you. A DPA becomes active any time you cannot make medical decisions for yourself. Sometimes it is called a Medical Power of Attorney or health care proxy. Only use a DPA if you have someone you trust to make these decisions. Talk to your DPA about their role and your health care wishes.

    *Do not resuscitate order (DNR).If a person’s heart stops or they stop breathing, hospital staff will give CPR, or cardiopulmonary resuscitation. If you have a DNR, you are telling hospital staff that you do not want CPR given to you. You do not have to have a living will or DPA to have a DNR.

    Some states do not consider living wills or DPAs to be official legal documents. Even if it’s not legal, an advance directive or DPA can be very helpful. It can help your family and/or doctor make decisions you want so you get the care you desire. Your doctor or an attorney can tell you about your state’s laws. All states recognize and honor DNR orders that are in a patient’s medical record. An attorney does not have to do a DPA or living will. Many people fill them out themselves.

    What do I put in an advance directive?

    If you’re thinking about getting an advance directive, you may be wondering what it should say. Your doctor or an attorney can help you, and you may want to think about it for a while.

    Health care items that are often listed in a living will include:

    *  Ventilation (artificial breathing machines)

    *  Dialysis (machines that work for kidneys that are failing)

    *  Tube feeding (used when a person  cannot eat or drink)

    *  Palliative care (care that keeps you comfortable, such as pain relief measures)

    *  Organ donation or donating organs to be used for research

    Why do I need an advance directive?

    Most medical experts agree that an advance directive is helpful. It makes your preferences about medical care known before you become sick or injured. It means your loved ones will not have to make hard decisions about your care while you are sick.

    An advance directive can give you peace of mind. If you feel strongly about receiving certain treatments, an advance directive helps ensure that your wishes will be honored. It gives you more control over your own health care.

    Where do I start?

    An advance directive doesn’t have to be hard. It can be short and simple. You can:

    *  Get a form from your doctor.

    *  Write down your own wishes yourself.

    *  Discuss your wishes with your DPA.

    *  Meet with an attorney to write an advance directive.

    *  Get a form from your local health department or Area Agency on Aging in your area.

    It’s a good idea to have your doctor or an attorney look at your advance directive. This ensures your wishes are in line with state laws. It also gives you a chance to answer questions and make sure your wishes are understood. When you are done, have your advance directive notarized. Give copies to your family and your doctor.

    You can change or cancel your advance directive. This can be done when you are of “sound mind,” which means you are able to think and communicate clearly. Any changes you make must be signed and notarized according to the laws in your state. Make sure that your doctor and family members know about the changes.

    Sources: Medicare.gov, American Academy of Family Physicians

    © American Institute for Preventive Medicine