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- Advance Directives
- Choices
- Sister Jane Connolly, Director, Spiritual Care
- Ricky Stachura, RN, Director, Case Management/Social Work
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- Planning in advance
- the kinds of treatment you would like
- if you are in a terminal condition
- and
- you are not able to speak for yourself.
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- Surrogate Decision Maker
- Living Will
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- Who will make medical decisions for me when
- I no longer can?
- Picking the right person…
- knows you well
- can make difficult decisions
- will advocate on your behalf to see that your
- wishes are followed
- will be available
- Those who are not eligible:
- the person who signed your document for you
- if you were unable to sign it
yourself
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- ² choices about
appropriate medical treatments
- interpret the instructions I’ve given in this
- document
- ² arrange for medical care
in hospitals, nursing homes, etc.
- make decisions about life-sustaining
- treatments
- ² see and release of my
medical records
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- ² move me to another
state for care
- authorize/refuse medications or procedures
- for pain management
- take legal action to assure my wishes are
- carried out
- ² make decisions about
organ donation
- apply for Medicare, Medicaid, etc. and have
- access to personal information needed to do that
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- What kinds of medical treatment do I want, or not
- want, if I have a terminal illness and am unable to
- speak for myself?
- Some basic things I want:
- I want to be free from pain, even if that means
- I may sleep more than usual;
- I do not want anything done or omitted with
- the intention of ending my
life.
- I want to be offered food and fluids by mouth
- I want to be kept clean and warm.
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- Life support treatment is any medical procedure,
- device or medication to keep me alive.
- breathing machine/ventilator
- feeding tube
- CPR
- major surgery
- blood transfusions
- kidney dialysis
- antibiotics
- anything else intended to keep me alive
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- CPR
- Intubation (insertion of tubes)
- Endotracheal
- Feeding
- Ventillator
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- C Circulation (pulse, heart
pumping)
- P Pulmonary (lungs, breathing)
- Cardiopulmonary Resuscitation is a technique
- of basic life support for the purpose of oxygenating the brain and
heart until definitive medical management can restore normal heart and
breathing action.
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- A responsiveness check is done
- The airway is cleared
- The rescue team then begins “mouth-to-
- mouth” - breathing into the
victim’s mouth.
- If no pulse is palpable, then external chest compressions are begun.
- Chest compressions are done by quickly, and with some force, depressing
the lower half of the patient’s sternum (breast bone) in an attempt to
restore circulation .
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- Endotracheal Intubation is the placement of a tube into the trachea (windpipe)
in order to maintain an open airway in patients who are unconscious or
unable to breathe on their own.
- The tube is inserted through the mouth into the trachea (the large
airway from the mouth to the lungs).
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- The tube that is used today is a flexible plastic tube, with a balloon
that is inflated to keep the tube in place in the patient’s throat.
- The doctor inserts the tube with the help of a laryngoscope, an
instrument that the doctor uses to see down the trachea.
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- The endotracheal tube serves as an open passage through the upper
airway.
- The purpose of endotracheal intubation is to permit air to pass freely
to and from the lungs in order to inflate the lungs. Endotracheal tubes can be connected to
ventilator machines to provide aeration and respiration (breathing).
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- A ventilator is a machine that breathes for the patient when the patient
is unable to breathe on their own or if assistance is needed to maintain
oxygen levels required to sustain life.
- The breathing machine is connected to an endotracheal tube and forces
air from the machine into the lungs and essentially breathes for the
patient.
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- A patient may be dependent on a ventilator temporarily or permanently.
- A temporary vent would be connected to the endotracheal tube.
- When the patient’s condition improves, he/she
- would be weaned from the
ventilator when they
- were able to breathe on their
own. If the patient cannot be weaned from the ventilator, a permanent
tube called a tracheostomy tube would be inserted directly into the
patient’s trachea and connected to a portable ventilator.
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- A tracheotomy is a surgically created opening in the neck which allows
direct access to the trachea (breathing tube).
- It is maintained open with a hollow tube called a tracheotomy tube.
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- A tracheotomy may be temporary or permanent
- if the person’s respiratory
system is paralyzed or
- if the patient will never be
able to breathe on their own again.
The tracheostomy becomes permanent and the patient is connected
to a portable ventilator.
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- Feeding tubes are inserted to facilitate meeting the patient’s
nutritional need when that patient is no
- longer able to take oral food or fluids.
- Feeding tubes may be inserted through the nasal passageway for
short-term use (nasogastric tube), through the nose into the stomach,
and intermittently liquid nutrition is inserted through the tube into
the stomach.
- A nosogastric tube is always temporary.
If the
- patient requires long-term nutritional support, then
- a permanent tube called a PEG tube would be surgically inserted.
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- For those patients who
require longer use
- of the tube, it is
customary to place the
- tube directly into the stomach through the
- abdominal wall. This method is called a PEG or percutaneous
endoscopic gastrostomy tube.
Feeding tubes are not painful and are not easily visible. The
tube extends from the interior of the stomach to the outside of the
body through a small incision in the abdomen.
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- The PEG tube feedings may be administered by a pump or a drip mechanism
to allow for controlled feedings.
Too-rapid feedings may cause the patient discomfort.
- A bag containing the liquid nutrition is connected to the tube and
allowed to infuse nutrients and water directly into the stomach.
- Problems and complications, such as infection, could develop if the
feedings are not administered properly or the tube site is not cared for
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- Three scenarios in which my Advance Directives would guide my medical
treatment:
- ² Two physicians decide I
am likely to
- die in a short period of
time (terminal
- condition) and life
support would only
- delay the moment of my
death.
- ² I am in a coma and not
expected to
- wake up.
- ² I have permanent and
severe brain
- damage and I am not
expected to
- recover.
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- The Five Wishes Document suggests
- three options:
- I want life support.
- I do not want life support; if
life
- support has already been started,
- please stop.
- Try it; if my doctor thinks it
might
- help, continue; if it does not help my
- condition or my symptoms, stop.
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- How comfortable do I wish to
be?
- Pain management
- Handling symptoms that can occur (nausea, depression, etc.)
- Mouth care and other personal care
- Cleanliness and comfort
- Other things that can add to my comfort
- (music and reading poetry is comforting to some, not others and prayer
is helpful to some people, but not others)
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- How do I want people to treat me?
- Do I want someone with me when it seems
- that the time of my death is near?
- Who do I want? My Family? Members of my
- church or synagogue? Someone
else?
- What do I want them to do?
Pray? Talk to me,
- even if I don’t respond? Play
music for me?
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- What do I want my loved ones to know?
- Thank my family, my friends and those who have been good to me.
- Ask and offer forgiveness.
- Encourage family members to reconcile their differences.
- Frame death, not so much as a time of fear,
- but as a time of growth for everyone concerned.
- Express any wishes for place of burial, funeral or memorial service,
organ donation, etc.
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- For your Advance
Directive to be a legal document
- it must be signed in the
presence of two witnesses.
- According to Pennsylvania law, neither witness can be
- the person who signs the document for you, in the event
- you are unable to sign it yourself.
- Although Pennsylvania law does not require an
- Advance Directive to be dated,
it is wise to do so.
- Pennsylvania law does not require that an Advance
- Directive be notarized.
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- Keep the original in your home, available to others who may need it;
- Give copies to significant people, including your agent, your family and
your physician;
- Discuss it with them so they do not have any surprises if the need
arises for it to be used;
- Present a copy any time you are admitted to a hospital or other
healthcare facility;
- Note to whom you have given the document.
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